JPWO2022191283A5 - - Google Patents
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- Publication number
- JPWO2022191283A5 JPWO2022191283A5 JP2023505632A JP2023505632A JPWO2022191283A5 JP WO2022191283 A5 JPWO2022191283 A5 JP WO2022191283A5 JP 2023505632 A JP2023505632 A JP 2023505632A JP 2023505632 A JP2023505632 A JP 2023505632A JP WO2022191283 A5 JPWO2022191283 A5 JP WO2022191283A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- residue
- salt
- atom
- bond
- 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
- 150000003839 salts Chemical class 0.000 claims 38
- 125000004432 carbon atom Chemical group C* 0.000 claims 35
- 229910052799 carbon Inorganic materials 0.000 claims 24
- 125000004430 oxygen atom Chemical group O* 0.000 claims 17
- 229910052717 sulfur Inorganic materials 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 14
- 125000004434 sulfur atom Chemical group 0.000 claims 14
- 108060003951 Immunoglobulin Proteins 0.000 claims 12
- 102000018358 immunoglobulin Human genes 0.000 claims 12
- 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 12
- 125000002947 alkylene group Chemical group 0.000 claims 10
- 108090000765 processed proteins & peptides Proteins 0.000 claims 10
- 150000001540 azides Chemical group 0.000 claims 9
- IVRMZWNICZWHMI-UHFFFAOYSA-N azide group Chemical group [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 claims 7
- 125000003275 alpha amino acid group Chemical group 0.000 claims 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 6
- 125000003277 amino group Chemical group 0.000 claims 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- COLNVLDHVKWLRT-QMMMGPOBSA-N phenylalanine group Chemical group N[C@@H](CC1=CC=CC=C1)C(=O)O COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 5
- 239000000126 substance Substances 0.000 claims 5
- 125000000637 arginyl group Chemical group N[C@@H](CCCNC(N)=N)C(=O)* 0.000 claims 4
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims 4
- 125000000613 asparagine group Chemical group N[C@@H](CC(N)=O)C(=O)* 0.000 claims 3
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims 3
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 claims 3
- 125000000487 histidyl group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C([H])=N1 0.000 claims 3
- 125000002349 hydroxyamino group Chemical group [H]ON([H])[*] 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims 2
- 239000004472 Lysine Substances 0.000 claims 2
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 2
- 125000000539 amino acid group Chemical group 0.000 claims 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N aspartic acid group Chemical group N[C@@H](CC(=O)O)C(=O)O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000000404 glutamine group Chemical group N[C@@H](CCC(N)=O)C(=O)* 0.000 claims 2
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- 125000000430 tryptophan group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 0.000 claims 2
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 2
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000001433 C-terminal amino-acid group Chemical group 0.000 claims 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 1
- 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 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 1
- 125000000729 N-terminal amino-acid group Chemical group 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
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- -1 pentafluorophenyloxy group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 claims 1
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 1
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 claims 1
- 229910052721 tungsten Inorganic materials 0.000 claims 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2024217693A JP2025038071A (ja) | 2021-03-11 | 2024-12-12 | 化合物またはその塩、およびそれらにより得られる抗体 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021039706 | 2021-03-11 | ||
| JP2021039706 | 2021-03-11 | ||
| PCT/JP2022/010574 WO2022191283A1 (ja) | 2021-03-11 | 2022-03-10 | 化合物またはその塩、およびそれらにより得られる抗体 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2024217693A Division JP2025038071A (ja) | 2021-03-11 | 2024-12-12 | 化合物またはその塩、およびそれらにより得られる抗体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2022191283A1 JPWO2022191283A1 (https=) | 2022-09-15 |
| JPWO2022191283A5 true JPWO2022191283A5 (https=) | 2024-08-06 |
| JP7605290B2 JP7605290B2 (ja) | 2024-12-24 |
Family
ID=83228078
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023505632A Active JP7605290B2 (ja) | 2021-03-11 | 2022-03-10 | 化合物またはその塩、およびそれらにより得られる抗体 |
| JP2024217693A Pending JP2025038071A (ja) | 2021-03-11 | 2024-12-12 | 化合物またはその塩、およびそれらにより得られる抗体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2024217693A Pending JP2025038071A (ja) | 2021-03-11 | 2024-12-12 | 化合物またはその塩、およびそれらにより得られる抗体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20240115719A1 (https=) |
| EP (1) | EP4306535A1 (https=) |
| JP (2) | JP7605290B2 (https=) |
| KR (1) | KR20230154853A (https=) |
| CN (1) | CN116964076A (https=) |
| AU (1) | AU2022234694B2 (https=) |
| CA (1) | CA3212822A1 (https=) |
| WO (1) | WO2022191283A1 (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2020090979A1 (ja) * | 2018-10-31 | 2021-09-24 | 味の素株式会社 | 抗体に対する親和性物質、切断性部分および反応性基を有する化合物またはその塩 |
| CA3212822A1 (en) * | 2021-03-11 | 2022-09-15 | Ajinomoto Co., Inc. | Compound or salt thereof, and antibody obtained by using the same |
| CN116947671A (zh) * | 2023-07-26 | 2023-10-27 | 四川轻化工大学 | 一种半刚性含氮的六元芳香羧酸配体及其制备方法 |
| WO2026058917A1 (ja) * | 2024-09-10 | 2026-03-19 | 味の素株式会社 | 抗体親和性物質を含む化合物、修飾抗体およびそれらの塩ならびに抗体誘導体または抗体-機能性物質コンジュゲートの製造方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL106992A (en) | 1988-02-11 | 1994-06-24 | Bristol Myers Squibb Co | Acylhydrazone derivatives of anthracycline and methods for their preparation |
| US5622929A (en) | 1992-01-23 | 1997-04-22 | Bristol-Myers Squibb Company | Thioether conjugates |
| US6214345B1 (en) | 1993-05-14 | 2001-04-10 | Bristol-Myers Squibb Co. | Lysosomal enzyme-cleavable antitumor drug conjugates |
| DK0871490T3 (da) | 1995-12-22 | 2003-07-07 | Bristol Myers Squibb Co | Forgrenede hydrazonlinkere |
| EP1243276A1 (en) | 2001-03-23 | 2002-09-25 | Franciscus Marinus Hendrikus De Groot | Elongated and multiple spacers containing activatible prodrugs |
| DK1545613T3 (da) | 2002-07-31 | 2011-11-14 | Seattle Genetics Inc | Auristatinkonjugater og deres anvendelse til behandling af cancer, en autoimmun sygdom eller en infektiøs sygdom |
| WO2004043493A1 (en) | 2002-11-14 | 2004-05-27 | Syntarga B.V. | Prodrugs built as multiple self-elimination-release spacers |
| EP2478912B1 (en) | 2003-11-06 | 2016-08-31 | Seattle Genetics, Inc. | Auristatin conjugates with anti-HER2 or anti-CD22 antibodies and their use in therapy |
| ES3058443T3 (es) | 2015-05-20 | 2026-03-10 | Univ Kagoshima | Modificación específica de anticuerpo con péptido de unión a IgG |
| JP7020403B2 (ja) | 2016-05-02 | 2022-02-16 | 味の素株式会社 | アジド基含有Fcタンパク質 |
| AU2018259856B2 (en) | 2017-04-28 | 2025-05-01 | Ajinomoto Co., Inc. | Compound having substance that has affinity for soluble protein, cleavable moiety, and reactive group, or salt thereof |
| JPWO2019240288A1 (ja) | 2018-06-14 | 2021-07-26 | 味の素株式会社 | 抗体に対する親和性物質、および生体直交性官能基を有する化合物またはその塩 |
| KR102921757B1 (ko) | 2018-06-14 | 2026-02-03 | 아지노모토 가부시키가이샤 | 항체에 대한 친화성 물질, 절단성 부분 및 반응성기를 갖는 화합물 또는 이의 염 |
| WO2020009165A1 (ja) | 2018-07-03 | 2020-01-09 | 味の素株式会社 | 修飾抗体およびその製造方法 |
| JPWO2020090979A1 (ja) | 2018-10-31 | 2021-09-24 | 味の素株式会社 | 抗体に対する親和性物質、切断性部分および反応性基を有する化合物またはその塩 |
| CA3212822A1 (en) * | 2021-03-11 | 2022-09-15 | Ajinomoto Co., Inc. | Compound or salt thereof, and antibody obtained by using the same |
-
2022
- 2022-03-10 CA CA3212822A patent/CA3212822A1/en active Pending
- 2022-03-10 CN CN202280020193.XA patent/CN116964076A/zh active Pending
- 2022-03-10 WO PCT/JP2022/010574 patent/WO2022191283A1/ja not_active Ceased
- 2022-03-10 KR KR1020237030639A patent/KR20230154853A/ko active Pending
- 2022-03-10 EP EP22767237.5A patent/EP4306535A1/en active Pending
- 2022-03-10 JP JP2023505632A patent/JP7605290B2/ja active Active
- 2022-03-10 AU AU2022234694A patent/AU2022234694B2/en active Active
-
2023
- 2023-09-08 US US18/463,903 patent/US20240115719A1/en active Pending
-
2024
- 2024-12-12 JP JP2024217693A patent/JP2025038071A/ja active Pending
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