|
US4943533A
(en)
|
1984-03-01 |
1990-07-24 |
The Regents Of The University Of California |
Hybrid cell lines that produce monoclonal antibodies to epidermal growth factor receptor
|
|
NZ226171A
(en)
|
1987-09-18 |
1990-06-26 |
Ethicon Inc |
Gel formulation containing polypeptide growth factor
|
|
GB8827305D0
(en)
|
1988-11-23 |
1988-12-29 |
British Bio Technology |
Compounds
|
|
CA2102780C
(en)
|
1991-05-10 |
2007-01-09 |
Alfred P. Spada |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase
|
|
NZ243082A
(en)
|
1991-06-28 |
1995-02-24 |
Ici Plc |
4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof
|
|
GB9300059D0
(en)
|
1992-01-20 |
1993-03-03 |
Zeneca Ltd |
Quinazoline derivatives
|
|
GB9215665D0
(en)
|
1992-07-23 |
1992-09-09 |
British Bio Technology |
Compounds
|
|
CN1038583C
(zh)
|
1993-08-09 |
1998-06-03 |
钟纺株式会社 |
酰基苯基甘氨酸衍生物及以其为有效成分的胶原酶活性亢进所致疾病的防治药物
|
|
FI960803L
(fi)
|
1993-08-23 |
1996-04-22 |
Immunex Corp |
TNF-alfa-sekreetion inhibiittoreita
|
|
JPH08503971A
(ja)
|
1993-10-01 |
1996-04-30 |
チバ−ガイギー アクチェンゲゼルシャフト |
ピリミジンアミン誘導体及びその調製のための方法
|
|
US5656643A
(en)
|
1993-11-08 |
1997-08-12 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
|
IL112248A0
(en)
|
1994-01-25 |
1995-03-30 |
Warner Lambert Co |
Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
|
|
IL112249A
(en)
|
1994-01-25 |
2001-11-25 |
Warner Lambert Co |
Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
|
|
WO1995024190A2
(en)
|
1994-03-07 |
1995-09-14 |
Sugen, Inc. |
Receptor tyrosine kinase inhibitors for inhibiting cell proliferative disorders and compositions thereof
|
|
DE59500788D1
(de)
|
1994-05-03 |
1997-11-20 |
Ciba Geigy Ag |
Pyrrolopyrimidinderivate mit antiproliferativer Wirkung
|
|
DE69536015D1
(de)
|
1995-03-30 |
2009-12-10 |
Pfizer Prod Inc |
Chinazolinone Derivate
|
|
JP4249804B2
(ja)
|
1995-04-03 |
2009-04-08 |
ノバルティス・アクチエンゲゼルシャフト |
ピラゾール誘導体およびその製造法
|
|
JP3814696B2
(ja)
|
1995-04-17 |
2006-08-30 |
住友精化株式会社 |
芳香族またはヘテロ芳香族スルホニルハライド類の製造方法
|
|
US5691381A
(en)
|
1995-04-18 |
1997-11-25 |
The Dupont Merck Pharmaceutical Company |
Hydroxamic and carbocyclic acids as metalloprotease inhibitors
|
|
DE69632821T2
(de)
|
1995-04-25 |
2005-08-25 |
Daiichi Fine Chemical Co., Ltd., Takaoka |
In wasser hochlöslicher metalloproteinase-inhibitor
|
|
GB9508538D0
(en)
|
1995-04-27 |
1995-06-14 |
Zeneca Ltd |
Quinazoline derivatives
|
|
US5747498A
(en)
*
|
1996-05-28 |
1998-05-05 |
Pfizer Inc. |
Alkynyl and azido-substituted 4-anilinoquinazolines
|
|
US5650415A
(en)
|
1995-06-07 |
1997-07-22 |
Sugen, Inc. |
Quinoline compounds
|
|
GB9513331D0
(en)
|
1995-06-30 |
1995-09-06 |
British Biotech Pharm |
Matrix metalloproteinase inhibitors
|
|
EP0836605B1
(en)
|
1995-07-06 |
2002-02-06 |
Novartis AG |
Pyrrolopyrimidines and processes for the preparation thereof
|
|
DK9500262U4
(da)
|
1995-07-07 |
1996-10-07 |
Bonus Energy As |
Bundramme til vindmøllehus samt vindmølle omfattende samme
|
|
AR004010A1
(es)
|
1995-10-11 |
1998-09-30 |
Glaxo Group Ltd |
Compuestos heterociclicos
|
|
SK63498A3
(en)
|
1995-11-14 |
1999-01-11 |
Du Pont Merck Pharma |
Novel macrocyclic compounds as metalloprotease inhibitors
|
|
US6281352B1
(en)
|
1995-11-14 |
2001-08-28 |
Dupont Pharmaceuticals Company |
Macrocyclic compounds as metalloprotease inhibitors
|
|
US5665777A
(en)
|
1995-11-14 |
1997-09-09 |
Abbott Laboratories |
Biphenyl hydroxamate inhibitors of matrix metalloproteinases
|
|
GB9523637D0
(en)
|
1995-11-18 |
1996-01-17 |
British Biotech Pharm |
Synthesis of carboxylic acid derivatives
|
|
GB9523675D0
(en)
|
1995-11-20 |
1996-01-24 |
Celltech Therapeutics Ltd |
Chemical compounds
|
|
JP2000500761A
(ja)
|
1995-11-23 |
2000-01-25 |
ブリティッシュ バイオテック ファーマシューティカルズ リミテッド |
金属タンパク質分解酵素阻害剤
|
|
DE69633947T2
(de)
|
1995-12-08 |
2005-12-01 |
Agouron Pharmaceuticals, Inc., San Diego |
Zwischenprodukte zur Herstellung von Metallproteinasehemmern
|
|
WO1997024117A1
(en)
|
1996-01-02 |
1997-07-10 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Substituted (aryl, heteroaryl, arylmethyl or heteroarylmethyl) hydroxamic acid compounds
|
|
AU1441497A
(en)
|
1996-01-23 |
1997-08-20 |
Novartis Ag |
Pyrrolopyrimidines and processes for their preparation
|
|
JP3406763B2
(ja)
|
1996-01-30 |
2003-05-12 |
東レ・ダウコーニング・シリコーン株式会社 |
シリコーンゴム組成物
|
|
GB9603097D0
(en)
|
1996-02-14 |
1996-04-10 |
Zeneca Ltd |
Quinazoline compounds
|
|
GB9603095D0
(en)
|
1996-02-14 |
1996-04-10 |
Zeneca Ltd |
Quinazoline derivatives
|
|
DE19608588A1
(de)
|
1996-03-06 |
1997-09-11 |
Thomae Gmbh Dr K |
Pyrimido [5,4-d]pyrimidine, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
|
|
DE19629652A1
(de)
|
1996-03-06 |
1998-01-29 |
Thomae Gmbh Dr K |
4-Amino-pyrimidin-Derivate, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
|
|
US6051577A
(en)
|
1996-03-15 |
2000-04-18 |
Novartis Ag |
N-7-heterocyclyl pyrrolo[2,3-D]pyrimidines and the use thereof
|
|
JP3370340B2
(ja)
|
1996-04-12 |
2003-01-27 |
ワーナー―ランバート・コンパニー |
チロシンキナーゼの不可逆的阻害剤
|
|
GB9607729D0
(en)
|
1996-04-13 |
1996-06-19 |
Zeneca Ltd |
Quinazoline derivatives
|
|
WO1997042168A1
(en)
|
1996-05-06 |
1997-11-13 |
Zeneca Limited |
Thio derivatives of hydroxamic acids
|
|
GB9609795D0
(en)
|
1996-05-10 |
1996-07-17 |
Smithkline Beecham Plc |
Novel compounds
|
|
GB9609794D0
(en)
|
1996-05-10 |
1996-07-17 |
Smithkline Beecham Plc |
Novel compounds
|
|
EP0907642B1
(en)
|
1996-06-24 |
2005-11-02 |
Pfizer Inc. |
Phenylamino-substituted tricyclic derivatives for treatment of hyperproliferative diseases
|
|
GB9613547D0
(en)
|
1996-06-27 |
1996-08-28 |
Pharmacia Spa |
Matrix metalloproteinase inhibitors
|
|
DE69716916T2
(de)
|
1996-07-13 |
2003-07-03 |
Glaxo Group Ltd., Greenford |
Kondensierte heterozyklische verbindungen als protein kinase inhibitoren
|
|
HRP970371A2
(en)
|
1996-07-13 |
1998-08-31 |
Kathryn Jane Smith |
Heterocyclic compounds
|
|
EA199900021A1
(ru)
|
1996-07-13 |
1999-08-26 |
Глаксо, Груп Лимитед |
Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы
|
|
GB9715962D0
(en)
|
1996-08-23 |
1997-10-01 |
Zeneca Ltd |
Sulfonamides
|
|
AU720429B2
(en)
|
1996-08-23 |
2000-06-01 |
Novartis Ag |
Substituted pyrrolopyrimidines and processes for their preparation
|
|
AU4779897A
(en)
|
1996-10-02 |
1998-04-24 |
Novartis Ag |
Fused pyrazole derivatives and processes for their preparation
|
|
ES2239779T3
(es)
|
1996-10-02 |
2005-10-01 |
Novartis Ag |
Derivados de pirimidina y procedimientos para la preparacion de los mismos.
