JP2016537388A5 - - Google Patents
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- JP2016537388A5 JP2016537388A5 JP2016533529A JP2016533529A JP2016537388A5 JP 2016537388 A5 JP2016537388 A5 JP 2016537388A5 JP 2016533529 A JP2016533529 A JP 2016533529A JP 2016533529 A JP2016533529 A JP 2016533529A JP 2016537388 A5 JP2016537388 A5 JP 2016537388A5
- Authority
- JP
- Japan
- Prior art keywords
- dioxo
- pyrido
- imidazo
- indole
- pharmaceutically acceptable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 150000001875 compounds Chemical class 0.000 claims 26
- 150000003839 salts Chemical class 0.000 claims 21
- 239000012453 solvate Substances 0.000 claims 21
- -1 3,5-dichlorophenyl Chemical group 0.000 claims 13
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 11
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 235000019260 propionic acid Nutrition 0.000 claims 7
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 125000005345 deuteroalkyl group Chemical group 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 claims 3
- FARUMNUOOCOIFR-UHFFFAOYSA-N 3-[8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]propanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)CC2N(C3)C(N(C2=O)CCC(=O)O)=O)C=C1 FARUMNUOOCOIFR-UHFFFAOYSA-N 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000006716 (C1-C6) heteroalkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- AILJKGFWQVGMIU-IBGZPJMESA-N 1-[[(15S)-8-[(6-methoxypyridin-3-yl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]methyl]cyclopropane-1-carboxylic acid Chemical compound COC1=CC=C(C=N1)CN1C2=C(C=3C=CC=CC1=3)C[C@@H]1N(C2)C(N(C1=O)CC1(CC1)C(=O)O)=O AILJKGFWQVGMIU-IBGZPJMESA-N 0.000 claims 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
- 125000006507 2,4-difluorobenzyl group Chemical group [H]C1=C(F)C([H])=C(F)C(=C1[H])C([H])([H])* 0.000 claims 1
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims 1
- YLYVSXXLTPESAN-UHFFFAOYSA-N 2-[8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]acetic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)CC2N(C3)C(N(C2=O)CC(=O)O)=O)C=C1 YLYVSXXLTPESAN-UHFFFAOYSA-N 0.000 claims 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims 1
- ZLHOPMRBMUIHIW-FQEVSTJZSA-N 3-[(15S)-8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]-2,2-dimethylpropanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C[C@@H]2N(C3)C(N(C2=O)CC(C(=O)O)(C)C)=O)C=C1 ZLHOPMRBMUIHIW-FQEVSTJZSA-N 0.000 claims 1
- XJYAVHBLBATKGO-FQEVSTJZSA-N 3-[(15S)-8-[(4-methoxyphenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]propanoic acid Chemical compound COC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C[C@@H]2N(C3)C(N(C2=O)CCC(=O)O)=O)C=C1 XJYAVHBLBATKGO-FQEVSTJZSA-N 0.000 claims 1
- UQBQGMVQMFLLNZ-KRWDZBQOSA-N 3-[(15S)-8-[(6-chloropyridin-3-yl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]propanoic acid Chemical compound ClC1=CC=C(C=N1)CN1C2=C(C=3C=CC=CC1=3)C[C@@H]1N(C2)C(N(C1=O)CCC(=O)O)=O UQBQGMVQMFLLNZ-KRWDZBQOSA-N 0.000 claims 1
- PYWWVCQEMKEUMW-KRWDZBQOSA-N 3-[(15S)-8-[(6-fluoropyridin-3-yl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]propanoic acid Chemical compound FC1=CC=C(C=N1)CN1C2=C(C=3C=CC=CC1=3)C[C@@H]1N(C2)C(N(C1=O)CCC(=O)O)=O PYWWVCQEMKEUMW-KRWDZBQOSA-N 0.000 claims 1
- OOBJTDBLYKSTAP-SFHVURJKSA-N 3-[(15S)-8-[(6-methoxypyridin-3-yl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]propanoic acid Chemical compound COC1=CC=C(C=N1)CN1C2=C(C=3C=CC=CC1=3)C[C@@H]1N(C2)C(N(C1=O)CCC(=O)O)=O OOBJTDBLYKSTAP-SFHVURJKSA-N 0.000 claims 1
- PVDVSFPLRHGBMD-UHFFFAOYSA-N 3-[8-[(4-fluorophenyl)methyl]-16,16-dimethyl-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]propanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C(C2N(C3)C(N(C2=O)CCC(=O)O)=O)(C)C)C=C1 PVDVSFPLRHGBMD-UHFFFAOYSA-N 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 1
- WZUKMQBZMZEAJU-HXUWFJFHSA-N 4-[(15R)-8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]butanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C[C@H]2N(C3)C(N(C2=O)CCCC(=O)O)=O)C=C1 WZUKMQBZMZEAJU-HXUWFJFHSA-N 0.000 claims 1
- JKLILFULYSLIJL-FQEVSTJZSA-N 4-[(15S)-5-chloro-8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2(7),3,5-tetraen-13-yl]butanoic acid Chemical compound ClC=1C=CC=2C3=C(N(C=2C=1)CC1=CC=C(C=C1)F)CN1[C@@H](C3)C(N(C1=O)CCCC(=O)O)=O JKLILFULYSLIJL-FQEVSTJZSA-N 0.000 claims 1
- ZSSCPNTVNYYVNQ-NRFANRHFSA-N 4-[(15S)-8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]-2,2-dimethylbutanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C[C@@H]2N(C3)C(N(C2=O)CCC(C(=O)O)(C)C)=O)C=C1 ZSSCPNTVNYYVNQ-NRFANRHFSA-N 0.000 claims 1
- GWCXAEUGQVRSLM-NRFANRHFSA-N 4-[(15S)-8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]-3,3-dimethylbutanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C[C@@H]2N(C3)C(N(C2=O)CC(CC(=O)O)(C)C)=O)C=C1 GWCXAEUGQVRSLM-NRFANRHFSA-N 0.000 claims 1
- WZUKMQBZMZEAJU-FQEVSTJZSA-N 4-[(15S)-8-[(4-fluorophenyl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]butanoic acid Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)C[C@@H]2N(C3)C(N(C2=O)CCCC(=O)O)=O)C=C1 WZUKMQBZMZEAJU-FQEVSTJZSA-N 0.000 claims 1
- IEZLOKTWFZIIDZ-IBGZPJMESA-N 4-[(15S)-8-[(6-methoxypyridin-3-yl)methyl]-12,14-dioxo-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]butanoic acid Chemical compound COC1=CC=C(C=N1)CN1C2=C(C=3C=CC=CC1=3)C[C@@H]1N(C2)C(N(C1=O)CCCC(=O)O)=O IEZLOKTWFZIIDZ-IBGZPJMESA-N 0.000 claims 1
- PFZOARDENKNXPK-UHFFFAOYSA-N 4-[12,14-dioxo-8-(3-phenylpropyl)-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraen-13-yl]butanoic acid Chemical compound O=C1N(C(N2CC=3N(C=4C=CC=CC=4C=3CC21)CCCC1=CC=CC=C1)=O)CCCC(=O)O PFZOARDENKNXPK-UHFFFAOYSA-N 0.000 claims 1
- WZUKMQBZMZEAJU-UHFFFAOYSA-N 4-[9-(4-fluorobenzyl)-1,3-diketo-4,10-dihydro-3ah-imidazo[1,5-b]$b-carbolin-2-yl]butyric acid Chemical compound C1N2C(=O)N(CCCC(=O)O)C(=O)C2CC(C2=CC=CC=C22)=C1N2CC1=CC=C(F)C=C1 WZUKMQBZMZEAJU-UHFFFAOYSA-N 0.000 claims 1
- UJCIHJDXVNITQQ-UHFFFAOYSA-N 8-[(4-fluorophenyl)methyl]-13-(2-hydroxyethyl)-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraene-12,14-dione Chemical compound FC1=CC=C(CN2C3=C(C=4C=CC=CC2=4)CC2N(C3)C(N(C2=O)CCO)=O)C=C1 UJCIHJDXVNITQQ-UHFFFAOYSA-N 0.000 claims 1
- BSTKPKFHNBHEGA-UHFFFAOYSA-N 8-[(4-fluorophenyl)methyl]-13-(2H-tetrazol-5-ylmethyl)-8,11,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(9),2,4,6-tetraene-12,14-dione Chemical compound N=1NN=NC=1CN1C(N2CC=3N(C=4C=CC=CC=4C=3CC2C1=O)CC1=CC=C(C=C1)F)=O BSTKPKFHNBHEGA-UHFFFAOYSA-N 0.000 claims 1
- 206010016654 Fibrosis Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims 1
- 230000004761 fibrosis Effects 0.000 claims 1
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims 1
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000004306 triazinyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361907947P | 2013-11-22 | 2013-11-22 | |
| US61/907,947 | 2013-11-22 | ||
| US201462038093P | 2014-08-15 | 2014-08-15 | |
| US62/038,093 | 2014-08-15 | ||
| PCT/US2014/066705 WO2015077502A1 (en) | 2013-11-22 | 2014-11-20 | Tetracyclic autotaxin inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016537388A JP2016537388A (ja) | 2016-12-01 |
| JP2016537388A5 true JP2016537388A5 (OSRAM) | 2017-12-28 |
Family
ID=53180151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016533529A Pending JP2016537388A (ja) | 2013-11-22 | 2014-11-20 | 四環系のオートタキシン阻害剤 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US9926318B2 (OSRAM) |
| EP (1) | EP3071569A4 (OSRAM) |
| JP (1) | JP2016537388A (OSRAM) |
| KR (1) | KR20160088878A (OSRAM) |
| CN (1) | CN105764903B (OSRAM) |
| AU (1) | AU2014352887A1 (OSRAM) |
| BR (1) | BR112016010221A2 (OSRAM) |
| CA (1) | CA2930735A1 (OSRAM) |
| CL (1) | CL2016001232A1 (OSRAM) |
| CR (1) | CR20160290A (OSRAM) |
| EA (1) | EA201690880A1 (OSRAM) |
| IL (1) | IL245389A0 (OSRAM) |
| MX (1) | MX2016006688A (OSRAM) |
| NI (1) | NI201600070A (OSRAM) |
| PE (1) | PE20160902A1 (OSRAM) |
| PH (1) | PH12016500863A1 (OSRAM) |
| WO (1) | WO2015077502A1 (OSRAM) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3046909A4 (en) | 2013-09-17 | 2017-03-29 | Pharmakea, Inc. | Heterocyclic vinyl autotaxin inhibitor compounds |
| US9714240B2 (en) | 2013-09-17 | 2017-07-25 | Pharmakea, Inc. | Vinyl autotaxin inhibitor compounds |
| JP2016531874A (ja) | 2013-09-26 | 2016-10-13 | ファーマケア,インク. | オートタキシン阻害剤化合物 |
| CA2930737C (en) | 2013-11-22 | 2023-02-21 | Pharmakea, Inc. | Autotaxin inhibitor compounds |
| EA201690880A1 (ru) | 2013-11-22 | 2016-12-30 | Фармакеа, Инк. | Тетрациклические ингибиторы аутотаксина |
| SG10201911204WA (en) | 2015-05-27 | 2020-02-27 | Pharmakea Inc | Autotaxin inhibitors and uses thereof |
| ES2782113T3 (es) * | 2015-07-11 | 2020-09-10 | Advenchen Pharmaceuticals Llc | Compuestos de quinolina fusionados como inhibidores de PI3K/mTor |
| CN105021735B (zh) * | 2015-07-21 | 2017-09-19 | 中国科学院西北高原生物研究所 | 白刺种子或其提取物中ss和rsMTCA的检测方法 |
| US20250002505A1 (en) * | 2021-10-05 | 2025-01-02 | Turning Point Therapeutics, Inc. | Synthesis of macroyclic compounds |
| CN119591596B (zh) * | 2024-12-04 | 2025-10-17 | 沈阳药科大学 | 4,5-二氢-3H-吡咯并[2,3-c]喹啉-4-酮衍生物及其应用 |
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| ATE332903T1 (de) | 2000-10-03 | 2006-08-15 | Lilly Icos Llc | Kondensierte pyridoindolderivate |
| US20060270634A1 (en) | 2005-05-06 | 2006-11-30 | Miller Duane D | Acetal phosphate-derived LPA mimics, PPARgamma activators, and autotaxin inhibitors |
| DE102007047737A1 (de) | 2007-10-05 | 2009-04-30 | Merck Patent Gmbh | Piperidin- und Piperazinderivate |
| US8268891B1 (en) | 2007-11-13 | 2012-09-18 | University Of Memphis Research Foundation | Autotaxin inhibitors |
| US8378100B2 (en) | 2008-01-09 | 2013-02-19 | University Of Virginia Patent Foundation | Phosphonate derivatives as autotaxin inhibitors |
| WO2009151644A2 (en) | 2008-06-13 | 2009-12-17 | Yale University | Small molecule inhibitors of autotaxin methods of use |
| US8022239B2 (en) | 2008-10-03 | 2011-09-20 | The University Of Memphis Research Foundation | Mechanism-based inactivators of autotaxin |
| DE102008059578A1 (de) | 2008-11-28 | 2010-06-10 | Merck Patent Gmbh | Benzo-Naphtyridin Verbindungen |
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| DE102009033392A1 (de) | 2009-07-16 | 2011-01-20 | Merck Patent Gmbh | Heterocyclische Verbindungen als Autotaxin-Inhibitoren II |
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| HK1212348A1 (en) | 2012-12-19 | 2016-06-10 | Novartis Ag | Autotaxin inhibitors |
| US9409895B2 (en) | 2012-12-19 | 2016-08-09 | Novartis Ag | Autotaxin inhibitors |
| US9714240B2 (en) | 2013-09-17 | 2017-07-25 | Pharmakea, Inc. | Vinyl autotaxin inhibitor compounds |
| EP3046909A4 (en) | 2013-09-17 | 2017-03-29 | Pharmakea, Inc. | Heterocyclic vinyl autotaxin inhibitor compounds |
| JP2016531874A (ja) | 2013-09-26 | 2016-10-13 | ファーマケア,インク. | オートタキシン阻害剤化合物 |
| EA201690880A1 (ru) | 2013-11-22 | 2016-12-30 | Фармакеа, Инк. | Тетрациклические ингибиторы аутотаксина |
| CA2930737C (en) | 2013-11-22 | 2023-02-21 | Pharmakea, Inc. | Autotaxin inhibitor compounds |
| US9051320B1 (en) | 2014-08-18 | 2015-06-09 | Pharmakea, Inc. | Methods for the treatment of metabolic disorders by a selective small molecule autotaxin inhibitor |
-
2014
- 2014-11-20 EA EA201690880A patent/EA201690880A1/ru unknown
- 2014-11-20 WO PCT/US2014/066705 patent/WO2015077502A1/en not_active Ceased
- 2014-11-20 US US15/036,370 patent/US9926318B2/en active Active
- 2014-11-20 AU AU2014352887A patent/AU2014352887A1/en not_active Abandoned
- 2014-11-20 CN CN201480063882.4A patent/CN105764903B/zh not_active Expired - Fee Related
- 2014-11-20 CA CA2930735A patent/CA2930735A1/en not_active Abandoned
- 2014-11-20 JP JP2016533529A patent/JP2016537388A/ja active Pending
- 2014-11-20 CR CR20160290A patent/CR20160290A/es unknown
- 2014-11-20 PE PE2016000667A patent/PE20160902A1/es not_active Application Discontinuation
- 2014-11-20 KR KR1020167014492A patent/KR20160088878A/ko not_active Ceased
- 2014-11-20 MX MX2016006688A patent/MX2016006688A/es unknown
- 2014-11-20 BR BR112016010221A patent/BR112016010221A2/pt not_active Application Discontinuation
- 2014-11-20 EP EP14863158.3A patent/EP3071569A4/en not_active Withdrawn
-
2016
- 2016-05-02 IL IL245389A patent/IL245389A0/en unknown
- 2016-05-10 PH PH12016500863A patent/PH12016500863A1/en unknown
- 2016-05-20 NI NI201600070A patent/NI201600070A/es unknown
- 2016-05-20 CL CL2016001232A patent/CL2016001232A1/es unknown
-
2018
- 2018-02-08 US US15/892,142 patent/US20180162859A1/en not_active Abandoned
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