RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
Home > Products
| Cat.No. | Product name | Product Description |
| R21082403 | CHF5074; CSP-1103;Itanapraced | Itanapraced (CHF5074) is A new type of γ-secretase modulator, which reduces Aβ42 |
| R21082404 | PJ34 | PJ34 is a potent and specific PARPl/2 inhibitor with IC50 of 110 nM and 86 nM, r |
| R21082405 | EHT5372 | EHT 5372 is a potent inhibitor of DYRK with IC50 values of 0.22 nM and 0.28 nM, |
| R21082406 | RRx-001 | Rrx-001 is a potent inhibitor of glucose 6-phosphate dehydrogenase (G6PD). Rrx- |
| R21082407 | FTBMT | FTBMT is a selective GPR52 agonist with an EC50 of 75 nM. Antipsychotic and cog |
| R21082408 | AST2818;Alflutinib | Alflutinib (AST-2818, ASK120067) is a third-generation EGFR mutant selective tyr |
| R21082409 | PD 168077 MALEATE | Pd-168077 maleate is a selective dopamine D4 receptor agonist with a Ki value of |
| R21082410 | PIH | Pyridoxal isonicotinoyl hydrazine (PIH) is a lipophilic ferric chelating agent e |
| R21082411 | SR0987 | SR0987 is an agonist of RORγ T with an EC50 value of 800 nM. |
| R21082412 | C-176 | C-176 is a potent covalent inhibitor of interferon gene - stimulating receptor ( |
| R21082413 | GSK805 | GSK805 is a potent RORγ T inhibitor. |
| R21082414 | Bobcat339 (Bobcat 339) | Bobcat339 (Bobcat339) is a novel cytosine-based TET enzyme inhibitor with IC50 o |
| 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 ( |
