CHEBI:142290 - anagrelide

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ChEBI Name anagrelide
ChEBI ID CHEBI:142290
Definition A 1,5-dihydroimidazo[2,1-]quinazoline having an oxo substituent at the 2-position and chloro substituents at the 6- and 7-positions.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H7Cl2N3O
Net Charge 0
Average Mass 256.08800
Monoisotopic Mass 254.99662
InChI InChI=1S/C10H7Cl2N3O/c11-6-1-2-7-5(9(6)12)3-15-4-8(16)14-10(15)13-7/h1-2H,3-4H2,(H,13,14,16)
InChIKey OTBXOEAOVRKTNQ-UHFFFAOYSA-N
SMILES Clc1ccc2N=C3NC(=O)CN3Cc2c1Cl
Roles Classification
Application(s): anticoagulant
An agent that prevents blood clotting.
platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
antifibrinolytic drug
A drug that prevent fibrinolysis or lysis of a blood clot or thrombus.
cardiovascular drug
A drug that affects the rate or intensity of cardiac contraction, blood vessel diameter or blood volume.
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ChEBI Ontology
Outgoing anagrelide (CHEBI:142290) has role anticoagulant (CHEBI:50249)
anagrelide (CHEBI:142290) has role antifibrinolytic drug (CHEBI:48675)
anagrelide (CHEBI:142290) has role cardiovascular drug (CHEBI:35554)
anagrelide (CHEBI:142290) has role platelet aggregation inhibitor (CHEBI:50427)
anagrelide (CHEBI:142290) is a imidazoquinazoline (CHEBI:47975)
Incoming anagrelide hydrochloride (CHEBI:55345) has part anagrelide (CHEBI:142290)
IUPAC Name
6,7-dichloro-1,5-dihydroimidazo[2,1-]quinazolin-2(3H)-one
INNs Sources
anagrelida ChemIDplus
anagrelide ChemIDplus
anagrelidum ChemIDplus
Manual Xrefs Databases
209 DrugCentral
Anagrelide Wikipedia
D07455 KEGG DRUG
DB00261 DrugBank
LSM-3380 LINCS
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Registry Numbers Types Sources
619582 Beilstein Registry Number Beilstein
68475-42-3 CAS Registry Number DrugBank
68475-42-3 CAS Registry Number ChemIDplus
68475-42-3 CAS Registry Number KEGG DRUG
Last Modified
22 February 2017