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Details

Stereochemistry ACHIRAL
Molecular Formula C28H56O2
Molecular Weight 424.743
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONTANIC ACID

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O

InChI

InChIKey=UTOPWMOLSKOLTQ-UHFFFAOYSA-N
InChI=1S/C28H56O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28(29)30/h2-27H2,1H3,(H,29,30)

HIDE SMILES / InChI

Molecular Formula C28H56O2
Molecular Weight 424.743
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Lupeol esters from the twig bark of Japanese pear (Pyrus serotina Rehd.) cv. Shinko.
2001 May
Inhibition of cholesterol biosynthesis in cultured fibroblasts by D003, a mixture of very long chain saturated fatty acids.
2001 Oct
Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on CL4C-induced liver acute injury in rats.
2002
Preliminary evaluation of the cytotoxic and genotoxic potential of D-003: Mixture of very long chain fatty acids.
2002
[Studies on chemical constituents of two plants from Costus].
2002 Feb
Inhibition of rat lipoprotein lipid peroxidation by the oral administration of D003, a mixture of very long-chain saturated fatty acids.
2002 Jan
Synergistic effect of D-003 and aspirin on experimental thrombosis models.
2003 May
Effect of D-003 on a subconvulsive dose of kainic Acid in rats.
2004
Partial phase behavior and micellar properties of tetrabutylammonium salts of fatty acids: unusual solubility in water and formation of unexpectedly small micelles.
2004 Jul 6
[Studies on chemical constituents from Eucommia ulmoides Oliv].
2004 May
D-003 and warfarin interaction on the bleeding time and venous thrombosis experimentally induced in rats.
2004 Summer
Lack of protective effect of D-003, a mixture of high-molecular-weight primary acids from sugar cane wax, on liver damage induced by galactosamine in rats.
2005 Fall
In vitro and in vivo study of octacosanol metabolism.
2005 Mar-Apr
Effect of D-003 on intimal thickening and circulating endothelial cells in rabbit cuffed carotid artery.
2005 Summer
[Studies on chemical constituents from roots of Craibiodendron henryi].
2007 Apr
Chemical constituents from aerial part of Curcuma wenyujin.
2007 Dec
[Studies on the chemical constituents from Inula cappa (II)].
2007 Jan
The influence of the long chain fatty acid on the antagonistic activities of Rhizobium sin-1 lipid A.
2007 Jul 15
Effects of radix adenophorae and cyclosporine A on an OVA-induced murine model of asthma by suppressing to T cells activity, eosinophilia, and bronchial hyperresponsiveness.
2008
Octacosanol attenuates disrupted hepatic reactive oxygen species metabolism associated with acute liver injury progression in rats intoxicated with carbon tetrachloride.
2008 Mar
Chemical constituents from the fruits of Hippophae rhamnoides.
2009
[Studies on chemical constituents from roots of Angelica polymorpha].
2009 Apr
Application of GC-MS for the detection of lipophilic compounds in diverse plant tissues.
2009 Apr 24
Trace quantification of 1-octacosanol and 1-triacontanol and their main metabolites in plasma by liquid-liquid extraction coupled with gas chromatography-mass spectrometry.
2009 Dec 15
Composition of diethyl ether flower extracts of Lonicera fragrantissima Lindl. & Paxton (caprifoliaceae).
2009 Nov
Assessment of anti-nociceptive efficacy of costus speciosus rhizome in swiss albino mice.
2010 Jan
Metabolic profiling of Arabidopsis thaliana epidermal cells.
2010 Mar
[Studies on the chemical constituents of the petroleum ether portion of Nervilia fordii].
2010 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:08:27 GMT 2023
Edited
by admin
on Fri Dec 15 18:08:27 GMT 2023
Record UNII
4BKL1A0KJY
Record Status Validated (UNII)
Record Version
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Name Type Language
MONTANIC ACID
Systematic Name English
NSC-407311
Code English
LICOWAX SFL
Common Name English
OCTACOSANOIC ACID
Systematic Name English
MONTAN ACID ESTER
Common Name English
N-OCTACOSANOIC ACID
Common Name English
Code System Code Type Description
MESH
C068792
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID2075051
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-041-8
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
PUBCHEM
10470
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
EVMPD
SUB91599
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
CAS
506-48-9
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
FDA UNII
4BKL1A0KJY
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
WIKIPEDIA
MONTANIC ACID
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
CHEBI
31001
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
SMS_ID
100000141377
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
NSC
407311
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY