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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- A61K47/6851—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
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- 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
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- 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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- 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)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cell Biology (AREA)
- Oncology (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Pulmonology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Nitrogen Condensed Heterocyclic Rings (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 (cg-RX-API-DMAC7.html) | 2020-09-24 |
| JP7023933B2 true JP7023933B2 (ja) | 2022-02-22 |
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| 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 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3500574B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP7023933B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR102493853B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN109641911B (cg-RX-API-DMAC7.html) |
| ES (1) | ES2902179T3 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2018035391A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI3886914T3 (fi) | 2018-11-30 | 2023-05-26 | Bristol Myers Squibb Co | Glutamiinin sisältävän kevytketjun c-terminaalisen jatkeen käsittävä vasta-aine, sen konjugaatteja, ja menetelmiä ja käyttöjä |
| 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 |
| WO2023054706A1 (ja) * | 2021-09-30 | 2023-04-06 | 味の素株式会社 | 抗体および機能性物質のコンジュゲートまたはその塩、ならびにその製造に用いられる抗体誘導体および化合物またはそれらの塩 |
| EP4475894A1 (en) * | 2022-02-11 | 2024-12-18 | 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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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO1981001145A1 (en) | 1979-10-18 | 1981-04-30 | Univ Illinois | Hydrolytic enzyme-activatible pro-drugs |
| 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 |
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|---|---|
| EP3500574B1 (en) | 2021-11-24 |
| EP3500574A1 (en) | 2019-06-26 |
| CN109641911B (zh) | 2023-02-21 |
| ES2902179T3 (es) | 2022-03-25 |
| US10287291B2 (en) | 2019-05-14 |
| CN109641911A (zh) | 2019-04-16 |
| KR20190039570A (ko) | 2019-04-12 |
| KR102493853B1 (ko) | 2023-01-30 |
| WO2018035391A1 (en) | 2018-02-22 |
| JP2019524845A (ja) | 2019-09-05 |
| US20180051031A1 (en) | 2018-02-22 |
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