AR068048A1 - Combinacion de agente antimitotico e inhibidor de aurora quinasa como tratamiento anticancerigeno - Google Patents
Combinacion de agente antimitotico e inhibidor de aurora quinasa como tratamiento anticancerigenoInfo
- Publication number
- AR068048A1 AR068048A1 ARP080103276A ARP080103276A AR068048A1 AR 068048 A1 AR068048 A1 AR 068048A1 AR P080103276 A ARP080103276 A AR P080103276A AR P080103276 A ARP080103276 A AR P080103276A AR 068048 A1 AR068048 A1 AR 068048A1
- Authority
- AR
- Argentina
- Prior art keywords
- nr4c
- nr4r5
- alkyl
- nr4or7
- heterocyclyl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 239000003080 antimitotic agent Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 23
- 125000003118 aryl group Chemical group 0.000 abstract 20
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 20
- 125000000623 heterocyclic group Chemical group 0.000 abstract 20
- 125000001072 heteroaryl group Chemical group 0.000 abstract 19
- 125000005843 halogen group Chemical group 0.000 abstract 11
- 229910052757 nitrogen Inorganic materials 0.000 abstract 11
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 10
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 10
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 10
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 10
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 229910052799 carbon Inorganic materials 0.000 abstract 8
- 125000004475 heteroaralkyl group Chemical group 0.000 abstract 8
- 229910052717 sulfur Inorganic materials 0.000 abstract 7
- -1 - (CR10R11) 0-4NR4R5 Chemical group 0.000 abstract 6
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 6
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000005103 alkyl silyl group Chemical group 0.000 abstract 4
- 150000001721 carbon Chemical group 0.000 abstract 4
- 125000005842 heteroatom Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- LOBCDGHHHHGHFA-LBPRGKRZSA-N (S)-monastrol Chemical compound CCOC(=O)C1=C(C)NC(=S)N[C@H]1C1=CC=CC(O)=C1 LOBCDGHHHHGHFA-LBPRGKRZSA-N 0.000 abstract 1
- 108010012934 Albumin-Bound Paclitaxel Proteins 0.000 abstract 1
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 1
- QJZRFPJCWMNVAV-HHHXNRCGSA-N N-(3-aminopropyl)-N-[(1R)-1-[7-chloro-4-oxo-3-(phenylmethyl)-2-quinazolinyl]-2-methylpropyl]-4-methylbenzamide Chemical compound NCCCN([C@H](C(C)C)C=1N(C(=O)C2=CC=C(Cl)C=C2N=1)CC=1C=CC=CC=1)C(=O)C1=CC=C(C)C=C1 QJZRFPJCWMNVAV-HHHXNRCGSA-N 0.000 abstract 1
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 229930012538 Paclitaxel Natural products 0.000 abstract 1
- 229940123237 Taxane Drugs 0.000 abstract 1
- 229940028652 abraxane Drugs 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 229940121375 antifungal agent Drugs 0.000 abstract 1
- 239000003429 antifungal agent Substances 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 229960003668 docetaxel Drugs 0.000 abstract 1
- 229930013356 epothilone Natural products 0.000 abstract 1
- 150000003883 epothilone derivatives Chemical class 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 229950007344 ispinesib Drugs 0.000 abstract 1
