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

Details

Stereochemistry ACHIRAL
Molecular Formula C10H12FN3
Molecular Weight 193.2208
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUTONIDINE

SMILES

CC1=CC=C(F)C=C1NC2=NCCN2

InChI

InChIKey=UYIZEUBMWCOJFF-UHFFFAOYSA-N
InChI=1S/C10H12FN3/c1-7-2-3-8(11)6-9(7)14-10-12-4-5-13-10/h2-3,6H,4-5H2,1H3,(H2,12,13,14)

HIDE SMILES / InChI

Molecular Formula C10H12FN3
Molecular Weight 193.2208
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Flutonidine, an alpha2-adrenergic receptor agonist was studied as an antihypertensive drug. However, information about the current use of this drug is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of flutonidine on ouabain-induced arrhythmias and lethality in guinea-pig.
1993-05-01
Diuretic effects of flutonidine, a newer clonidine analog.
1987-01
[Long-term treatment with a new antihypertensive drug: flutonidin].
1983-05-19
alpha-Adrenoceptor activity of flutonidine (ST 600) in rat anococcygeus muscle and rabbit jejunum.
1982-04
A comparative trial of timolol and flutonidin as antihypertensive agents.
1982-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:08:46 GMT 2025
Edited
by admin
on Mon Mar 31 18:08:46 GMT 2025
Record UNII
ZCC19F3X8K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUTONIDINE
INN  
INN  
Official Name English
ST-600
Preferred Name English
2-(5-FLUORO-O-TOLUIDINO)-2-IMIDAZOLINE
Common Name English
flutonidine [INN]
Common Name English
ST 600
Code English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
Code System Code Type Description
FDA UNII
ZCC19F3X8K
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106760
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID90182405
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
PUBCHEM
65761
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
EVMPD
SUB07763MIG
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
SMS_ID
100000080405
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
MESH
C010227
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
NCI_THESAURUS
C65741
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
CAS
28125-87-3
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
INN
3590
Created by admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY