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(C=C(OC)C(OC)=C4OC)C3=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
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Mon Mar 31 18:16:46 GMT 2025
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| Record UNII |
UJ1O5LVT0G
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| Record Status |
Validated (UNII)
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Preferred Name | English | ||
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Common Name | English |
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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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PRIMARY |
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ENANTIOMER -> RACEMATE |
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ACTIVE MOIETY |