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Cas Index 1

• 178606-66-1 | U-104 (Catalog# : 010440)U-104 is a potent carbonic anhydrase (CA) inhibitor for CA IX and CA XII with Ki of 4
• 1431612-23-5 | UNC1999 (Catalog# : 111901)UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 wit
• 112648-68-7 | U73122 (Catalog# : 102201)U73122 is a potent phospholipase C (PLC) inhibitor, which reduces agonist-induced Ca2
• 1197196-48-7 | UNC0224 (Catalog# : 82404)UNC0224 is a potent and selective G9a inhibitor with IC50 of 15 nM in the G9a Thioglo
• 1255580-76-7 | UNC0638 (Catalog# : 82403)UNC0638 is an inhibitor of G9a and GLP with excellent potency and selectivity over a
• 1429881-91-3 | UNC-2025 (Catalog# : 72807)UNC-2025 is a novel potent and highly orally bioavailable Mer/FLT3 dual inhibitor, ca
• 1493694-70-4 | UNC2250 (Catalog# : 52738)UNC2250 is a phosphorylation of endogenous Mer inhibitor with an IC50 of 9.8 nM and b
• 1320288-17-2 | UNC0646 (Catalog# : 52710)UNC0646 is a potent and selective G9a inhibitor with IC50 of 6 nM.
• 1320288-19-4 | UNC 0631 (Catalog# : 52709)UNC 0631 is a potent G9a inhibitor with IC50 value of 4 nM.
• 1238673-32-9 | UNC0321 (Catalog# : 52708)UNC0321 is a potent and selective G9a inhibitor with Ki of 63 pM, UNC0321 is the firs
• 1493764-08-1 | UNC2881 (Catalog# : 52574)UNC2881 is a potent and specific Mer kinase inhibitor; inhibits steady-state Mer kina
• 1430089-64-7 | UNC0064-12 (Catalog# : 52214)UNC0064-12 is useful chemical agent for research use.
• 1620401-82-2 | UNC0379 (Catalog# : 51801)UNC0379 is a selective, substrate competitive inhibitor ofN-lysine methyltransferase
• 1383716-40-2 | Vps34-PIK-III (Catalog# : 26A029)Vps34-PIK-III is a selective inhibitor of VPS34 that binds a unique hydrophobic pocke
• 1868065-21-7 | Vicadrostat (Catalog# : 25142)Vicadrostat is an aldosterone synthase inhibitor.
• 1628606-05-2 | Vimseltinib free base (Catalog# : 25047)Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
• 1644545-52-7 | Vorasidenib (Catalog# : 20631)Vorasidenib, also known as AG-881, is a potent and selective orally available inhibit
• 1809336-93-3 | Valemetostat tosylayte (Catalog# : 20612)Valemetostat, also known as DS-3201 is a potent, selective and orally active EZH1/2 i
• 1062444-54-5 | 1V209 (Catalog# : 20566)1V209, also known as TLR7 agonist T7, is a novel Toll-like receptor 7 (TLR7) agonist,
• 1629063-78-0 | Venglustat malate (Catalog# : 20547)Venglustat, also known as Ibiglustat, GZ402671, GZ-452; Genz-682452 and SAR402671, is
• 1321924-70-2 | VTX-27 (Catalog# : G20377)VTX-27 is a novel potent and selective PKCθ inhibitor.
• 1401090-53-6 | Venglustat ( ibiglustat ) (Catalog# : 822223)Venglustat(ibiglustat)is an oral inhibitor of an enzyme called glucosylceramide synth
• 1681017-83-3 | Venadaparib (Catalog# : 20299)Venadaparib, also known as IDX-1197, is a potent, selective and orally active PARP in
• 1213269-98-7 | Vatiquinone (Catalog# : 20284)Vatiquinone, also known as EPI 743, is an orally bioavailable para-benzoquinone being
• 1160247-92-6 | VU0238429 (Catalog# : 2071548)VU0238429 is a selective positive allosteric modulator of M5 receptors (EC50 values a
• 1192171-69-9 | Vonafexor (Catalog# : 2071543)Vonafexor, also known as EYP001, is a farnesoid X receptor agonist.
• 1228585-88-3 | Vesatolimod(GS-9620) (Catalog# : 19529)DescriptionGS-9620 is a potent and selective orally active small molecule agonist ofT
• 1188371-47-2 | Valecobulin (Catalog# : 193114)Valecobulin is an anti-neoplastic beta-tubulin polymerization inhibitor. Tubulin poly
• 1510829-06-7 | Vecabrutinib (Catalog# : 192154)Vecabrutinib, also known as SNS-062; FP-182, BSK-4841 and BIIB-062; is a potent, nonc
• 1809336-39-7 | Valemetostat (Catalog# : 192141)Valemetostat is an antineoplastic drug candidate.