Indomethacin morpholinylamide; IMMA MedChemExpress (MCE)

Product Name	BML-190
Synonyms	IMMA BML-190 INDOMETHACIN MORPHOLINYLAMIDE 4-((2-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indolyl)acetyl)-morpholin 1h-indole,1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1-(2-(4-morpholinyl)-2-oxoe Synonyms IMMA BML-190 INDOMETHACIN MORPHOLINYLAMIDE 4-((2-(p-chlorobenzoyl)-5-methoxy-2-methyl-3-indolyl)acetyl)-morpholin 1h-indole,1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1-(2-(4-morpholinyl)-2-oxoe BML-190, N-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetyl]morpholine 1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETIC ACID, MORPHOLINEAMIDE 1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1-[2-(4-MORPHOLINYL)-2-OXOETHYL]-1H-INDOLE
CAS	2854-32-2
EINECS
Chemical Formula	C23H23ClN2O4
Molecular Weight	426.89
inchi
Package	10 mM * 1 mL;5 mg;10 mg;25 mg;50 mg;100 mg;500 mg
Price	Email to quote
Descriptions	BML-190 BML-190 MedChemExpress (MCE) HY-15420 2854-32-2 Indomethacin morpholinylamide Descriptions BML-190 BML-190 MedChemExpress (MCE) HY-15420 2854-32-2 Indomethacin morpholinylamide IMMA 99.53% Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year Room temperature in continental US may vary elsewhere. BML-190(IMMA) is a potent and selective CB2 receptor ligand (Ki values are 435 nM and > 2 μM for CB2 and CB1 respectively). \| \| \| \| \| \| \| \| \| \| [1]. Zhang, Qiang Ma, Peng Cole, Richard B. Wang, Guangdi In vitro metabolism of indomethacin morpholinylamide (BML-190), an inverse agonist for the peripheral cannabinoid receptor (CB2) in rat liver microsomes. European Journal of Pharmaceutical Sciences ( [2]. Klegeris, Andis Bissonnette, Christopher J. McGeer, Patrick L. Reduction of human monocytic cell neurotoxicity and cytokine secretion by ligands of the cannabinoid-type CB2 receptor. British Journal of Pharmacology (2003), 139(4), 775-786. [Content Brief] [3]. New DC, Wong YH. BML-190 and AM251 act as inverse agonists at the human cannabinoid CB2 receptor: signalling via cAMP and inositol phosphates. FEBS Lett. 2003 Feb 11 536(1-3):157-60. [Content Brief]
Last Update	2025-04-01 14:45:47

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