- 229960001592 paclitaxel Drugs 0.000 abstract 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- DKPFODGZWDEEBT-QFIAKTPHSA-N taxane Chemical class C([C@]1(C)CCC[C@@H](C)[C@H]1C1)C[C@H]2[C@H](C)CC[C@@H]1C2(C)C DKPFODGZWDEEBT-QFIAKTPHSA-N 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Reivindicacion 1: Una composicion farmacéutica para tratar o mejorar cáncer, que comprende en combinacion (a) al menos un agente antimicotico seleccionado del grupo que consiste en un taxano, paclitaxel, docetaxel, un inhibidor de Cenp-E, abraxano, epotilona, monastrol, un inhibidor de KSP, ispinesib y un compuesto de las formulas (A) - (D) mostradas en los puntos a) - d) que figuran más abajo: a) Un compuesto representado por la formula estructural (A) o una de sus sales, solvatos o ésteres farmacéuticamente aceptables, en donde el anillo Y es un arilo de 5 o 6 miembros o un heteroarilo de 5 o 6 miembros fusionado tal como se indica en la formula (A), en donde en dichos arilo y heteroarilo cada carbono del anillo sustituible está sustituido, de modo independiente, con R2 y cada nitrogeno del anillo sustituible está sustituido, de modo independiente, con R6; W es N o C(R12); X es N o N-oxido; Z es S, S(=O) o S(=O)2; R1 es H, alquilo, alcoxi, hidroxi, halo, -CN, -S(O)m-alquilo, -C(O)NR9R10, -(CR9R10)1-6OH o -NR4(CR9R10)1-2OR9; cada R2 está seleccionado, de modo independiente, del grupo que consiste en H, halo, alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo, heteroaralquilo, -(CR10R11)0-6-OR7, -C(O)R4, -C(S)R4, -C(O)OR7, -C(S)OR7, -OC(O)R7, -OC(S)R7, -C(O)NR4R5, -C(S)NR4R5, -C(O)NR4OR7, -C(S)NR4OR7, -C(O)NR7NR4R5, -C(S)NR7NR4R5, -C(S)NR4OR7, -C(O)SR7, -NR4R5, -NR4C(O)R5, -NR4C(S)R5, -NR4C(O)OR7, -NR4C(S)OR7, -OC(O)NR4R5, -OC(S)NR4R5, -NR4C(O)NR4R5, -NR4C(S)NR4R5, -NR4C(O)NR4OR7, -NR4C(S)NR4OR7, -(CR10R11)0-6SR7, -SO2R7, -S(O)1-2NR4R5, -N(R7)SO2R7, -S(O)1-2NR5OR7, -CN, -OCF3, -SCF3, -C(=NR7)NR4, -C(O)NR7(CH2)1-10NR4R5, -C(O)NR7(CH2)1-10OR7, -C(S)NR7(CH2)1-10NR4R5, -C(S)NR7(CH2)1-10OR7, haloalquilo y alquilsililo, en donde cada uno de dichos alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo o heteroarilalquilo está opcionalmente sustituido, de modo independiente, con 1-5 restos R9; cada R3 está seleccionado, de modo independiente, del grupo que consiste en H, halo, alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo, heteroaralquilo, -(CR10R11)0-6-OR7, -C(O)R4, -C(S)R4, -C(O)OR7, -C(S)OR7, -OC(O)R7, -OC(S)R7, -C(O)NR4R5, -C(S)NR4R5, -C(O)NR4OR7, -C(S)NR4OR7, -C(O)NR7NR4R5, -C(S)NR7NR4R5, -C(S)NR4OR7, -C(O)SR7, -NR4R5, -NR4C(O)R5, -NR4C(S)R5, -NR4C(O)OR7, -NR4C(S)OR7, -OC(O)NR4R5, -OC(S)NR4R5, -NR4C(O)NR4R5, -NR4C(S)NR4R5, -NR4C(O)NR4OR7, -NR4C(S)NR4OR7, -(CR10R11)0-6SR7, SO2R7, -S(O)1-2NR4R5, -N(R7)SO2R7, -S(O)1-2NR5OR7, -CN, -OCF3, -SCF3, -C(=NR7)NR4R5, -C(O)NR7(CH2)1-10NR4R5, -C(O)NR7(CH2)1-10OR7, -C(S)NR7(CH2)1-10NR4R5, -C(S)NR7(CH2)1-10OR7, haloalquilo y alquilsililo, en donde cada uno de dichos alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo o heteroaralquilo está opcionalmente sustituido, de modo independiente, con 1-5 restos R9; cada R4 y R5 está seleccionado, de modo independiente, del grupo que consiste en H, alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo, heteroaralquilo, -OR7, -C(O)R7 y -C(O)OR7, en donde cada uno de dichos alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo o heteroaralquilo está opcionalmente sustituido con 1-4 restos R8; o R4 y R5, cuando están unidos al mismo átomo de nitrogeno, se toman opcionalmente juntos con el átomo de nitrogeno al que están unidos para formar un anillo heterocíclico de 3-6 miembros que tiene 0-2 heteroátomos adicionales seleccionados de N, O o S; cada R6 está seleccionado, de modo independiente, del grupo que consiste en H, alquilo, arilo, aralquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, heteroarilo, heteroaralquilo, -(CH2)1-6CF3, -C(O)R7, -C(O)OR7 y -SO2R7; cada R7 está seleccionado, de modo independiente, del grupo que consiste en H, alquilo, arilo, aralquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, heteroarilo y heteroaralquilo, en donde cada miembro de R7 excepto H está opcionalmente sustituido con 1-4 restos R8; cada R8 está seleccionado, de modo independiente, del grupo que consiste en halo, alquilo, cicloalquilo, heterociclilo, arilo, heteroarilo, -NO2, -OR10, -(alquil C1-6)-OR10, -CN, -NR10R11, -C(O)R10, -C(O)OR10, -C(O)NR10R11, -CF3, -OCF3, -CF2CF3, -C(=NOH)R10, -N(R10)C(O)R11, -C(=NR10)NR10R11 y -NR10C(O)OR11, en donde cada uno de dichos alquilo, cicloalquilo, heterociclilo, arilo y heteroarilo está opcionalmente sustituido, de modo independiente, con 1-3 restos seleccionados del grupo que consiste en halo, alquilo, cicloalquilo, heterociclilo, arilo, heteroarilo, -NO2, -OR10, -(alquil C1-6)-OR10, -CN, -NR10R11, -C(O)OR10, -C(O)NR10R11, -CF3, -OCF3, -NR10C(O)OR11 y -NR10(O)R40; o dos grupos R8, cuando están unidos al mismo átomo de carbono, se toman opcionalmente juntos con el átomo de carbono al que están unidos para formar un grupo C=O o un grupo C=S; cada R9 está seleccionado, de modo independiente, del grupo que consiste en H, alquilo, alcoxi, OH, CN, halo, -(CR10R11)0-4NR4R5, haloalquilo, hidroxialquilo, alcoxialquilo, -C(O)NR4R5, -C(O)OR7, -OC(O)NR4R5, -NR4C(O)R5 y -NR4C(O)NR4R5; cada R10 es, de modo independiente, H o alquilo; o R9 y R10, cuando están unidos al mismo átomo de nitrogeno, se toman opcionalmente juntos con el átomo de nitrogeno al que están unidos para formar un anillo heterocíclico de 3-6 miembros que tiene 0-2 heteroátomos adicionales seleccionados de N, O o S; cada R11 es, de modo independiente, H o alquilo; o R10 y R11 cuando están unidos al mismo átomo de nitrogeno, se toman opcionalmente juntos con el átomo de nitrogeno al que están unidos para formar un anillo heterocíclico de 3-6 miembros que tiene 0-2 heteroátomos adicionales seleccionados de N, O o S; cada R12 está seleccionado, de modo independiente, del grupo que consiste en H, halo, alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo, heteroaralquilo, -(CR10R11)0-6-OR7, -C(O)R4, -C(S)R4, -C(O)OR7, -C(S)OR7, -OC(O)R7, -OC(S)R7, -C(O)NR4R5, -C(S)NR4R5, -C(O)NR4OR7, -C(S)NR4OR7, -C(O)NR7NR4R5, -C(S)NR7NR4R5, -C(S)NR4OR7, -C(O)SR7, -NR4R5, -NR4C(O)R5, -NR4C(S)R5, NR4C(O)OR7, -NR4C(S)OR7, -OC(O)NR4R5, -OC(S)NR4R5, -NR4C(O)NR4R5, -NR4C(S)NR4R5, -NR4C(O)NR4OR7, -NR4C(S)NR4OR7, -(CR10R11)0-6SR7, SO2R7, -S(O)1-2NR4R5, -N(R7)SO2R7, -S(O)1-2NR5OR7, -CN, -OCF3, -SCF3, -C(NR7)NR4, -C(O)NR7(CH2)1-10NR4R5, -C(O)NR7(CH2)1-10OR7, -C(S)NR7(CH2)1-10NR4R5, -C(S)NR7(CH2)1-10OR7, haloalquilo y alquilsililo, en donde cada uno de dichos alquilo, cicloalquilo, cicloalquilalquilo, heterociclilo, heterociclilalquilo, arilo, aralquilo, heteroarilo o heteroarilalquilo está opcionalmente sustituido, de modo independiente, con 1-5 restos R9; y R40 está seleccionado del grupo que consiste en cicloalquilo, heterociclilo, arilo y heteroarilo, en donde cada uno de dichos cicloalquilo, heterociclilo, arilo y heteroarilo está opcionalmente sustituidos, de modo independiente, con 1-3 restos seleccionados, de modo independiente, del grupo que consiste en -CN, -OH, halo, alquilo, haloalquilo, alcoxi y -NR10R11; b) Un compuesto representado por la formula estructural (B) o una de sus sales, solvatos o ésteres farmacéuticamente aceptables, en donde el anillo Y es un anillo de 5 a 7 miembros seleccionado del grupo que consiste en cicloalquilo, cicloalquenilo, heterociclilo o heterociclenilo fusionado tal como se indica en la formula (B), en donde en cada uno de dichos anillos de 5 a 7 miembros, cada carbono del anillo sustituible está sustituido, de modo independiente, con 1-2 restos R2 y cada heteroátomo del anillo sustituible está sustituido, de modo independiente, con R6; W es N o C(R12); X es N o N-oxido; Z es S, S(=O) o S(=O)2; R1 es H, alquilo, alcoxi, hidroxi, halo, -CN, -S(O)m-alquilo, -C(O)NR9R10, -(CR9R10)1-6OH o -NR4(CR9R10)1-2OR9; en donde m es 0 a 2; cada R2 está seleccionado, de modo independiente, del grupo que consiste en H, halo, alquilo, cicloalquilo, alquilsililo, cicloalquenilo, heterociclilo, heterociclenilo, arilo, heteroarilo, -(CR10R11)0-6-OR7, -C(O)R4, -C(S)R4, -C(O)OR7, -C(S)ORT, -OC(O)R7, -OC(S)R7, -C(O)NR4R5, -C(S)NR4R5, -C(O)NR4OR7, -C(S)NR4OR7, -C(O)NR7NR4R5, -C(S)NR7NR4R5, -C(S)NR4OR7, -C(O)SR7, -NR4R5, -NR4C(O)R5, -NR4C(S)R5, -NR4C(O)OR7, -NR4C(S)OR7, -OC(O)NR4R5, -OC(S)NR4R5, -NR4C(O)NR4R5, -NR4C(S)NR4R5, -NR4C(O)NR4OR7, -NR4C(S)NR4OR7, -(CR10R11)0-6SR7, SO2R7, -S(O)1-2NR4R5, -N(R7)SO2R7, -S(O)1-2NR5OR7, -CN, -OCF3, -SCF3, -C(=NR7)NR4, -C(O)NR7(CH2)1-10NR4R5, -C(O)NR7(CH2)1-10OR7, -C(S)NR7(CH2)1-10NR4R5 y -C(S)NR7(CH2)1-10OR7, en donde cada uno de dichos alquilo, cicloalquilo, cicloalquenilo, heterociclilo, heterociclenilo, arilo y heteroarilo está opcionalmente sustituido, de modo independiente, con 1-5 restos R9; o dos grupos R2 en el mismo átomo de carbono se toman opcionalmente juntos con el átomo de carbono al que están unidos para formar un grupo C=O, un grupo C=S o un grupo etilendioxi; R3 está seleccionado, de modo independiente, del grupo que consiste en H, halo, alquilo, cicloalquilo, cicloalquenilo, heterociclilo, heterociclenilo, arilo, heteroarilo, -(CR10R11)0-6-OR7, -C(O)R4, -C(S)R4, -C(O)OR7, -C(S)OR7, -OC(O)R7, -OC(S)R7, -C(O)NR4R5, -C(S)NR4R, -C(O)NR4OR7, -C(S)NR4OR7, -C(O)NR7NR4R5 -C(S)NR7NR4R5, -C(S)NR4OR7, -C(O)SR7, -NR4R5, -NR4C(O)R5, -NR4C(S)R5, -NR4C(O)OR7, -NR4C(S)OR7, -OC(O)NR4R5, -OC(S)NR4R5, -NR4C(O)NR4R5, -NR4C(S)NR4R5, -NR4C(O)NR4OR7, -NR4C(S)NR4OR7, -(CR10R11)0-6SR7, SO2R7, -S(O)1-2NR4R5, -N(R7)SO2R7, -S(O)1-2NR5OR7, -CN, -C(=NR7)NR4R5, -C(O)N(R7)-(CR40R41)1-5-C(=NR7)NR4R5, -C(O)N(R7)(CR40R41)1-5-NR4R5-C(O)N(R7)(CR40R41)1-5-C(O)-NR4R5, -C(O)N(R7)(CR40R41)1-5-OR7, -C(S)NR7(CH2)1-5NR4R5 y -C(S)NR7(CH2)1-5OR7, en donde cada uno de dichos alquilo, cicloalquilo, cicloalquenilo, heter
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| CL2008002224A1 (es) | 2009-07-17 |
| CO6331446A2 (es) | 2011-10-20 |
| EP2182986A2 (en) | 2010-05-12 |
| US20100249030A1 (en) | 2010-09-30 |
| BRPI0814874A2 (pt) | 2019-09-24 |
| TW200911241A (en) | 2009-03-16 |
| MX2010001340A (es) | 2010-06-02 |
| CN101808666A (zh) | 2010-08-18 |
| AU2008282885A1 (en) | 2009-02-05 |
| WO2009017701A3 (en) | 2009-05-07 |
| KR20100042287A (ko) | 2010-04-23 |
| WO2009017701A2 (en) | 2009-02-05 |
| JP2010535201A (ja) | 2010-11-18 |
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