200,000+ products from a single source!

sales@angenechem.com

Home > Other Building Blocks > 58436-28-5

58436-28-5

58436-28-5 | Dihydroresveratrol

CAS No: 58436-28-5 Catalog No: AG0038MU MDL No:MFCD25973128

Product Description

Catalog Number:
AG0038MU
Chemical Name:
Dihydroresveratrol
CAS Number:
58436-28-5
Molecular Formula:
C14H14O3
Molecular Weight:
230.2592
MDL Number:
MFCD25973128
IUPAC Name:
5-[2-(4-hydroxyphenyl)ethyl]benzene-1,3-diol
InChI:
InChI=1S/C14H14O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h3-9,15-17H,1-2H2
InChI Key:
HITJFUSPLYBJPE-UHFFFAOYSA-N
SMILES:
Oc1ccc(cc1)CCc1cc(O)cc(c1)O
EC Number:
611-651-0
NSC Number:
723534

Properties

Complexity:
214  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
230.094g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
230.263g/mol
Monoisotopic Mass:
230.094g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
60.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  

Literature

Title Journal
Hydroxystilbenes and methoxystilbenes activate human aryl hydrocarbon receptor and induce CYP1A genes in human hepatoma cells and human hepatocytes. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20170501
Effects of long-term consumption of low doses of resveratrol on diet-induced mild hypercholesterolemia in pigs: a transcriptomic approach to disease prevention. The Journal of nutritional biochemistry 20120701
The journey of resveratrol from yeast to human. Aging 20120301
Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets. Bioorganic & medicinal chemistry 20120101
Resveratrol, but not dihydroresveratrol, induces premature senescence in primary human fibroblasts. Age (Dordrecht, Netherlands) 20111201
Metabolites and tissue distribution of resveratrol in the pig. Molecular nutrition & food research 20110801
A study of resveratrol-copper complexes by electrospray ionization mass spectrometry and density functional theory calculations. Rapid communications in mass spectrometry : RCM 20110227
Investigation of piceid metabolites in rat by liquid chromatography tandem mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20110101
Bioavailability of resveratrol. Annals of the New York Academy of Sciences 20110101
Dihydro-resveratrol--a potent dietary polyphenol. Bioorganic & medicinal chemistry letters 20101015
trans-Resveratrol reduces precancerous colonic lesions in dimethylhydrazine-treated rats. Journal of agricultural and food chemistry 20100714
Determination of dihydroresveratrol in rat plasma by HPLC. Journal of agricultural and food chemistry 20100623
A theoretical study of the structure-radical scavenging activity of trans-resveratrol analogues and cis-resveratrol in gas phase and water environment. European journal of medicinal chemistry 20100301
Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography. Journal of medicinal chemistry 20090813
Interaction of dietary resveratrol with animal-associated bacteria. FEMS microbiology letters 20090801
Biocatalytic production of acyclic bis[bibenzyls] from dihydroresveratrol by crude Momordica charantia peroxidase. Chemistry & biodiversity 20090801
[Studies on constituents of Dendrobium gratiosissimum]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20070401
Identification of the major metabolites of resveratrol in rat urine by HPLC-MS/MS. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20051227
Phytotoxic activity of bibenzyl derivatives from the orchid Epidendrum rigidum. Journal of agricultural and food chemistry 20050810
Resveratrol derivatives and their role as potassium channels modulators. Journal of natural products 20040301
Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii. Journal of natural products 20040201
Specific structural determinants are responsible for the antioxidant activity and the cell cycle effects of resveratrol. The Journal of biological chemistry 20010622

© 2019 Angene International Limited. All rights Reserved.