JP2005526857A5 - - Google Patents
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- JP2005526857A5 JP2005526857A5 JP2004507431A JP2004507431A JP2005526857A5 JP 2005526857 A5 JP2005526857 A5 JP 2005526857A5 JP 2004507431 A JP2004507431 A JP 2004507431A JP 2004507431 A JP2004507431 A JP 2004507431A JP 2005526857 A5 JP2005526857 A5 JP 2005526857A5
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- Japan
- Prior art keywords
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- pharmaceutically acceptable
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- 239000008194 pharmaceutical composition Substances 0.000 claims 29
- 125000001931 aliphatic group Chemical group 0.000 claims 28
- 150000001875 compounds Chemical class 0.000 claims 22
- 150000003839 salts Chemical class 0.000 claims 21
- 239000011780 sodium chloride Substances 0.000 claims 21
- 239000012453 solvate Substances 0.000 claims 21
- 125000005843 halogen group Chemical group 0.000 claims 16
- 125000001188 haloalkyl group Chemical group 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 12
- 125000001072 heteroaryl group Chemical group 0.000 claims 9
- 125000001424 substituent group Chemical group 0.000 claims 9
- 125000004429 atoms Chemical group 0.000 claims 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims 8
- 125000005842 heteroatoms Chemical group 0.000 claims 8
- -1 aliphatic ester Chemical class 0.000 claims 6
- 230000002401 inhibitory effect Effects 0.000 claims 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 5
- 200000000018 inflammatory disease Diseases 0.000 claims 5
- 210000000265 Leukocytes Anatomy 0.000 claims 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 4
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims 4
- 125000004104 aryloxy group Chemical group 0.000 claims 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 4
- 125000006575 electron-withdrawing group Chemical group 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 101700040666 ACKR2 Proteins 0.000 claims 3
- 102100008149 CCR9 Human genes 0.000 claims 3
- 101700076302 CCR9 Proteins 0.000 claims 3
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims 3
- 230000027455 binding Effects 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 125000004971 nitroalkyl group Chemical group 0.000 claims 3
- 125000004385 trihaloalkyl group Chemical group 0.000 claims 3
- 102000004900 CC chemokine receptor 9 Human genes 0.000 claims 2
- 108090001026 CC chemokine receptor 9 Proteins 0.000 claims 2
- 206010011401 Crohn's disease Diseases 0.000 claims 2
- 210000004400 Mucous Membrane Anatomy 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- 230000001404 mediated Effects 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 206010009839 Coeliac disease Diseases 0.000 claims 1
- 201000008260 Crohn's colitis Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US38357302P | 2002-05-24 | 2002-05-24 | |
US60/383,573 | 2002-05-24 | ||
PCT/US2003/016090 WO2003099773A1 (en) | 2002-05-24 | 2003-05-21 | Ccr9 inhibitors and methods of use thereof |
Related Child Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006124437A Division JP4818798B2 (ja) | 2002-05-24 | 2006-04-27 | Ccr9インヒビターおよびその使用方法 |
JP2009235795A Division JP2010047584A (ja) | 2002-05-24 | 2009-10-09 | Ccr9インヒビターおよびその使用方法 |
JP2010265823A Division JP5544283B2 (ja) | 2002-05-24 | 2010-11-29 | Ccr9インヒビターおよびその使用方法 |
JP2011167759A Division JP5432221B2 (ja) | 2002-05-24 | 2011-07-29 | Ccr9インヒビターおよびその使用方法 |
JP2011167760A Division JP5548169B2 (ja) | 2002-05-24 | 2011-07-29 | Ccr9インヒビターおよびその使用方法 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2005526857A JP2005526857A (ja) | 2005-09-08 |
JP2005526857A5 true JP2005526857A5 (US07794700-20100914-C00152.png) | 2006-06-22 |
JP4828822B2 JP4828822B2 (ja) | 2011-11-30 |
Family
ID=29584585
Family Applications (7)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004507431A Expired - Lifetime JP4828822B2 (ja) | 2002-05-24 | 2003-05-21 | Ccr9インヒビターおよびその使用方法 |
JP2006124437A Expired - Fee Related JP4818798B2 (ja) | 2002-05-24 | 2006-04-27 | Ccr9インヒビターおよびその使用方法 |
JP2009235795A Pending JP2010047584A (ja) | 2002-05-24 | 2009-10-09 | Ccr9インヒビターおよびその使用方法 |
JP2010265823A Expired - Fee Related JP5544283B2 (ja) | 2002-05-24 | 2010-11-29 | Ccr9インヒビターおよびその使用方法 |
JP2011167759A Expired - Fee Related JP5432221B2 (ja) | 2002-05-24 | 2011-07-29 | Ccr9インヒビターおよびその使用方法 |
JP2011167760A Expired - Fee Related JP5548169B2 (ja) | 2002-05-24 | 2011-07-29 | Ccr9インヒビターおよびその使用方法 |
JP2014036198A Pending JP2014132018A (ja) | 2002-05-24 | 2014-02-27 | Ccr9インヒビターおよびその使用方法 |
Family Applications After (6)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006124437A Expired - Fee Related JP4818798B2 (ja) | 2002-05-24 | 2006-04-27 | Ccr9インヒビターおよびその使用方法 |
JP2009235795A Pending JP2010047584A (ja) | 2002-05-24 | 2009-10-09 | Ccr9インヒビターおよびその使用方法 |
JP2010265823A Expired - Fee Related JP5544283B2 (ja) | 2002-05-24 | 2010-11-29 | Ccr9インヒビターおよびその使用方法 |
JP2011167759A Expired - Fee Related JP5432221B2 (ja) | 2002-05-24 | 2011-07-29 | Ccr9インヒビターおよびその使用方法 |
JP2011167760A Expired - Fee Related JP5548169B2 (ja) | 2002-05-24 | 2011-07-29 | Ccr9インヒビターおよびその使用方法 |
JP2014036198A Pending JP2014132018A (ja) | 2002-05-24 | 2014-02-27 | Ccr9インヒビターおよびその使用方法 |
Country Status (9)
Families Citing this family (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2003229767A1 (en) * | 2002-05-14 | 2003-11-11 | Bayer Healthcare Ag | Diagnostics and therapeutics for diseases associated with chemokine receptor 9(ccr9) |
WO2003099773A1 (en) * | 2002-05-24 | 2003-12-04 | Millennium Pharmaceuticals, Inc. | Ccr9 inhibitors and methods of use thereof |
US7227035B2 (en) | 2002-11-18 | 2007-06-05 | Chemocentryx | Bis-aryl sulfonamides |
ATE517102T1 (de) * | 2002-11-18 | 2011-08-15 | Chemocentryx Inc | Arylsulfonamide |
US7741519B2 (en) | 2007-04-23 | 2010-06-22 | Chemocentryx, Inc. | Bis-aryl sulfonamides |
US7420055B2 (en) * | 2002-11-18 | 2008-09-02 | Chemocentryx, Inc. | Aryl sulfonamides |
US7288538B2 (en) | 2003-02-20 | 2007-10-30 | Encysive Pharmaceuticals, Inc. | Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists |
CA2767153A1 (en) | 2003-02-20 | 2004-09-02 | Encysive Pharmaceuticals Inc. | Phenylenediamine urotensin-ii receptor antagonists and ccr-9 antagonists |
US7265122B2 (en) | 2003-02-28 | 2007-09-04 | Encysive Pharmaceuticals, Inc. | Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists |
US7320989B2 (en) | 2003-02-28 | 2008-01-22 | Encysive Pharmaceuticals, Inc. | Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists |
DE102004027119A1 (de) | 2003-06-06 | 2004-12-30 | Schott Ag | UV-Strahlung absorbierendes Glas mit geringer Absorption im sichtbaren Bereich, ein Verfahren zu seiner Herstellung sowie dessen Verwendung |
US7393873B2 (en) | 2003-07-02 | 2008-07-01 | Merck & Co., Inc. | Arylsulfonamide derivatives |
WO2005060963A1 (en) * | 2003-12-19 | 2005-07-07 | Pfizer Inc. | Benzenesulfonylamino-pyridin-2-yl derivatives and related compounds as inhibitors of 11-beta-hydroxysteroid dehydrogenase type 1 (11-beta-hsd-1) for the treatment of diabetes and obesity |
US7479496B2 (en) | 2004-02-19 | 2009-01-20 | Bristol-Myers Squibb Company | Substituted spiro azabicyclics as modulators of chemokine receptor activity |
US7288563B2 (en) | 2004-02-19 | 2007-10-30 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
US7381738B2 (en) | 2004-02-19 | 2008-06-03 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
US7230022B2 (en) | 2004-02-19 | 2007-06-12 | Bristol-Myers Squibb Company | Substituted fused bicyclic amines as modulators of chemokine receptor activity |
EP1748989A2 (en) * | 2004-05-12 | 2007-02-07 | ChemoCentryx Inc | Aryl sulfonamides |
CA2571361C (en) | 2004-06-28 | 2011-07-26 | F. Hoffmann-La Roche Ag | Pyrimidine derivatives as 11beta-hsd1 inhibitors |
DE602005012292D1 (de) | 2004-09-29 | 2009-02-26 | Hoffmann La Roche | Indozolonderivate als 11b-hsd1-inhibitoren |
SE0402635D0 (sv) * | 2004-10-29 | 2004-10-29 | Astrazeneca Ab | Chemical compounds |
EP2270512B1 (en) * | 2004-12-08 | 2016-03-23 | Cedars-Sinai Medical Center | Methods for diagnosis of Crohn's disease |
US7622583B2 (en) * | 2005-01-14 | 2009-11-24 | Chemocentryx, Inc. | Heteroaryl sulfonamides and CCR2 |
ATE503741T1 (de) * | 2005-01-14 | 2011-04-15 | Chemocentryx Inc | Heteroarylsulfonamide und ccr2 |
EP1893609B1 (en) | 2005-06-16 | 2009-11-18 | Pfizer, Inc. | N-(pyridin-2-yl)-sulfonamide derivatives |
FI20055498A0 (fi) * | 2005-09-16 | 2005-09-16 | Biotie Therapies Corp | Sulfonamidijohdannaisia |
GB0524786D0 (en) * | 2005-12-05 | 2006-01-11 | Glaxo Group Ltd | Compounds |
GB0526252D0 (en) * | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
GB0526255D0 (en) * | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
GB0526445D0 (en) * | 2005-12-23 | 2006-02-08 | Novartis Ag | Organic compounds |
KR101433392B1 (ko) | 2006-07-14 | 2014-08-29 | 케모센트릭스, 인크. | 트리아졸릴 페닐 벤젠설폰아마이드 |
US8519135B2 (en) * | 2006-07-14 | 2013-08-27 | Chemocentryx, Inc. | Heteroaryl sulfonamides and CCR2/CCR9 |
WO2008008374A2 (en) * | 2006-07-14 | 2008-01-17 | Chemocentryx, Inc. | Ccr2 inhibitors and methods of use thereof |
HUP0600810A3 (en) * | 2006-10-27 | 2008-09-29 | Richter Gedeon Nyrt | New sulfonamide derivatives as bradykinin antagonists, process and intermediates for their preparation and pharmaceutical compositions containing them |
TW200829578A (en) | 2006-11-23 | 2008-07-16 | Astrazeneca Ab | Chemical compounds 537 |
JO2754B1 (en) | 2006-12-21 | 2014-03-15 | استرازينكا ايه بي | Amylendazoleil derivatives for the treatment of glucocorticoid-mediated disorders |
NZ578744A (en) | 2007-01-31 | 2012-02-24 | Vertex Pharma | 2-aminopyridine derivatives useful as kinase inhibitors |
US20100021917A1 (en) * | 2007-02-14 | 2010-01-28 | Cedars-Sinai Medical Center | Methods of using genes and genetic variants to predict or diagnose inflammatory bowel disease |
US20100190162A1 (en) * | 2007-02-26 | 2010-07-29 | Cedars-Sinai Medical Center | Methods of using single nucleotide polymorphisms in the tl1a gene to predict or diagnose inflammatory bowel disease |
WO2010039931A2 (en) * | 2008-10-01 | 2010-04-08 | Cedars-Sinai Medical Center | Methods of using il17rd and il23-il17 pathway genes to diagnose crohn's disease |
WO2008137762A2 (en) * | 2007-05-04 | 2008-11-13 | Cedars-Sinai Medical Center | Methods of diagnosis and treatment of crohn's disease |
US20100015156A1 (en) * | 2007-03-06 | 2010-01-21 | Cedars-Sinai Medical Center | Diagnosis of inflammatory bowel disease in children |
US8486640B2 (en) | 2007-03-21 | 2013-07-16 | Cedars-Sinai Medical Center | Ileal pouch-anal anastomosis (IPAA) factors in the treatment of inflammatory bowel disease |
US20100184050A1 (en) * | 2007-04-26 | 2010-07-22 | Cedars-Sinai Medical Center | Diagnosis and treatment of inflammatory bowel disease in the puerto rican population |
US7776877B2 (en) | 2007-06-22 | 2010-08-17 | Chemocentryx, Inc. | N-(2-(hetaryl)aryl) arylsulfonamides and N-(2-(hetaryl) hetaryl arylsulfonamides |
CA2692761C (en) * | 2007-07-12 | 2013-04-30 | Chemocentryx, Inc. | Fused heteroaryl pyridyl and phenyl benzenesulfonamides as ccr2 modulators for the treament of inflammation |
US20090028866A1 (en) * | 2007-07-27 | 2009-01-29 | John Wayne Cancer Institute | USE OF CCR9, CCL25/TECK, AND NITEGRIN alpha4 IN DIAGNOSIS AND TREATMENT OF MELANOMA METASTASIS IN THE SMALL INTESTINE |
US20100080786A1 (en) | 2008-05-20 | 2010-04-01 | Markus Berger | Phenyl or Pyridinyl Substituted Indazoles Derivatives |
WO2010011768A1 (en) | 2008-07-23 | 2010-01-28 | Vertex Pharmaceuticals Incorporated | Tri-cyclic pyrazolopyridine kinase inhibitors |
CA2731451A1 (en) | 2008-07-23 | 2010-01-28 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridine kinase inhibitors |
US8569337B2 (en) | 2008-07-23 | 2013-10-29 | Vertex Pharmaceuticals Incorporated | Tri-cyclic pyrazolopyridine kinase inhibitors |
MX2011001319A (es) | 2008-08-06 | 2011-04-05 | Vertex Pharma | Inhibidores de aminopiridina cinasa. |
US20110189685A1 (en) * | 2008-10-22 | 2011-08-04 | Cedars-Sinai Medical Center | Methods of using jak3 genetic variants to diagnose and predict crohn's disease |
US20110229471A1 (en) | 2008-11-26 | 2011-09-22 | Cedars-Sinai Medical Center | Methods of determining responsiveness to anti-tnf alpha therapy in inflammatory bowel disease |
WO2010075579A2 (en) | 2008-12-24 | 2010-07-01 | Cedars-Sinai Medical Center | Methods of predicting medically refractive ulcerative colitis (mr-uc) requiring colectomy |
CN102459259A (zh) | 2009-05-06 | 2012-05-16 | 沃泰克斯药物股份有限公司 | 吡唑并吡啶类 |
ES2547072T3 (es) * | 2009-07-21 | 2015-10-01 | The Board Of Trustees Of The Leland Stanford Junior University | Heteroaril benzamidas, composiciones y métodos de utilización |
WO2011017120A1 (en) * | 2009-07-27 | 2011-02-10 | Cedars-Sinai Medical Center | Use of ccr9, ccl25, batf and il17/il23 pathway variants to diagnose and treat inflammatory bowel disease |
AU2011209649A1 (en) | 2010-01-27 | 2012-08-09 | Vertex Pharmaceuticals Incorporated | Pyrazolopyrazine kinase inhibitors |
US9067932B2 (en) | 2010-01-27 | 2015-06-30 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridine kinase inhibitors |
WO2011094290A1 (en) | 2010-01-27 | 2011-08-04 | Vertex Pharmaceuticals Incorporated | Pyrazolopyrimidine kinase inhibitors |
CN108383828A (zh) | 2010-12-16 | 2018-08-10 | 阿勒根公司 | 作为趋化因子受体调节剂的新的1,2-双-磺酰胺衍生物 |
AU2011344148B2 (en) | 2010-12-16 | 2017-04-27 | Allergan, Inc. | Phosphorous derivatives as chemokine receptor modulators |
KR101303991B1 (ko) | 2011-03-18 | 2013-09-04 | 성균관대학교산학협력단 | 포스포리파제C의 활성인자인 m-3M3FBS를 유효성분으로 포함하는 염증성 질환 또는 감염성 질환의 예방 또는 치료용 약학적 조성물 |
UY34054A (es) | 2011-05-02 | 2012-11-30 | Millennium Pharm Inc | FORMULACIÓN PARA ANTICUERPO ANTI-a(alfa)4B(Beta)7 |
UA116189C2 (uk) | 2011-05-02 | 2018-02-26 | Мілленніум Фармасьютікалз, Інк. | КОМПОЗИЦІЯ АНТИ-α4β7 АНТИТІЛА |
MX2014000659A (es) | 2011-07-22 | 2014-07-09 | Chemocentrix Inc | Formas polimorficas de la sal de sodio de 4-ter-butil-[4-cloro-2-( 1-oxi-piridina-4-carbonil)-fenil]-bencensulfonamida. |
DK2748146T3 (en) * | 2011-07-22 | 2017-05-22 | Chemocentryx Inc | CRYSTALLINE FORM OF THE SODIUM SALT OF 4-TERT-BUTYL-N- [4-CHLOR-2- (1-OXY-PYRIDINE-4-CARBONYL) -PHENYL] -BENZEN SULPHONAMIDE |
WO2013016156A1 (en) * | 2011-07-22 | 2013-01-31 | Glaxo Group Limited | Polymorphic forms of the sodium salt of 4-tert- butyl -n-[4-chloro-2-(1-oxy-pyridine-4-carbonyl)-phenyl]-benzene sulfonamide |
AU2013225938B2 (en) | 2012-02-29 | 2017-08-10 | Chemocentryx, Inc. | Pyrazol-1-yl benzene sulfonamides as CCR9 antagonists |
HUE038700T2 (hu) | 2012-03-01 | 2018-11-28 | Allergan Inc | Benzofuran-2-szulfonamid származékok, mint kemokinreceptor-modulációk |
WO2014008417A1 (en) | 2012-07-04 | 2014-01-09 | Concert Pharmaceuticals, Inc. | Deuterated vercirnon |
WO2014088113A1 (en) | 2012-12-04 | 2014-06-12 | Millennium Pharmaceuticals, Inc. | Prophylactic or therapeutic method for sjogren's syndrome using specific ccr9 receptor inhibitors/antagonists |
EP2970239B1 (en) * | 2013-03-12 | 2018-10-10 | Allergan, Inc. | Sulfonamide derivatives as chemokine receptor modulators |
KR20210157418A (ko) | 2013-03-27 | 2021-12-28 | 세다르스-신나이 메디칼 센터 | Tl1a 기능 및 관련된 신호전달 경로의 저해에 의한 섬유증 및 염증의 완화 및 반전 |
EP4105236A1 (en) | 2013-07-19 | 2022-12-21 | Cedars-Sinai Medical Center | Anti-tl1a (tnfsf15) antibody for treatment of inflammatory bowel disease |
EP3087074A1 (en) | 2013-12-23 | 2016-11-02 | Norgine BV | Benzene sulfonamides as ccr9 inhibitors |
WO2015097121A1 (en) | 2013-12-23 | 2015-07-02 | Norgine B.V. | Compounds useful as ccr9 modulators |
NZ768528A (en) * | 2014-10-06 | 2024-03-22 | Chemocentryx Inc | Combination therapy of inhibitors of c-c chemokine receptor type 9 (ccr9) and anti-α4β7 integrin blocking antibodies |
US20170327584A1 (en) | 2014-11-26 | 2017-11-16 | Millennium Pharmaceuticals, Inc. | Vedolizumab for the Treatment of Fistulizing Crohn's Disease |
MA41636A (fr) | 2015-03-06 | 2018-01-09 | Millennium Pharm Inc | Méthode de traitement de la cholangite sclérosante primitive |
CA3017743A1 (en) | 2016-03-14 | 2017-09-21 | Millennium Pharmaceuticals, Inc. | Method of preventing graft versus host disease |
WO2017160700A1 (en) | 2016-03-14 | 2017-09-21 | Millennium Pharmaceuticals, Inc. | Methods of treating or preventing graft versus host disease |
EP3430172A4 (en) | 2016-03-17 | 2019-08-21 | Cedars-Sinai Medical Center | METHOD FOR DIAGNOSIS OF INFLAMMATORY ENDURANCE THROUGH RNASET2 |
IL266751B (en) | 2016-11-23 | 2022-07-01 | Chemocentryx Inc | A method for the treatment of focal segmental tuberous sclerosis |
MX2019012749A (es) | 2017-04-28 | 2020-02-03 | Millennium Pharm Inc | Metodos para tratar trastornos pediatricos. |
JP2020536919A (ja) | 2017-10-11 | 2020-12-17 | ケモセントリックス, インコーポレイテッド | Ccr2アンタゴニストによる巣状分節性糸球体硬化症の治療 |
US20210154292A1 (en) * | 2019-11-21 | 2021-05-27 | Chemocentryx, Inc. | Compositions and Methods for Treating CCR9-Mediated Diseases using CCR9 Inhibitor and Anti-TNF-Alpha Blocking Antibodies |
US10792360B1 (en) | 2019-11-21 | 2020-10-06 | Chemocentryx, Inc. | Compositions and methods for treating inflammatory bowel disease using CCR9 inhibitor and anti-TNF-alpha blocking antibodies |
Family Cites Families (118)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2997368A (en) | 1956-12-20 | 1961-08-22 | Barent Mark | Production of manganese hydroxide |
GB884847A (en) * | 1958-04-14 | 1961-12-20 | Ciba Ltd | Mercapto compounds |
CH408029A (de) * | 1959-12-10 | 1966-02-28 | Hoffmann La Roche | Verfahren zur Herstellung von 1,4-Benzodiazepinen |
DE1145626B (de) * | 1959-12-10 | 1963-03-21 | Hoffmann La Roche | Verfahren zur Herstellung von 3H-1, 4-Benzodiazepin-2(1H)-on-derivaten |
US3121077A (en) | 1961-10-20 | 1964-02-11 | Hoffmann La Roche | Substituted-1, 4-benzodiazepine-2-one compounds |
US3442946A (en) | 1960-04-26 | 1969-05-06 | Hoffmann La Roche | 2-aminomercapto- and 2-aminoalkylcaptobenzophenone oximes |
US3336295A (en) | 1960-12-02 | 1967-08-15 | Hoffmann La Roche | Hydroxy or alkoxy substituted 5-phenyl-3h-1, 4-benzodiazepin-2(1h)-ones |
US3402171A (en) * | 1960-12-02 | 1968-09-17 | Hoffmann La Roche | Process for preparing 5-aryl-3h-1, 4-benzodiazepin-2(1h)-ones |
NL124621C (US07794700-20100914-C00152.png) * | 1962-11-13 | |||
US3534062A (en) | 1967-05-16 | 1970-10-13 | Upjohn Co | Dibenzothiadiazocines |
US3551427A (en) | 1969-05-09 | 1970-12-29 | Sandoz Ag | 4-thienyl-2-(1h)-quinazolones |
CH561703A5 (en) | 1970-12-11 | 1975-05-15 | Hoffmann La Roche | 7-Iodobenzodiazepin-2-ones - sedatives etc prepd by cyclising iodobenzophenones with glycine (esters) |
GB1332697A (en) | 1970-12-21 | 1973-10-03 | Hoffmann La Roche | Benzodiazepine derivatives |
BE791902A (fr) | 1971-11-26 | 1973-05-24 | Wander Ag Dr A | Nouveaux derives de la thieno (3,2-c) (1)benzazepine, leur preparation et leur application comme medicaments |
US3846477A (en) * | 1972-09-20 | 1974-11-05 | Robins Co Inc A H | 2-alkylamino benzophenones |
CH585222A5 (en) | 1973-02-14 | 1977-02-28 | Wander Ag Dr A | Prepn. of antipsychotic heterocyclic piperazine derivs. - by reaction of heterocyclic ketones with metal piperazine complexes |
US4166452A (en) | 1976-05-03 | 1979-09-04 | Generales Constantine D J Jr | Apparatus for testing human responses to stimuli |
US4256108A (en) | 1977-04-07 | 1981-03-17 | Alza Corporation | Microporous-semipermeable laminated osmotic system |
FR2403330A1 (fr) | 1977-06-16 | 1979-04-13 | Fabre Sa Pierre | Nouveaux derives de benzoyl-2-chloro-4-glycinanilides substitues, leur procede de preparation et leur application en tant que medicaments |
FR2449677B1 (fr) | 1979-02-26 | 1986-03-28 | Fabre Sa Pierre | Nouveaux derives de benzoyl-2 glycylanilides substitues, leur preparation et leur application en tant que medicaments anxiolytiques |
US4265874A (en) | 1980-04-25 | 1981-05-05 | Alza Corporation | Method of delivering drug with aid of effervescent activity generated in environment of use |
US4312996A (en) * | 1980-12-29 | 1982-01-26 | Schering Corporation | Benzodiazepine intermediates |
DD251126A1 (de) | 1984-12-21 | 1987-11-04 | Univ Berlin Humboldt | Verfahren zur herstellung neuer 2-arylsulfonamido-benzo- und -acetophenone und deren oxime, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
US5010195A (en) | 1988-05-25 | 1991-04-23 | The Dow Chemical Company | Herbicidal alkoxy-1,2,4-triazolo(1,5-c)primidine-2-sulfonamides |
US5021591A (en) | 1986-07-11 | 1991-06-04 | The Dow Chemical Company | Pyrazolo[1,5-a]pyrimidine-2-sulfide compounds |
US4997940A (en) | 1986-07-11 | 1991-03-05 | The Dow Chemical Company | Pyrazolo[1,5-a]pyrimidine-2-sulfonyl chloride and -2-sulfide compounds |
US4992091A (en) | 1986-07-11 | 1991-02-12 | The Dow Chemical Company | Substituted pyrazolo[1,5-a]pyrimidine-2-sulfonamides and compositions and methods of controlling undesired vegetation |
JPH01156953A (ja) * | 1987-09-01 | 1989-06-20 | Hokko Chem Ind Co Ltd | ベンゼンスルホンアニリド誘導体および農園芸用殺菌剤 |
JPH0753725B2 (ja) | 1987-10-08 | 1995-06-07 | 富山化学工業株式会社 | 4h―1―ベンゾピラン―4―オン誘導体およびその塩、それらの製造法並びにそれらを含有する抗炎症剤 |
DE3825041A1 (de) | 1988-07-20 | 1990-02-15 | Schering Ag | Pyrido(3,2-e)(1,2,4)triazolo(1,5-a)pyrimidin- 2-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider, pflanzenwachstumsregulierender und fungizider wirkung |
