Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H30O2 |
Molecular Weight | 302.451 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 5 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O
InChI
InChIKey=JAZBEHYOTPTENJ-JLNKQSITSA-N
InChI=1S/C20H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-19H2,1H3,(H,21,22)/b4-3-,7-6-,10-9-,13-12-,16-15-
Molecular Formula | C20H30O2 |
Molecular Weight | 302.451 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 5 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:35:07 UTC 2023
by
admin
on
Fri Dec 15 16:35:07 UTC 2023
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Record UNII |
AAN7QOV9EA
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Code | English |
Classification Tree | Code System | Code | ||
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LOINC |
75097-6
Created by
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LOINC |
88998-0
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FDA ORPHAN DRUG |
283409
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LOINC |
90911-9
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LIVERTOX |
342
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EU-Orphan Drug |
EU/3/09/666
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LOINC |
88996-4
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admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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NCI_THESAURUS |
C67080
Created by
admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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DSLD |
3820 (Number of products:4)
Created by
admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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LOINC |
35173-4
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LOINC |
90908-5
Created by
admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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DSLD |
1011 (Number of products:2641)
Created by
admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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LOINC |
90909-3
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admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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LOINC |
88999-8
Created by
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LOINC |
88997-2
Created by
admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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LOINC |
90912-7
Created by
admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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Code System | Code | Type | Description | ||
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36006
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PRIMARY | |||
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1234293
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100000079270
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PRIMARY | |||
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D015118
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PRIMARY | |||
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AAN7QOV9EA
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PRIMARY | |||
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28364
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PRIMARY | |||
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6328
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PRIMARY | |||
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10417-94-4
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PRIMARY | |||
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EICOSAPENTAENOIC ACID
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PRIMARY | |||
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CHEMBL460026
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PRIMARY | |||
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61330
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PRIMARY | |||
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DTXSID9041023
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PRIMARY | |||
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AAN7QOV9EA
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PRIMARY | |||
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3174
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PRIMARY | |||
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SUB13664MIG
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PRIMARY | |||
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25378-27-2
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NON-SPECIFIC SUBSTITUTION | |||
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m4848
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PRIMARY | Merck Index | ||
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58562
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84883
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PRIMARY | |||
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C68434
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PRIMARY | |||
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1553-41-9
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NON-SPECIFIC STEREOCHEMISTRY | |||
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618597
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ALTERNATIVE | |||
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7441
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PRIMARY | |||
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90
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PRIMARY | |||
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DB00159
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PRIMARY | |||
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446284
Created by
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
USP
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SALT/SOLVATE -> PARENT | |||
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LIPID -> FATTY ACID | |||
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DERIVATIVE -> PARENT |
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PARENT -> CONSTITUENT ALWAYS PRESENT |
USP
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SALT/SOLVATE -> PARENT |
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Related Record | Type | Details | ||
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PARENT -> METABOLITE ACTIVE |
EPA is mainly metabolized by the liver via beta-oxidation similar to dietary fatty acids. Beta oxidation splits the long carbon chain of EPA into acetyl Coenzyme A, which is converted into energy via the Krebs cycle. Cytochrome P450-mediated metabolism is a minor pathway of elimination of EPA.
MAJOR
PLASMA
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Related Record | Type | Details | ||
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ACTIVE MOIETY |