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Neurobiology and Neurodiseases

  • (±)-2-Methylarachidonoyl-2'-fluoroethylamide
    An analog of arachidonylethanolamide that is a strong, selective CB1 cannabinoid receptor agonist. The methyl group at the C-2 position of arachidonic acid enhances the metabolic stability of the compound. It can fully substitute for 9-THC in animal self-administration tests.
    Katalog #CAS NummerSummenformelMenge
    sc-251783166100-39-6C23H38NOF5 mg
  • (2S,3S)-3-Methylglutamic Acid Hydrochloride Salt
    A potent agonist for kainate receptors. Is highly selective.
    Katalog #CAS NummerSummenformelMenge
    sc-216336n.n.C6H12ClNO45 mg
  • (2S,3S)-trans-3-(Carboxymethyl)-azetidine-2-acetic Acid
    Effective inhibitor of sodium dependent glu uptake and KA receptor agonist.
    Katalog #CAS NummerSummenformelMenge
    sc-206577185387-36-4C6H9NO45 mg
  • (-)-2β-Carbomethoxy-3β-(4-iodophenyl)nortropane
    This compound inhibits the serotonin (5-HT) transporter.
    Katalog #CAS NummerSummenformelMenge
    sc-206587136794-87-1C15H18INO2500 µg
  • (-)-3,4,4a,5,6,10b-Hexahydro-2H-naphtho[1,2-b][1,4]oxazin-9-ol, HCl
    A dopamine antagonist. A dopaminergic ligand. This compound has been used as a precursor for the PET radiotracer, 11C-(-)-4-Propyl-3,4,4a,5,6,10b-hexahydro-2H-naphtho[1,2-b][1,4]oxazin-9-ol.
    Katalog #CAS NummerSummenformelMenge
    sc-216586n.n.C12H16ClNO25 mg
  • (-)-3,4,4a,5,6,10b-Hexahydro-9-methoxy-2H-naphtho[1,2-b][1,4]oxazin-3-one
    A dopamine antagonist and dopaminergic ligand.
    Katalog #CAS NummerSummenformelMenge
    sc-216587n.n.C13H15NO35 mg
  • (+)-3,4,4a,5,6,10b-Hexahydro-9-methoxy-2H-naphtho[1,2-b][1,4]oxazin-3-one
    A dopamine antagonist and a dopaminergic ligand.
    Katalog #CAS NummerSummenformelMenge
    sc-216588153153-60-7C13H15NO35 mg
  • (-)-3,4,4a,5,6,10b-Hexahydro-9-methoxy-2H-naphtho[1,2-b][1,4]oxazin, HCl
    A dopamine antagonist and dopaminergic ligand.
    Katalog #CAS NummerSummenformelMenge
    sc-216589n.n.C13H18ClNO25 mg
  • (+)-3,4,4a,5,6,10b-Hexahydro-9-methoxy-2H-naphtho[1,2-b][1,4]oxazin, HCl
    A dopamine antagonist and dopaminergic ligand.
    Katalog #CAS NummerSummenformelMenge
    sc-216590n.n.C13H18ClNO25 mg
  • 4-Benzoylpiperidine Hydrochloride
    Synthetic intermediate in the preparation of CNS depressants.
    Katalog #CAS NummerSummenformelMenge
    sc-21678325519-80-6C12H16ClNO100 mg
  • 4-Formylphenyl b-D-allopyranoside
    Katalog #CAS NummerSummenformelMenge
    sc-27740580154-34-3C13H16O71 g/5 g
  • 5-Chloro Bifeprunox Mesylate
    Used as an antipsychotic compound. Activates the serotonin 5-hydroxytryptamine (5-HT)1A receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-217164n.n.C25H26ClN3O5S25 mg
  • 5-Fluoro-2'-deoxycytidine
    Mechanism-based DNMT inhibitor, shown to form covalent links with the cysteine residue in the DNMT active site.
    Katalog #CAS NummerSummenformelMenge
    sc-25226710356-76-0C9H12FN3O45 mg
  • 6-Iodonordihydrocapsaicin
    TRPV1 (V1) vanilloid receptor antagonist.
    Katalog #CAS NummerSummenformelMenge
    sc-252297859171-97-4C17H26INO35 mg
  • 6-Nitro-7-sulfamoylbenzo[f]quinoxaline-2,3-dione, Disodium Salt
    A discriminating and potent antagonist for AMPA binding sites.
    Katalog #CAS NummerSummenformelMenge
    sc-217370479347-86-9C12H6N4Na2O6S5 mg
  • 9-(Benzylamino)-1,2,3,4-tetrahydroacridin-1-ol Maleate
    Exhibits biochemical and pharmacological profile similar to THA except that it is far less toxic.
    Katalog #CAS NummerSummenformelMenge
    sc-207210113108-86-4C24H24N2O5100 mg
  • α-Methadol-d3
    An analgesic, labeled reduction product of Methadone.
    Katalog #CAS NummerSummenformelMenge
    sc-220441n.n.C21H26D3NO1 mg
  • AC-93253 iodide
    A potent, cell permeable, subtype selective RAR agonist.
    Katalog #CAS NummerSummenformelMenge
    sc-257044108527-83-9C23H25N2SI10 mg/50 mg
  • Angiotensin II, Human
    Katalog #CAS NummerSummenformelMenge
    sc-3636434474-91-3n.n.1 mg/5 mg
  • Arachidonyl-2'-chloroethylamide hydrate
    A potent and selective neuronal CB1 cannabinoid receptor agonist.
    Katalog #CAS NummerSummenformelMenge
    sc-252384220556-69-4 (anhydrous)C22H36ClNO25 mg
  • BATCP
    HDAC 6 selective substrate (over HDAC 1, Class II over Class I).
    Katalog #CAS NummerSummenformelMenge
    sc-252405787549-23-9C23H28F3N3O62 mg
  • BAY U6751 hydrate
    Katalog #CAS NummerSummenformelMenge
    sc-257117114290-51-6 (anhydrous)C20H20ClNNa2O6•xH2O5 mg
  • Benztropine mesylate
    A derivative of Atropine and an antagonist of the mAChR which also demonstrates anti-nicotinic action at the nAChR.
    Katalog #CAS NummerSummenformelMenge
    sc-202495132-17-2C21H25NO ·CH4SO3 ·H2O1 g/5 g
  • Bretazenil
    A benzodiazepine partial agonist.
    Katalog #CAS NummerSummenformelMenge
    sc-25251284379-13-5C19H20N3O3Br5 mg
  • Carbasalate calcium
    Katalog #CAS NummerSummenformelMenge
    sc-2788095749-67-7C19H18CaO9N220 mg
  • Citral
    Katalog #CAS NummerSummenformelMenge
    sc-2526205392-40-5C10H16O1 kg
  • CPTH2
    CPTH2 is a histone acetyltransferase (HAT) inhibitor modulating the Gcn5 network where HATs act as transcriptional coactivators. Histone acetylation plays an important role in regulating the chromatin structure and is tightly regulated by two classes of enzyme, histone acetyltransferases (HAT) and histone deacetylases (HDAC). Deregulated HAT and HDAC activity plays a role in the development of a range of cancers. Consequently, inhibitors of these enzymes have potential as anticancer agents.
    Katalog #CAS NummerSummenformelMenge
    sc-255032357649-93-5C14H14ClN3S5 mg
  • Cys-Gly-Tyr-Gly-Pro-Lys-Lys-Lys-Arg-Lys-Val-Gly-Gly
    SV40 T-antigen homolog that can induce nuclear transport.
    Katalog #CAS NummerSummenformelMenge
    sc-257276104914-40-1C60H104N20O15S500 µg
  • Cytosporone B
    The first naturally occurring agonist for nuclear orphan receptor Nur77 is Cytosporone B. The molecule binds with high affinity (IC50=0.278 nM) to the ligand-binding domain of Nur77 and stimulates Nur77-dependent activities. Nur77 is a nuclear receptor/transcription factor. A physiological ligand for Nur77 is as yet unknown, but there is increasing interest in Nur77 because of its known activities. Translocation of Nur77 from the nucleus to mitochondria initiates cell apoptosis, making it a potential target for cancer treatment. Nur77 is also involved in glucose homeostasis, where it induces genes involved in gluconeogenesis. Csn-B physically binds to Nur77 and activates its transactivational activity and translocation to mitochondria to induce apoptosis. It inhibits cancer cell proliferation and tumor growth.
    Katalog #CAS NummerSummenformelMenge
    sc-252653321661-62-5C18H26O55 mg
  • D-α-Tocotrienol
    Widely used for their strong antioxidant properties. The various isoforms of tocotrienols differ in their methyl substitution in the chromanol head. α-tocotrienol demonstrates neuroprotective properties by blocking glutamate-induced cell death in neuronal cells.
    Katalog #CAS NummerSummenformelMenge
    sc-2526561721-51-3C29H44O210 mg
  • D,L N-Desmethyl Venlafaxine
    A metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-207483149289-30-5C16H25NO25 mg
  • D,L N,O-Didesmethyl Venlafaxine
    A metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-207484135308-74-6C15H23NO25 mg
  • D,L N,O-Didesmethyl Venlafaxine-d3
    A deuterium-labeled metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine with reported weak inhibitory effect on dopamine reuptake.
    Katalog #CAS NummerSummenformelMenge
    sc-218040n.n.C15H20D3NO21 mg
  • D,L-N-Desmethyl Venlafaxine-d3
    A deuterium-labeled metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-218052n.n.C16H22D3NO21 mg
  • D,L-N,N-Didesmethyl Venlafaxine-d6
    A deuterium-labeled metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-218053n.n.C15H17D6NO21 mg
  • D,L-N,N-Didesmethyl-N-(4-methoxyphenethyl) Venlafaxine
    An impurity of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-218054n.n.C24H33NO310 mg
  • D,L-N,N-Didesmethyl-O-desmethyl Venlafaxine Hydrochloride
    A metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-211199135308-76-8C14H21NO2•HCl2.5 mg
  • D,L-O-Desmethyl Venlafaxine
    A metabolite of the serotonin and noradrenaline reuptake inhibitor Venlafaxine.
    Katalog #CAS NummerSummenformelMenge
    sc-20749493413-62-8C16H25NO25 mg
  • D,L-O-Desmethyl Venlafaxine-d6
    A deuterium-labeled metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-218055n.n.C16H19D6NO21 mg
  • Dansyl-NECA
    Fluorescent ligand for adenosine receptors with a marked selectivity for the A1 receptor subtype. Has been successfully applied in fluorescence microscopy assays.
    Katalog #CAS NummerSummenformelMenge
    sc-202570219982-12-4C30H40N8O6S500 µg
  • DCHC
    A SIRT1 activator which increases peroxisome proliferator-activated receptor gamma co-activator 1å (PGC1å) expression, resulting in mitochondrial biogenesis. Activates SIRT1 at low micromolar concentrations and increases SIRT1 activity at 100 µM. It induces the activation of recombinant SIRT1, but does not increase SIRT1 expression.
    Katalog #CAS NummerSummenformelMenge
    sc-255067302953-06-6C15H8Cl2O310 mg
  • Dehydro Venlafaxine
    A degradation product of the neuroamine reuptake inhibitor Venlafaxine.
    Katalog #CAS NummerSummenformelMenge
    sc-21123093413-57-1C17H25NO•HCl1 mg
  • Deoxy Venlafaxine
    An impurity of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-218117n.n.C17H27NO1 mg
  • Desethylene Aripiprazole
    A derivative of Aripiprazole.
    Katalog #CAS NummerSummenformelMenge
    sc-2181381216394-63-6C21H25Cl2N3O21 mg
  • Dimebolin
    Katalog #CAS NummerSummenformelMenge
    sc-2789723613-73-8C21H25N325 mg
  • Dimethyl Cabergoline
    An analogue of Cabergoline.
    Katalog #CAS NummerSummenformelMenge
    sc-218234n.n.C28H41N5O210 mg
  • DM 235
    Potent nootropic agent.
    Katalog #CAS NummerSummenformelMenge
    sc-300499314728-85-3C14H18N2O25 mg
  • Donepezil
    A noncompetitive acetylcholineesterase inhibitor, which can readily cross the blood brain barrier and increases the concentration of cortical acetylcholine.
    Katalog #CAS NummerSummenformelMenge
    sc-279006120014-06-4C24H29NO310 mg
  • Donepezil Hydrochloride
    A noncompetitive acetylcholineesterase inhibitor, which can readily cross the blood brain barrier and increases the concentration of cortical acetylcholine.
    Katalog #CAS NummerSummenformelMenge
    sc-218265120011-70-3C24H30ClNO310 mg
  • Doxapram
    Katalog #CAS NummerSummenformelMenge
    sc-279007309-29-5C24H30N2O25 mg
  • Doxapram hydrochloride
    Katalog #CAS NummerSummenformelMenge
    sc-279008113-07-5C24H31ClN2O25 mg
  • Droxidopa
    Katalog #CAS NummerSummenformelMenge
    sc-27901023651-95-8C9H11NO5100 mg
  • Duloxetine
    Katalog #CAS NummerSummenformelMenge
    sc-279011116539-59-4C18H19NOS10 mg
  • (-)-Eseroline fumarate
    Metabolite of physostigmine (eserine). Potent analgesic.
    Katalog #CAS NummerSummenformelMenge
    sc-202155104015-29-4C13H18N2O ·C4H4O410 mg/50 mg
  • Ethyl gallate
    Katalog #CAS NummerSummenformelMenge
    sc-239928831-61-8C9H10O5100 g
  • Fadrozole hydrochloride
    Nonsteroidal aromatase inhibitor exhibiting a very potent and selective inhibitory effect of the aromatase enzyme system in vivo and estrogen biosynthesis in vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-252819102676-31-3C14H13N3 ·HCl10 mg
  • FH535
    FH535 is a reversible dual inhibitor of Wnt/β-catenin and PPARγ and PPARδ signaling antagonist; β-catenin/Tcf inhibitor. FH535 has been shown to inhibit the Wnt/b-catenin pathway. The compound is selectively toxic to some carcinomas expressing the Wnt/B-catenin pathway. FH535 is a more potent Wnt/h-catenin inhibitor than NO-aspirin.
    Katalog #CAS NummerSummenformelMenge
    sc-300691108409-83-2C13H10Cl2N2O4S5 mg
  • FIPI hydrochloride hydrate
    A potent inhibitor of PLD (phospholipase D) specifically PLD 1 and PLD 2. FIPI hydrochloride hydrate can block the production of phosphatidic acid with subnanomolar potency.
    Katalog #CAS NummerSummenformelMenge
    sc-300694n.n.C23H24FN5O2 ·HCl ·xH2O5 mg
  • Fluoxetine
    A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-27916654910-89-3C17H18F3NO500 mg
  • Fluoxetine HCl
    A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-20112556296-78-7C17H18F3NO•HCl50 mg/250 mg
  • Fluoxetine-d5 Hydrochloride
    A deuterium-labeled 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-21850956296-78-7 (unlabeled)C17H14D5ClF3NO1 mg
  • Fluphenazine
    A neuroleptic drug that is a dopamine receptor antagonist. Acts as an antimutagen, which may be explained by its ability to reduce the level of free radicals.
    Katalog #CAS NummerSummenformelMenge
    sc-20570069-23-8C22H26F3N3OS1 g/5 g
  • Fluphenazine decanoate
    Katalog #CAS NummerSummenformelMenge
    sc-2791675002-47-1C32H44F3N3O2S10 mg
  • fluphenazine enanthate
    Katalog #CAS NummerSummenformelMenge
    sc-2791682746-81-8C29H38F3N3O2S10 mg
  • Gabapentin Related Compound B
    A Gabapentin analogue used in the treatment of neurological disorders.
    Katalog #CAS NummerSummenformelMenge
    sc-211550133481-09-1C9H13NO22.5 mg
  • Gabapentin Related Compound D
    A Gabapentin analogue.
    Katalog #CAS NummerSummenformelMenge
    sc-2185521076198-17-8C18H29NO35 mg
  • Gabapentin Related Compound E
    A Gabapentin analogue.
    Katalog #CAS NummerSummenformelMenge
    sc-21155167950-95-2C9H14O410 mg
  • Gly-Pro-Glu
    Gly-Pro-Glu is a neuroprotective compound and the N-terminal tripeptide of IGF-1. Gly-Pro-Glu is neuroprotective after central administration in animal models of neurodegenerative processes, such as Huntington's, Parkinson's, Alzheimer's diseases, and varies acute brain injury animal models. The neuroprotective activity is not related to its affinity to glutamate receptor. Findings indicate that GPE mimics insulin-like growth factor I effects on the somatostatin system through a mechanism independent of β-amyloid clearance that involves modulation of calcium and glycogen synthase kinase 3β signaling.
    Katalog #CAS NummerSummenformelMenge
    sc-25285932302-76-4C12H19N3O610 mg
  • HR-73
    HR-73 is a splitomycin derivative and a SIRT1 inhibitor. HR-73 induces p53 hyperacetylation and decreases HIV transcription.
    Katalog #CAS NummerSummenformelMenge
    sc-255207959571-93-8C19H13BrO25 mg
  • Hypaconitine
    A diterpene alkaloid isolated from Aconiti Carmichaeli Praeparata which is a neuromuscular blocker.
    Katalog #CAS NummerSummenformelMenge
    sc-2057176900-87-4C33H45NO1010 mg/25 mg
  • IIK7
    IIK7 is a melatonin receptor agonist.
    Katalog #CAS NummerSummenformelMenge
    sc-300823n.n.C22H24N2O21 mg
  • iso-Talipexole, Dihydrochloride
    An analogue of Talipexole, an alpha 2-Adrenoceptor and dopamine D2-receptor agonist. Used as an antiparkinson reagent.
    Katalog #CAS NummerSummenformelMenge
    sc-280851n.n.C10H17Cl2N3S50 mg
  • IWP-2
    Inhibits Wnt production; useful in both regenerative medicine and anticancer efforts.
    Katalog #CAS NummerSummenformelMenge
    sc-252928686770-61-6C22H18N4O2S35 mg
  • JNJ 17203212
    Katalog #CAS NummerSummenformelMenge
    sc-300853n.n.C17H15F6N5O5 mg
  • JZL 184 hydrate
    Katalog #CAS NummerSummenformelMenge
    sc-300854n.n.C27H24N2O9•xH2O5 mg
  • K 185
    K 185 is a melatonin receptor antagonist.
    Katalog #CAS NummerSummenformelMenge
    sc-30085532223-82-8C24H28N2O21 mg
  • KH7
    A selective peptide inhibitor of soluble adenylyl cyclase and transepithelial Na+ current.
    Katalog #CAS NummerSummenformelMenge
    sc-252933330676-02-3C17H15BrN4O2S5 mg
  • (±)-L-Alliin
    Sulfur-containing amino acid that is converted to allicin by alliinase. Constituent of garlic (Alliumsativum).
    Katalog #CAS NummerSummenformelMenge
    sc-25293717795-26-5C6H11NO3S10 mg
  • L-BMAA hydrochloride
    A neurotoxic amino acid originally isolated from Cycas circinalis, which may cause Guam disease, a form of amyotrophic lateral sclerosis.
    Katalog #CAS NummerSummenformelMenge
    sc-25293816012-55-8C4H10N2O2•HCl10 mg
  • L-Kynurenine
    Key intermediate in the breakdown pathway of tryptophan.
    Katalog #CAS NummerSummenformelMenge
    sc-2026882922-83-0C10H12N2O350 mg
  • LED209 hydrate
    Sensor histidine kinase QseC is conserved in many bacterial pathogens. QseC upon presence of the bacterial aromatic signal autoinducer (AI-3) and/or host norepinephrine or epinephrine autophosphorylates and subsequently phosphorylates transcription factor QseB. These result in transcription of key virulence genes. LED209 antagonizes NE binding to QseC. It does not inhibits the pathogen growth but markedly inhibits virulence (for example Shiga toxin which is induced in EHEC by treatment with traditional antibiotics). LED209 does not interfere with mammalian adrenergic signaling, is orally bioavailable, and is non toxic to mice.
    Katalog #CAS NummerSummenformelMenge
    sc-252950245342-14-7 (anhydrous)C19H17N3O2S2•xH2O5 mg
  • lomerizine
    Katalog #CAS NummerSummenformelMenge
    sc-279282101477-55-8C27H30F2N2O31 g
  • Meta Fluoxetine Hydrochloride
    A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor derivative.
    Katalog #CAS NummerSummenformelMenge
    sc-21180379088-29-2C17H19ClF3NO25 mg
  • Methoprene acid
    Retinoic acid receptor (RXR) agonist used in gene regulation research. Analog of juvenile hormone, an insect growth hormone.
    Katalog #CAS NummerSummenformelMenge
    sc-25300753092-52-7C16H28O35 mg
  • MOCPAC
    Selective HDAC1 substrate (over HDAC6, class I over class II).
    Katalog #CAS NummerSummenformelMenge
    sc-253051787549-26-2C27H31N3O62 mg
  • Muscimol hydrobromide
    A potent but toxic structural analog of g-aminobutyric acid (GABA), with a zwitterionic structure that can cross the blood-brain barrier.
    Katalog #CAS NummerSummenformelMenge
    sc-21889418174-72-6C4H6N2O2•HBr10 mg
  • Myra A hydrochloride
    Myra A hydrochloride is a small molecule transcription factor inhibitor (c-Myc/Max DNA binding).
    Katalog #CAS NummerSummenformelMenge
    sc-301177n.n.C19H20N2O4•xHCl5 mg
  • N-(3X-Oxooctanoyl)-DL-homoserine lactone
    It is an autoinducer and potent antagonist. This stimulates the tra gene expression.
    Katalog #CAS NummerSummenformelMenge
    sc-257812106983-27-1C12H19NO425 mg
  • N-(4-Amino-2-chlorophenyl)phthalimide
    An anticonvulsant.
    Katalog #CAS NummerSummenformelMenge
    sc-25306819348-53-9C14H9ClN2O25 mg
  • N,N-Didesmethyl-O-desmethyl-(rac-Venlafaxine) Glucuronide
    A metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-219275n.n.C20H29NO81 mg
  • N,O-Didesmethyl-(rac-venlafaxine) Glucuronide Hydrochloride
    A metabolite of Venlafaxine which may at as a reuptake inhibitor of serotonin and noradrenaline.
    Katalog #CAS NummerSummenformelMenge
    sc-2080721021933-99-2C21H32ClNO81 mg
  • N2-Ethyl-2'-deoxyguanosine
    Adduct between DNA and acetaldehyde, the first metabolite of ethanol, that strongly blocks transcription by RNAPs (including RNAPII, both mammalian and yeast, E. coli RNAP, and T7 RNAP).
    Katalog #CAS NummerSummenformelMenge
    sc-253167101803-03-6C12H17N5O45 mg
  • Naphmethonium dibromide
    Very potent allosteric modulator of muscarinic receptors, selective for M2-receptors. Retards the dissociation of the antagonist N-methylscopolamine and exhibits positive cooperativity.
    Katalog #CAS NummerSummenformelMenge
    sc-202726505059-27-8C38H50Br2N4O45 mg
  • NIDA-41020
    NIDA-41020 is a CB1 cannabinoid receptor antagonist. NIDA-41020 is structurally similar to Rimonabant, which is currently in clinical development. NIDA-41020 is less lipophilic; developed at NIDA as a potential radioligand for CB1 receptors, Ki = 4.1 nM [in comparison AM 251, AM 281, SR 141716 (Rimonabant) have Ki of 0.6, 4.5 and 1.8 nM respectively].
    Katalog #CAS NummerSummenformelMenge
    sc-253189502486-89-7C23H24Cl2N4O210 mg
  • Norharmane hydrochloride
    Inhibitor of indoleamine 2,3-dioxygenase (IDO).
    Katalog #CAS NummerSummenformelMenge
    sc-2532017259-44-1C11H8N2•HCl100 mg
  • NSC 295642
    A potent inhibitor of cell migration.
    Katalog #CAS NummerSummenformelMenge
    sc-25320477111-29-6C30H28Cl2Cu2N6S45 mg
  • NVP-231
    Ceramide kinase presents an attractive target for drug development because of its involvement in cell growth and inflammation. CerK biology is still poorly understood thus discovery and availability of inhibitors will facilitate research at this area. NVP-231 is a newly discovered potent, specific and reversible CerK inhibitor that competitively inhibits binding of ceraminde to CerK.
    Katalog #CAS NummerSummenformelMenge
    sc-255397362003-83-6C25H25N3O2S5 mg
  • OPC 4392 Hydrochloride
    An analogue of Aripiprazole, a selective dopamine D2-receptor antagonist with dopamine autoreceptor agonist activity.
    Katalog #CAS NummerSummenformelMenge
    sc-219492n.n.C24H30ClN3O210 mg
  • OU749
    Gamma-glutamyl transpeptidase (GGT; aka gamma-glutamyl transferase) cleaves the gamma-glutamyl bond of glutathione, making extracellular glutathione available for intracellular use. Elevated intracellular glutathione contributes to resistance of tumors to chemotherapy and radiation. GGT is a therapeutic target for treatment-resistance cancers, as treatment with GGT inhibitors prior to chemotherapy or radiation could sensitize GGT-positive tumors to treatment by decreasing glutathione levels. Previously, all GGT inhibitors have been glutamine analogues, which are competitive for the gamma-glutamyl site. Due to high toxicity, these compounds cannot be used in the clinic. OU749 is the first non-glutamine GGT inhibitor. It is also non-competitive for the gamma-glutamyl site. OU749 inhibits human GGT in an enzyme assay and is much less toxic than other GGT inhibitors, including azaserine (glutamine analogue, Sigma catalog).
    Katalog #CAS NummerSummenformelMenge
    sc-253219519170-13-9C16H15N3O3S25 mg
  • Oxiracetam
    Nootropic agent shown to exhibit learning and memory improvement and cognitive function impairment prevention. Mechanism of action has not been quantified, but current theories suggest a modulation of glutamatergic and cholinergic neurotransmissions with the possibility of PKC involvement.
    Katalog #CAS NummerSummenformelMenge
    sc-26999662613-82-5C6H10N2O310 mg
  • Palmitoyl chloride
    Katalog #CAS NummerSummenformelMenge
    sc-281122112-67-4C16H31ClO100 ml/500 ml
  • Pergolide Sulfone
    A metabolite of Pergolide, a dopaminergic agonist that also decrease plasma prolactin concentrations. An antiparkinsonian agent.
    Katalog #CAS NummerSummenformelMenge
    sc-219576n.n.C19H26N2O2S1 mg
  • perospirone
    Katalog #CAS NummerSummenformelMenge
    sc-279959150915-41-6C23H30N4O2S1 g
  • Philanthotoxin 433 tris(trifluoroacetate) salt
    A polyamine-containing toxin that blocks NMDA-gated ion channels. Originally isolated from the venom of the wasp Philanthus triangulum.
    Katalog #CAS NummerSummenformelMenge
    sc-255421276684-27-6C23H41N5O3•3C2HF3O2777 µg
  • Phorbol
    A mammary tumor promoter used in experimental models.1
    Katalog #CAS NummerSummenformelMenge
    sc-25326717673-25-5C20H28O65 mg
  • Phorbol 12,13-dinonanoate 20-homovanillate
    This product is a resiniferatoxin-type vanilloid phorbol ester that displays capsaicin-like selectivity for the vanilloid receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-301544251362-87-5C47H68O111 mg/5 mg
  • PHPS1 sodium salt hydrate
    A phenylhydrazonopyrazolone sulfonate, which inhibits the phosphatase and cellular activities of Shp2.
    Katalog #CAS NummerSummenformelMenge
    sc-253272314291-83-3 (non-salt)C21H14N5O6SNa ·xH2O5 mg
  • Physostigmine
    An alkaloid that acts as a potent and reversible inhibitor of cholinesterase. Forms an enzyme complex with aetylcholinesterase (AChE).
    Katalog #CAS NummerSummenformelMenge
    sc-20276457-47-6C15H21N3O2100 mg
  • Phytoceramide C2
    This product has been shown to inhibit yeast growth, and to act as a ceramide-activated protein phosphatase (CAPP) activator.
    Katalog #CAS NummerSummenformelMenge
    sc-301547n.n.C20H41NO45 mg
  • pikamilone sodium salt
    Katalog #CAS NummerSummenformelMenge
    sc-27998362936-56-5C10H11NaN2O31 g
  • PNU-74654
    Inhibits the Wnt-βcatenin pathway by blocking the interaction between β-catenin and TCF (T cell factor). Also an anti-tumor agent.
    Katalog #CAS NummerSummenformelMenge
    sc-258020113906-27-7C19H16N2O35 mg
  • PP121
    PP121 has been shown to be anl inhibitor of tyrosine and phosphoinositide kinases. PP121 is the first inhibitor active on both Tyrosine kinases and the phosphatidylinositol-3-OH kinase (PI(3)K) family. The inhibitor is not effecting other serine-threonine protein kinases.
    Katalog #CAS NummerSummenformelMenge
    sc-3016051092788-83-4C17H17N75 mg
  • PP242 hydrate
    PP242 has been shown to be a potent and selective mTOR inhibitor. PP242 is a first selective inhibitor that targets ATP domain of mTOR.
    Katalog #CAS NummerSummenformelMenge
    sc-3016061092351-67-1 (anhydrous)C16H16N6O•xH2O5 mg/1 mg
  • pramiracetam
    Katalog #CAS NummerSummenformelMenge
    sc-28001668497-62-1C14H27N3O2200 mg
  • Psammaplin A
    An antibiotic, anti-tumor, DNA methyltransferase inhibitor. It is a bromotyrosine-derived, symmetrical conjugate of cystamine, which was first isolated from the Psammaplinaplysilla sponge. Impedes angiogenesis as well as bacterial and tumor cell growth. Inhibits the activities of several key enzymes in prokaryotic and eukaryotic systems including those involved in epigenetic control of gene expression, DNA replication, angiogensis, and microbial detoxification.
    Katalog #CAS NummerSummenformelMenge
    sc-258049110659-91-1C22H24Br2N4O6S21 mg/5 mg
  • QBP1
    QBP1 is an inhibitor of polyglutamine protein aggregation and cell death. QBP1 inhibits polyglutamine aggregation in COS-7 cells at a concentration of 25 µM, as shown by complete inhibition of thioredoxin-Q62 aggregation assayed by turbidity at 405 nm. QBP1 reduces cell death of these cells by 50% and increases median life span from 5.5-52 days in Drosophilla melanogaster that expresses the expanded polyglutamine; can be shortened to 8 amino acids (Trp-Ley-Trp-Trp-Pro-Gly-Ile-Phe) without the loss of ability to inhibit polyglutamine aggregation. Several inherited neurodegenerative diseases, Huntington's dentatorubral pallidoluysian atrophy, spinobulbar muscular atrophy, and spinocerebellar ataxia are caused by the expanded CAG repeats in the coding region of the gene, leading to accumulation of polyglutamine.
    Katalog #CAS NummerSummenformelMenge
    sc-301629274914-75-9C72H90N16O16•xC2HF3O21 mg
  • quetiapine
    Katalog #CAS NummerSummenformelMenge
    sc-280046111974-69-7C21H25N3O2S2.5 mg
  • R-Venlafaxine
    An isomer of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine with reported weak inhibitory effect on dopamine reuptake.
    Katalog #CAS NummerSummenformelMenge
    sc-20820993413-46-8C17H27NO25 mg
  • R-Venlafaxine-di-p-toluoyl-D-tartrate Salt
    A (-)-Venlafaxine derivative which may act as a reuptake inhibitor of serotonin and noradrenaline.
    Katalog #CAS NummerSummenformelMenge
    sc-208210272788-00-8C37H45NO105 mg
  • (R)-Fluoxetine Hydrochloride
    A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-208240114247-09-5C17H19ClF3NO2.5 mg
  • (R)-Fluoxetine-d5 Hydrochloride
    A deuterium-labeled 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-219754114247-09-5 (unlabeled)C17H14D5ClF3NO1 mg
  • rac O-Desmethyl Venlafaxine 2,3,4-Tri-O-acetyl-β-D-glucuronide Methyl Ester
    A metabolic intermediate of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
    Katalog #CAS NummerSummenformelMenge
    sc-219870n.n.C29H41NO111 mg
  • rac O-Desmethyl Venlafaxine β-D-Glucuronide
    A metabolite of the serotonin and noradrenalin reuptake inhibitor, Venlafaxine.
    Katalog #CAS NummerSummenformelMenge
    sc-2082791021933-98-1C22H33NO81 mg
  • rac α-Methyl DOPA
    An antihypertensive agent.
    Katalog #CAS NummerSummenformelMenge
    sc-21987255-40-3C10H13NO42.5 mg
  • Retrorsine
    A pyrrolizidine alkaloid that contains antimitotic, cytotoxic, mutagenic properties. Retrorsine activation results after metabolism by cytochrome P450.
    Katalog #CAS NummerSummenformelMenge
    sc-215805480-54-6C18H25NO6100 mg/500 mg
  • Rizatriptan Benzoate
    A selective serotonin 5-HTID receptor agonist which is structurally derived from tryptamine.
    Katalog #CAS NummerSummenformelMenge
    sc-219983145202-66-0C22H25N5O210 mg
  • RM-65
    Compound is of interest to Broad researchers studying chromatin modifying compounds (e.g. BIX-01294). Cell (HepG2) permeable. Not selective between human and fungal PRMT, unlike AMI-1 (CLIC 2931). Paper tests diastereomeric mixture, yet models the R,R isomer. Compound does not hit lysine methyltransferase SET7/9.: Compound is of interest to Broad researchers studying chromatin modifying compounds (e.g. BIX-01294). Cell (HepG2) permeable.
    Katalog #CAS NummerSummenformelMenge
    sc-255522947508-41-0C34H32N2O4S25 mg
  • S-(+)-O-Desmethyl Venlafaxine
    A metabolite of the neuroamine inhibitor Venlafaxine. May potentially inhibit reuptake of serotonin and norepinephrine with reported weak inhibitory effect on dopamine reuptake.
