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Details

Stereochemistry RACEMIC
Molecular Formula C14H17NO2.ClH
Molecular Weight 267.751
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZOCLIDINE HYDROCHLORIDE

SMILES

Cl.O=C(OC1CN2CCC1CC2)C3=CC=CC=C3

InChI

InChIKey=DGPMCYQIJOUUFY-UHFFFAOYSA-N
InChI=1S/C14H17NO2.ClH/c16-14(12-4-2-1-3-5-12)17-13-10-15-8-6-11(13)7-9-15;/h1-5,11,13H,6-10H2;1H

HIDE SMILES / InChI
Benzoclidine (Oxylidin) exerts tranquilizing and hypotensive actions. It reduces the excitability of the central nervous system, enhances the effect of hypnotic drugs, analgesics and local anesthetics, has a moderate antihypertensive effect, reduces the excitability of the vasomotor centers, has anti-arrhythmic activity. Benzoclidine is marke indicated for the treatment of anxiety and depression of various origins (particularly mild expressed and associated with cerebrovascular insufficiency), neurosis, personality disorder, cyclothymia, hypertension with cerebral disorders, sinus tachycardia, paroxysmal tachycardia.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Benzoclidine

Approved Use

Anxiety and depression of various origins (particularly mild expressed and associated with cerebrovascular insufficiency), neurosis, personality disorder, cyclothymia, hypertension with cerebral disorders, sinus tachycardia, paroxysmal tachycardia.
Primary
Benzoclidine

Approved Use

Anxiety and depression of various origins (particularly mild expressed and associated with cerebrovascular insufficiency), neurosis, personality disorder, cyclothymia, hypertension with cerebral disorders, sinus tachycardia, paroxysmal tachycardia.
Primary
Benzoclidine

Approved Use

Anxiety and depression of various origins (particularly mild expressed and associated with cerebrovascular insufficiency), neurosis, personality disorder, cyclothymia, hypertension with cerebral disorders, sinus tachycardia, paroxysmal tachycardia.
PubMed

PubMed

TitleDatePubMed
[ON THE RELATIONSHIP BETWEEN THE HYPOTENSIVE EFFECT OF OXYLIDIN AND ITS EFFECT ON CENTERS OF THE MEDULLA OBLONGATA AND CARDIAC ACTIVITY].
1964 Jan-Feb
[OXYLIDIN THERAPY OF PATIENTS WITH CEREBROVASCULAR DISEASES WITH MENTAL DISORDERS].
1965
[CLINICAL TESTING OF OXYLIDIN, A NEW HYPOTENSIVE AGENT, IN THE TREATMENT OF HYPERTENSION].
1965 Feb
[Experience in the treatment of hypertensive patients with oxylidin under polyclinical conditions].
1965 Nov
[Oxylidin--a new preparation of tranquilizing and hypotensive action].
1966 Feb
[The use of oxylidin in psychiatric practice].
1968
[Chromatographic analysis of aceclidine and oxylidin solutions for injections].
1971 Jan-Feb
[Antiarrhythmic action of oxylidin].
1973 Apr
[Effect of antihypertensive compounds on the hypothalamic regulation of baroreceptor reflexes].
1980 Jan-Feb
[Effect of antihypertensive agents on indices of systemic hemodynamics and baroreceptors reflexes in man].
1981 Jan-Feb
[Effect of hypotensive preparations on hemodynamics in persons of different sexes and ages].
1982 Nov-Dec
[Effectiveness of health resort climatic treatment including oxylidin electrophoresis and the correction of the climatic adaptation of patients with the sequelae of viral encephalitis].
1988 Jul-Aug

Sample Use Guides

Average therapeutic dose oral, subcutaneous and intramuscular injection 0.02 - 0.3 grams daily, the duration of treatment 3-8 weeks.
Route of Administration: Other
In Vitro Use Guide
Unknown
Name Type Language
BENZOCLIDINE HYDROCHLORIDE
Common Name English
(±)-3-QUINUCLIDINOL BENZOATE HYDROCHLORIDE
Systematic Name English
3-QUINUCLIDINOL DL-FORM BENZOATE HYDROCHLORIDE [MI]
Common Name English
1-AZABICYCLO(2.2.2)OCTAN-3-OL, 3-BENZOATE, HYDROCHLORIDE (1:1)
Systematic Name English
OKSILIDIN
Brand Name English
DL-3-QUINUCLIDINOL BENZOATE HYDROCHLORIDE
Common Name English
OXYLIDINE
Brand Name English
3-QUINUCLIDINOL, BENZOATE (ESTER), HYDROCHLORIDE
Common Name English
Code System Code Type Description
CAS
25333-48-6
Created by admin on Sat Dec 16 09:58:11 GMT 2023 , Edited by admin on Sat Dec 16 09:58:11 GMT 2023
SUPERSEDED
CAS
7348-26-7
Created by admin on Sat Dec 16 09:58:11 GMT 2023 , Edited by admin on Sat Dec 16 09:58:11 GMT 2023
PRIMARY
MERCK INDEX
m9469
Created by admin on Sat Dec 16 09:58:11 GMT 2023 , Edited by admin on Sat Dec 16 09:58:11 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID60994234
Created by admin on Sat Dec 16 09:58:11 GMT 2023 , Edited by admin on Sat Dec 16 09:58:11 GMT 2023
PRIMARY
FDA UNII
9ZYM70P491
Created by admin on Sat Dec 16 09:58:11 GMT 2023 , Edited by admin on Sat Dec 16 09:58:11 GMT 2023
PRIMARY
PUBCHEM
10199264
Created by admin on Sat Dec 16 09:58:11 GMT 2023 , Edited by admin on Sat Dec 16 09:58:11 GMT 2023
PRIMARY