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Details

Stereochemistry ACHIRAL
Molecular Formula C9H12Cl2N4O
Molecular Weight 263.124
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUANOCLOR

SMILES

NC(=N)NNCCOC1=C(Cl)C=CC=C1Cl

InChI

InChIKey=XIHXRRMCNSMUET-UHFFFAOYSA-N
InChI=1S/C9H12Cl2N4O/c10-6-2-1-3-7(11)8(6)16-5-4-14-15-9(12)13/h1-3,14H,4-5H2,(H4,12,13,15)

HIDE SMILES / InChI

Molecular Formula C9H12Cl2N4O
Molecular Weight 263.124
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Guanoclor is an anti-hypertensive agent developed by Pfizer Ltd. (U.K.). It seems to be effective in various types of hypertension (unknown aetiology, renal, and malignant). It affects both systolic blood-pressure and diastolic blood-pressure. It is an adrenergic neurone-blocking agent, which also interferes with noradrenaline synthesis by inhibition of the enzyme dopamine beta-hydroxylase. Clinical use of the compound was first reported by Lawrie et al. (1964), who achieved satisfactory blood-pressure control in 60% of their cases with guanoclor alone, and in a further 18% with the addition of a thiazide diuretic. They also noted a significant reduction in urinary noradrenaline levels during guanoclor administration. Guanochlor has an affinity for the Na+/H+ exchanger ranging between 0.5 uM and 6 uM in different systems and is more potent than amiloride in all systems studied. It is suggested that guanochlor recognizes a binding site on the Na+/H+ exchanger that is distinct from the amiloride binding site.

CNS Activity

Curator's Comment: Guanoclor induced depletion of noradrenaline in the C.N.S.,

Approval Year

PubMed

PubMed

TitleDatePubMed
Clinical assessment of the new antihypertensive Compound--1029 (Vatensol)--Guanoclor.
1967 Oct
A comparison of guanoclor and methyldopa in the treatment of severe hypertension.
1971 Mar
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: The drug has been administered to 35 hypertensive subjects in doses of from 20 to 240 mg orally each day.
The smallest effective dose used was 20 mg and the largest 240 mg daily
Route of Administration: Oral
In Vitro Use Guide
Guanochlor has an affinity for the Na+/H+ exchanger ranging between 0.5 uM and 6 uM in different systems and is more potent than amiloride in all systems studied. Half-maximum inhibition by guanochlor of 45Ca2+ uptake is observed at 30 uM. Half-maximum inhibition of the NaC/H+ exchange system in rabbit renal brush border membrane vesicles is observed at 6 uM guanochlor.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:42:09 GMT 2023
Edited
by admin
on Fri Dec 15 15:42:09 GMT 2023
Record UNII
M4HBT852YO
Record Status Validated (UNII)
Record Version
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Name Type Language
GUANOCLOR
INN   WHO-DD  
INN  
Official Name English
3-01029
Code English
GUANOCHLOR [MI]
Common Name English
guanoclor [INN]
Common Name English
HYDRAZINECARBOXIMIDAMIDE, 2-(2-(2,6-DICHLOROPHENOXY)ETHYL)-,(2:1)
Common Name English
Guanoclor [WHO-DD]
Common Name English
NSC-108163
Code English
((2-(2,6-DICHLOROPHENOXY)ETHYL)AMINO)GUANIDINE (2:1)
Common Name English
Classification Tree Code System Code
WHO-VATC QC02CC05
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
NCI_THESAURUS C270
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
WHO-ATC C02CC05
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
Code System Code Type Description
CAS
5001-32-1
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
PUBCHEM
71835
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
EVMPD
SUB07987MIG
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
DRUG CENTRAL
4564
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID10198184
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
FDA UNII
M4HBT852YO
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
SMS_ID
100000084475
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
MESH
C012340
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
NSC
108163
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110641
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
WIKIPEDIA
Guanoclor
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
INN
1827
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
NCI_THESAURUS
C65833
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
ECHA (EC/EINECS)
225-667-7
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
DRUG BANK
DB13779
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY
MERCK INDEX
m223
Created by admin on Fri Dec 15 15:42:09 GMT 2023 , Edited by admin on Fri Dec 15 15:42:09 GMT 2023
PRIMARY Merck Index
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