Details
Stereochemistry | RACEMIC |
Molecular Formula | C27H34N4O10 |
Molecular Weight | 574.5797 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC(OC)=C1OC)C(=O)OC(CN2CCOCC2)CN3N=NC4=C(OC)C(OC)=C(OC)C=C4C3=O
InChI
InChIKey=KUUKBTYSAHIXTN-UHFFFAOYSA-N
InChI=1S/C27H34N4O10/c1-34-19-11-16(12-20(35-2)23(19)37-4)27(33)41-17(14-30-7-9-40-10-8-30)15-31-26(32)18-13-21(36-3)24(38-5)25(39-6)22(18)28-29-31/h11-13,17H,7-10,14-15H2,1-6H3
Molecular Formula | C27H34N4O10 |
Molecular Weight | 574.5797 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
DescriptionCurator's Comment: Publication in URI also on PubMed, but title only: https://www.ncbi.nlm.nih.gov/pubmed/7196735
Curator's Comment: Publication in URI also on PubMed, but title only: https://www.ncbi.nlm.nih.gov/pubmed/7196735
Razinodil was developed as a coronary vasodilator, a drug that reduces blood pressure by dilating blood vessels. It was tested for its potential as a drug in ischemic myocardial diseases. In a canine heart-lung laboratory model, it increased coronary blood flow without increasing oxygen consumption. Only slight negative chronotropic (heart rate) and inotropic (cardiac contraction) effects were reported. Razinodil also improved the survival rate of miniature pigs after an induced heart attack.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:01:48 GMT 2023
by
admin
on
Fri Dec 15 16:01:48 GMT 2023
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Record UNII |
UJ1O5LVT0G
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29707
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SUB10264MIG
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65771
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CHEMBL2104773
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310409
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100000080821
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C77078
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4294
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C031048
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DTXSID40865534
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UJ1O5LVT0G
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30271-85-3
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |