Glutamatergics

• (±)-1-(1,2-Diphenylethyl)piperidine maleate
  NMDA receptor ion channel blocker.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203732	36794-52-2	C19H23N ·C4H4O4	10 mg/50 mg

• 1-Aminocyclobutane-cis-1,3-dicarboxylic acid
  A very potent, competitive and selective inhibitor of glutamate uptake.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200438	117488-23-0	C6H9NO4	5 mg/25 mg

• 1-Aminocyclobutane-trans-1,3-dicarboxylic acid
  A very potent, competitive and selective inhibitor of glutamate uptake.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361072	73550-55-7	C6H9NO4	10 mg/50 mg

• 1-Aminocyclopentanecarboxylic acid
  NMDA receptor antagonist acting at the glycine site.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202392	52-52-8	C6H11NO2	10 mg

• 1-Aminocyclopropane-1-carboxylic Acid
  An agonist at the glycine modulatory site of the NMDA receptor. Mimics the effects of glycine on the NMDA_R and competitively inhibits glycine-NMDA_R binding.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202393	22059-21-8	C4H7NO2	500 mg

• 1-BCP
  Centrally active selective potentiator of AMPA-mediated responses. Facilitates memory retention in rats.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203454	34023-62-6	C13H15NO3	10 mg/50 mg

• 1-Benzyl-APDC hydrochloride
  A selective ligand of mGlu6 receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-220463	n.n.	C13H16N2O4•HCl	1 mg/5 mg

• (1R,3R)-homo-ACPD

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-206296	n.n.	C8H13NO4	5 mg

• (1R,3S)-homo-ACPD
  Inactive isomer of trans-1,3-homo-ACPD.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-206299	n.n.	C8H13NO4	5 mg

• (1S,3R)-ACPD
  A rigid analog of glutamate. Excites metabotropic receptors with α-kainic acid-like action.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202009	111900-32-4	C7H11NO4	5 mg/25 mg

• (1S,3R)-homo-ACPD
  Active isomer of trans-1,2-homo-ACPD. Highly selective agonist for group II mGluRs and has no effect at ionotropic excitatory amino acid receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205919	n.n.	C8H13NO4	5 mg

• (1S,3S)-homo-ACPD
  Isomer of cis-1,3-homo-ACPD. Partial agonist for group II mGluRs. Displays no effect at ionotropic excitatory amino acid receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-206307	n.n.	C8H13NO4	5 mg

• (-/+)-2-amino-7-phosphonoheptanoic acid
  This product is a NMDA antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-287806	85797-13-3	C7H16NO5P	2 mg/5 mg

• 2,4-Dihydroxyphenylacetyl-L-asparagine
  Component of various spider toxins and purported specific blocker of glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203468	111872-98-1	C12H14N2O6	10 mg/50 mg

• (2R,3S)-Chlorpheg
  A weakly active NMDA receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203775	n.n.	C11H12ClNO4	10 mg

• (2R,4R)-(+)-Azetidine-2,4-dicarboxylic acid
  A selective pharmacological agent of the metabotropic glutamate (mGlu) receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205922	161596-63-0	C5H7NO4	1 mg

• (2R,4R)-APDC
  A highly selective agonist for group II metabotropic glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202408	169209-63-6	C6H10N2O4	1 mg/5 mg

• (2S,3S,4S)-2-Methyl-2-(carboxycyclopropyl)glycine
  Selective group II mGluR antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202014	157141-16-7	C7H11NO4	1 mg/5 mg

• (2S,4R)-4-Methylglutamic Acid
  A highly selective and potent agonist for kainate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-216338	31137-74-3	C6H11NO4	5 mg

• (2S,4S)-(-)-Azetidine-2,4-dicarboxylic acid

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-220844	161596-62-9	C5H7NO4	1 mg

• (2S)-2-Hydroxyglutaric Acid
  Potential inhibitor of glutamate carboxypeptidase.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-311696	13095-48-2	C5H8O5	25 mg

• (2S)-α-Ethylglutamic acid
  Group II mGluR antagonist

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-220848	n.n.	C7H13NO4	1 mg

• (+)-3-(2-Carboxypiperazin-4-yl)-propyl-1-phosphoric Acid
  Displays NMDA antagonistic activity.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-288641	100828-16-8	C8H17N2O5P	10 mg

• 3-MATIDA
  Potent metabotropic glutamate mGlu1 receptor antagonist (IC50 = 6.3 μM at rat mGlu1a).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203470	518357-51-2	C8H9NO4S•xH20	10 mg/50 mg

• 5,7-Dichlorokynurenic acid
  A potent antagonist at the NMDA receptor glycine modulatory site. Noncompetitively antagonizes NMDA-stimulated responses.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200440	131123-76-7	C10H5Cl2NO3	10 mg/50 mg

• 5,7-Dichlorokynurenic acid sodium salt
  A sodium salt of 5,7-Dichlorokynurenic acid (sc-200440). Acts as a potent antagonist at the glycine site of the NMDA receptor (Ki = 79 nM vs. [3H]-glycine).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-291018	131123-76-7 (non-salt)	C10H4Cl2NNaO3	10 mg/50 mg

• 6,7-Dinitroquinoxaline-2,3-dione (DNQX)
  A non-NMDA receptor complex antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200444	2379-57-9	C8H4N4O6	10 mg/50 mg

• 7-Chlorokynurenic acid
  NMDA receptor antagonist acting at the glycine site.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358717	18000-24-3	C10H6CINO3	10 mg/50 mg

• 7-Chlorokynurenic acid sodium salt
  Sodium salt of 7-Chlorokynurenic acid (sc-202893), an NMDA receptor antagonist acting at the glycine site. Acts as a potent competitive inhibitor of L-glutamate transport into synaptic vesicles.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-291578	n.n.	C10H5CINNaO3	10 mg/50 mg

• 7-Chlorothiokynurenic acid hydrochloride
  NMDA receptor antagonist acting at the glycine site. More potent than the corresponding kynurenic acid analog.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202430	135025-56-8	C10H6ClNO2S ·HCl	5 mg

• A 841720
  Potent, non-competitive mGlu1 receptor antagonist that displays 34-fold selectivity over mGlu5 (IC₅₀ values are 10 and 342 nM respectively). Displays no significant activity at a range of other GPCRs, ion channels and transporters. Exhibits analgesic effects; decreases mechanical allodynia in models of neuropathic pain;impairs cognitive function

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203792	869802-58-4	C17H21N5OS	10 mg/50 mg

• ACBC
  NMDA receptor antagonist acting at the glycine site.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203493	22264-50-2	C5H9NO2	25 mg

• ACDPP hydrochloride
  Antagonist at the mGlu5 receptor (K_i = 295 nM). Inhibits human mGlu5 receptor-mediated calcium flux with an IC₅₀ of 134 nM.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203494	37804-11-8	C12H13ClN6O•HCl•xH20	10 mg/50 mg

• ACET
  Potent and selective GluR5-containing kainate receptor antagonist (IC₅₀ = 7 nM) that displays selectivity over GluR6-containing kainate, NMDA, AMPA and group I mGlu receptors. Reversibly blocks induction of NMDA recptor-independent long term potentiation (LTP) in vitro at nanomolar concentrations.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203801	n.n.	C20H19N3O6S	10 mg

• AIDA
  A selective antagonist of the mGluR1. Competitively antagonizes the stimulatory response of glutamate at mGluR1a.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202047	168560-79-0	C11H11NO4	5 mg

• (+/-)-alpha-Amino-3-hydroxy-5-methylisoxazole- 4-propionic Acid Hydrobromide
  Shows highly potent agonist activity towards central glutamate/quisqualate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-291862	118896-96-1	C7H10N2O4 ·HBr	1 mg/5 mg

• α-Benzylquisqualic acid
  Selective antagonist of group II mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-221178	n.n.	C12H13N3O5	1 mg/5 mg

• α-Ketoglutaric acid sodium salt

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-214449	22202-68-2	C5H5NaO5	1 g/5 g

• AMN082 Dihydrochloride
  Potent and selective agonist at mGluR7 acting at an allosteric site.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200483	83027-13-8	C28H28N2 ·2HCl	10 mg/50 mg

• AMPA
  A potent agonist of the AMPA receptor, a glutamate-recognizing ionotropic receptor. Agonism of the AMPA receptor produces neuronal excitation.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200437	74341-63-2	C7H10N2O4	5 mg/50 mg

• Aniracetam
  Nootropic with modulatory actions through allosteric potentiation of reduction of glutamate receptor desensitization, AMPA specific receptors, and potentiation of metabotropic glutamate receptor activity. Anxiolytic following systemic administration.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203514	72432-10-1	C12H13NO3	50 mg/250 mg

• Arcaine sulfate
  Arcaine is a novel and potent antagonist of the polyamine site on the NMDA receptor. it can inhibit [3H]MK801 binding in the absence of added polyamines.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200475	14923-17-2	C6H16N6 ·H2SO4	20 mg/50 mg

• BINA

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361121	866823-73-6	C30H30O4	10 mg/50 mg

• Boc-L-Glutamic acid 5-fluorenyl methyl ester

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-285175	123417-18-5	C24H27NO6	1 g/5 g

• CBiPES hydrochloride
  Positive allosteric modulator of the mGlu2 receptor

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358830	856702-40-4	C21H19N3O2S•HCl	10 mg/50 mg

• CCMQ
  Acts selectively when inhibiting homoquinolinic acid binding to non-NMDA sensitive sites. Works in combination with [3H]-homoquinolinic acid to characterize NR2B-containing NMDA receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205625	n.n.	C12H9NO4	10 mg/50 mg

• CFM-2
  A novel, selective, non-competitive AMPA antagonist1.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203429	178616-26-7	C17H17N3O3	10 mg

• CGP 37849
  Potent, competitive and selective NMDA antagonist. Orally active anticonvulsive.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203880	127910-31-0	C6H12NO5P	10 mg/50 mg

• CGP 39551

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361139	127910-32-1	C8H16NO5P	10 mg/50 mg

• CGP 78608 hydrochloride

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361144	206648-13-7	C11H13BrN3O5P.HCl	10 mg/50 mg

• CGS 19755
  Potent, competitive NMDA antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203882	110347-85-8	C7H14NO5P	10 mg/50 mg

• Chicago Sky Blue 6B

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361146	2610-05-1	C34H24N6Na4O16S4	25 g

• CHPG
  A selective metabotropic glutamate receptor agonist, mGlu5. Inactive at mGlu1a receptors which are expressed in CHO cells. Active in vivo.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205931	170846-74-9	C8H8NO3Cl	10 mg/50 mg

• CHPG Sodium salt

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361148	n.n.	C8H7ClNO3 ·Na	10 mg/50 mg

• cis-(+/-)-3,4-Dichloro-N-Methyl-N-(2-[1-Pyrrolidinyl]Cyclo- Hexyl)Benzeneacetamide Hydrochloride
  Shown to be a potent antagonist of NMDA and displays anticonvulsant effects.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-294036	92953-41-8	C18H24Cl2N2O	1 mg/5 mg

• cis-1,3-homo-ACPD
  An equimolar mixture of (1R,3R)-homo-ACPD and (1S,3S)-homo-ACPD. This compound is a selective agonist for group II mGluRs and has no effect at ionotropic excitatory amino acid receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205932	n.n.	C8H13NO4	5 mg

• cis-ACPD
  Potent NMDA agonist. Equimolar mixture of (1R,3R)-ACPD

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202102	39026-63-6	C7H11NO4	5 mg

• Cl-HIBO
  Highly desensitising AMPA receptor agonist. Subtype selective for GluR1 and GluR2 subunit-containing receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205934	n.n.	C6H7ClN2O4	10 mg/50 mg

• CNQX disodium salt
  Water soluble, potent competitive kainate/quisqualate (non-NMDA) receptor antagonist. More soluble form of CNQX

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203003	115066-14-3 (non-salt)	C9H2N4O4Na2	5 mg/10 mg

• Co 101244 hydrochloride
  Highly selective N-methyl-D-aspartate (NMDA) NR2B subtype antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203899	193359-26-1	C21H27NO3 ·HCl	10 mg/50 mg

• CP 465022 hydrochloride
  AMPA antagonist which is selective, non-competitive and displays anti-convulsant activity.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205272	199655-36-2	C26H24ClFN4O ·HCl	10 mg/50 mg

• CPCCOEt
  The compound CPCCOEt is a reversible and non-competitive antagonist of type 1α metabotropic glutamate receptor activation.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200481	179067-99-3	C13H13NO4	5 mg/25 mg

• CX546
  AMPA receptor potentiator which is specifically bound to agonist bound non-desensitized receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205278	215923-54-9	C14H17NO3	10 mg/50 mg

• D-AP3

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-211171	128241-72-5	C3H8NO5P	5 mg

• D-AP7
  More active form of DL-AP7

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203016	81338-23-0	C7H16NO5P	5 mg

• D-Aspartic acid
  Endogenous NMDA receptor agonist with similar activity to the L-isomer. Also a non-metabolizable substrate for EAA uptake systems. Modulates melatonin synthesis in the pineal gland.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202562	1783-96-6	C4H7NO4	1 g

• D-CPP-ene
  Potent, competitive N-methyl-D-aspartic acid (NMDA) antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203910	117414-74-1	C8H15N2O5P	10 mg

• D-Cycloserine
  Reported to improve memory-dependent tasks in rats. Partial agonist of NMDA receptors at the glycine modulatory site.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-221470	68-41-7	C3H6N2O2	200 mg/1 g

• D-Quisqualic acid

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358857	52809-07-1 (L-isomer)	C5H7N3O5	10 mg

• D(-)-2-Amino-4-phosphonobutanoic acid (D-AP4)
  NMDA antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200429	78739-01-2	C4H8NO5P-2	5 mg

• D(-)-2-Amino-5-phosphonovaleric acid (D-AP5)
  A selective antagonist of the NMDA receptors. Antagonizes amino acid- and electrically-induced synaptic excitations. Protects neurons against oxidative damage, increasing levels of SOD, catalase, and GSH.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200434	79055-68-8	C5H12NO5P	5 mg

• DCB
  Allosteric ligand for the metabotropic glutamate receptor mGlu5; displays neutral modulation. Does not affect agonist-stimulated mGlu5 responses, but blocks regulation of the receptor by other allosteric modulators such as DFB and DMeOB.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203560	6971-97-7	C14H10Cl2N2	10 mg/50 mg

• Desmethyl-YM 298198

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361167	299901-57-8	C17H20N4OS.HCl	10 mg/50 mg

• Dextromethorphan Hydrobromide
  An NMDA receptor agonist that is the d-form of racemethorphan, where it is widely used as a cough suppressant. Newer uses include its anticonvulsive and neuro-protective properties. It was also found to improve cerebral ischemia.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204716	125-69-9	C18H25NO ·HBr	5 g/10 g

• DFB
  Selective allosteric potentiator of metabotropic glutamate receptor subtype 5 (mGlu5).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203918	15332-10-2	C14H10F2N2	10 mg/50 mg

• DL-2-Amino-3-phosphonopropionic acid (AP3)
  An inhibitor of phosphoserine phosphatase and antagonist of mGluR, blocking mGluR-mediated phosphoinositide turnover. D-AP3 produces phosphoserine phosphatase inhibition and L-AP3 both antagonizes mGluR and inhibits phosphoserine phosphatase with similar potency.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200433	20263-06-3	C3H8NO5P	50 mg

• DL-2-Amino-5-phosphonovaleric acid (AP5)
  Shown to be a potent and selective NMDA antagonist which causes antagonism of synaptic and amino-acid induced excitation in nerves.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-201503	76326-31-3	C5H12NO5P	10 mg/50 mg

• DL-2-Aminoadipic acid
  An excitatory amino acid analogue, which functions as a glutamine synthetase inhibitor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-255121	542-32-5	C6H11NO4	1 g/5 g

• DL-AP7
  A competitive antagonist of the ionotropic glutamate receptor, NMDA.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203028	78966-69-5	C7H16NO5P	5 mg

• DMEOB
  Negative allosteric modulator at mGlu5. Exhibits reversible non-competitive inhibition of mGlu5-mediated responses.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203569	40252-74-2	C16H16N2O2	10 mg/50 mg

• Domoic acid
  An analogue of the neurotransmitter glutamate and an effective excitatory neurotransmitter that activates kainate subtype glutamate receptors

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200446	14277-97-5	C15H21NO6	1 mg/5 mg

• E4CPG
  Group I/group II metabotropic glutamate receptor antagonist which is more potent than (RS)-MCPG.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205943	n.n.	C11H13NO4	10 mg/50 mg

• EGLU
  Selective antagonist of presynaptically-mediated (1S,3S)-ACPD-induced depression of motoneuron excitation in neonatal rat spinal cord. Assumed to be a group II mGlu receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205944	n.n.	C7H13NO4	10 mg/50 mg

• Eliprodil
  Non-competitive NR2B-selective NMDA antagonist. Noncardiac drug with neuroprotective properties.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203939	119431-25-3	C20H23ClFNO	10 mg/50 mg

• Felbamate
  Anticonvulsant, acting as an antagonist at the NMDA-associated glycine binding site.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203579	25451-15-4	C11H14N2O4	10 mg/50 mg

• Fenobam
  A selective non-competitive antagonist of the mGluR-5 receptor. Produces inverse agonist activity through an allosteric modulatory site. Demonstrates anxiolytic effects.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202608	57653-26-6	C11H11ClN4O2	5 mg/25 mg

• gamma-D-Glutamylaminomethylsulfonic acid
  This product is a selective antagonist of kainate/quisqualate.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-295005	90237-02-8	C6H12N2O6S	1 mg/5 mg

• γDGG
  Broad spectrum glutamate receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203728	6729-55-1	C7H12N2O5	50 mg

• Gavestinel

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361183	153436-22-7	C18H11Cl2N2O3Na	10 mg/50 mg

• GYKI 47261 dihydrochloride
  Non-competitive AMPA antagonist receptor (IC₅₀ = 2.5 μM). In vivo, displays broad spectrum anticonvulsive activity and neuroprotective effects.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203993	220445-20-5	C18H15ClN4 ·2HCl ·xH2O	10 mg/50 mg

• GYKI 52466 dihydrochloride
  Selective non-competitive allosteric AMPA receptor antagonist. Anticonvulsant; skeletal muscle relaxant. Exhibits anti-proliferative effects in transformed cells.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203591	102771-26-6	C17H15N3O2•2HCl•xH2O	10 mg/50 mg

• HexylHIBO
  Group I mGlu antagonist (receptor). In vitro, decreases sEPSCs in rat pyramidal neurons.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203597	334887-43-3	C12H20N2O4	10 mg/50 mg

• (±)-HIP-A
  Potent, non-competitive excitatory amino acid transporter (EAAT) blocker. Preferentially inhibits glutamate-induced [3H]D-aspartate release (IC₅₀ = 1.6 μM) rather than [3H]L-glutamate uptake (IC₅₀ = 18 μM). Moderately selective; displays no affinity for NMDA and metabotropic glutamate receptors, and low affinity for AMPA and kainate receptors (IC₅₀ values are 43 and 8 μM respectively).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203598	227619-64-9	C6H8N2O4	10 mg

• HIP-B
  Potent, non-competitive excitatory amino acid transporter (EAAT) blocker. Preferentially inhibits glutamate-induced [3H]D-aspartate release (IC5₅₀= 1.2 μM) rather than [3H]L-glutamate uptake (IC₅₀ = 16.9 μM). Moderately selective; displays no affinity for NMDA and metabotropic glutamate receptors, and low affinity for AMPA and kainate receptors (IC₅₀ values are 35 and 45 μM respectively).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203599	227619-65-0	C6H8N2O4	10 mg

• HomoAMPA
  Higher homologue of AMPA. Compound is completely inactive at ionotropic glutamate receptors but instead is a relatively potent and highly mGlu6 subtype selective metabotropic glutamate receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204001	n.n.	C8H12N2O4	10 mg/50 mg

• Homoquinolinic acid
  An analog of glutamic acid shown to excite rat cortical neurons and also be a neurotoxic agent. Found to specifically target the NR2A/B subunit of NMDA.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200456	490-75-5	C8H7NO4	5 mg/25 mg

• Ibotenic acid
  A conformationally restricted analogue of glutamic acid which is a useful tool in morphological and functional analysis of central neuronal systems in vivo and in vitro.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200449	2552-55-8	C5H6N2O4	1 mg/5 mg

• Ibotenic acid monohydrate
  A hydrate of Ibotenic acid and a conformationally restricted analogue of glutamic acid which is a useful tool in morphological and functional analysis of central neuronal systems in vivo and in vitro.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-295172	60573-88-8	n.n.	1 mg/5 mg

• IEM 1460
  Adamantane derivative. Open-channel blocker of AMPA currents; selectively blocks GluR2-lacking, Ca²⁺-permeable AMPA receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204007	121034-89-7	C19H37N2Br•HBr	10 mg/50 mg

• IEM 1754 dihydrobromide

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362747	C16H30N2.2HBr	162831-31-4	10 mg/50 mg

• IEM 1925 dihydrobromide

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362748	258282-23-4	C17H28N2.2HBr	10 mg/50 mg

• Ifenprodil Tartrate Salt
  Shown to be a NMDA receptor antagonist, believed to act at the polyamine site. A neuroprotective agent, an alpha-adrenergic central and peripheral vasodilator, and an alpha ligand.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-295173	23210-56-2	C21H27NO2	5 mg/10 mg

• Ifenprodil hemitartrate
  NMDA receptor antagonist, acting at the polyamine site. Also an α-adrenergic vasodilator. σ2 ligand displaying about 3-fold selectivity over σ 1 sites.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203601	23210-58-4	(C21H27NO2)2 ·C4H6O6	10 mg/50 mg

• Ivermectin
  Positive allosteric modulator of the α7 neuronal nicotinic acetylcholine receptor and the purinergic P2X4 receptor. Antihelmintic. Also modulates glutamate- and GABA-activated chloride channels. Potentiates glycine-gated currents at low concentrations (30 nM).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203609	70288-86-7	C48H74O14 ·(B1a ·form)	100 mg/1 g

• JNJ 16259685
  Sub-nanomolar potent, non-competitive mGlu1 antagonist. Inhibits glutamate-induced Ca²⁺ response at the human mGluR1. Selective over mGluR5.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202670	409345-29-5	C20H23NO3	5 mg/25 mg

• Joro Spider Toxin
  Originally isolated from the spider Nephila clavata, shown to selectively block postsynaptic glutamate potentials and quisqualate-sensitive glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200453	112163-33-4	C27H47N7O6	100 µg

• Kynurenic acid
  A potential ligand of GPR35 G-protein-coupled receptor, antagonist of excitatory amino acids (EAA) and N-methyl-D-aspartate (NMDA) receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202683	492-27-3	C10H7NO3	250 mg/1 g

• Kynurenic acid sodium salt
  A sodium salt of Kynurenic acid. A potential ligand of GPR35 G-protein-coupled receptor, antagonist of excitatory amino acids (EAA) and N-methyl-D-aspartate (NDMA) receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358835	492-27-3 (non-salt)	C10H6NO3•Na	100 mg

• L-(-)-threo-3-Hydroxyaspartic acid
  Potent, competitive, transportable EAAT1-4 inhibitor/non-transportable EAAT5 inhibitor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204033	7298-99-9	C4H7NO5	10 mg

• L-689,560
  A selective antagonist at the glycine-binding site of the NMDA receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202684	139051-78-8	C17H15N3O3Cl2	1 mg

• L-701,252
  NMDA receptor antagonist acting at the glycine site1. Anticonvulsant.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205726	151057-13-5	C13H10ClNO3	10 mg/50 mg

• L-701,324

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361224	142326-59-8	C21H14CINO3	10 mg/50 mg

• L-AP3
  Selective antagonist of the PI-linked metabotropic glutamate response.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202201	23052-80-4	C3H8NO5P	5 mg/25 mg

• L-AP6
  QUIS-sensitized L-AP4 receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202202	78944-89-5	C6H14NO5P	5 mg/1 mg

• L-BMAA hydrochloride
  Monocarboxylic, neurotoxic amino acid; can act at the strychnine-insensitive glycine modulatory site to modify the activity of N-methyl-D-aspartate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204049	15920-93-1	C4H10N2O2.HCl	10 mg

• L-CCG-I
  Potent group II mGluR agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203097	117857-93-9	C6H9NO4	1 mg

• L-CCG-IV
  Potent NMDA receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203098	117857-95-1	C6H9NO4	1 mg

• L-Cysteinesulfinic acid
  An amino acid neurotransmitter.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203620	1115-65-7	C3H7NO4S	100 mg

• L-Glutamic acid γ-(α-naphthylamide) monohydrate

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-215217	81012-91-1	C15H16N2O3⋅H2O	25 mg/1 g

• L-Glutamic acid γ-(β-naphthylamide)

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-215219	14525-44-1	C15H16N2O3	100 mg/1 g

• L-Glutamic acid γ-(3-carboxy-4-hydroxyanilide)

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-215215	74929-17-2	C12H14N2O6	10 mg/250 mg

• L-Pyroglutamic acid 4-nitroanilide

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-211711	66642-35-1	C11H11N3O4	25 mg

• L-Quisqualic acid
  Quisqualate acts as an agonist for metabotropic glutamate receptor 1 (mGluR1), and can be used to differentiate between mGluR1 and mGluR4.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200467	52809-07-1	C5H7N3O5	5 mg/25 mg

• L-trans-Pyrrolidine-2,4-dicarboxylic acid
  An inhibitior of glutamate transport. Demonstrates an increase in extracellular glutamate levels, leading to massive NMDA_R-mediated neuronal death with no observed agonism of NMDA_R.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200477	64769-66-0	C6H9NO4	5 mg/25 mg

• L(+)-2-Amino-4-phosphonobutanoic acid (L-AP4)
  An amino-acid derivative and a mGluR4 and mGluR6 metabotropic glutamate receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200432	23052-81-5	C4H10NO5P	5 mg

• L(+)-2-Amino-5-phosphonovaleric acid
  This product has been shown to be an NMDA antagonist. It has also been oberved to be an agonist at quisqualate-sensitized AP6 site, where it is more potent than the D-isomer. There is evidence that L-AP5 can preferentially block cone signals in the rat retina.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358599	79055-67-7	C5H12NO5P	5 mg/50 mg

• Lamotrigine isethionate
  A water soluble phenyltriazine compound, which functions as an inhibitor of voltage gated sodium channels of presynaptic neurons.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-218654	113170-86-8	C9H7Cl2N5.C2H6O4S	10 mg

• LY 233053

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361238	125546-04-5	C8H13N5O2	1 mg/10 mg

• LY 235959

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361239	137433-06-8	C11H20NO5P	10 mg/50 mg

• LY 341495

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361244	201943-63-7	C20H19NO5	1 mg/10 mg

• LY 341495 disodium salt

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362765	n.n.	C20H17NNa2O5	1 mg/10 mg

• LY 354740
  This compound is a highly selective and potent group II (mGlu 2/3) receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204064	176199-48-7	C8H11NO4	10 mg/50 mg

• LY 367385

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361246	198419-91-9	C10H11NO4	10 mg/50 mg

• LY 379268

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361247	191471-52-0	C7H9NO5	10 mg/50 mg

• LY 395756

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-359013	842679-66-4	C9H13NO4	10 mg/50 mg

• LY 456236 hydrochloride
  Selective mGlu1 antagonist. Reduces formalin-induced hyperalgesic behavior in both mouse and rat with ED50 values of 28 and 16.3 mg/kg, respectively.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203625	338738-57-1	C16H15N3O2.HCl	10 mg/50 mg

• LY 487379 hydrochloride
  Positive allosteric modulator selective for mGlu2 receptors. Potentiates glutamate-stimulated [35S]GTPγS binding (EC₅₀ values are 1.7 and > 10 μM for mGlu2 and mGlu3 receptors respectively). Devoid of any activity at mGlu5 and mGlu7 receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204065	353231-17-1	C21H19F3N2O4S ·HCl	10 mg/50 mg

• MAP4
  Selective agonist for group III mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202221	157381-42-5	C5H12NO5P	5 mg

• Matrine
  An alkaloid. Has antiulcerogenic activity against stress ulcer in rat. It depresses both glutamate-induced responses and neurally evoked excitatory junctional potentials.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205741	519-02-8	C15H24N2O	100 mg/500 mg

• Memantine hydrochloride
  An antagonist at the NMDA receptor, binding to the ion channel site. Used in the treatment of Parkinsonism.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203628	41100-52-1	C12H21N ·HCl	50 mg

• mGluR5 Ligand, CDPPB
  A pyrazole amide compound that crosses the blood-brain barrier and acts as a potent, selective, reversible, positive allosteric modulator for metabotropic glutamate receptor subtype 5 (mGluR5). This also exerts anti-psychotic-like effects. It is reported to potentiate the response to glutamate (~300 nM) in CHO-mGluR5 cells (EC₅₀ = 10 nM for human, 4-fold potentiation; 20 nM for rat, 4.3-fold potentiation) and reverse amphetamine-induced disruption of pre-pulse inhibition (PPI) in rats. The specificity was determined using a panel of kinases and receptors. It does not potentiate the activity of other glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-221942	781652-57-1	C23H16N4O	1 mg

• (-)-MK 801 maleate

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361253	77086-19-2	C16H15N.C4H4O4	10 mg/50 mg

• (+)-MK 801 Maleate
  A selective non-competitive antagonist of the NMDA receptor. Interacts with NMDA-associated ion channel, blocking Ca²⁺ flux and NMDA-induced depolarization. Demonstrates neuroprotective effects.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203137	77086-22-7	C16H15N•C4H4O4	10 mg

• MMPIP hydrochloride
  Potent allosteric mGlu7-selective receptor antagonist. Inhibits agonist-induced intracellular calcium mobilization and cAMP accumulation (IC₅₀ values are 26 and 610 nM). Displays intrinsic activity; increases forskolin-induced cAMP accumulation in the absence of an agonist (IC₅₀ = 15 nM), indicating inverse agonist activity.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204093	479077-02-6	C19H15N3O3 ·HCl	1 mg/10 mg

• MNI caged kainic acid

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-359014	487-79-6 (uncaged)	C19H23N3O6	10 mg

• MNI-caged-L-glutamate

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361257	295325-62-1	C14H17N3O6	10 mg/50 mg

• MNI-caged-NMDA

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361258	n.n.	C14H17N3O6	10 mg

• MPDC
  A strong inhibitor of the Na+-dependent high-affinity synaptosomal glutamate transporter.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204097	n.n.	C7H9NO4	10 mg

• MPPG
  Potent antagonist of L-AP4-induced effects in rat spinal cord, thalamic and hippocampal neurons. Antagonist of mGlu receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203143	169209-65-8	C9H12NO5P	10 mg/50 mg

• MSOP
  Selective group III metabotropic glutamate receptor antagonist. Displays an apparent K_d of 51 μM for the L-AP4-sensitive presynaptic mGluR on primary afferent terminals in spinal cord compared to > 700 μM for the (1S,3S)-ACPD-sensitive presynaptic mGlu in the same system. Has no activity on postsynaptic mGlu receptors or on ionotropic glutamate receptors on neonatal rat motoneurons.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203637	66515-29-5	C4H10NO6P	10 mg/50 mg

• MTEP
  A brain-permeable (thiazole-pyridine)alkyne compound that acts as a potent, selective and non-competitive mGluR5 antagonist with in vivo anxiolytic activity in a rodent model. Highly selective and potent with a 5-fold higher anxiolytic activity than MPEP. Shows fewer off-target effects than MPEP.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205956	n.n.	C11H8N2S	5 mg/25 g

• MTEP hydrochloride

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361267	n.n.	C11H8N2S.HCl	10 mg/50 mg

• MTPG
  Group II/group III mGlu antagonist, showing selectivity for group II in electrophysiological studies. Potent antagonist for (1S,3S)-ACPD-sensitive receptors; preference for GluR2 and GluR3 subtypes.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204106	169209-66-9	C10H11N5O2	10 mg/50 mg

• N-(3-Aminopropyl)cyclohexylamine
  An inhibitor of spermine synthase. Described to specifically deplete spermidine and spermine levels in cultured rat hepatoma cells. Anatagonizes the facilitating effect of spermidine on NMDLA-induced seizures.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202715	3312-60-5	C9H20N2	1 g

• N-(4-Hydroxyphenylacetyl)-spermine
  A wasp toxin analog of naturally occurring PhTX-433. This is a very potent glutamate antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200466	130210-32-1	C18H32N4O2	250 µg

• N-(4-Hydroxyphenylpropanoyl) spermine trihydrochloride
  Wasp toxin analog. More potent than PhTX-343 at locust NMJ. Antagonist of the quisqualate-sensitive L-glutamate receptor (quis-GluR) of locust muscle.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204109	130631-59-3	C19H34N4O2 ·3HCl	250 µg

• N-Acetyl-Asp-Glu-OH
  Endogenous neurotransmitter with high affinity for the brain glutamate receptor. mGluR3 activator. NMDA receptor antagonist. Neuroprotective.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202717	3106-85-2	C11H16N2O8	10 mg/50 mg

• N-Acetylglycyl-D-glutamic acid
  Excitatory peptide, more potent than L-glutamic acid at inducing seizures in mice.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204111	135701-69-8	C9N14N2O6	10 mg/50 mg

• N-Glutaryl-Gly-Phe-4-methoxy-β-naphthylamide

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-215459	100940-58-7	C27H29N3O6	10 mg/25 mg

• N-Glutaryl-L-phenylalanine p-nitroanilide

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-215460	5800-34-0	C20H21N3O6	1 g/5 g

• N20C hydrochloride
  Non-competitive NMDA receptor open-channel blocker. Binds to receptor-associated ion channels and prevents glutamate-induced Ca²⁺ influx. Displays neuroprotective activity in vivo, and reportedly to be a brain-penetrant.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204116	76991-05-4	C17H20N2O•HCl	10 mg/50 mg

• Neuronal Differentiation Inducer III
  A cell-permeable isoxazole compound that selectively induces robust neuronal differentiation in various stem/progenitor cells.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222058	n.n.	C11H10N2O2S	10 mg

• NPEC-caged-(1S,3R)-ACPD

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-359016	n.n.	C16H18N2O8	10 mg/50 mg

• NPEC-caged-(S)-3,4-DCPG

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-359017	n.n.	C19H16N2O10	10 mg/50 mg

• NPEC-caged-(S)-AMPA
  Caged compound; a 1-(2-nitrophenyl)ethyl caged version of (S)-AMPA agonist at the AMPA receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358838	n.n.	C16H17N3O8	10 mg

• NPEC-caged-D-AP5

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362772	n.n.	C14H19N2O9P	10 mg/50 mg

• NPEC-caged-LY 379268

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-359019	n.n.	C16H16N2O9	10 mg

• NS 3763
  Selective non-competitive kainate receptor antagonist; displays selectivity for GLUK5 subunit-containing receptors (IC₅₀ values are 1.6 and > 30 mM for homomeric GLUK5 and GLUK6 receptors respectively). Has minimal activity at AMPA and NMDA receptors (IC₅₀ >> 30 mM).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203651	70553-45-6	C22H16N2O6	10 mg/50 mg

• O-Phospho-L-serine
  L-AP4 agonist. Competitive NMDA antagonist. Has affinity for type IV, but not type I, metabotropic glutamate receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202257	407-41-0	C3H8NO6P	1 g

• PCCG-13
  A potent, selective and competitive antagonist of PLD-coupled mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205962	n.n.	C12H13NO4	1 mg

• PCCG-4
  Selective group II mGluR antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222130	n.n.	C12H13NO4	1 mg/5 mg

• Pentamidine isethionate
  Exhibits inhibitory actions on constitutive nitric oxide synthase in the brain and acts as a NMDA Glu antagonist. Antimicrobial, neuroprotective agent.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204176	140-64-7	C19H24N4O2•2C2H6O4S	50 mg

• PEPA
  Allosteric potentiator of AMPA desensitization. Decreases rate of onset of desensitization and potentiates steady-state equilibrium currents induced by Glu with splic variant and subunit selectivity. Enhances post-ischemic memory impairment in rats post i.v. administration.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204178	141286-78-4	C16H16F2N2O4S2	10 mg/50 mg

• PHCCC

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361292	n.n.	C17H14N2O3	10 mg/50 mg

• Philanthotoxin 74
  Subtype-selective AMPA receptor antagonist that inhibits GluR1/2 but not GluR2/3 receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204189	401601-12-5	C24H42N4O3 ·2HCl	1 mg/10 mg

• Piracetam
  Nootropic that displays cognitive enhancing properties. Proposed to enhance neurotransmission via modulation of ion flux. Through AMPA receptors, potentiates Na+ influx. Facilitates efficiency of cholinergic neurotransmission at muscarinic receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204196	7491-74-9	C6H10N2O2	5 g/25 g

• PMPA (NMDA antagonist)
  Short-chain competitive NMDA antagonist. Displays K_i values of 0.84, 2.74, 3.53 and 4.16 μM at NR2A, NR2B, NR2C and NR2D subunit-containing receptors respectively. Selective over AMPA receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204850	113919-36-1	C6H13N2O5P	10 mg/50 mg

• PPDA
  Subtype-selective NMDA receptor antagonist that preferentially binds to NR2C/NR2D-containing receptors (Ki values are 0.096, 0.125, 0.31 and 0.55 μM for NR2C, NR2D, NR2B and NR2A subunits respectively).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204210	n.n.	C21H18N2O5 ·xH2O	10 mg/50 mg

• PPPA
  Competitive NMDA receptor antagonist that displays moderate selectivity for NR2A-containing receptors (Ki values are 0.13, 0.47, 1.10 and 3.86 μM for NR2A, NR2B, NR2C and NR2D subunits respectively).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204212	n.n.	C9H18NO5P	10 mg/50 mg

• Putrescine dihydrochloride
  A compound that binds to the polyamine modulatory site of the NMDA (N-methyl D-aspartate) receptor and potentiate NMDA-induced currents.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202786	333-93-7	C4H12N2 ·2HCl	1 g

• Quinolinic acid
  Metabolite of tryptophan. Putative NMDA receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203226	89-00-9	C7H5NO4	1 g

• (R,S)-ATPA
  Potent and selective agonist of the GluR5 subtype of the kainate receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203232	140158-50-5	C10H16N2O4	1 mg/5 mg

• (R)-(+)-HA-966

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361303	123931-04-4	C4H8N2O2	10 mg/50 mg

• (R)-3-Carboxy-4-hydroxyphenylglycine
  Moderately potent NMDA and AMPA/kainate receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204871	13861-03-5	C9H9NO5	10 mg/50 mg

• (R)-3,4-DCPG
  AMPA receptor antagonist with little activity at kainate receptors and weak activity at NMDA receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204227	n.n.	C10H9NO6	10 mg/50 mg

• (R)-4-Carboxyphenylglycine

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361304	134052-68-9	C9H9NO4	10 mg/50 mg

• (R)-AMPA

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361305	83654-13-1	C7H10N2O4	10 mg

• (R)-CPP
  Highly potent NMDA receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202308	126453-07-4	C8H17N2O5P	1 mg/10 mg

• Remacemide hydrochloride

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361307	111686-79-4	C17H20N2O.HCl	10 mg/50 mg

• Ro 01-6128

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362789	302841-86-7	C17H17NO3	10 mg/50 mg

• Ro 04-5595 hydrochloride
  Selective antagonist for NR2B-containing NMDA receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204885	194089-07-1	C19H22ClNO2.HCl	10 mg/50 mg

• Ro 25-6981 maleate
  NMDA agonist. Potent and selective activity-dependent blocker NR2B subunit-containing NMDA receptors . IC₅₀ values are 0.009 and 52 μM for cloned receptor subunit combinations NR1C/NR2B and NR1C/NR2A respectively. Acts as a neuroprotectant in vivo and in vitro.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204887	169274-78-6	C22H29NO2 ·C4H4O4	1 mg/10 mg/50 mg

• Ro 67-4853

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362790	302841-89-0	C19H19NO4	10 mg/50 mg

• Ro 8-4304 Hydrochloride
  NMDA receptor antagonist (IC₅₀ = 0.4 μM) that displays > 100 fold selectivity for NR2B-containing receptors over NR2A-containing receptors. Displays an activity-dependent mechanism of NMDA antagonism and is competitive with respect to spermine.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204241	195988-65-9	C21H23FN2O3 ·HCl	10 mg/50 mg

• (RS)-(Tetrazol-5-yl)glycine
  Highly potent NMDA receptor agonist Potent NMDA receptor agonist, approximately 20 times more active than NMDA.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205495	138199-51-6	C3H5N5O2	10 mg/50 mg

• (RS)-α-Methyl-3-carboxy-4-hydroxyphenylglycine
  This is a potent antagonist of both L-AP4 and L-CCG-I-induced depressions of forskolin-stimulated cAMP production. It shows preferential antagonist activity versus L-CCG-I. Group I/group II mGluR antagonist at cloned receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222264	n.n.	C10H11NO5	5 mg

• (RS)-3-Hydroxyphenylglycine
  Agonist at PI-linked metabotropic glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204246	31932-87-3	C8H9NO3	10 mg/50 mg

• (RS)-3,4-DCPG
  Systemically active anticonvulsant that is 30-100-fold more potent in vivo than the separate enantiomers (S)-3,4-DCPG (mGlu8-selective agonist) or (R)-3,4,-DCPG (AMPA/NMDA antagonist).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204247	n.n.	C10H9NO6	10 mg/50 mg

• (RS)-3,5-DHPG
  Selective group I metabotropic glutamate receptor agonist which activates both mGlu1 and mGlu5.Reported to be an antagonist at metabotropic glutamate receptors linked to phospholipase D.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205496	19641-83-9	C8H9NO4	10 mg/50 mg

• (RS)-4-Bromo-homo-ibotenic acid
  Potent AMPA receptor agonist. Selective but relatively non-potent group I mGluR agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203244	71366-32-0	C6H7N2O4Br	5 mg

• (RS)-4-Carboxyphenylglycine

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361319	7292-81-1	C9H9NO4	10 mg/50 mg

• (RS)-4C3H-PG
  'Broad spectrum' EAA ligand

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203245	134052-66-7	C9H9NO5	10 mg/50 mg

• (RS)-AMPA hydrobromide
  More water soluble form of sc-200437.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203246	77521-29-0	C7H10N2O4 ·HBr	1 mg

• (RS)-APICA
  A rigidified analog of MPPG; a selective group II metabotropic glutamate receptor antagonist (IC₅₀ = 30 μM) with no significant effect on group I and III mGlu receptors at concentrations up to 1 mM. Increases extracellular glutamate concentrations and possesses an unusual inverse agonist-like action.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204248	n.n.	C10H12NO5P	10 mg/50 mg

• (RS)-CPPG
  Most potent group II/III mGluR antagonist, with approx. 20-fold selectivity for group III over group II.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203448	183364-82-1	C11H14NO5P	5 mg/25 mg

• (RS)-MCPG
  A non-selective antagonist of group I/II mGluRs. Used as a tool for probing the mGluR system.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202325	146669-29-6	C10H11NO4	5 mg

• (RS)-MCPG disodium salt
  A non-selective group I/group II metabotropic glutamate receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358840	n.n.	C10H9NNa2O4	10 mg

• (RS)-MSPG
  A non-selective antagonist of mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203247	169209-64-7	C9H11NO5S	10 mg

• (RS)-PPG
  Potent and selective group III mGluR agonist, with a subtype specificity towards the mGlu₃ receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202797	120667-15-4	C8H10NO5P	5 mg

• S-(+)-CBPG
  This is a potent and selective, structurally new group I mGluR antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222268	n.n.	C8H11NO4	1 mg/5 mg

• S-(N,N-Diethylcarbamoyl)glutathione

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-220012	157723-51-8	C15H26N4O7S	5 mg

• S-(N,N-Diethylcarbamoyl)glutathione Sulfoxide

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-220013	n.n.	C14H26N4O8S	5 mg

• S-Sulfo-L-cysteine sodium salt
  EAA receptor agonist. Agonist at mGlu1α and mGlu5a subtypes expressed in clonal RGT cell lines.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205498	1637-71-4	C3H6NO5S2Na.xH2O	10 mg/50 mg

• (S)-(-)-5-Fluorowillardiine

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361326	140187-23-1	C7H8FN3O4	10 mg/50 mg

• (S)-(-)-5-Iodowillardiine

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361327	140187-25-3	C7H8IN3O4	10 mg/50 mg

• (S)-3-Carboxy-4-hydroxyphenylglycine
  Mixed group II mGlu agonist and group I metabotropic glutamate receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203689	55136-48-6	C9H9NO5	10 mg/50 mg

• (S)-3-Hydroxyphenylglycine
  Agonist at group I metabotropic glutamate receptors (mGlu1) having no effect at mGlu2 or mGlu4.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204254	71301-82-1	C8H9NO3	10 mg/50 mg

• (S)-3,4-DCPG
  Potent, selective mGlu8a agonist (EC₅₀ = 31 nM). Displays > 100-fold selectivity over mGlu1-7 and displays little/no activity at NMDA and kainate receptors. Increases c-Fos expression in stress-related brain areas following systemic administration in mice in vivo. Also a potent anticonvulsant in mice in vivo.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204255	201730-11-2	C10H9NO6	10 mg/50 mg

• (S)-3,5-DHPG
  Selective group I mGlu receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204256	162870-29-3	C8H9NO4	5 mg/10 mg

• (S)-4C-PG
  Competitve group I mGluR antagonist, with selectivity for mGlu1 over mGlu5 receptor.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203449	134052-73-6	C9H9NO4	1 mg/5 mg/50 mg

• (S)-4C3H-PG
  Agonist for group II mGluRs. Competitive antagonist for group I mGluR1; mixed effects at mGluR5.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203249	85148-82-9	C9H9NO5	1 mg/5 mg

• (S)-CPW 399
  Subtype-selective weakly desensitising AMPA agonist. At GluR1 and GluR2 subunit-containing AMPA receptors, exhibits potent agonist activity. Excitotoxic in vitro.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203690	389888-02-2	C10H13N3O4	10 mg/50 mg

• (S)-HexylHIBO
  Group I mGlu antagonist. Enantiomer of hexylHIBO.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203691	334887-48-8	C12H20N2O4	10 mg/50 mg

• (S)-MCPG
  An antagonist of the group I/II mGluRs. Active isomer of (RS)-MCPG preparations. Affects spatial learning and blocks induction of LTP through interaction with the mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202329	150145-89-4	C10H11NO4	5 mg/25 mg

• (S)-MPPG
  This is the active isomer of (RS)-MPPG. It is a highly potent L-AP4-sensitive receptor antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222283	201608-25-5	C9H12NO5P	1 mg/5 mg

• (S)-MPPG (cyclic)
  This is a selective antagonist of group II mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222284	n.n.	C10H12NO5P	1 mg

• Salsolinol-1-carboxylic acid
  An amino acid that occurs naturally in the CNS.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204259	57256-34-5	C11H13NO4	10 mg/50 mg

• SDZ 220-040

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361354	174575-40-7	C16H16Cl2NO6P	10 mg/50 mg

• SDZ 220-581

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361355	n.n.	n.n.	10 mg/50 mg

• SIB 1757
  A highly selective antagonist for the mGlu5 metabotropic glutamate receptor subtype; displays an IC₅₀ value of 0.4 μM at hmGlu5 compared with > 30 μM at hmGlu1b, hmGlu2, hmGlu4, hmGlu6, hmGlu7 and hmGlu8.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204277	31993-01-8	C12H11N3O	10 mg/50 mg

• SIB 1893
  Highly selective non-competitive antagonist for the metabotropic glutamate mGlu5 receptor subtype.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203262	6266-99-5	C14H13N	10 mg/50 mg

• Spermidine trihydrochloride

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-360822	334-50-9	C7H19N3•3HCl	1 g/5 g

• SYM 2206

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361369	173952-44-8	C20H22N4O3	10 mg/50 mg

• t-CAA
  This is a potent in vivo inhibitor of glutamate uptake and a Kainate receptor agonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222334	n.n.	C6H9NO4	1 mg

• TCN 238

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-362803	125404-04-8	C12H11N3	10 mg/50 mg

• TCS 46b
  Orally active, subtype-selective NR1A/NR2B NMDA receptor antagonist (IC₅₀ values are 5.3, 35000 and > 100000 nM for NR1A/2B, NR1A/2A and NR1A/2C receptor subtypes respectively). Potentiates the effect of L-DOPA in 6-OHDA-lesioned rats following oral administration.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204328	302799-86-6	C22H23N3O	10 mg/50 mg

• Threo Ifenprodil hemitartrate

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361381	74991-34-7	C21H27NO2.½C4H6O6	10 mg/50 mg

• (±)-threo-3-Methylglutamic acid
  A potent blocker of glutamate transport. Selective for EAAT2 and EAAT4 (IC₅₀ values are 90, 109, 1600 and 1080 μM for EAAT2, EAAT4, EAAT1 and EAAT3 respectively).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204344	63088-04-0	C6H11NO4	10 mg/50 mg

• Topiramate
  Anticonvulsant that antagonizes GluR5 kainate receptors (IC₅₀ = 0.46 μM), acts as a positive allosteric modulator of GABA_A receptor-mediated currents, inhibits Nav channels (IC₅₀ = 48.9 μM) and inhibits L-type Ca²⁺ channels. Inhibits carbonic anhydrase (CA) (K_i values are 0.1 and 0.2 μM at rat CA II and CA IV respectively), which lowers intracellular neuronal pH.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204350	97240-79-4	C12H21NO8S	10 mg/50 mg

• trans-1,2-homo-ACPD
  Selective antagonist for group II mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-208456	n.n.	C8H13NO4	5 mg

• trans-1,3-homo-ACPD
  Equimolar mixture of (1R,3S)-homo-ACPD and (1S,3R)-homo-ACPD.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-205981	n.n.	C8H13NO4	5 mg

• TRANS-ACPD
  An equimolar mixture of Trans-(1S,3R)-ACPD and Trans-(1R,3S)-APCD. Agonist of metabotropic glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-202367	67684-64-4	C7H11NO4	10 mg/50 mg

• (±)-trans-Azetidine-2,4-dicarboxylic acid
  Selective agonist for group I mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203300	161596-62-9	C5H7NO4	1 mg

• U-54494A hydrochloride
  NMDA antagonist.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-200479	112465-94-8	C18H24Cl2N2O··HCl	5 mg/25 mg

• UBP 282
  AMPA and kainate receptor antagonist that distinguishes between motoneuron and dorsal root kainate receptors. Inhibits AMPA receptor-, but not kainate receptor-mediated currents on spinal neonatal motoneurons yet antagonizes kainate-induced responses on dorsal root C-fibres.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203715	544697-47-4	C15H15N3O6	10 mg/50 mg

• UBP 296
  Potent and selective GluR5-subunit containing kainate receptor antagonist (apparent K_d = 1.09 mM). Displays ~ 90-fold selectivity over AMPA receptors and recombinant human GluR6- and KA2-containing kainate receptors. Selectively blocks kainate receptor-mediated LTP induction in rat hippocampal mossy fibres. Has little or no action at NMDA or group I mGlu receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204366	n.n.	C15H15N3O6	10 mg/50 mg

• UBP 301
  Kainate potent receptor antagonist (apparent Kd = 5.94 mM). Displays ~ 30-fold selectivity over AMPA receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203716	569371-10-4	C15H14IN3O6	10 mg/50 mg

• UBP 302
  Potent and selective GLUK5 (GluR5)-subunit containing kainate receptor antagonist; active enantiomer of UBP 296.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204367	n.n.	C15H15N3O6	10 mg/50 mg

• UBP1112
  A group III mGlu receptor antagonist that is selective (apparent K_d values are 5.1 and 488 μM for group III and group II mGlu receptors respectively; IC₅₀ > 1 mM for group I, NMDA, AMPA and kainate receptors).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204368	n.n.	C10H14NO5P	10 mg/50 mg

• VU 0155041
  Potent, positive allosteric modulator/allosteric agonist at mGlu4 receptors (EC₅₀ = 798 and 693 nM at human and rat mGlu4 receptors respectively). In vivo models of Parkinson's disease, active following i.c.v. administration.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204385	n.n.	C14H15Cl2NO3	10 mg/50 mg

• VU 0155041 sodium salt
  A positive allosteric modulator of the metabotropic glutamate receptor 4 (mGluR4).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204386	n.n.	C14H14Cl2NNaO3	10 mg/50 mg

• VU 0361737
  A selective positive allosteric modulator at mGlu4 receptors (EC50 values are 240 and 110 nM at human and rat receptors respectively). Inactive at mGlu1, mGlu2, mGlu3, mGlu6 and mGlu7 receptors and displays weak activity at mGlu5 and mGlu8 receptors. Also a brain penetrant.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-301976	1161205-04-4	C13H11CIN2O2	10 mg/50 mg

• VU 1545
  Positive allosteric modulator of metabotropic glutamate receptor 5 (mGlu5) (EC₅₀ = 9.6 nM, K_i = 156 nM at rat mGlu5).

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204388	890764-63-3	C22H15FN4O3	10 mg/50 mg

• WAY 213613
  Strong, non-substrate inhibitor of EAAT2 (GLT-1) that displays > 44-fold selectivity over EAAT1 and EAAT3 (IC₅₀ values are 85, 3787 and 5004 nM for EAAT2, EAAT3 and EAAT1 respectively). Exhibits no activity towards metabotropic and ionotropic glutamate receptors.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-203720	868359-05-1	C16H13BrF2N2O4	10 mg/50 mg

• XE-CCG-I
  Selective and highly active group II mGluR antagonist with a subtype specificity towards the mGlu3 receptor. XE-CCG-I has no activity towards group I and group III mGluRs.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-222421	n.n.	C21H21NO5	1 mg

• YM 230888
  A selective mGLU1 antagonist reported to inhibit mGlu1-mediated inositol phosphate production.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-358843	446257-23-4	C19H28N4OS	10 mg/50 mg

• YM 298198 hydrochloride

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361412	748758-45-4	C18H22N4OS.HCl	10 mg/50 mg

• YM 90K hydrochloride

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361415	154164-30-4	C11H7N5O4.HCl	10 mg/50 mg

• Z-Cyclopentyl-AP4
  Group III mGlu receptor agonist that displays higher potency at mGlu4 than mGlu8 (EC₅₀ values are 49 and 124 μM respectively) with no activity at mGlu7. Selectively inhibits synaptic activity in the lateral perforant pathway (IC₅₀ values are 130 and 1859 μM in the lateral and medial perforant pathways respectively). Conformationally restrained analog of L-AP4.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204413	103439-17-4	C6H12NO5P	10 mg/50 mg

• ZJ 43
  Has been shown to be a potent inhibitor of glutamate carboxypeptidase II and III. a potent inhibitor of glutamate carboxypeptidase II and III.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-361420	723331-20-2	C12H20N2O7	1 mg/10 mg

• ZK 200775
  Competitive AMPA/kainate antagonist; inhibits currents induced by AMPA, kainate and NMDA; Displays anxiolytic, anticonvulsant and muscle relaxant activity in vivo.

  Katalog #	CAS Nummer	Summenformel	Menge
  sc-204421	161605-73-8	C14H15N3O6F3P	10 mg/50 mg