Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H13NO4 |
| Molecular Weight | 283.2787 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(O)C=C(CC2=NC=CC3=CC(O)=C(O)C=C23)C=C1
InChI
InChIKey=MXQKCNCLQIHHJA-UHFFFAOYSA-N
InChI=1S/C16H13NO4/c18-13-2-1-9(6-14(13)19)5-12-11-8-16(21)15(20)7-10(11)3-4-17-12/h1-4,6-8,18-21H,5H2
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/7237948
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7237948
Papaveroline was developed in Italy. It was shown that this compound produced a dose-related inhibition of the aggregation of platelets. This compound is also studied in mental disorders caused by a deficit of non-focalized cerebral circulation. However, information about the further development of papaveroline is not available.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Cerebral ischemic vasculopathy: clinical and thermographic study in patients treated with papaveroline]. | 1981-07-31 |
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| [Papaveroline in mental disorders caused by a deficit of non-focalized cerebral circulation]. | 1981-01-15 |
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| [Some effects of papaveroline on blood circulation in patients with arteriosclerosis]. | 1974-05 |
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| [Action of N-methylglucamine, papaveroline and their association on spontaneous motility of isolated arteries]. | 1969-12 |
|
| [Study of the hemodynamic changes induced with a new drug: papaveroline]. | 1967 |
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NCI_THESAURUS |
C29707
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ACTIVE MOIETY