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 |
| R2032564 | Walrycin B | Walrycin B is a novel antibacterial compound specifically targeting the essentia |
| R2032565 | WAY100635 | WAY-100635 maleate is a potent and selective 5-hydroxytryptamine 1A (5-HT1A) rec |
| R2032566 | WHI-P154 | WHI-P154 is a potent EGFR inhibitor, and also modestly blocks JAK3, with IC50s o |
| R2032567 | Wnt-c59 | Wnt-C59 (C59) is a highly potent and oral porcupine (PORCN) inhibitor with an IC |
| R2032568 | WYE125132(WYE-132) | WYE-132 (WYE-125132) is a highly potent, ATP-competitive, and specific mTOR kina |
| R2032569 | XCT790 | XCT-790 is a potent and selective inverse agonist for ERRα with an IC50 value of |
| R2032570 | XL388 | XL388 is a highly potent and ATP-competitive mTOR inhibitor with an IC50 of 9.9 |
| R2032571 | XMD17-109 | XMD17-109 is a novel, specific ERK-5 inhibitor, with an IC50 of 162 nM. |
| R2032572 | YH239-EE | YH239-EE, ethyl ester of the free carboxylic acid compound YH239, is a potent p5 |
| R2032573 | YM155 | YM-155 is a survivin inhibitor with an IC50 of 0.54 nM. |
| R2032574 | z-fa-fMk | Z-FA-FMK is an irreversible cysteine protease inhibitor, and also inhibits effec |
| R2032575 | ZK-811752 hydrochloride(BX471 hydrochloride) | BX471 hydrochloride (ZK-811752 hydrochloride) is a potent, selective non-peptide |
| R2032576 | ZM39923 hydrochloride | ZM 39923 HCl is an JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to |
| R2032577 | z-vad -fMk | Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan |
| R2032578 | AS602801(BentaMapiMod) | Bentamapimod (AS 602801) is an ATP-competitive JNK inhibitor with IC50 of 80 nM, |
| R2032579 | PF670462 | PF-670462 is a potent and selective inhibitor of casein kinase (CK1ε and CK1δ), |
| R2032580 | SBC110,736 | SBC-110736 is a proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitor |
| R2032581 | Y-27632 | Y-27632 dihydrochloride is a cell-permeable, ATP-competitive inhibitor of ROCK-I |
| R2032584 | VidofludiMus(4SC-101;SC12267) | Vidofludimus(4SC-101; SC12267) is a novel immunosuppressive drug that inhibits D |
| R2032585 | FK3311 | FK 3311 (COX-2 Inhibitor V) is a selective inhibitor of COX-2 with antiinflammat |
| R2032586 | CYT997(Lexibulin) | Lexibulin(CYT-997) is a potent tubulin polymerisation inhibitor with IC50 of 10- |
| R2032587 | Mutant IDH1-IN-1 | Mutant IDH1-IN-1 is a mutant-selective IDH1 inhibitor with with IC50s of 4, 42, |
| R2032588 | SAR125844 | SAR125844 is a potent, highly selective, reversible and ATP-competitive MET rece |
| R2032589 | Acalisib(GS-9820) | Acalisib is a potent and selective PI3Kδ inhibitor with an IC50 of 12.7 nM. |
| R2032590 | A77-01 | A 77-01 is a potent inhibitor of transforming growth factor (TGF)-β type I recep |
