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Triacetyl resveratrol - 10mM in DMSO, high purity , CAS No.42206-94-0
Basic Description
Synonyms
triacetylresveratrol | 42206-94-0 | Acetyl-trans-resveratrol | Triacetyl resveratrol | (E)-5-(4-ACETOXYSTYRYL)-1,3-PHENYLENE DIACETATE | trans-Resveratrol triacetate | 54443-64-0 | 63366-83-6 | 3,4',5-Triacetoxy-trans-stilbene | [4-[(E)-2-(3,5-diacetyloxyphenyl)ethenyl]phe
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Triacetyl resveratrol displays superior bioavailability to the parent compound, resveratrol. The compound induces p53 activity and inhibits proliferation in breast and prostate tumor cell lines.
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Resveratrol (RSV) is a natural polyphenolic antioxidant.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Stilbenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Stilbenes
Alternative Parents
Phenol esters Tricarboxylic acids and derivatives Styrenes Phenoxy compounds Carboxylic acid esters Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Stilbene - Phenol ester - Tricarboxylic acid or derivatives - Phenoxy compound - Styrene - Benzenoid - Monocyclic benzene moiety - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
[4-[(E)-2-(3,5-diacetyloxyphenyl)ethenyl]phenyl] acetate
INCHI
InChI=1S/C20H18O6/c1-13(21)24-18-8-6-16(7-9-18)4-5-17-10-19(25-14(2)22)12-20(11-17)26-15(3)23/h4-12H,1-3H3/b5-4+
InChIKey
PDAYUJSOJIMKIS-SNAWJCMRSA-N
Smiles
CC(=O)OC1=CC=C(C=C1)C=CC2=CC(=CC(=C2)OC(=O)C)OC(=O)C
Isomeric SMILES
CC(=O)OC1=CC=C(C=C1)/C=C/C2=CC(=CC(=C2)OC(=O)C)OC(=O)C
WGK Germany
3
PubChem CID
5962587
Molecular Weight
354.35
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
light sensitive
Melt Point(°C)
117.0-121.0℃
Molecular Weight
354.400 g/mol
XLogP3
3.400
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
8
Exact Mass
354.11 Da
Monoisotopic Mass
354.11 Da
Topological Polar Surface Area
78.900 Ų
Heavy Atom Count
26
Formal Charge
0
Complexity
508.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
1
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
1
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Yajie Zhang, Changjiao Shang, Chaofan Sun, Lingling Wang.
(2024)
Simultaneously regulating absorption capacities and antioxidant activities of four stilbene derivatives utilizing substitution effect: A theoretical and experimental study against UVB radiation. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,
304
(123325).
2.
Chai Ran, Chen Yafei, Yuan Hongbo, Wang Xuzhao, Guo Shuai, Qi Jinlong, Zhang Hailin, Zhan Yong, An Hailong.
(2017)
Identification of Resveratrol, an Herbal Compound, as an Activator of the Calcium-Activated Chloride Channel, TMEM16A. JOURNAL OF MEMBRANE BIOLOGY,
250
(5):
(483-492).
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2 Citations