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Details

Stereochemistry ACHIRAL
Molecular Formula C24H50
Molecular Weight 338.6538
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TETRACOSANE

SMILES

CCCCCCCCCCCCCCCCCCCCCCCC

InChI

InChIKey=POOSGDOYLQNASK-UHFFFAOYSA-N
InChI=1S/C24H50/c1-3-5-7-9-11-13-15-17-19-21-23-24-22-20-18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C24H50
Molecular Weight 338.6538
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
128.7 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Intramolecular diffusive motion in alkane monolayers studied by high-resolution quasielastic neutron scattering and molecular dynamics simulations.
2004 Jan 30
Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted mice.
2005 Aug
Emissions of organic compounds and trace metals in fine particulate matter from motor vehicles: a tunnel study in Houston, Texas.
2005 Jan
A synthetic route to size-controlled fcc and fct FePt nanoparticles.
2005 Jul 27
Variation of chemical composition of the lipophilic extracts from yellow birch (Betula alleghaniensis) foliage.
2005 Jun 15
Rheological and structural studies of liquid decane, hexadecane, and tetracosane under planar elongational flow using nonequilibrium molecular-dynamics simulations.
2005 May 8
Calculation the surface tension of heptane, eicosane, docosane, tetracosane, and their asymmetric mixtures.
2005 Sep 1
Late opacification of a silicone intraocular lens caused by ophthalmic ointment.
2006 Feb
Characterization of waxes used in pictorial artworks according to their relative amount of fatty acids and hydrocarbons by gas chromatography.
2006 Jan 6
[Studies on chemical constituents in flower of Abelmoschus manihot].
2006 Oct
Gramicidin A channel in a matrix from a semifluorinated surfactant monolayer.
2006 Oct 5
A Staphylococcus aureus ypfP mutant with strongly reduced lipoteichoic acid (LTA) content: LTA governs bacterial surface properties and autolysin activity.
2007 Aug
Raman spectroscopy of natural accumulated paraffins from rocks: evenkite, ozokerite and hatchetine.
2007 Dec 15
Kairomones extracted from rice yellow stem borer and their influence on egg parasitization by Trichogramma japonicum ashmead.
2007 Jan
Biochemical evaluation of borage (Borago officinalis) rosette leaves through their essential oil and fatty acid composition.
2007 Jun
Comparative study of normal and branched alkane monolayer films adsorbed on a solid surface. I. Structure.
2007 Mar 14
The odor of origin: kinship and geographical distance are reflected in the marking pheromone of male beewolves (Philanthus triangulum F., Hymenoptera, Crabronidae).
2007 Oct 10
Gas chromatography-mass spectrometry with supersonic molecular beams.
2008 Feb
Structural and phase properties of tetracosane (C24H50) monolayers adsorbed on graphite: an explicit hydrogen molecular dynamics study.
2008 Nov 4
Silencing of StKCS6 in potato periderm leads to reduced chain lengths of suberin and wax compounds and increased peridermal transpiration.
2009
Conferols A and B, new anti-inflammatory 4-hydroxyisoflavones from Caragana conferta.
2009 Apr
Structure and phase transitions of monolayers of intermediate-length n-alkanes on graphite studied by neutron diffraction and molecular dynamics simulation.
2009 Aug 28
[Study on the chemical constituents of the leaves of Ipomoea batatas].
2009 Jun
Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae).
2009 Jun
Chemical Examination of Citrus sinensis Flavedo Variety Pineapple.
2009 Nov
Confinement-driven weakening of the rotator phase transitions in an alkane through a possible tricritical point.
2010 Dec 7
[Study on the chemical constituents qf Spongilla Wagner].
2010 Jan
Comprehensive compositional analysis of plant cell walls (Lignocellulosic biomass) part I: lignin.
2010 Mar 11
Chemical composition of the essential oils of Rhodiola rosea L. of three different origins.
2010 Oct
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 07:32:43 GMT 2023
Edited
by admin
on Sat Dec 16 07:32:43 GMT 2023
Record UNII
YQ5H1M1D7I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TETRACOSANE
Systematic Name English
NSC-2984
Code English
N-TETRACOSANE
Common Name English
Code System Code Type Description
WIKIPEDIA
TETRACOSANE
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
PUBCHEM
12592
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID8060955
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
CHEBI
32936
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
HSDB
8354
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
NSC
2984
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
CAS
646-31-1
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
FDA UNII
YQ5H1M1D7I
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-474-5
Created by admin on Sat Dec 16 07:32:43 GMT 2023 , Edited by admin on Sat Dec 16 07:32:43 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
9.7% of chemical composition of the leaf essential oil from Moringa oleifera.