GB8820129D0 (en) | 1988-08-24 | 1988-09-28 | Schering Agrochemicals Ltd | Fungicides |
GB8830182D0 (en) | 1988-12-23 | 1989-02-22 | Shell Int Research | Heterocyclic herbicides |
US5217521A (en) | 1989-12-22 | 1993-06-08 | Ciba-Geigy Corporation | Triazolylsulfonamides |
US5338755A (en) | 1990-07-31 | 1994-08-16 | Elf Sanofi | N-sulfonylindoline derivatives, their preparation and the pharmaceutical compositions in which they are present |
FR2679903B1 (fr) * | 1991-08-02 | 1993-12-03 | Elf Sanofi | Derives de la n-sulfonyl indoline portant une fonction amidique, leur preparation, les compositions pharmaceutiques en contenant. |
FR2665441B1 (fr) * | 1990-07-31 | 1992-12-04 | Sanofi Sa | Derives de la n-sulfonyl indoline, leur preparation, les compositions pharmaceutiques en contenant. |
US5481005A (en) | 1990-07-31 | 1996-01-02 | Sanofi | N-sulfonylindoline derivatives, their preparation and the pharmaceutical compositions in which they are present |
US5185348A (en) | 1990-08-16 | 1993-02-09 | Bayer Aktiengesellschaft | Phenylsulphonamide substituted pyridinealkene- and -aminooxyalkanecarboxylic acid derivatives |
DE4025818A1 (de) | 1990-08-16 | 1992-02-20 | Bayer Ag | Phenylsulfonamid substituierte pyridinalken- und -aminooxyalkancarbonsaeure-derivate |
JPH04248984A (ja) * | 1991-02-05 | 1992-09-04 | Kuraray Co Ltd | スーパーオキシドジスムターゼ誘導体およびその製造方法 |
IE920175A1 (en) | 1991-02-11 | 1992-08-12 | Zeneca Ltd | Nitrogen heterocycles |
IL101860A0 (en) * | 1991-05-31 | 1992-12-30 | Ici Plc | Heterocyclic derivatives |
RU2086544C1 (ru) * | 1991-06-13 | 1997-08-10 | Хоффманн-Ля Рош АГ | Бензолсульфонамидные производные пиримидина или их соли, фармацевтическая композиция для лечения заболеваний, связанных с активностью эндотелина |
JPH06145145A (ja) | 1991-12-27 | 1994-05-24 | Ishihara Sangyo Kaisha Ltd | アミノトリフルオロメチルピリジン誘導体又はその塩、それらの製造方法及びそれらを含有するホスホリパーゼa▲2▼阻害剤、抗炎症剤並びに抗膵炎剤 |
JPH06135934A (ja) * | 1991-12-27 | 1994-05-17 | Ishihara Sangyo Kaisha Ltd | ピリジン誘導体又はその塩を含有するホスホリパーゼ▲a2▼阻害剤、抗炎症剤又は抗膵炎剤 |
DE59307360D1 (de) | 1992-02-15 | 1997-10-23 | Hoechst Ag | Ortho-substituierte Benzoylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
JP3229668B2 (ja) | 1992-09-25 | 2001-11-19 | 株式会社リコー | テレライティング装置 |
TW287160B (US07794700-20100914-C00152.png) * | 1992-12-10 | 1996-10-01 | Hoffmann La Roche | |
NZ250916A (en) | 1993-02-27 | 1995-08-28 | Nihon Nohyaku Co Ltd | N-heteroaryl-n'-phenylureas, their use as acat inhibitors |
US5514555A (en) | 1993-03-12 | 1996-05-07 | Center For Blood Research, Inc. | Assays and therapeutic methods based on lymphocyte chemoattractants |
TW394761B (en) * | 1993-06-28 | 2000-06-21 | Hoffmann La Roche | Novel Sulfonylamino Pyrimidines |
IL111959A (en) * | 1993-12-17 | 2000-07-16 | Tanabe Seiyaku Co | N-(polysubstituted pyrimidin-4-yl) benzenesulfonamide derivatives their preparation and pharmaceutical compositions containing them |
WO1995033462A1 (en) | 1994-06-02 | 1995-12-14 | Smithkline Beecham Corporation | Anti-inflammatory compounds |
JPH089412A (ja) | 1994-06-22 | 1996-01-12 | Nec Eng Ltd | 自動色信号補正回路 |
US5571775A (en) | 1994-07-11 | 1996-11-05 | Dowelanco | N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide herbicides |
FR2724654B1 (fr) | 1994-09-16 | 1997-12-12 | Roussel Uclaf | Nouveaux derives de l'acide gallique, leur procede de preparation, les nouveaux intermediaires obtenus, leur application a titre de medicaments et les compositions pharmaceutiques les renfermant |
