Informations sur le produit
- (4-chlorophenyl)[5-methoxy-2-methyl-3-(2-morpholin-4-yl-2-oxoethyl)-2H-indol-2-yl]methanone
- 1H-Indole, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-3-[2-(4-morpholinyl)-2-oxoethyl]-
- 2-(1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)-1-morpholinoethanone
- 2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)ethanone
- 2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(morpholin-4-yl)ethan-1-one
- 2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]-1-morpholin-4-ylethanone
- Bml 190
- Ethanone, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)-
- Indole, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-[(morpholinocarbonyl)methyl]-
- Lm-4131
- Voir d'autres synonymes
BML-190 is a quinoline compound that inhibits the growth of cancer cells. It has antimicrobial activity and can bind to the CB2 receptor on cells, preventing the binding of endogenous cannabinoids. BML-190 also blocks the production of certain growth factors and erythropoietin, which may inhibit tumor proliferation. BML-190 has been shown to have anti-inflammatory properties in animal models. This drug has been shown to have anticancer effects in rat liver microsomes and colorectal carcinoma cells in vitro. BML-190 is not active against cryptococcus neoformans, although it inhibits pluripotent stem cell growth in vitro.
Propriétés chimiques
Question d’ordre technique sur : 3D-CAA85432 BML-190
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