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

Details

Stereochemistry ACHIRAL
Molecular Formula C27H22F4N4O3S
Molecular Weight 558.547
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LOSULAZINE

SMILES

FC1=CC=C(C=C1)S(=O)(=O)N2CCN(CC2)C(=O)C3=CC=C(NC4=C5C=CC(=CC5=NC=C4)C(F)(F)F)C=C3

InChI

InChIKey=SYJKIRZBDWNJSB-UHFFFAOYSA-N
InChI=1S/C27H22F4N4O3S/c28-20-4-8-22(9-5-20)39(37,38)35-15-13-34(14-16-35)26(36)18-1-6-21(7-2-18)33-24-11-12-32-25-17-19(27(29,30)31)3-10-23(24)25/h1-12,17H,13-16H2,(H,32,33)

HIDE SMILES / InChI

Molecular Formula C27H22F4N4O3S
Molecular Weight 558.547
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Losulazine (U-54,669F) is an antihypertensive agent acting by a sympatholytic mechanism. It appears to alter peripheral sympathetic neurogenic function but apparently does not enter the central nervous system. Losulazine effectively lowered the blood pressure in patients with hypertension.

Approval Year

PubMed

PubMed

TitleDatePubMed
Study on the activities of testes and accessory sex glands after losulazine treatment in rats.
1994-09
Comparison of the effects of losulazine and reserpine on central aminergic neurons.
1993-11
Mechanism of anestrus in rats treated with an antihypertensive agent, losulazine hydrochloride.
1987-01
7-(Trifluoromethyl)-4-aminoquinoline hypotensives: novel peripheral sympatholytics.
1986-01
Losulazine, a new antihypertensive.
1985-08
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:32:40 GMT 2025
Edited
by admin
on Mon Mar 31 19:32:40 GMT 2025
Record UNII
O2978JQ9B7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-((P-FLUOROPHENYL)SULFONYL)-4-(P-((7-(TRIFLUOROMETHYL)-4-QUINOLYL)AMINO)BENZOYL)PIPERAZINE
Preferred Name English
LOSULAZINE
INN  
INN  
Official Name English
losulazine [INN]
Common Name English
Code System Code Type Description
CAS
72141-57-2
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
PUBCHEM
54750
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
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FDA UNII
O2978JQ9B7
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
EVMPD
SUB08598MIG
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
ChEMBL
CHEMBL287419
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
INN
5362
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
SMS_ID
100000082038
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID20868088
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
NCI_THESAURUS
C174780
Created by admin on Mon Mar 31 19:32:40 GMT 2025 , Edited by admin on Mon Mar 31 19:32:40 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY