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Cas Index 1

• 1312005-62-1 | YF-2 hydrochloride (Catalog# : 193151)YF-2 hydrochloride is a highly selective, blood-brain-barrier permeable histone acety
• 1364488-67-4 | YH239-EE (Catalog# : 192213)YH239-EE is a highly potent p53-MDM2 antagonist.
• 199433-58-4 | Y-39983 free base (Catalog# : 185172)Y-39983 (free base), also known as Y-33075, is a potent and selective inhibitor of RO
• 1339058-04-6 | YL-0919 (Catalog# : 18578)YL-0919 is a novel 5-HT1A receptor agonist and selective serotonin reuptake inhibitor.
• 1943733-16-1 | YU-238259 (Catalog# : 1710139)YU238259 exhibits potent synthetic lethality in the setting of DNA damage response an
• 143984-17-2 | Y-29794 Tosylate (Catalog# : 1791521)Y-29794 Tosylate is an orally active, potent and specific non-peptide prolyl endopept
• 173897-44-4 | Y-39983 HCl (Catalog# : 17021305)Y-39983 is a selective rho-associated protein kinase(ROCK) inhibitor with an IC50 o
• 1236188-16-1 | 740 Y-P (PDGFR 740Y-P) (Catalog# : 17021302)740 Y-P is cell-permeable phosphopeptide activator ofPI3K. The PDGFR 740Y-P peptide s
• 163769-88-8 | YM-90709 (Catalog# : 16122849)YM-90709 is an interleukin-5 receptor antagonist. YM-90709 inhibits the binding of IL
• 129184-48-1 | Y-29794 Tosylate (Catalog# : 16122848)Y-29794 Tosylate is an orally active, potent and specific non-peptide prolyl endopept
• 1346753-00-1 | YHO-13351 (Catalog# : 6111512)YHO-13351 is the water-soluble prodrug of YHO-13177, which is a potent and specific i
• 1273323-67-3 | YLF-466D (Catalog# : 611813)YLF-466D is an allosteric AMPK activator.YLF466D activated recombinant human 111, 211
• 146986-50-7 | Y27632(free base) (Catalog# : 16070918)Y27632 is a selective ROCK inhibitor, which inhibits ET-1-induced increases in natriu
• 1370003-76-1 | YK11 (Catalog# : 030910)Coming soon!
• 129830-38-2 | Y-27632 dihydrochloride (Catalog# : 010421)Y-27632 2Hcl is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM, exhibits &g
• 1802650-31-2 | ZY-444 (Catalog# : 26A020)ZY-444 is an anti-cancer agent by inhibiting PC ( pyruvate carboxylase ) activity.
• 1016340-64-9 | Z57346765 (Catalog# : 25191)Z57346765 is a PGK1-specific inhibitor that reduces the activity of metabolic enzymes
• 167354-41-8 | Zosuquidar ( LY-335979 ) (Catalog# : 25127)Zosuquidar is a potent modulator of P-glycoprotein-mediated multi-drug resistance.
• 1640282-42-3 | Zunsemetinib (Catalog# : 24012)Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr
• 1606974-33-7 | Zatolmilast (Catalog# : 20651)Zatolmilast is a phosphodiesterase IV inhibitor.
• 1851412-93-5 | Zavondemstat (Catalog# : 20610)Zavondemstat is a KDM4 inhibitor with potential as an antineoplastic agent.
• 1438280-73-9 | 1Z105 (Catalog# : 20567)1Z105 is a TLR4/MD2 ligand, significantly reducing the IL-6 secretion by subsequent c
• 1211825-25-0 | ZINC40099027 (ZN27) (Catalog# : 20513)ZINC40099027 (ZN27) is a specific focal adhesion kinase (FAK) activator that promotes
• 1661854-97-2 | Zipalertinib (Catalog# : 20317)Zipalertinib, also known as TAS6417, CLN-081, is a Novel EGFR Inhibitor Targeting Exo
• 1713240-67-5 | Zegocractin ( CM-4620 ) (Catalog# : 204504)Zegocractin (CM-4620, Auxora(TM)) is a small-molecule inhibitor of the calcium releas
• 1802632-22-9 | Zervimesine ( CT1812 ) (Catalog# : 193283)CT-1812 is a first-in-class, orally available sigma-2/PGRMC1 antagonist (alpha beta o
• 1080028-80-3 | Zamicastat (Catalog# : 189271)Zamicastat is a potent and selective dopamine β-mono-oxygenase inhibitor.
• 101975-10-4 | Zardaverine (Catalog# : 185186)Zardaverine is a Phosphodiesterase 3/4 inhibitor.
• 1691249-45-2 | Zanubrutinib (Catalog# : 18577)Zanubrutinib, aslo known as BGB-3111, is a potent and highly selective small molecule
• 139180-30-6 | ZM241385 (Catalog# : 17022714)ZM241385 is an adenosine A2A-receptor antagonist. ZM241385 enhances neuronal survival