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

morusinol
oxydihydromorusi

Supplier Sponsors

CAS Number: 62949-93-3Picture of molecule3D/inchi
FDA UNII: IA6I4SG21V
Nikkaji Web:J1.046.905H
XlogP3-AA:4.10 (est)
Molecular Weight:438.47662000
Formula:C25 H26 O7
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
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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, 0.4867 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.
Morusinol 98%
BOC Sciences
For experimental / research use only.
Morusinol >98%
Odor: characteristic
Use: Morusinol is a natural flavonoid found in the root bark of Morus alba L, it inhibits arterial thrombosis in vivo due to antiplatelet activity. antiplatelet
 
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 morusinol usage levels up to:
 not for fragrance use.
 
Recommendation for morusinol 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 :5481968
National Institute of Allergy and Infectious Diseases:Data
2-(2,4-dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one
Chemidplus:0062949933
 
References:
 2-(2,4-dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5481968
Pubchem (cas):62949-93-3
 
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
KEGG (GenomeNet):C17868
HMDB (The Human Metabolome Database):HMDB30620
FooDB:FDB002518
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
 morus alba root bark
Search Trop Picture
 
Synonyms:
oxydihydromorusi
2-(2,4-dihydroxy-phenyl)-5-hydroxy-3-(3-hydroxy-3-methyl-butyl)-8,8-dimethyl-8H-benzo(1,2-b:4,3-b')dipyran-4-one
2-(2,4-dihydroxyphenyl)-5-hydroxy-3-(3-hydroxy-3-methylbutyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one
 

Articles:

PubMed:Synergism of prenylflavonoids from Morus alba root bark against clinical MRSA isolates.
PubMed:Two new prenylflavonoids from Morus alba.
PubMed:Evaluation of anti-inflammatory activity of prenylated substances isolated from Morus alba and Morus nigra.
PubMed:Morusinol extracted from Morus alba inhibits arterial thrombosis and modulates platelet activation for the treatment of cardiovascular disease.
PubMed:Isolation of cholinesterase-inhibiting flavonoids from Morus lhou.
PubMed:Root turnover: an important source of microbial substrates in rhizosphere remediation of recalcitrant contaminants.
PubMed:Morusinol, isoprenoid flavone from Morus root barks.
 
Notes:
None found
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