Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H31O2.K |
Molecular Weight | 318.5358 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 2 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O
InChI
InChIKey=BAYJYBALPIYBQQ-NBTZWHCOSA-M
InChI=1S/C18H32O2.K/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h6-7,9-10H,2-5,8,11-17H2,1H3,(H,19,20);/q;+1/p-1/b7-6-,10-9-;
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL612426 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26412702 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Ascorbic acid and copper in linoleate oxidation. 3. Catalysts in combination. | 1969 Sep |
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Effect of hemoglobin concentration on the oxidation of linoleic acid. | 1971 Mar |
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Enzymatic properties of the lipoxygenase from pea seeds. | 1985 |
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Antibacterial Effect of Fatty Acid Salts on Oral Bacteria. | 2015 |
Patents
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26412702
Potassium linoleate (C18:2K), used at a concentration of 175 mM, resulted in a 7 log-unit reduction of S. mutans after a 10-min incubation. The minimum inhibitory concentration (MIC) of C18:2K was 5.5 mM.
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD