GUANISOQUIN

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H12BrN3
Molecular Weight	254.126
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of GUANISOQUIN

Structure Search

SMILES

NC(=N)N1CCC2=C(C1)C=C(Br)C=C2

InChI

InChIKey=ICLLENNEPRZLAP-UHFFFAOYSA-N

InChI=1S/C10H12BrN3/c11-9-2-1-7-3-4-14(10(12)13)6-8(7)5-9/h1-2,5H,3-4,6H2,(H3,12,13)

HIDE SMILES / InChI

Molecular Formula	C10H12BrN3
Molecular Weight	254.126
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14259507 | https://books.google.ru/books?id=YpzyCAAAQBAJ&pg=PA189&lpg=PA189&dq=GUANISOQUIN&source=bl&ots=pQ8c3yJLW4&sig=ACfU3U2RrsocrZgmuePbkek1aBo64DDErg&hl=ru&sa=X&ved=2ahUKEwjwmr6n3KriAhVylosKHYUwDDM4ChDoATABegQIBxAB#v=onepage&q=GUANISOQUIN&f=false

Guanisoquin was found to be an effective antihypertensive agent that inhibited the monoamine oxidase.

Approval Year

PubMed

PubMed

Title	Date	PubMed
PHARMACOLOGICAL STUDIES WITH GUANISOQUIN.	1965-02	14259507

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:15:45 GMT 2025` Edited by `admin` on `Mon Mar 31 18:15:45 GMT 2025`
Record UNII	307YLU08D8
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

GUANISOQUIN

Common Name

English

GUANISOQUINE

Preferred Name

English

2(1H)-ISOQUINOLINECARBOXIMIDAMIDE, 7-BROMO-3,4-DIHYDRO-

Systematic Name

English

guanisoquine [INN]

Common Name

English

7-BROMO-3,4-DIHYDRO-2(1H)-ISOQUINOLINECARBOXAMIDE

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C270

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

Code System Code Type Description

PUBCHEM

10422416

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

EVMPD

SUB07986MIG

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

CAS

154-73-4

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

SMS_ID

100000084494

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

NCI_THESAURUS

C72807

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

FDA UNII

307YLU08D8

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

ChEMBL

CHEMBL2110964

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

EPA CompTox

DTXSID60165508

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

INN

1825

Created by admin on Mon Mar 31 18:15:45 GMT 2025 , Edited by admin on Mon Mar 31 18:15:45 GMT 2025

PRIMARY

Related Record Type Details


					E4E8GE5LVJ

GUANISOQUIN SULFATE

SALT/SOLVATE -> PARENT

Related Record Type Details


					307YLU08D8

ACTIVE MOIETY