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
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
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:37:22 GMT 2023
by
admin
on
Fri Dec 15 17:37:22 GMT 2023
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Record UNII |
H3H80F5CTY
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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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
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Code System | Code | Type | Description | ||
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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
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PRIMARY | |||
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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
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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
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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
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PRIMARY | |||
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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
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PRIMARY | |||
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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
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PRIMARY | |||
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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
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PRIMARY | |||
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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
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |