ChemicalBook--->CAS DataBase List--->146204-42-4

146204-42-4

146204-42-4 Structure

146204-42-4 Structure
IdentificationBack Directory
[Name]

BM 212
[CAS]

146204-42-4
[Synonyms]

BM 212
BM 212;BM-212
1-((1,5-bis(4-chlorophenyl)-2-methyl-1H-pyrrol-3-yl)methyl)-4-methylpiperazine
Piperazine, 1-[[1,5-bis(4-chlorophenyl)-2-methyl-1H-pyrrol-3-yl]methyl]-4-methyl-
[Molecular Formula]

C23H25Cl2N3
[MDL Number]

MFCD30489752
[MOL File]

146204-42-4.mol
[Molecular Weight]

414.37
Chemical PropertiesBack Directory
[Boiling point ]

528.3±50.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:0.75(Max Conc. mg/mL);1.81(Max Conc. mM)
Ethanol:3.03(Max Conc. mg/mL);7.31(Max Conc. mM)
[form ]

A crystalline solid
[pka]

7.60±0.10(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

BM212 is a potent Mycobacterial membrane protein Large 3 (MmpL3) inhibitor. BM212 has strong bactericidal activity against both M. tuberculosis and some nontuberculosis mycobacteria. BM212 exhibits antimycobacterial activity against M. tuberculosis H37Rv with an MIC of 5 μM[1][2].
[References]

[1] Deidda D et al. Bactericidal activities of the pyrrole derivative BM212 against multidrug-resistant and intramacrophagic Mycobacterium tuberculosis strains. Antimicrob Agents Chemother. 1998 Nov;42(11):3035-7. DOI:10.1128/AAC.42.11.3035
[2] Poce G et al. Improved BM212 MmpL3 inhibitor analogue shows efficacy in acute murine model of tuberculosis infection. PLoS One. 2013;8(2) DOI:10.1371/journal.pone.0056980
[3] Albertus Viljoen, et al. Fast chemical force microscopy demonstrates that glycopeptidolipids define nanodomains of varying hydrophobicity on mycobacteria. Nanoscale Horiz. 2020 Jun 1;5(6):944-953. DOI:10.1039/c9nh00736a
[4] Delia Deidda, et al. Bactericidal activities of the pyrrole derivative BM212 against multidrug-resistant and intramacrophagic Mycobacterium tuberculosis strains. Antimicrob Agents Chemother. 1998 Nov;42(11):3035-7. DOI:10.1128/AAC.42.11.3035
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