JP2015506960A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015506960A5 JP2015506960A5 JP2014555666A JP2014555666A JP2015506960A5 JP 2015506960 A5 JP2015506960 A5 JP 2015506960A5 JP 2014555666 A JP2014555666 A JP 2014555666A JP 2014555666 A JP2014555666 A JP 2014555666A JP 2015506960 A5 JP2015506960 A5 JP 2015506960A5
- Authority
- JP
- Japan
- Prior art keywords
- pro
- alanine
- isoleucine
- methionine
- valine
- 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
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 18
- 108090000765 processed proteins & peptides Proteins 0.000 claims 18
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims 17
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 claims 17
- 229960000310 isoleucine Drugs 0.000 claims 17
- 229930182817 methionine Natural products 0.000 claims 17
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims 16
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 16
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 16
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 16
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims 16
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 16
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims 16
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims 16
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims 16
- 239000004473 Threonine Substances 0.000 claims 16
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims 16
- 235000004279 alanine Nutrition 0.000 claims 16
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims 16
- 239000004474 valine Substances 0.000 claims 16
- 239000000816 peptidomimetic Substances 0.000 claims 13
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 10
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 claims 10
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 10
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims 9
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 claims 8
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims 8
- 239000004471 Glycine Substances 0.000 claims 8
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims 8
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 8
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 8
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 8
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims 8
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 8
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 8
- 239000004472 Lysine Substances 0.000 claims 8
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 claims 8
- 235000009582 asparagine Nutrition 0.000 claims 8
- 229960001230 asparagine Drugs 0.000 claims 8
- 235000003704 aspartic acid Nutrition 0.000 claims 8
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims 8
- 235000013922 glutamic acid Nutrition 0.000 claims 8
- 239000004220 glutamic acid Substances 0.000 claims 8
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims 8
- 235000018977 lysine Nutrition 0.000 claims 8
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 8
- QNAYBMKLOCPYGJ-UWTATZPHSA-N D-alanine Chemical compound C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims 6
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims 6
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- KSPIYJQBLVDRRI-UHFFFAOYSA-N N-methylisoleucine Chemical compound CCC(C)C(NC)C(O)=O KSPIYJQBLVDRRI-UHFFFAOYSA-N 0.000 claims 2
- 102000004196 processed proteins & peptides Human genes 0.000 claims 2
- 239000004475 Arginine Substances 0.000 claims 1
- 208000024172 Cardiovascular disease Diseases 0.000 claims 1
- XUJNEKJLAYXESH-UWTATZPHSA-N D-Cysteine Chemical compound SC[C@@H](N)C(O)=O XUJNEKJLAYXESH-UWTATZPHSA-N 0.000 claims 1
- 125000000030 D-alanine group Chemical group [H]N([H])[C@](C([H])([H])[H])(C(=O)[*])[H] 0.000 claims 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims 1
- 125000000539 amino acid group Chemical group 0.000 claims 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 1
- 235000018417 cysteine Nutrition 0.000 claims 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261592887P | 2012-01-31 | 2012-01-31 | |
| US61/592,887 | 2012-01-31 | ||
| PCT/US2013/023808 WO2013116312A1 (en) | 2012-01-31 | 2013-01-30 | ß-ARRESTIN EFFECTORS AND COMPOSITIONS AND METHODS OF USE THEREOF |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015506960A JP2015506960A (ja) | 2015-03-05 |
| JP2015506960A5 true JP2015506960A5 (enExample) | 2016-03-10 |
| JP6225121B2 JP6225121B2 (ja) | 2017-11-01 |
Family
ID=48870731
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014555666A Expired - Fee Related JP6225121B2 (ja) | 2012-01-31 | 2013-01-30 | β−アレスチンエフェクターおよび組成物ならびにそれらの使用方法 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8946142B2 (enExample) |
| EP (1) | EP2809337A4 (enExample) |
| JP (1) | JP6225121B2 (enExample) |
| KR (1) | KR20140132340A (enExample) |
| CN (1) | CN104168907A (enExample) |
| AU (1) | AU2013215269A1 (enExample) |
| BR (1) | BR112014018709A8 (enExample) |
| CA (1) | CA2862933A1 (enExample) |
| EA (1) | EA201491455A1 (enExample) |
| HK (1) | HK1203379A1 (enExample) |
| IL (1) | IL233826A0 (enExample) |
| MX (1) | MX2014009233A (enExample) |
| NZ (1) | NZ627995A (enExample) |
| WO (1) | WO2013116312A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA201491455A1 (ru) * | 2012-01-31 | 2015-01-30 | Тревена, Инк. | ЭФФЕКТОРЫ β-АРРЕСТИНА, КОМПОЗИЦИИ, ИХ СОДЕРЖАЩИЕ, И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
| EP3208861A1 (en) | 2016-02-19 | 2017-08-23 | Novaled GmbH | Electron transport layer comprising a matrix compound mixture for an organic light-emitting diode (oled) |
| US11116737B1 (en) | 2020-04-10 | 2021-09-14 | University Of Georgia Research Foundation, Inc. | Methods of using probenecid for treatment of coronavirus infections |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3925345A (en) * | 1974-05-10 | 1975-12-09 | Francis Merlin Bumpus | (sar' 1',thr' 8'+9 angiotensin ii as an angiotensin antagonist |
| US3932624A (en) | 1974-06-17 | 1976-01-13 | Morton-Norwich Products, Inc. | Method for prolonging the inhibitory effect of saralasin on angiotensin II |
| JPS5825980B2 (ja) | 1976-02-12 | 1983-05-31 | ヤマサ醤油株式会社 | サイクリックヌクレオチドの定量法 |
| US4547489A (en) | 1984-06-11 | 1985-10-15 | Ortho Pharmaceutical Corporation | Conformationally restricted thymopentin-like compounds |
| US5182264A (en) | 1986-03-07 | 1993-01-26 | Schering Corporation | Angiotensin II receptor blockers as antiglaucoma agents |
| EP0358418B1 (en) * | 1988-09-05 | 1992-12-16 | Sankyo Company Limited | Cyclic peptide, its preparation and its use in the treatment of cardiovascular disorders |
| GB8822483D0 (en) | 1988-09-24 | 1988-10-26 | Medical Res Council | Developments relating to mas oncogene |
| US5401629A (en) | 1990-08-07 | 1995-03-28 | The Salk Institute Biotechnology/Industrial Associates, Inc. | Assay methods and compositions useful for measuring the transduction of an intracellular signal |
| CA2090401A1 (en) | 1990-08-27 | 1992-02-28 | Deborah A. Rathjen | Method of treating viral infection |
| AU1256692A (en) | 1991-02-06 | 1992-09-07 | Schering Corporation | Combination of an angiotensin II antagonist or renin inhibitor with a neutral endopeptidase inhibitor |
| PT730465E (pt) | 1993-09-24 | 2002-06-28 | Univ Southern California | Utilizacao de angiotensina iii e de analogos desta em cicatrizacao de tecidos |
| US5955430A (en) | 1993-09-24 | 1999-09-21 | University Of Southern California | Use of angiotensin II fragments and analogs thereof in tissue repair |
| US5958884A (en) | 1997-04-11 | 1999-09-28 | The Brigham And Women's Hospital, Inc. | Compositions and methods for treating erectile dysfunction |
| US6165978A (en) | 1997-12-12 | 2000-12-26 | University Of Southern California | Wound healing composition |
| US20040214836A1 (en) | 1998-05-29 | 2004-10-28 | Cheresh David A. | Method of treatment of myocardial infarction |
| US6362371B1 (en) | 1998-06-08 | 2002-03-26 | Advanced Medicine, Inc. | β2- adrenergic receptor agonists |
| US20050202029A1 (en) | 2003-10-03 | 2005-09-15 | The Board Of Trustees Of The Leland Stanford Junior University | Family of cystatin-related chemoattractant proteins |
| US20070286863A1 (en) | 2006-05-17 | 2007-12-13 | Christopher Sinal | CMKLR regulation of adipogenesis and adipocyte metabolic function |
| WO2008130217A1 (en) | 2006-08-08 | 2008-10-30 | Applied Nanosystems B.V. | Cyclic angiotensin analogs |
| GB0705488D0 (en) | 2007-03-22 | 2007-05-02 | Isis Innovation | Treatment of inflammation and/or endotoxic shock |
| US8038992B2 (en) | 2008-05-10 | 2011-10-18 | The Board Of Trustees Of The Leland Stanford Junior University | Target for regulating multiple sclerosis |
| US20100092974A1 (en) | 2008-08-15 | 2010-04-15 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for screening for modulators of ccrl2 |
| CN102333536B (zh) * | 2008-12-29 | 2014-08-13 | 特维那公司 | β-抑制蛋白效应器和组合物以及其应用方法 |
| US8293925B2 (en) | 2009-09-21 | 2012-10-23 | Chemocentryx, Inc. | Pyrrolidinone carboxamide derivatives |
| JP5925771B2 (ja) * | 2010-06-24 | 2016-05-25 | トラスティーズ オブ タフツ カレッジ | ナイアシン模倣体、およびその使用方法 |
| EA201491455A1 (ru) * | 2012-01-31 | 2015-01-30 | Тревена, Инк. | ЭФФЕКТОРЫ β-АРРЕСТИНА, КОМПОЗИЦИИ, ИХ СОДЕРЖАЩИЕ, И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
-
2013
- 2013-01-30 EA EA201491455A patent/EA201491455A1/ru unknown
- 2013-01-30 KR KR20147023251A patent/KR20140132340A/ko not_active Withdrawn
- 2013-01-30 CN CN201380014614.9A patent/CN104168907A/zh active Pending
- 2013-01-30 AU AU2013215269A patent/AU2013215269A1/en not_active Abandoned
- 2013-01-30 MX MX2014009233A patent/MX2014009233A/es unknown
- 2013-01-30 BR BR112014018709A patent/BR112014018709A8/pt active Search and Examination
- 2013-01-30 HK HK15103956.9A patent/HK1203379A1/xx unknown
- 2013-01-30 JP JP2014555666A patent/JP6225121B2/ja not_active Expired - Fee Related
- 2013-01-30 WO PCT/US2013/023808 patent/WO2013116312A1/en not_active Ceased
- 2013-01-30 EP EP13743852.9A patent/EP2809337A4/en not_active Withdrawn
- 2013-01-30 NZ NZ627995A patent/NZ627995A/en not_active IP Right Cessation
- 2013-01-30 CA CA2862933A patent/CA2862933A1/en not_active Abandoned
- 2013-01-31 US US13/755,637 patent/US8946142B2/en not_active Expired - Fee Related
-
2014
- 2014-07-27 IL IL233826A patent/IL233826A0/en unknown
- 2014-12-22 US US14/579,956 patent/US20150105316A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL262805B2 (en) | Agonist agents of cd47 inducing programmed cell death and their use in the treatments of diseases associated with defects in programmed cell death | |
| MX2020010806A (es) | Peptidos anti-inflamatorios y usos de los mismos. | |
| PE20190355A1 (es) | Derivado de glucagon, conjugado del mismo, composicion que comprende el mismo y uso terapeutico del mismo | |
| IL276294B2 (en) | Human CD30 ligand antigen-binding proteins | |
| PE20120358A1 (es) | Mutantes fgf21 y usos de los mismos | |
| CA2489227A1 (en) | Hla-a24-restricted cancer antigen peptides | |
| NZ628987A (en) | Extended recombinant polypeptides and compositions comprising same | |
| JP2014510518A5 (enExample) | ||
| RU2011100126A (ru) | Применение мимотопов для лечения бетта-амилоидозов | |
| WO2014080376A3 (en) | Pro-pigmenting peptides | |
| JP2006525288A5 (enExample) | ||
| RU2011100125A (ru) | Соединения для лечения амилоидозов | |
| RU2016140627A (ru) | Бета-лактамазы с улучшенными свойствами для лечения | |
| IL276170B2 (en) | Lipid-modified relaxin B peptide chains and their medical use | |
| JP2019533722A5 (enExample) | ||
| NZ579566A (en) | Modified fgf-21 polypeptides and their uses | |
| RU2009141595A (ru) | Пептиды тем8 и содержащие их вакцины | |
| JP2017534675A5 (enExample) | ||
| WO2017032856A3 (en) | Compounds for inducing tissue formation and uses thereof | |
| JP2015506960A5 (enExample) | ||
| FI3737399T3 (fi) | ATF5-peptidivariantit ja niiden käytöt | |
| JP2013541528A5 (enExample) | ||
| CA3010982A1 (en) | Alpha chain of the high-affinity ige receptor (fceria) | |
| NZ736652A (en) | Short synthetic peptide for treating diseases and/or conditions related to angiogenesis | |
| EA201492068A1 (ru) | Гидрохлоридная соль пептида и ее применение в комбинации с другими пептидами в иммунотерапии |