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Details

Stereochemistry ACHIRAL
Molecular Formula C21H18ClNO6
Molecular Weight 415.824
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACEMETACIN

SMILES

COC1=CC2=C(C=C1)N(C(=O)C3=CC=C(Cl)C=C3)C(C)=C2CC(=O)OCC(O)=O

InChI

InChIKey=FSQKKOOTNAMONP-UHFFFAOYSA-N
InChI=1S/C21H18ClNO6/c1-12-16(10-20(26)29-11-19(24)25)17-9-15(28-2)7-8-18(17)23(12)21(27)13-3-5-14(22)6-4-13/h3-9H,10-11H2,1-2H3,(H,24,25)

HIDE SMILES / InChI

Molecular Formula C21H18ClNO6
Molecular Weight 415.824
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 Sat Dec 16 18:02:26 UTC 2023
Edited
by admin
on Sat Dec 16 18:02:26 UTC 2023
Record UNII
5V141XK28X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACEMETACIN
EP   INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
Acemetacin [WHO-DD]
Common Name English
RANTUDIL
Brand Name English
acemetacin [INN]
Common Name English
NSC-757413
Code English
1-(P-CHLOROBENZOYL)-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID ESTER WITH GLYCOLIC ACID
Common Name English
ACEMETACIN [JAN]
Common Name English
ACEMETACIN [MI]
Common Name English
ACEMETACIN [EP MONOGRAPH]
Common Name English
ACEMETACIN [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
WHO-VATC QM01AB11
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
WHO-ATC M01AB11
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
Code System Code Type Description
MESH
C026784
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
ChEMBL
CHEMBL189171
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
ECHA (EC/EINECS)
258-403-4
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
NCI_THESAURUS
C73068
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
WIKIPEDIA
ACEMETACIN
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
CHEBI
31162
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
DRUG CENTRAL
47
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
PUBCHEM
1981
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
SMS_ID
100000087912
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
CAS
53164-05-9
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
INN
3664
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
FDA UNII
5V141XK28X
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
NSC
757413
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
MERCK INDEX
m1298
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY Merck Index
EVMPD
SUB05209MIG
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
EPA CompTox
DTXSID7022540
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
DRUG BANK
DB13783
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY
RXCUI
16695
Created by admin on Sat Dec 16 18:02:27 UTC 2023 , Edited by admin on Sat Dec 16 18:02:27 UTC 2023
PRIMARY RxNorm
Related Record Type Details
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity C = 1.3
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity F = 1.3
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity D = 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY