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ChemicalBook--->CAS DataBase List--->1061318-81-7

1061318-81-7

1061318-81-7 Structure

1061318-81-7 Structure
IdentificationBack Directory
[Name]

Debio 0932 ,CUDC-305
[CAS]

1061318-81-7
[Synonyms]

CS-1423
CUDC-305
bio 0932
Debio 0932
Debio 0932 ,CUDC-305
CUDC-305 (DEBIO-0932 )
1H-Imidazo[4,5-c]pyridine-1-ethanamine, 4-amino-2-[[6-(dimethylamino)-1,3-benzodioxol-5-yl]thio]-N-(2,2-dimethylpropyl)-
[Molecular Formula]

C22H30N6O2S
[MOL File]

1061318-81-7.mol
[Molecular Weight]

442.58
Chemical PropertiesBack Directory
[Boiling point ]

654.8±65.0 °C(Predicted)
[density ]

1.32±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:33.0(Max Conc. mg/mL);74.56(Max Conc. mM)
[form ]

A crystalline solid
[pka]

10.02±0.19(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

Debio 0932 (CUDC-305) is an orally active HSP90 inhibitor, with IC50s of 100 and 103 nM for HSP90α and HSP90β, respectively[1].
[in vivo]

Debio 0932 (CUDC-305, 30 mg/kg, p.o.) exhibits favorable pharmacokinetic profiles in tumor-bearing nude mice. Debio 0932 (160 mg/kg, p.o.) causes degradation of HSP90 client proteins, suppresses tumor growth, and also prolongs survival in various animal models of U87MG glioblastoma. Debio 0932 (40, 80, or 160 mg/kg, p.o.) also dose-dependently inhibits tumor growth in the U87MG s.c. tumor model by every-other-day (q2d) dosing[1]. Debio 0932 (80 mg/kg, p.o.) significantly alleviates psoriasis by day 11 and decreases epidermal thickness in psoriasis xenograft transplantation model[2]. Debio 0932 (CUDC-305) is able to cross the blood-brain barrier. Debio 0932 (80, 120, and 160 mg/kg, p.o.) shows dose-dependent inhibition of tumor growth in the H1975 subcutaneous tumor model. Debio 0932 (160 mg/kg, p.o.) also promotes antitumor activity in the erlotinib-resistant H1975 subcutaneous tumor model[3].

[IC 50]

HSP90α: 100 nM (IC50); HSP90β: 103 nM (IC50)
[storage]

Store at -20°C
[References]

[1] Bao R, et al. CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacologic properties for cancer therapy. Clin Cancer Res. 2009 Jun 15;15(12):4046-57. DOI:10.1158/1078-0432.CCR-09-0152
[2] Stenderup K, et al. Debio 0932, a new oral Hsp90 inhibitor, alleviates psoriasis in a xenograft transplantation model. Acta Derm Venereol. 2014 Nov;94(6):672-6. DOI:10.2340/00015555-1838
[3] Bao R, et al. Targeting heat shock protein 90 with CUDC-305 overcomes erlotinib resistance in non-small cell lung cancer. Mol Cancer Ther. 2009 Dec;8(12):3296-306. DOI:10.1158/1535-7163.MCT-09-0538
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