3',4',7-trihydroxyisoflavone
4H-1-benzopyran-4-one, 3-(3,4-dihydroxyphenyl)-7-hydroxy-
 
Notes:
from streptomyces sp oh-1049. A polyphenol metabolite detected in biological fluids [PhenolExplorer]
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CAS Number: 485-63-2Picture of molecule3D/inchi
FDA UNII: T08Y239E7Y
Nikkaji Web: J91.438J
Beilstein Number: 00251800
MDL: MFCD00143002
XlogP3-AA: 2.10 (est)
Molecular Weight: 270.24070000
Formula: C15 H10 O5
BioActivity Summary: listing
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
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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
Boiling Point: 572.80 °C. @ 760.00 mm Hg (est)
Flash Point: 435.00 °F. TCC ( 224.00 °C. ) (est)
logP (o/w): 2.580 (est)
Soluble in:
 water, 1188 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:
ExtraSynthese
For experimental / research use only.
3',4',7-Trihydroxyisoflavone (HPLC) ≥90%
Santa Cruz Biotechnology
For experimental / research use only.
3',4',7-Trihydroxyisoflavone
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Safety Information:
Preferred SDS: View
 
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 3',4',7-trihydroxyisoflavone usage levels up to:
 not for fragrance use.
 
Recommendation for 3',4',7-trihydroxyisoflavone flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5284648
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 3-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one
Chemidplus: 0000485632
RTECS: DJ3002500 for cas# 485-63-2
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References:
 3-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5284648
Pubchem (sid): 135227189
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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): C14313
HMDB (The Human Metabolome Database): HMDB41655
FooDB: FDB029811
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
 found in nature
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Synonyms:
4H-1-benzopyran-4-one, 3-(3,4-dihydroxyphenyl)-7-hydroxy-
3-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one
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Articles:
PubMed: Pharmacological chaperones increase residual β-galactocerebrosidase activity in fibroblasts from Krabbe patients.
PubMed: Production of a novel O-methyl-isoflavone by regioselective sequential hydroxylation and O-methylation reactions in Streptomyces avermitilis host system.
PubMed: Transcriptomic study for screening genes involved in the oxidative bioconversions of Streptomyces avermitilis.
PubMed: Inhibitory effects of isoflavonoids on rat prostate testosterone 5α-reductase.
PubMed: 7,3',4'-Trihydroxyisoflavone modulates multidrug resistance transporters and induces apoptosis via production of reactive oxygen species.
PubMed: [Interaction between three isoflavones and different isomers of human serum albumin].
PubMed: 7,3',4'-Trihydroxyisoflavone, a metabolite of the soy isoflavone daidzein, suppresses ultraviolet B-induced skin cancer by targeting Cot and MKK4.
PubMed: 7,3',4'-Trihydroxyisoflavone inhibits epidermal growth factor-induced proliferation and transformation of JB6 P+ mouse epidermal cells by suppressing cyclin-dependent kinases and phosphatidylinositol 3-kinase.
PubMed: A-ring ortho-specific monohydroxylation of daidzein by cytochrome P450s of Nocardia farcinica IFM10152.
PubMed: Regioselective hydroxylation of isoflavones by Streptomyces avermitilis MA-4680.
PubMed: ortho-dihydroxyisoflavone derivatives from aged Doenjang (Korean fermented soypaste) and its radical scavenging activity.
PubMed: Biochemical characterization of 60S acidic ribosomal P proteins associated with CK-II from bamboo shoots and potent inhibitors of their phosphorylation in vitro.
PubMed: Urinary metabolites of daidzin orally administered in rats.
PubMed: Structural study of isoflavonoids possessing antioxidant activity isolated from the fermentation broth of Streptomyces sp.
PubMed: Isolation of isoflavonoids possessing antioxidant activity from the fermentation broth of Streptomyces sp.
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