EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

cajanin
isoflavone, 2,',4',5-trihydroxy-7-methoxy-

Supplier Sponsors

CAS Number: 32884-36-9Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J20.651B
XlogP3-AA:2.60 (est)
Molecular Weight:300.26684000
Formula:C16 H12 O6
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, 147.7 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.
Cajanin >98%
Odor: characteristic
Use: Cajanin is a natural flavonoid found in the herbs of Kadsura interior. It has been shown to be promising anticancer compound with low toxicity. anticancer
 
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 cajanin usage levels up to:
 not for fragrance use.
 
Recommendation for cajanin 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 :5281706
National Institute of Allergy and Infectious Diseases:Data
3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one
Chemidplus:0032884369
 
References:
 3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5281706
Pubchem (cas):32884-36-9
 
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):C10203
HMDB (The Human Metabolome Database):HMDB32696
FooDB:FDB010653
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 cajanus cajan
Search Trop Picture
 
Synonyms:
3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one
isoflavone, 2,',4',5-trihydroxy-7-methoxy-
 

Articles:

PubMed:Activity of the antiestrogenic cajanin stilbene acid towards breast cancer.
PubMed:Cell cycle arrest and induction of apoptosis by cajanin stilbene acid from Cajanus cajan in breast cancer cells.
PubMed:Cytotoxicity of natural products and derivatives toward MCF-7 cell monolayers and cancer stem-like mammospheres.
PubMed:Synthetic cajanin stilbene acid derivatives inhibit c-MYC in breast cancer cells.
PubMed:Prenylated isoflavonoids from Rhynchosia edulis.
PubMed:Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa.
PubMed:Flavonoids and isoflavonoids from Sophorae Flos improve glucose uptake in vitro.
PubMed:Methoxylated isoflavones, cajanin and isoformononetin, have non-estrogenic bone forming effect via differential mitogen activated protein kinase (MAPK) signaling.
PubMed:Antimicrobial activity of the crude extract, fractions and compounds from stem bark of Ficus ovata (Moraceae).
PubMed:Estrogenic constituents of the heartwood of Dalbergia parviflora.
PubMed:Isoflavones from Ficus nymphaefolia.
PubMed:Indicanines B and C, two isoflavonoid derivatives from the root bark of Erythrina indica.
 
Notes:
None found
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