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 |
| Cat.No. | Product name | Product Description |
| R11668 | AZD1080 | AZD1080 is a potent and selective GSK3 inhibitor. AZD1080 inhibits recombinant h |
| R11669 | Erastin | Erastin is a ferroptosis inducer. Erastin binds and inhibits voltage-dependent a |
| R11670 | Merestinib (Synonyms: LY2801653) | Merestinib (LY2801653) is a potent, orally bioavailable c-Met inhibitor (Ki=2 nM |
| R11671 | Molidustat(BAY 85-3934) | Molidustat是一种新型的HIF-PH抑制剂，对PHD1, PHD2, PHD3的IC50值分别为480 nM, 280 nM和450 nM。 |
| R11672 | NVP-BAW2881 (Synonyms: BAW2881) | NVP-BAW2881 (BAW2881) is a potent and selective VEGFR2 inhibitor with an IC50 of |
| R11673 | AMG-47A | AMG-47a is a potent inhibitor of Lck and T cell proliferation; exhibits anti-inf |
| R11674 | APY29 | APY29, an ATP-competitive inhibitor, is an allosteric modulator of IRE1α which i |
| R11675 | R1487 Hydrochloride | R1487 (Hydrochloride) is highly potent and highly selective inhibitors of p38α. |
| R11676 | FH535 | FH535 is an inhibitor of Wnt/β-catenin and PPAR, with anti-tumor activities.&nbs |
| R11677 | BIX01294 3hydrochloride | BIX01294 is an inhibitor of G9a histone methyltransferase with IC |
| R11678 | Tandutinib;MLN518; CT53518 | Tandutinib (MLN518) is a potent and selective inhibitor of the FLT3 wi |
| R11679 | KR-33494 | KR-33493 is a potent inhibitor of Fas-mediated cell death (FAF1). |
| R11680 | MK 0557 | MK-0557 is a highly selective, orally available neuropeptide Y5 recept |
| R11681 | Doravirine (MK-1439) | Doravirine (MK-1439) is a highly specific HIV-1 nonnucleoside reverse trans |
| R11682 | H-89 | H-89 is a potent and selective inhibitor of cyclic AMP-dependent protein kinase |
| R11683 | KN92 phosphate | KN-92 phosphate is an inactive derivative of KN-93. KN-93 is a selective inhibit |
| R11684 | BMS-687453;BMS687453 | BMS-687453 is a potent and selective PPARα agonist, with an EC50 and IC50 of 10 |
| R11685 | XMU-MP-1 | XMU-MP-1 is a reversible and selective MST1/2 inhibitor with IC50s of 71.1 and 3 |
| R11687 | SD 0006 (Synonyms: SD-06) | SD 0006 (SD-06) is an orally active, selective, ATP-competitive and potent diary |
| R11688 | JTE-013 | JTE-013 is a potent and specific S1P2 (Sphingosine-1-Phosphate 2; EDG- |
| R11689 | Vps34 | |
| R11690 | Bilastine | Bilastine is a selective histamine H1 receptor antagonist used for treatment of |
| R11691 | PD0166285 | PD0166285 is a WEE1 inhibitor and a weak Myt1 inhibitor with IC50s of 24 and 72 |
| R11692 | Tirbanibulin (KX2-391) | Tirbanibulin (KX2-391) is an inhibitor of Src that targets the peptide |
| R11693 | Vps34-IN-1 | Vps34-IN-1 is an inhibitor of Vps34 extracted from patent WO2012085815 |
