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Details

Stereochemistry ACHIRAL
Molecular Formula C9H8ClN5
Molecular Weight 221.646
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORAZANIL

SMILES

NC1=NC=NC(NC2=CC=C(Cl)C=C2)=N1

InChI

InChIKey=YRZQHIVOIFJEEE-UHFFFAOYSA-N
InChI=1S/C9H8ClN5/c10-6-1-3-7(4-2-6)14-9-13-5-12-8(11)15-9/h1-5H,(H3,11,12,13,14,15)

HIDE SMILES / InChI

Molecular Formula C9H8ClN5
Molecular Weight 221.646
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Chlorazanil is a triazine derivative and diuretic agent. Chlorazanil appears to prevent the absorption of sodium and chloride in the distal convoluted tubule. As nonmercurial orally effective diuretic agent, Chlorazanil is prohibited in sport according to the regulations of the World Anti-Doping Agency (WADA).

Approval Year

PubMed

PubMed

TitleDatePubMed
[Acute interstitial nephritis caused by drugs].
1983 May 20

Sample Use Guides

In conscious unloaded Sprague-Dawley female rats chlorazanil (10 mg/kg orally) markedly increased urinary prostaglandin E2-excretion from 51 +/- 9 to 813 +/- 112 ng/kg/6 hrs. Urinary flow rate increased from 12.8 +/- 0.6 to 42.0 +/- 1.4 ml/kg/6 hrs and urinary sodium excretion from 0.96 +/- 0.12 to 3.86 +/- 0.33 mmol/kg/6 hrs. Urinary potassium excretion was unchanged.
Route of Administration: Oral
In Vitro Use Guide
In vitro chlorazanil (10(-4) M) exhibited a moderate inhibition of 15-OH-prostaglandin dehydrogenase.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:12:29 GMT 2023
Edited
by admin
on Fri Dec 15 16:12:29 GMT 2023
Record UNII
48SN4K3W0E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORAZANIL
INN   MI   WHO-DD  
INN  
Official Name English
Chlorazanil [WHO-DD]
Common Name English
2-AMINO-4-P-CHLOROANILINO-S-TRIAZINE
Common Name English
chlorazanil [INN]
Common Name English
CHLORAZANIL [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C448
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
Code System Code Type Description
INN
724
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
PRIMARY
MERCK INDEX
m635
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
PRIMARY Merck Index
PUBCHEM
10374
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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MESH
C017837
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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CAS
500-42-5
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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ChEMBL
CHEMBL1984344
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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EVMPD
SUB06174MIG
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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FDA UNII
48SN4K3W0E
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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ECHA (EC/EINECS)
207-904-6
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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NCI_THESAURUS
C79796
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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EPA CompTox
DTXSID0049026
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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DRUG CENTRAL
591
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
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SMS_ID
100000081558
Created by admin on Fri Dec 15 16:12:29 GMT 2023 , Edited by admin on Fri Dec 15 16:12:29 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY