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| 目录号 | 产品名称 | 产品描述 |
| R10311 | E7080; E7080; Lenvatinib Intermediate3 | Neratinib (HKI-272) is a highly selective HER2 and EGFR inhibitor with IC50 of 5 |
| R10312 | E7080; E7080; Lenvatinib Intermediate4 | Neratinib (HKI-272) is a highly selective HER2 and EGFR inhibitor with IC50 of 5 |
| R10313 | KU0059436; AZD2281; OlaparibIntermediate | Olaparib (AZD2281, KU0059436) is a selective inhibitor of PARP1/2 with IC50 of 5 |
| R10314 | PD0332991; PD0332991; Palbociclib | Palbociclib (PD0332991) Isethionate is a highly selective inhibitor of CDK4/6 wi |
| R10315 | PD0332991; Palbociclib Intermediate1 | Palbociclib (PD0332991) Isethionate is a highly selective inhibitor of CDK4/6 wi |
| R10316 | PD0332991; Palbociclib Intermediate2 | Palbociclib (PD0332991) Isethionate is a highly selective inhibitor of CDK4/6 wi |
| R10317 | PD0332991; Palbociclib Intermediate3 | Palbociclib (PD0332991) Isethionate is a highly selective inhibitor of CDK4/6 wi |
| R10318 | Valsartan/sacubitril; LCZ696 Intermediate1 | LCZ696, consisting of valsartan and sacubitril in 1:1 molar ratio, is an orally |
| R10319 | Valsartan/sacubitril; LCZ696 Intermediate2 | LCZ696, consisting of valsartan and sacubitril in 1:1 molar ratio, is an orally |
| R10320 | Valsartan/sacubitril; LCZ696 Intermediate3 | LCZ696, consisting of valsartan and sacubitril in 1:1 molar ratio, is an orally |
| R10321 | MS37452 | |
| R10322 | Ryuvidine | Ryuvidine 是一种含有的 SET 结构域的蛋白质 8 (SETD8) 的有效抑制剂，其 IC50 为 0.5 µM，并在体外抑制 H4K20 的甲基化。 |
| R10323 | ML190; Indomethacin morpholinylamide | |
| R10329 | Elafibranor;GFT505;GFT-505;GFT 505 | Elafibranor is an agonist of the peroxisome proliferator-activated receptor-α an |
| R10330 | GFT505; elafibranor E | Elafibranor是 PPARα/δ 的激动剂，EC50 分别为 45 和 175 nM。 |
| R10331 | Cabozantinib S-malate (XL184 S-malate; BMS-907351 S-malate) | Cabozantinib S-malate (XL184 S-malate) 是一种有效的多受体酪氨酸激酶抑制剂， 抑制VEGFR2，c-Met，Kit，Axl |
| R10332 | Molibresib (Synonyms: GSK 525762A; I-BET 762) | Molibresib (GSK 525762A; I-BET 762) 是 BET 溴结构域 抑制剂，IC50 为32.5-42.5 nM。 |
| R10333 | Navitoclax (Synonyms: ABT-263) | Navitoclax (ABT-263) 是有效，可口服的 Bcl-2 抑制剂，可与Bcl-xL，Bcl-2， Bcl-w等多种Bcl-2家族蛋白结合，Ki 值 |
| R10334 | SU6656 | SU 6656 is a selective Src family kinase inhibitor with IC50 of 280 nM, 20 nM, 1 |
| R10336 | Felbamate; Felbatol | Felbamate (Felbatol) is an anticonvulsant drug used in the treatment of epilepsy |
| R10339 | PLX-3397; Pexidartinib | Pexidartinib (PLX3397) is an oral, potent mutil-targeted receptor tyrosine kinas |
| R10341 | BS-181 hydrochloride | BS-181盐酸盐是CDK7高效选择性抑制剂，IC50值21nM，对CDK1/92/4/5/6/9作用弱。 |
| R10342 | GW 627368 | GW627368 (GW627368X) 是前列腺素受体 EP4 高效选择竞争性抑制剂，还对血栓素受体 TP 有亲和力。 |
| R10343 | Bikinin; Abrasin | Bikinin 是一种非甾体类的，植物性 GSK-3/Shaggy-like kinases 的 ATP 竞争性抑制剂，可激活 BR 信号通路。 |
| R10344 | GW9662 | GW9662 is a selective PPAR antagonist for PPARγ with IC50 of 3.3 nM in a cell-fr |
