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Details

Stereochemistry ACHIRAL
Molecular Formula C15H14N2O2
Molecular Weight 254.2839
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NEPAFENAC

SMILES

NC(=O)CC1=C(N)C(=CC=C1)C(=O)C2=CC=CC=C2

InChI

InChIKey=QEFAQIPZVLVERP-UHFFFAOYSA-N
InChI=1S/C15H14N2O2/c16-13(18)9-11-7-4-8-12(14(11)17)15(19)10-5-2-1-3-6-10/h1-8H,9,17H2,(H2,16,18)

HIDE SMILES / InChI

Molecular Formula C15H14N2O2
Molecular Weight 254.2839
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:45:15 UTC 2023
Edited
by admin
on Fri Dec 15 15:45:15 UTC 2023
Record UNII
0J9L7J6V8C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEPAFENAC
EMA EPAR   INN   JAN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
INN   USAN  
Official Name English
nepafenac [INN]
Common Name English
Nepafenac [WHO-DD]
Common Name English
NEPAFENAC [USAN]
Common Name English
NEPAFENAC [EMA EPAR]
Common Name English
2-(2-Amino-3-benzoylphenyl)acetamide
Systematic Name English
NEVANAC
Brand Name English
NEPAFENAC [MART.]
Common Name English
AL-6515
Code English
NEPAFENAC [ORANGE BOOK]
Common Name English
2-AMINO-3-BENZOYLBENZENEACETAMIDE
Systematic Name English
NEPAFENAC [USP-RS]
Common Name English
NEPAFENAC [MI]
Common Name English
NEPAFENAC [VANDF]
Common Name English
NEPAFENAC [JAN]
Common Name English
AHR-9434
Code English
Classification Tree Code System Code
NDF-RT N0000000160
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
NDF-RT N0000175721
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
NDF-RT N0000175722
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
WHO-VATC QS01BC10
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
EMA ASSESSMENT REPORTS NEVANAC (AUTHORIZED: PAIN, POSTOPERATIVE)
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
WHO-ATC S01BC10
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
EMA ASSESSMENT REPORTS NEVANAC (AUTHORIZED: OPTHALMOLOGIC SURGICAL PROCEDURES)
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
Code System Code Type Description
MESH
C414203
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
PUBCHEM
151075
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
LACTMED
Nepafenac
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
CHEBI
75922
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
INN
7685
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
SMS_ID
100000085451
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
WIKIPEDIA
Nepafenac
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
DRUG BANK
DB06802
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
NCI_THESAURUS
C66228
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
RXCUI
298665
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID0048638
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
RS_ITEM_NUM
1460317
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
EVMPD
SUB09197MIG
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
DAILYMED
0J9L7J6V8C
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
DRUG CENTRAL
1899
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
ChEMBL
CHEMBL1021
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
FDA UNII
0J9L7J6V8C
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
MERCK INDEX
m7823
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY Merck Index
IUPHAR
7564
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
CAS
78281-72-8
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
USAN
II-86
Created by admin on Fri Dec 15 15:45:15 UTC 2023 , Edited by admin on Fri Dec 15 15:45:15 UTC 2023
PRIMARY
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC SINGLE DOSE

Tmax PHARMACOKINETIC SINGLE DOSE