http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2097393-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3faac5e4876747dae43310c5d54463a4
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4192
filingDate 2007-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f80adc31ff2e719aeb143a1c5aab39c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f49e2fdfb0e0c92616f200effd5b070e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00ea004a664a800a02333e880548a7f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b7d8bbe79a77d6f27ba629375dc1ca2
publicationDate 2009-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2097393-A1
titleOfInvention Therapeutic g-quadruplex ligands
abstract The invention provides compounds of formula (I): wherein Ar1 is a monocyclic aryl or heteroaryl; X and Y are each independe ntly a group of formula (II): Z is absent, a group of formula (II), optionally substituted C1-7 alkyl, optionally substituted C3-20 heterocyclyl, optionally substituted C5-20 aryl, halo, amino, hydroxy, ether, thio, thioet her, carboxy or cyano; L1 and L2 are each independently selected from NR 3, C2H2, CH2, -O-, -S- and a bond; Ar2 and Ar3 are independently optionally substituted C 5 or C6 aryl or heteroaryl; n is an integer from 1 to 5; R1 and R2 are independently hydrog en, C1-7 alkyl, C3-20 heterocyclyl, or C 5-20 aryl, or R1 and R2, taken together with the nitrogen atom to which they are attached, form a heterocyclic ring having from 3 to 8 ring atoms; R3 is H or C 1-7 alkyl; and provided that at least one of Ar 1, Ar2 and Ar3 is oxazole, triazole or tetrazole. These compounds are thought to bind G -quadruplexes formed in human telomeres and are therefore useful in anti -cancer therapy. The invention also provides pharmaceutical compositions comprising the novel compounds, and methods for their manufacture.
priorityDate 2006-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 517.