JP2020143066A5 - - Google Patents
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- JP2020143066A5 JP2020143066A5 JP2020075470A JP2020075470A JP2020143066A5 JP 2020143066 A5 JP2020143066 A5 JP 2020143066A5 JP 2020075470 A JP2020075470 A JP 2020075470A JP 2020075470 A JP2020075470 A JP 2020075470A JP 2020143066 A5 JP2020143066 A5 JP 2020143066A5
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- JP
- Japan
- Prior art keywords
- absent
- aib
- glu
- substituted
- unsubstituted
- 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.)
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- 108090000765 processed proteins & peptides Proteins 0.000 claims 39
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 27
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 claims 12
- 239000008194 pharmaceutical composition Substances 0.000 claims 8
- ODKSFYDXXFIFQN-UHFFFAOYSA-N Arginine Chemical compound OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 7
- 239000002253 acid Substances 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 150000001720 carbohydrates Chemical class 0.000 claims 7
- 239000004094 surface-active agent Substances 0.000 claims 7
- 125000004171 alkoxy aryl group Chemical group 0.000 claims 6
- 150000001413 amino acids Chemical class 0.000 claims 6
- 125000006239 protecting group Chemical group 0.000 claims 6
- 150000003431 steroids Chemical class 0.000 claims 5
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims 3
- SCIFESDRCALIIM-VIFPVBQESA-N N-methyl-L-phenylalanine Chemical compound C[NH2+][C@H](C([O-])=O)CC1=CC=CC=C1 SCIFESDRCALIIM-VIFPVBQESA-N 0.000 claims 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- -1 linker amino acid Chemical class 0.000 claims 3
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 3
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- QNAYBMKLOCPYGJ-UWTATZPHSA-N D-alanine Chemical compound C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 2
- 125000000539 amino acid group Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000000524 functional group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- 108010087791 pyroglutamylhistidine Proteins 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 2
- PPIIOFOWNPKGDP-IBEHDNSVSA-N (2R,3R,4S,5S,6R)-2-decyl-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound C(CCCCCCCCC)[C@]1(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO PPIIOFOWNPKGDP-IBEHDNSVSA-N 0.000 claims 1
- QYICFPNWZRKTDX-QMCAAQAGSA-N (2R,3R,4S,5S,6R)-2-hexadecyl-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound C(CCCCCCCCCCCCCCC)[C@]1(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO QYICFPNWZRKTDX-QMCAAQAGSA-N 0.000 claims 1
- KJFNPHUIPRFEEI-GNADVCDUSA-N (2R,3R,4S,5S,6R)-6-(hydroxymethyl)-2-octadecyloxane-2,3,4,5-tetrol Chemical compound C(CCCCCCCCCCCCCCCCC)[C@]1(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO KJFNPHUIPRFEEI-GNADVCDUSA-N 0.000 claims 1
- NZRRQTWJVNMISZ-OUUBHVDSSA-N (2R,3R,4S,5S,6R)-6-(hydroxymethyl)-2-tetradecyloxane-2,3,4,5-tetrol Chemical compound C(CCCCCCCCCCCCC)[C@]1(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO NZRRQTWJVNMISZ-OUUBHVDSSA-N 0.000 claims 1
- OOUZMUGHCDPALG-VZGLXOSZSA-N (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxy-6-octadecyloxane-2-carboxylic acid Chemical compound C(CCCCCCCCCCCCCCCCC)[C@]1(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O1)C(=O)O OOUZMUGHCDPALG-VZGLXOSZSA-N 0.000 claims 1
- ALYRJYOQVDSVBI-UYTYNIKBSA-N (2r,3r,4s,5s,6r)-2-dodecyl-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound CCCCCCCCCCCC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O ALYRJYOQVDSVBI-UYTYNIKBSA-N 0.000 claims 1
- KITVZRVDBQNSDD-RKQHYHRCSA-N (2r,3r,4s,5s,6r)-6-(hydroxymethyl)-2-octyloxane-2,3,4,5-tetrol Chemical compound CCCCCCCC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O KITVZRVDBQNSDD-RKQHYHRCSA-N 0.000 claims 1
- CLRWZDLKTLJVEF-ZXPJVPCYSA-N (2s,3s,4s,5r,6r)-3,4,5,6-tetrahydroxy-6-octyloxane-2-carboxylic acid Chemical compound CCCCCCCC[C@@]1(O)O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O CLRWZDLKTLJVEF-ZXPJVPCYSA-N 0.000 claims 1
- FCQMGQZEJINDNN-KVIJGQROSA-N (2s,3s,4s,5r,6r)-3,4,5,6-tetrahydroxy-6-tetradecyloxane-2-carboxylic acid Chemical compound CCCCCCCCCCCCCC[C@@]1(O)O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O FCQMGQZEJINDNN-KVIJGQROSA-N 0.000 claims 1
- KZPCPTBVXOXXOY-GRYWWWGRSA-N (2s,3s,4s,5r,6r)-6-decyl-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid Chemical compound CCCCCCCCCC[C@@]1(O)O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O KZPCPTBVXOXXOY-GRYWWWGRSA-N 0.000 claims 1
- ZWSXIJDIJOZWHM-YIUJWAEMSA-N (2s,3s,4s,5r,6r)-6-hexadecyl-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid Chemical compound CCCCCCCCCCCCCCCC[C@@]1(O)O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O ZWSXIJDIJOZWHM-YIUJWAEMSA-N 0.000 claims 1
- MTCFGRXMJLQNBG-UWTATZPHSA-N D-Serine Chemical compound OC[C@@H](N)C(O)=O MTCFGRXMJLQNBG-UWTATZPHSA-N 0.000 claims 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 1
- 206010022489 Insulin Resistance Diseases 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000007306 functionalization reaction Methods 0.000 claims 1
- 229930182470 glycoside Natural products 0.000 claims 1
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims 1
- 230000000302 ischemic effect Effects 0.000 claims 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 1
- 230000004580 weight loss Effects 0.000 claims 1
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022127266A JP2022172128A (ja) | 2014-05-28 | 2022-08-09 | インスリン抵抗性のための改善されたペプチド医薬品 |
| JP2024067692A JP2024102119A (ja) | 2014-05-28 | 2024-04-18 | インスリン抵抗性のための改善されたペプチド医薬品 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462004156P | 2014-05-28 | 2014-05-28 | |
| US62/004,156 | 2014-05-28 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016569787A Division JP6697807B2 (ja) | 2014-05-28 | 2015-05-28 | インスリン抵抗性のための改善されたペプチド医薬品 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022127266A Division JP2022172128A (ja) | 2014-05-28 | 2022-08-09 | インスリン抵抗性のための改善されたペプチド医薬品 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2020143066A JP2020143066A (ja) | 2020-09-10 |
| JP2020143066A5 true JP2020143066A5 (OSRAM) | 2020-11-05 |
Family
ID=54699825
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016569787A Active JP6697807B2 (ja) | 2014-05-28 | 2015-05-28 | インスリン抵抗性のための改善されたペプチド医薬品 |
| JP2020075470A Pending JP2020143066A (ja) | 2014-05-28 | 2020-04-21 | インスリン抵抗性のための改善されたペプチド医薬品 |
| JP2022127266A Pending JP2022172128A (ja) | 2014-05-28 | 2022-08-09 | インスリン抵抗性のための改善されたペプチド医薬品 |
| JP2024067692A Pending JP2024102119A (ja) | 2014-05-28 | 2024-04-18 | インスリン抵抗性のための改善されたペプチド医薬品 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016569787A Active JP6697807B2 (ja) | 2014-05-28 | 2015-05-28 | インスリン抵抗性のための改善されたペプチド医薬品 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022127266A Pending JP2022172128A (ja) | 2014-05-28 | 2022-08-09 | インスリン抵抗性のための改善されたペプチド医薬品 |
| JP2024067692A Pending JP2024102119A (ja) | 2014-05-28 | 2024-04-18 | インスリン抵抗性のための改善されたペプチド医薬品 |
Country Status (18)
| Country | Link |
|---|---|
| US (5) | US9856306B2 (OSRAM) |
| EP (2) | EP4397374A3 (OSRAM) |
| JP (4) | JP6697807B2 (OSRAM) |
| KR (3) | KR20230084337A (OSRAM) |
| CN (5) | CN106661097A (OSRAM) |
| AU (3) | AU2015266854B2 (OSRAM) |
| BR (1) | BR112016027595B1 (OSRAM) |
| CA (1) | CA2949701C (OSRAM) |
| DK (1) | DK3155017T3 (OSRAM) |
| ES (1) | ES2985732T3 (OSRAM) |
| FI (1) | FI3155017T3 (OSRAM) |
| HU (1) | HUE066179T2 (OSRAM) |
| IL (3) | IL285613B2 (OSRAM) |
| MX (2) | MX384236B (OSRAM) |
| NZ (2) | NZ726623A (OSRAM) |
| PL (1) | PL3155017T3 (OSRAM) |
| PT (1) | PT3155017T (OSRAM) |
| WO (1) | WO2015184177A1 (OSRAM) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012158962A2 (en) | 2011-05-18 | 2012-11-22 | Eumederis Pharmaceuticals, Inc. | Improved peptide pharmaceuticals |
| KR20240110072A (ko) | 2011-05-18 | 2024-07-12 | 메더리스 다이어비티즈, 엘엘씨 | 인슐린 저항성에 대한 개선된 펩티드 제약 |
| WO2014081864A1 (en) * | 2012-11-20 | 2014-05-30 | Eumederis Pharmaceuticals, Inc. | Improved peptide pharmaceuticals |
| JP6525456B2 (ja) * | 2012-11-20 | 2019-06-05 | メデリス ダイアビーティーズ，エルエルシー | インスリン抵抗性のための改善されたペプチド製剤 |
| US9856306B2 (en) | 2014-05-28 | 2018-01-02 | Spitfire Pharma, Inc. | Peptide pharmaceuticals for insulin resistance |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| WO2019018350A1 (en) | 2017-07-17 | 2019-01-24 | Keith Roizman | TOPICAL ADMINISTRATION OF THERAPEUTIC AGENTS COMPRISING CELL PENETRATION PEPTIDES, FOR USE IN THE TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND OTHER OCULAR DISEASES |
| EP3735295B1 (en) | 2018-01-03 | 2024-08-21 | Mederis Diabetes, LLC | Improved peptide pharmaceuticals for treatment of nash and other disorders |
| KR20220143923A (ko) * | 2020-02-21 | 2022-10-25 | 스핏파이어 파마, 엘엘씨 | Glp-1r 및 gcgr 효능제, 제형 및 사용 방법 |
| WO2022125598A1 (en) * | 2020-12-07 | 2022-06-16 | Spitfire Pharma Llc | Therapeutic regimens and methods for lowering blood glucose and or body weight using glp-1r and gcgr balanced agonists |
| US12171806B2 (en) | 2021-09-28 | 2024-12-24 | Spitfire Pharma Llc | Therapeutic regimens and methods for lowering blood glucose and/or body weight using GLP-1R and GCGR balanced agonists |
| CN113461747B (zh) * | 2021-07-12 | 2023-02-03 | 吉林化工学院 | 刺玫果中2个具有降血糖活性的化合物 |
| WO2024239961A1 (zh) * | 2023-05-24 | 2024-11-28 | 联邦生物科技(珠海横琴)有限公司 | 一种胰岛素衍生物及其应用 |
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| JP6525456B2 (ja) | 2012-11-20 | 2019-06-05 | メデリス ダイアビーティーズ，エルエルシー | インスリン抵抗性のための改善されたペプチド製剤 |
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| US9856306B2 (en) | 2014-05-28 | 2018-01-02 | Spitfire Pharma, Inc. | Peptide pharmaceuticals for insulin resistance |
| CA3093383A1 (en) * | 2014-10-24 | 2016-04-28 | Merck Sharp & Dohme Corp. | Co-agonists of the glucagon and glp-1 receptors |
| EP3735295B1 (en) * | 2018-01-03 | 2024-08-21 | Mederis Diabetes, LLC | Improved peptide pharmaceuticals for treatment of nash and other disorders |
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2015
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