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

Details

Stereochemistry ACHIRAL
Molecular Formula C10H13N3O2
Molecular Weight 207.2291
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUABENXAN

SMILES

NC(=N)NCC1=CC=C2OCCOC2=C1

InChI

InChIKey=WTDYJDLUNYALPM-UHFFFAOYSA-N
InChI=1S/C10H13N3O2/c11-10(12)13-6-7-1-2-8-9(5-7)15-4-3-14-8/h1-2,5H,3-4,6H2,(H4,11,12,13)

HIDE SMILES / InChI

Molecular Formula C10H13N3O2
Molecular Weight 207.2291
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Guabenxan was developed as an oral antihypertensive drug.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Double-blind controlled study of the therapeutic effectiveness and tolerance of the guabenxan-bemetizid combination as compared with guanethidine-hydrochlorothiazide in arterial hypertension in the aged].
1982-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:01:31 GMT 2025
Edited
by admin
on Mon Mar 31 18:01:31 GMT 2025
Record UNII
SAW16W26X6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GUABENXAN
INN   MART.   WHO-DD  
INN  
Official Name English
GUABENXAN [MART.]
Preferred Name English
(1,4-BENZODIOXAN-6-YLMETHYL)GUANIDINE
Systematic Name English
guabenxan [INN]
Common Name English
Guabenxan [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
Code System Code Type Description
PUBCHEM
28563
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
INN
3544
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
SMS_ID
100000084259
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
NCI_THESAURUS
C65820
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
CAS
19889-45-3
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
DRUG CENTRAL
1332
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
FDA UNII
SAW16W26X6
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
MESH
C036327
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID60173643
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105111
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
EVMPD
SUB07967MIG
Created by admin on Mon Mar 31 18:01:31 GMT 2025 , Edited by admin on Mon Mar 31 18:01:31 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY