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首页
抑制剂/受体激动剂
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Anti-infection
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Cas号索引 1
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Cas号索引 1
1034442-21-1 | Basimglurant
(Catalog# : 187121)
Basimglurant,又称RO 4917523和RG-7090,是一种新型的mGlu5阴性变构调制
1923833-60-6 | BMS-986205
(Catalog# : 185314)
BMS-986205是一种抗癌药物。
1260251-31-7 | Birinapant
(Catalog# : 185182)
Birinapant,也被称为TL32711,是一种合成的小分子,具有潜在的抗肿
1286279-29-5 | BMS-813160
(Catalog# : 1842812)
BMS-813160是一种有效的选择性CCR2/CCR5拮抗剂,具有潜在的免疫调节
198480-56-7 | 盐酸巴多昔芬
(Catalog# : 18496)
Bazedoxifene,又名WAY-140424,是第三代选择性雌激素受体调节剂(SERM)
1513879-21-4 | BQR695
(Catalog# : 184218)
BQR695, also known as NVP-BQR695, is a potent and selective PI4K inhibitor.
1414943-88-6 | BAY1143572
(Catalog# : 181242)
Atuveciclib, also known as BAY1143572, is a highly selective, potent and orally avail
1803274-65-8 | BAY-1436032
(Catalog# : 181181)
BAY-1436032是一个强有力的,有选择性的,有效的突变异柠檬酸脱氢酶
1446090-77-2;1446090-79-4 | BGB-283
(Catalog# : 17101620)
BGB-283,也称为Beigene-283或Lifirafenib,是一种新的有效的和选择性的
1357920-84-3 | Belizatinib
(Catalog# : 17101619)
Belizatinib,也称为TSR-011,具有受体酪氨酸激酶间变性淋巴瘤激酶(
1420071-30-2 | Bioymifi
(Catalog# : 1710165)
Bioymifi是DR5的活性剂(Kd = 1.2 µM; IC50 = 2 µM). Bioymifi诱导凋亡的肿瘤
1707289-21-1 | BLU-554
(Catalog# : 1710162)
BLU-554是针对肝癌治疗的成纤维细胞生长因子受体4(FGFR4)抑制剂
1632118-69-4 | BAR-501
(Catalog# : 179821)
BAR-501是一种选择性GPBAR1激动剂,没有任何的FXR激动剂活性。BAR-50
1207293-36-4 | BI-847325
(Catalog# : 83101)
BI-847325是一种口服、具有选择性的日常生物MEK/Aurora激酶抑制剂,
1906919-67-2 | BAY-598
(Catalog# : 17982)
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
1906920-28-2 | BAY-598 R-异构体
(Catalog# : 17981)
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
171655-91-7 | 布索芬新
(Catalog# : 17916)
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
1290541-46-6 | B02
(Catalog# : 1783013)
B02,也叫RAD51 - in - 02,是一种RAD51抑制剂。B02能增强MM细胞的DOX敏
1703793-34-3 | BLU-285
(Catalog# : 1781003)
BLU-285是一种有效、具有选择性的抑制剂。
1876467-74-1 | BAY-1895344
(Catalog# : 1781002)
BAY-1895344是一种有效的、具有选择性的ATM抑制剂。
1263871-36-8 | BMS-932481
(Catalog# : 2017877)
BMS-932481调节Aβ肽在血浆和脑脊液的健康志愿者。
1334493-07-0 | BP-1-102
(Catalog# : 17030606)
BP-1-102是一种有效的口服生物和选择性抑制剂。
1799753-84-6 | BAY-876
(Catalog# : 17030604)
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
1137359-47-7 | BRD-7552
(Catalog# : 17030312)
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
1821496-27-8 | BDA-366
(Catalog# : 17030305)
BDA - 366是BCL - BH4拮抗剂。BDA - 366抑制人骨髓瘤的生长。BDA - 366诱导
1225037-39-7 | Bimiralisib
(Catalog# : 17030116)
Bimiralisib,也被称为PQR309,是一种口服生物可用的磷脂- 3 -激酶抑
1197953-54-0 | Brigatinib (AP-26113)
(Catalog# : 16122905)
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
189232-42-6 | Bohemine
(Catalog# : 16122903)
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
1000998-59-3 | BMS-687453
(Catalog# : 16122902)
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
130370-60-4 | Batimastat
(Catalog# : 16122804)
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th
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-- Metabolism
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Lipoxygenase
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HMG-CoA Reductase
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Carbonic Anhydrase
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Newest added products
抑制剂/受体激动剂
中间体
分子砌块
--
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新产品
天然化合物
最新产品
845959-55-9 | Mitoquinol mesylate (MitoQ)
(Catalog# : 26A042)
Mitoquinol mesylate (MitoQ) 是一种线粒体靶向抗氧化剂,具体而言,它
1246960-09-7 | SPG-601 ( VSN-16R )
(Catalog# : 24042)
SPG-601(原名VSN-16R)是一种口服给药、同类首创的小分子药物,是
1421438-81-4 | LY3039478 ( Crenigacestat )
(Catalog# : 17021601)
LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂,通过阻断 VEGFA/
72882-78-1 | PF-9366
(Catalog# : 184107)
PF-9366是一种新型的人蛋氨酸腺苷转移酶2A (Mat2A),肝外同种型。
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
| Pantothenate kinase-IN-3
(Catalog# : 26A041)
泛酸激酶-IN-3(亦称化合物21,https://doi.org/10.1021/acs.jmedchem.5c03452)
2361124-03-8 | Claziprotamidum ( Claziprotamide ; BBP-671 )
(Catalog# : 26A040)
Claziprotamidum(Claziprotamide;BBP-671)是一种强效、口服有效且能透过
2170608-85-0 | PZ-3022
(Catalog# : 26A039)
PZ-3022是一种别构型的PanK激活剂,能够抵消C3-CoA的抑制作用。
2170608-82-7 | PZ-2891
(Catalog# : 193282)
PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂,
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2是一种泛酸激酶抑制剂,对PanK2的IC50值为92 nM,