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Details

Stereochemistry RACEMIC
Molecular Formula C22H24ClN3OS.2ClH
Molecular Weight 486.885
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZACLORZINE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=UERHIZBSLAGDLU-UHFFFAOYSA-N
InChI=1S/C22H24ClN3OS.2ClH/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;2*1H

HIDE SMILES / InChI

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
[Use of nonachlazine in the acute period of myocardial infarction].
1990
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.
Name Type Language
AZACLORZINE HYDROCHLORIDE
MART.   USAN  
USAN  
Official Name English
2-CHLORO-10-(3-(HEXAHYDROPYRROLO(1,2-A)YRAZIN-2(1H)-YL)-PROPIONYL)HENOTHIAZINE DIHYDROCHLORIDE
Common Name English
AZACLORZINE HYDROCHLORIDE [USAN]
Common Name English
AZACLORZINE HCL
Common Name English
10H-PHENOTHIAZINE, 2-CHLORO-10-(3-(HEXAHYDROPYRROLO(1,2-A)PYRAZIN-2(1H)-YL)-1-OXOPROPYL)-, DIHYDROCHLORIDE
Common Name English
AZACLORZINE HYDROCHLORIDE [MART.]
Common Name English
AY-25,329
Code English
AY-25329
Code English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 15:38:56 GMT 2023 , Edited by admin on Fri Dec 15 15:38:56 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL1615867
Created by admin on Fri Dec 15 15:38:56 GMT 2023 , Edited by admin on Fri Dec 15 15:38:56 GMT 2023
PRIMARY
CAS
49780-10-1
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PUBCHEM
39525
Created by admin on Fri Dec 15 15:38:56 GMT 2023 , Edited by admin on Fri Dec 15 15:38:56 GMT 2023
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EPA CompTox
DTXSID40964399
Created by admin on Fri Dec 15 15:38:56 GMT 2023 , Edited by admin on Fri Dec 15 15:38:56 GMT 2023
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NCI_THESAURUS
C72709
Created by admin on Fri Dec 15 15:38:56 GMT 2023 , Edited by admin on Fri Dec 15 15:38:56 GMT 2023
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FDA UNII
7531I37BK3
Created by admin on Fri Dec 15 15:38:56 GMT 2023 , Edited by admin on Fri Dec 15 15:38:56 GMT 2023
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