Db07107

Modify Date: 2025-08-26 08:39:41

Db07107 Structure
Db07107 structure
Common Name Db07107
CAS Number 552332-71-5 Molecular Weight 370.45
Density N/A Boiling Point N/A
Molecular Formula C23H22N4O Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Db07107


DB07107 is a potent drug resistant T315I mutant Bcr-Abl tyrosine kinase inhibitor. DB07107 is also a potent Akt1 inhibitor with an IC50 value of 360 nM[1][2].

 Names

Name DB07107

 Db07107 Biological Activity

Description DB07107 is a potent drug resistant T315I mutant Bcr-Abl tyrosine kinase inhibitor. DB07107 is also a potent Akt1 inhibitor with an IC50 value of 360 nM[1][2].
Related Catalog
Target

Bcr-AblT315I

Akt1:360 nM (IC50)

In Vitro DB07107 is more effective in blocking drug-resistant T315I mutant than the wild-type Bcr-Abl. DB07107 (C23H22N4O) from DrugBank showed the highest binding energy with XP score of -14.045 kcal/mol[1].
References

[1]. Banavath HN, et al. Identification of novel tyrosine kinase inhibitors for drug resistant T315I mutant BCR-ABL: a virtual screening and molecular dynamics simulations study. Sci Rep. 2014 Nov 10;4:6948.

[2]. Li Q, et al. Discovery of trans-3,4'-bispyridinylethylenes as potent and novel inhibitors of protein kinase B (PKB/Akt) for the treatment of cancer: Synthesis and biological evaluation. Bioorg Med Chem Lett. 2006 Mar 15;16(6):1679-85.

 Chemical & Physical Properties

Molecular Formula C23H22N4O
Molecular Weight 370.45

 Safety Information

Hazard Codes Xi
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