OA10786A - Method of inhibiting cathepsin k - Google Patents
Method of inhibiting cathepsin k Download PDFInfo
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- OA10786A OA10786A OA70040A OA70040A OA10786A OA 10786 A OA10786 A OA 10786A OA 70040 A OA70040 A OA 70040A OA 70040 A OA70040 A OA 70040A OA 10786 A OA10786 A OA 10786A
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- 239000007858 starting material Substances 0.000 description 1
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- 210000001258 synovial membrane Anatomy 0.000 description 1
- QQUYJNCVRFJDSA-QMMMGPOBSA-N tert-butyl n-[(2s)-2-amino-4-methylpentanoyl]carbamate Chemical compound CC(C)C[C@H](N)C(=O)NC(=O)OC(C)(C)C QQUYJNCVRFJDSA-QMMMGPOBSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 150000004905 tetrazines Chemical class 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 125000006090 thiamorpholinyl sulfone group Chemical group 0.000 description 1
- 125000006089 thiamorpholinyl sulfoxide group Chemical group 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 125000001984 thiazolidinyl group Chemical group 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
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- 241000701447 unidentified baculovirus Species 0.000 description 1
- 238000003828 vacuum filtration Methods 0.000 description 1
- 239000004474 valine Chemical class 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
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Classifications
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- C07—ORGANIC CHEMISTRY
- 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
- C07D207/18—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 one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—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 one double bond between ring members or between a ring member and a non-ring member 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- 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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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/34—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a carbon skeleton further substituted by nitrogen atoms
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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- C07D211/96—Sulfur atom
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen 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
- C07D215/36—Sulfur atoms
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- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members 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
- C07D241/24—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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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
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- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
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- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
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- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- 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
- C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
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- C07D333/30—Hetero atoms other than halogen
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Applications Claiming Priority (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US810895P | 1995-10-30 | 1995-10-30 | |
| US747395P | 1995-11-22 | 1995-11-22 | |
| US899295P | 1995-12-21 | 1995-12-21 | |
| US1374896P | 1996-03-20 | 1996-03-20 | |
| US1374796P | 1996-03-20 | 1996-03-20 | |
| US1376496P | 1996-03-20 | 1996-03-20 | |
| US1789296P | 1996-05-17 | 1996-05-17 | |
| US1745596P | 1996-05-17 | 1996-05-17 | |
| US2047896P | 1996-06-13 | 1996-06-13 | |
| US2204796P | 1996-07-22 | 1996-07-22 | |
| US2349496P | 1996-08-07 | 1996-08-07 | |
| US2374296P | 1996-08-08 | 1996-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| OA10786A true OA10786A (en) | 2002-12-24 |
Family
ID=27583607
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| OA70040A OA10786A (en) | 1995-10-30 | 1997-06-27 | Method of inhibiting cathepsin k |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6274336B1 (de) |
| EP (1) | EP0804180A4 (de) |
| JP (1) | JPH10512300A (de) |
| CN (1) | CN1177293A (de) |
| AU (1) | AU711014B2 (de) |
| BG (1) | BG101712A (de) |
| CA (1) | CA2209109A1 (de) |
| CZ (1) | CZ206097A3 (de) |
| EA (1) | EA199700087A1 (de) |
| HU (1) | HUP9802488A3 (de) |
| IL (1) | IL121167A0 (de) |
| NO (1) | NO973009L (de) |
| NZ (1) | NZ324921A (de) |
| OA (1) | OA10786A (de) |
| PL (1) | PL328877A1 (de) |
| SK (2) | SK88997A3 (de) |
| WO (1) | WO1997016177A1 (de) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5948669A (en) * | 1997-02-26 | 1999-09-07 | Smithkline Beecham Corporation | Rat cathepsin K polynucleotide and polypeptide sequence |
| US6566373B2 (en) | 1997-05-06 | 2003-05-20 | Smithkline Beecham Corporation | Protease inhibitors |
| AR013079A1 (es) * | 1997-05-06 | 2000-12-13 | Smithkline Beecham Corp | Derivados sustituidos de tetrahidrofurano-3-onas, de tetrahidropirano-3- onas y tetrahidrotiofen-3-onas, un procedimiento para su preparacion unacomposicion farmaceutica de un medicamento util como inhibidores de proteasas e intermediarios |
| CA2301201A1 (en) * | 1998-08-14 | 2000-02-24 | Smithkline Beecham Corporation | Method of inhibiting cathepsin k |
| US6735530B1 (en) | 1998-09-23 | 2004-05-11 | Sarnoff Corporation | Computational protein probing to identify binding sites |
| US6117870A (en) | 1998-11-12 | 2000-09-12 | Fujirebio Kabushiki Kaisha | Cyclic amide derivatives |
| US20030144175A1 (en) * | 1998-12-23 | 2003-07-31 | Smithkline Beecham Corporation | Protease inhibitors |
| US6720139B1 (en) | 1999-01-27 | 2004-04-13 | Elitra Pharmaceuticals, Inc. | Genes identified as required for proliferation in Escherichia coli |
| AU2041901A (en) | 1999-11-09 | 2001-06-06 | Elitra Pharmaceuticals, Inc. | Genes essential for microbial proliferation and antisense thereto |
| JP2003513924A (ja) | 1999-11-10 | 2003-04-15 | スミスクライン・ビーチャム・コーポレイション | プロテア−ゼ阻害剤 |
| WO2001034600A1 (en) | 1999-11-10 | 2001-05-17 | Smithkline Beecham Corporation | Protease inhibitors |
| AU1588901A (en) | 1999-11-10 | 2001-06-06 | Smithkline Beecham Corporation | Protease inhibitors |
| OA12323A (en) | 2000-03-21 | 2006-05-15 | Smithkline Beecham Corp | Protease inhibitors. |
| US6605589B1 (en) * | 2000-03-31 | 2003-08-12 | Parker Hughes Institute | Cathepsin inhibitors in cancer treatment |
| AU2001253739A1 (en) * | 2000-04-20 | 2001-11-07 | Salman Baig | Method for the identification of active site protease inactivators |
| AU2002330085A1 (en) * | 2001-09-24 | 2003-05-26 | Mount Sinai School Of Medicine | Methods and compositions for therapeutic treatment of cathepsin k complex-mediated disorders |
| US7282512B2 (en) | 2002-01-17 | 2007-10-16 | Smithkline Beecham Corporation | Cycloalkyl ketoamides derivatives useful as cathepsin K inhibitors |
| US7109243B2 (en) * | 2003-03-24 | 2006-09-19 | Irm Llc | Inhibitors of cathepsin S |
| US7384970B2 (en) * | 2003-03-24 | 2008-06-10 | Irm Llc | Inhibitors of cathepsin S |
| US7173051B2 (en) * | 2003-06-13 | 2007-02-06 | Irm, Llc | Inhibitors of cathepsin S |
| US7256207B2 (en) * | 2003-08-20 | 2007-08-14 | Irm Llc | Inhibitors of cathepsin S |
| US7415361B2 (en) | 2003-12-09 | 2008-08-19 | Locus Pharmaceuticals, Inc. | Methods and systems for analyzing and determining ligand-residue interaction |
| US7029902B2 (en) * | 2004-03-26 | 2006-04-18 | Applera Corporation | Isolated monkey cathepsin S proteins, nucleic acid molecules encoding monkey cathepsin S proteins, and uses thereof |
| JP4047365B2 (ja) | 2006-01-11 | 2008-02-13 | 生化学工業株式会社 | シクロアルカンカルボキサミド誘導体及びその製造方法 |
| CA2636765C (en) | 2006-01-11 | 2014-03-18 | Seikagaku Corporation | Cycloalkylcarbonylamino acid ester derivative and process for producing the same |
| JP4012239B2 (ja) | 2006-01-11 | 2007-11-21 | 生化学工業株式会社 | オキサゾロン誘導体 |
| JP3975226B2 (ja) | 2006-01-11 | 2007-09-12 | 生化学工業株式会社 | シクロアルキルカルボニルアミノ酸誘導体及びその製造方法 |
| WO2007137149A2 (en) * | 2006-05-22 | 2007-11-29 | Velcura Therapeutics, Inc. | Use of cathepsin k antagonists in bone production |
| BRPI0807477A2 (pt) * | 2007-02-14 | 2014-05-13 | Karolinska Innovations Ab | Uso de um polipeptídeo isolado, polipeptídeo isolado, composição farmacêutica, e, métdo de tratamento de um mamífero |
| GB0800277D0 (en) | 2008-01-08 | 2008-02-13 | Imagination Tech Ltd | Video motion compensation |
| GB0900425D0 (en) | 2009-01-12 | 2009-02-11 | Ucb Pharma Sa | Biological products |
| US10048253B2 (en) | 2012-06-28 | 2018-08-14 | Ucb Biopharma Sprl | Method for identifying compounds of therapeutic interest |
| FR3127580B1 (fr) * | 2021-09-30 | 2024-02-09 | Ateq | Sonde active pour la mesure de tension en impédances élevées |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3650901A (en) * | 1968-09-27 | 1972-03-21 | Yeda Res & Dev | Polymeric enzyme products |
| EP0356595A1 (de) * | 1988-09-01 | 1990-03-07 | Merrell Dow Pharmaceuticals Inc. | Peptidase-Hemmer |
| US5223486A (en) * | 1988-11-01 | 1993-06-29 | University Research Corporation | Inhibition of cancer procoagulant |
| WO1990007330A1 (en) * | 1989-01-06 | 1990-07-12 | The Regents Of The University Of California | Selection method for specific useful pharmaceutical compounds |
| CA2047226A1 (en) * | 1989-12-27 | 1991-06-28 | Jun-Ichi Haruta | 1,3,2-dioxathiolane oxide derivative |
| US5331573A (en) * | 1990-12-14 | 1994-07-19 | Balaji Vitukudi N | Method of design of compounds that mimic conformational features of selected peptides |
| EP0504938A3 (en) | 1991-03-22 | 1993-04-14 | Suntory Limited | Prophylactic and therapeutic agent for bone diseases comprising di- or tripeptide derivative as active ingredient |
| JPH05140063A (ja) * | 1991-11-19 | 1993-06-08 | Suntory Ltd | ジペプチド誘導体及びそれを有効成分とする骨疾患の予防及び治療剤 |
| DK0603769T3 (da) * | 1992-12-25 | 1999-06-14 | Mitsubishi Chem Corp | Alfa-aminoketonderivater |
| CA2111930A1 (en) | 1992-12-25 | 1994-06-26 | Ryoichi Ando | Aminoketone derivatives |
| EP0693124A1 (de) | 1993-04-06 | 1996-01-24 | Forsyth Dental Infirmary For Children | Menschliche osteoklast-spezifische und zugehörende gene |
| US5501969A (en) * | 1994-03-08 | 1996-03-26 | Human Genome Sciences, Inc. | Human osteoclast-derived cathepsin |
| CA2187451A1 (en) * | 1994-04-13 | 1995-10-26 | Shigetoshi Tsubotani | Aziridine derivatives, their production and use |
| CA2190151A1 (en) * | 1994-05-31 | 1995-12-07 | Shigetoshi Tsubotani | Epoxysuccinic acid derivatives, their production and use |
| US6544767B1 (en) | 1994-10-27 | 2003-04-08 | Axys Pharmaceuticals, Inc. | Cathespin O2 protease |
| TW438591B (en) | 1995-06-07 | 2001-06-07 | Arris Pharm Corp | Reversible cysteine protease inhibitors |
| US5830850A (en) * | 1996-08-28 | 1998-11-03 | Mount Sinai School Of Medicine Of The City Of New York | Methods for the treatment of bone resorption disorders, including osteoporosis |
-
1996
- 1996-10-30 CZ CZ972060A patent/CZ206097A3/cs unknown
- 1996-10-30 JP JP9517568A patent/JPH10512300A/ja not_active Withdrawn
- 1996-10-30 WO PCT/US1996/017512 patent/WO1997016177A1/en not_active Ceased
- 1996-10-30 IL IL12116796A patent/IL121167A0/xx unknown
- 1996-10-30 US US08/860,255 patent/US6274336B1/en not_active Expired - Fee Related
- 1996-10-30 HU HU9802488A patent/HUP9802488A3/hu unknown
- 1996-10-30 SK SK889-97A patent/SK88997A3/sk unknown
- 1996-10-30 PL PL96328877A patent/PL328877A1/xx unknown
- 1996-10-30 AU AU12707/97A patent/AU711014B2/en not_active Ceased
- 1996-10-30 CN CN96192191A patent/CN1177293A/zh active Pending
- 1996-10-30 CA CA002209109A patent/CA2209109A1/en not_active Abandoned
- 1996-10-30 EP EP96943476A patent/EP0804180A4/de not_active Withdrawn
- 1996-10-30 NZ NZ324921A patent/NZ324921A/xx unknown
- 1996-10-30 EA EA199700087A patent/EA199700087A1/ru unknown
- 1996-10-30 SK SK481-98A patent/SK48198A3/sk unknown
-
1997
- 1997-06-27 NO NO973009A patent/NO973009L/no not_active Application Discontinuation
- 1997-06-27 OA OA70040A patent/OA10786A/en unknown
- 1997-07-01 BG BG101712A patent/BG101712A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL328877A1 (en) | 1999-03-01 |
| NO973009D0 (no) | 1997-06-27 |
| NO973009L (no) | 1997-08-27 |
| EP0804180A1 (de) | 1997-11-05 |
| HUP9802488A3 (en) | 2001-10-29 |
| SK88997A3 (en) | 1998-05-06 |
| CN1177293A (zh) | 1998-03-25 |
| CZ206097A3 (cs) | 1999-02-17 |
| AU711014B2 (en) | 1999-10-07 |
| IL121167A0 (en) | 1997-11-20 |
| CA2209109A1 (en) | 1997-05-09 |
| US6274336B1 (en) | 2001-08-14 |
| WO1997016177A1 (en) | 1997-05-09 |
| JPH10512300A (ja) | 1998-11-24 |
| NZ324921A (en) | 2000-07-28 |
| EP0804180A4 (de) | 2001-09-05 |
| AU1270797A (en) | 1997-07-17 |
| BG101712A (en) | 1998-02-27 |
| EA199700087A1 (ru) | 1998-04-30 |
| HUP9802488A2 (hu) | 1999-02-01 |
| SK48198A3 (en) | 1998-10-07 |
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