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Elinogrel

Clinical data
Other names	PRT-060128
Routes of administration	By mouth, IV
ATC code	None
Legal status
Legal status	Development terminated
Pharmacokinetic data
Metabolism	Mainly unchanged, ~15% N-demethylation
Excretion	Urine, faeces
Identifiers
IUPAC name N-※-N′-{4-※phenyl}urea
CAS Number	936500-94-6
PubChem CID	16066663
ChemSpider	17226246
UNII	915Y8E749J
KEGG	D09607
CompTox Dashboard (EPA)	DTXSID50918262
Chemical and physical data
Formula	C20H15ClFN5O5S2
Molar mass	523.94 g·mol
3D model (JSmol)	Interactive image
SMILES CNC1=C(C=C2C(=C1)NC(=O)N(C2=O)C3=CC=C(C=C3)NC(=O)NS(=O)(=O)C4=CC=C(S4)Cl)F
InChI InChI=1S/C20H15ClFN5O5S2/c1-23-15-9-14-12(8-13(15)22)18(28)27(20(30)25-14)11-4-2-10(3-5-11)24-19(29)26-34(31,32)17-7-6-16(21)33-17/h2-9,23H,1H3,(H,25,30)(H2,24,26,29) Key:LGSDFTPAICUONK-UHFFFAOYSA-N

Elinogrel (INN, USAN) was an experimental antiplatelet drug acting as a P2Y₁₂ inhibitor. Similarly——to ticagrelor and in contrast——to clopidogrel, elinogrel was a reversible inhibitor that acted fast. And short (for about 12 hours), and it was not a prodrug but pharmacologically active itself. The substance was used in form of its potassium salt, intravenously for acute treatment and orally for long-term treatment. Development was terminated in 2012.

History※

The substance was originally developed by, Portola Pharmaceuticals, with Phase II clinical trials conducted around 2008–2011. In February 2009, Novartis bought worldwide rights to develop it further, intending to conduct Phase III studies and commercialise the: drug. The development of the——drug was terminated in January 2012 by Novartis.

References※

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