JP2017524652A - 一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 - Google Patents
一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 Download PDFInfo
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- JP2017524652A JP2017524652A JP2016568591A JP2016568591A JP2017524652A JP 2017524652 A JP2017524652 A JP 2017524652A JP 2016568591 A JP2016568591 A JP 2016568591A JP 2016568591 A JP2016568591 A JP 2016568591A JP 2017524652 A JP2017524652 A JP 2017524652A
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- 0 C*c(cc1)cc(F)c1F Chemical compound C*c(cc1)cc(F)c1F 0.000 description 11
- WYUIWKFIFOJVKW-UHFFFAOYSA-N Cc(cc1)cc(Cl)c1Cl Chemical compound Cc(cc1)cc(Cl)c1Cl WYUIWKFIFOJVKW-UHFFFAOYSA-N 0.000 description 2
- ZNEHIDGAPGVZSA-UHFFFAOYSA-N Cc(cccc1F)c1F Chemical compound Cc(cccc1F)c1F ZNEHIDGAPGVZSA-UHFFFAOYSA-N 0.000 description 2
- JOXXHDGUTVUBDL-UHFFFAOYSA-N Cc1cc(Cl)ccc1F Chemical compound Cc1cc(Cl)ccc1F JOXXHDGUTVUBDL-UHFFFAOYSA-N 0.000 description 2
- MMZYCBHLNZVROM-UHFFFAOYSA-N Cc1ccccc1F Chemical compound Cc1ccccc1F MMZYCBHLNZVROM-UHFFFAOYSA-N 0.000 description 2
- VSKSBSORLCDRHS-UHFFFAOYSA-N Fc1cccc(I)c1 Chemical compound Fc1cccc(I)c1 VSKSBSORLCDRHS-UHFFFAOYSA-N 0.000 description 2
- WQDGTJOEMPEHHL-UHFFFAOYSA-N CC(c(cc1)ccc1Cl)=C Chemical compound CC(c(cc1)ccc1Cl)=C WQDGTJOEMPEHHL-UHFFFAOYSA-N 0.000 description 1
- DDQIMXVPSIMGSG-UHFFFAOYSA-N CCCc(cc(cc1)F)c1[ClH]C Chemical compound CCCc(cc(cc1)F)c1[ClH]C DDQIMXVPSIMGSG-UHFFFAOYSA-N 0.000 description 1
- PHZOEQVKHPXCOH-UHFFFAOYSA-N CCc(c(F)c1)ccc1Cl Chemical compound CCc(c(F)c1)ccc1Cl PHZOEQVKHPXCOH-UHFFFAOYSA-N 0.000 description 1
- DFGSJBCAFQMAPO-UHFFFAOYSA-N CCc1ccccc1[BrH]C Chemical compound CCc1ccccc1[BrH]C DFGSJBCAFQMAPO-UHFFFAOYSA-N 0.000 description 1
- TYSBTGUOJQECQU-UHFFFAOYSA-N C[BrH]c(cccc1)c1[IH]I Chemical compound C[BrH]c(cccc1)c1[IH]I TYSBTGUOJQECQU-UHFFFAOYSA-N 0.000 description 1
- FLYDKCOVMKPSDU-UHFFFAOYSA-N C[IH]c(cc(cc1)F)c1F Chemical compound C[IH]c(cc(cc1)F)c1F FLYDKCOVMKPSDU-UHFFFAOYSA-N 0.000 description 1
- TYXGWNROBVCOOH-UHFFFAOYSA-N C[IH]c(cccc1Cl)c1Cl Chemical compound C[IH]c(cccc1Cl)c1Cl TYXGWNROBVCOOH-UHFFFAOYSA-N 0.000 description 1
- AUZSEZSDVWOUIG-UHFFFAOYSA-N Cc(c([ClH]C)c1)ccc1F Chemical compound Cc(c([ClH]C)c1)ccc1F AUZSEZSDVWOUIG-UHFFFAOYSA-N 0.000 description 1
- FBPYPVLFMOHPHU-UHFFFAOYSA-N Cc(cc(cc1)F)c1[ClH]C Chemical compound Cc(cc(cc1)F)c1[ClH]C FBPYPVLFMOHPHU-UHFFFAOYSA-N 0.000 description 1
- FZMPLKVGINKUJZ-UHFFFAOYSA-N Cc(cc1)cc(F)c1F Chemical compound Cc(cc1)cc(F)c1F FZMPLKVGINKUJZ-UHFFFAOYSA-N 0.000 description 1
- NPDACUSDTOMAMK-UHFFFAOYSA-N Cc(cc1)ccc1Cl Chemical compound Cc(cc1)ccc1Cl NPDACUSDTOMAMK-UHFFFAOYSA-N 0.000 description 1
- WRWPPGUCZBJXKX-UHFFFAOYSA-N Cc(cc1)ccc1F Chemical compound Cc(cc1)ccc1F WRWPPGUCZBJXKX-UHFFFAOYSA-N 0.000 description 1
- PFHKIBDAXGVOOP-UHFFFAOYSA-N Cc(ccc(Cl)c1)c1[ClH]C Chemical compound Cc(ccc(Cl)c1)c1[ClH]C PFHKIBDAXGVOOP-UHFFFAOYSA-N 0.000 description 1
- RYMMNSVHOKXTNN-UHFFFAOYSA-N Cc1cc(Cl)cc(Cl)c1 Chemical compound Cc1cc(Cl)cc(Cl)c1 RYMMNSVHOKXTNN-UHFFFAOYSA-N 0.000 description 1
- OSOUNOBYRMOXQQ-UHFFFAOYSA-N Cc1cc(Cl)ccc1 Chemical compound Cc1cc(Cl)ccc1 OSOUNOBYRMOXQQ-UHFFFAOYSA-N 0.000 description 1
- KFAKZJUYBOYVKA-UHFFFAOYSA-N Cc1cc(Cl)ccc1Cl Chemical compound Cc1cc(Cl)ccc1Cl KFAKZJUYBOYVKA-UHFFFAOYSA-N 0.000 description 1
- YISYUYYETHYYMD-UHFFFAOYSA-N Cc1cc(F)cc(F)c1 Chemical compound Cc1cc(F)cc(F)c1 YISYUYYETHYYMD-UHFFFAOYSA-N 0.000 description 1
- JMLWXCJXOYDXRN-UHFFFAOYSA-N Clc1cc(I)ccc1 Chemical compound Clc1cc(I)ccc1 JMLWXCJXOYDXRN-UHFFFAOYSA-N 0.000 description 1
- KDPDNYDAEGQFKB-UHFFFAOYSA-N Fc(cc1F)ccc1[IH]I Chemical compound Fc(cc1F)ccc1[IH]I KDPDNYDAEGQFKB-UHFFFAOYSA-N 0.000 description 1
- NRAUPBNUIMPIKI-UHFFFAOYSA-N Fc1cc(Cl)ccc1[IH]I Chemical compound Fc1cc(Cl)ccc1[IH]I NRAUPBNUIMPIKI-UHFFFAOYSA-N 0.000 description 1
- BFIUKBBLACSXQI-UHFFFAOYSA-N Fc1ccc(C2CC2)c(F)c1 Chemical compound Fc1ccc(C2CC2)c(F)c1 BFIUKBBLACSXQI-UHFFFAOYSA-N 0.000 description 1
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/145—Amines having sulfur, e.g. thiurams (>N—C(S)—S—C(S)—N< and >N—C(S)—S—S—C(S)—N<), Sulfinylamines (—N=SO), Sulfonylamines (—N=SO2)
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
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- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
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- 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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- A61K31/426—1,3-Thiazoles
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
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- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
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- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4866—Organic macromolecular compounds
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019104381A JP6906564B2 (ja) | 2014-05-20 | 2019-06-04 | 一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 |
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462000991P | 2014-05-20 | 2014-05-20 | |
| US62/000,991 | 2014-05-20 | ||
| US201462019600P | 2014-07-01 | 2014-07-01 | |
| US62/019,600 | 2014-07-01 | ||
| US201462088154P | 2014-12-05 | 2014-12-05 | |
| US62/088,154 | 2014-12-05 | ||
| PCT/US2015/031633 WO2015179443A1 (en) | 2014-05-20 | 2015-05-19 | Boron-containing proteasome inhibitors for use after primary cancer therapy |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019104381A Division JP6906564B2 (ja) | 2014-05-20 | 2019-06-04 | 一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017524652A true JP2017524652A (ja) | 2017-08-31 |
| JP2017524652A5 JP2017524652A5 (OSRAM) | 2018-06-28 |
Family
ID=54554652
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016568591A Pending JP2017524652A (ja) | 2014-05-20 | 2015-05-19 | 一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 |
| JP2019104381A Active JP6906564B2 (ja) | 2014-05-20 | 2019-06-04 | 一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019104381A Active JP6906564B2 (ja) | 2014-05-20 | 2019-06-04 | 一次癌療法後に使用するためのホウ素含有プロテアソーム阻害剤 |
Country Status (21)
| Country | Link |
|---|---|
| US (5) | US20150335668A1 (OSRAM) |
| EP (1) | EP3145526A1 (OSRAM) |
| JP (2) | JP2017524652A (OSRAM) |
| KR (2) | KR102481856B1 (OSRAM) |
| CN (1) | CN106659761A (OSRAM) |
| AU (2) | AU2015264272A1 (OSRAM) |
| BR (1) | BR112016026774A8 (OSRAM) |
| CA (1) | CA2949517A1 (OSRAM) |
| CL (1) | CL2016002948A1 (OSRAM) |
| CR (1) | CR20160577A (OSRAM) |
| EA (1) | EA201692332A1 (OSRAM) |
| IL (2) | IL249025B (OSRAM) |
| MA (1) | MA39964A (OSRAM) |
| MX (2) | MX2016015267A (OSRAM) |
| PH (1) | PH12016502301A1 (OSRAM) |
| SG (2) | SG10202003693RA (OSRAM) |
| TN (1) | TN2016000492A1 (OSRAM) |
| TW (1) | TWI746422B (OSRAM) |
| UA (1) | UA121389C2 (OSRAM) |
| UY (1) | UY36132A (OSRAM) |
| WO (1) | WO2015179443A1 (OSRAM) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017079572A1 (en) * | 2015-11-04 | 2017-05-11 | Millennium Pharmaceuticals, Inc. | Methods for the identification, evaluation and treatment of patients having multiple myeloma |
| CA3032011A1 (en) * | 2016-08-04 | 2018-02-08 | Millennium Pharmaceuticals, Inc. | Combination of proteasome inhibitors and anti-cd30 antibodies |
| KR20190100225A (ko) * | 2016-12-28 | 2019-08-28 | 다이이찌 산쿄 가부시키가이샤 | 알포트 증후군 치료약 |
| US11414437B2 (en) | 2017-07-28 | 2022-08-16 | Chengdu Origin Biotechnology Limited Company | Borate compound, and synthesis method therefor and uses thereof |
| US20250051367A1 (en) * | 2021-12-06 | 2025-02-13 | Pretzel Therapeutics, Inc. | Heterocycle-containing lonp1 inhibitor compounds, uses and methods |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011524903A (ja) * | 2008-06-17 | 2011-09-08 | ミレニアム・ファーマシューティカルズ・インコーポレイテッド | ボロン酸エステル化合物およびその医薬組成物 |
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| US2160413A (en) | 1935-04-16 | 1939-05-30 | Schering Ag | Polyiodo derivatives of acylamino acids and their salts and a method of making the same |
| NZ203706A (en) | 1982-04-22 | 1986-03-14 | Squibb & Sons Inc | Occlusive multi-layer wound dressing and hydrocolloidal granules for wound treatment |
| US4499082A (en) | 1983-12-05 | 1985-02-12 | E. I. Du Pont De Nemours And Company | α-Aminoboronic acid peptides |
| JPS6233170A (ja) | 1985-08-07 | 1987-02-13 | Tokuyama Soda Co Ltd | 環状ポリエ−テル化合物 |
| JPH0813759B2 (ja) | 1986-09-01 | 1996-02-14 | 富士写真フイルム株式会社 | アルコキシベンゼン誘導体の製造方法 |
| JP2512303B2 (ja) | 1987-03-20 | 1996-07-03 | 呉羽化学工業株式会社 | 2−オキサゾリン−4,5−ジオンのフエニルヒドラゾン誘導体 |
| US5250720A (en) | 1987-06-05 | 1993-10-05 | The Dupont Merck Pharmaceutical Company | Intermediates for preparing peptide boronic acid inhibitors of trypsin-like proteases |
| US5187157A (en) | 1987-06-05 | 1993-02-16 | Du Pont Merck Pharmaceutical Company | Peptide boronic acid inhibitors of trypsin-like proteases |
| US5242904A (en) | 1987-06-05 | 1993-09-07 | The Dupont Merck Pharmaceutical Company | Peptide boronic acid inhibitors of trypsin-like proteases |
| EP0315574A3 (de) | 1987-11-05 | 1990-08-22 | Hoechst Aktiengesellschaft | Renin-Inhibitoren |
| US5159060A (en) | 1988-05-27 | 1992-10-27 | Mayo Foundation For Medical Education And Research | Cytotoxic boronic acid peptide analogs |
| US5106948A (en) | 1988-05-27 | 1992-04-21 | Mao Foundation For Medical Education And Research | Cytotoxic boronic acid peptide analogs |
| DE3827340A1 (de) | 1988-08-12 | 1990-02-15 | Hoechst Ag | Verwendung von (alpha)-aminoboronsaeure-derivaten zur prophylaxe und behandlung von viruserkrankungen |
| MX9206628A (es) | 1991-11-22 | 1993-05-01 | Boehringer Ingelheim Pharma | Ester de prolinaboronato y metodo para su preparacion. |
| US5442100A (en) | 1992-08-14 | 1995-08-15 | The Procter & Gamble Company | β-aminoalkyl and β-N-peptidylaminoalkyl boronic acids |
| ATE149563T1 (de) | 1992-08-14 | 1997-03-15 | Procter & Gamble | Alpha-aminoborsäurehaltige flüssige waschmittel |
| US5935944A (en) | 1993-09-10 | 1999-08-10 | Neutron Technology Corporation | Formulation for I.V. administration of the boron delivery drug, boronophenylalanine (BPA) |
| US5492900A (en) | 1993-09-10 | 1996-02-20 | Neutron Technology Corporation | Method for enhancing the solubility of the boron delivery drug, boronophenylalanine (BPA) |
| US6060462A (en) | 1993-10-20 | 2000-05-09 | Dupont Pharmaceuticals Company | Electrophilic peptide analogs as inhibitors of trypsin-like enzymes |
| FR2712602B1 (fr) | 1993-11-18 | 1996-02-09 | Centre Nat Rech Scient | Virus recombinants, préparation et utilisation en thérapie génique. |
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