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Cas号索引 1

• 153437-55-9 | WHI-P180 hydrochloride (Catalog# : 611927)WHI-P180 hydrochloride is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0
• 1062159-35-6 | WAY-600 (Catalog# : 161009014)WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 of 9 n
• 1062161-90-3 | WYE-687 (Catalog# : 1610912)WYE-687 is a potent and ATP-competitive and selective inhibitor of mTOR with IC50 of
• 1144068-46-1 | WYE-125132 (Catalog# : 161009008)WYE-132 inhibited mTORC1 and mTORC2 in diverse cancer models in vitro and in vivo. Im
• 1062169-56-5 | WYE-354 (Catalog# : 1610101)WYE-354 is a potent cell-permeable inhibitor of mTOR (IC50 = 4.3 nM) which blocks sig
• 19545-26-7 | Wortmannin (Catalog# : 160926005)It has an in vitro inhibitory concentration (IC50) of around 5 nM, making it a more p
• 1213269-23-8 | WZ4002 (Catalog# : 52822)WZ4002 is a novel, mutant-selective EGFR inhibitor for EGFR(L858R)/(T790M) with IC50
• 1123231-07-1 | WAY-262611 (Catalog# : 52726)WAY-262611 is a wingless -Catenin agonist that increases bone formation rate; with EC
• 1421227-53-3 | WS6 (Catalog# : 52224)WS6 is a novel small molecule that promotes cell proliferation in rodent and human p
• 152854-19-8 (tartrate) | Xanomeline tartrate (Catalog# : 2112067)Xanomeline (LY-246,708) 是一种正构毒蕈碱乙酰胆碱受体 (mAChR) 激动剂，
• 1208229-58-6 | XP-23829 (Catalog# : 192143)XP-23829，又称福马酸替吡胺，是一种羟羧酸受体2配体，可用于银屑
• 192939-46-1 | 希美加群 (Catalog# : 185282)希美加群是一种抗凝剂，它被作为warfarin[1]的替代品进行了广泛的
• 1234480-50-2 | XMD8-92 (Catalog# : 17030608)XMD8-92是一种BMK1抑制剂，是ERK5活性的高选择性抑制剂。
• 1345098-78-3 | XMD16-5 (Catalog# : 17021312)XMD16-5是一种新型的酪氨酸激酶非受体2(TNK2)抑制剂，对于D163E和R80
• 1234480-46-6 | XMD8-87 (Catalog# : 17021311)XMD8-87是一种新型的酪氨酸激酶非受体2(TNK2)抑制剂，ic50为38nmol / L
• 1251156-08-7 | XL388 (Catalog# : 161009016)XL388 inhibited cellular phosphorylation of mTOR complex 1 (p-p70S6K, pS6, and p-4E-B
• 1435488-37-1 | XMD17-109 (Catalog# : 16071410)XMD17-109 is a novel, specific inhibitor of ERK-5 with an EC50 value of 4.2 M in HEK2
• 1624117-53-8 | XY1 (Catalog# : 021803)XY1 is a very close analogue of SGC707 (a potent, selective, and non-competitive inhi
• 1365267-27-1 | X-396 (Catalog# : 011804)X-396 is an orally available small molecule inhibitor of the receptor tyrosine kinase
• 1123889-87-1 | XL765 (Catalog# : 111910)XL765 is a PI3K/mTOR dual kinase inhibitor with IC50 values of 157 nM, 39 nM, 113 nM,
• 1515856-92-4 | XEN445 (Catalog# : 52501)XEN445 is a potent and selective EL inhibitor(IC50=0.237 uM), that showed good ADME a
• 1936529-65-5 | YKL-05-099 (Catalog# : 21241)YKL-05-099 is a selective inhibitor of Salt-Inducible Kinase (SIK).
• 181147-28-4 | YCN47284 (Catalog# : 2073105)YCN47284 is an aromatic guanylhydrazone compounds with antimalarial activity.
• 1312005-62-1 | YF-2盐酸盐 (Catalog# : 193151)YF-2盐酸盐是一个具有高度选择性,血脑屏障渗透组蛋白乙酰转移酶
• 1364488-67-4 | YH239-EE (Catalog# : 192213)YH239-EE是一种高效的p53-MDM2拮抗剂。
• 199433-58-4 | Y-39983游离 (Catalog# : 185172)Y-39983 (游离)，也被称为Y-33075，是一种有效的、选择性的ROCK家族抑
• 1339058-04-6 | YL-0919 (Catalog# : 18578)YL-0919是一种日常5-HT1A受体拮抗剂，具有选择性的 5 -羟色胺再摄取
• 1943733-16-1 | YU-238259 (Catalog# : 1710139)YU238259表现出有效的合成致死性设置中的DNA损伤反应和DNA修复缺陷
• 143984-17-2 | Y-29794 甲苯磺酸酯 (Catalog# : 1791521)Y-29794甲苯磺酸酯是一种口服有效的，强有力的和特定的非肽脯氨
• 173897-44-4 | Y-39983盐酸盐 (Catalog# : 17021305)Y-39983是一种选择性的与之相关的蛋白激酶(ROCK)抑制剂，其IC50为3.