编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
17982 | BAY-598 | 1906919-67-2 | 98.0% | |
BAY-598是一种强效的针对SMYD2中肽-竞争的化学探测器。BAY-598拥有一 | ||||
17981 | BAY-598 R-异构体 | 1906920-28-2 | 98.0% | |
BAY-598 R-异构体是BAY589 R-异构体。bay-598 R-异构体可以作为一个参照 | ||||
17916 | 布索芬新 | 171655-91-7 | 98.0% | |
布索芬新是一种充分的单胺再摄取阻滞剂,已被开发用于治疗帕金 | ||||
1783013 | B02 | 1290541-46-6 | 98.0% | |
B02,也叫RAD51 - in - 02,是一种RAD51抑制剂。B02能增强MM细胞的DOX敏 | ||||
1781003 | BLU-285 | 1703793-34-3 | 98.0% | |
BLU-285是一种有效、具有选择性的抑制剂。 | ||||
1781002 | BAY-1895344 | 1876467-74-1 | 98.0% | |
BAY-1895344是一种有效的、具有选择性的ATM抑制剂。 | ||||
178813 | BIBR1532 | 321674-73-1 | 98.0% | |
BIBR1132对端粒酶的抑制具有很强的选择性,导致肿瘤细胞延迟生长 | ||||
2017877 | BMS-932481 | 1263871-36-8 | 98.0% | |
BMS-932481调节Aβ肽在血浆和脑脊液的健康志愿者。 | ||||
20178216 | B-1613 | 214066-78-1 | 98.0% | |
(2S,4S)-4-(氨基甲基)吡咯烷-1,2-二羧酸 1-叔丁酯 2-甲酯;(2S,4S)-1-tert | ||||
2017822 | Balamapimod | 863029-99-6 | 98.0% | |
<span style="color:#34495E;font-family:" font-Balamapimod, 也称为MKI-822,是一种 | ||||
17030606 | BP-1-102 | 1334493-07-0 | 98% | |
BP-1-102是一种有效的口服生物和选择性抑制剂。 | ||||
17030604 | BAY-876 | 1799753-84-6 | 98% | |
BAY-876是一种有效的、选择性的谷氨酸抑制剂。BAY- 876在体外具有良 | ||||
17030312 | BRD-7552 | 1137359-47-7 | 98% | |
BRD-7552是一种PDX1转录诱导因子。它主要在人类胰岛和导管细胞中调 | ||||
17030305 | BDA-366 | 1821496-27-8 | 98% | |
BDA - 366是BCL - BH4拮抗剂。BDA - 366抑制人骨髓瘤的生长。BDA - 366诱导 | ||||
17030116 | Bimiralisib | 1225037-39-7 | 98% | |
Bimiralisib,也被称为PQR309,是一种口服生物可用的磷脂- 3 -激酶抑 | ||||
17030110 | BEC HCl | 222638-67-7 | 98% | |
BEC,也称为S -(2-boronoethyl)-L-cysteine,是一个慢结合和竞争力的精氨酸 | ||||
17109003 | BGP-15 | 66611-37-8 | 98% | |
BGP-15, 是一种带有PARP抑制活性的烟碱类胺肟衍生物。已经证明BGP- | ||||
16122908 | Butylphthalide | 6066-49-5 | 98% | |
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of | ||||
16122907 | Buthionine Sulphoximine | 5072-26-4 | 98% | |
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe | ||||
16122906 | 布瓦西坦 | 357336-20-0 | 98% | |
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra | ||||
16122905 | Brigatinib (AP-26113) | 1197953-54-0 | 98% | |
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL | ||||
16122904 | Brevianamide F | 38136-70-8 | 98% | |
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o | ||||
16122903 | Bohemine | 189232-42-6 | 98% | |
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh | ||||
16122902 | BMS-687453 | 1000998-59-3 | 98% | |
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR | ||||
16122901 | BML-210 | 537034-17-6 | 98% | |
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition | ||||
16122868 | BIIB021 | 848695-25-0 | 98% | |
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule | ||||
16122867 | BI605906 | 960293-88-3 | 98% | |
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre | ||||
16122866 | Benzbromarone | 3562-84-3 | 98% | |
Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase | ||||
16122805 | BAY-59-3074 | 406205-74-1 | 98% | |
BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr | ||||
16122804 | Batimastat | 130370-60-4 | 98% | |
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th |