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Details

Stereochemistry RACEMIC
Molecular Formula C22H24ClN3OS
Molecular Weight 413.963
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZACLORZINE

SMILES

ClC1=CC=C2SC3=C(C=CC=C3)N(C(=O)CCN4CCN5CCCC5C4)C2=C1

InChI

InChIKey=ZQTOZLYOIRKCPL-UHFFFAOYSA-N
InChI=1S/C22H24ClN3OS/c23-16-7-8-21-19(14-16)26(18-5-1-2-6-20(18)28-21)22(27)9-11-24-12-13-25-10-3-4-17(25)15-24/h1-2,5-8,14,17H,3-4,9-13,15H2

HIDE SMILES / InChI

Molecular Formula C22H24ClN3OS
Molecular Weight 413.963
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: The description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/2293393 | https://www.ncbi.nlm.nih.gov/pubmed/3758337

Nonachlazine is an original drug synthesized in the Institute of Pharmacology, Academy of Medical Sciences of the USSR. The results of clinical trials have shown that Nonachlazine is an antianginal agent distinguished by its high efficacy in the treatment of ischemic heart disease. Experimental studies have shown that an important role in the mechanism of the antianginal effect of nonachlazine is played by its effect on adrenergic processes of regulation of the circulation and cardiac activity. Nonachlazine increases the noradrenalin concentration and activity of phosphorylase "a" in the myocardium. These findings suggest that the beneficial effect of nonachlazine is evidently associated with its ability to activate adrenergic mechanisms in the regulation of glycogenolysis. Yonahlazin is used in patients who do not tolerate nitroglycerin or who have contraindications to its use. Nonahlazin in solution, unlike nitroglycerin, does not lower arterial pressure and does not cause dizziness, but often nitroglycerin more effectively eliminates an attack than Nonachlazine.

Originator

Sources: Khimiko-Farmatsevticheskii Zhurnal (1978), 12, (7), 97-101

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Азаклорзин

Approved Use

Unknown
Primary
Азаклорзин

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: https://www.piluli.kharkov.ua/drugs/drug/393/
Chronic ischemic heart disease: 0,03 g (1 tablet) for 1 hour before meals 3-4 times a day for 3-4 weeks. Preinfarction angina: 5ml of 1,5% solution 3 times per day for 3 days. After that 1 tablet 4-8 times per day for 3-4 weeks. Angina pectoris: 5-10 ml of 1,5% solution. Repeat after 4-5 hours. Do not exceed daily dose - 30 ml.
Route of Administration: Oral
In Vitro Use Guide
Experiments on the ischemic myocardial tissue of the rat in vitro showed that despite the fact that reserpine-induced depletion of the tissue catecholamine storage failed to affect the stability of lysosomal membranes, a combination of reserpine pretreatment of the animals with subsequent administration of nonachlazine at the low dose yielded stabilization of lysosomal membranes to a greater extent than administration of nonachlazine alone. The effects of nonachlazine (0.25 mg/kg) on the activity of creatine phosphokinase and total activity of acid phosphatase with and without reserpine pretreatment were similar.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:38:57 GMT 2023
Edited
by admin
on Fri Dec 15 15:38:57 GMT 2023
Record UNII
7N4BHX8N3L
Record Status Validated (UNII)
Record Version
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Name Type Language
AZACLORZINE
INN   MART.  
INN  
Official Name English
AZACLORZINE [MART.]
Common Name English
2-CHLORO-10-(3-(HEXAHYDROPYRROLO(1,2-A)PYRAZIN-2(1H)-YL)-PROPIONYL)PHENOTHIAZINE
Systematic Name English
azaclorzine [INN]
Common Name English
10H-PHENOTHIAZINE, 2-CHLORO-10-(3-(HEXAHYDROPYRROLO(1,2-A)PYRAZIN-2(1H)-YL)-1-OXOPROPYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
Code System Code Type Description
INN
3510
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
PUBCHEM
39526
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID1046423
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
EVMPD
SUB05625MIG
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
CAS
49864-70-2
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
FDA UNII
7N4BHX8N3L
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
ChEMBL
CHEMBL1615867
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
SMS_ID
100000086886
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
NCI_THESAURUS
C74421
Created by admin on Fri Dec 15 15:38:57 GMT 2023 , Edited by admin on Fri Dec 15 15:38:57 GMT 2023
PRIMARY
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ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
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ACTIVE MOIETY