phaseollidin
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      37831-70-2 Phaseollidin >98%
      Phaseollidin, also called 3,9-Dihydroxy-10-prenylpterocarpan, is a natural flavonoid isolated from the fruits of Phaseolus vulgaris. Phaseollidin exhibits the activity of antimicrobial. anti-microbial
       
       
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CAS Number: 37831-70-2Picture of molecule3D/inchi
Nikkaji Web: J18.400D
MDL: MFCD00272171
XlogP3-AA: 4.20 (est)
Molecular Weight: 324.37620000
Formula: C20 H20 O4
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.514 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
Phaseollidin >98%
Odor: characteristic
Use: Phaseollidin, also called 3,9-Dihydroxy-10-prenylpterocarpan, is a natural flavonoid isolated from the fruits of Phaseolus vulgaris. Phaseollidin exhibits the activity of antimicrobial. anti-microbial
Carbosynth
For experimental / research use only.
Phaseollidin
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for phaseollidin usage levels up to:
 not for fragrance use.
 
Recommendation for phaseollidin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 119268
National Institute of Allergy and Infectious Diseases: Data
 (6aR,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
Chemidplus: 0037831702
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References:
 (6aR,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 119268
Pubchem (cas): 37831-70-2
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C05230
HMDB (The Human Metabolome Database): HMDB33669
FooDB: FDB011772
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 phaseolus aureus
Search Trop  Picture
 phaseolus calcaratus
Search Trop  Picture
 phaseolus vulgaris
Search Trop  Picture
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Synonyms:
6H-benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-10-(3-methyl-2-butenyl)-, (6aR,11aR)-
(6aR,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
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Articles:
PubMed: [Chemical constituents from EtOAc fraction of Sophora dunnii].
PubMed: Cytotoxic evaluation of alkaloids and isoflavonoids from the Australian tree Erythrina vespertilio.
PubMed: Prenylated pterocarpanes from Erythrina melanacantha.
PubMed: Flavanoids and pterocarpans from the bark of Erythrina fusca.
PubMed: Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii.
PubMed: Homohesperetin and phaseollidin from Erythrina velutina.
PubMed: Prenylated isoflavanone from the roots of Erythrina sigmoidea.
PubMed: Two bioactive pterocarpans from Erythrina burana.
PubMed: An extracellular enzyme from Fusarium solani f. sp. phaseoli which catalyses hydration of the isoflavonoid phytoalexin, phaseollidin.
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