ATE479651T1 - Dipeptide nitrile - Google Patents
Dipeptide nitrileInfo
- Publication number
- ATE479651T1 ATE479651T1 AT98958887T AT98958887T ATE479651T1 AT E479651 T1 ATE479651 T1 AT E479651T1 AT 98958887 T AT98958887 T AT 98958887T AT 98958887 T AT98958887 T AT 98958887T AT E479651 T1 ATE479651 T1 AT E479651T1
- Authority
- AT
- Austria
- Prior art keywords
- dipeptide nitriles
- dipeptide
- nitriles
- Prior art date
Links
- 108010016626 Dipeptides Proteins 0.000 title 1
- 150000002825 nitriles Chemical class 0.000 title 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/325—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
- C07D207/327—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
- C07C255/29—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups and acylated amino groups bound to the carbon skeleton
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- C07C255/42—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms
- C07C255/44—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms at least one of the singly-bound nitrogen atoms being acylated
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- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D307/85—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D333/40—Thiophene-2-carboxylic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
- C07K5/06043—Leu-amino acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Physical Education & Sports Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Pyrrole Compounds (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9723407.4A GB9723407D0 (en) | 1997-11-05 | 1997-11-05 | Organic compounds |
| US98597397A | 1997-12-05 | 1997-12-05 | |
| PCT/EP1998/006937 WO1999024460A2 (en) | 1997-11-05 | 1998-11-03 | Dipeptide nitriles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE479651T1 true ATE479651T1 (de) | 2010-09-15 |
Family
ID=26312558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT98958887T ATE479651T1 (de) | 1997-11-05 | 1998-11-03 | Dipeptide nitrile |
Country Status (22)
| Country | Link |
|---|---|
| EP (1) | EP1028942B1 (https=) |
| JP (1) | JP4450988B2 (https=) |
| KR (1) | KR100518690B1 (https=) |
| CN (1) | CN1273444C (https=) |
| AR (1) | AR016665A1 (https=) |
| AT (1) | ATE479651T1 (https=) |
| AU (1) | AU751669B2 (https=) |
| BR (1) | BR9813197A (https=) |
| CA (1) | CA2306313C (https=) |
| CO (1) | CO4970837A1 (https=) |
| DE (1) | DE69841871D1 (https=) |
| HU (1) | HUP0004400A3 (https=) |
| ID (1) | ID24931A (https=) |
| IL (1) | IL135508A (https=) |
| MY (1) | MY133174A (https=) |
| NO (1) | NO20002320L (https=) |
| NZ (1) | NZ503889A (https=) |
| PE (1) | PE123699A1 (https=) |
| PL (1) | PL202226B1 (https=) |
| SK (1) | SK6572000A3 (https=) |
| TR (1) | TR200001189T2 (https=) |
| WO (1) | WO1999024460A2 (https=) |
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| EP1155011A1 (en) * | 1999-02-20 | 2001-11-21 | AstraZeneca AB | Di- and tripeptide nitrile derivatives as inhibitors of cathepsin l and cathepsin s |
| EP1159273A1 (en) | 1999-03-02 | 2001-12-05 | Boehringer Ingelheim Pharmaceuticals Inc. | Compounds useful as reversible inhibitors of cathepsin s |
| EP1452522A3 (en) * | 1999-03-15 | 2005-02-09 | Axys Pharmaceuticals, Inc. | Novel compounds and compositions as protease inhibitors |
| DE60021254T2 (de) * | 1999-03-15 | 2006-04-20 | AXYS Pharmaceuticals, Inc., South San Francisco | N-cyanomethylamide als protease inhibitoren |
| CA2379747C (en) | 1999-07-30 | 2008-09-23 | Boehringer Ingelheim Pharmaceuticals, Inc. | Novel succinate derivative compounds useful as cysteine protease inhibitors |
| US6420364B1 (en) | 1999-09-13 | 2002-07-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compound useful as reversible inhibitors of cysteine proteases |
| GB9925264D0 (en) * | 1999-10-26 | 1999-12-29 | Zeneca Ltd | Chemical compounds |
| ES2270898T3 (es) | 1999-12-24 | 2007-04-16 | F. Hoffmann-La Roche Ag | Derivados de nitrilo como inhibidores de catepsina k. |
| GB0003111D0 (en) * | 2000-02-10 | 2000-03-29 | Novartis Ag | Organic compounds |
| WO2001058869A2 (en) * | 2000-02-11 | 2001-08-16 | Bristol-Myers Squibb Company | Cannabinoid receptor modulators, their processes of preparation, and use of cannabinoid receptor modulators in treating respiratory and non-respiratory diseases |
| AU2001245764A1 (en) * | 2000-03-15 | 2001-09-24 | Axys Pharmaceuticals, Inc. | Novel compounds and compositions as protease inhibitors |
| ATE304526T1 (de) * | 2000-05-15 | 2005-09-15 | Novartis Pharma Gmbh | N-substituierte peptidylnitrile als cystein- cathepsin-inhibitoren |
| US6812237B2 (en) | 2000-05-15 | 2004-11-02 | Novartis Ag | N-substituted peptidyl nitriles as cysteine cathepsin inhibitors |
| US6462076B2 (en) | 2000-06-14 | 2002-10-08 | Hoffmann-La Roche Inc. | Beta-amino acid nitrile derivatives as cathepsin K inhibitors |
| EP1309593B1 (en) | 2000-08-14 | 2006-03-15 | Ortho-McNeil Pharmaceutical, Inc. | Substituted pyrazoles |
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| US7332494B2 (en) | 2000-08-14 | 2008-02-19 | Janssen Pharmaceutica, N.V. | Method for treating allergies using substituted pyrazoles |
| US7199102B2 (en) | 2000-08-24 | 2007-04-03 | The Regents Of The University Of California | Orally administered peptides synergize statin activity |
| US6369032B1 (en) * | 2000-09-06 | 2002-04-09 | Ortho-Mcneil Pharmaceutical, Inc. | Method for treating allergies |
| MXPA03005601A (es) | 2000-12-22 | 2004-12-02 | Axys Pharm Inc | Nuevos compuestos y composiciones como inhibidores de catepsina. |
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| CA2439415C (en) | 2001-03-02 | 2011-09-20 | Merck Frosst Canada & Co. | Cathepsin cysteine protease inhibitors |
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| JP2005504078A (ja) | 2001-09-14 | 2005-02-10 | アベンティス・ファーマスーティカルズ・インコーポレイテツド | カテプシン阻害剤としての新規化合物および組成物 |
| CA2459825A1 (en) | 2001-10-02 | 2003-04-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as reversible inhibitors of cysteine proteases |
| CA2463770A1 (en) | 2001-10-29 | 2003-05-08 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as reversible inhibitors of cysteine proteases |
| US6780985B2 (en) | 2001-11-08 | 2004-08-24 | Ortho-Mcneil Pharmaceutical, Inc. | Polynucleotide and polypeptide sequences of Canine Cathepsin S |
| US6784288B2 (en) | 2001-11-08 | 2004-08-31 | Ortho-Mcneil Pharmaceutical, Inc. | Polynucleotide and polypeptide sequences of monkey cathepsin S |
| MXPA04004450A (es) | 2001-11-14 | 2004-08-11 | Aventis Pharma Inc | Nuevos compuestos y composiciones como inhibidores de catepsina s. |
| HUP0402344A2 (hu) | 2001-12-04 | 2005-02-28 | F. Hoffmann-La Roche Ag | Helyettesített 2-amino-cikloalkán-karboxamidok, felhasználásuk cisztein-proteáz-inhibitorként, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények |
| US6759428B2 (en) | 2001-12-04 | 2004-07-06 | Roche Palo Alto Llc | Indole nitriles |
| EP1465862A1 (en) | 2002-01-17 | 2004-10-13 | SmithKline Beecham Corporation | Cycloalkyl ketoamides derivatives useful as cathepsin k inhibitors |
| CN100430052C (zh) * | 2002-03-05 | 2008-11-05 | 默克弗罗斯特加拿大有限公司 | 组织蛋白酶半胱氨酸蛋白酶抑制剂 |
| WO2004052921A1 (en) * | 2002-12-05 | 2004-06-24 | Axys Pharmaceuticals, Inc. | Cyanomethyl derivatives as cysteine protease inhibitors |
| US7465745B2 (en) | 2003-03-13 | 2008-12-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Cathepsin S inhibitors |
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| JP2006527704A (ja) * | 2003-06-18 | 2006-12-07 | プロザイメックス・アクティーゼルスカブ | プロテアーゼ阻害剤 |
| KR100738230B1 (ko) * | 2003-06-30 | 2007-07-12 | 주식회사 오스코텍 | 메톡시아크릴레이트계 화합물을 포함하는, 골다공증 예방 또는 치료용 조성물 |
| US7317019B2 (en) | 2003-08-21 | 2008-01-08 | Bristol Myers Squibb Co. | N-alkylated diaminopropane derivatives as modulators of chemokine receptor activity |
| PT1663958E (pt) | 2003-09-18 | 2015-06-01 | Virobay Inc | Compostos contendo haloalquilo como inibidores de protease de cisteína |
| US7186827B2 (en) | 2003-10-30 | 2007-03-06 | Boehringer Ingelheim Pharmaceuticals, Inc. | Dipeptide synthesis |
| CA2545723A1 (en) * | 2003-11-19 | 2005-06-02 | Novartis Ag | Use of cathepsin k inhibitors in severe bone loss diseases |
| JP2007513890A (ja) | 2003-12-12 | 2007-05-31 | メルク フロスト カナダ リミテツド | カテプシンシステインプロテアーゼ阻害剤 |
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| WO2006034004A2 (en) * | 2004-09-17 | 2006-03-30 | Schering Aktiengesellschaft | Processes and intermediates for preparing cysteine protease inhibitors |
| AR055283A1 (es) * | 2004-11-23 | 2007-08-15 | Merck Frosst Canada Ltd | Inhibidores de cisteinproteasa de catepsina |
| EP1819667B1 (en) | 2004-12-02 | 2012-10-17 | ViroBay, Inc. | Sulfonamide compounds as cysteine protease inhibitors |
| KR20070089996A (ko) | 2004-12-06 | 2007-09-04 | 더 리전트 오브 더 유니버시티 오브 캘리포니아 | 세동맥의 구조 및 기능의 개선 방법 |
| GB0427380D0 (en) * | 2004-12-14 | 2005-01-19 | Novartis Ag | Organic compounds |
| EP1841419A4 (en) * | 2005-01-19 | 2009-02-25 | Merck Frosst Canada Ltd | CATHEPSIN K AND ADIPOSITAS INHIBITORS |
| EP1841730A4 (en) * | 2005-01-19 | 2010-10-27 | Merck Frosst Canada Ltd | CATHEPSIN K INHIBITORS AND ATHEROSCLEROSIS |
| US7488848B2 (en) | 2005-03-21 | 2009-02-10 | Virobay, Inc. | Alpha ketoamide compounds as cysteine protease inhibitors |
| US7893093B2 (en) | 2005-03-22 | 2011-02-22 | Virobay, Inc. | Sulfonyl containing compounds as cysteine protease inhibitors |
| JP5311822B2 (ja) | 2005-07-19 | 2013-10-09 | 第一三共株式会社 | 置換プロパンアミド誘導体及びそれを含む医薬組成物 |
| WO2007081530A2 (en) * | 2006-01-03 | 2007-07-19 | Med Institute, Inc. | Endoluminal medical device for local delivery of cathepsin inhibitors |
| UA100669C2 (ru) | 2006-06-01 | 2013-01-25 | Санофі-Авентіс | Спироциклические нитрилы как ингибиторы протеазы, способ их получения (варианты) и лекарственное средство на их основе |
| US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| EP2079683B1 (en) | 2006-10-04 | 2015-01-21 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| EP2240491B1 (en) | 2008-01-09 | 2015-07-15 | Amura Therapeutics Limited | TETRAHYDROFURO(2,3-b)PYRROL-3-ONE DERIVATIVES AS INHIBITORS OF CYSTEINE PROTEINASES |
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| EP2198879A1 (en) | 2008-12-11 | 2010-06-23 | Institut Curie | CD74 modulator agent for regulating dendritic cell migration and device for studying the motility capacity of a cell |
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| WO2011094426A1 (en) * | 2010-01-29 | 2011-08-04 | The United State Of America, As Represented By The Secretary, Department Of Health & Human Services | Caspase inhibitors |
| US9330026B2 (en) * | 2013-03-05 | 2016-05-03 | Qualcomm Incorporated | Method and apparatus for preventing unauthorized access to contents of a register under certain conditions when performing a hardware table walk (HWTW) |
| EP3342765B1 (en) * | 2015-08-29 | 2021-09-15 | Sunshine Lake Pharma Co., Ltd. | Cathepsin k inhibitor and application thereof |
| CN106478564B (zh) * | 2015-08-29 | 2021-11-12 | 广东东阳光药业有限公司 | 组织蛋白酶k抑制剂及其用途 |
| WO2017089389A1 (en) * | 2015-11-26 | 2017-06-01 | F. Hoffmann-La Roche Ag | Trypanosomes inhibitors |
| EP3878836B1 (en) * | 2018-11-07 | 2025-07-23 | Chugai Seiyaku Kabushiki Kaisha | O-substituted serine derivative production method |
| US11124497B1 (en) | 2020-04-17 | 2021-09-21 | Pardes Biosciences, Inc. | Inhibitors of cysteine proteases and methods of use thereof |
| US11174231B1 (en) | 2020-06-09 | 2021-11-16 | Pardes Biosciences, Inc. | Inhibitors of cysteine proteases and methods of use thereof |
| BR112021023814A2 (pt) * | 2020-06-09 | 2022-12-20 | Pardes Biosciences Inc | Inibidores de proteases de cisteína e métodos de uso das mesmas |
| GB202107385D0 (en) * | 2021-05-24 | 2021-07-07 | Heptares Therapeutics Ltd | Sars-cov-2 mpro inhibitor compounds |
| US20240083845A1 (en) * | 2020-12-18 | 2024-03-14 | Heptares Therapeutics Limited | Sars-cov-2 mpro inhibitor compounds |
| KR20220115062A (ko) | 2021-02-09 | 2022-08-17 | (주)오스티오뉴로젠 | 크로몬 구조의 화합물을 포함하는 골다공증의 예방 및 치료용 약학적 조성물 |
| CN116589425B (zh) * | 2022-12-29 | 2026-03-24 | 百放英库医药科技(北京)有限公司 | 组织蛋白酶l抑制剂 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3467691A (en) * | 1964-04-22 | 1969-09-16 | Tsutomu Irikura | N-(n-acylaminoacyl)-aminoacetonitriles |
| JP2848232B2 (ja) * | 1993-02-19 | 1999-01-20 | 武田薬品工業株式会社 | アルデヒド誘導体 |
| WO1997027200A1 (en) * | 1996-01-26 | 1997-07-31 | Smithkline Beecham Plc | Thienoxazinone derivatives useful as antiviral agents |
| JP2001504498A (ja) * | 1996-11-22 | 2001-04-03 | エラン・ファーマシューティカルズ・インコーポレイテッド | N―(アリール/ヘテロアリール/アルキルアセチル)アミノ酸アミドおよびその医薬組成物、並びに該化合物を用いたβ―アミロイドペプチドの放出および/またはその合成を阻害する方法 |
-
1998
- 1998-11-03 SK SK657-2000A patent/SK6572000A3/sk unknown
- 1998-11-03 CN CNB988107686A patent/CN1273444C/zh not_active Expired - Fee Related
- 1998-11-03 HU HU0004400A patent/HUP0004400A3/hu unknown
- 1998-11-03 WO PCT/EP1998/006937 patent/WO1999024460A2/en not_active Ceased
- 1998-11-03 NZ NZ503889A patent/NZ503889A/en unknown
- 1998-11-03 AU AU14873/99A patent/AU751669B2/en not_active Ceased
- 1998-11-03 JP JP2000520468A patent/JP4450988B2/ja not_active Expired - Fee Related
- 1998-11-03 BR BR9813197-4A patent/BR9813197A/pt not_active Application Discontinuation
- 1998-11-03 KR KR10-2000-7004868A patent/KR100518690B1/ko not_active Expired - Fee Related
- 1998-11-03 DE DE69841871T patent/DE69841871D1/de not_active Expired - Lifetime
- 1998-11-03 CA CA002306313A patent/CA2306313C/en not_active Expired - Fee Related
- 1998-11-03 IL IL135508A patent/IL135508A/en not_active IP Right Cessation
- 1998-11-03 PL PL340819A patent/PL202226B1/pl not_active IP Right Cessation
- 1998-11-03 TR TR2000/01189T patent/TR200001189T2/xx unknown
- 1998-11-03 ID IDW20000830A patent/ID24931A/id unknown
- 1998-11-03 EP EP98958887A patent/EP1028942B1/en not_active Expired - Lifetime
- 1998-11-03 AT AT98958887T patent/ATE479651T1/de not_active IP Right Cessation
- 1998-11-04 AR ARP980105565A patent/AR016665A1/es not_active Application Discontinuation
- 1998-11-04 MY MYPI98005030A patent/MY133174A/en unknown
- 1998-11-05 CO CO98065245A patent/CO4970837A1/es unknown
- 1998-11-05 PE PE1998001066A patent/PE123699A1/es not_active Application Discontinuation
-
2000
- 2000-05-02 NO NO20002320A patent/NO20002320L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| PL202226B1 (pl) | 2009-06-30 |
| TR200001189T2 (tr) | 2000-09-21 |
| DE69841871D1 (en) | 2010-10-14 |
| EP1028942A2 (en) | 2000-08-23 |
| SK6572000A3 (en) | 2000-10-09 |
| NZ503889A (en) | 2002-07-26 |
| AU751669B2 (en) | 2002-08-22 |
| CA2306313A1 (en) | 1999-05-20 |
| ID24931A (id) | 2000-08-31 |
| KR100518690B1 (ko) | 2005-10-05 |
| HUP0004400A2 (hu) | 2002-04-29 |
| CO4970837A1 (es) | 2000-11-07 |
| BR9813197A (pt) | 2000-08-29 |
| CN1278244A (zh) | 2000-12-27 |
| WO1999024460B1 (en) | 1999-10-28 |
| EP1028942B1 (en) | 2010-09-01 |
| WO1999024460A3 (en) | 1999-09-02 |
| IL135508A0 (en) | 2001-05-20 |
| AR016665A1 (es) | 2001-07-25 |
| NO20002320L (no) | 2000-07-04 |
| JP4450988B2 (ja) | 2010-04-14 |
| NO20002320D0 (no) | 2000-05-02 |
| IL135508A (en) | 2006-12-10 |
| PL340819A1 (en) | 2001-02-26 |
| HUP0004400A3 (en) | 2002-10-28 |
| WO1999024460A2 (en) | 1999-05-20 |
| PE123699A1 (es) | 1999-12-17 |
| CN1273444C (zh) | 2006-09-06 |
| JP2001522862A (ja) | 2001-11-20 |
| CA2306313C (en) | 2010-03-09 |
| MY133174A (en) | 2007-10-31 |
| AU1487399A (en) | 1999-05-31 |
| KR20010031800A (ko) | 2001-04-16 |
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