HD2 | DCN1 inhibitor

CAS:
 2543578-57-8
Catalog Number:
 10-4370
HD2 chemical structure

Available Options

Size:PriceQuantity 
5 mg$75.00
25 mg$250.00

HD2 (2543578-57-8) is a potent (IC50 = 2.96 nM) inhibitor of DCN1, an important co-E3 ligase of neddylation.  Displays favorable pharmacokinetics and low toxicity (including no hepatotoxicity).  Selective against other DCN family members as well as ACE. HD2 reduced the migration and proliferation of Ang II-treated cardiac fibroblasts. Active in an isoproterenol-induced pathological cardiac remodeling and fibrosis mouse model. HD2 is a promising new therapeutic option for treatment of cardiac remodeling and fibrosis.

References/CItations:

  1. He et al. (2024), Discovery of 1,2,4-Triazole-3-thione Derivatives AS Potent and Selective DCN1 Inhibitors for Pathological Cardiac Fibrosis and Remodeling; J. Med. Chem. 67 18699
CAS:
2543578-57-8
Catalog Number:
10-4370
Activity:
DCN1 inhibitor
Chemical Names:
3-(3-(4-Chlorophenyl)-5-mercapto-4H-1,2,4-triazol-4-yl)-N-(3-(trifluoromethyl)phenyl)propanamide
Molecular Weight:
426.84
Molecular Formula:

C18H14ClF3N4OS

Solubility:
Soluble in DMSO (at least 60 mg/ml)
Physical Properties:
White solid
Purity:

>98% HPLC
NMR: (Conforms)

Storage Temperature:
-20°C
Stability:
Stable for up to 2 years when stored as supplied @ -20°C. Solutions in DMSO may be stored at -20°C for up to 3 months.
Shipping Code:
RT

Safety Data Sheet:

N/A

Product Data Sheet:

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