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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
Structure of ICOSAPENT

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-

HIDE SMILES / InChI

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 Fri Dec 15 16:35:07 UTC 2023
Edited
by admin
on Fri Dec 15 16:35:07 UTC 2023
Record UNII
AAN7QOV9EA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ICOSAPENT
INN  
INN  
Official Name English
EPA
Common Name English
EICOSAPENTAENOIC ACID (EPA) (C20:5) (CONSTITUENT OF KRILL OIL) [DSC]
Common Name English
TIMNODONIC ACID
Common Name English
Eicosapentaenoic acid [WHO-DD]
Common Name English
ALL-CIS-FATTY ACID 20:5 OMEGA-3
Common Name English
INCROMEGA E 7010SR
Common Name English
ROPUFA 70
Common Name English
icosapent [INN]
Common Name English
(5Z,8Z,11Z,14Z,17Z)-5,8,11,14,17-EICOSAPENTAENOIC ACID
Systematic Name English
(ALL-Z)-5,8,11,14,17-EICOSAPENTAENOIC ACID
Common Name English
EICOSAPENTAENOATE
Systematic Name English
EICOSAPENTAENOIC ACID [INCI]
Common Name English
EICOSAPENTAENOIC ACID [MI]
Common Name English
EICOSAPENTAENOIC ACID (EPA) (C20:5 N3)
Common Name English
EICOSAPENTAENOIC ACID [USP-RS]
Common Name English
C20:5 (N-3)
Common Name English
EICOSAPENTAENOIC ACID
INCI   MART.   MI   VANDF   WHO-DD  
INCI  
Official Name English
EICOSAPENTAENOIC ACID (C20:5 N3)
Common Name English
EICOSAPENTAENOIC ACID [VANDF]
Common Name English
EICOSAPENTAENOIC ACID [MART.]
Common Name English
EPA 45G
Code English
Classification Tree Code System Code
LOINC 75097-6
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
LOINC 88998-0
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
FDA ORPHAN DRUG 283409
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
LOINC 90911-9
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
LIVERTOX 342
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
EU-Orphan Drug EU/3/09/666
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
LOINC 88996-4
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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
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
LOINC 35173-4
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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
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
LOINC 90909-3
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
LOINC 88999-8
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
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
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
Code System Code Type Description
CHEBI
36006
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
RS_ITEM_NUM
1234293
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
SMS_ID
100000079270
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
MESH
D015118
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
FDA UNII
AAN7QOV9EA
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
CHEBI
28364
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
INN
6328
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
CAS
10417-94-4
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
WIKIPEDIA
EICOSAPENTAENOIC ACID
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
ChEMBL
CHEMBL460026
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
CHEBI
61330
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
EPA CompTox
DTXSID9041023
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
DAILYMED
AAN7QOV9EA
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
DRUG CENTRAL
3174
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
EVMPD
SUB13664MIG
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
CAS
25378-27-2
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
NON-SPECIFIC SUBSTITUTION
MERCK INDEX
m4848
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY Merck Index
CHEBI
58562
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
CHEBI
84883
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
NCI_THESAURUS
C68434
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
CAS
1553-41-9
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
RXCUI
618597
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
ALTERNATIVE
IUPHAR
7441
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
RXCUI
90
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
DRUG BANK
DB00159
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
PUBCHEM
446284
Created by admin on Fri Dec 15 16:35:07 UTC 2023 , Edited by admin on Fri Dec 15 16:35:07 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
USP
SALT/SOLVATE -> PARENT
LIPID -> FATTY ACID
DERIVATIVE -> PARENT
PARENT -> CONSTITUENT ALWAYS PRESENT
USP
SALT/SOLVATE -> PARENT
Related Record Type Details
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
Related Record Type Details
ACTIVE MOIETY