U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C15H9ClO2
Molecular Weight 256.684
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLORINDIONE

SMILES

ClC1=CC=C(C=C1)C2C(=O)C3=C(C=CC=C3)C2=O

InChI

InChIKey=NJDUWAXIURWWLN-UHFFFAOYSA-N
InChI=1S/C15H9ClO2/c16-10-7-5-9(6-8-10)13-14(17)11-3-1-2-4-12(11)15(13)18/h1-8,13H

HIDE SMILES / InChI
Clorindione belongs to a class of drugs which are known to be vitamin K antagonists, and is a derivative of phenindione. It has been demonstrated as effective in reducing prothrombin levels in humans and also to reduce serum cholesterol and triglycerides in mice.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Hypolipidemic activity of indan-1,3-dione derivatives in rodents.
1985-11
A Trial of Clorindione-A Long Acting Oral Anticoagulant.
1965-12
[ON THE VALUE OF CHLORPHENYLINDANDIONE IN THE THERAPY OF THROMBOEMBOLISM].
1964-02-29
Patents

Patents

Sample Use Guides

32 patients were treated in hospital and administered oral tablets of clorindione; 12 mg on the first day, 8 mg on the second day, and 4 mg on the third day. Because of the delayed action of clorindione, Heparin 10,000 iu was given by intramuscular injection on admission and then 5,000 iu every 6 hours for 3 days at 24-hour intervals. Clorindione effectively reduced the prothrombin levels in the patient population back to the desired therapeutic range by the fourth day.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
CLORINDIONE
INN   MI   WHO-DD  
INN  
Official Name English
CLORINDIONE [MI]
Preferred Name English
Clorindione [WHO-DD]
Common Name English
clorindione [INN]
Common Name English
NSC-758878
Code English
G-25766
Code English
2-(P-CHLOROPHENYL)-1,3-INDANDION
Common Name English
Classification Tree Code System Code
WHO-ATC B01AA09
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
WHO-VATC QB01AA09
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
NCI_THESAURUS C263
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL278519
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-553-2
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
FDA UNII
541C7WS64R
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
MESH
C004665
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
INN
1534
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PRIMARY
CAS
1146-99-2
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PRIMARY
DRUG CENTRAL
3111
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID0046228
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
EVMPD
SUB06760MIG
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
NCI_THESAURUS
C81463
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
MERCK INDEX
m1085
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY Merck Index
PUBCHEM
70846
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
SMS_ID
100000084027
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
WIKIPEDIA
CLORINDIONE
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
NSC
758878
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
DRUG BANK
DB13275
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY
RXCUI
402527
Created by admin on Mon Mar 31 18:50:39 GMT 2025 , Edited by admin on Mon Mar 31 18:50:39 GMT 2025
PRIMARY