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| Cat.No. | Product name | Product Description |
| R21082463 | ASP4132 | ASP4132 is an orally active, potent AMPK activator with an EC50 of 18 nM. ASP41 |
| R21082464 | MYCI975 | MYCi975 (NUCC-0200975) is an orally active MYC inhibitor that disrupts the MYC/M |
| R21082465 | MYCI361 | MYCi361 (NUCC-0196361) is a MYC inhibitor with a Kd of 3.2 μM. MYCi361 (NUCC-01 |
| R21082466 | GSK2837808A | GSK2837808A is A potent and selective lactate dehydrogenase A (LDHA) inhibitor w |
| R21082467 | ML-9 hydrochloride | Ml-9 is a potent and selective inhibitor of Akt kinase that inhibits myosin ligh |
| R21082468 | PRI-724 | PRI-724, an isomer or enantiomer of ICG-001, is a potent, specific inhibitor of |
| R21082469 | Picropodophyllotoxin(PPP) | Picropodophyllin (AXL1717) is a selective insulin-like growth factor-1 receptor |
| R21082470 | GCN2iB | GCN2iB is an ATP-competitive inhibitor of stress response kinase (GCN2), a serin |
| R21082471 | Fatostatin HBr | Fatostatin hydrobromide (125B11 hydrobromide) is a specific inhibitor of SREBP a |
| R21082472 | MYF-01-37 | MYF-01-37 is a novel covalent inhibitor of TEAD targeting Cys380 when incubated |
| R21082473 | Valemetostat | Valemetostat is an antitumor agent. |
| R21082474 | HS-243 | HS-243 is an inhibitor of transforming growth factor-beta kinase. HS-243 can be |
| R21082475 | LY-3381916 | Ly-3381916 is an effective, selective, transbbB IDO1 inhibitor that can bind to |
| R21082476 | CU-CPT-9a | CU-CPT9b is an antagonist of toll-like receptor 8 (TLR8; Kd = 21 nM). It inhibit |
| R21082477 | Pitstop 2 | Pitstop 2 is a small molecule inhibitor of clathrin terminal domain and inhibits |
| R21082478 | TAS4464 | TAS4464 is a highly selective inhibitor of NEDD8 activase (NAE) with an IC50 val |
| R21082479 | BTK inhibitor 17 | BTK inhibitor 17 is a potent oral active irreversible BTK inhibitor with IC50 of |
| R21082480 | A922500 | A 922500 is an effective, selective and orally available dgat-1 inhibitor with a |
| R21082481 | BI-3812 | Bi-3812 is a highly effective inhibitor of BCL6, which can inhibit the BTB domai |
| R21082482 | EN4 | EN4 MYC inhibitor is a covalent ligand that targets cysteine 171 (C171) of MYC. |
| R21082483 | pamiparib | Pamiparib is a PARP inhibitor that can be used to treat a variety of cancers, in |
| R21082484 | U0126 | U0126 is a potent, non-ATP-competitive, selective inhibitor of MEK1 and MEK2 wit |
| R21082485 | TPX-0022 | Csf1r-in-2 (Compound 5) is an oral effective inhibitor of SRC, MET and C-FMS, wi |
| R21082486 | AGI1067;Succinobucol | Succinobucol is a phenolic antioxidant that has anti-inflammatory and anti-plate |
| R21082487 | CBP-IN-1 | Cbp-in-1 is a highly effective p300/CBP bromine domain inhibitor. |
