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| Cat.No. | Product name | Product Description |
| R21082415 | SGC-GAK-1 | Sgc-gak-1 is a potent selective cyclin G-associated kinase (GAK) inhibitor with |
| R21082416 | S-GBOXIN | S-gboxin is an active analogue of Gboxin and has potent antitumor activity. |
| R21082417 | Voxelotor | GBT 440 (Voxelotor) is an orally available regulator of sickle cell hemoglobin. |
| R21082418 | NSC23766 3HCL | NSC 23766 trihydrochloride is an inhibitor of Rac1 activation. |
| R21082419 | IC-87201 | IC87201 is an inhibitor of psD95-NNOS interaction, which inhibits the formation |
| R21082420 | AMG837 (calcium hydrate) | AMG 837 calcium hydroxide is a GPR40 agonist with EC50 of 13 nM and has good pha |
| R21082421 | CAY10650 | CAY10650 is a cPLA2α inhibitor with IC50 of 12 nM. |
| R21082422 | DKM2-93 | DKM 2-93 is a relatively selective inhibitor of UBA5 with IC50 value of 430 μM. |
| R21082423 | PF429242 dihydrochloride | PF429242 dihydrochloride is a reversible and competitive inhibitor of S1P (IC50 |
| R21082424 | AZ1 | USP25/28 inhibitor AZ1 (AZ1) is a potent, selective, and non-competitive dual ub |
| R21082425 | MB-07811 ( VK-2809) | Mb-07811 (VK-2809) is a HepDirect prodrug with oral activity of MB07344, a liver |
| R21082426 | Udenafil | Udenafil(DA8159) is a PDE5 inhibitor. |
| R21082427 | RHC-80267 | RHC 80267 (U-57908) is an effective selective diacylglycerase (DAGL) inhibitor ( |
| 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 |
