U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of PAPAVEROLINE

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

HIDE SMILES / InChI

Molecular Formula C16H13NO4
Molecular Weight 283.2787
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

PubMed

TitleDatePubMed
[Cerebral ischemic vasculopathy: clinical and thermographic study in patients treated with papaveroline].
1981-07-31
[Papaveroline in mental disorders caused by a deficit of non-focalized cerebral circulation].
1981-01-15
[Some effects of papaveroline on blood circulation in patients with arteriosclerosis].
1974-05
[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
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:20:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:20:28 GMT 2025
Record UNII
A0CR5J8X17
Record Status Validated (UNII)
Record Version
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Name Type Language
PAPAVEROLINE
INN   MART.   WHO-DD  
INN  
Official Name English
PAPAVEROLINE [MART.]
Preferred Name English
papaveroline [INN]
Common Name English
Papaveroline [WHO-DD]
Common Name English
1-(3,4-DIHYDROXYBENZYL)-6,7-ISOQUINOLINEDIOL
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
Code System Code Type Description
EVMPD
SUB09610MIG
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-374-1
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
NCI_THESAURUS
C66306
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
MESH
C011054
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID50972889
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
DRUG CENTRAL
2057
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
ChEMBL
CHEMBL351585
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
INN
3408
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
SMS_ID
100000082789
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
CAS
574-77-6
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
PUBCHEM
5459346
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
FDA UNII
A0CR5J8X17
Created by admin on Mon Mar 31 18:20:28 GMT 2025 , Edited by admin on Mon Mar 31 18:20:28 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY