phaseollidin, 37831-70-2

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CODE183756 CODE183756
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

CAS Number:	37831-70-2	3D/inchi
FDA UNII:	Search
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, Edge 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

Physical Properties:

Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Soluble in:
	water, 1.514 mg/L @ 25 °C (est)

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

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

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

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.

Safety References:

EPI System: View

AIDS Citations:Search

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

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

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

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

	phaseolus aureus Search Trop Picture
	phaseolus calcaratus Search Trop Picture
	phaseolus vulgaris Search Trop Picture

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

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.

Notes:

None found