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Home > Products
| Cat.No. | Product name | Product Description |
| R2032554 | UMI-77 | UMI-77 is a selective Mcl-1 inhibitor, which shows high binding affinity to Mcl- |
| R2032555 | UNC0631 | UNC 0631 is a potent G9a inhibitor with IC50 value of 4 nM.IC50 value: 4 nM Targ |
| R2032556 | UNC2250 | UNC2250 is a potent and selective Mer inhibitor with an IC50 of 1.7 nM, about 16 |
| R2032557 | UNC2881 | UNC2881 is a potent and specific Mer kinase inhibitor; inhibits steady-state Mer |
| R2032558 | VE-821 | VE-821 is a potent ATP-competitive inhibitor of ATR with Ki/IC50 of 13 nM/26 nM. |
| R2032559 | Verdinexor(KPT-335) | Verdinexor(KPT-335) is a novel, orally bioavailable selective inhibitor of nucle |
| R2032560 | VS-5584 | VS-5584 is a pan-PI3K/mTOR kinase inhibitor with IC50s of 16 nM, 68 nM, 42 nM, 2 |
| R2032561 | VX-702 | VX-702 is a highly selective inhibitor of p38α MAPK, 14-fold higher potency agai |
| R2032562 | VX745;Neflamapimod(VX-745) | Neflamapimod (VX-745) is a potent, blood-brain barrier penetrant, highly selecti |
| R2032563 | Belnacasan(VX-765) | Belnacasan (VX-765) is an orally bioactive prodrug of VRT-043198, which is a pot |
| 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, |
