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Home > Products
| Cat.No. | Product name | Product Description |
| R21082428 | JWG-071 | Jwg-071 is the first reported ERK5 kinase selective chemical probe. Jwg-071 imp |
| R21082429 | RIPASUDIL | Ripasudil Free Base (K-115 Free Base) is a rock-specific inhibitor that inhibits |
| R21082430 | JDTIC | JDTic is a κ- opioid receptor antagonist, but has no effect on μ- and δ- opioid |
| R21082431 | Dual Specificity Protein Phosphatase 1/6 Inhibitor | (E/Z)-BCI (NSC 150117) is a DUSP6 inhibitor with anti-inflammatory activity. (E |
| R21082432 | VAS2870 | VAS2870 is NADPH oxidase (NOX) inhibitor. |
| R21082433 | Nelonicline | Nelonicline (ABT-126) is a selective agonist of neuronal nicotinic receptors. |
| R21082434 | VBIT-12 | Vbit-12 is a potent inhibitor of VDAC1. Vbit-12 interacts directly with VDAC1 a |
| R21082435 | SR-18292 | Sr-18292 is an inhibitor of PPARγ co-activator -1α (PGC-1α), which promotes the |
| R21082436 | Belvarafenib | Belvarafenib is an effective, widespread rapidly accelerating fibrosarcoma kinas |
| R21082437 | Ingliforib | Ingliforib is a glycogen phosphorylase inhibitor with IC50 values of 52,352 nM a |
| R21082438 | GSK3117391A | Dac-in-3 is an inhibitor of histone deacetylase (HDAC). For details, please refe |
| R21082439 | Vindesine | The semi-synthetic vinblastine derivatives have higher anti-cancer spectrum, hig |
| R21082440 | Vindesine sulfate | Vindesine sulfate is a vinca alkaloid which is a synthetic derivative of vinblas |
| R21082441 | EOAI3402143 | EOAI3402143 is a deubiquitination enzyme (DUB) inhibitor that inhibits Usp9x/Usp |
| R21082442 | KY-226 | KY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0. |
| R21082443 | TP-003 | TP003 is a potent, functional selectivity for α3 subunit-containing GABAA recept |
| R21082444 | RMS060 | Protein kinase Affinity Probe 1 is a novel Protein kinase affinity probe used fo |
| R21082445 | SRT1460 | SRT 1460 is an effective sirTUin-1 (SIRT1) agonist with an EC1.5 value of 2.9 μM |
| R21082446 | Curcumin analog C1 | TFEB Activator 1 is an orally effective, mTOR independent TFEB activator. TFEB |
| R21082447 | Probe 388-9 | |
| R21082448 | OMO-1 | Jnj-38877618 is a potent, highly selective, orally available (Met) kinase inhibi |
| R21082449 | ARQ-531 | ARQ 531 is a reversible non-covalent inhibitor of BTK, with IC50 values of 0.85 |
| R21082450 | RU320521 | RU.521 (RU320521) is a potent dsDNA inhibitor (IC50 : 700 nM), inhibition of the |
| R21082451 | SNDX-5613 | Sndx-5613 is a potent and specific menin-MLL inhibitor, binding Ki at 0.149 nM a |
| R21082452 | mitoNEET Inhibitor NL-1, Thi | Nl-1 is a mitoNEET inhibitor with anti-leukemia effects. Nl-1 inhibited the gro |
