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)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Oncology (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)
- Pyridine Compounds (AREA)
- Furan Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole 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 (de) |
| JP (1) | JP4450988B2 (de) |
| KR (1) | KR100518690B1 (de) |
| CN (1) | CN1273444C (de) |
| AR (1) | AR016665A1 (de) |
| AT (1) | ATE479651T1 (de) |
| AU (1) | AU751669B2 (de) |
| BR (1) | BR9813197A (de) |
| CA (1) | CA2306313C (de) |
| CO (1) | CO4970837A1 (de) |
| DE (1) | DE69841871D1 (de) |
| HU (1) | HUP0004400A3 (de) |
| ID (1) | ID24931A (de) |
| IL (1) | IL135508A (de) |
| MY (1) | MY133174A (de) |
| NO (1) | NO20002320L (de) |
| NZ (1) | NZ503889A (de) |
| PE (1) | PE123699A1 (de) |
| PL (1) | PL202226B1 (de) |
| SK (1) | SK6572000A3 (de) |
| TR (1) | TR200001189T2 (de) |
| WO (1) | WO1999024460A2 (de) |
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| AU2560000A (en) * | 1999-02-20 | 2000-09-04 | Astrazeneca Ab | Di- and tripeptide nitrile derivatives as inhibitors of cathepsin l and cathepsin |
| WO2000051998A1 (en) * | 1999-03-02 | 2000-09-08 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as reversible inhibitors of cathepsin s |
| CN1362947A (zh) | 1999-03-15 | 2002-08-07 | Axys药物公司 | 用作蛋白酶抑制剂的n-氰基甲基酰胺 |
| SI1178958T1 (en) * | 1999-03-15 | 2004-08-31 | Axys Pharmaceuticals, Inc. | N-cyanomethyl amides as protease inhibitors |
| JP2003506364A (ja) | 1999-07-30 | 2003-02-18 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | システインプロテアーゼインヒビターとして有益な新規スクシネート誘導体化合物 |
| 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 |
| AU783145B2 (en) | 1999-12-24 | 2005-09-29 | F. Hoffmann-La Roche Ag | Nitrile derivatives as cathepsin K inhibitors |
| 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 |
| WO2001068645A2 (en) * | 2000-03-15 | 2001-09-20 | Axys Pharmaceuticals, Inc. | N-cyanomethylcarboxamides and their use as protease inhibitors |
| US6812237B2 (en) | 2000-05-15 | 2004-11-02 | Novartis Ag | N-substituted peptidyl nitriles as cysteine cathepsin inhibitors |
| JP2003533506A (ja) * | 2000-05-15 | 2003-11-11 | ノバルティス アクチエンゲゼルシャフト | N−置換ペプチジルニトリル |
| US6462076B2 (en) * | 2000-06-14 | 2002-10-08 | Hoffmann-La Roche Inc. | Beta-amino acid nitrile derivatives as cathepsin K inhibitors |
| HK1052509B (en) | 2000-08-14 | 2007-09-07 | Ortho-Mcneil Pharmaceutical, Inc. | Substituted pyrazole |
| DK1309592T3 (da) | 2000-08-14 | 2006-08-21 | Ortho Mcneil Pharm Inc | Substituerede pyrazoler |
| EP1309593B1 (de) | 2000-08-14 | 2006-03-15 | Ortho-McNeil Pharmaceutical, Inc. | Substituierte pyrazole |
| 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 |
| MXPA03001960A (es) | 2000-09-06 | 2004-03-18 | Johnson & Johnson | Un metodo para tratar alergias. |
| JP2004523506A (ja) | 2000-12-22 | 2004-08-05 | アクシス・ファーマシューティカルズ・インコーポレイテッド | カテプシン阻害剤としての新規な化合物と組成物 |
| US7030116B2 (en) | 2000-12-22 | 2006-04-18 | Aventis Pharmaceuticals Inc. | Compounds and compositions as cathepsin inhibitors |
| EP1372655B1 (de) | 2001-03-02 | 2008-10-01 | Merck Frosst Canada Ltd. | Cathepsincystein-proteasehemmer |
| US6982263B2 (en) | 2001-06-08 | 2006-01-03 | Boehringer Ingelheim Pharmaceuticals, Inc. | Nitriles useful as reversible inhibitors of cysteine proteases |
| EP1436255A1 (de) | 2001-09-14 | 2004-07-14 | Aventis Pharmaceuticals, Inc. | Neue verbindungen und zusammensetzungen als cathepsininhibitoren |
| AU2002340031A1 (en) | 2001-10-02 | 2003-04-14 | 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 |
| YU34604A (sh) | 2001-11-14 | 2006-08-17 | Aventis Pharmaceuticals Inc. | Oligopeptidi kao inhibitori katepsina s i kompozicije koje ih sadrže |
| US6759428B2 (en) | 2001-12-04 | 2004-07-06 | Roche Palo Alto Llc | Indole nitriles |
| JP2005517640A (ja) | 2001-12-04 | 2005-06-16 | エフ.ホフマン−ラ ロシュ アーゲー | 置換2−アミノ−シクロアルカンカルボキサアミドならびにシステインプロテアーゼインヒビターとしてのその使用 |
| WO2003062192A1 (en) | 2002-01-17 | 2003-07-31 | Smithkline Beecham Corporation | Cycloalkyl ketoamides derivatives useful as cathepsin k inhibitors |
| US7375134B2 (en) * | 2002-03-05 | 2008-05-20 | Axys Pharmaceuticals, Inc. | Cathepsin cysteine protease inhibitors |
| 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 |
| US7326719B2 (en) | 2003-03-13 | 2008-02-05 | Boehringer Ingelheim Pharmaceuticals, Inc. | Cathepsin S inhibitors |
| 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 |
| DK1663958T3 (da) | 2003-09-18 | 2015-04-07 | Virobay Inc | Haloalkylholdige forbindelser som cysteinproteasehæmmere |
| DE602004024916D1 (de) | 2003-10-30 | 2010-02-11 | Boehringer Ingelheim Pharma | Synthese von dipeptidanaloga |
| CN1882343A (zh) * | 2003-11-19 | 2006-12-20 | 诺瓦提斯公司 | 组织蛋白酶k抑制剂在严重骨损失疾病中的用途 |
| CA2548600A1 (en) | 2003-12-12 | 2005-06-23 | Merck Frosst Canada & Co. | Cathepsin cysteine protease inhibitors |
| JP2007514692A (ja) * | 2003-12-19 | 2007-06-07 | ビーエーエスエフ アクチェンゲゼルシャフト | ヘテロアロイル置換フェニルアラニンアミド除草剤 |
| JP2008513472A (ja) * | 2004-09-17 | 2008-05-01 | バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト | システインプロテアーゼインヒビターの調製のための方法及び中間体 |
| AR055283A1 (es) * | 2004-11-23 | 2007-08-15 | Merck Frosst Canada Ltd | Inhibidores de cisteinproteasa de catepsina |
| WO2006060810A1 (en) | 2004-12-02 | 2006-06-08 | Schering Aktiengesellschaft | Sulfonamide compounds as cysteine protease inhibitors |
| WO2006063132A2 (en) | 2004-12-06 | 2006-06-15 | The Regents Of The University Of California | Methods for improving the structure and function of arterioles |
| GB0427380D0 (en) * | 2004-12-14 | 2005-01-19 | Novartis Ag | Organic compounds |
| EP1841730A4 (de) * | 2005-01-19 | 2010-10-27 | Merck Frosst Canada Ltd | Cathepsin-k-inhibitoren und atherosklerose |
| US20090005323A1 (en) * | 2005-01-19 | 2009-01-01 | Michael David Percival | Cathepsin K Inhibitors and Obesity |
| US7488848B2 (en) | 2005-03-21 | 2009-02-10 | Virobay, Inc. | Alpha ketoamide compounds as cysteine protease inhibitors |
| JP5215167B2 (ja) | 2005-03-22 | 2013-06-19 | ビロベイ,インコーポレイティド | システインプロテアーゼ阻害剤としてのスルホニル基含有化合物 |
| CA2615991C (en) * | 2005-07-19 | 2011-02-08 | Daiichi Sankyo Company, Limited | Substituted propanamide derivative and pharmaceutical composition comprising the same |
| WO2007081530A2 (en) * | 2006-01-03 | 2007-07-19 | Med Institute, Inc. | Endoluminal medical device for local delivery of cathepsin inhibitors |
| DK2032535T3 (da) | 2006-06-01 | 2012-11-05 | Sanofi Sa | Spiro-cycliske nitriler som protease-inhibitorer |
| US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
| EP2079683B1 (de) | 2006-10-04 | 2015-01-21 | Virobay, Inc. | Difluorhaltige verbindungen als cysteinproteasehemmer |
| EP2719700A1 (de) | 2008-01-09 | 2014-04-16 | Amura Therapeutics Limited | Tetrahydrofuro(3,2-b)pyrrol-3-one derivate als cysteine proteinase inhibitoren |
| WO2009103432A2 (en) * | 2008-02-21 | 2009-08-27 | Sanofi-Aventis | Covalently binding imaging probes |
| EP2198879A1 (de) | 2008-12-11 | 2010-06-23 | Institut Curie | CD74-modulierender Wirkstoff zur Regulierung der Dendritenzellmigration und Verfahren zur Untersuchung der Bewegungsfähigkeit einer Zelle |
| US8324417B2 (en) | 2009-08-19 | 2012-12-04 | Virobay, Inc. | Process for the preparation of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid and alkyl esters and acid salts thereof |
| 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) |
| 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 |
| WO2017036357A1 (zh) * | 2015-08-29 | 2017-03-09 | 广东东阳光药业有限公司 | 组织蛋白酶k抑制剂及其用途 |
| CN108368056A (zh) * | 2015-11-26 | 2018-08-03 | 豪夫迈·罗氏有限公司 | 锥虫抑制剂 |
| EP3878836B1 (de) * | 2018-11-07 | 2025-07-23 | Chugai Seiyaku Kabushiki Kaisha | Verfahren zur herstellung von o-substituierten serinderivaten |
| 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 |
| GB2595975B (en) * | 2020-06-09 | 2022-12-07 | Pardes Biosciences Inc | Inhibitors of cysteine proteases and methods of use thereof |
| JP2024500136A (ja) * | 2020-12-18 | 2024-01-04 | ヘプタレス セラピューティクス リミテッド | Sars-cov-2 mpro阻害薬化合物 |
| GB202107385D0 (en) * | 2021-05-24 | 2021-07-07 | Heptares Therapeutics Ltd | 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 |
| AU1595997A (en) | 1996-01-26 | 1997-08-20 | Smithkline Beecham Plc | Thienoxazinone derivatives useful as antiviral agents |
| KR20000069075A (ko) * | 1996-11-22 | 2000-11-25 | 진 엠. 듀발 | N-(아릴/헤테로아릴/알킬아세틸)아미노산 아미드, 이들을 함유하는 제약 조성물, 및 이들 화합물을 사용하여 베타-아밀로이드 펩티드의 방출 및(또는) 합성의 억제 방법 |
-
1998
- 1998-11-03 TR TR2000/01189T patent/TR200001189T2/xx unknown
- 1998-11-03 AU AU14873/99A patent/AU751669B2/en not_active Ceased
- 1998-11-03 PL PL340819A patent/PL202226B1/pl not_active IP Right Cessation
- 1998-11-03 SK SK657-2000A patent/SK6572000A3/sk unknown
- 1998-11-03 HU HU0004400A patent/HUP0004400A3/hu unknown
- 1998-11-03 JP JP2000520468A patent/JP4450988B2/ja not_active Expired - Fee Related
- 1998-11-03 CA CA002306313A patent/CA2306313C/en not_active Expired - Fee Related
- 1998-11-03 CN CNB988107686A patent/CN1273444C/zh not_active Expired - Fee Related
- 1998-11-03 AT AT98958887T patent/ATE479651T1/de not_active IP Right Cessation
- 1998-11-03 DE DE69841871T patent/DE69841871D1/de not_active Expired - Lifetime
- 1998-11-03 KR KR10-2000-7004868A patent/KR100518690B1/ko not_active Expired - Fee Related
- 1998-11-03 IL IL135508A patent/IL135508A/en not_active IP Right Cessation
- 1998-11-03 BR BR9813197-4A patent/BR9813197A/pt not_active Application Discontinuation
- 1998-11-03 NZ NZ503889A patent/NZ503889A/en unknown
- 1998-11-03 ID IDW20000830A patent/ID24931A/id unknown
- 1998-11-03 WO PCT/EP1998/006937 patent/WO1999024460A2/en not_active Ceased
- 1998-11-03 EP EP98958887A patent/EP1028942B1/de not_active Expired - Lifetime
- 1998-11-04 MY MYPI98005030A patent/MY133174A/en unknown
- 1998-11-04 AR ARP980105565A patent/AR016665A1/es not_active Application Discontinuation
- 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 |
|---|---|
| KR20010031800A (ko) | 2001-04-16 |
| IL135508A0 (en) | 2001-05-20 |
| EP1028942A2 (de) | 2000-08-23 |
| DE69841871D1 (en) | 2010-10-14 |
| WO1999024460A3 (en) | 1999-09-02 |
| ID24931A (id) | 2000-08-31 |
| JP4450988B2 (ja) | 2010-04-14 |
| CN1273444C (zh) | 2006-09-06 |
| HUP0004400A3 (en) | 2002-10-28 |
| CO4970837A1 (es) | 2000-11-07 |
| AU751669B2 (en) | 2002-08-22 |
| PL340819A1 (en) | 2001-02-26 |
| CA2306313A1 (en) | 1999-05-20 |
| SK6572000A3 (en) | 2000-10-09 |
| KR100518690B1 (ko) | 2005-10-05 |
| HUP0004400A2 (hu) | 2002-04-29 |
| JP2001522862A (ja) | 2001-11-20 |
| NO20002320D0 (no) | 2000-05-02 |
| IL135508A (en) | 2006-12-10 |
| AR016665A1 (es) | 2001-07-25 |
| PL202226B1 (pl) | 2009-06-30 |
| MY133174A (en) | 2007-10-31 |
| NZ503889A (en) | 2002-07-26 |
| AU1487399A (en) | 1999-05-31 |
| EP1028942B1 (de) | 2010-09-01 |
| PE123699A1 (es) | 1999-12-17 |
| CA2306313C (en) | 2010-03-09 |
| CN1278244A (zh) | 2000-12-27 |
| BR9813197A (pt) | 2000-08-29 |
| WO1999024460B1 (en) | 1999-10-28 |
| NO20002320L (no) | 2000-07-04 |
| TR200001189T2 (tr) | 2000-09-21 |
| WO1999024460A2 (en) | 1999-05-20 |
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