ChemicalBook--->CAS DataBase List--->1253491-42-7

1253491-42-7

1253491-42-7 Structure

1253491-42-7 Structure
IdentificationBack Directory
[Name]

SP 141
[CAS]

1253491-42-7
[Synonyms]

SP 141
SP 141;SP141;
6-Methoxy-1-(1-naphthyl)-9H-β-carboline
6-Methoxy-1-(1-naphthalenyl)-9H-pyrido[3,4-b]indole
9H-Pyrido[3,4-b]indole, 6-methoxy-1-(1-naphthalenyl)-
[Molecular Formula]

C22H16N2O
[MDL Number]

MFCD29059920
[MOL File]

1253491-42-7.mol
[Molecular Weight]

324.38
Chemical PropertiesBack Directory
[Boiling point ]

571.2±45.0 °C(Predicted)
[density ]

1.284±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

≤100mg/ml in ethanol;30mg/ml in DMSO;50mg/ml in dimethyl formamide
[form ]

crystalline solid
[pka]

15.04±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Description]

Mouse double minute 2 protein (MDM2) is an E3 ubiquitin-protein ligase that binds and ubiquitinates the tumor suppressor p53, leading to its degradation by the proteasome. SP 141 is a cell-permeable inhibitor of MDM2 (Ki = 28 nM). Binding of MDM2 by SP 141 promotes its auto-ubiquitination and proteasomal degradation. SP 141 induces cell cycle arrest and apoptosis in breast and pancreatic cancer cell lines and inhibits xenograft tumor growth in vivo. This compound has a short half-life in plasma and wide tissue distribution in tumor-bearing nude mice.
[Uses]

SP 141 induces cell cycle arrest and apoptosis in breast and pancreatic cancer cell lines, inhibiting xenograft tumor growth in vivo.
[storage]

Store at -20°C
[References]

[1]. vassilev lt, vu bt, graves b, et al. in vivo activation of the p53 pathway by small-molecule antagonists of mdm2. science. 2004 feb 6;303(5659):844-8.
[2]. wang w, qin jj, voruganti s, et al. the pyrido[b]indole mdm2 inhibitor sp-141 exerts potent therapeutic effects in breast cancer models. nat commun. 2014 oct 1;5:5086.
[3]. wang w, qin jj, voruganti s, et al. identification of a new class of mdm2 inhibitor that inhibits growth of orthotopic pancreatic tumors in mice. gastroenterology. 2014 oct;147(4):893-902.e2.
[4]. nag s, qin jj, voruganti s, et al. development and validation of a rapid hplc method for quantitation of sp-141, a novel pyrido[b]indole anticancer agent, and an initial pharmacokinetic study in mice. biomed chromatogr. 2015 may;29(5):654-63.
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