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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H26ClNO5
Molecular Weight 395.877
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLORICROMEN

SMILES

CCOC(=O)COC1=C(Cl)C2=C(C=C1)C(C)=C(CCN(CC)CC)C(=O)O2

InChI

InChIKey=GYNNRVJJLAVVTQ-UHFFFAOYSA-N
InChI=1S/C20H26ClNO5/c1-5-22(6-2)11-10-15-13(4)14-8-9-16(26-12-17(23)25-7-3)18(21)19(14)27-20(15)24/h8-9H,5-7,10-12H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C20H26ClNO5
Molecular Weight 395.877
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cloricromen a drug that inhibits platelet aggregation in man and in experimental thrombosis. Experiments on rodents have revealed that cloricromene which reduced tumor necrosis factor production, could be useful in the treatment of periodontitis. In addition, it could be potentially useful in ischemic-retinal diseases where amelioration of blood flow and inflammation is desirable. However, experiments with patients with cerebrovascular occlusive disease didn’t shown any effect of cloricromen on coagulative variables.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cloricromene in endotoxemia: role of NF-kappaB.
2004 Aug
Protective effects of a coumarin derivative in diabetic rats.
2009 Aug

Sample Use Guides

Twenty patients with a history of atherothrombotic stroke received cloricromen (100 mg, twice daily) for 30 days in order to evaluate its effects on plasma fibrinogen, antithrombin III, and other variables of the haemostatic system
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:30:49 GMT 2023
Edited
by admin
on Fri Dec 15 16:30:49 GMT 2023
Record UNII
B9454PE93C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLORICROMEN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
CLORICROMEN [MART.]
Common Name English
Cloricromen [WHO-DD]
Common Name English
CLORICROMENE
Common Name English
AD-6
Code English
ETHYL ((8-CHLORO-3-(2-(DIETHYLAMINO)ETHYL)-4-METHYL-2-OXO-2H-1-BENZOPYRAN-7-YL)OXY)ACETATE
Systematic Name English
cloricromen [INN]
Common Name English
CLORICROMEN [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QB01AC02
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
WHO-ATC B01AC02
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
NCI_THESAURUS C1327
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
Code System Code Type Description
FDA UNII
B9454PE93C
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
WIKIPEDIA
Cloricromen
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
ChEMBL
CHEMBL255066
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
MERCK INDEX
m3663
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY Merck Index
PUBCHEM
68876
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
DRUG CENTRAL
713
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
SMS_ID
100000084025
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
EVMPD
SUB06756MIG
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID2048373
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
CAS
68206-94-0
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
INN
5623
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
DRUG BANK
DB13367
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
NCI_THESAURUS
C78091
Created by admin on Fri Dec 15 16:30:49 GMT 2023 , Edited by admin on Fri Dec 15 16:30:49 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY