About 10 results found for searched term "58-55-9" (0.068 seconds)
Cat.No. | Name | Target |
---|---|---|
M4568 | Aescin-IIA | Others |
Escin IIa, isolated from horse chestnut seed horse chestnut, has a positive effect on acute inflammation in animals. Escin IIa has obvious protective effect on gastric mucosa injury induced by ethanol. | ||
M11355 | EEDi-5273 | PRC2/EED |
Eedi-5273 is a potent and orally effective EED inhibitor (IC50 = 0.2 nM) that can achieve complete and sustained tumor regression. | ||
M6007 | Theophylline | PDE |
1,3-Dimethylxanthine; Theo-24 | ||
Theophylline is a methylated xanthine derivative; competitive nonselective phosphodiesterase inhibitor and nonselective adenosine receptor antagonist. | ||
M8689 | JJKK-048 | MAGL |
JJKK-048 is a cell penetrant ultrapotent and highly selective inhibitor of monoacylglycerol lipase (MAGL) that exhibits a low cross-reactivity with other endocannabinoid targets. | ||
M18664 | Saikosaponin B4 | Others |
Saikosaponin B4 | ||
M30326 | Carboprost tromethamine | Prostaglandin Receptor |
Carboprost tromethamine is the synthetic 15-methyl analogue of prostaglandin F2α. Carboprost tromethamine can effectively promote law contraction of the uterus and significantly reduce the amount of bleeding during and after delivery. | ||
M30471 | CLZ-8 | Bcl-2 |
CLZ-8 (Compound 8) is an orally active Mcl-1-PUMA interface inhibitor, with a Ki of 0.3 μM. CLZ-8 exhibits dual activity on reduce PUMA-dependent apoptosis while deactivating Mcl-1-mediated anti-apoptosis in cancer cells. | ||
M43435 | PROTAC BRD4 Degrader-17 | PROTAC |
PROTAC BRD4 Degrader-17 is a potent PROTAC BRD4 Degrader, with IC50 values of 29.54 nM (BRD4 (BD1)) and 3.82 nM (BRD4 (BD2)). | ||
M53490 | Cys-TAT(47-57) | Anti-infection |
Cys-TAT(47-57) (Cys-[HIV-Tat (47-57)]) is an arginine rich cell penetrating peptide derived from the HIV-1 transactivating protein. | ||
M54396 | LDV | Integrin |
LDV, a tripeptide, is a non-fluorescent analog of LDV-FITC. |
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