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acetyl ursolic acid
(3beta)-3-(acetyloxy)urs-12-en-28-oic acid

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Name:(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
CAS Number: 7372-30-7Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J143.977D
XlogP3-AA:7.90 (est)
Molecular Weight:498.74730000
Formula:C32 H50 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
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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, 4.333e-005 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.
3-Acetylursolic acid 98%
BOC Sciences
For experimental / research use only.
Ursolic acid acetate >98%
Odor: characteristic
Use: Acetylursolic acid,that can be isolated from the herbs of Ilex paraguariensis, has several biological activities such as antimalarial, cytotoxic, antitumor, anticancer and NO production inhibitory activities. It maybe a potential anti-cholinesterase agent Antimalarial/cytotoxic/antitumor/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 acetyl ursolic acid usage levels up to:
 not for fragrance use.
 
Recommendation for acetyl ursolic acid 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 :6475119
National Institute of Allergy and Infectious Diseases:Data
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
Chemidplus:0007372307
 
References:
 (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):6475119
Pubchem (cas):7372-30-7
 
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):HMDB36008
FooDB:FDB014823
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
 leptospermum scoparium
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 persimmon
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 rosemary shoot
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 sage
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 verbena
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Synonyms:
(3beta)-3-(acetyl oxy) urs-12-en-28-oic acid
(3beta)-3-(acetyloxy)urs-12-en-28-oic acid
 acetylursolic acid
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
 urs-12-en-28-oic acid, 3-(acetyloxy)-, (3beta)-
 

Articles:

PubMed:Evaluation of the anti-Listeria potentials of some plant-derived triterpenes.
PubMed:[Chemical constituents from the roots of Ilex pubescens].
PubMed:Anti-plasmodial activity of some Zulu medicinal plants and of some triterpenes isolated from them.
PubMed:One new pyrroline compound from Callistemon viminalis (Sol. Ex Gaertner) G.Don Ex Loudon.
PubMed:[Study on the triterpenoids from the fruits of Ligustrum lucidum].
PubMed:Inhibitory effect of ursolic acid derivatives on hydrogen peroxide- and glutathione-mediated degradation of hemin: a possible additional mechanism of action for antimalarial activity.
PubMed:[Chemical constituents from root of Actinidia chinensis].
PubMed:Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents.
PubMed:Jacaranone and related compounds from the fresh fruits of Ternstroemia japonica and their antioxidative activity.
PubMed:Suppression of the SOS-inducing activity of mutagenic heterocyclic amine, Trp-P-1, by triterpenoid from Uncaria sinensis in the Salmonella typhimurium TA1535/pSK1002 Umu test.
PubMed:[Studies on chemical constituents from branch of Trema angustifolia].
PubMed:Cytotoxic triterpenes from the aerial roots of Ficus microcarpa.
PubMed:Triterpenoids from Brazilian Ilex species and their in vitro antitrypanosomal activity.
PubMed:[Studies on chemical constituents from the stems of Schisandra sphaerandra].
 
Notes:
Isol. from various plants, e.g. Leptospermum scoparium (red tea)
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