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ChemicalBook--->CAS DataBase List--->308246-52-8

308246-52-8

308246-52-8 Structure

308246-52-8 Structure
IdentificationBack Directory
[Name]

LMP744
[CAS]

308246-52-8
[Synonyms]

LMP744
NSC-706744
5H-[1,3]Dioxolo[5,6]indeno[1,2-c]isoquinoline-5,12(6H)-dione, 6-[3-[(2-hydroxyethyl)amino]propyl]-2,3-dimethoxy-
6-(3-((2-hydroxyethyl)amino)propyl)-2,3-dimethoxy-5H-[1,3]dioxolo[4,5:5,6]indeno[1,2-c]isoquinoline-5,12(6H)-dione(WXG02929)
[Molecular Formula]

C24H24N2O7
[MDL Number]

MFCD32645133
[MOL File]

308246-52-8.mol
[Molecular Weight]

452.46
Chemical PropertiesBack Directory
[Melting point ]

231-234 °C
[Boiling point ]

748.1±60.0 °C(Predicted)
[density ]

1.46±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

14.79±0.10(Predicted)
[color ]

Brown to dark brown
Hazard InformationBack Directory
[Uses]

LMP744 (MJ-III65) is a DNA intercalator and Topoisomerase I (Top1) inhibitor with antitumor activity[1].
[in vivo]

LMP744 (MJ-III65) (10-50 mg/kg) administered i.v. push once a week for 4 weeks in nude mice moderately actives against human A253 and FaDu tumor xenografts without significant toxicity[1].

Animal Model:Athymic nude mice (nu/nu, female, 20-25 g, 8-12 weeks old) transplanted with A253 and FaDu human head and neck xenografts[1].
Dosage:10, 25, or 50 mg/kg/week, 4 weeks
Administration:I.V. push via tail vein
Result:Moderately actived against human A253 and FaDu tumor xenografts without significant toxicity.
[IC 50]

Top1
[storage]

Store at -20°C
[References]

[1] Antony S, et al. Cellular topoisomerase I inhibition and antiproliferative activity by MJ-III-65 (NSC 706744), an indenoisoquinoline topoisomerase I poison. Mol Pharmacol. 2005 Feb;67(2):523-30. DOI:10.1124/mol.104.003889
[2] Antony S, et al. Novel indenoisoquinolines NSC 725776 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance. Cancer Res. 2007 Nov 1;67(21):10397-405. DOI:10.1158/0008-5472.CAN-07-0938
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