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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
Structure of 12-METHOXYDODECANOATE

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)

HIDE SMILES / InChI

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

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
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 Tue Apr 01 19:45:18 GMT 2025
Edited
by admin
on Tue Apr 01 19:45:18 GMT 2025
Record UNII
T5D2P5P2A8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-666070
Preferred Name English
12-METHOXYDODECANOATE
Systematic Name English
12-METHOXYDODECANOIC ACID
Systematic Name English
13-OXATETRADECANOIC ACID
Systematic Name English
DODECANOIC ACID, 12-METHOXY-
Systematic Name English
13-OXAMYRISTIC ACID
Systematic Name English
Code System Code Type Description
PUBCHEM
1420
Created by admin on Tue Apr 01 19:45:18 GMT 2025 , Edited by admin on Tue Apr 01 19:45:18 GMT 2025
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FDA UNII
T5D2P5P2A8
Created by admin on Tue Apr 01 19:45:18 GMT 2025 , Edited by admin on Tue Apr 01 19:45:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID20238909
Created by admin on Tue Apr 01 19:45:18 GMT 2025 , Edited by admin on Tue Apr 01 19:45:18 GMT 2025
PRIMARY
NSC
666070
Created by admin on Tue Apr 01 19:45:18 GMT 2025 , Edited by admin on Tue Apr 01 19:45:18 GMT 2025
PRIMARY
CAS
92169-28-3
Created by admin on Tue Apr 01 19:45:18 GMT 2025 , Edited by admin on Tue Apr 01 19:45:18 GMT 2025
PRIMARY