    Katalog #CAS NummerSummenformelMenge
    sc-208319142761-12-4C16H25NO25 mg
  • S-Venlafaxine
    An isomer of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine with reported weak inhibitory effect on dopamine reuptake.
    Katalog #CAS NummerSummenformelMenge
    sc-20833093413-44-6C17H27NO25 mg
  • S-Venlafaxine-di-p-toluoyl-L-tartrate Salt
    A (+)-Venlafaxine derivative that may act as a serotonin and noradrenaline reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-208331272788-02-0C37H45NO105 mg
  • (S)-Citalopram Oxalate
    A derivative of Citalopram and a potential selective inhibitor of the 5-hydroxytryptamine transporter (serotonin).
    Katalog #CAS NummerSummenformelMenge
    sc-208365219861-08-2C22H23FN2O510 mg/100 mg
  • (S)-Fluoxetine Hydrochloride
    A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-208367114247-06-2C17H19ClF3NO2.5 mg
  • (S)-Fluoxetine-d5 Hydrochloride
    A deuterium-labeled 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-220069114247-06-2C17H14D5ClF3NO1 mg
  • salicylsalicylic acid
    Katalog #CAS NummerSummenformelMenge
    sc-281146552-94-3C14H10O525 g
  • Sarcosine
    Endogenous inhibitor of GlyT1 that displays antipsychotic activity. Potentiates the action of glycine on the NMDA glycine binding site.
    Katalog #CAS NummerSummenformelMenge
    sc-204262107-97-1C3H7NO250 mg
  • Sazetidine A dihydrochloride
    Novel ligand of nACh receptors. Potent agonist of native and recombinant α4β2 nACHRs.
    Katalog #CAS NummerSummenformelMenge
    sc-203256820231-95-6C15H20N2O2 ·2HCl1 mg
  • tardan
    Katalog #CAS NummerSummenformelMenge
    sc-280109113-59-7C18H18ClNS5 mg
  • Terodiline hydrochloride
    Terodiline hydrochloride is a non-selective calcium channel antagonist that has anticholinergic and vasodilatory activity.
    Katalog #CAS NummerSummenformelMenge
    sc-2536247082-21-5C20H27N··HCl5 mg
  • Thapsigargicin
    Mobilizes intracellular Ca2+.
    Katalog #CAS NummerSummenformelMenge
    sc-25369267526-94-7C32H46O121 mg
  • TPBM
    An effective inhibitor of the alpha estrogen receptor via blockage of the ER-alpha dinging to consensus estrogen response element DNA. Displays minimal cellular toxicity and no effect on estrogen-independent cell growth.
    Katalog #CAS NummerSummenformelMenge
    sc-2726206466-43-9C15H16N4O2S5 mg
  • Tryptamine hydrochloride
    The prototypical indole of the Tryptamine family. Described to produce vasocontriction, potentially through the TAAR-1 receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-202843343-94-2C10H12N2 ·HCl5 g
  • Vacuolin-1
    Alters the morphology of lysosomes, but not cell resealing.
    Katalog #CAS NummerSummenformelMenge
    sc-216045351986-85-1C26H24IN7O1 mg
  • Valpromide
    A derivative of Valproic acid (VPA) and is employed as an antiepileptic drug. It is hydrolyzed quickly to VPA in vivo, but has intrinsic anticonvulsant activity.
    Katalog #CAS NummerSummenformelMenge
    sc-2538222430-27-5C8H17NO10 mg
  • Vanillic acid diethylamide
    A stimulant reactive to the CNS and respiratory.
    Katalog #CAS NummerSummenformelMenge
    sc-253824304-84-7C12H17NO310 g
  • Vecuronium Bromide
    A nonpolarizing neuromuscular relaxant.
    Katalog #CAS NummerSummenformelMenge
    sc-20588050700-72-6C34H57BrN2O410 mg/50 mg
  • Venlafaxine Cyclic Impurity H
    An impurity of Venlafaxine, the neuroamine reuptake inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-21315193413-70-8C17H25NO21 mg
  • Venlafaxine Hydrochloride
    A reuptake inhibitor of neurotransmitters such as serotonin and norepinephrine with reported weak inhibitory effect on dopamine reuptake.
    Katalog #CAS NummerSummenformelMenge
    sc-20110299300-78-4C17H27NO2 ·HCl10 mg/50 mg
  • ω-Agatoxin IVA
    This toxin is found in the venom of the funnel web spider, Agelenopsis aptera. It is a potent, selective blocker of mammalian P-type voltage-dependent calcium channels.
    Katalog #CAS NummerSummenformelMenge
    sc-302015145017-83-0C217H360N68O60S10100 µg
  • Zonisamide sodium salt
    Zonisamide sodium salt is an anti-epileptic, that is effective in various animal epilepsy models and humans with both partial and generalized epileptic seizures. Zonisamide sodium salt scavenges nitric oxide (NO) as well.
    Katalog #CAS NummerSummenformelMenge
    sc-25385768291-98-5C8H7N2NaO3S10 mg