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

ailanthone
picrasa-3,13(21)-dien-2,16-dione, 11,20-epoxy-1,11,12-trihydroxy-, (1b,11b,12a)

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CAS Number: 981-15-7Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J21.167B
XlogP3-AA:-1.10 (est)
Molecular Weight:376.40568000
Formula:C20 H24 O7
BioActivity Summary:listing
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 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
Boiling Point: 641.00 °C. @ 760.00 mm Hg (est)
Flash Point: 449.00 °F. TCC ( 231.60 °C. ) (est)
logP (o/w): -0.760 (est)
Soluble in:
 water, 2637 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.
Ailanthone 98%
BOC Sciences
For experimental / research use only.
Ailanthone
ExtraSynthese
For experimental / research use only.
Ailanthone
 
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:
intraperitoneal-mouse LD50 31400 ug/kg
European Journal of Medicinal Chemistry--Chimie Therapeutique. Vol. 26, Pg. 345, 1991.

oral-mouse LD50 9800 ug/kg
Parassitologia. Vol. 10, Pg. 215, 1968.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for ailanthone usage levels up to:
 not for fragrance use.
 
Recommendation for ailanthone 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 :72965
National Institute of Allergy and Infectious Diseases:Data
Chemidplus:0000981157
 
References:
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):72965
Pubchem (sid):135030641
 
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):C08747
HMDB (The Human Metabolome Database):Search
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
 ailanthus altissima
Search Trop Picture
 
Synonyms:
 ailantone
(1-beta,11-beta,12-alpha)-11,20-epoxy-1,11,12-trihydroxypicrasa-3,13(21)-diene-2,16-dione
2H-1,11c-(epoxymethano)phenanthro(10,1-bc)pyran-5,10(3H,6ah)-dione, 1,3a,4,7,7a,11,11a,11b-octahydro-8,11a-b-dimethyl-3-methylene-1-a,2-b,11-b-trihydroxy-
 picrasa-3,13(21)-dien-2,16-dione, 11,20-epoxy-1,11,12-trihydroxy-, (1b,11b,12a)
 

Articles:

PubMed:Herbicide activity of extracts from Ailanthus altissima (Simaroubaceae).
PubMed:Quassinoids can induce mitochondrial membrane depolarisation and caspase 3 activation in human cells.
PubMed:Antiplasmodial activity of extracts and quassinoids isolated from seedlings of Ailanthus altissima (Simaroubaceae).
PubMed:Isolation of phytotoxic compounds from tree-of-heaven (Ailanthus altissima swingle).
PubMed:Anti-tuberculosis activity of quassinoids.
PubMed:Quassinoids as inhibitors of Epstein-Barr virus early antigen activation.
PubMed:Antitumor activity of novel ailanthone derivatives in vitro and in vivo.
PubMed:[Antiamebic properties of some derivatives of ailantone and quassin].
 
Notes:
None found
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