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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
[Studies on the chemical constituents of the petroleum ether portion of Nervilia fordii].
2010-05
Metabolic profiling of Arabidopsis thaliana epidermal cells.
2010-03
Assessment of anti-nociceptive efficacy of costus speciosus rhizome in swiss albino mice.
2010-01
Trace quantification of 1-octacosanol and 1-triacontanol and their main metabolites in plasma by liquid-liquid extraction coupled with gas chromatography-mass spectrometry.
2009-12-15
Composition of diethyl ether flower extracts of Lonicera fragrantissima Lindl. & Paxton (caprifoliaceae).
2009-11
Application of GC-MS for the detection of lipophilic compounds in diverse plant tissues.
2009-04-24
[Studies on chemical constituents from roots of Angelica polymorpha].
2009-04
Chemical constituents from the fruits of Hippophae rhamnoides.
2009
Octacosanol attenuates disrupted hepatic reactive oxygen species metabolism associated with acute liver injury progression in rats intoxicated with carbon tetrachloride.
2008-03
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
Chemical constituents from aerial part of Curcuma wenyujin.
2007-12
The influence of the long chain fatty acid on the antagonistic activities of Rhizobium sin-1 lipid A.
2007-07-15
[Studies on chemical constituents from roots of Craibiodendron henryi].
2007-04
[Studies on the chemical constituents from Inula cappa (II)].
2007-01
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
Effect of D-003 on intimal thickening and circulating endothelial cells in rabbit cuffed carotid artery.
2005
Partial phase behavior and micellar properties of tetrabutylammonium salts of fatty acids: unusual solubility in water and formation of unexpectedly small micelles.
2004-07-06
In vitro and in vivo study of octacosanol metabolism.
2004-06-27
[Studies on chemical constituents from Eucommia ulmoides Oliv].
2004-05
Effect of D-003 on a subconvulsive dose of kainic Acid in rats.
2004
D-003 and warfarin interaction on the bleeding time and venous thrombosis experimentally induced in rats.
2004
Synthesis and biological evaluation of Rhizobium sin-1 lipid A derivatives.
2003-05-21
Synergistic effect of D-003 and aspirin on experimental thrombosis models.
2003-05
Lack of developmental toxicity of D-003: a mixture of long-chain fatty acids in rats.
2003-01
Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on paracetamol-induced liver damage in rats.
2003
D-003, a potential antithrombotic compound isolated from sugar cane wax with effects on arachidonic acid metabolites.
2002-07
[Studies on chemical constituents of two plants from Costus].
2002-02
Inhibition of rat lipoprotein lipid peroxidation by the oral administration of D003, a mixture of very long-chain saturated fatty acids.
2002-01
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
Inhibition of cholesterol biosynthesis in cultured fibroblasts by D003, a mixture of very long chain saturated fatty acids.
2001-10
[Non-anthraquinone constituents from Rheum sublanceolatum C. Y. Cheng et Kao].
2001-08
Lupeol esters from the twig bark of Japanese pear (Pyrus serotina Rehd.) cv. Shinko.
2001-05
[Studies on chemical constituents from Buddleja lindleyana Fert].
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:04:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:04:30 GMT 2025
Record UNII
4BKL1A0KJY
Record Status Validated (UNII)
Record Version
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Name Type Language
MONTANIC ACID
Systematic Name English
NSC-407311
Preferred Name 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 Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID2075051
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-041-8
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
PUBCHEM
10470
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
EVMPD
SUB91599
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
CAS
506-48-9
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
FDA UNII
4BKL1A0KJY
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
WIKIPEDIA
MONTANIC ACID
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
CHEBI
31001
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
SMS_ID
100000141377
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
NSC
407311
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY