JP2019206547A5 - - Google Patents
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- JP2019206547A5 JP2019206547A5 JP2019129901A JP2019129901A JP2019206547A5 JP 2019206547 A5 JP2019206547 A5 JP 2019206547A5 JP 2019129901 A JP2019129901 A JP 2019129901A JP 2019129901 A JP2019129901 A JP 2019129901A JP 2019206547 A5 JP2019206547 A5 JP 2019206547A5
- Authority
- JP
- Japan
- Prior art keywords
- moiety
- peg
- compstatin analog
- cyclic peptide
- terminus
- 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
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- RDTRHBCZFDCUPW-KWICJJCGSA-N 2-[(4r,7s,10s,13s,19s,22s,25s,28s,31s,34r)-4-[[(2s,3r)-1-amino-3-hydroxy-1-oxobutan-2-yl]carbamoyl]-34-[[(2s,3s)-2-amino-3-methylpentanoyl]amino]-25-(3-amino-3-oxopropyl)-7-[3-(diaminomethylideneamino)propyl]-10,13-bis(1h-imidazol-5-ylmethyl)-19-(1h-indol Chemical class C([C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CSSC[C@@H](C(N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=2C3=CC=CC=C3NC=2)C(=O)NCC(=O)N[C@@H](CC=2NC=NC=2)C(=O)N1)C(C)C)C(C)C)=O)NC(=O)[C@@H](N)[C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=CN=CN1 RDTRHBCZFDCUPW-KWICJJCGSA-N 0.000 claims description 28
- 229920001223 polyethylene glycol Polymers 0.000 claims 24
- 239000002202 Polyethylene glycol Substances 0.000 claims 23
- 238000000034 method Methods 0.000 claims 22
- 108010069514 Cyclic Peptides Proteins 0.000 claims 14
- 102000001189 Cyclic Peptides Human genes 0.000 claims 14
- 150000001413 amino acids Chemical group 0.000 claims 13
- 125000006850 spacer group Chemical group 0.000 claims 9
- 229940024606 amino acid Drugs 0.000 claims 8
- 235000001014 amino acid Nutrition 0.000 claims 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 150000003335 secondary amines Chemical class 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical class C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 2
- QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical compound CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 claims 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 claims 2
- 125000000524 functional group Chemical group 0.000 claims 2
- 150000002905 orthoesters Chemical class 0.000 claims 2
- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims 2
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims 2
- IYKLZBIWFXPUCS-VIFPVBQESA-N (2s)-2-(naphthalen-1-ylamino)propanoic acid Chemical compound C1=CC=C2C(N[C@@H](C)C(O)=O)=CC=CC2=C1 IYKLZBIWFXPUCS-VIFPVBQESA-N 0.000 claims 1
- RWLSBXBFZHDHHX-VIFPVBQESA-N (2s)-2-(naphthalen-2-ylamino)propanoic acid Chemical compound C1=CC=CC2=CC(N[C@@H](C)C(O)=O)=CC=C21 RWLSBXBFZHDHHX-VIFPVBQESA-N 0.000 claims 1
- SPHNJDOWMOXSMT-NETXQHHPSA-N (2s)-2-amino-3-(2,3-dihydro-1h-indol-3-yl)propanoic acid Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)CNC2=C1 SPHNJDOWMOXSMT-NETXQHHPSA-N 0.000 claims 1
- ZADWXFSZEAPBJS-JTQLQIEISA-N 1-methyl-L-tryptophan Chemical compound C1=CC=C2N(C)C=C(C[C@H](N)C(O)=O)C2=C1 ZADWXFSZEAPBJS-JTQLQIEISA-N 0.000 claims 1
- INPQIVHQSQUEAJ-UHFFFAOYSA-N 5-fluorotryptophan Chemical group C1=C(F)C=C2C(CC(N)C(O)=O)=CNC2=C1 INPQIVHQSQUEAJ-UHFFFAOYSA-N 0.000 claims 1
- HUNCSWANZMJLPM-UHFFFAOYSA-N 5-methyltryptophan Chemical compound CC1=CC=C2NC=C(CC(N)C(O)=O)C2=C1 HUNCSWANZMJLPM-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 1
- 108010077895 Sarcosine Proteins 0.000 claims 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 229960003767 alanine Drugs 0.000 claims 1
- 235000004279 alanine Nutrition 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 150000001408 amides Chemical group 0.000 claims 1
- 125000000539 amino acid group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 230000001588 bifunctional effect Effects 0.000 claims 1
- 210000004899 c-terminal region Anatomy 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 150000002148 esters Chemical group 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 150000002466 imines Chemical group 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 125000006574 non-aromatic ring group Chemical group 0.000 claims 1
- TVIDEEHSOPHZBR-AWEZNQCLSA-N para-(benzoyl)-phenylalanine Chemical compound C1=CC(C[C@H](N)C(O)=O)=CC=C1C(=O)C1=CC=CC=C1 TVIDEEHSOPHZBR-AWEZNQCLSA-N 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- ZADWXFSZEAPBJS-UHFFFAOYSA-N racemic N-methyl tryptophan Natural products C1=CC=C2N(C)C=C(CC(N)C(O)=O)C2=C1 ZADWXFSZEAPBJS-UHFFFAOYSA-N 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 150000003568 thioethers Chemical group 0.000 claims 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims 1
- 239000012528 membrane Substances 0.000 description 2
- 201000008171 proliferative glomerulonephritis Diseases 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161484836P | 2011-05-11 | 2011-05-11 | |
| US61/484,836 | 2011-05-11 | ||
| JP2017111625A JP6653294B2 (ja) | 2011-05-11 | 2017-06-06 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017111625A Division JP6653294B2 (ja) | 2011-05-11 | 2017-06-06 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019206547A JP2019206547A (ja) | 2019-12-05 |
| JP2019206547A5 true JP2019206547A5 (enExample) | 2020-05-07 |
| JP6905554B2 JP6905554B2 (ja) | 2021-07-21 |
Family
ID=47139714
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014510520A Active JP6522337B2 (ja) | 2011-05-11 | 2012-05-11 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
| JP2017111625A Active JP6653294B2 (ja) | 2011-05-11 | 2017-06-06 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
| JP2019129901A Active JP6905554B2 (ja) | 2011-05-11 | 2019-07-12 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014510520A Active JP6522337B2 (ja) | 2011-05-11 | 2012-05-11 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
| JP2017111625A Active JP6653294B2 (ja) | 2011-05-11 | 2017-06-06 | 細胞反応性、長時間作用型または標的化コンプスタチン類似体およびその使用 |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US10125171B2 (enExample) |
| EP (2) | EP2707384B1 (enExample) |
| JP (3) | JP6522337B2 (enExample) |
| CN (2) | CN107050422B (enExample) |
| AU (3) | AU2012253294B2 (enExample) |
| BR (1) | BR112013028816B1 (enExample) |
| CA (1) | CA2835627C (enExample) |
| DK (1) | DK2707384T3 (enExample) |
| ES (1) | ES2915265T3 (enExample) |
| IL (3) | IL265344B2 (enExample) |
| MX (2) | MX356528B (enExample) |
| RU (1) | RU2653439C9 (enExample) |
| WO (1) | WO2012155107A1 (enExample) |
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| US20150330989A1 (en) * | 2012-11-15 | 2015-11-19 | The Brigham And Women's Hospital, Inc. | Method and system for diagnosing and treating preeclampsia |
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| US11499964B2 (en) * | 2015-02-27 | 2022-11-15 | The Johns Hopkins University | Assay to diagnose and treat disorders of the alternative pathway of complement activation |
| WO2017035405A1 (en) | 2015-08-26 | 2017-03-02 | Achillion Pharmaceuticals, Inc. | Amino compounds for treatment of immune and inflammatory disorders |
| AR106018A1 (es) | 2015-08-26 | 2017-12-06 | Achillion Pharmaceuticals Inc | Compuestos de arilo, heteroarilo y heterocíclicos para el tratamiento de trastornos médicos |
| EP3340983B1 (en) | 2015-08-26 | 2023-10-04 | Achillion Pharmaceuticals, Inc. | Aryl, heteroaryl, and heterocyclic compounds for treatment of immune and inflammatory disorders |
| WO2017035401A1 (en) | 2015-08-26 | 2017-03-02 | Achillion Pharmaceuticals, Inc. | Amide compounds for treatment of immune and inflammatory disorders |
| JP6968787B2 (ja) * | 2015-10-07 | 2021-11-17 | アペリス・ファーマシューティカルズ・インコーポレイテッドApellis Pharmaceuticals, Inc. | 投与レジメン |
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| CN107722262B (zh) * | 2017-09-18 | 2020-11-24 | 华南理工大学 | 一种聚碳二亚胺类聚合物及其制备方法与应用 |
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| MX2021002640A (es) | 2018-09-06 | 2021-07-16 | Achillion Pharmaceuticals Inc | Formas morficas de los inhibidores del factor d del complemento. |
| US11814391B2 (en) | 2018-09-06 | 2023-11-14 | Achillion Pharmaceuticals, Inc. | Macrocyclic compounds for the treatment of medical disorders |
| EP3856164B1 (en) | 2018-09-25 | 2024-08-07 | Achillion Pharmaceuticals, Inc. | Morphic forms of complement factor d inhibitors |
| US12239645B2 (en) | 2018-12-17 | 2025-03-04 | Achillion Pharmaceuticals, Inc. | Targeted dosing for the treatment of complement mediated disorders |
| JP7635138B2 (ja) | 2019-03-22 | 2025-02-25 | アキリオン ファーマシューティカルズ， インコーポレーテッド | 補体媒介性障害の治療のための医薬化合物 |
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| US20250197403A1 (en) | 2020-02-20 | 2025-06-19 | Achillion Pharmaceuticals, Inc. | Heteroaryl compounds for treatment of complement factor d mediated disorders |
| CN116437913A (zh) | 2020-09-23 | 2023-07-14 | 艾其林医药公司 | 用于治疗补体介导的病症的药物化合物 |
| CA3237642A1 (en) * | 2021-11-03 | 2023-05-11 | Apellis Pharmaceuticals, Inc. | Complement inhibitor dosing regimens |
| CN118812653A (zh) * | 2023-04-18 | 2024-10-22 | 成都奥达生物科技有限公司 | 一种长效坎普他汀化合物 |
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| WO2015006915A1 (zh) | 2013-07-16 | 2015-01-22 | 北京机械设备研究所 | 适用于高层和超高层建筑火灾扑救的消防车 |
| US9806963B2 (en) | 2013-10-18 | 2017-10-31 | Cellco Partnership | Feature activation on device |
| US11040107B2 (en) | 2017-04-07 | 2021-06-22 | Apellis Pharmaceuticals, Inc. | Dosing regimens and related compositions and methods |
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2012
- 2012-05-11 CN CN201611160681.3A patent/CN107050422B/zh active Active
- 2012-05-11 CN CN201280033181.7A patent/CN103687867B/zh active Active
- 2012-05-11 AU AU2012253294A patent/AU2012253294B2/en active Active
- 2012-05-11 EP EP12782170.0A patent/EP2707384B1/en active Active
- 2012-05-11 MX MX2013013084A patent/MX356528B/es active IP Right Grant
- 2012-05-11 RU RU2013149956A patent/RU2653439C9/ru active
- 2012-05-11 CA CA2835627A patent/CA2835627C/en active Active
- 2012-05-11 ES ES12782170T patent/ES2915265T3/es active Active
- 2012-05-11 WO PCT/US2012/037648 patent/WO2012155107A1/en not_active Ceased
- 2012-05-11 US US14/116,591 patent/US10125171B2/en active Active
- 2012-05-11 DK DK12782170.0T patent/DK2707384T3/da active
- 2012-05-11 EP EP22159092.0A patent/EP4105224A1/en active Pending
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2013
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2017
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