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

Details

Stereochemistry MIXED
Molecular Formula C13H20ClN3O4S2
Molecular Weight 381.899
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEBUTIZIDE

SMILES

CCC(C)C(C)C1NC2=CC(Cl)=C(C=C2S(=O)(=O)N1)S(N)(=O)=O

InChI

InChIKey=KJLLKLRVCJAFRY-UHFFFAOYSA-N
InChI=1S/C13H20ClN3O4S2/c1-4-7(2)8(3)13-16-10-5-9(14)11(22(15,18)19)6-12(10)23(20,21)17-13/h5-8,13,16-17H,4H2,1-3H3,(H2,15,18,19)

HIDE SMILES / InChI

Molecular Formula C13H20ClN3O4S2
Molecular Weight 381.899
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:54:01 GMT 2023
Edited
by admin
on Fri Dec 15 16:54:01 GMT 2023
Record UNII
7738AS8324
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEBUTIZIDE
INN   MART.   WHO-DD  
INN  
Official Name English
NEONIAGAR
Brand Name English
MEBUTHIAZIDE
Common Name English
MEBUTIZIDE [MART.]
Common Name English
2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE, 6-CHLORO-3-(1,2-DIMETHYLBUTYL)-3,4-DIHYDRO-, 1,1-DIOXIDE
Systematic Name English
mebutizide [INN]
Common Name English
MEBUTIZID
Common Name English
MINUSTEN
Brand Name English
BETALEVO
Brand Name English
6-CHLORO-3,4-DIHYDRO-3-(1,2-DIMETHYLBUTYL)-2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE 1,1-DIOXIDE
Systematic Name English
DEVALENE
Brand Name English
TRINIAGAR
Brand Name English
Mebutizide [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC C03AA13
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
WHO-VATC QC03EA05
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
WHO-VATC QC03AA13
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
NCI_THESAURUS C49185
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
WHO-ATC C03EA05
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
Code System Code Type Description
PUBCHEM
71652
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
DRUG CENTRAL
1645
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
MESH
C008338
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
SMS_ID
100000081773
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID90863202
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
INN
1859
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105212
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
WIKIPEDIA
MEBUTIZIDE
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
NCI_THESAURUS
C83910
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
ECHA (EC/EINECS)
222-660-0
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
EVMPD
SUB08669MIG
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
FDA UNII
7738AS8324
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
CAS
3568-00-1
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
DRUG BANK
DB13430
Created by admin on Fri Dec 15 16:54:01 GMT 2023 , Edited by admin on Fri Dec 15 16:54:01 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY