http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2392873-A1

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filingDate 2000-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16b948025cd481f28e2d339c4fc6b7ee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b42d607bb933ae094ec614e930b9171b
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27595bd58147f2a512fd9ae8801b36a6
publicationDate 2001-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2392873-A1
titleOfInvention Benzo[a]phenazin-11-carboxamide derivatives and their use as joint inhibitors of topomerase i and ii
abstract A compound which is a benzo[a]phenazine-11-carboxamide derivative of formula (I) wherein each of R1 to R4, which are the same or different, is selected from hydrogen, halogen, hydroxyl, C1-C6 alkoxy which is unsubstituted or substituted, heteroaryloxy, C1-C6 alkyl which is unsubstituted or substitute d, nitro, cyano, azido, amidoxime, CO2R10, CON(R12)2, OCON(R12), SR10, SOR11, SO2(R11), SO2N(R12)2, N(R12)2, NR10SO2R11, N(SO2R11)2NR10(CH2)nCN, NR10COR11 , OCOR11 or COR10; each of R5 to R7, which are the same or different, is selected from hydrogen, halogen, hydroxy, C1-C6 alkoxy, C1-C6 alkyl, SR10 an d N(R12)2; Q is C1-C6 alkylene which is unsubstituted or substituted by (i) C1 - C6 alkyl which is unsubstituted or substituted, (ii) hydroxy, provided that the hydroxy group is not .alpha. to either of the N atoms adjacent to Q in formula (I), (iii) CO2R10, or (iv) CON(R12); R8 and R9, which are the same o r different, are each hydrogen or C1-C6 alkyl, or R8 and R9 together with the nitrogen atom to which they are attached form a saturated 5- or 6-membered N - containing heterocyclic ring which may include one additional heteroatom selected from O, N and S, or one of R8 and R9 is an alkylene chain optionall y interrupted by O, N or S, which is attached to a carbon atom on the alkylene chain representedby Q to complete a saturated 5- or 6-membered N-containing heterocyclic ring as defined above; or a pharmaceutically acceptable salt thereof; with the proviso that at least one R1 to R4 is other than hydrogen. These compounds are inhibitors of topoisomerase I and/or topoisomerase II an d can be used to treat tumours, including tumours which express MDR.
priorityDate 1999-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10136807
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP20109
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11534
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21412
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8022
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10135495
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422025924
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID60505
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422367621
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID171040
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424468363
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11446470
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451290595
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422352530
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457444288
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424429440
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422025922
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450863681
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10270443
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422352531
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID103802
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558386
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426688023
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Total number of triples: 675.