Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H11O2.Na |
Molecular Weight | 138.1401 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CCCCCC([O-])=O
InChI
InChIKey=UDWXLZLRRVQONG-UHFFFAOYSA-M
InChI=1S/C6H12O2.Na/c1-2-3-4-5-6(7)8;/h2-5H2,1H3,(H,7,8);/q;+1/p-1
Molecular Formula | C6H11O2 |
Molecular Weight | 115.1503 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Expression of human plasminogen in Drosophila Schneider S2 cells. | 1999 Jun |
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Biosynthesis and structural characterization of medium-chain-length poly(3-hydroxyalkanoates) produced by Pseudomonas aeruginosa from fatty acids. | 2001 Aug 20 |
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Competitive binding of aroma compounds by beta-cyclodextrin. | 2001 Dec |
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A C-H...O=C hydrogen bond? Intramolecular hydrogen bonding in a novel semirubin. | 2001 Dec 14 |
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[Determination of organic acids in cigarette smoke]. | 2001 Jul |
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[Desulfacinum subterraneum sp.nov.--a new thermophilic sulfate-reducing bacterium isolated from a high temperature oil field ]. | 2001 Jul-Aug |
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Cometabolic biosynthesis of copolyesters consisting of 3-hydroxyvalerate and medium-chain-length 3-hydroxyalkanoates by Pseudomonas sp. DSY-82. | 2001 Oct |
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[Chiral separation by capillary electrochromatography on stationary phase adsorbed with protein]. | 2001 Sep |
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Saturated triglycerides and fatty acids activate neutrophils depending on carbon chain-length. | 2002 Apr |
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Study of competitive binding of enantiomers to protein by affinity capillary electrochromatography. | 2002 Jan 15 |
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Effects of acylation on the structure, lipid binding, and transfer activity of wheat lipid transfer protein. | 2002 Mar |
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Enhancement of NGF- and cholera toxin-induced neurite outgrowth by butyrate in PC12 cells. | 2002 Oct 4 |
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Hydrogen production from wastewater by acidogenic granular sludge. | 2003 |
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Immunology of term and preterm labor. | 2003 Dec 2 |
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Enhanced transdermal delivery of phenylalanyl-glycine by chemical modification with various fatty acids. | 2003 Jan 2 |
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Actinidia arguta: volatile compounds in fruit and flowers. | 2003 Jun |
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Chemical composition of precloacal secretions of two Liolaemus fabiani populations: are they different? | 2003 Mar |
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Role of the fuel utilized by tissues on coronary vessel response to physical stimuli in isolated rat hearts. | 2004 |
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Functional effects of 17alpha-hydroxyprogesterone caproate (17P) on human myometrial contractility in vitro. | 2004 Dec 7 |
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2-ammonio-6-(3-oxidopyridinium-1-yl)hexanoate (OP-lysine) is a newly identified advanced glycation end product in cataractous and aged human lenses. | 2004 Feb 20 |
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Impact of unusual fatty acid synthesis on futile cycling through beta-oxidation and on gene expression in transgenic plants. | 2004 Jan |
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Sampling and analysis of volatile organic compounds in bovine breath by solid-phase microextraction and gas chromatography-mass spectrometry. | 2004 Jan 30 |
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Impairment of male reproduction in adult rats exposed to hydroxyprogesterone caproate in utero. | 2004 May |
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Evaluation of antioxidant activity of Australian tea tree (Melaleuca alternifolia) oil and its components. | 2004 May 19 |
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Design and chemical synthesis of a magnetic resonance contrast agent with enhanced in vitro binding, high blood-brain barrier permeability, and in vivo targeting to Alzheimer's disease amyloid plaques. | 2004 May 25 |
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Orientation behaviour of the blood-sucking bug triatoma infestans to short-chain fatty acids: synergistic effect of L-lactic acid and carbon dioxide. | 2004 Nov |
|
Peroxisomal and mitochondrial oxidation of fatty acids in the heart, assessed from the 13C labeling of malonyl-CoA and the acetyl moiety of citrate. | 2005 Mar 11 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:43:31 GMT 2023
by
admin
on
Fri Dec 15 19:43:31 GMT 2023
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Record UNII |
E00CG11S66
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Record Status |
Validated (UNII)
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Record Version |
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4087444
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233-179-0
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E00CG11S66
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DTXSID8064933
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10051-44-2
Created by
admin on Fri Dec 15 19:43:31 GMT 2023 , Edited by admin on Fri Dec 15 19:43:31 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |