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garcinone C

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CAS Number: 76996-27-5Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J2.284.473C
XlogP3-AA:4.60 (est)
Molecular Weight:414.45462000
Formula:C23 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:
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Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 0.0183 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.
Garcinone C 98%
BOC Sciences
For experimental / research use only.
Garcinone C 97%
Odor: characteristic
Use: Garcinone C isolated from the fruits of Garcinia mangostana. It is the most potent inhibitor of AChE, and it exhibits either significant or moderate cytotoxicity against MCF-7, A549, Hep-G2 and CNEhuman cancer cell lines.
 
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 garcinone C usage levels up to:
 not for fragrance use.
 
Recommendation for garcinone C 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 :44159808
National Institute of Allergy and Infectious Diseases:Data
1,3,6,7-tetrahydroxy-8-(3-hydroxy-3-methylbutyl)-2-(3-methylbut-2-enyl)xanthen-9-one
 
References:
 1,3,6,7-tetrahydroxy-8-(3-hydroxy-3-methylbutyl)-2-(3-methylbut-2-enyl)xanthen-9-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):44159808
Pubchem (cas):76996-27-5
 
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
HMDB (The Human Metabolome Database):HMDB29511
FooDB:FDB000646
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
 garcinia mangostana
Search Trop Picture
 
Synonyms:
1,3,6,7-tetrahydroxy-8-(3-hydroxy-3-methylbutyl)-2-(3-methylbut-2-enyl)xanthen-9-one
 

Articles:

PubMed:Mangostanaxanthone VIII, a new xanthone from Garcinia mangostana and its cytotoxic activity.
PubMed:Garcinone C exerts antitumor activity by modulating the expression of ATR/Stat3/4E‑BP1 in nasopharyngeal carcinoma cells.
PubMed:Garcixanthone A, a new cytotoxic xanthone from the pericarps of Garcinia mangostana.
PubMed:α-Mangostin, A Natural Xanthone, Induces Apoptosis and ROS Accumulation in Human Rheumatoid Fibroblast-Like Synoviocyte MH7A Cells.
PubMed:Mangostanaxanthones III and IV: advanced glycation end-product inhibitors from the pericarp of Garcinia mangostana.
PubMed:Xanthones Isolated from the Pericarp of Mangosteen Inhibit Neurotransmitter Receptors Expressed in Xenopus Oocytes.
PubMed:Natural Xanthones from Garcinia mangostana with Multifunctional Activities for the Therapy of Alzheimer's Disease.
PubMed:A virtual screening approach for identifying plants with anti H5N1 neuraminidase activity.
PubMed:Prenylated xanthones from mangosteen as promising cholinesterase inhibitors and their molecular docking studies.
PubMed:A new xanthone from the pericarp of Garcinia mangostana.
PubMed:Antileptospiral activity of xanthones from Garcinia mangostana and synergy of gamma-mangostin with penicillin G.
 
Notes:
None found
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