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831217-40-4

831217-40-4 Structure

831217-40-4 Structure
IdentificationBack Directory
[Name]

5-PyriMidinecarboxylic acid, 4-[1,1'-biphenyl]-4-yl-1-[6-[[2-(butylaMino)-1-[3-(Methoxycarbonyl)-4-(2-Methoxy-2-oxoethoxy)phenyl]-2-oxoethyl]hexylaMino]-6-oxohexyl]-1,2,3,4-tetrahydro-6-Methyl-2-oxo-, phenylMethyl ester
[CAS]

831217-40-4
[Synonyms]

MAL3-101
benzyl 4-([1,1'-biphenyl]-4-yl)-1-(6-((2-(butylamino) -1-(4-(2-methoxy-2-oxoethoxy)-3-(methoxycarbonyl)phenyl)-2-oxoethyl)(hexyl)amino)-6-oxohexyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
5-PyriMidinecarboxylic acid, 4-[1,1'-biphenyl]-4-yl-1-[6-[[2-(butylaMino)-1-[3-(Methoxycarbonyl)-4-(2-Methoxy-2-oxoethoxy)phenyl]-2-oxoethyl]hexylaMino]-6-oxohexyl]-1,2,3,4-tetrahydro-6-Methyl-2-oxo-, phenylMethyl ester
[Molecular Formula]

C54H66N4O10
[MDL Number]

MFCD20257231
[MOL File]

831217-40-4.mol
[Molecular Weight]

931.123
Chemical PropertiesBack Directory
[Boiling point ]

1037.1±65.0 °C(Predicted)
[density ]

1.165±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

11.16±0.70(Predicted)
[color ]

Off-white to light brown
Hazard InformationBack Directory
[Description]

MAL3-101 is a heat shock protein 70 molecular chaperone inhibitor.
[Uses]

MAL3-101 is a potent HSP70 allosteric inhibitor. MAL3-101 inhibits HSP70 ATPase activity by blocking Hsp40 co-chaperone interaction. MAL3-101 can be used for researching muscle invasive bladder cancer (MIBC)[1].
[IC 50]

HSP70
[References]

[1] Prince T, et al. Dual targeting of HSP70 does not induce the heat shock response and synergistically reduces cell viability in muscle invasive bladder cancer. Oncotarget. 2018 Aug 24;9(66):32702-32717. DOI:10.18632/oncotarget.26021
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