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Details

Stereochemistry ACHIRAL
Molecular Formula C9H16O3
Molecular Weight 172.2215
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEXACYCLONIC ACID

SMILES

OCC1(CC(O)=O)CCCCC1

InChI

InChIKey=WMJPAYUKEVEBCN-UHFFFAOYSA-N
InChI=1S/C9H16O3/c10-7-9(6-8(11)12)4-2-1-3-5-9/h10H,1-7H2,(H,11,12)

HIDE SMILES / InChI

Molecular Formula C9H16O3
Molecular Weight 172.2215
Charge 0
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.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[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
Patents

Sample Use Guides

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
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:38:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:38:28 GMT 2025
Record UNII
2K0FP9UB6A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HEXACYCLONIC ACID
Common Name English
CYCLOHEXANEACETIC ACID, 1-(HYDROXYMETHYL)-
Preferred Name English
1-(HYDROXYMETHYL)CYCLOHEXANEACETATE
Systematic Name English
HEXACYCLONATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47795
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C83747
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
FDA UNII
2K0FP9UB6A
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID30225885
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
CHEBI
167168
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
CAS
7491-42-1
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
WIKIPEDIA
HEXACYCLONATE
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
PUBCHEM
23444
Created by admin on Mon Mar 31 18:38:28 GMT 2025 , Edited by admin on Mon Mar 31 18:38:28 GMT 2025
PRIMARY
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY