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Details

Stereochemistry RACEMIC
Molecular Formula C10H12ClN3O6S2
Molecular Weight 369.802
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARMETIZIDE

SMILES

COC(=O)C1NC2=C(C=C(C(Cl)=C2)S(N)(=O)=O)S(=O)(=O)N1C

InChI

InChIKey=PFRBORHNFYMVOA-UHFFFAOYSA-N
InChI=1S/C10H12ClN3O6S2/c1-14-9(10(15)20-2)13-6-3-5(11)7(21(12,16)17)4-8(6)22(14,18)19/h3-4,9,13H,1-2H3,(H2,12,16,17)

HIDE SMILES / InChI

Molecular Formula C10H12ClN3O6S2
Molecular Weight 369.802
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Carmetizide is benzothiadiazine derivative patented by pharmaceutical company Abbott Laboratories as a diuretic. In preclinical studies, Carmetizide demonstrates perfect safety profile. Administration of Carmetizide (10,000 mg/kg, orally or 5000 mg/kg, s.c. or i.p.) to rats had no toxic effect. Carmetizide had no effect on the central nervous system and the cardiovascular system of guinea pigs or on the heart-lung preparation of dogs. These drugs did not affect the body temperature of rats and the blood coagulation of rabbits. Carmetizide had no effect on the spontaneous movement of smooth muscles.

Approval Year

Patents

Sample Use Guides

In Vivo Use Guide
Sources: Oyo Yakuri (1973), 7, (2), 231-44.
rat (acute tox. study) 10,​000 mg​/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:24:03 GMT 2023
Edited
by admin
on Fri Dec 15 16:24:03 GMT 2023
Record UNII
8695816VMO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARMETIZIDE
INN  
INN  
Official Name English
carmetizide [INN]
Common Name English
Code System Code Type Description
NCI_THESAURUS
C171770
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
CAS
42583-55-1
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
EPA CompTox
DTXSID20866100
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
PUBCHEM
68670
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
INN
3495
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
EVMPD
SUB06129MIG
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104012
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
FDA UNII
8695816VMO
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
SMS_ID
100000081321
Created by admin on Fri Dec 15 16:24:03 GMT 2023 , Edited by admin on Fri Dec 15 16:24:03 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY