编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
1712141 | Benzetimide HCl | 5633-14-7 | >98% | |
Benzetimide HCl, also known as EINECS 227-072-8, Spasmentral, and Dioxatrine, is a mu | ||||
17022714 | ZM241385 | 139180-30-6 | 98% | |
ZM241385是一种腺苷A2A受体拮抗剂。ZM241385在大鼠CA1海马区缺氧后增 | ||||
17021304 | Y-27632二盐酸盐 | 557782-81-7 | 98% | |
ZINC00881524是一个Y-27632二盐酸盐抑制剂。 | ||||
16122852 | ZLN005 | 49671-76-3 | 98% | |
ZLN005 is a PGC-1 Transcriptional Regulator, which shoed some beneficialfEffects on d | ||||
16122851 | ZL006 | 1181226-02-7 | 98% | |
ZL006 is a PSD95-nNOS protein-protein interaction inhibitor. ZL006 (EC50: 12.88 M) di | ||||
16122850 | ZK-756326 dihydrochloride | 1780259-94-0 | 98% | |
ZK-756326 is a potent, selective and non-peptide CCR8 chemokine receptor agonist. ZK | ||||
16122771 | Z-IETD-FMK | 210344-98-2 | 98% | |
Z-IETD-FMK is a specific Caspase-8 inhibitor.Z-IETD-FMK, which inhibits the cleavage | ||||
16122725 | ZK756326 | 874911-96-3 | 98% | |
ZK756326 is a full agonist of CCR8Chemokine receptor 8 with an IC50 of 1.8 M, dose-re | ||||
611814 | ZLN024 hydrochloride | 98% | ||
ZLN024 Hcl is a novel AMPK allosteric activator; activated 111 and 211 by around 2C2. | ||||
161009018 | Zotarolimus | 221877-54-9 | 98% by HPLC | |
It is a semi-synthetic derivative of rapamycin. It was designed for use in stents wit | ||||
160926006 | ZSTK474 | 475110-96-4 | 98% by HPLC | |
Combination treatment using X-rays then ZSTK474 given orally for 8 days, starting 2 | ||||
16071403 | Z-Vad-fmk, non-methylated | 161401-82-7 | 98% by HPLC | |
Z-Vad-fmk, non-methylated | ||||
16062112 | Z-DEVD-FMK | 210344-95-9 | 98% by HPLC | |
Z-DEVD-FMK(Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and | ||||
16062111 | Z-FA-FMK | 105637-38-5 | 98% by HPLC | |
Z-FA-FMK | ||||
16062110 | Z-VAD(OH)-FMK | 634911-81-2 | 98% by HPLC | |
Z-VAD(OH)-FMK | ||||
011908 | Zibotentan | 186497-07-4 | 98% | |
Zibotentan is an orally available selective antagonist of the endothelin-A (ET-A) rec | ||||
122923 | ZM 306416 | 690206-97-4 | 98% | |
ZM-306416 is a VEGFR inhibitor that inhibits Flk-1 (KDR) (IC50=100 nM) and Flt (IC50 | ||||
122214 | ZM 323881 hydrochloride | 324077-30-7 | 98% | |
 ZM323881 is a potent and selective inhibitor of VEGF-R2 tyrosine kinase in vitr | ||||
121415 | Zucapsaicin | 25775-90-0 | 98% | |
Comig soon! | ||||
111008 | ZM323881 hydrochloride | 193000-39-4 | 98% | |
ZZZM 323881 Hcl is a potent and selective VEGFR2 inhibitor with IC50 of <2 nM, alm | ||||
110604 | Z-VAD-FMK | 187389-52-2 | 98% | |
Z-VAD-FMK is a cell-permeable, irreversible broad-spectrum caspase inhibitor, blocks | ||||
101201 | 1088965-37-0 | 1088965-37-0 | 98% | |
Coming soon! | ||||
52555 | ZCL278 | 587841-73-4 | 98% | |
ZCL278 is a Cdc42 small molecule modulator that directly binds to Cdc42 (Kd=11.4 uM) | ||||
52239 | ZM 336372 | 208260-29-1 | 98% | |
ZM 336372 is a potent and selective c-Raf inhibitor with IC50 of 70 nM, 10-fold selec | ||||
52003 | Zosuquidar trihydrochloride | 167465-36-3 | 99% | |
zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl |