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ChemicalBook--->CAS DataBase List--->1391108-10-3

1391108-10-3

1391108-10-3 Structure

1391108-10-3 Structure
IdentificationBack Directory
[Name]

BM-1074
[CAS]

1391108-10-3
[Synonyms]

BM-1074
1H-Pyrrole-3-carboxamide, 5-(4-chlorophenyl)-4-[3-[4-[4-[[[4-[[(1R)-3-(dimethylamino)-1-[(phenylthio)methyl]propyl]amino]-3-nitrophenyl]sulfonyl]amino]phenyl]-1-piperazinyl]phenyl]-2-methyl-1-(1-methylethyl)-N-(methylsulfonyl)-
[Molecular Formula]

C50H57ClN8O7S3
[MDL Number]

MFCD26960894
[MOL File]

1391108-10-3.mol
[Molecular Weight]

1013.68
Chemical PropertiesBack Directory
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO mg/mL Water mg/mL Ethanol mg/mL
[pka]

2.32±0.40(Predicted)
Hazard InformationBack Directory
[Uses]

BM-1074 is a potent Bcl-2/Bcl-xL inhibitor which is capable of achieving rapid, complete, and durable tumor regression in vivo.
[in vivo]

BM-1074 (i.v., 15 mg/kg, daily, 5 days a week for 2 weeks) exhibits the maximum tolerated dose (MTD) (15 mg/kg) and strong antitumor activity in H146 tumor xenograft mice, as well as shows no significant weight loss (<5%) or other signs of toxicity[1].
BM-1074 (i.v., 15 mg/kg, single) induces strong apoptosis in H146 tumor tissues[1].

Animal Model:SCID mice (injected with 5 x 106 H146 cancer cells with Matrigel, subcutaneously)[1]
Dosage:15 mg/kg
Administration:i.v., 15 mg/kg, daily, 5 days a week for 2 weeks
Result:Showed good toleration and did not cause significant weight loss or other signs of toxicity, also induced completely and persistent tumor regression in the H146 xenograft model.
Animal Model:SCID mice (injected with 5 x 106 H146 cancer cells with Matrigel, subcutaneously)[1]
Dosage:15 mg/kg
Administration:i.v., 15 mg/kg, single dosage
Result:Induced robust cleavage of PARP and caspase-3 at both 3 and 6-hr time-points in H146 tumor tissues.
[IC 50]

Bcl-2: 1.8 nM (IC50); Bcl-xL: 6.9 nM (IC50)
[storage]

Store at -20°C
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