BAY-8040 (R)

  Cat. No.:  DC11857   Featured
Chemical Structure
1194453-23-0
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More than 5000 active chemicals with high quality for research!
Field of application
Bay-8040 is a potent, selective human neutrophil elastase (HNE) inhibitor with IC50 of 28 nM; displays no significant inhibition toward 68 other pharmacologically relevant targets (>10 uM), and a panel of related serine proteases; shows in vivo efficacy with regard to decreasing cardiac remodeling and amelioration of cardiac function in monocrotaline-induced rat model for pulmonary arterial hypertension.
Cas No.: 1194453-23-0
Chemical Name: (R)-4-(7-methyl-2,5-dioxo-1-(3-(trifluoromethyl)phenyl)-1,2,3,4,5,6,7,8-octahydropyrimido[4,5-d]pyridazin-4-yl)benzonitrile
Synonyms: BAY 8040;BAY8040
SMILES: C(C1C=CC([C@@H]2NC(=O)N(C3C=C(C(F)(F)F)C=CC=3)C3=C2C(NN(C3)C)=O)=CC=1)#N
Formula: C21H16F3N5O2
M.Wt: 427.379
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Publication: 1. von Nussbaum F, et al. ChemMedChem. 2016 Jan 19;11(2):199-206.
Description: Bay-8040 is a potent, selective human neutrophil elastase (HNE) inhibitor with IC50 of 28 nM; displays no significant inhibition toward 68 other pharmacologically relevant targets (>10 uM), and a panel of related serine proteases; shows in vivo efficacy with regard to decreasing cardiac remodeling and amelioration of cardiac function in monocrotaline-induced rat model for pulmonary arterial hypertension.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC46984 Lonodelestat Lonodelestat (POL6014) is a potent, orally active and selective peptide inhibitor of human neutrophil elastase (hNE).
DC11858 BAY-678 BAY-678 is a cell-permeable inhibitor of human neutrophil elastase (HNE).
DC11857 BAY-8040 (R) Bay-8040 is a potent, selective human neutrophil elastase (HNE) inhibitor with IC50 of 28 nM; displays no significant inhibition toward 68 other pharmacologically relevant targets (>10 uM), and a panel of related serine proteases; shows in vivo efficacy with regard to decreasing cardiac remodeling and amelioration of cardiac function in monocrotaline-induced rat model for pulmonary arterial hypertension.
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