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Details

Stereochemistry RACEMIC
Molecular Formula C11H9Cl4NO2
Molecular Weight 329.007
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOPONONE

SMILES

ClCC(NC(=O)C(Cl)Cl)C(=O)C1=CC=C(Cl)C=C1

InChI

InChIKey=MLVKMSCFQIQULM-UHFFFAOYSA-N
InChI=1S/C11H9Cl4NO2/c12-5-8(16-11(18)10(14)15)9(17)6-1-3-7(13)4-2-6/h1-4,8,10H,5H2,(H,16,18)

HIDE SMILES / InChI

Molecular Formula C11H9Cl4NO2
Molecular Weight 329.007
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Cloponone is chloramphenicol derivative with antibacterial activity. It was used in combination with chloramphenicol and myralact for the treatment of trichomonal vaginitis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Trichomonal vaginitis treated with one dose of metronidazole.
1971-12
Influence of dichloroacetylation on the antimicrobial activity of chloramphenicol derivatives and of various amines.
1961-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:31:54 GMT 2025
Edited
by admin
on Mon Mar 31 18:31:54 GMT 2025
Record UNII
V51W472X6D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(±)-2,2-DICHLORO-N-(PARA-CHLORO-ALPHA-(CHLOROMETHYL)PHENACYL)ACETAMIDE
Preferred Name English
CLOPONONE
INN   MART.   WHO-DD  
INN  
Official Name English
cloponone [INN]
Common Name English
ACETAMIDE, 2,2-DICHLORO-N-(1-(CHLOROMETHYL)-2-(4-CHLOROPHENYL)-2-OXOETHYL)-
Systematic Name English
Cloponone [WHO-DD]
Common Name English
CLOPONONE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
Code System Code Type Description
FDA UNII
V51W472X6D
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
PUBCHEM
160412
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
SMS_ID
100000084019
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
NCI_THESAURUS
C76259
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
ECHA (EC/EINECS)
287-113-0
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104693
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
CAS
85409-44-5
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
INN
1762
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
EVMPD
SUB06743MIG
Created by admin on Mon Mar 31 18:31:54 GMT 2025 , Edited by admin on Mon Mar 31 18:31:54 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY