JP2019523260A5 - - Google Patents
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- JP2019523260A5 JP2019523260A5 JP2019503646A JP2019503646A JP2019523260A5 JP 2019523260 A5 JP2019523260 A5 JP 2019523260A5 JP 2019503646 A JP2019503646 A JP 2019503646A JP 2019503646 A JP2019503646 A JP 2019503646A JP 2019523260 A5 JP2019523260 A5 JP 2019523260A5
- Authority
- JP
- Japan
- Prior art keywords
- amino acid
- item
- amino acids
- peptide agent
- amino
- 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.)
- Ceased
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- 108090000765 processed proteins & peptides Proteins 0.000 claims description 83
- 239000003795 chemical substances by application Substances 0.000 claims description 79
- 150000001413 amino acids Chemical class 0.000 claims description 77
- -1 cationic amino acids Chemical class 0.000 claims description 18
- 230000002209 hydrophobic effect Effects 0.000 claims description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 16
- 150000008574 D-amino acids Chemical class 0.000 claims description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 8
- AHLPHDHHMVZTML-SCSAIBSYSA-N D-Ornithine Chemical compound NCCC[C@@H](N)C(O)=O AHLPHDHHMVZTML-SCSAIBSYSA-N 0.000 claims description 7
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 claims description 6
- 150000003839 salts Chemical group 0.000 claims description 6
- 210000004899 c-terminal region Anatomy 0.000 claims description 5
- COLNVLDHVKWLRT-MRVPVSSYSA-N D-phenylalanine Chemical compound OC(=O)[C@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-MRVPVSSYSA-N 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 239000012472 biological sample Substances 0.000 claims description 4
- 201000010099 disease Diseases 0.000 claims description 4
- 208000035475 disorder Diseases 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 230000006540 mitochondrial respiration Effects 0.000 claims description 4
- OUYCCCASQSFEME-MRVPVSSYSA-N D-tyrosine Chemical compound OC(=O)[C@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-MRVPVSSYSA-N 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000001433 C-terminal amino-acid group Chemical group 0.000 claims description 2
- 125000001429 N-terminal alpha-amino-acid group Chemical group 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- 230000004065 mitochondrial dysfunction Effects 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 5
- 150000008575 L-amino acids Chemical class 0.000 claims 2
- 229940024606 amino acid Drugs 0.000 description 74
- 238000000034 method Methods 0.000 description 9
- 125000002091 cationic group Chemical group 0.000 description 8
- 238000009472 formulation Methods 0.000 description 6
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 5
- 230000002438 mitochondrial effect Effects 0.000 description 4
- SFVLTCAESLKEHH-WKAQUBQDSA-N (2s)-6-amino-2-[[(2s)-2-[[(2r)-2-amino-5-(diaminomethylideneamino)pentanoyl]amino]-3-(4-hydroxy-2,6-dimethylphenyl)propanoyl]amino]-n-[(2s)-1-amino-1-oxo-3-phenylpropan-2-yl]hexanamide Chemical compound CC1=CC(O)=CC(C)=C1C[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(N)=O)CC1=CC=CC=C1 SFVLTCAESLKEHH-WKAQUBQDSA-N 0.000 description 3
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 3
- 108010033284 arginyl-2,'6'-dimethyltyrosyl-lysyl-phenylalaninamide Proteins 0.000 description 3
- ZGSPNIOCEDOHGS-UHFFFAOYSA-L disodium [3-[2,3-di(octadeca-9,12-dienoyloxy)propoxy-oxidophosphoryl]oxy-2-hydroxypropyl] 2,3-di(octadeca-9,12-dienoyloxy)propyl phosphate Chemical compound [Na+].[Na+].CCCCCC=CCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COP([O-])(=O)OCC(O)COP([O-])(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COC(=O)CCCCCCCC=CCC=CCCCCC ZGSPNIOCEDOHGS-UHFFFAOYSA-L 0.000 description 3
- ROHFNLRQFUQHCH-RXMQYKEDSA-N D-leucine Chemical compound CC(C)C[C@@H](N)C(O)=O ROHFNLRQFUQHCH-RXMQYKEDSA-N 0.000 description 2
- 241001559542 Hippocampus hippocampus Species 0.000 description 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 description 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 206010053961 Mitochondrial toxicity Diseases 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 229940124280 l-arginine Drugs 0.000 description 2
- 231100000296 mitochondrial toxicity Toxicity 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Chemical group 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000037050 permeability transition Effects 0.000 description 2
- 230000000241 respiratory effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
- 229910052717 sulfur Chemical group 0.000 description 2
- 239000011593 sulfur Chemical group 0.000 description 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 1
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 description 1
- SJZRECIVHVDYJC-UHFFFAOYSA-M 4-hydroxybutyrate Chemical compound OCCCC([O-])=O SJZRECIVHVDYJC-UHFFFAOYSA-M 0.000 description 1
- ODKSFYDXXFIFQN-SCSAIBSYSA-N D-arginine Chemical compound OC(=O)[C@H](N)CCCNC(N)=N ODKSFYDXXFIFQN-SCSAIBSYSA-N 0.000 description 1
- KDXKERNSBIXSRK-RXMQYKEDSA-N D-lysine Chemical compound NCCCC[C@@H](N)C(O)=O KDXKERNSBIXSRK-RXMQYKEDSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 210000003470 mitochondria Anatomy 0.000 description 1
- 230000004898 mitochondrial function Effects 0.000 description 1
- 125000001620 monocyclic carbocycle group Chemical group 0.000 description 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 description 1
- 230000036284 oxygen consumption Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662321168P | 2016-04-11 | 2016-04-11 | |
| US62/321,168 | 2016-04-11 | ||
| PCT/US2017/026869 WO2017180535A1 (en) | 2016-04-11 | 2017-04-10 | Chiral peptides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2019523260A JP2019523260A (ja) | 2019-08-22 |
| JP2019523260A5 true JP2019523260A5 (enExample) | 2020-03-12 |
Family
ID=60042852
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019503646A Ceased JP2019523260A (ja) | 2016-04-11 | 2017-04-10 | キラルペプチド |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10870678B2 (enExample) |
| EP (1) | EP3442990A4 (enExample) |
| JP (1) | JP2019523260A (enExample) |
| CN (1) | CN109563131A (enExample) |
| AU (2) | AU2017249218B2 (enExample) |
| CA (1) | CA3020393A1 (enExample) |
| WO (1) | WO2017180535A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7606966B2 (ja) | 2018-12-18 | 2024-12-26 | ステルス バイオセラピューティクス インコーポレイテッド | ミトコンドリア病を標的とするアナログ |
| KR20210093957A (ko) | 2018-12-18 | 2021-07-28 | 스텔스 바이오테라퓨틱스 코포레이션 | 미토콘드리아-표적화 펩타이드 |
| US12215173B2 (en) | 2019-08-07 | 2025-02-04 | HUMANWELL PHARMACEUTICAL US, Inc. | Kappa opioid receptor peptide amide ligands |
| US20210255196A1 (en) * | 2020-01-17 | 2021-08-19 | Waters Technologies Corporation | Low binding surfaces for peptide mapping |
| KR20220151628A (ko) * | 2020-03-06 | 2022-11-15 | 알레그로 파마슈티칼스, 엘엘씨 | 미토콘드리아 기능의 손상을 개선하거나 감소시키기 위한 치료 |
| AU2020454871A1 (en) | 2020-06-25 | 2023-01-19 | Humanwell Pharmaceutical US | Peptides for treatment of medical disorders |
| CN117881411A (zh) | 2021-06-01 | 2024-04-12 | 艾迪雅生物有限责任公司 | 用于眼部药物的延长释放药物递送系统和使用方法 |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2865385B1 (en) | 2003-02-04 | 2016-11-16 | Cornell Research Foundation, Inc. | Uses of aromatic-cationic peptide |
| EP2197451A1 (en) | 2007-06-07 | 2010-06-23 | Institute For Hepatitis And Virus Research | 2-amino-2,7-dideoxy-alpha-d-glycero-d-gluco-heptopyranosyl inhibitors of positive sense single-stranded rna envelope viruses |
| JP5697450B2 (ja) * | 2007-10-02 | 2015-04-08 | マリーナ バイオテック，インコーポレイテッド | 核酸の送達のためのリポペプチド |
| JP5677096B2 (ja) | 2008-02-26 | 2015-02-25 | コーネル ユニヴァーシティー | 急性腎障害を予防および治療するための方法 |
| JP5238297B2 (ja) | 2008-03-04 | 2013-07-17 | シャープ株式会社 | 認証方法および入力装置 |
| EP3563862B1 (en) * | 2009-03-20 | 2021-05-05 | The General Hospital Corporation d/b/a Massachusetts General Hospital | D-arg-2'6'-dimethyltyrosine-lys-phe-nh2 for use in the prevention of secondary complications of burn injuries |
| CN105031605A (zh) * | 2009-08-12 | 2015-11-11 | 康奈尔大学 | 预防或治疗代谢综合症的方法 |
| EP3150215A1 (en) | 2009-08-24 | 2017-04-05 | Stealth Peptides International, Inc. | Methods and compositions for preventing or treating opthalmic conditions |
| CN102711785A (zh) | 2009-10-05 | 2012-10-03 | 康奈尔大学 | 预防或治疗心力衰竭的方法 |
| EP3100739A1 (en) | 2009-12-31 | 2016-12-07 | Stealth Peptides International, Inc. | Methods for performing a coronary artery bypass graft procedure |
| CN104725472A (zh) | 2010-01-25 | 2015-06-24 | 康奈尔大学 | 芳香族阳离子肽及其用途 |
| WO2011106717A1 (en) | 2010-02-26 | 2011-09-01 | University Of Florida Research Foundation, Inc. | Mitochondrial-targeted antioxidants protect against mechanical ventilation-induced diaphragm dysfunction and skeletal muscle atrophy |
| EP3290433A1 (en) | 2010-05-03 | 2018-03-07 | Stealth Peptides International, Inc. | Aromatic-cationic peptides and uses of same |
| CN105879008A (zh) | 2010-07-09 | 2016-08-24 | 康德生物医疗技术公司 | 预防或治疗缺血/再灌注损伤之后无复流的方法 |
| EP3488941A1 (en) | 2011-03-24 | 2019-05-29 | Cornell University | Aromatic-cationic peptides and uses of same |
| CN103764159A (zh) | 2011-06-14 | 2014-04-30 | 康肽德生物医药技术有限公司 | 芳香族阳离子肽及其用途 |
| CN107496899A (zh) | 2011-09-29 | 2017-12-22 | 梅约医学教育与研究基金会 | 芳族阳离子肽和使用它们的方法 |
| WO2013059071A1 (en) | 2011-10-17 | 2013-04-25 | Cornell University | Aromatic-cationic peptides and uses of same |
| EP2788013A4 (en) * | 2011-12-09 | 2015-08-19 | Stealth Peptides Int Inc | AROMATIC-CATIONIC PEPTIDES AND USES THEREOF |
| EP3078384A1 (en) | 2012-02-22 | 2016-10-12 | Stealth Peptides International, Inc. | Methods and compositions for preventing or treating ophthalmic conditions |
| WO2013126775A1 (en) | 2012-02-23 | 2013-08-29 | Cornell University | Aromatic-cationic peptides and uses of same |
| EP3170506B1 (en) | 2012-03-30 | 2018-05-16 | Stealth Peptides International, Inc. | Methods and compositions for the prevention and treatment neuropathy |
| WO2013155334A1 (en) | 2012-04-12 | 2013-10-17 | Stealth Peptides International, Inc. | Aromatic-cationic peptides and uses of same |
| JP6272853B2 (ja) * | 2012-07-11 | 2018-01-31 | ジェムバックス アンド カエル カンパニー，リミティド | 細胞透過性ペプチド、それを含んだコンジュゲート、及びそれを含んだ組成物 |
| US20140034183A1 (en) | 2012-07-31 | 2014-02-06 | Viz Enterprises, Llc | Cap assembly for dispensing a dispensable component and method of making and using the same |
| MX2015005102A (es) | 2012-10-22 | 2016-02-09 | Stealth Peptides Int Inc | Metodos para la reduccion de los riesgos asociados con el insuficiencia cardiaca y factores asociado con el mismo. |
| WO2014088631A1 (en) | 2012-12-06 | 2014-06-12 | Stealth Peptides International, Inc. | Peptide therapeutics and methods for using same |
| CN117752766A (zh) | 2013-03-01 | 2024-03-26 | 康德生物医疗有限公司 | 治疗线粒体疾病的方法 |
| WO2014165607A2 (en) | 2013-04-02 | 2014-10-09 | Stealth Peptides International, Inc. | Aromatic-cationic peptide formulations, compositions and methods of use |
| US20160193278A1 (en) | 2013-08-01 | 2016-07-07 | Stealth Biotherapeutics Corp | Methods and compositions for preventing or treating leber's hereditary optic neuropathy |
| US20160175379A1 (en) | 2013-08-12 | 2016-06-23 | Stealth Bio Therapeutics Corp | Combination therapy for the treatment of ischemia-reperfusion injury |
| EP3049096B1 (en) | 2013-09-27 | 2018-12-12 | Cornell University | Use of aromatic-cationic peptides to treat niemann-pick disease characterised by cholesterol-induced mitochondrial dysfunction |
| CN106163537A (zh) * | 2013-09-30 | 2016-11-23 | 康奈尔大学 | 心磷脂靶向肽抑制β‑淀粉样蛋白寡聚物毒性 |
| JP2016539931A (ja) | 2013-10-23 | 2016-12-22 | 株式会社カネカ | テトラペプチド化合物及びその製造方法 |
| EP3077049B1 (en) | 2013-12-02 | 2019-06-19 | Stealth BioTherapeutics Corp | Compositions for use in treating vitiligo |
| CN112457368A (zh) | 2013-12-27 | 2021-03-09 | 康德生物医疗技术公司 | 药学相关的芳香族阳离子肽 |
| EP2913287B1 (en) | 2014-02-26 | 2018-01-03 | Otis Elevator Company | Governor for controlling the speed of a hoisted object relative to a guide member |
| CA2942143A1 (en) | 2014-03-03 | 2015-09-11 | Stealth Biotherapeutics Corp | Pharmaceutically relevant aromatic-cationic peptides and methods of generating the same |
| WO2016004441A1 (en) | 2014-07-03 | 2016-01-07 | Stealth Peptides International, Inc. | Methods for the prevention or treatment of acute myocardial infarction injury |
-
2017
- 2017-04-10 AU AU2017249218A patent/AU2017249218B2/en not_active Ceased
- 2017-04-10 WO PCT/US2017/026869 patent/WO2017180535A1/en not_active Ceased
- 2017-04-10 CN CN201780031671.6A patent/CN109563131A/zh active Pending
- 2017-04-10 CA CA3020393A patent/CA3020393A1/en not_active Abandoned
- 2017-04-10 US US16/092,093 patent/US10870678B2/en not_active Expired - Fee Related
- 2017-04-10 JP JP2019503646A patent/JP2019523260A/ja not_active Ceased
- 2017-04-10 EP EP17782934.8A patent/EP3442990A4/en not_active Withdrawn
-
2020
- 2020-09-03 US US17/011,264 patent/US20200407395A1/en not_active Abandoned
- 2020-10-29 AU AU2020260489A patent/AU2020260489A1/en not_active Abandoned
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