1598422-94-6

Basic information

• Product Name: (S,E)-methyl 3-(4-(2-([1,1′-biphenyl]-4-ylsulfonamido)-3-(1H-indol-3-yl)propoxy)phenyl)acrylate
• CAS NO: 1598422-94-6
• Molecular Weight: 566.678
• Mol File: 1598422-94-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S,E)-methyl 3-(4-(2-([1,1′-biphenyl]-4-ylsulfonamido)-3-(1H-indol-3-yl)propoxy)phenyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (S,E)-methyl 3-(4-(2-([1,1′-biphenyl]-4-ylsulfonamido)-3-(1H-indol-3-yl)propoxy)phenyl)acrylate(1598422-94-6)
• EPA Substance Registry System: (S,E)-methyl 3-(4-(2-([1,1′-biphenyl]-4-ylsulfonamido)-3-(1H-indol-3-yl)propoxy)phenyl)acrylate(1598422-94-6)

Safety Data

• Hazardous Substances Data: 1598422-94-6(Hazardous Substances Data)

Upstream product

• 110659-38-6 N-t-butoxycarbonyl-tryptophanol 
• 141215-69-2 methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(1H-indol-3-yl)propanoate 
• 7524-52-9 (S)-tryptophan methyl ester hydrochloride 
• 73-22-3 L-Tryptophan 
• 1526901-52-9 (S,E)-methyl 3-(4-(2-((tert-butoxycarbonyl)amino)-3-(1H-indol-3yl)propoxy)phenyl)acrylate 
• 3943-97-3 methyl 4-hydroxycinnamate 
• 7400-08-0 p-Coumaric Acid 
• 2113-68-0 4-biphenylmonosulfonic acid 
• 1526901-56-3 (S,E)-methyl 3-(4-(2-amino-3-(1H-indol-3-yl)propoxy)phenyl)acrylate hydrochloride 

Relevant articles and documents

Discovery of the first N -hydroxycinnamamide-based histone deacetylase 1/3 dual inhibitors with potent oral antitumor activity

In our previous study, we designed and synthesized a novel series of N-hydroxycinnamamide-based HDAC inhibitors (HDACIs), among which the representative compound 14a exhibited promising HDACs inhibition and antitumor activity. In this current study, we report the development of a more potent class of N-hydroxycinnamamide-based HDACIs, using 14a as lead, among which, compound 11r gave IC50 values of 11.8, 498.1, 3.9, 2000.8, 5700.4, 308.2, and 900.4 nM for the inhibition of HDAC1, HDAC2, HDAC3, HDAC8, HDAC4, HDAC6, and HDAC11, exhibiting dual HDAC1/3 selectivity. Compounds 11e, 11r, 11w, and 11y showed excellent growth inhibition in multiple tumor cell lines. In vivo antitumor assay in U937 xenograft model identified compound 11r as a potent, orally active HDACI. To the best of our knowledge, this work constitutes the first report of oral active N-hydroxycinnamamide-based HDACIs with dual HDAC1/3 selectivity.