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Cas号索引 1

• 1448440-52-5 | UAMC-1110 (Catalog# : 21249)UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro
• 1616413-96-7 | UCB9608 (Catalog# : 2071515)UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
• 142878-12-4 | U-73343 (Catalog# : 112591)U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
• 1612782-86-1 | UNC2541 (Catalog# : 6111901)UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
• 1890169-95-5 | UPGL00004 (Catalog# : 193251)UPGL00004是谷氨酰胺酶C (GAC)的有效抑制剂。
• 1387560-01-1 | Umibecestat游离 (Catalog# : 193223)Umibecestat，也被称为CNP-520，是一种β分泌酶抑制剂，是预防阿尔茨
• 1333218-50-0 | Upacicalcet ( 别名 SK-1403 ; AJT240) (Catalog# : 192142)Upacicalcet（别名 SK-1403/AJT240）是一种新型非肽拟钙剂，作为钙敏感
• 1229582-33-5 | URMC-099 (Catalog# : 1810252)URMC-099是一种口服生物可用的、脑内渗透混合谱系激酶(MLK)抑制剂
• 1184136-10-4 | UNC-926游离 (Catalog# : 18584)UNC-926是一种L3MBTL1域抑制剂. UNC-926联结L3MBTL1蛋白的MBT域。(Kd = 3.9
• 1310726-60-3 | 乌帕替尼 (Catalog# : 184105)乌帕替尼，也被称为ABT-494，是一种强力和选择性的JAK抑制剂，用
• 1048371-03-4 | UPF-1069 (Catalog# : 1791520)UPF-1069是一种选择性的强效PARP2抑制剂。UPF-1069诱导细胞凋亡。UPF-
• 1956366-10-1 | Ulixertinib HCl (Catalog# : 179153)Ulixertinib，也称为BVD-523和VRT752271，是ERK蛋白激酶抑制剂。对ERK蛋白
• 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