Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H26O3 |
| Molecular Weight | 230.3437 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COCCCCCCCCCCCC(O)=O
InChI
InChIKey=OGLQEYICTWWJQB-UHFFFAOYSA-N
InChI=1S/C13H26O3/c1-16-12-10-8-6-4-2-3-5-7-9-11-13(14)15/h2-12H2,1H3,(H,14,15)
| Molecular Formula | C13H26O3 |
| Molecular Weight | 230.3437 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2096973 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10611737 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Myristic acid analogs are inhibitors of Junin virus replication. | 1999-07 |
|
| Antiviral phospholipids. Anti-HIV drugs conjugated to the glycerobackbone of phospholipids. | 1993-04-15 |
|
| Incorporation of 12-methoxydodecanoate into the human immunodeficiency virus 1 gag polyprotein precursor inhibits its proteolytic processing and virus production in a chronically infected human lymphoid cell line. | 1991-03-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 19:45:18 GMT 2025
by
admin
on
Tue Apr 01 19:45:18 GMT 2025
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| Record UNII |
T5D2P5P2A8
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| Record Status |
Validated (UNII)
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| Record Version |
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92169-28-3
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