|
|
ID18494A
(id)
|
1996-10-02 |
1998-04-16 |
Novartis Ag |
Turunan pirazola leburan dan proses pembuatannya
|
|
AU743901B2
(en)
|
1996-10-16 |
2002-02-07 |
Wyeth Holdings Corporation |
Ortho-sulfonamido bicyclic heteroaryl hydroxamic acids as matrix metalloprote inase and tace inhibitors
|
|
CN1105101C
(zh)
|
1996-10-16 |
2003-04-09 |
美国氰胺公司 |
作为基质金属蛋白质酶和TACE抑制剂的β-亚磺酰氨基异羟肟酸
|
|
AU743898B2
(en)
|
1996-10-16 |
2002-02-07 |
American Cyanamid Company |
The preparation and use of ortho-sulfonamido heteroaryl hydroxamic acids as matrix metalloproteinase and tace inhibitors
|
|
HUP0000641A3
(en)
|
1996-10-16 |
2001-02-28 |
American Cyanamid Company Madi |
Ortho-sulfonamido aryl hydroxamic acid derivatives, their use, as matrix metalloproteinase and tace inhibitors and pharmaceutical compositions containing them
|
|
EP0837063A1
(en)
|
1996-10-17 |
1998-04-22 |
Pfizer Inc. |
4-Aminoquinazoline derivatives
|
|
GB9621757D0
(en)
|
1996-10-18 |
1996-12-11 |
Ciba Geigy Ag |
Phenyl-substituted bicyclic heterocyclyl derivatives and their use
|
|
ZA9818B
(en)
|
1997-01-07 |
1998-07-02 |
Abbott Lab |
C-terminal ketone inhibitors of matrix metalloproteinases and tnf alpha secretion
|
|
ZA9820B
(en)
|
1997-01-07 |
1998-07-02 |
Abbott Lab |
Macrocyclic inhibitors of matrix metalloproteinases and tnf x secretion
|
|
IL130802A0
(en)
|
1997-01-23 |
2001-01-28 |
Hoffmann La Roche |
Sulfamide-metalloprotease inhibitors
|
|
KR20000070751A
(ko)
|
1997-02-05 |
2000-11-25 |
로즈 암스트롱, 크리스틴 에이. 트러트웨인 |
세포 증식 억제제로서의 피리도[2,3-d]피리미딘 및 4-아미노피리미딘
|
|
KR20000075681A
(ko)
|
1997-02-26 |
2000-12-26 |
그레이엄 브레레톤, 레슬리 에드워즈 |
메탈로프로테아제 억제제로서의 후위 히드록사메이트 유도체
|
|
GEP20022626B
(en)
|
1997-02-27 |
2002-02-25 |
American Cyanamid Company Us |
N-Hydroxy-2-(Alkyl, Aryl, or Heteroaryl Sulfanyl, Sulfinil or Sulfonyl)-3-Substituted Alkyl, Aryl or Heteroarylamides as Matrix Metalloproteinase Inhibitors
|
|
US7115632B1
(en)
|
1999-05-12 |
2006-10-03 |
G. D. Searle & Co. |
Sulfonyl aryl or heteroaryl hydroxamic acid compounds
|
|
US6362183B1
(en)
|
1997-03-04 |
2002-03-26 |
G. D. Searle & Company |
Aromatic sulfonyl alpha-hydroxy hydroxamic acid compounds
|
|
CA2285372A1
(en)
|
1997-04-01 |
1998-10-08 |
Melwyn A. Abreo |
Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
|
|
AUPO721997A0
(en)
|
1997-06-06 |
1997-07-03 |
Queensland Institute Of Medical Research, The |
Anticancer compounds
|
|
AU8858398A
(en)
|
1997-07-10 |
1999-02-08 |
Pharmacia & Upjohn S.P.A. |
Matrix metalloproteinase inhibitors
|
|
IT1296305B1
(it)
|
1997-07-17 |
1999-06-25 |
Polifarma Spa |
Inibitori di metalloproteinasi loro uso terapeutico e procedimento per la produzione del composto di partenza nella loro
|
|
WO1999006410A1
(en)
|
1997-08-04 |
1999-02-11 |
Amgen Inc. |
Hydroxamic acid substituted fused heterocyclic metalloproteinase inhibitors
|
|
WO1999007701A1
(en)
|
1997-08-05 |
1999-02-18 |
Sugen, Inc. |
Tricyclic quinoxaline derivatives as protein tyrosine kinase inhibitors
|
|
DE59703834D1
(de)
|
1997-08-25 |
2001-07-19 |
Hydac Filtertechnik Gmbh |
Filterelement mit kunststoff-filtermantel
|
|
DK1021413T3
(da)
|
1997-10-06 |
2003-10-06 |
Wyeth Corp |
Fremstilling og anvendelse af ortho-sulfonamido-bicykliske heteroarylhydroxamsyrer som matrixmetalloproteinase- og TACE-inhibitorer
|
|
US6750228B1
(en)
|
1997-11-14 |
2004-06-15 |
Pharmacia Corporation |
Aromatic sulfone hydroxamic acid metalloprotease inhibitor
|
|
EP1038864A1
(en)
|
1997-12-12 |
2000-09-27 |
Fuji Yakuhin Kogyo Kabushiki Kaisha |
Novel metalloproteinase inhibitors
|
|
GB9800575D0
(en)
|
1998-01-12 |
1998-03-11 |
Glaxo Group Ltd |
Heterocyclic compounds
|
|
RS49779B
(sr)
|
1998-01-12 |
2008-06-05 |
Glaxo Group Limited, |
Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze
|
|
BR9907746A
(pt)
|
1998-01-27 |
2000-10-17 |
American Cyanamid Co |
ácidos 2,3,4,5-tetraidro-1h[1,4]-benzodiazepina-3-hidroxâmic os como inibidores de matriz de metaloproteinase
|
|
ID25639A
(id)
|
1998-02-19 |
2000-10-19 |
American Cyanamid Co |
Alkil, aril atau heteroarilamida tersubstitusi n-hidroksi-2-(alkil, aril, atau heteroaril sulfanil, sulfinil atau sulfonil)-3 sebagai inhibitor matriks mataloproteinase
|
|
CN1301265A
(zh)
|
1998-05-14 |
2001-06-27 |
杜邦药品公司 |
新的用作金属蛋白酶抑制剂的取代的芳基异羟肟酸
|
|
CA2332946A1
(en)
|
1998-05-22 |
1999-12-02 |
Welfide Corporation |
Hydroxamic acid derivative and pharmaceutical use thereof
|
|
US6552223B1
(en)
|
1998-08-31 |
2003-04-22 |
Astrazeneca Ab |
N-hydroxacylamino compounds, process for their preparation and pharmaceutical compositions containing them
|
|
GB9919776D0
(en)
|
1998-08-31 |
1999-10-27 |
Zeneca Ltd |
Compoujnds
|
|
JP3913983B2
(ja)
|
1998-12-11 |
2007-05-09 |
エフ.ホフマン−ラ ロシュ アーゲー |
TNF−α阻害剤としての環式ヒドラジン誘導体
|
|
PT1144369E
(pt)
|
1999-01-27 |
2004-11-30 |
Wyeth Corp |
Acidos hidroxamicos de arilsulfonamidas acetilenicas e de amidas de acido fosfinico acetilenicas inibidores de tace
|
|
AR035478A1
(es)
|
1999-01-27 |
2004-06-02 |
Wyeth Corp |
Acido amida-hidroxamico, acido acetilenico, beta-sulfonamido y fosfinico como inhibidores de la tace, uso de los mismos para la manufactura de un medicamento y composicion farmaceutica que los contiene
|
|
AR022423A1
(es)
|
1999-01-27 |
2002-09-04 |
American Cyanamid Co |
Compuestos derivados de acidos 2,3,4,5-tetrahidro-1h-[1,4]benzodiazepina-3-hidroxamicos, composicion farmaceutica que los comprenden, y el uso de losmismos para la manufactura de un medicamento
|
|
CN1224612C
(zh)
|
1999-01-27 |
2005-10-26 |
惠氏控股有限公司 |
炔基磺酰胺硫醇tace抑制剂
|
|
AR035313A1
(es)
|
1999-01-27 |
2004-05-12 |
Wyeth Corp |
Inhibidores de tace acetilenicos de acido hidroxamico de sulfonamida a base de alfa-aminoacidos, composiciones farmaceuticas y el uso de los mismos para la manufactura de medicamentos.
|
|
AR022422A1
(es)
|
1999-01-27 |
2002-09-04 |
American Cyanamid Co |
Inhibidores de tace acetilenicos de acido hidroxamico de heteroarilfulfonamida y amida del acido fosfinico
|
|
AR022424A1
(es)
|
1999-01-27 |
2002-09-04 |
American Cyanamid Co |
Compuestos derivados de acidos ortosulfonamido acetilenico e hidroxamico biciclico heteroarilo amido de acido fosfinico como inhibidores tace, composicionfarmaceutica que los comprende y el uso de los mismos para la manufactura de un medicamento
|
|
US6358980B1
(en)
|
1999-01-27 |
2002-03-19 |
American Cyanamid Company |
Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase/tace inhibitors
|
|
AR035311A1
(es)
|
1999-01-27 |
2004-05-12 |
Wyeth Corp |
Derivados de acido hidroxamico que contienen alquinilo, como inhibidores de las metalloproteinasas de matriz y de la tace, composicion farmaceutica y el uso de los mismos para la manufactura de un medicamento
|
|
AU2320500A
(en)
|
1999-02-02 |
2000-08-25 |
Shionogi & Co., Ltd. |
Sulfonamide derivatives having cyclic structures
|
|
AP2001002240A0
(en)
|
1999-02-08 |
2001-09-30 |
Searle & Co |
Sufamato hydroxamic acid metalloprotease inhibitor.
|
|
CA2367963A1
(en)
|
1999-03-22 |
2000-09-28 |
Darwin Discovery Limited |
Hydroxamic and carboxylic acid derivatives
|
|
WO2000059285A2
(en)
|
1999-04-02 |
2000-10-12 |
Du Pont Pharmaceuticals Company |
NOVEL LACTAM INHIBITORS OF MATRIX METALLOPROTEINASES, TNF-α, AND AGGRECANASE
|
|
GB9911073D0
(en)
|
1999-05-12 |
1999-07-14 |
Darwin Discovery Ltd |
Hydroxamic and carboxylic acid derivatives
|
|
EP1177173A1
(en)
|
1999-05-12 |
2002-02-06 |
G.D. Searle & Co. |
Hydroxamic acid derivatives as matrix metalloprotease inhibitors
|
|
GB9911071D0
(en)
|
1999-05-12 |
1999-07-14 |
Darwin Discovery Ltd |
Hydroxamic and carboxylic acid derivatives
|
|
GB9911075D0
(en)
|
1999-05-12 |
1999-07-14 |
Darwin Discovery Ltd |
HYdroxamic and carboxylic acid derivatives
|
|
AU4614000A
(en)
|
1999-05-17 |
2000-12-05 |
Daiichi Fine Chemical Co., Ltd. |
Novel hydroxamic acid derivatives
|
|
US6583299B1
(en)
|
1999-05-20 |
2003-06-24 |
G.D. Searle & Co. |
α-amino-β-sulfonyl hydroxamic acid compounds
|
|
KR20020005769A
(ko)
|
1999-06-04 |
2002-01-17 |
다비드 에 질레스 |
메탈로프로테이나제의 억제제
|
|
TR200202164T2
(tr)
|
1999-08-18 |
2002-11-21 |
Warner-Lambert Company |
Matris metaloproteinaz inhibitörleri olarak kullanışlı olan hidroksamik asit bileşikleri.
|
|
GB9922825D0
(en)
|
1999-09-25 |
1999-11-24 |
Smithkline Beecham Biolog |
Medical use
|
|
US6632667B1
(en)
|
1999-10-28 |
2003-10-14 |
Isis Pharmaceuticals, Inc. |
Modulation of L-selectin shedding via inhibition of tumor necrosis factor-α converting enzyme (TACE)
|
|
UA74803C2
(uk)
|
1999-11-11 |
2006-02-15 |
Осі Фармасьютікалз, Інк. |
Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування
|
|
GB9929979D0
(en)
|
1999-12-17 |
2000-02-09 |
Darwin Discovery Ltd |
Hydroxamic acid derivatives
|
|
EP1252143A1
(en)
|
2000-01-27 |
2002-10-30 |
American Cyanamid Company |
Method for preparing alpha-sulfonyl hydroxamic acid derivatives
|
|
US6989139B2
(en)
|
2000-02-15 |
2006-01-24 |
Bristol-Myers Squibb Pharma Company |
Matrix metalloproteinase inhibitors
|
|
JP2003524008A
(ja)
|
2000-02-21 |
2003-08-12 |
アストラゼネカ・アクチエボラーグ |
アリールピペラジンおよびアリールピペリジン、およびそれらのメタロプロテイナーゼ阻害剤としての使用
|
|
AU2001232113A1
(en)
|
2000-02-21 |
2001-09-03 |
Astrazeneca Ab |
Arylpiperazines and their use as metalloproteinase inhibiting agents (mmp)
|
|
MXPA02008111A
(es)
|
2000-02-21 |
2002-11-29 |
Astrazeneca Ab |
N-hidroxiformamidas substituidas con piperidina y piperazina como inhibidores de metaloproteinasas.
|
|
AR027943A1
(es)
|
2000-02-25 |
2003-04-16 |
Wyeth Corp |
Acidos orto-sulfonamido aril hidroxamicos como inhibidores de metaloproteinasa de matriz y preparacion de los mismos
|
|
CN1481377A
(zh)
|
2000-03-17 |
2004-03-10 |
����˹�ж�-����˹˹����ҩƷ��˾ |
作为基质金属蛋白酶和TNF-α的抑制剂的环β-氨基酸衍生物
|
|
AU2001250850A1
(en)
|
2000-03-17 |
2001-10-03 |
Dupont Pharmaceuticals Company |
Beta-amino acid derivatives as inhibitors of matrix metalloproteases and tnf-alpha
|
|
EP1286994A1
(en)
|
2000-05-15 |
2003-03-05 |
Darwin Discovery Limited |
Hydroxamic and carboxylic acid derivatives having mmp and tnf inhibitory activity
|
|
WO2001087870A1
(en)
|
2000-05-15 |
2001-11-22 |
Darwin Discovery Limited |
Hydroxamic acid derivatives
|
|
US6620823B2
(en)
|
2000-07-11 |
2003-09-16 |
Bristol-Myers Squibb Pharme Company |
Lactam metalloprotease inhibitors
|
|
GB0017435D0
(en)
|
2000-07-14 |
2000-08-30 |
Pharmacia & Upjohn Spa |
3-arylsulfonyl-2-hydroxy-2-methylpropanoic acid derivatives
|
|
KR101822444B1
(ko)
|
2010-07-08 |
2018-01-26 |
가켄 세이야쿠 가부시키가이샤 |
N-히드록시포름아미드 유도체 및 그를 함유하는 의약
|