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

Details

Stereochemistry RACEMIC
Molecular Formula C9H20N4
Molecular Weight 184.2819
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUANAZODINE

SMILES

NC(=N)NCC1CCCCCCN1

InChI

InChIKey=ZCVAIGPGEINFCX-UHFFFAOYSA-N
InChI=1S/C9H20N4/c10-9(11)13-7-8-5-3-1-2-4-6-12-8/h8,12H,1-7H2,(H4,10,11,13)

HIDE SMILES / InChI
Guanazodine is a new antihypertensive drug. Guanazodine caused a sustained decrease in the systemic blood pressure of spontaneously hypertensive rats, renal hypertensive dogs and normal cats. No tachyphylaxis developed when the drug was administered orally. The heart rate decreased. Guanazodine relaxed the cat nictitating membrane, attenuated the positive chronotropic response to sympathetic nerve stimulation in anesthetized dogs and in isolated rabbit aorta to transmural electrical stimulation. Guanazodine potentiated the pressor response to noradrenaline but attenuated the response to tyramine in anesthetized cats. It may be concluded that the hypotensive effect of guanazodine is related to adrenergic neuron blocking action, the noradrenaline-depleting action in peripheral tissues is similar to the effect of guanethidine and bethanidine. However, this drug is less potent than guanethidine. Toxicity and side effects appear to be less with guanazodine than with guanethidine and bethanidine.

Approval Year

Name Type Language
GUANAZODINE
INN   MI   WHO-DD  
INN  
Official Name English
GUANAZODINE [MI]
Common Name English
1-AZACYCLOOCT-2-YLMETHYLGUANIDINE
Systematic Name English
guanazodine [INN]
Common Name English
.ALPHA.-GUANIDINOMETHYLHEPTAMETHYLENIMINE
Common Name English
((OCTAHYDRO-2-AZOCINYL)METHYL)GUANIDINE
Systematic Name English
Guanazodine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QC02CC06
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
WHO-ATC C02CC06
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
NCI_THESAURUS C29713
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3455
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
INN
3127
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL2008565
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
EVMPD
SUB07981MIG
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID30953934
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
MESH
C014017
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
DRUG BANK
DB13604
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
PUBCHEM
36054
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
WIKIPEDIA
GUANAZODINE
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
CAS
32059-15-7
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
NCI_THESAURUS
C83741
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
MERCK INDEX
m222
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY Merck Index
SMS_ID
100000084452
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY
FDA UNII
7N05KQ38YI
Created by admin on Fri Dec 15 16:52:38 GMT 2023 , Edited by admin on Fri Dec 15 16:52:38 GMT 2023
PRIMARY