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

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
[Non-anthraquinone constituents from Rheum sublanceolatum C. Y. Cheng et Kao].
2001 Aug
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
[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
D-003, a potential antithrombotic compound isolated from sugar cane wax with effects on arachidonic acid metabolites.
2002 Jul
Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on paracetamol-induced liver damage in rats.
2003
Lack of developmental toxicity of D-003: a mixture of long-chain fatty acids in rats.
2003 Jan
Synthesis and biological evaluation of Rhizobium sin-1 lipid A derivatives.
2003 May 21
Effect of D-003 on a subconvulsive dose of kainic Acid in rats.
2004
[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
Chemical constituents from aerial part of Curcuma wenyujin.
2007 Dec
[Studies on the chemical constituents from Inula cappa (II)].
2007 Jan
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 the fruits of Hippophae rhamnoides.
2009
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
  • Download
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