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COVID-19 Ontology
Last uploaded:
February 25, 2021
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Preferred Name | dipyridamole | |
Synonyms |
Dypyridamol Dipyudamine Cleridium 150 dipyridamolum dipyridamole Dipyridamine dipiridamol Cardoxin Curantyl Persantin 2,2',2'',2'''-[(4,8-dipiperidin-1-ylpyrimido[5,4-d]pyrimidine-2,6-diyl)dinitrilo]tetraethanol |
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Definitions |
A pyrimidopyrimidine that is 2,2',2'',2'''-(pyrimido[5,4-d]pyrimidine-2,6-diyldinitrilo)tetraethanol substituted by piperidin-1-yl groups at positions 4 and 8 respectively. A vasodilator agent, it inhibits the formation of blood clots. |
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ID |
http://purl.obolibrary.org/obo/CHEBI_4653 |
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alternative_term |
2,2',2'',2'''-[(4,8-dipiperidin-1-ylpyrimido[5,4-d]pyrimidine-2,6-diyl)dinitrilo]tetraethanol
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charge |
0
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database_cross_reference |
KEGG:D00302 Drug_Central:924 PMID:11709364 Wikipedia:Dipyridamole Reaxys:68373 Patent:US3031450 DrugBank:DB00975 PMID:11098344 LINCS:LSM-3927 Patent:GB807826 CAS:58-32-2 Beilstein:0068373
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definition |
A pyrimidopyrimidine that is 2,2',2'',2'''-(pyrimido[5,4-d]pyrimidine-2,6-diyldinitrilo)tetraethanol substituted by piperidin-1-yl groups at positions 4 and 8 respectively. A vasodilator agent, it inhibits the formation of blood clots.
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formula |
C24H40N8O4
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fromArticle |
true
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has_obo_namespace |
chebi_ontology
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has_related_synonym |
Dypyridamol Dipyudamine Cleridium 150 dipyridamolum dipyridamole Dipyridamine dipiridamol Cardoxin Curantyl Persantin
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id |
CHEBI:4653
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imported from | ||
in_subset | ||
inchi |
InChI=1S/C24H40N8O4/c33-15-11-31(12-16-34)23-26-20-19(21(27-23)29-7-3-1-4-8-29)25-24(32(13-17-35)14-18-36)28-22(20)30-9-5-2-6-10-30/h33-36H,1-18H2
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inchikey |
IZEKFCXSFNUWAM-UHFFFAOYSA-N
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label |
dipyridamole
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mass |
504.62592
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monoisotopicmass |
504.31725
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notation |
CHEBI:4653
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preferred label |
dipyridamole
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prefLabel |
dipyridamole
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see also |
https://www.medrxiv.org/content/10.1101/2020.02.27.20027557v1 |
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smiles |
OCCN(CCO)c1nc(N2CCCCC2)c2nc(nc(N3CCCCC3)c2n1)N(CCO)CCO
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textual definition |
A pyrimidopyrimidine that is 2,2',2'',2'''-(pyrimido[5,4-d]pyrimidine-2,6-diyldinitrilo)tetraethanol substituted by piperidin-1-yl groups at positions 4 and 8 respectively. A vasodilator agent, it inhibits the formation of blood clots.
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subClassOf |
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