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Cas号索引 1

• 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.
• 1236188-16-1 | 740 Y-P (PDGFR 740Y-P) (Catalog# : 17021302)740 Y-P是PI3K的细胞渗透磷肽激活剂。
• 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
• 1632051-40-1 | Zuranolone (Catalog# : 24105)
• 1640282-42-3 | Zunsemetinib (Catalog# : 24012)Zunsemetinib是一种在研口服丝裂原活化蛋白激酶活化蛋白激酶2（MK2
• 1606974-33-7 | Zatolmilast (Catalog# : 20651)Zatolmilast is a phosphodiesterase IV inhibitor.
• 1851412-93-5 | Zavondemstat (Catalog# : 20610)Zavondemstat 是一种 KDM4 抑制剂，具有抗肿瘤药物的潜力。
• 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) 是一种特异性粘着斑激酶 (FAK) 激活剂，可促进缺血
• 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)) 是钙释放激活钙通道蛋白 1（CRAC 通道，
• 1199236-64-0 | Z944 (Catalog# : 181233)Z944是一种T型钙通道拮抗剂，有望用于疼痛的治疗。Z944对癫痫大鼠