按首字母搜索

Cas号索引 1

• 1872382-47-2 | UNC3866 (Catalog# : 17011102)UNC3866是一种强力拮抗剂，对多梳型CBX和CDY家族染色体组的阅读功
• 126784-99-4 | Ulipristal acetate (Catalog# : 16122843)Ulipristal acetate, also known as CDB-2914, is a selective progesterone receptor modu
• 152273-12-6 | U-93631 (Catalog# : 16122841)U-93631 is a GABAA receptor antagonist. U-93631 causes rapid decay of gamma-aminobuty
• 1381291-36-6 | USP7-IN-1 (Catalog# : 611931)USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; l
• 1481677-78-4 | UNC0642 (Catalog# : 16071013)UNC0642 is a potent, selective inhibitor of G9a/GLP with improved PK properties. UNC0
• 1047634-65-0 | Uprosertib (GSK2141795) (Catalog# : 16070901)Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailableAktin
• 178870-32-1 | UC-781 (Catalog# : 011311)UC-781 is a thiocarboxanilide non-nucleoside reverse transcriptase inhibitor. It is a
• 1415800-43-9 | UNC1215 (Catalog# : 011123)UNC1215 is a potent and selective chemical probe for the methyllysine (Kme) reading f
• 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
• 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)Ibiglustat (Venglustat) 是一种具有口服活性的，可透过血脑屏障的葡萄
• 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