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| Cat.No. | Product name | Product Description |
| R2032999 | AT406 hydrochloride | AT-406 is a potent and orally bioavailable Smac mimetic and an antagonist of IAP |
| R2033000 | BS194 | BS194 is as a potent cyclin-dependent protein kinases (CDKs) inhibitor. |
| R2033001 | Cambinol | Cambinol is a SIRT1 and SIRT2 inhibitor with IC50 values of 56 and 59 μM, respec |
| R2033002 | CCT241736 | CCT241736 is a potent and orally bioavailable dual FLT3 and Aurora kinase inhibi |
| R2033003 | CFI-400437 | CFI-400437 is potent against PLK4 (IC50 = 0.6 nM) and selective against other me |
| R2033004 | Derazantinib | Derazantinib (ARQ-087) is an ATP competitive tyrosine kinase inhibitor; exhibits |
| R2033005 | DGAT1-IN-1 | DGAT1-IN-1 is a potent DGAT1 inhibitor with IC50 of < 10 nM(cell lysate from |
| R2033006 | GNE-490 | GNE-490 is a highly selective pan-PI3K inhibitor that demonstrates selectivity o |
| R2033007 | GSK-F1 | GSK-F1 is a potent inhibitor of PI4KA.It has markedly better pharmacokinetic pro |
| R2033008 | GW441756 | GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC |
| R2033009 | GW806742X | GW806742X is a Mixed Lineage Kinase Domain-Like protein (MLKL) inhibitor which b |
| R2033010 | JBSNF-000088 | JBSNF-000088 (6-Methoxynicotinamide), a analog of nicotinamide (NA), is a potent |
| R2033011 | JNJ-38158471 | JNJ-38158471 is a well tolerated, orally available, highly selective VEGFR-2 inh |
| R2033012 | LXH254 | LXH254 is a potent B/C RAF inhibitor extracted from patent WO2018051306A1, Compo |
| R2033013 | LY2510924 | LY2510924 is a potent and selective CXCR4 antagonist that blocks SDF-1 binding t |
| R2033014 | MBP146-78 | MBP146-78 is a potent and selective inhibitor of cGMP dependent protein kinases. |
| R2033015 | MI463 | MI-463 is a highly potent and orally bioavailable small molecule inhibitor of th |
| R2033016 | MI503 | MI-503 is a highly potent and orally bioavailable small molecule inhibitor of th |
| R2033017 | MPI-5a | MPI_5a is a potent and selective HDAC6 inhibitor (IC50=36 nM).MPI_5a weakly inhi |
| R2033018 | NIBR-17 | NIBR-17 is a pan class I PI3K inhibitor with IC(50) values of 1, 9.2, 9 and 20nM |
| R2033019 | PF-04979064 | PF-04979064 is a potent and selective PI3K/mTOR dual kinase inhibitor with Kis o |
| R2033020 | PF4618433 | PF 4618433 is an inhibitor of proline-rich tyrosine kinase 2 (PYK2) and focal ad |
| R2033021 | RO495 | RO495 is a very potent TYK2 inhibitor with a IC50 of 1.5nM on TYK2 as tested in |
| R2033022 | S6K-18 | S6K-18 is a highly selective inhibitor of S6K1, with an IC50 of 52nM. |
| R2033023 | SSR240612 | SSR240612 is a potent, and orally active specific non-peptide bradykinin B1 rece |
