ChemicalBook--->CAS DataBase List--->1883650-95-0

1883650-95-0

1883650-95-0 Structure

1883650-95-0 Structure
IdentificationBack Directory
[Name]

CDDO-2-P-Im
[CAS]

1883650-95-0
[Synonyms]

CPD1589
CPDB1589
CDDO-2-P-Im
CDDO-3P-Imidazolide
Oleana-1,9(11)-diene-2-carbonitrile, 3,12,28-trioxo-28-[4-(3-pyridinyl)-1H-imidazol-1-yl]-
[Molecular Formula]

C39H46N4O3
[MOL File]

1883650-95-0.mol
[Molecular Weight]

618.81
Chemical PropertiesBack Directory
[Boiling point ]

771.1±70.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 250 mg/mL (404.00 mM)
[form ]

Solid
[pka]

3.34±0.12(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

CDDO-3P-Im is an analogue of CDDO-Imidazolide with chemopreventive effect. CDDO-3P-Im can reduce the size and the severity of the lung tumors in mouse lung cancer model[1]. CDDO-3P-Im is a orally active necroptosis inhibitor that can be used for the research of ischemia/reperfusion (I/R)[2].
[in vivo]

CDDO-3P-Im is more stable than CDDO-Im in pharmacokinetic studies[1].
CDDO-3P-Im significantly elevates heme oxygenase-1 (HO-1) and quinone reductase (NQO1) mRNA and protein levels in various mouse tissues in vivo[1].
CDDO-3P-Im (50-200 mg/kg; diet; for 16 weeks) decreases the number, the size and the severity of tumors in A/J mice[1].

Animal Model:Seven week-old female A/J mice[1]
Dosage:50 mg/kg, 200 mg/kg
Administration:Diet; for 16 weeks
Result:Decreased the number, the size and the severity of tumors.
[References]

[1] Cao M , et al. Novel synthetic pyridyl analogues of CDDO-Imidazolide are useful new tools in cancer prevention. Pharmacol Res. 2015 Oct;100:135-47. DOI:10.1016/j.phrs.2015.07.024
[2] Yuanyuan Wang, et al. Discovery of bardoxolone derivatives as novel orally active necroptosis inhibitors. Eur J Med Chem. 2020 Nov 21;113030. DOI:10.1016/j.ejmech.2020.113030
Spectrum DetailBack Directory
[Spectrum Detail]

CDDO-2-P-Im(1883650-95-0)1HNMR
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