CHEBI:73282 - DPCPX

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ChEBI Name DPCPX
ChEBI ID CHEBI:73282
Definition An oxopurine that is 7H-xanthine substituted at positions 1 and 3 by propyl groups and at position 8 by a cyclohexyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Margaret Duesbury
Supplier Information ChemicalBook:CB8327518, eMolecules:501674, ZINC000000900692
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2,6-Xylidine is an organic compound with the formula C6H3(CH3)2NH2. It is one of several isomeric xylidines. It is a colorless viscous liquid. Commercially significant derivatives are the anesthetics lidocaine, bupivacaine, mepivacaine, and etidocaine.
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Formula C16H24N4O2
Net Charge 0
Average Mass 304.38740
Monoisotopic Mass 304.18993
InChI InChI=1S/C16H24N4O2/c1-3-9-19-14-12(15(21)20(10-4-2)16(19)22)17-13(18-14)11-7-5-6-8-11/h11H,3-10H2,1-2H3,(H,17,18)
InChIKey FFBDFADSZUINTG-UHFFFAOYSA-N
SMILES CCCn1c2nc([nH]c2c(=O)n(CCC)c1=O)C1CCCC1
Roles Classification
Biological Role(s): adenosine A1 receptor antagonist
An antagonist at the A1 receptor.
EC 3.1.4.* (phosphoric diester hydrolase) inhibitor
An EC 3.1.* (ester hydrolase) inhibitor that interferes with the action of a phosphoric diester hydrolase (EC 3.1.4.*).
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ChEBI Ontology
Outgoing DPCPX (CHEBI:73282) has functional parent 7H-xanthine (CHEBI:48517)
DPCPX (CHEBI:73282) has role adenosine A1 receptor antagonist (CHEBI:63957)
DPCPX (CHEBI:73282) has role EC 3.1.4.* (phosphoric diester hydrolase) inhibitor (CHEBI:50218)
DPCPX (CHEBI:73282) is a oxopurine (CHEBI:25810)
IUPAC Name
8-cyclopentyl-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione
Synonyms Sources
1,3-Dipropyl-8-cyclopentylxanthine ChemIDplus
1,3-Dpcpx ChemIDplus
8-Cyclopentyl-1,3-dipropylxanthine KEGG COMPOUND
CPX KEGG COMPOUND
dipropylcyclopentylxanthine ChEBI
PD-116,948 ChemIDplus
PD-116948 ChemIDplus
Manual Xrefs Databases
C13709 KEGG COMPOUND
Dipropylcyclopentylxanthine Wikipedia
LSM-19971 LINCS
US2004259889 Patent
US5470579 Patent
View more database links
Registry Numbers Types Sources
102146-07-6 CAS Registry Number KEGG COMPOUND
102146-07-6 CAS Registry Number ChemIDplus
4298634 Reaxys Registry Number Reaxys
Citation Type Source
23597562 PubMed citation Europe PMC
Last Modified
25 February 2016