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

lupiwighteone
5,7,4'-trihydroxy-8-prenylisoflavone

Supplier Sponsors

CAS Number: 104691-86-3Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J397.729C
XlogP3-AA:4.60 (est)
Molecular Weight:338.35946000
Formula:C20 H18 O5
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, 1.008 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
8-Isopentenylgenistein 98%
BOC Sciences
For experimental / research use only.
Lupiwighteone 0.975
Odor: characteristic
Use: Lupiwighteone isolated from the roots of Glycyrrhiza glabra. It has anticancer and cancer preventive effects on SH-SY5Y cells. anti-angiogenesis potential; anticancer and cancer preventive effects
 
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 lupiwighteone usage levels up to:
 not for fragrance use.
 
Recommendation for lupiwighteone 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 :5317480
National Institute of Allergy and Infectious Diseases:Data
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
 
References:
 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5317480
Pubchem (cas):104691-86-3
 
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
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB38902
FooDB:FDB018366
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
 glycyrrhiza uralensis
Search Trop Picture
 vigna angularis
Search Trop Picture
 
Synonyms:
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
5,7,4'-trihydroxy-8-prenylisoflavone
 

Articles:

PubMed:Isoflavone lupiwighteone induces cytotoxic, apoptotic, and antiangiogenic activities in DU-145 prostate cancer cells.
PubMed:Lupiwighteone induces cell cycle arrest and apoptosis and activates the Nrf2/ARE pathway in human neuroblastoma cells.
PubMed:New antifungal pyranoisoflavone from Ficus tikoua Bur.
PubMed:bis-Sigmodiol: a new prenylflavanone dimer from Erythrina sigmoidea Hua (Fabaceae) of Nigeria.
PubMed:Four new isoflavonoids from the stem bark of Erythrina variegata.
PubMed:Dihydrostilbene derivatives from Glycyrrhiza glabra leaves.
PubMed:Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus speciosus.
 
Notes:
None found
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