编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
262401 | MRTX1719 | 2630904-45-7 | ≧96.0% | |
MRTX1719 is a potent and selective binder to the PRMT5•MTA complex and selectively | ||||
20637 | (R)-4-((3-丙烯酰胺基哌啶-1-基)甲基)-N-(4-(4-吗啉-7H-吡咯并[2,3-D]嘧啶-6-基)苯基)吡啶-2-甲酰胺 | 2448172-22-1 | 98% Min. | |
20615 | Mavodelpar | 942594-93-6 | 98% Min. | |
Mavodelpar is a peroxisome proliferator activated receptor (PPAR) delta agonist. | ||||
20611 | MRTX849 | 2326521-71-3 | 98% Min. | |
Adagrasib, also known as MRTX849, is a potent, highly selective, oral available KRAS | ||||
20592 | Migoprotafib | 2377352-49-1 | 98% Min. | |
Migoprotafib, also known as GDC-1971 and RLY-1971, is a SHP2 allosteric inhibitor. GD | ||||
20572 | Mtb-IN-2 | 2861190-30-7 | 98% Min. | |
Mtb-IN-2 (compound 10c) is an antimicrobial agent against Mycobacterium tuberculosis | ||||
20542 | MBX-8025 lysine anhydrous | 928821-41-4 | 98% Min. | |
MBX-8025 lysine anhydrous is a selective PPAR-delta agonist. | ||||
20529 | Milademetan free base | 1398568-47-2 | 98% Min. | |
Milademetan, also known as DS-3032b or DS-3032, is a potent and selective MDM2 inhibi | ||||
20528 | muvalaplin | 2565656-70-2 | 98% Min. | |
20503 | MK-8189 | 1424371-93-6 | 98% Min. | |
MK-8189 is a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizo | ||||
20473 | 4-N-BOC-哌啶-4-甲酸甲酯 | 98% Min. | ||
20470 | MCUF-651 | 2747162-85-0 | 98% Min. | |
MCUF-651 is a small molecule guanylyl cyclase A receptor positive allosteric modulato | ||||
20466 | Moracin C | 69120-06-5 | 98% Min. | |
Moracin C is a phenolic compound isolated from Artocarpus heterophyllus. Moracin C su | ||||
20464 | ML192 | 460331-61-7 | 98% Min. | |
ML192, also known as MLS000526305 and CID1434953, is a selective ligands for GPR55. T | ||||
20459 | 3-甲基-1,2,4-噻二唑-5-羧酸甲酯 | 352356-71-9 | 98% Min. | |
20457 | Mitiperstat | 1933460-19-5 | 98% Min. | |
Mitiperstat is a myeloperoxidase inhibitor. | ||||
171462 | MRTX0902 | 2654743-22-1 | ≧98.0% | |
MRTX0902 是一种口服有效的 SOS1 的抑制剂,IC50 为 46 nM。 | ||||
20414 | Methanone, (3,5-dibromophenyl)(2-methoxy-4-pyridinyl)- | 915412-80-5 | 98% Min. | |
20407 | 4-(2-氨基乙氧基)苯甲酸甲酯盐酸盐 | 210113-85-2 | 98% Min. | |
20398 | 4-(4-甲氧苯甲基)-3-甲氧基苯甲醛 | 129047-38-7 | 98% Min. | |
20395 | methyl (3-chloropyrazin-2-yl)acetate | 235748-94-4 | 98% Min. | |
20394 | 7-methoxy-8-[3-(4-morpholinyl)propoxy]-Imidazo[1,2-c]quinazolin-5-amine | 1032570-74-3 | 98% Min. | |
20364 | methyl 3-bromo-4-ethoxy-5-formylbenzoate | 2385682-18-6 | 98% Min. | |
20363 | 3-溴-5-甲酰基-4-羟基苯甲酸甲酯 | 706820-79-3 | 98% Min. | |
20362 | 3-醛基-4-羟基苯甲酸甲酯 | 24589-99-9 | 98% Min. | |
L20346 | Mycro3 | 944547-46-0 | 98% Min. | |
Mycro3 is an inhibitor of Myc-Max dimerization. | ||||
L20331 | MELK-8a | 1922153-17-0 | 98% Min. | |
MELK-8a Dihydrochloride is a novel inhibitor of maternal embryonic leucine zipper kin | ||||
L20329 | MTI-31 | 1567915-38-1 | 98% Min. | |
MTI-31 is a bioactive chemical. | ||||
20325 | MKC-8866 | 1338934-59-0 | 98% Min. | |
MKC-8866, also known as IRE1-IN-8866, is an inhibitor of IRE1 RNase activity. MKC8866 | ||||
20320 | MDK-7553 | 1700637-55-3 | 98% Min. | |
MDK-7553, also known as CD38 inhibitor 78c and Compound-78c, is a potent CD38 inhibit |