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
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)
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.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Losulazine, a new antihypertensive. | 1985 Aug |
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7-(Trifluoromethyl)-4-aminoquinoline hypotensives: novel peripheral sympatholytics. | 1986 Jan |
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Mechanism of anestrus in rats treated with an antihypertensive agent, losulazine hydrochloride. | 1987 Jan |
|
Study on the activities of testes and accessory sex glands after losulazine treatment in rats. | 1994 Sep |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:07:07 GMT 2023
by
admin
on
Fri Dec 15 19:07:07 GMT 2023
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Record UNII |
O2978JQ9B7
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Record Status |
Validated (UNII)
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Record Version |
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |