JP7023933B2 - セコ-シクロプロパピロロインドール化合物、その抗体-薬物コンジュゲート、ならびに製造および使用方法 - Google Patents
セコ-シクロプロパピロロインドール化合物、その抗体-薬物コンジュゲート、ならびに製造および使用方法 Download PDFInfo
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- JP7023933B2 JP7023933B2 JP2019509530A JP2019509530A JP7023933B2 JP 7023933 B2 JP7023933 B2 JP 7023933B2 JP 2019509530 A JP2019509530 A JP 2019509530A JP 2019509530 A JP2019509530 A JP 2019509530A JP 7023933 B2 JP7023933 B2 JP 7023933B2
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- 0 CCN1c2cc(O)c3[n]ccc3c2[C@](CN(C=NC2=N)c3c2nc[n]3*)C1 Chemical compound CCN1c2cc(O)c3[n]ccc3c2[C@](CN(C=NC2=N)c3c2nc[n]3*)C1 0.000 description 32
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- WHKWMTXTYKVFLK-UHFFFAOYSA-N CC(C)N1CCNCC1 Chemical compound CC(C)N1CCNCC1 WHKWMTXTYKVFLK-UHFFFAOYSA-N 0.000 description 1
- XLZMWNWNBXSZKF-UHFFFAOYSA-N CC(C)N1CCOCC1 Chemical compound CC(C)N1CCOCC1 XLZMWNWNBXSZKF-UHFFFAOYSA-N 0.000 description 1
- WRASSQXOVNVAGD-UHFFFAOYSA-N CC(C)NC(C(CC(C)=O)SC)=O Chemical compound CC(C)NC(C(CC(C)=O)SC)=O WRASSQXOVNVAGD-UHFFFAOYSA-N 0.000 description 1
- LHEAKOCZFQCLGM-UHFFFAOYSA-N CC(C)ON=C(C)C Chemical compound CC(C)ON=C(C)C LHEAKOCZFQCLGM-UHFFFAOYSA-N 0.000 description 1
- RWGFKTVRMDUZSP-UHFFFAOYSA-N CC(C)c1ccccc1 Chemical compound CC(C)c1ccccc1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 1
- IQBIBKCEOZEYOR-UHFFFAOYSA-N CC1N(CCOCCO)CCN1C Chemical compound CC1N(CCOCCO)CCN1C IQBIBKCEOZEYOR-UHFFFAOYSA-N 0.000 description 1
- SGBUPPPJULFBCI-QGZVFWFLSA-N CCCOc(cc1)cc2c1[nH]c(C(N1c3cc(O)c4[nH]c(C(N5CCOCC5)=O)cc4c3[C@H](CCl)C1)=O)c2 Chemical compound CCCOc(cc1)cc2c1[nH]c(C(N1c3cc(O)c4[nH]c(C(N5CCOCC5)=O)cc4c3[C@H](CCl)C1)=O)c2 SGBUPPPJULFBCI-QGZVFWFLSA-N 0.000 description 1
- TXIOGJHPPVXTOY-UHFFFAOYSA-N CCN1CCN(C)CC1 Chemical compound CCN1CCN(C)CC1 TXIOGJHPPVXTOY-UHFFFAOYSA-N 0.000 description 1
- CQRNPUSDYPNGDN-UHFFFAOYSA-N CCNCCOCCO Chemical compound CCNCCOCCO CQRNPUSDYPNGDN-UHFFFAOYSA-N 0.000 description 1
- UJWHLERCFNIFNJ-UHFFFAOYSA-N CCNc(cc1)ccc1O Chemical compound CCNc(cc1)ccc1O UJWHLERCFNIFNJ-UHFFFAOYSA-N 0.000 description 1
- SJVXBSOZYHQKSR-UHFFFAOYSA-N CCOCc(cc1)ccc1N Chemical compound CCOCc(cc1)ccc1N SJVXBSOZYHQKSR-UHFFFAOYSA-N 0.000 description 1
- VVMDKUYMBJVSSL-NSKGRQOBSA-N CCOc(cc1)cc2c1[nH]c(C(N1c3cc(OCc(cc4)ccc4NC([C@@H](C)NC([C@@H](C(C)C)NC(C(C)(C)CCOC(C)(C)CCN)=O)=O)=O)c4[nH]c(C(N5CCOCC5)=O)cc4c3[C@H](CCl)C1)=O)c2 Chemical compound CCOc(cc1)cc2c1[nH]c(C(N1c3cc(OCc(cc4)ccc4NC([C@@H](C)NC([C@@H](C(C)C)NC(C(C)(C)CCOC(C)(C)CCN)=O)=O)=O)c4[nH]c(C(N5CCOCC5)=O)cc4c3[C@H](CCl)C1)=O)c2 VVMDKUYMBJVSSL-NSKGRQOBSA-N 0.000 description 1
- XTGCJRCYGWLUHJ-UHFFFAOYSA-N CN1CCOCCC1 Chemical compound CN1CCOCCC1 XTGCJRCYGWLUHJ-UHFFFAOYSA-N 0.000 description 1
- OYAGYLOQGQMMJW-OAHLLOKOSA-N COc(cc(cc(C(N1c2cc(O)c3[nH]c(C(N4CCOCC4)=O)cc3c2[C@H](CCl)C1)=O)[nH]1)c1c1OC)c1OC Chemical compound COc(cc(cc(C(N1c2cc(O)c3[nH]c(C(N4CCOCC4)=O)cc3c2[C@H](CCl)C1)=O)[nH]1)c1c1OC)c1OC OYAGYLOQGQMMJW-OAHLLOKOSA-N 0.000 description 1
- AEAPOYNCUWVXRP-UHFFFAOYSA-N CS(C)N1CCOCC1 Chemical compound CS(C)N1CCOCC1 AEAPOYNCUWVXRP-UHFFFAOYSA-N 0.000 description 1
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
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- A61K47/6851—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
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- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6851—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
- A61K47/6857—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell the tumour determinant being from lung cancer cell
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- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
- A61K47/6851—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
- A61K47/6863—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell the tumour determinant being from stomach or intestines cancer cell
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- A61K47/6869—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell the tumour determinant being from a cell of the reproductive system: ovaria, uterus, testes, prostate
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Cell Biology (AREA)
- Oncology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pulmonology (AREA)
- General Chemical & Material Sciences (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662377052P | 2016-08-19 | 2016-08-19 | |
| US62/377,052 | 2016-08-19 | ||
| PCT/US2017/047465 WO2018035391A1 (en) | 2016-08-19 | 2017-08-18 | Seco-cyclopropapyrroloindole compounds, antibody-drug conjugates thereof, and methods of making and use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019524845A JP2019524845A (ja) | 2019-09-05 |
| JP2019524845A5 JP2019524845A5 (enExample) | 2020-09-24 |
| JP7023933B2 true JP7023933B2 (ja) | 2022-02-22 |
Family
ID=59714170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019509530A Active JP7023933B2 (ja) | 2016-08-19 | 2017-08-18 | セコ-シクロプロパピロロインドール化合物、その抗体-薬物コンジュゲート、ならびに製造および使用方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10287291B2 (enExample) |
| EP (1) | EP3500574B1 (enExample) |
| JP (1) | JP7023933B2 (enExample) |
| KR (1) | KR102493853B1 (enExample) |
| CN (1) | CN109641911B (enExample) |
| ES (1) | ES2902179T3 (enExample) |
| WO (1) | WO2018035391A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2019386945B9 (en) | 2018-11-30 | 2025-10-23 | Bristol-Myers Squibb Company | Antibody comprising a glutamine-containing light chain C-terminal extension, conjugates thereof, and methods and uses |
| KR20210102334A (ko) | 2018-12-12 | 2021-08-19 | 브리스톨-마이어스 스큅 컴퍼니 | 트랜스글루타미나제 접합을 위해 변형된 항체, 그의 접합체, 및 방법 및 용도 |
| US20240377413A1 (en) | 2019-09-16 | 2024-11-14 | Bristol-Myers Squibb Company | Dual capture method for analysis of antibody-drug conjugates |
| EP4410830A1 (en) * | 2021-09-30 | 2024-08-07 | Ajinomoto Co., Inc. | Conjugate of antibody and functional substance or salt thereof, and antibody derivative and compound or salts thereof to be used in producing conjugate or salt thereof |
| AU2023218463A1 (en) * | 2022-02-11 | 2024-08-29 | Shenzhen Enduring Biotech , Ltd. | Pegylated antibody hydroxyl-bearing drug conjugate |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011103557A1 (en) | 2010-02-22 | 2011-08-25 | Advanced Cancer Therapeutics, Llc | Small molecule inhibitors of pfkfb3 and glycolytic flux and their methods of use as anti-cancer therapeutics |
| JP2013525347A (ja) | 2010-04-21 | 2013-06-20 | シンタルガ・ビーブイ | Cc−1065類似体の新規の複合体および二官能性リンカー |
| JP2016520533A (ja) | 2013-03-19 | 2016-07-14 | ベイジン シェノゲン ファーマ グループ リミテッド | エストロゲン受容体関連疾患を処置するための抗体及び方法 |
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| US4475196A (en) | 1981-03-06 | 1984-10-02 | Zor Clair G | Instrument for locating faults in aircraft passenger reading light and attendant call control system |
| US4447233A (en) | 1981-04-10 | 1984-05-08 | Parker-Hannifin Corporation | Medication infusion pump |
| US5144011A (en) | 1981-06-26 | 1992-09-01 | Boston University | Acidity-sensitive spacer molecule to control the release of pharmaceuticals from molecular carriers |
| US4631190A (en) | 1981-06-26 | 1986-12-23 | Shen Wei C | Acidity-sensitive spacer molecule to control the release of pharmaceuticals from molecular carriers |
| US4439196A (en) | 1982-03-18 | 1984-03-27 | Merck & Co., Inc. | Osmotic drug delivery system |
| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
| US4447224A (en) | 1982-09-20 | 1984-05-08 | Infusaid Corporation | Variable flow implantable infusion apparatus |
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| US4486194A (en) | 1983-06-08 | 1984-12-04 | James Ferrara | Therapeutic device for administering medicaments through the skin |
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| US20180051031A1 (en) | 2018-02-22 |
| JP2019524845A (ja) | 2019-09-05 |
| KR20190039570A (ko) | 2019-04-12 |
| KR102493853B1 (ko) | 2023-01-30 |
| WO2018035391A1 (en) | 2018-02-22 |
| EP3500574B1 (en) | 2021-11-24 |
| US10287291B2 (en) | 2019-05-14 |
| EP3500574A1 (en) | 2019-06-26 |
| CN109641911B (zh) | 2023-02-21 |
| ES2902179T3 (es) | 2022-03-25 |
| CN109641911A (zh) | 2019-04-16 |
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