DI-82

Modify Date: 2024-01-08 19:15:46

DI-82 Structure
DI-82 structure
Common Name DI-82
CAS Number 1638148-50-1 Molecular Weight 510.65
Density N/A Boiling Point N/A
Molecular Formula C20H26N6O4S3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of DI-82


DI-82 is a potent deoxycytidine kinase (dCK) inhibitor with an IC50app of 27.8 nM and Kiapp of 9.2 nM. DI-82 has antitumor activity[1].

 Names

Name DI-82

 DI-82 Biological Activity

Description DI-82 is a potent deoxycytidine kinase (dCK) inhibitor with an IC50app of 27.8 nM and Kiapp of 9.2 nM. DI-82 has antitumor activity[1].
Related Catalog
Target

IC50app: 27.8 nM (dCK)[1] Kiapp: 9.2 nM (dCK)[1]

In Vitro DI-82 (compound 12R) has an IC50 of 3.7 nM in CCRF-CEM acute lymphoblastic leukemia cells[1]. DI-82 (1 μM) has a NADPH-dependent CLint of 22.7 μL/min•mg and a NADPH-dependent T1/2 of 102 mins in a standard microsomal liver clearance assay[1]. DI-82 (200 μM) completely blunts the ability of decitabine to bind human thymidylate synthase (TS)[2].
References

[1]. Julian Nomme, et al. Structure-guided Development of Deoxycytidine Kinase Inhibitors With Nanomolar Affinity and Improved Metabolic Stability. J Med Chem. 2014 Nov 26;57(22):9480-94.

[2]. Helena Almqvist, et al. CETSA Screening Identifies Known and Novel Thymidylate Synthase Inhibitors and Slow Intracellular Activation of 5-fluorouracil. Nat Commun. 2016 Mar 24;7:11040.

 Chemical & Physical Properties

Molecular Formula C20H26N6O4S3
Molecular Weight 510.65
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