CAS 2854-32-2

2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)ethanone

Description:

The chemical substance known as 2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)ethanone, with the CAS number 2854-32-2, is a complex organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This substance features a chlorobenzoyl group, a methoxy group, and a morpholinyl group, contributing to its diverse chemical properties and potential biological activities. The presence of the chlorobenzoyl moiety may enhance its lipophilicity, while the morpholinyl group can influence its pharmacological profile. The compound may exhibit various interactions with biological targets, making it of interest in medicinal chemistry and drug development. Its synthesis and characterization typically involve standard organic reactions, and it may be evaluated for its efficacy in various applications, including as a potential therapeutic agent. Safety and handling precautions should be observed due to the presence of halogenated and nitrogen-containing groups, which may pose specific health risks.

Formula: C₂₃H₂₃ClN₂O₄

InChI: InChI=1S/C23H23ClN2O4/c1-15-19(14-22(27)25-9-11-30-12-10-25)20-13-18(29-2)7-8-21(20)26(15)23(28)16-3-5-17(24)6-4-16/h3-8,13H,9-12,14H2,1-2H3

InChI key: InChIKey=BJSDNVVWJYDOLK-UHFFFAOYSA-N

SMILES: C(=O)(N1C=2C(C(CC(=O)N3CCOCC3)=C1C)=CC(OC)=CC2)C4=CC=C(Cl)C=C4

Synonyms:

• (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

Ethanone, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)-

CAS: 2854-32-2

Formula: C₂₃H₂₃ClN₂O₄

Purity: 99%

Color and Shape: Solid

Molecular weight: 426.8927

Ref: IN-DA002VNX

2-(1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-1H-Indol-3-Yl)-1-Morpholinoethanone

CAS: 2854-32-2

2-(1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-1H-Indol-3-Yl)-1-Morpholinoethanone

Purity: 99%

Molecular weight: 426.89g/mol

Ref: 54-OR1025600

BML-190

CAS: 2854-32-2

BML-190

Purity: ≥95%

Molecular weight: 426.89g/mol

Ref: 54-BUP11373

BML-190

CAS: 2854-32-2

BML-190 (Indomethacin morpholinylamide) 是一种 CB2 受体的配体，其对 CB2 受体 (Ki:435 nM) 和 CB1受体 (Ki> 2 μM)。

Formula: C₂₃H₂₃ClN₂O₄

Purity: 97.70%

Color and Shape: Solid

Molecular weight: 426.89

Ref: TM-T6417

BML-190

CAS: 2854-32-2

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.

Formula: C₂₃H₂₃ClN₂O₄

Purity: Min. 95%

Molecular weight: 426.89 g/mol

Ref: 3D-CAA85432