52250-35-8

Basic information

• Product Name: ISOMUCRONULATOL
• Synonyms: ISOMUCRONULATOL;(3R)-2,3-Dihydro-3β-(2-hydroxy-3,4-dimethoxyphenyl)-7-hydroxy-4H-1-benzopyran;(3R)-3β-(2-Hydroxy-3,4-dimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol;(3R)-3β-(2-Hydroxy-3,4-dimethoxyphenyl)chroman-7-ol;(+/-)-2',7-Dihydroxy-3',4'-dimethoxyisoflavan;7,2'-Dihydroxy-3',4'-dimethoxyisoflavan;DL-Isomucronulatol;2'-Dihydroxy-3'
• CAS NO: 52250-35-8
• Molecular Formula: C17H18O5
• Molecular Weight: 302.32
• Mol File: 52250-35-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Density: 1.279
• CAS DataBase Reference: ISOMUCRONULATOL(CAS DataBase Reference)
• NIST Chemistry Reference: ISOMUCRONULATOL(52250-35-8)
• EPA Substance Registry System: ISOMUCRONULATOL(52250-35-8)

Safety Data

• Hazardous Substances Data: 52250-35-8(Hazardous Substances Data)

Usage

Uses

Isomucronulatol is Codonopsis pilosula and Astragalus membranaceus compound.

Upstream product

• 101153-41-7 odoriflavene 
• 73340-41-7 (-)-6aR,11aR-dihydro-3-hydroxy-9,10-dimethoxy-6H-benzofuro<3,2-c><1>-benzopyran 
• 485-72-3 7-Hydroxy-3-(4-methoxy-phenyl)-chromen-4-on 
• 52250-21-2 7,2'-dibenzyloxy-3',4'-dimethoxyisoflavone 

Relevant articles and documents

A PTEROCARPAN AND TWO ISOFLAVANS FROM ALFALFA

(-)-6aR,11aR-Dihydro-3-hydroxy-9,10-dimethoxy-6H-benzofuro-benzopyran (10-methoxymedicarpin), (+)-(2,3,4-trimethoxyphenyl)-2,3-dihydro-7-hydroxy-4H-1-benzopyran (7-hydroxy-2',3',4'-trimethoxyisoflavan) and (+)-(2,3,4-trimethoxy-5-hydroxyphenyl)-

Inhibitors of prostaglandin biosynthesis from Dalbergia odorifera

The root heartwood of Dalbergia odorifera T. CHEN (Leguminosae) is a Chinese medicinal drug (Japanese name koshinko) used for a stagnant blood syndrome (stagnation of disordered blood; Japanese, oketsu). In addition to 10 known compounds, five new phenolic compounds, isomucronustyrene and hydroxyobtustyrene (cinnamylphenols), (+)-isoduartin (isoflavan), odoriflavene (isoflav-3-ene) and (-)-odoricarpan (pterocarpan) were isolated and their structures were elucidated on the basis of chemical and spectroseopic methods. Of the fifteen compounds isolated, cinnamylphenols, isoflavans, isoflavene and benzoic acid derivative significantly inhibited prostaglandin biosynthesis as well as platelet aggregation induced by arachidonic acid.