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
| Molecular Formula | C9H15O3 |
| Molecular Weight | 171.2136 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
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 |
|---|---|---|
| [Hypolipidemic effect of gevilon]. | 1993 |
|
| Therapeutic effect of gevilon in patients with hyperlipoproteinaemia. | 1992-04-01 |
|
| [ELECTROENCEPHALOGRAPHIC EXPERIMENTATION WITH 2 NEW ACTIVATORS: TOCEN AND HEXACYCLONATE (GEVILON)]. | 1963 |
|
| Adjunctive treatment of the chronic alcoholic with hexacyclonate sodium. | 1962-05 |
|
| Pharmaco-motivation of the geriatric patient: a preliminary report on hexacyclonate. | 1962-01 |
|
| Effects of hexacyclonate on regressed patients. | 1961-10 |
|
| [Sodium hexacyclonate as coadjuvant in the treatment and rehabilitation of the chronic alcoholic]. | 1961-06-20 |
|
| [Special clinical a spects of old age and their treatment with sodium-beta,beta-pentamethylene-beta-hydroxybutyrate (Gevilon) in internal medicine]. | 1960-10-28 |
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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 07:30:11 GMT 2025
by
admin
on
Wed Apr 02 07:30:11 GMT 2025
|
| Record UNII |
6XI46H39BZ
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C47795
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
134805
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110826
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
m233
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | Merck Index | ||
|
C082676
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
3459
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
DTXSID60220363
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
7009-49-6
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
100000083531
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
6XI46H39BZ
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
947
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
C83746
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
23675742
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY | |||
|
SUB10564MIG
Created by
admin on Wed Apr 02 07:30:11 GMT 2025 , Edited by admin on Wed Apr 02 07:30:11 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |