PE20180796A1 - Macrociclos peptidicos contra acinetobacter baumannii - Google Patents
Macrociclos peptidicos contra acinetobacter baumanniiInfo
- Publication number
- PE20180796A1 PE20180796A1 PE2018000242A PE2018000242A PE20180796A1 PE 20180796 A1 PE20180796 A1 PE 20180796A1 PE 2018000242 A PE2018000242 A PE 2018000242A PE 2018000242 A PE2018000242 A PE 2018000242A PE 20180796 A1 PE20180796 A1 PE 20180796A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- hydrogen
- individually selected
- acinetobacter baumannii
- cyano
- Prior art date
Links
- 241000588626 Acinetobacter baumannii Species 0.000 title abstract 2
- 150000002678 macrocyclic compounds Chemical class 0.000 title 1
- 108090000765 processed proteins & peptides Proteins 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 150000002431 hydrogen Chemical class 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61K31/04—Nitro compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06086—Dipeptides with the first amino acid being basic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0806—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/081—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0815—Tripeptides with the first amino acid being basic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0821—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Abstract
Referido a un compuesto de Formula (I), en donde X1 es C-L1-R11 o N; X2 es C-L2-R12 o N; X3 es C-L3-R13 o N; X4 es C-L4-R14 o N, con la salvedad de que no mas de tres de X1, X2, X3 y X4 sean N; X5 es C-L5-R15 o N; X6 es C-L6-R16 o N; X7 es C-L7-R17 o N; X8 es C-L8-R18 o N, con la salvedad de que no mas de tres de X5, X6, X7 y X8 sean N; R1 es -(CH2)m-heteroarilo o -(CH2)m-heterocicloalquilo, entre otros; R2, R4 y R6 se seleccionan cada uno de forma individual entre hidrogeno, alquilo C1-7, entre otros; R3 es alquilo C1-7, -(CH2)n-NR20R21, entre otros; R5 es hidrogeno, alquilo C1-7, hidroxi-alquilo C1-7, entre otros; R5´ es hidrogeno o alquilo C1-7; R7 y R8 se seleccionan cada uno de forma individualmente hidrogeno, alquilo C1-7, haloalquilo C1-7, entre otros; R11, R12, R13, R14, R15 Y R16 se seleccionan cada uno de forma individual entre hidrogeno, halogeno, ciano, alquilo C1-7, entre otros; R17 es hidrogeno, halogeno, ciano, entre otros; R18 es hidrogeno, halogeno, ciano, alquilo C1-7, haloalquiloC1-7, entre otros. R21 y R23 se selecciona cada uno individualmente entre hidrogeno y alquilo C1-7; L1, L2, L3, L4, L5, L6, L7 y L8 se seleccionan cada uno individualmente entre un enlace simple, -C(O)-, -SO2-, -(CH2)p-, -CH=CH-, entre otros; m es 1, 2, 3, o 4; n es 1, 2, 3, o 4; o es 0, 1, 2, 3, o 4; p es 1, 2, 3, o 4; q es 1, 2, 3, o 4; r es 1, 2, 3, o 4; asi como sales farmaceuticamente aceptables de los mismos. Tambien se refiere a un proceso para la fabricacion de dicho compuesto, composiciones farmaceuticas que los comprenden, y su uso como medicamento para el tratamiento de enfermedades e infecciones causadas por Acinetobacter baumannii.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15191743 | 2015-10-27 | ||
| CN2016100125 | 2016-09-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20180796A1 true PE20180796A1 (es) | 2018-05-09 |
Family
ID=57200005
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2018000242A PE20180796A1 (es) | 2015-10-27 | 2016-10-24 | Macrociclos peptidicos contra acinetobacter baumannii |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US10030047B2 (es) |
| EP (1) | EP3368544B1 (es) |
| JP (2) | JP7286317B2 (es) |
| KR (1) | KR102701379B1 (es) |
| CN (1) | CN108350028B (es) |
| AU (1) | AU2016347456B2 (es) |
| CL (1) | CL2018000978A1 (es) |
| CO (1) | CO2017013708A2 (es) |
| CR (1) | CR20180232A (es) |
| DK (1) | DK3368544T3 (es) |
| ES (1) | ES2811911T3 (es) |
| HR (1) | HRP20201273T1 (es) |
| HU (1) | HUE050053T2 (es) |
| IL (1) | IL258060B (es) |
| MX (2) | MX2018005236A (es) |
| MY (1) | MY193014A (es) |
| PE (1) | PE20180796A1 (es) |
| PH (1) | PH12018500904A1 (es) |
| PL (1) | PL3368544T3 (es) |
| PT (1) | PT3368544T (es) |
| RS (1) | RS60662B1 (es) |
| RU (1) | RU2729609C2 (es) |
| SI (1) | SI3368544T1 (es) |
| TW (1) | TWI720042B (es) |
| UA (1) | UA124303C2 (es) |
| WO (1) | WO2017072062A1 (es) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2659352C1 (ru) * | 2014-08-13 | 2018-07-03 | Хуавей Текнолоджиз Ко., Лтд. | Передатчик и приемник, способ приема и способ передачи через fbmc сигнала |
| MY193014A (en) * | 2015-10-27 | 2022-09-22 | Hoffmann La Roche | Peptide macrocycles against acinetobacter baumannii |
| CA3045970A1 (en) | 2016-12-21 | 2018-06-28 | F. Hoffmann-La Roche Ag | Method for in vitro glycoengineering of antibodies |
| CN110100007B (zh) | 2016-12-21 | 2024-05-28 | 豪夫迈·罗氏有限公司 | 用于体外糖工程化抗体的酶的再使用 |
| EP3388444A1 (en) * | 2017-04-10 | 2018-10-17 | F. Hoffmann-La Roche AG | Anti-bacterial peptide macrocycles and use thereof |
| US11505573B2 (en) | 2018-03-28 | 2022-11-22 | Hoffmann-La Roche Inc. | Peptide macrocycles against Acinetobacter baumannii |
| US11819532B2 (en) * | 2018-04-23 | 2023-11-21 | Hoffmann-La Roche Inc. | Peptide macrocycles against Acinetobacter baumannii |
| WO2020126956A1 (en) * | 2018-12-17 | 2020-06-25 | F. Hoffmann-La Roche Ag | Imidazopyrazine derivatives as antibacterial agents |
| CN113613722A (zh) | 2019-03-08 | 2021-11-05 | 豪夫迈·罗氏有限公司 | 新型咪唑-吡唑衍生物 |
| JP7715715B2 (ja) | 2020-01-22 | 2025-07-30 | エフ． ホフマン－ラ ロシュ アーゲー | 新規複素環式化合物 |
| JP7771084B2 (ja) | 2020-04-29 | 2025-11-17 | エフ． ホフマン－ラ ロシュ アーゲー | 抗菌８－フェニルアミノ－３－（ピラゾール－４－イル）イミダゾ［１，２－ａ］ピラジン誘導体 |
| EP4157846A1 (en) | 2020-06-01 | 2023-04-05 | F. Hoffmann-La Roche AG | Novel imidazopyrazne derivatives |
| CN115667264A (zh) | 2020-06-08 | 2023-01-31 | 豪夫迈·罗氏有限公司 | 新型咪唑并-吡嗪衍生物 |
| EP4161931A1 (en) | 2020-06-09 | 2023-04-12 | F. Hoffmann-La Roche AG | Novel imidazopyrazine derivatives |
| EP4204090A1 (en) | 2020-08-31 | 2023-07-05 | F. Hoffmann-La Roche AG | Imidazole-pyrazole derivatives as antibacterials |
| EP4208454A1 (en) | 2020-09-01 | 2023-07-12 | F. Hoffmann-La Roche AG | Imidazole-pyrazole derivatives with anti-bacterial properties |
| WO2022049272A1 (en) | 2020-09-07 | 2022-03-10 | F. Hoffmann-La Roche Ag | Novel heterocyclic antibiotics |
| CN116829546A (zh) | 2021-02-07 | 2023-09-29 | 豪夫迈·罗氏有限公司 | 新型杂芳基取代的咪唑衍生物 |
| CN117715892A (zh) | 2021-07-06 | 2024-03-15 | 豪夫迈·罗氏有限公司 | 用于治疗细菌感染的季铵阳离子取代化合物 |
| EP4370514A1 (en) | 2021-07-15 | 2024-05-22 | F. Hoffmann-La Roche AG | Imidazole derivatives and their use as antibiotics |
| WO2023161316A1 (en) | 2022-02-25 | 2023-08-31 | F. Hoffmann-La Roche Ag | Zwitterionic antibacterial compounds |
| EP4568984A1 (en) * | 2022-08-09 | 2025-06-18 | F. Hoffmann-La Roche AG | Process for manufacturing an antibiotic macrocyclic peptide |
| CN119708122A (zh) * | 2023-09-27 | 2025-03-28 | 武汉人福创新药物研发中心有限公司 | 抗鲍曼不动杆菌的环肽及其应用 |
| WO2025162366A1 (zh) * | 2024-02-02 | 2025-08-07 | 武汉人福创新药物研发中心有限公司 | 抗鲍曼不动杆菌的含羧酸取代的环肽及其应用 |
Family Cites Families (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6660832B1 (en) * | 1999-08-20 | 2003-12-09 | Isis Pharmaceuticals, Inc. | Macrocyclic compounds and preparation methods thereof |
| DE10226921A1 (de) | 2002-06-17 | 2003-12-24 | Bayer Ag | Antibakterielle Amid-Makrozyklen |
| DE10234422A1 (de) | 2002-07-29 | 2004-02-12 | Bayer Ag | Antibakterielle Ester-Makrozyklen |
| ES2281692T3 (es) | 2002-08-23 | 2007-10-01 | Sloan-Kettering Institute For Cancer Research | Sintesis de epotilones, sus intermediarios, sus analogos y sus usos. |
| RU2462463C2 (ru) * | 2002-08-23 | 2012-09-27 | Слоан-Кеттеринг Инститьют Фор Кэнсер Рисерч | Синтез эпотилонов, их промежуточных продуктов, аналогов и их применения |
| US7476653B2 (en) | 2003-06-18 | 2009-01-13 | Tranzyme Pharma, Inc. | Macrocyclic modulators of the ghrelin receptor |
| WO2004111077A1 (en) | 2003-06-18 | 2004-12-23 | Tranzyme Pharma Inc. | Macrocyclic antagonists of the motilin receptor |
| US7491695B2 (en) | 2003-06-18 | 2009-02-17 | Tranzyme Pharma Inc. | Methods of using macrocyclic modulators of the ghrelin receptor |
| EP1498422A1 (de) | 2003-07-17 | 2005-01-19 | Jerini AG | C5a-Rezeptor-Antagonisten |
| DK1648922T3 (da) | 2003-07-31 | 2011-03-14 | Tranzyme Pharma Inc | Rumligt definerede makrocykliske forbindelser, der er anvendelige til opdagelse af lægemidler |
| CA2533820C (en) | 2003-07-31 | 2016-12-13 | Tranzyme Pharma | Spatially-defined macrocycles incorporating peptide bond surrogates |
| CA2540646A1 (en) | 2003-10-01 | 2005-04-14 | Bayer Healthcare Ag | Antibacterial amide macrocycles |
| EP1737884B1 (en) | 2004-03-19 | 2016-10-19 | The University Of Queensland | Alpha helical mimics, their uses and methods for their production |
| DE102004025731A1 (de) * | 2004-05-26 | 2005-12-15 | Bayer Healthcare Ag | Antibakterielle Amid-Makrozyklen III |
| US20060004185A1 (en) | 2004-07-01 | 2006-01-05 | Leese Richard A | Peptide antibiotics and peptide intermediates for their prepartion |
| SG158191A1 (en) | 2005-01-17 | 2010-01-29 | Jerini Ag | C5a receptor antagonists |
| DE102005014245A1 (de) | 2005-03-30 | 2006-10-05 | Aicuris Gmbh & Co. Kg | Antibakterielle Amid-Makrozyklen V |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| US8937080B2 (en) | 2007-02-08 | 2015-01-20 | Medivir Ab | Pyrimidine substituted macrocyclic HCV inhibitors |
| DE112009000300T5 (de) | 2008-02-08 | 2011-01-20 | Aileron Therapeutics, Inc., Cambridge | Therapeutische Peptidomimetische Makrocyclen |
| US8338565B2 (en) | 2008-08-20 | 2012-12-25 | Ensemble Therapeutics Corporation | Macrocyclic compounds for inhibition of tumor necrosis factor alpha |
| JP2013508409A (ja) | 2009-10-23 | 2013-03-07 | トランザイム・ファーマ，インコーポレイテッド | セリンプロテアーゼ酵素の大環状阻害剤 |
| CA2778990A1 (en) | 2009-10-30 | 2011-05-05 | Tranzyme Pharma, Inc. | Macrocyclic ghrelin receptor antagonists and inverse agonists and methods of using the same |
| SI2603600T1 (sl) | 2010-08-13 | 2019-04-30 | Aileron Therapeutics, Inc. | Peptidomimetični makrocikli |
| US20130123196A1 (en) | 2011-08-31 | 2013-05-16 | New York University | Thioether-, ether-, and alkylamine-linked hydrogen bond surrogate peptidomimetics |
| US8927500B2 (en) | 2012-02-15 | 2015-01-06 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles |
| CN103387601B (zh) | 2012-05-11 | 2017-01-11 | 南开大学 | 抗登革热病毒(denv)杂环肽类化合物及其制备方法和用途 |
| EP2922829B1 (en) | 2012-11-21 | 2021-08-11 | RQX Pharmaceuticals, Inc. | Macrocyclic broad spectrum antibiotics |
| US9493510B2 (en) | 2013-01-10 | 2016-11-15 | Noliva Therapeutics Llc | Peptidomimetic compounds |
| WO2016016291A1 (en) | 2014-07-30 | 2016-02-04 | Ferrer Internacional, S.A. | Arylhydrazides containing a 2-pyridone moiety as selective antibacterial agents |
| MY193014A (en) | 2015-10-27 | 2022-09-22 | Hoffmann La Roche | Peptide macrocycles against acinetobacter baumannii |
| EP3388444A1 (en) | 2017-04-10 | 2018-10-17 | F. Hoffmann-La Roche AG | Anti-bacterial peptide macrocycles and use thereof |
| US11505573B2 (en) | 2018-03-28 | 2022-11-22 | Hoffmann-La Roche Inc. | Peptide macrocycles against Acinetobacter baumannii |
| US11819532B2 (en) | 2018-04-23 | 2023-11-21 | Hoffmann-La Roche Inc. | Peptide macrocycles against Acinetobacter baumannii |
-
2016
- 2016-10-24 MY MYPI2018701615A patent/MY193014A/en unknown
- 2016-10-24 RS RS20200964A patent/RS60662B1/sr unknown
- 2016-10-24 AU AU2016347456A patent/AU2016347456B2/en active Active
- 2016-10-24 RU RU2018113426A patent/RU2729609C2/ru active
- 2016-10-24 JP JP2018521507A patent/JP7286317B2/ja active Active
- 2016-10-24 EP EP16785469.4A patent/EP3368544B1/en active Active
- 2016-10-24 PL PL16785469T patent/PL3368544T3/pl unknown
- 2016-10-24 MX MX2018005236A patent/MX2018005236A/es unknown
- 2016-10-24 SI SI201630882T patent/SI3368544T1/sl unknown
- 2016-10-24 HU HUE16785469A patent/HUE050053T2/hu unknown
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- 2016-10-24 ES ES16785469T patent/ES2811911T3/es active Active
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