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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H18N4
Molecular Weight 182.266
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUANACLINE

SMILES

CC1=CCN(CCNC(N)=N)CC1

InChI

InChIKey=WQVAYGCXSJMPRT-UHFFFAOYSA-N
InChI=1S/C9H18N4/c1-8-2-5-13(6-3-8)7-4-12-9(10)11/h2H,3-7H2,1H3,(H4,10,11,12)

HIDE SMILES / InChI

Molecular Formula C9H18N4
Molecular Weight 182.266
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Guanacline was studied in the treatment of hypertension. However, information about the current use of this compound is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Guanacline, a new hypotensive drug.
1969 Jan 25
Clinical experiences with Leron (guanacline) in the treatment of hypertension.
1970 May 9
Species and structural specificity of the lipopigment accumulation and neuronal destruction induced by N-(2-guanidinoethyl)-4-methyl-1,2,5,6-tetrahydropyridine (guanacline).
1986 Sep 24
Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:05 UTC 2023
Edited
by admin
on Fri Dec 15 14:59:05 UTC 2023
Record UNII
2S93M1DW13
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GUANACLINE
INN   MI   WHO-DD  
INN  
Official Name English
guanacline [INN]
Common Name English
(2-(3,6-DIHYDRO-4-METHYL-1(2H)-PYRIDYL)ETHYL)GUANIDINE
Systematic Name English
GUANIDINE, (2-(3,6-DIHYDRO-4-METHYL-1(2H)-PYRIDINYL)ETHYL)-
Systematic Name English
GUANACLINE [MI]
Common Name English
Guanacline [WHO-DD]
Common Name English
Code System Code Type Description
MERCK INDEX
m221
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY Merck Index
EVMPD
SUB07979MIG
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
MESH
C004943
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
NCI_THESAURUS
C166589
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
PUBCHEM
15102
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
FDA UNII
2S93M1DW13
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
SMS_ID
100000084451
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
CAS
1463-28-1
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
ChEMBL
CHEMBL1160385
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
INN
2150
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
EPA CompTox
DTXSID90163350
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
DRUG CENTRAL
3454
Created by admin on Fri Dec 15 14:59:05 UTC 2023 , Edited by admin on Fri Dec 15 14:59:05 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY