JP2012502974A5 - - Google Patents
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- Publication number
- JP2012502974A5 JP2012502974A5 JP2011527431A JP2011527431A JP2012502974A5 JP 2012502974 A5 JP2012502974 A5 JP 2012502974A5 JP 2011527431 A JP2011527431 A JP 2011527431A JP 2011527431 A JP2011527431 A JP 2011527431A JP 2012502974 A5 JP2012502974 A5 JP 2012502974A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- ylmethoxy
- dihydroxy
- biphenyl
- group
- 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.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 31
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 22
- 125000001072 heteroaryl group Chemical group 0.000 claims 20
- 150000001875 compounds Chemical class 0.000 claims 15
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 15
- 150000003839 salts Chemical class 0.000 claims 13
- 125000002947 alkylene group Chemical group 0.000 claims 12
- 125000003118 aryl group Chemical group 0.000 claims 11
- 125000001475 halogen functional group Chemical group 0.000 claims 11
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- -1 -OH Chemical group 0.000 claims 5
- 125000005647 linker group Chemical group 0.000 claims 4
- 125000001960 7 membered carbocyclic group Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- HKHLJBBDUOPRQN-ACJLOTCBSA-N (2s,3r)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]butanamide Chemical compound C1=CC(CO[C@@](C)([C@H](O)C)C(=O)NO)=CC=C1C1=CC=CC=C1 HKHLJBBDUOPRQN-ACJLOTCBSA-N 0.000 claims 1
- SIXFEBVKDCSUST-ICSRJNTNSA-N (2s,3r)-n,3-dihydroxy-2-methyl-3-(1,2-oxazol-5-yl)-2-[(4-phenylphenyl)methoxy]propanamide Chemical compound O([C@@](C)([C@@H](O)C=1ON=CC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 SIXFEBVKDCSUST-ICSRJNTNSA-N 0.000 claims 1
- SYCHQJMHORHPDP-FPOVZHCZSA-N (2s,3s)-3-(furan-2-yl)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]propanamide Chemical compound O([C@@](C)([C@@H](O)C=1OC=CC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 SYCHQJMHORHPDP-FPOVZHCZSA-N 0.000 claims 1
- GSUWLVYTJTWUHP-ICSRJNTNSA-N (2s,3s)-3-cyclopropyl-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]propanamide Chemical compound O([C@@](C)([C@@H](O)C1CC1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 GSUWLVYTJTWUHP-ICSRJNTNSA-N 0.000 claims 1
- JCZKNQBVKSRKGG-WMZOPIPTSA-N (2s,3s)-5,5,5-trifluoro-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]pentanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)CC(F)(F)F)C(=O)NO)=CC=C1C1=CC=CC=C1 JCZKNQBVKSRKGG-WMZOPIPTSA-N 0.000 claims 1
- KXQHQOVKEMSLRA-FPOVZHCZSA-N (2s,3s)-5-ethoxy-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]pentanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)CCOCC)C(=O)NO)=CC=C1C1=CC=CC=C1 KXQHQOVKEMSLRA-FPOVZHCZSA-N 0.000 claims 1
- OEIHVBMZXNURRL-ICSRJNTNSA-N (2s,3s)-n,3-dihydroxy-2,4-dimethyl-2-[(4-phenylphenyl)methoxy]pentanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)C(C)C)C(=O)NO)=CC=C1C1=CC=CC=C1 OEIHVBMZXNURRL-ICSRJNTNSA-N 0.000 claims 1
- JGQMWGGZNFCDEO-UNMCSNQZSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]-3-pyridin-2-ylpropanamide Chemical compound O([C@@](C)([C@@H](O)C=1N=CC=CC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 JGQMWGGZNFCDEO-UNMCSNQZSA-N 0.000 claims 1
- XDHPXTDIDHKVFF-UNMCSNQZSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]-3-pyridin-3-ylpropanamide Chemical compound O([C@@](C)([C@@H](O)C=1C=NC=CC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 XDHPXTDIDHKVFF-UNMCSNQZSA-N 0.000 claims 1
- RKDZGGUXXBBZTR-FPOVZHCZSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]-3-pyrimidin-5-ylpropanamide Chemical compound O([C@@](C)([C@@H](O)C=1C=NC=NC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 RKDZGGUXXBBZTR-FPOVZHCZSA-N 0.000 claims 1
- HKHLJBBDUOPRQN-UGSOOPFHSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]butanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)C)C(=O)NO)=CC=C1C1=CC=CC=C1 HKHLJBBDUOPRQN-UGSOOPFHSA-N 0.000 claims 1
- LPHYIYSLVMHHIT-FPOVZHCZSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]heptanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)CCCC)C(=O)NO)=CC=C1C1=CC=CC=C1 LPHYIYSLVMHHIT-FPOVZHCZSA-N 0.000 claims 1
- UZEYYYATUXVBCZ-ICSRJNTNSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]hexanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)CCC)C(=O)NO)=CC=C1C1=CC=CC=C1 UZEYYYATUXVBCZ-ICSRJNTNSA-N 0.000 claims 1
- VKJROWRLVCWQPU-HKUYNNGSSA-N (2s,3s)-n,3-dihydroxy-2-methyl-2-[(4-phenylphenyl)methoxy]pentanamide Chemical compound C1=CC(CO[C@@](C)([C@@H](O)CC)C(=O)NO)=CC=C1C1=CC=CC=C1 VKJROWRLVCWQPU-HKUYNNGSSA-N 0.000 claims 1
- WFVASGYQNPHMCF-GMAHTHKFSA-N (2s,3s)-n,3-dihydroxy-2-methyl-3-phenyl-2-[(4-phenylphenyl)methoxy]propanamide Chemical compound O([C@@](C)([C@@H](O)C=1C=CC=CC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 WFVASGYQNPHMCF-GMAHTHKFSA-N 0.000 claims 1
- IYOHQOLEWXCJEG-ICSRJNTNSA-N (2s,3s)-n,3-dihydroxy-3-(1h-imidazol-5-yl)-2-methyl-2-[(4-phenylphenyl)methoxy]propanamide Chemical compound O([C@@](C)([C@@H](O)C=1N=CNC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 IYOHQOLEWXCJEG-ICSRJNTNSA-N 0.000 claims 1
- MRYZMLDBJLIIPW-UNMCSNQZSA-N (2s,3s)-n,3-dihydroxy-3-[5-(hydroxymethyl)furan-2-yl]-2-methyl-2-[(4-phenylphenyl)methoxy]propanamide Chemical compound O([C@@](C)([C@@H](O)C=1OC(CO)=CC=1)C(=O)NO)CC(C=C1)=CC=C1C1=CC=CC=C1 MRYZMLDBJLIIPW-UNMCSNQZSA-N 0.000 claims 1
- 208000035143 Bacterial infection Diseases 0.000 claims 1
- 208000022362 bacterial infectious disease Diseases 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- KIXXNPCYAPCLLP-UHFFFAOYSA-N CCC(C)C(C1)N1NN Chemical compound CCC(C)C(C1)N1NN KIXXNPCYAPCLLP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9824908P | 2008-09-19 | 2008-09-19 | |
| US61/098,249 | 2008-09-19 | ||
| PCT/IB2009/053809 WO2010032147A2 (en) | 2008-09-19 | 2009-09-01 | Hydroxamic acid derivatives useful as antibacterial agents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012502974A JP2012502974A (ja) | 2012-02-02 |
| JP2012502974A5 true JP2012502974A5 (enExample) | 2012-10-04 |
| JP5524215B2 JP5524215B2 (ja) | 2014-06-18 |
Family
ID=41664561
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011527431A Expired - Fee Related JP5524215B2 (ja) | 2008-09-19 | 2009-09-01 | 抗菌剤として有用なヒドロキサム酸誘導体 |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US8722686B2 (enExample) |
| EP (1) | EP2334636A2 (enExample) |
| JP (1) | JP5524215B2 (enExample) |
| CA (1) | CA2735929C (enExample) |
| WO (1) | WO2010032147A2 (enExample) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2602615T3 (es) | 2007-06-12 | 2017-02-21 | Achaogen, Inc. | Agentes antibacterianos |
| EP2334636A2 (en) | 2008-09-19 | 2011-06-22 | Pfizer Inc. | Hydroxamic acid derivatives useful as antibacterial agents |
| JP5793766B2 (ja) | 2009-12-16 | 2015-10-14 | ファイザー・インク | 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体 |
| TW201609079A (zh) | 2010-04-20 | 2016-03-16 | 大正製藥股份有限公司 | 新穎之異羥肟酸（ｈｙｄｒｏｘａｍｉｃ ａｃｉｄ）衍生物 |
| AP3336A (en) | 2011-03-07 | 2015-07-31 | Pfizer | Fluoro-pyridinone derivatives useful as antibacterial agents |
| CN103717582B (zh) * | 2011-04-08 | 2015-09-30 | 辉瑞大药厂 | 用作抗菌剂的异*唑衍生物 |
| WO2012137099A1 (en) * | 2011-04-08 | 2012-10-11 | Pfizer Inc. | Imidazole, pyrazole, and triazole derivatives useful as antibacterial agents |
| EP2847168A1 (en) | 2012-05-10 | 2015-03-18 | Achaogen, Inc. | Antibacterial agents |
| CN102993052B (zh) * | 2012-12-29 | 2014-07-09 | 吉首大学 | 芳基丙酰氧肟酸类尿素酶抑制剂及其合成和用途 |
| CN103012207B (zh) * | 2012-12-29 | 2015-05-27 | 吉首大学 | 二芳基丙酰-n-甲基氧肟酸类尿素酶抑制剂及其合成和用途 |
| WO2014165075A1 (en) | 2013-03-12 | 2014-10-09 | Achaogen, Inc. | Antibacterial agents |
| RS58930B1 (sr) | 2013-03-15 | 2019-08-30 | Fujifilm Toyama Chemical Co Ltd | Novi derivati hidroksaminske kiseline ili njihova so |
| WO2015051045A2 (en) | 2013-10-04 | 2015-04-09 | Novartis Ag | 3'END CAPS FOR RNAi AGENTS FOR USE IN RNA INTERFERENCE |
| WO2015050871A2 (en) | 2013-10-04 | 2015-04-09 | Novartis Ag | Organic compounds to treat hepatitis b virus |
| EP3134401B1 (en) | 2014-04-22 | 2018-06-13 | Novartis AG | Isoxazoline hydroxamic acid derivatives as lpxc inhibitors |
| WO2016039432A1 (ja) | 2014-09-12 | 2016-03-17 | 富山化学工業株式会社 | 新規なヒドロキサム酸誘導体および抗菌性物質を組み合わせて使用する方法 |
| SG11201701956TA (en) | 2014-09-12 | 2017-04-27 | Toyama Chemical Co Ltd | Novel pharmaceutical composition containing hydroxamic acid derivative or salt thereof |
| CR20170260A (es) | 2014-12-16 | 2017-08-21 | Novartis Ag | COMPUESTOS DE ISOXAZOL DE ÁCIDO HIDROXÁMICO COMO INHIBIDORES DE LpxC |
| HRP20211864T1 (hr) | 2015-07-06 | 2022-03-04 | Alkermes, Inc. | Inhibitori hetero-halo histonske deacetilaze |
| EP3319968A1 (en) | 2015-07-06 | 2018-05-16 | Rodin Therapeutics, Inc. | Heterobicyclic n-aminophenyl-amides as inhibitors of histone deacetylase |
| AR105646A1 (es) | 2015-08-11 | 2017-10-25 | Actelion Pharmaceuticals Ltd | Agentes antibacterianos de 1,2-dihidro-3h-pirrolo[1,2-c]imidazol-3-ona sustituida |
| ES2820502T3 (es) | 2016-06-14 | 2021-04-21 | Novartis Ag | Forma cristalina de (R)-4-(5-(ciclopropiletilinil)isoxazol-3-il)-N-hidroxi-2-metil-2-(metilsulfonil)butanamida como agente antibacteriano |
| WO2017223349A1 (en) | 2016-06-23 | 2017-12-28 | Achaogen, Inc. | Antibacterial agents |
| KR102526032B1 (ko) | 2017-01-11 | 2023-04-25 | 로딘 테라퓨틱스, 인크. | 히스톤 데아세틸라제의 바이시클릭 억제제 |
| US10085999B1 (en) | 2017-05-10 | 2018-10-02 | Arixa Pharmaceuticals, Inc. | Beta-lactamase inhibitors and uses thereof |
| CN107226845B (zh) * | 2017-05-31 | 2020-10-09 | 成都雅途生物技术有限公司 | 一种抗多重耐药菌的化合物yt-011及其制备方法 |
| SI3664802T1 (sl) | 2017-08-07 | 2022-10-28 | Alkermes, Inc. | Biciklični zaviralci histon deacetilaze |
| JP6991345B2 (ja) | 2017-10-02 | 2022-01-12 | アリクサ ファーマシューティカルズ、インコーポレイテッド | アズトレオナム誘導体およびその使用 |
| US11180500B2 (en) | 2018-10-01 | 2021-11-23 | Arixa Pharmaceuticals, Inc. | Derivatives of relebactam and uses thereof |
| EP3938366A1 (en) | 2019-03-12 | 2022-01-19 | Arixa Pharmaceuticals, Inc. | Crystalline form of an avibactam derivative |
| US11565999B2 (en) | 2019-04-25 | 2023-01-31 | Arixa Pharmaceuticals, Inc. | Methods of synthesizing aztreonam derivatives |
| CA3186854A1 (en) * | 2020-07-24 | 2022-01-27 | Mindset Pharma Inc. | Scalable synthetic route for psilocin and psilocybin |
| CN116730870B (zh) * | 2023-08-08 | 2023-10-13 | 中国医学科学院医药生物技术研究所 | 异羟肟酸类化合物或其可药用盐、及其用途和制备方法 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS50121218A (enExample) * | 1974-03-01 | 1975-09-23 | ||
| US4769461A (en) * | 1986-09-16 | 1988-09-06 | American Home Products Corporation | Quinolinyl benzene hydroxamic acids as anti-inflammatory/antiallergic agents |
| US5110831A (en) | 1990-11-30 | 1992-05-05 | Du Pont Merck Pharmaceutical Company | Vinylogous hydroxamic acids and derivatives thereof as 5-lipoxygenase inhibitors |
| AU749699B2 (en) | 1998-02-07 | 2002-07-04 | British Biotech Pharmaceuticals Limited | Antibacterial agents |
| GB9925470D0 (en) | 1999-10-27 | 1999-12-29 | Smithkline Beecham Plc | Novel compounds |
| WO2002074298A1 (en) * | 2001-03-21 | 2002-09-26 | Ono Pharmaceutical Co., Ltd. | Il-6 production inhibitors |
| ES2180456B1 (es) | 2001-07-20 | 2004-05-01 | Laboratorios S.A.L.V.A.T., S.A. | Isoxazoles sustituidos y su utilizacion como antibioticos. |
| KR101076018B1 (ko) | 2003-01-08 | 2011-10-21 | 유니버시티 오브 워싱톤 | 항균제 |
| GB0302431D0 (en) | 2003-01-30 | 2003-03-05 | Glaxo Group Ltd | Novel compounds |
| US7495006B2 (en) | 2004-12-10 | 2009-02-24 | Emory University | 2′ and 3′-substituted cyclobutyl nucleoside analogs for the treatment of viral infections and abnormal cellular proliferation |
| WO2006118155A1 (ja) * | 2005-04-27 | 2006-11-09 | Ishihara Sangyo Kaisha, Ltd. | ビフェニル誘導体又はその塩、並びにそれらを有効成分として含有する農園芸用殺菌剤 |
| WO2006124897A2 (en) | 2005-05-13 | 2006-11-23 | Lexicon Genetics Incorporated | Methods and compositions for improving cognition |
| JP2009520695A (ja) | 2005-12-15 | 2009-05-28 | ヴィキュロン ファーマシューティカルズ インコーポレイテッド | 抗菌活性を有するｎ−ヒドロキシアミド誘導体 |
| WO2007093904A1 (en) | 2006-02-14 | 2007-08-23 | Pfizer Products Inc. | Benzoxazinone and benzoxazepinone oxazolidinones as antibacterial agents |
| US20080085893A1 (en) | 2006-10-06 | 2008-04-10 | Shyh-Ming Yang | Matrix metalloprotease inhibitors |
| CN101016270B (zh) | 2006-12-30 | 2012-05-09 | 天津药物研究院 | 取代的哌嗪基苯基异噁唑啉衍生物及其用途 |
| US7879911B2 (en) | 2007-02-01 | 2011-02-01 | Johnson Alan T | Hydroxamic acid derivatives of phenoxy-acetic acids and analogs useful as therapeutic agents for treating anthrax poisoning |
| WO2008105515A1 (ja) | 2007-02-28 | 2008-09-04 | Taisho Pharmaceutical Co., Ltd. | 新規なヒドロキサム酸誘導体 |
| US20080234297A1 (en) | 2007-03-20 | 2008-09-25 | Changgeng Qian | HSP90 Inhibitors Containing a Zinc Binding Moiety |
| JP2011529964A (ja) | 2008-08-04 | 2011-12-15 | シェーリング コーポレイション | 抗菌剤としての尿素誘導体 |
| WO2010024356A1 (ja) | 2008-08-27 | 2010-03-04 | 大正製薬株式会社 | ナフチリジン－ｎ－オキシドを有する新規ヒドロキサム酸誘導体 |
| US8372885B2 (en) | 2008-09-17 | 2013-02-12 | Novartis Ag | Organic compounds and their uses |
| EP2334636A2 (en) | 2008-09-19 | 2011-06-22 | Pfizer Inc. | Hydroxamic acid derivatives useful as antibacterial agents |
| WO2010100475A1 (en) | 2009-03-02 | 2010-09-10 | Astrazeneca Ab | Hydroxamic acid derivatives as gram-negative antibacterial agents |
| JP5793766B2 (ja) | 2009-12-16 | 2015-10-14 | ファイザー・インク | 抗菌剤として有用なｎ−結合型ヒドロキサム酸誘導体 |
| AP3336A (en) | 2011-03-07 | 2015-07-31 | Pfizer | Fluoro-pyridinone derivatives useful as antibacterial agents |
| WO2012137099A1 (en) | 2011-04-08 | 2012-10-11 | Pfizer Inc. | Imidazole, pyrazole, and triazole derivatives useful as antibacterial agents |
| CN103717582B (zh) | 2011-04-08 | 2015-09-30 | 辉瑞大药厂 | 用作抗菌剂的异*唑衍生物 |
-
2009
- 2009-09-01 EP EP09787063A patent/EP2334636A2/en not_active Withdrawn
- 2009-09-01 WO PCT/IB2009/053809 patent/WO2010032147A2/en not_active Ceased
- 2009-09-01 CA CA2735929A patent/CA2735929C/en not_active Expired - Fee Related
- 2009-09-01 JP JP2011527431A patent/JP5524215B2/ja not_active Expired - Fee Related
- 2009-09-01 US US13/119,484 patent/US8722686B2/en not_active Expired - Fee Related
-
2014
- 2014-03-24 US US14/223,061 patent/US9340493B2/en not_active Expired - Fee Related