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Details

Stereochemistry ACHIRAL
Molecular Formula C17H17N.ClH
Molecular Weight 271.785
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZAPETINE HYDROCHLORIDE

SMILES

Cl.C=CCN1CC2=C(C=CC=C2)C3=C(C1)C=CC=C3

InChI

InChIKey=PAGNTBKVOFUKLT-UHFFFAOYSA-N
InChI=1S/C17H17N.ClH/c1-2-11-18-12-14-7-3-5-9-16(14)17-10-6-4-8-15(17)13-18;/h2-10H,1,11-13H2;1H

HIDE SMILES / InChI

Molecular Formula C17H17N
Molecular Weight 235.3236
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

AZAPETINE, a benzazepine derivative, is an alpha-1 adrenoceptor antagonist. It is a potent arterial vasodilator in the treatment of peripheral vascular diseases.

Approval Year

Conditions

Conditions

PubMed

PubMed

TitleDatePubMed
DDT-induced myoclonus: serotonin and alpha noradrenergic interaction.
1979 Feb
An in vivo model for investigating alpha 1- and alpha 2-receptors in the CNS: studies with mianserin.
1979 Nov
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:06:55 UTC 2023
Edited
by admin
on Fri Dec 15 15:06:55 UTC 2023
Record UNII
KN855K6HSO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AZAPETINE HYDROCHLORIDE
Common Name English
AZAPENTINE HYDROCHLORIDE
Common Name English
AZAPETINE HCL
Common Name English
5H-DIBENZ(C,E)AZEPINE, 6,7-DIHYDRO-6-(2-PROPENYL)-, HYDROCHLORIDE
Systematic Name English
5H-DIBENZ(C,E)AZEPINE, 6-ALLYL-6,7-DIHYDRO-, HYDROCHLORIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29713
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
Code System Code Type Description
MESH
C004448
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID40215313
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
PRIMARY
PUBCHEM
120163
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
PRIMARY
FDA UNII
KN855K6HSO
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
PRIMARY
CAS
65-15-6
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
PRIMARY
NCI_THESAURUS
C83541
Created by admin on Fri Dec 15 15:06:55 UTC 2023 , Edited by admin on Fri Dec 15 15:06:55 UTC 2023
PRIMARY
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