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Details

Stereochemistry ACHIRAL
Molecular Formula C28H38N2O2.ClH
Molecular Weight 471.074
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTOPROZINE HYDROCHLORIDE

SMILES

Cl.CCCCN(CCCC)CCCOC1=CC=C(C=C1)C(=O)C2=C(CC)C=C3C=CC=CN23

InChI

InChIKey=DXHWOBBGGCYHNV-UHFFFAOYSA-N
InChI=1S/C28H38N2O2.ClH/c1-4-7-17-29(18-8-5-2)19-11-21-32-26-15-13-24(14-16-26)28(31)27-23(6-3)22-25-12-9-10-20-30(25)27;/h9-10,12-16,20,22H,4-8,11,17-19,21H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula C28H38N2O2
Molecular Weight 434.6135
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

Butoprozine increased the action potential duration like amiodarone, depressed the plateau phase like verapamil and decreased the amplitude and the maximum rate of depolarization. Butoprozine injected intravenously depressed sino-atrial node function, lengthened A-V nodal conduction time and the A-V nodal refractory period, and prolonged the atrial refractory period. Thus butoprozine acted preferentially on parts of the myocardial tissue where the slow inward current seems to be particularly involved. In this respect, butoprozine was more active than amiodarone, but in contrast to this drug, butoprozine did neither prolong the ventricular monophasic action potential duration nor the ventricular refractory period.

Approval Year

PubMed

PubMed

TitleDatePubMed
Amiodarone-like haemodynamic and non-competitive antiadrenergic properties of a benzoyl-indolizine.
1977 Jul
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:37:22 GMT 2023
Edited
by admin
on Fri Dec 15 17:37:22 GMT 2023
Record UNII
H3H80F5CTY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTOPROZINE HYDROCHLORIDE
USAN  
USAN  
Official Name English
P-(3-(DIBUTYLAMINO)PROPOXY)PHENYL 2-ETHYL-3-INDOLIZINYL KETONE MONOHYDROCHLORIDE
Common Name English
L-9394
Code English
METHANONE, (4-(3-(DIBUTYLAMINO)-PROPOXY)PHENYL)(2-ETHYL-3-INDOLIZINYL)-, MONOHYDROCHLORIDE
Common Name English
BUTOPROZINE HCL
Common Name English
BUTOPROZINE HYDROCHLORIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
Code System Code Type Description
MESH
C014921
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
CAS
62134-34-3
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
FDA UNII
H3H80F5CTY
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
PUBCHEM
71958
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID80211192
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110811
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
263-427-3
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
NCI_THESAURUS
C79925
Created by admin on Fri Dec 15 17:37:22 GMT 2023 , Edited by admin on Fri Dec 15 17:37:22 GMT 2023
PRIMARY
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