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
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
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Code | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C29707
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
SUB10264MIG
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
65771
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
CHEMBL2104773
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
310409
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
100000080821
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
C77078
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
4294
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
C031048
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
DTXSID40865534
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
UJ1O5LVT0G
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY | |||
|
30271-85-3
Created by
admin on Fri Dec 15 16:01:48 GMT 2023 , Edited by admin on Fri Dec 15 16:01:48 GMT 2023
|
PRIMARY |
ACTIVE MOIETY