Home Other Building Blocks 58436-28-5
58436-28-5,MFCD25973128
Catalog No.:AA0038K2

58436-28-5 | Dihydroresveratrol

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1mg
95%
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$74.00   $52.00
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5mg
≥98%
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$82.00   $57.00
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10mg
≥98%
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$153.00   $107.00
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25mg
≥98%
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$276.00   $193.00
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100mg
95%
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$364.00   $255.00
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250mg
95%
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$556.00   $389.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0038K2
Chemical Name:
Dihydroresveratrol
CAS Number:
58436-28-5
Molecular Formula:
C14H14O3
Molecular Weight:
230.2592
MDL Number:
MFCD25973128
SMILES:
Oc1ccc(cc1)CCc1cc(O)cc(c1)O
NSC Number:
723534
Properties
Computed Properties
 
Complexity:
214  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
3  
XLogP3:
3.1  

Downstream Synthesis Route

[1]Chemistryandbiodiversity,2009,vol.6,p.1193-1201

[2]BiochemicalJournal,1959,vol.72,p.369,370

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.1437-1443

[2]Patent:JP6527347,2019,B2.Locationinpatent:Paragraph0016

[3]Patent:US9526706,2016,B1.Locationinpatent:Page/Pagecolumn7;8

[4]Patent:JP6591173,2019,B2.Locationinpatent:Paragraph0018

[5]Phytochemistry,1993,vol.33,p.813-816

[6]RapidCommunicationsinMassSpectrometry,2011,vol.25,p.526-532

[7]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.3167-3172

[8]Phytochemistry,1976,vol.15,p.1791-1793

[9]BioorganicandMedicinalChemistry,2001,vol.9,p.41-50

[10]JournalofNaturalProducts,2004,vol.67,p.421-426

[11]BioorganicChemistry,2005,vol.33,p.22-33

[12]ProceedingsoftheNationalAcademyofSciencesoftheUnitedStatesofAmerica,2011,vol.108,p.6615-6620

[13]ArchivesofPharmacalResearch,2012,vol.35,p.1763-1770

[14]ChemBioChem,2013,vol.14,p.1094-1104

[15]BioorganicandMedicinalChemistry,2014,vol.22,p.1276-1284

[16]EuropeanJournalofMedicinalChemistry,2014,vol.87,p.862-867

58436-28-5    100-39-0   
5-2-(4-benzyloxy-phenyl)-ethyl-benzene-1,3-diol 
 
3-benzyloxy-5-2-(4-benzyloxy-phenyl)-ethyl-phenol 
 
4-2-(3,5-bis-benzyloxy-phenyl)-ethyl-phenol 
 
1,3-Bis-benzyloxy-5-2-(4-benzyloxy-phenyl)-ethyl-benzene 

[1]JournalofNaturalProducts,2004,vol.67,p.421-426

58436-28-5    870-63-3   
5-{2-4-(3-methyl-but-2-enyloxy)-phenyl-ethyl}-benzene-1,3-diol 
 
3-2-(4-Hydroxy-phenyl)-ethyl-5-(3-methyl-but-2-enyloxy)-phenol 
 
4-(3-methyl-2-buten-1-yl)-3,4',5-trihydroxydihydrostilbene 

[1]JournalofNaturalProducts,2004,vol.67,p.421-426

Literature

Title: Hydroxystilbenes and methoxystilbenes activate human aryl hydrocarbon receptor and induce CYP1A genes in human hepatoma cells and human hepatocytes.

Journal: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20170501

Title: Effects of long-term consumption of low doses of resveratrol on diet-induced mild hypercholesterolemia in pigs: a transcriptomic approach to disease prevention.

Journal: The Journal of nutritional biochemistry 20120701

Title: The journey of resveratrol from yeast to human.

Journal: Aging 20120301

Title: Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets.

Journal: Bioorganic & medicinal chemistry 20120101

Title: Resveratrol, but not dihydroresveratrol, induces premature senescence in primary human fibroblasts.

Journal: Age (Dordrecht, Netherlands) 20111201

Title: Metabolites and tissue distribution of resveratrol in the pig.

Journal: Molecular nutrition & food research 20110801

Title: A study of resveratrol-copper complexes by electrospray ionization mass spectrometry and density functional theory calculations.

Journal: Rapid communications in mass spectrometry : RCM 20110227

Title: Investigation of piceid metabolites in rat by liquid chromatography tandem mass spectrometry.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20110101

Title: Bioavailability of resveratrol.

Journal: Annals of the New York Academy of Sciences 20110101

Title: Dihydro-resveratrol--a potent dietary polyphenol.

Journal: Bioorganic & medicinal chemistry letters 20101015

Title: trans-Resveratrol reduces precancerous colonic lesions in dimethylhydrazine-treated rats.

Journal: Journal of agricultural and food chemistry 20100714

Title: Determination of dihydroresveratrol in rat plasma by HPLC.

Journal: Journal of agricultural and food chemistry 20100623

Title: A theoretical study of the structure-radical scavenging activity of trans-resveratrol analogues and cis-resveratrol in gas phase and water environment.

Journal: European journal of medicinal chemistry 20100301

Title: Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography.

Journal: Journal of medicinal chemistry 20090813

Title: Interaction of dietary resveratrol with animal-associated bacteria.

Journal: FEMS microbiology letters 20090801

Title: Biocatalytic production of acyclic bis[bibenzyls] from dihydroresveratrol by crude Momordica charantia peroxidase.

Journal: Chemistry & biodiversity 20090801

Title: [Studies on constituents of Dendrobium gratiosissimum].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20070401

Title: Identification of the major metabolites of resveratrol in rat urine by HPLC-MS/MS.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20051227

Title: Phytotoxic activity of bibenzyl derivatives from the orchid Epidendrum rigidum.

Journal: Journal of agricultural and food chemistry 20050810

Title: Resveratrol derivatives and their role as potassium channels modulators.

Journal: Journal of natural products 20040301

Title: Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii.

Journal: Journal of natural products 20040201

Title: Specific structural determinants are responsible for the antioxidant activity and the cell cycle effects of resveratrol.

Journal: The Journal of biological chemistry 20010622

Title: Anisimova NY, et al. Trans-, cis-, and dihydro-resveratrol: a comparative study. Chem Cent J. 2011 Dec 20;5:88.

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