Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H15O3.Na |
Molecular Weight | 194.2034 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].OCC1(CC([O-])=O)CCCCC1
InChI
InChIKey=YPKROQTVZNJPNX-UHFFFAOYSA-M
InChI=1S/C9H16O3.Na/c10-7-9(6-8(11)12)4-2-1-3-5-9;/h10H,1-7H2,(H,11,12);/q;+1/p-1
Hexacyclonic Acid (aka gevilon) has been clinically demonstrated to produce hypolipidemic effects. It has been investigated as a treatment for coronary heart disease, and hypertensive disease with severe lipid metabolic disturbances. Gevilon has been found to have a hypolipidemic effect in reducing the levels of total cholesterol, beta-cholesterol, triglycerides, increasing alpha-cholesterol levels and normalizing the atherogenicity coefficient; especially in patients with Type IIb dyslipoproteinemia.
CNS Activity
Approval Year
PubMed
Title | Date | PubMed |
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[Special clinical a spects of old age and their treatment with sodium-beta,beta-pentamethylene-beta-hydroxybutyrate (Gevilon) in internal medicine]. | 1960 Oct 28 |
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Effects of hexacyclonate on regressed patients. | 1961 Oct |
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Pharmaco-motivation of the geriatric patient: a preliminary report on hexacyclonate. | 1962 Jan |
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Adjunctive treatment of the chronic alcoholic with hexacyclonate sodium. | 1962 May |
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[ELECTROENCEPHALOGRAPHIC EXPERIMENTATION WITH 2 NEW ACTIVATORS: TOCEN AND HEXACYCLONATE (GEVILON)]. | 1963 |
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Therapeutic effect of gevilon in patients with hyperlipoproteinaemia. | 1992 Apr-Jun |
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[Hypolipidemic effect of gevilon]. | 1993 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1307777
Patients with hyperlipoproteinemia were divided according to hyperlipoproteinemia type IIA, IIB, and IV. After one month of isocaloric diet, the patients were given a single night gevilon dose of 900 mg for a period of 3 months. In all groups increased levels of cholesterol, beta-lipoproteins and triglycerides were significantly reduced after 3 months of gevilon treatment. In all patients, the HDL/LDL ratio increased close to normal values.
Route of Administration:
Oral
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C47795
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD