JP2013523761A5 - - Google Patents
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- Publication number
- JP2013523761A5 JP2013523761A5 JP2013502803A JP2013502803A JP2013523761A5 JP 2013523761 A5 JP2013523761 A5 JP 2013523761A5 JP 2013502803 A JP2013502803 A JP 2013502803A JP 2013502803 A JP2013502803 A JP 2013502803A JP 2013523761 A5 JP2013523761 A5 JP 2013523761A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkylene
- heterocyclyl
- hydrogen
- ring
- 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 25
- 229910052739 hydrogen Inorganic materials 0.000 claims 21
- 239000001257 hydrogen Substances 0.000 claims 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 16
- 125000000623 heterocyclic group Chemical group 0.000 claims 15
- 125000002947 alkylene group Chemical group 0.000 claims 14
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000001153 fluoro group Chemical group F* 0.000 claims 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 9
- 125000004452 carbocyclyl group Chemical group 0.000 claims 9
- 208000015181 infectious disease Diseases 0.000 claims 9
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- -1 methoxy, methyl Chemical group 0.000 claims 5
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 241001430197 Mollicutes Species 0.000 claims 4
- 241000186359 Mycobacterium Species 0.000 claims 4
- 241000204031 Mycoplasma Species 0.000 claims 4
- 241000193996 Streptococcus pyogenes Species 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- 238000011282 treatment Methods 0.000 claims 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 4
- 241001156739 Actinobacteria <phylum> Species 0.000 claims 3
- 241000193830 Bacillus <bacterium> Species 0.000 claims 3
- 206010057190 Respiratory tract infections Diseases 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000003386 piperidinyl group Chemical group 0.000 claims 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 206010040872 skin infection Diseases 0.000 claims 3
- 241000894007 species Species 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 claims 2
- 241000304886 Bacilli Species 0.000 claims 2
- 241000894006 Bacteria Species 0.000 claims 2
- 241001112696 Clostridia Species 0.000 claims 2
- 241000194033 Enterococcus Species 0.000 claims 2
- 241000194032 Enterococcus faecalis Species 0.000 claims 2
- 241000194031 Enterococcus faecium Species 0.000 claims 2
- 241000606768 Haemophilus influenzae Species 0.000 claims 2
- 241000589248 Legionella Species 0.000 claims 2
- 241000589242 Legionella pneumophila Species 0.000 claims 2
- 241000186781 Listeria Species 0.000 claims 2
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 claims 2
- 241000588655 Moraxella catarrhalis Species 0.000 claims 2
- 206010035664 Pneumonia Diseases 0.000 claims 2
- 241000191940 Staphylococcus Species 0.000 claims 2
- 241000194017 Streptococcus Species 0.000 claims 2
- 241000193985 Streptococcus agalactiae Species 0.000 claims 2
- 241000193998 Streptococcus pneumoniae Species 0.000 claims 2
- 239000004098 Tetracycline Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 229940115932 legionella pneumophila Drugs 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 229960003085 meticillin Drugs 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 229960002180 tetracycline Drugs 0.000 claims 2
- 229930101283 tetracycline Natural products 0.000 claims 2
- 235000019364 tetracycline Nutrition 0.000 claims 2
- 150000003522 tetracyclines Chemical class 0.000 claims 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 2
- SOVUOXKZCCAWOJ-HJYUBDRYSA-N (4s,4as,5ar,12ar)-9-[[2-(tert-butylamino)acetyl]amino]-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1C2=C(N(C)C)C=C(NC(=O)CNC(C)(C)C)C(O)=C2C(O)=C2[C@@H]1C[C@H]1[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]1(O)C2=O SOVUOXKZCCAWOJ-HJYUBDRYSA-N 0.000 claims 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- ITHCSGCUQDMYAI-ZMIZWQJLSA-N 2-carboxy-D-arabinitol 1,5-bisphosphate Chemical compound OP(=O)(O)OC[C@@H](O)[C@@H](O)[C@](O)(COP(O)(O)=O)C(O)=O ITHCSGCUQDMYAI-ZMIZWQJLSA-N 0.000 claims 1
- 241000589291 Acinetobacter Species 0.000 claims 1
- 108700042778 Antimicrobial Peptides Proteins 0.000 claims 1
- 102000044503 Antimicrobial Peptides Human genes 0.000 claims 1
- 241000606125 Bacteroides Species 0.000 claims 1
- 241000589968 Borrelia Species 0.000 claims 1
- 241000589876 Campylobacter Species 0.000 claims 1
- 241001185363 Chlamydiae Species 0.000 claims 1
- 241000498849 Chlamydiales Species 0.000 claims 1
- 241000193403 Clostridium Species 0.000 claims 1
- 241000186216 Corynebacterium Species 0.000 claims 1
- 241000588921 Enterobacteriaceae Species 0.000 claims 1
- 241000589989 Helicobacter Species 0.000 claims 1
- 208000007764 Legionnaires' Disease Diseases 0.000 claims 1
- 208000016604 Lyme disease Diseases 0.000 claims 1
- 241000187479 Mycobacterium tuberculosis Species 0.000 claims 1
- 241000202934 Mycoplasma pneumoniae Species 0.000 claims 1
- 241000204003 Mycoplasmatales Species 0.000 claims 1
- 241000588656 Neisseriaceae Species 0.000 claims 1
- 241000187654 Nocardia Species 0.000 claims 1
- 241000606752 Pasteurellaceae Species 0.000 claims 1
- 241000186429 Propionibacterium Species 0.000 claims 1
- 102100021486 Protein S100-G Human genes 0.000 claims 1
- 101710122252 Protein S100-G Proteins 0.000 claims 1
- 241000606651 Rickettsiales Species 0.000 claims 1
- 241000589973 Spirochaeta Species 0.000 claims 1
- 241000589970 Spirochaetales Species 0.000 claims 1
- 241000191967 Staphylococcus aureus Species 0.000 claims 1
- 241000589886 Treponema Species 0.000 claims 1
- 108010059993 Vancomycin Proteins 0.000 claims 1
- 241000607493 Vibrionaceae Species 0.000 claims 1
- 230000001154 acute effect Effects 0.000 claims 1
- 150000001413 amino acids Chemical group 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 230000001580 bacterial effect Effects 0.000 claims 1
- 230000003115 biocidal effect Effects 0.000 claims 1
- 229960000106 biosimilars Drugs 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229940124307 fluoroquinolone Drugs 0.000 claims 1
- 229940041010 fourth-generation cephalosporins Drugs 0.000 claims 1
- 206010022000 influenza Diseases 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000003910 polypeptide antibiotic agent Substances 0.000 claims 1
- 238000011321 prophylaxis Methods 0.000 claims 1
- 150000007660 quinolones Chemical class 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229940041008 second-generation cephalosporins Drugs 0.000 claims 1
- 125000003003 spiro group Chemical group 0.000 claims 1
- 229940031000 streptococcus pneumoniae Drugs 0.000 claims 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 229940072172 tetracycline antibiotic Drugs 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 229940041007 third-generation cephalosporins Drugs 0.000 claims 1
- 229960004089 tigecycline Drugs 0.000 claims 1
- 201000008827 tuberculosis Diseases 0.000 claims 1
- 229960003165 vancomycin Drugs 0.000 claims 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 claims 1
- MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 claims 1
- 150000003952 β-lactams Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31961410P | 2010-03-31 | 2010-03-31 | |
| US61/319,614 | 2010-03-31 | ||
| PCT/US2011/030532 WO2011123536A1 (en) | 2010-03-31 | 2011-03-30 | Polycyclic tetracycline compounds |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015196859A Division JP2016014058A (ja) | 2010-03-31 | 2015-10-02 | 多環式テトラサイクリン化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013523761A JP2013523761A (ja) | 2013-06-17 |
| JP2013523761A5 true JP2013523761A5 (enExample) | 2014-05-15 |
| JP5820462B2 JP5820462B2 (ja) | 2015-11-24 |
Family
ID=43929063
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013502803A Expired - Fee Related JP5820462B2 (ja) | 2010-03-31 | 2011-03-30 | 多環式テトラサイクリン化合物 |
| JP2015196859A Withdrawn JP2016014058A (ja) | 2010-03-31 | 2015-10-02 | 多環式テトラサイクリン化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015196859A Withdrawn JP2016014058A (ja) | 2010-03-31 | 2015-10-02 | 多環式テトラサイクリン化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US9371283B2 (enExample) |
| EP (1) | EP2552890B1 (enExample) |
| JP (2) | JP5820462B2 (enExample) |
| KR (1) | KR101879751B1 (enExample) |
| CN (2) | CN103180295B (enExample) |
| AR (1) | AR081064A1 (enExample) |
| AU (1) | AU2011235176B2 (enExample) |
| BR (1) | BR112012025045A2 (enExample) |
| CA (1) | CA2799727C (enExample) |
| DK (1) | DK2552890T3 (enExample) |
| ES (1) | ES2621409T3 (enExample) |
| MX (1) | MX2012011453A (enExample) |
| NZ (1) | NZ603323A (enExample) |
| PL (1) | PL2552890T3 (enExample) |
| SG (1) | SG184372A1 (enExample) |
| TW (1) | TWI592390B (enExample) |
| WO (1) | WO2011123536A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7607243B2 (en) | 2006-05-03 | 2009-10-27 | Nike, Inc. | Athletic or other performance sensing systems |
| CA2761241C (en) | 2009-05-08 | 2018-02-27 | Tetraphase Pharmaceuticals, Inc. | Tetracycline compounds |
| US9624166B2 (en) | 2009-08-28 | 2017-04-18 | Tetraphase Pharmaceuticals, Inc. | Tetracycline compounds |
| KR101879751B1 (ko) | 2010-03-31 | 2018-08-16 | 테트라페이즈 파마슈티컬스, 인코포레이티드 | 폴리사이클릭 테트라사이클린 화합물 |
| HUE042600T2 (hu) | 2012-08-31 | 2019-07-29 | Tetraphase Pharmaceuticals Inc | Tetraciklin vegyületek |
| US9580758B2 (en) | 2013-11-12 | 2017-02-28 | Luc Montagnier | System and method for the detection and treatment of infection by a microbial agent associated with HIV infection |
| MA40836A (fr) * | 2014-10-23 | 2017-08-29 | Tetraphase Pharmaceuticals Inc | Procédures de semi-synthèse |
| SG11201901390TA (en) * | 2016-08-30 | 2019-03-28 | Tetraphase Pharmaceuticals Inc | Tetracycline compounds and methods of treatment |
| EP3529236B1 (en) | 2016-10-19 | 2024-02-07 | Tetraphase Pharmaceuticals, Inc. | Crystalline forms of eravacycline |
| US20220401457A1 (en) * | 2019-08-30 | 2022-12-22 | Emory University | Use of Deoxycholic Acid, Derivatives, or Salts Thereof in Managing Bacterial Infections and Compositions Related Thereto |
| WO2021207217A1 (en) * | 2020-04-06 | 2021-10-14 | University Of Virginia Patent Foundation | Compositions and methods for treating viruses |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3304227A (en) | 1965-07-15 | 1967-02-14 | Loyal E Loveless | Antibiotic-containing animal feed |
| US4704383A (en) | 1983-12-29 | 1987-11-03 | The Research Foundation Of State University Of New York | Non-antibacterial tetracycline compositions possessing anti-collagenolytic properties and methods of preparing and using same |
| US4666897A (en) | 1983-12-29 | 1987-05-19 | Research Foundation Of State University | Inhibition of mammalian collagenolytic enzymes by tetracyclines |
| US4925833A (en) | 1983-12-29 | 1990-05-15 | The Research Foundation Of State University Of New York | Use of tetracycline to enhance bone protein synthesis and/or treatment of osteoporosis |
| USRE34656E (en) | 1983-12-29 | 1994-07-05 | The Research Foundation Of State University Of New York | Use of tetracycline to enhance bone protein synthesis and/or treatment of bone deficiency |
| US4935412A (en) | 1983-12-29 | 1990-06-19 | The Research Foundation Of State University Of New York | Non-antibacterial tetracycline compositions possessing anti-collagenolytic properties and methods of preparing and using same |
| JP3016587B2 (ja) | 1989-12-04 | 2000-03-06 | ザ・リサーチ・ファンデーション・オブ・ステート・ユニバーシティ・オブ・ニューヨーク | 非ステロイド抗炎症剤及びテトラサイクリンの配合 |
| US5308839A (en) | 1989-12-04 | 1994-05-03 | The Research Foundation Of State University Of New York | Composition comprising non-steroidal anti-inflammatory agent tenidap and effectively non-antibacterial tetracycline |
| US5770588A (en) | 1991-02-11 | 1998-06-23 | The Research Foundation Of State University Of New York | Non-antibacterial tetracycline compositions of the prevention and treatment of root caries |
| US5231017A (en) | 1991-05-17 | 1993-07-27 | Solvay Enzymes, Inc. | Process for producing ethanol |
| US5258371A (en) | 1992-05-29 | 1993-11-02 | Kuraray Co., Ltd. | Method to reduce connective tissue destruction |
| US6043225A (en) | 1992-06-12 | 2000-03-28 | Board Of Regents Of The University Of Washington | Diagnosis and treatment of arterial chlamydial granuloma |
| DK0599397T3 (da) | 1992-11-17 | 1996-09-16 | Univ New York State Res Found | Tetracycliner, herunder non-mikrobielle, kemisk-modificerede tetracycliner, inhiberer overdreven collagentværbinding ved diabetes |
| US5523297A (en) | 1993-03-02 | 1996-06-04 | The Research Foundation Of State University Of New York | Inhibition of excessive phospholipase A2 activity and/or production by non-antimicrobial tetracyclines |
| US6043231A (en) | 1993-03-02 | 2000-03-28 | The Research Foundation Of State Univ. Of New York | Inhibition of excessive phospholipase A2 activity and/or production by non-antimicrobial tetracyclines |
| US5668122A (en) | 1993-07-28 | 1997-09-16 | Fife; Rose S. | Method to treat cancer with tetracyclines |
| WO1995022529A1 (en) | 1994-02-17 | 1995-08-24 | Pfizer Inc. | 9-(substituted amino)-alpha-6-deoxy-5-oxy tetracycline derivatives, their preparation and their use as antibiotics |
| US5843925A (en) | 1994-12-13 | 1998-12-01 | American Cyanamid Company | Methods for inhibiting angiogenesis, proliferation of endothelial or tumor cells and tumor growth |
| US5834449A (en) | 1996-06-13 | 1998-11-10 | The Research Foundation Of State University Of New York | Treatment of aortic and vascular aneurysms with tetracycline compounds |
| US5827840A (en) | 1996-08-01 | 1998-10-27 | The Research Foundation Of State University Of New York | Promotion of wound healing by chemically-modified tetracyclines |
| US5789395A (en) | 1996-08-30 | 1998-08-04 | The Research Foundation Of State University Of New York | Method of using tetracycline compounds for inhibition of endogenous nitric oxide production |
| US5919774A (en) | 1996-12-10 | 1999-07-06 | Eli Lilly And Company | Pyrroles as sPLA2 inhibitors |
| US5837696A (en) | 1997-01-15 | 1998-11-17 | The Research Foundation Of State University Of New York | Method of inhibiting cancer growth |
| US5773430A (en) | 1997-03-13 | 1998-06-30 | Research Foundation Of State University Of New York | Serine proteinase inhibitory activity by hydrophobic tetracycline |
| US5929055A (en) | 1997-06-23 | 1999-07-27 | The Research Foundation Of State University Of New York | Therapeutic method for management of diabetes mellitus |
| US6277061B1 (en) | 1998-03-31 | 2001-08-21 | The Research Foundation Of State University Of New York | Method of inhibiting membrane-type matrix metalloproteinase |
| US6015804A (en) | 1998-09-11 | 2000-01-18 | The Research Foundation Of State University Of New York | Method of using tetracycline compounds to enhance interleukin-10 production |
| US5977091A (en) | 1998-09-21 | 1999-11-02 | The Research Foundation Of State University Of New York | Method of preventing acute lung injury |
| US5998390A (en) | 1998-09-28 | 1999-12-07 | The Research Foundation Of State University Of New York | Combination of bisphosphonate and tetracycline |
| US6231894B1 (en) | 1999-10-21 | 2001-05-15 | Duke University | Treatments based on discovery that nitric oxide synthase is a paraquat diaphorase |
| CN103214409B (zh) * | 2004-05-21 | 2015-10-21 | 哈佛大学校长及研究员协会 | 四环素及其类似物的合成 |
| AU2007235279B2 (en) * | 2006-04-07 | 2012-12-06 | President And Fellows Of Harvard College | Synthesis of tetracyclines and analogues thereof |
| KR101879751B1 (ko) | 2010-03-31 | 2018-08-16 | 테트라페이즈 파마슈티컬스, 인코포레이티드 | 폴리사이클릭 테트라사이클린 화합물 |
-
2011
- 2011-03-30 KR KR1020127028516A patent/KR101879751B1/ko not_active Expired - Fee Related
- 2011-03-30 CN CN201180026893.1A patent/CN103180295B/zh not_active Expired - Fee Related
- 2011-03-30 US US13/075,886 patent/US9371283B2/en not_active Expired - Fee Related
- 2011-03-30 CN CN201610322618.9A patent/CN106008317B/zh not_active Expired - Fee Related
- 2011-03-30 CA CA2799727A patent/CA2799727C/en not_active Expired - Fee Related
- 2011-03-30 PL PL11715112T patent/PL2552890T3/pl unknown
- 2011-03-30 ES ES11715112.6T patent/ES2621409T3/es active Active
- 2011-03-30 EP EP11715112.6A patent/EP2552890B1/en not_active Not-in-force
- 2011-03-30 SG SG2012072740A patent/SG184372A1/en unknown
- 2011-03-30 WO PCT/US2011/030532 patent/WO2011123536A1/en not_active Ceased
- 2011-03-30 JP JP2013502803A patent/JP5820462B2/ja not_active Expired - Fee Related
- 2011-03-30 TW TW100110964A patent/TWI592390B/zh not_active IP Right Cessation
- 2011-03-30 BR BR112012025045A patent/BR112012025045A2/pt not_active Application Discontinuation
- 2011-03-30 DK DK11715112.6T patent/DK2552890T3/en active
- 2011-03-30 AU AU2011235176A patent/AU2011235176B2/en not_active Ceased
- 2011-03-30 NZ NZ603323A patent/NZ603323A/en not_active IP Right Cessation
- 2011-03-30 MX MX2012011453A patent/MX2012011453A/es active IP Right Grant
- 2011-03-31 AR ARP110101090A patent/AR081064A1/es active IP Right Grant
-
2015
- 2015-10-02 JP JP2015196859A patent/JP2016014058A/ja not_active Withdrawn
-
2016
- 2016-05-25 US US15/164,183 patent/US20170107179A1/en not_active Abandoned
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