| | 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 Nummer | Summenformel | Menge |
|---|
| sc-251783 | 166100-39-6 | C23H38NOF | 5 mg |
- (2S,3S)-3-Methylglutamic Acid Hydrochloride Salt
A potent agonist for kainate receptors. Is highly selective.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-216336 | n.n. | C6H12ClNO4 | 5 mg |
- (2S,3S)-trans-3-(Carboxymethyl)-azetidine-2-acetic Acid
Effective inhibitor of sodium dependent glu uptake and KA receptor agonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-206577 | 185387-36-4 | C6H9NO4 | 5 mg |
- (-)-2β-Carbomethoxy-3β-(4-iodophenyl)nortropane
This compound inhibits the serotonin (5-HT) transporter.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-206587 | 136794-87-1 | C15H18INO2 | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-216586 | n.n. | C12H16ClNO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-216587 | n.n. | C13H15NO3 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-216588 | 153153-60-7 | C13H15NO3 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-216589 | n.n. | C13H18ClNO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-216590 | n.n. | C13H18ClNO2 | 5 mg |
- 4-Benzoylpiperidine Hydrochloride
Synthetic intermediate in the preparation of CNS depressants.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-216783 | 25519-80-6 | C12H16ClNO | 100 mg |
- 4-Formylphenyl b-D-allopyranoside
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-277405 | 80154-34-3 | C13H16O7 | 1 g/5 g |
- 5-Chloro Bifeprunox Mesylate
Used as an antipsychotic compound. Activates the serotonin 5-hydroxytryptamine (5-HT)1A receptor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-217164 | n.n. | C25H26ClN3O5S | 25 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 Nummer | Summenformel | Menge |
|---|
| sc-252267 | 10356-76-0 | C9H12FN3O4 | 5 mg |
- 6-Iodonordihydrocapsaicin
TRPV1 (V1) vanilloid receptor antagonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252297 | 859171-97-4 | C17H26INO3 | 5 mg |
- 6-Nitro-7-sulfamoylbenzo[f]quinoxaline-2,3-dione, Disodium Salt
A discriminating and potent antagonist for AMPA binding sites.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-217370 | 479347-86-9 | C12H6N4Na2O6S | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-207210 | 113108-86-4 | C24H24N2O5 | 100 mg |
- α-Methadol-d3
An analgesic, labeled reduction product of Methadone.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-220441 | n.n. | C21H26D3NO | 1 mg |
- AC-93253 iodide
A potent, cell permeable, subtype selective RAR agonist. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-257044 | 108527-83-9 | C23H25N2SI | 10 mg/50 mg |
- Angiotensin II, Human
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-363643 | 4474-91-3 | n.n. | 1 mg/5 mg |
- Arachidonyl-2'-chloroethylamide hydrate
A potent and selective neuronal CB1 cannabinoid receptor agonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252384 | 220556-69-4 (anhydrous) | C22H36ClNO | 25 mg |
- BATCP
HDAC 6 selective substrate (over HDAC 1, Class II over Class I). | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252405 | 787549-23-9 | C23H28F3N3O6 | 2 mg |
- BAY U6751 hydrate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-257117 | 114290-51-6 (anhydrous) | C20H20ClNNa2O6•xH2O | 5 mg |
- Benztropine mesylate
A derivative of Atropine and an antagonist of the mAChR which also demonstrates anti-nicotinic action at the nAChR.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202495 | 132-17-2 | C21H25NO ·CH4SO3 ·H2O | 1 g/5 g |
- Bretazenil
A benzodiazepine partial agonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252512 | 84379-13-5 | C19H20N3O3Br | 5 mg |
- Carbasalate calcium
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-278809 | 5749-67-7 | C19H18CaO9N2 | 20 mg |
- Citral
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252620 | 5392-40-5 | C10H16O | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-255032 | 357649-93-5 | C14H14ClN3S | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-257276 | 104914-40-1 | C60H104N20O15S | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-252653 | 321661-62-5 | C18H26O5 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-252656 | 1721-51-3 | C29H44O2 | 10 mg |
- D,L N-Desmethyl Venlafaxine
A metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-207483 | 149289-30-5 | C16H25NO2 | 5 mg |
- D,L N,O-Didesmethyl Venlafaxine
A metabolite of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-207484 | 135308-74-6 | C15H23NO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-218040 | n.n. | C15H20D3NO2 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-218052 | n.n. | C16H22D3NO2 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-218053 | n.n. | C15H17D6NO2 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-218054 | n.n. | C24H33NO3 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-211199 | 135308-76-8 | C14H21NO2•HCl | 2.5 mg |
- D,L-O-Desmethyl Venlafaxine
A metabolite of the serotonin and noradrenaline reuptake inhibitor Venlafaxine.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-207494 | 93413-62-8 | C16H25NO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-218055 | n.n. | C16H19D6NO2 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-202570 | 219982-12-4 | C30H40N8O6S | 500 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 Nummer | Summenformel | Menge |
|---|
| sc-255067 | 302953-06-6 | C15H8Cl2O3 | 10 mg |
- Dehydro Venlafaxine
A degradation product of the neuroamine reuptake inhibitor Venlafaxine.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-211230 | 93413-57-1 | C17H25NO•HCl | 1 mg |
- Deoxy Venlafaxine
An impurity of Venlafaxine, the reuptake inhibitor of neuroamines such as serotonin and norepinephrine.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-218117 | n.n. | C17H27NO | 1 mg |
- Desethylene Aripiprazole
A derivative of Aripiprazole.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-218138 | 1216394-63-6 | C21H25Cl2N3O2 | 1 mg |
- Dimebolin
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-278972 | 3613-73-8 | C21H25N3 | 25 mg |
- Dimethyl Cabergoline
An analogue of Cabergoline.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-218234 | n.n. | C28H41N5O2 | 10 mg |
- DM 235
Potent nootropic agent.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300499 | 314728-85-3 | C14H18N2O2 | 5 mg |
- Donepezil
A noncompetitive acetylcholineesterase inhibitor, which can readily cross the blood brain barrier and increases the concentration of cortical acetylcholine.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279006 | 120014-06-4 | C24H29NO3 | 10 mg |
- Donepezil Hydrochloride
A noncompetitive acetylcholineesterase inhibitor, which can readily cross the blood brain barrier and increases the concentration of cortical acetylcholine.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-218265 | 120011-70-3 | C24H30ClNO3 | 10 mg |
- Doxapram
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279007 | 309-29-5 | C24H30N2O2 | 5 mg |
- Doxapram hydrochloride
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279008 | 113-07-5 | C24H31ClN2O2 | 5 mg |
- Droxidopa
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279010 | 23651-95-8 | C9H11NO5 | 100 mg |
- Duloxetine
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279011 | 116539-59-4 | C18H19NOS | 10 mg |
- (-)-Eseroline fumarate
Metabolite of physostigmine (eserine). Potent analgesic.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202155 | 104015-29-4 | C13H18N2O ·C4H4O4 | 10 mg/50 mg |
- Ethyl gallate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-239928 | 831-61-8 | C9H10O5 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-252819 | 102676-31-3 | C14H13N3 ·HCl | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-300691 | 108409-83-2 | C13H10Cl2N2O4S | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-300694 | n.n. | C23H24FN5O2 ·HCl ·xH2O | 5 mg |
- Fluoxetine
A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279166 | 54910-89-3 | C17H18F3NO | 500 mg |
- Fluoxetine HCl
A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201125 | 56296-78-7 | C17H18F3NO•HCl | 50 mg/250 mg |
- Fluoxetine-d5 Hydrochloride
A deuterium-labeled 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-218509 | 56296-78-7 (unlabeled) | C17H14D5ClF3NO | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-205700 | 69-23-8 | C22H26F3N3OS | 1 g/5 g |
- Fluphenazine decanoate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279167 | 5002-47-1 | C32H44F3N3O2S | 10 mg |
- fluphenazine enanthate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279168 | 2746-81-8 | C29H38F3N3O2S | 10 mg |
- Gabapentin Related Compound B
A Gabapentin analogue used in the treatment of neurological disorders.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-211550 | 133481-09-1 | C9H13NO2 | 2.5 mg |
- Gabapentin Related Compound D
A Gabapentin analogue.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-218552 | 1076198-17-8 | C18H29NO3 | 5 mg |
- Gabapentin Related Compound E
A Gabapentin analogue.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-211551 | 67950-95-2 | C9H14O4 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-252859 | 32302-76-4 | C12H19N3O6 | 10 mg |
- HR-73
HR-73 is a splitomycin derivative and a SIRT1 inhibitor. HR-73 induces p53 hyperacetylation and decreases HIV transcription.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-255207 | 959571-93-8 | C19H13BrO2 | 5 mg |
- Hypaconitine
A diterpene alkaloid isolated from Aconiti Carmichaeli Praeparata which is a neuromuscular blocker.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-205717 | 6900-87-4 | C33H45NO10 | 10 mg/25 mg |
- IIK7
IIK7 is a melatonin receptor agonist.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300823 | n.n. | C22H24N2O2 | 1 mg |
- iso-Talipexole, Dihydrochloride
An analogue of Talipexole, an alpha 2-Adrenoceptor and dopamine D2-receptor agonist. Used as an antiparkinson reagent.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-280851 | n.n. | C10H17Cl2N3S | 50 mg |
- IWP-2
Inhibits Wnt production; useful in both regenerative medicine and anticancer efforts.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252928 | 686770-61-6 | C22H18N4O2S3 | 5 mg |
- JNJ 17203212
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300853 | n.n. | C17H15F6N5O | 5 mg |
- JZL 184 hydrate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300854 | n.n. | C27H24N2O9•xH2O | 5 mg |
- K 185
K 185 is a melatonin receptor antagonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300855 | 32223-82-8 | C24H28N2O2 | 1 mg |
- KH7
A selective peptide inhibitor of soluble adenylyl cyclase and transepithelial Na+ current.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252933 | 330676-02-3 | C17H15BrN4O2S | 5 mg |
- (±)-L-Alliin
Sulfur-containing amino acid that is converted to allicin by alliinase.
Constituent of garlic (Alliumsativum).| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-252937 | 17795-26-5 | C6H11NO3S | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-252938 | 16012-55-8 | C4H10N2O2•HCl | 10 mg |
- L-Kynurenine
Key intermediate in the breakdown pathway of tryptophan.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202688 | 2922-83-0 | C10H12N2O3 | 50 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 Nummer | Summenformel | Menge |
|---|
| sc-252950 | 245342-14-7 (anhydrous) | C19H17N3O2S2•xH2O | 5 mg |
- lomerizine
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279282 | 101477-55-8 | C27H30F2N2O3 | 1 g |
- Meta Fluoxetine Hydrochloride
A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor derivative.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-211803 | 79088-29-2 | C17H19ClF3NO | 25 mg |
- Methoprene acid
Retinoic acid receptor (RXR) agonist used in gene regulation research. Analog of juvenile hormone, an insect growth hormone.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253007 | 53092-52-7 | C16H28O3 | 5 mg |
- MOCPAC
Selective HDAC1 substrate (over HDAC6, class I over class II).| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253051 | 787549-26-2 | C27H31N3O6 | 2 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 Nummer | Summenformel | Menge |
|---|
| sc-218894 | 18174-72-6 | C4H6N2O2•HBr | 10 mg |
- Myra A hydrochloride
Myra A hydrochloride is a small molecule transcription factor inhibitor (c-Myc/Max DNA binding).
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-301177 | n.n. | C19H20N2O4•xHCl | 5 mg |
- N-(3X-Oxooctanoyl)-DL-homoserine lactone
It is an autoinducer and potent antagonist. This stimulates the tra gene expression. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-257812 | 106983-27-1 | C12H19NO4 | 25 mg |
- N-(4-Amino-2-chlorophenyl)phthalimide
An anticonvulsant.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253068 | 19348-53-9 | C14H9ClN2O2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-219275 | n.n. | C20H29NO8 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-208072 | 1021933-99-2 | C21H32ClNO8 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-253167 | 101803-03-6 | C12H17N5O4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-202726 | 505059-27-8 | C38H50Br2N4O4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-253189 | 502486-89-7 | C23H24Cl2N4O2 | 10 mg |
- Norharmane hydrochloride
Inhibitor of indoleamine 2,3-dioxygenase (IDO).| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253201 | 7259-44-1 | C11H8N2•HCl | 100 mg |
- NSC 295642
A potent inhibitor of cell migration. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253204 | 77111-29-6 | C30H28Cl2Cu2N6S4 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-255397 | 362003-83-6 | C25H25N3O2S | 5 mg |
- OPC 4392 Hydrochloride
An analogue of Aripiprazole, a selective dopamine D2-receptor antagonist with dopamine autoreceptor agonist activity.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-219492 | n.n. | C24H30ClN3O2 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-253219 | 519170-13-9 | C16H15N3O3S2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-269996 | 62613-82-5 | C6H10N2O3 | 10 mg |
- Palmitoyl chloride
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-281122 | 112-67-4 | C16H31ClO | 100 ml/500 ml |
- Pergolide Sulfone
A metabolite of Pergolide, a dopaminergic agonist that also decrease plasma prolactin concentrations. An antiparkinsonian agent.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-219576 | n.n. | C19H26N2O2S | 1 mg |
- perospirone
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279959 | 150915-41-6 | C23H30N4O2S | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-255421 | 276684-27-6 | C23H41N5O3•3C2HF3O2 | 777 µg |
- Phorbol
A mammary tumor promoter used in experimental models.1| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253267 | 17673-25-5 | C20H28O6 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-301544 | 251362-87-5 | C47H68O11 | 1 mg/5 mg |
- PHPS1 sodium salt hydrate
A phenylhydrazonopyrazolone sulfonate, which inhibits the phosphatase and cellular activities of Shp2.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253272 | 314291-83-3 (non-salt) | C21H14N5O6SNa ·xH2O | 5 mg |
- Physostigmine
An alkaloid that acts as a potent and reversible inhibitor of cholinesterase. Forms an enzyme complex with aetylcholinesterase (AChE).| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202764 | 57-47-6 | C15H21N3O2 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-301547 | n.n. | C20H41NO4 | 5 mg |
- pikamilone sodium salt
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-279983 | 62936-56-5 | C10H11NaN2O3 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-258020 | 113906-27-7 | C19H16N2O3 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-301605 | 1092788-83-4 | C17H17N7 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-301606 | 1092351-67-1 (anhydrous) | C16H16N6O•xH2O | 5 mg/1 mg |
- pramiracetam
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-280016 | 68497-62-1 | C14H27N3O2 | 200 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 Nummer | Summenformel | Menge |
|---|
| sc-258049 | 110659-91-1 | C22H24Br2N4O6S2 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-301629 | 274914-75-9 | C72H90N16O16•xC2HF3O2 | 1 mg |
- quetiapine
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-280046 | 111974-69-7 | C21H25N3O2S | 2.5 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 Nummer | Summenformel | Menge |
|---|
| sc-208209 | 93413-46-8 | C17H27NO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-208210 | 272788-00-8 | C37H45NO10 | 5 mg |
- (R)-Fluoxetine Hydrochloride
A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-208240 | 114247-09-5 | C17H19ClF3NO | 2.5 mg |
- (R)-Fluoxetine-d5 Hydrochloride
A deuterium-labeled 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-219754 | 114247-09-5 (unlabeled) | C17H14D5ClF3NO | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-219870 | n.n. | C29H41NO11 | 1 mg |
- rac O-Desmethyl Venlafaxine β-D-Glucuronide
A metabolite of the serotonin and noradrenalin reuptake inhibitor, Venlafaxine.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-208279 | 1021933-98-1 | C22H33NO8 | 1 mg |
- rac α-Methyl DOPA
An antihypertensive agent.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-219872 | 55-40-3 | C10H13NO4 | 2.5 mg |
- Retrorsine
A pyrrolizidine alkaloid that contains antimitotic, cytotoxic, mutagenic properties. Retrorsine activation results after metabolism by cytochrome P450.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-215805 | 480-54-6 | C18H25NO6 | 100 mg/500 mg |
- Rizatriptan Benzoate
A selective serotonin 5-HTID receptor agonist which is structurally derived from tryptamine.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-219983 | 145202-66-0 | C22H25N5O2 | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-255522 | 947508-41-0 | C34H32N2O4S2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-208319 | 142761-12-4 | C16H25NO2 | 5 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 Nummer | Summenformel | Menge |
|---|
| sc-208330 | 93413-44-6 | C17H27NO2 | 5 mg |
- S-Venlafaxine-di-p-toluoyl-L-tartrate Salt
A (+)-Venlafaxine derivative that may act as a serotonin and noradrenaline reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-208331 | 272788-02-0 | C37H45NO10 | 5 mg |
- (S)-Citalopram Oxalate
A derivative of Citalopram and a potential selective inhibitor of the 5-hydroxytryptamine transporter (serotonin).| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-208365 | 219861-08-2 | C22H23FN2O5 | 10 mg/100 mg |
- (S)-Fluoxetine Hydrochloride
A 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-208367 | 114247-06-2 | C17H19ClF3NO | 2.5 mg |
- (S)-Fluoxetine-d5 Hydrochloride
A deuterium-labeled 5-hydroxytryptamine (serotonin, 5-HT) reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-220069 | 114247-06-2 | C17H14D5ClF3NO | 1 mg |
- salicylsalicylic acid
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-281146 | 552-94-3 | C14H10O5 | 25 g |
- Sarcosine
Endogenous inhibitor of GlyT1 that displays antipsychotic activity. Potentiates the action of glycine on the NMDA glycine binding site.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204262 | 107-97-1 | C3H7NO2 | 50 mg |
- Sazetidine A dihydrochloride
Novel ligand of nACh receptors. Potent agonist of native and recombinant
α4β2 nACHRs.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203256 | 820231-95-6 | C15H20N2O2 ·2HCl | 1 mg |
- tardan
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-280109 | 113-59-7 | C18H18ClNS | 5 mg |
- Terodiline hydrochloride
Terodiline hydrochloride is a non-selective calcium channel antagonist that has anticholinergic and vasodilatory activity.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253624 | 7082-21-5 | C20H27N··HCl | 5 mg |
- Thapsigargicin
Mobilizes intracellular Ca2+.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253692 | 67526-94-7 | C32H46O12 | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-272620 | 6466-43-9 | C15H16N4O2S | 5 mg |
- Tryptamine hydrochloride
The prototypical indole of the Tryptamine family. Described to produce vasocontriction, potentially through the TAAR-1 receptor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202843 | 343-94-2 | C10H12N2 ·HCl | 5 g |
- Vacuolin-1
Alters the morphology of lysosomes, but not cell resealing.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-216045 | 351986-85-1 | C26H24IN7O | 1 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 Nummer | Summenformel | Menge |
|---|
| sc-253822 | 2430-27-5 | C8H17NO | 10 mg |
- Vanillic acid diethylamide
A stimulant reactive to the CNS and respiratory.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-253824 | 304-84-7 | C12H17NO3 | 10 g |
- Vecuronium Bromide
A nonpolarizing neuromuscular relaxant. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-205880 | 50700-72-6 | C34H57BrN2O4 | 10 mg/50 mg |
- Venlafaxine Cyclic Impurity H
An impurity of Venlafaxine, the neuroamine reuptake inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-213151 | 93413-70-8 | C17H25NO2 | 1 mg |
- Venlafaxine Hydrochloride
A reuptake inhibitor of neurotransmitters such as serotonin and norepinephrine with reported weak inhibitory effect on dopamine reuptake.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-201102 | 99300-78-4 | C17H27NO2 ·HCl | 10 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 Nummer | Summenformel | Menge |
|---|
| sc-302015 | 145017-83-0 | C217H360N68O60S10 | 100 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 Nummer | Summenformel | Menge |
|---|
| sc-253857 | 68291-98-5 | C8H7N2NaO3S | 10 mg |
|