U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C21H36O2
Molecular Weight 320.5093
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-PENTADECYLRESORCINOL

SMILES

CCCCCCCCCCCCCCCC1=CC(O)=CC(O)=C1

InChI

InChIKey=KVVSCMOUFCNCGX-UHFFFAOYSA-N
InChI=1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-16-20(22)18-21(23)17-19/h16-18,22-23H,2-15H2,1H3

HIDE SMILES / InChI

Molecular Formula C21H36O2
Molecular Weight 320.5093
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Irreversible competitive inhibitory kinetics of cardol triene on mushroom tyrosinase.
2010-12-22
Two new resorcinol derivatives with strong cytotoxicity from the roots of Ardisia brevicaulis Diels.
2010-12
Chromatographic techniques for the determination of alkyl-phenols, tocopherols and other minor polar compounds in raw and roasted cold pressed cashew nut oils.
2010-11-19
PEG-immobilization of cardol and soluble polymer-supported synthesis of some cardol-coumarin derivatives: preliminary evaluation of their inhibitory activity on mushroom tyrosinase.
2009-01-01
The effect of alkylresorcinol on lipid metabolism in Azotobacter chroococcum.
2008-11-13
Membrane perturbing properties of natural phenolic and resorcinolic lipids.
2008-10-29
The higher level of organization of the oxidative phosphorylation system: mitochondrial supercomplexes.
2008-10
Effects of immature cashew nut-shell liquid (Anacardium occidentale) against oxidative damage in Saccharomyces cerevisiae and inhibition of acetylcholinesterase activity.
2008-09-09
Parental use of the Internet to seek health information and primary care utilisation for their child: a cross-sectional study.
2008-08-28
A codon-optimized luciferase from Gaussia princeps facilitates the in vivo monitoring of gene expression in the model alga Chlamydomonas reinhardtii.
2008-06
A semisynthetic 5-n-alkylresorcinol derivative and its effect upon biomembrane properties.
2008-02-16
Striking variations in consultation rates with general practice reveal family influence.
2007-01-18
Biosynthesis of lipid resorcinols and benzoquinones in isolated secretory plant root hairs.
2007
Characterization of alkyl phenols in cashew (Anacardium occidentale) products and assay of their antioxidant capacity.
2006-02
Emulsions of oil from Adenanthera pavonina L. seeds and their protective effect.
2006
Detection of sensitivity to cardol in north-eastern and south-eastern Brazil.
2005-05
Alkyl- and alkenylresorcinols of wheat grains and their chemotaxonomic significance.
2004-07-10
Chalcones, coumarins, and flavanones from the exudate of Angelica keiskei and their chemopreventive effects.
2003-11-25
Process for isolation of cardanol from technical cashew (Anacardium occidentale L.) nut shell liquid.
2002-07-31
Botanical briefs: The cashew tree--Anacardium occidentale L.
2001-11
Formation of liposomes by resorcinolic lipids, single-chain phenolic amphiphiles from Anacardium occidentale L.
2001-07-02
Novel method for isolation of major phenolic constituents from cashew (Anacardium occidentale L.) nut shell liquid.
2001-05
Influence of chemical reactivity of urushiol-type haptens on sensitization and the induction of tolerance.
1986-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:19:43 GMT 2025
Edited
by admin
on Mon Mar 31 19:19:43 GMT 2025
Record UNII
U1FU33YCG0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-776
Preferred Name English
5-PENTADECYLRESORCINOL
Systematic Name English
RESORCINOL, 5-PENTADECYL-
Systematic Name English
ADIPOSTATIN A
Common Name English
HYDROGENATED CARDOL
Common Name English
3-N-PENTADECYL-5-HYDROXYPHENOL
Common Name English
5-(N-PENTADECYL)RESORCINOL
Common Name English
1,3-BENZENEDIOL, 5-PENTADECYL-
Systematic Name English
Code System Code Type Description
CAS
3158-56-3
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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WIKIPEDIA
ADIPOSTATIN A
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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NSC
776
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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ECHA (EC/EINECS)
221-599-7
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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PUBCHEM
76617
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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FDA UNII
U1FU33YCG0
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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CHEBI
2120
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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EPA CompTox
DTXSID7062875
Created by admin on Mon Mar 31 19:19:43 GMT 2025 , Edited by admin on Mon Mar 31 19:19:43 GMT 2025
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