编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
111913 | AR-12 | 742112-33-0 | 98% | ![]() |
AR-12 is an orally available, targeted anti-cancer agent that has been shown in pre-c | ||||
110909 | AR 231453 | 733750-99-7 | 98% | ![]() |
AR231453 is a potent and selective small molecule agonist of GPR119 that enhances glu | ||||
110906 | AZD6738 | 1352226-88-0 | 97% | ![]() |
AZD6738 is an orally available morpholino-pyrimidine-based inhibitor of ataxia telang | ||||
110217 | 3-Amino-2,6-dibromopyridine | 39856-57-0 | 98% | ![]() |
Coming soon! | ||||
110214 | 2-Amino-4-(trifluoromethyl)pyridine | 106447-97-6 | 98% | ![]() |
Coming soon! | ||||
110211 | 1-aminocyclopropanecarboxylic acid | 22059-21-8 | 98% | ![]() |
Coming soon! | ||||
110207 | 3-Amino-1-propanesulfonic acid | 3687-18-1 | 98% | ![]() |
Coming soon! | ||||
102702 | Alda 1 | 349438-38-6 | 98% | ![]() |
Alda 1 is a cell-permeable benzamide compound that selectively enhances the activity | ||||
102619 | ACTB-1003 | 939805-30-8 | 98% | ![]() |
ACTB-1003 is a potent inhibitor of FGFR1 with IC50 <10 nM in FGFR-1 biochemical as | ||||
102613 | ABT-751 | 141430-65-1 | 98% | ![]() |
ABT-751 is a novel bioavailable tubulin-binding and antimitotic sulfonamide agent wit | ||||
102604 | AZD1981 | 802904-66-1 | 98% | ![]() |
AZD1981 is a potent and selective CRTh2 antagonist; displaces radio-labelled PGD2 fro | ||||
101921 | AL 082D06 | 256925-03-8 | 98% | ![]() |
AL 082D06(D-06) is the first selective, nonsteroidal glucocorticoid receptor (GR) ant | ||||
101910 | ANA-12 | 219766-25-3 | 98% | ![]() |
ANA-12 is aTrkB receptor antagonist, which showed direct and selective binding to Trk | ||||
91823 | (3aR,5S)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole | 1613393-51-3 | 98% | ![]() |
Coming soon! | ||||
91803 | (3aR,5R)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole | 1220327-45-6 | 98% | ![]() |
Coming soon! | ||||
91411 | Amoxanox | 68302-57-8 | 98% | ![]() |
Amlexanox inhibits mast cell release of allergic mediators, which is also an antialle | ||||
91404 | (3aR,4S,7R,7aS)-Hexahydro-4,7-methanoisobenzofuran-1,3-dione | 14166-28-0 | 98% | ![]() |
The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3 | ||||
91401 | (3aR,4S,7R,7aS)-Hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione | 14805-29-9 | 98% | ![]() |
The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3 | ||||
901301 | AZD3759 | 1626387-80-1 | ≧99.0% | ![]() |
AZD3759 isan orally available inhibitor of the epidermal growth factor receptor (EGFR | ||||
90702 | 3-(4-Acetoxyphenyl)propanoic acid | 7249-16-3 | 98% | ![]() |
Coming soon! | ||||
90607 | 3-(3-Aminophenyl)propanoic acid | 1664-54-6 | 98% | ![]() |
Coming soon! | ||||
90102 | 3-Azetidinecarboxylic Acid | 36476-78-5 | 98% | ![]() |
Coming soon! | ||||
83110 | 1-aminocyclohexane-1-carboxylic acid | 2756-85-6 | 98% | ![]() |
Coming soon! | ||||
83109 | 2-amino-2-ethylbutanoic acid | 2566-29-2 | 98% | ![]() |
Coming soon! | ||||
82801 | 8-(2-aminoethyl)-5-hydroxy-4H-1,4-benzoxazin-3-one,hydrochloride | 1035229-35-6 | 98% | ![]() |
Coming soon! | ||||
82708 | Aliskiren | 173334-57-1 | 98% | ![]() |
Aliskiren(CGP 60536) is a direct renin inhibitor with IC50 of 1.5 nM. | ||||
82706 | Abiraterone | 154229-19-3 | 98% | ![]() |
Abiraterone is a potent steroidal cytochrome P450 17alpha-hydroxylase-17,20-lyase (CY | ||||
82702 | AT7519 Hydrochloride | 902135-91-5 | 98% | ![]() |
AT7519 hydrochloride is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10 | ||||
82405 | AZ191 | 1594092-37-1 | 98% | ![]() |
AZ191 selectively inhibits DYRK1B serine/threonine kinase activity with no effect on | ||||
81940 | 4-Amino-2,3-dihydro-1H-inden-1-one | 51135-91-2 | 98% | ![]() |
Coming soon! |