ES2647927T3 - Conjugados enlazadores del fármaco auriestatina - Google Patents
Conjugados enlazadores del fármaco auriestatina Download PDFInfo
- Publication number
- ES2647927T3 ES2647927T3 ES14182732.9T ES14182732T ES2647927T3 ES 2647927 T3 ES2647927 T3 ES 2647927T3 ES 14182732 T ES14182732 T ES 14182732T ES 2647927 T3 ES2647927 T3 ES 2647927T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- group
- heterocycle
- aryl
- carbocycle
- 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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- 239000003814 drug Substances 0.000 title abstract description 24
- 150000001413 amino acids Chemical class 0.000 abstract description 11
- 150000001875 compounds Chemical class 0.000 abstract description 9
- 150000003839 salts Chemical class 0.000 abstract description 9
- 239000003446 ligand Substances 0.000 abstract description 4
- 108090000765 processed proteins & peptides Proteins 0.000 abstract description 4
- 239000012453 solvate Substances 0.000 abstract description 4
- 108091005804 Peptidases Proteins 0.000 abstract description 2
- 239000004365 Protease Substances 0.000 abstract description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 abstract description 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 9
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 230000003834 intracellular effect Effects 0.000 abstract 1
- 125000005647 linker group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229920001184 polypeptide Polymers 0.000 abstract 1
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 150000003334 secondary amides Chemical class 0.000 abstract 1
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- -1 trityl ethers Chemical class 0.000 description 17
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- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
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- 150000008575 L-amino acids Chemical class 0.000 description 2
- RHGKLRLOHDJJDR-BYPYZUCNSA-N L-citrulline Chemical group NC(=O)NCCC[C@H]([NH3+])C([O-])=O RHGKLRLOHDJJDR-BYPYZUCNSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
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- 229910019142 PO4 Inorganic materials 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 108010044540 auristatin Proteins 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 2
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- 150000002148 esters Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 2
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 2
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- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
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| US3770508P | 2008-03-18 | 2008-03-18 | |
| US37705P | 2008-03-18 | ||
| US4443108P | 2008-04-11 | 2008-04-11 |
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| ES09721267.4T Active ES2523033T3 (es) | 2008-03-18 | 2009-03-18 | Conjugados enlazadores del fármaco auriestatina |
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| NO (1) | NO2842575T3 (show.php) |
| PL (2) | PL2265283T3 (show.php) |
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| CN101098854B (zh) | 2004-07-23 | 2012-12-05 | 恩多塞特公司 | 二价连接体及其轭合物 |
| EP2176293B1 (en) | 2007-06-25 | 2019-04-03 | Endocyte, Inc. | Conjugates containing hydrophilic spacer linkers |
| US9877965B2 (en) | 2007-06-25 | 2018-01-30 | Endocyte, Inc. | Vitamin receptor drug delivery conjugates for treating inflammation |
| JP5727786B2 (ja) | 2007-10-19 | 2015-06-03 | シアトル ジェネティクス,インコーポレーテッド | Cd19結合性物質およびその使用 |
| US8765432B2 (en) | 2009-12-18 | 2014-07-01 | Oligasis, Llc | Targeted drug phosphorylcholine polymer conjugates |
| AU2011239525B2 (en) | 2010-04-15 | 2015-04-09 | Medimmune Limited | Pyrrolobenzodiazepines used to treat proliferative diseases |
| KR102562175B1 (ko) | 2010-04-15 | 2023-07-31 | 코디악 사이언시스 인코포레이티드 | 고분자량 쌍성이온-함유 중합체 |
| ES2528956T3 (es) | 2010-06-10 | 2015-02-13 | Seattle Genetics, Inc. | Nuevos derivados de auristatina y su uso |
| JP5933562B2 (ja) | 2010-09-29 | 2016-06-15 | シアトル ジェネティックス, インコーポレイテッド | N−カルボキシアルキル−アウリスタチンおよびその使用 |
| CA2815363C (en) | 2010-10-22 | 2020-07-14 | Seattle Genetics, Inc. | Synergistic effects between auristatin-based antibody drug conjugates and inhibitors of the pi3k-akt mtor pathway |
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| HK1207976A1 (en) | 2016-02-19 |
| EP2265283A1 (en) | 2010-12-29 |
| PL2842575T3 (pl) | 2018-02-28 |
| EP2842575A1 (en) | 2015-03-04 |
| EP2265283A4 (en) | 2012-04-25 |
| DK2265283T3 (da) | 2014-10-20 |
| DK2842575T3 (da) | 2017-11-27 |
| US8609105B2 (en) | 2013-12-17 |
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