US5739333A (en) * | 1995-05-16 | 1998-04-14 | Tanabe Seiyaku Co., Ltd. | Sulfonamide derivative and process for preparing the same |
US5883092A (en) * | 1995-09-06 | 1999-03-16 | Kowa Co., Ltd. | Pyrimidine derivatives as endothelin antagonists |
GB9602166D0 (en) | 1996-02-02 | 1996-04-03 | Zeneca Ltd | Aminoheterocyclic derivatives |
US5780488A (en) | 1996-04-03 | 1998-07-14 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
DE19629144A1 (de) | 1996-07-19 | 1998-01-22 | Bayer Ag | Substituierte Triazoloazinsulfonamide |
JP4502408B2 (ja) | 1996-09-10 | 2010-07-14 | テオドーア−コッヒャー インスティトゥーテ | Cxcr3ケモカイン受容体、抗体、核酸および使用方法 |
AR015104A1 (es) | 1996-11-13 | 2001-04-18 | Dowelanco | Compuestos de n-arilsulfilimina sustituidos, utiles como catalizadores en la preparacion de compuestos de n-arilarilsulfonamida; proceso para preparar dichos compuestos y su uso para catalizar dicha preparacion. |
TW523506B (en) | 1996-12-18 | 2003-03-11 | Ono Pharmaceutical Co | Sulfonamide or carbamide derivatives and drugs containing the same as active ingredients |
SE9604786D0 (sv) | 1996-12-20 | 1996-12-20 | Astra Pharma Inc | New compounds |
US6696475B2 (en) | 1997-04-22 | 2004-02-24 | Neurosearch A/S | Substituted phenyl derivatives, their preparation and use |
AU7473398A (en) | 1997-05-07 | 1998-11-27 | University Of Pittsburgh | Inhibitors of protein isoprenyl transferases |
PL338016A1 (en) | 1997-07-11 | 2000-09-25 | Smithkline Beecham Plc | Novel chemical compounds |
US6297239B1 (en) | 1997-10-08 | 2001-10-02 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
JP2001526255A (ja) | 1997-12-23 | 2001-12-18 | ワーナー−ランバート・カンパニー | 炎症性疾患およびアテローム性動脈硬化症を治療または予防するチオ尿素およびベンズアミド化合物、組成物並びに方法 |
WO1999038845A1 (en) | 1998-01-29 | 1999-08-05 | Tularik Inc. | Ppar-gamma modulators |
GB9803411D0 (en) | 1998-02-18 | 1998-04-15 | Smithkline Beecham Plc | Novel compounds |
JP4327915B2 (ja) | 1998-03-30 | 2009-09-09 | 株式会社デ・ウエスタン・セラピテクス研究所 | スルフォンアミド誘導体 |
CA2329777A1 (en) | 1998-04-27 | 1999-11-04 | Dashyant Dhanak | Ccr-3 receptor antagonists |
EP1076641A1 (en) | 1998-04-29 | 2001-02-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of impdh enzyme |
US6136971A (en) * | 1998-07-17 | 2000-10-24 | Roche Colorado Corporation | Preparation of sulfonamides |
WO2000005214A2 (en) | 1998-07-24 | 2000-02-03 | Pfizer Inc. | Isoquinolines as urokinase inhibitors |
US6294192B1 (en) | 1999-02-26 | 2001-09-25 | Lipocine, Inc. | Triglyceride-free compositions and methods for improved delivery of hydrophobic therapeutic agents |
US6329159B1 (en) * | 1999-03-11 | 2001-12-11 | Millennium Pharmaceuticals, Inc. | Anti-GPR-9-6 antibodies and methods of identifying agents which modulate GPR-9-6 function |
MXPA01010292A (es) | 1999-04-15 | 2002-10-23 | Squibb Bristol Myers Co | Inhibidores ciclicos de la proteina tirosina cinasa. |
US7041691B1 (en) | 1999-06-30 | 2006-05-09 | Amgen Inc. | Compounds for the modulation of PPARγ activity |
NZ530833A (en) | 1999-06-30 | 2005-08-26 | Tularik Inc | Compounds for the modulation of PPARgamma activity |
AU6076000A (en) | 1999-07-30 | 2001-02-19 | Vertex Pharmaceuticals Incorporated | Cyclic amine derivatives for the treatment of neurological diseases |
ATE342257T1 (de) * | 1999-08-27 | 2006-11-15 | Chemocentryx Inc | Heterozyclische verbindungen und verfahren zur modulierung von cxcr3 funktion |
AU6870500A (en) | 1999-09-06 | 2001-04-10 | Takeda Chemical Industries Ltd. | Process for the preparation of 2,3-dihydroazepine derivatives |
TR200201413T2 (tr) | 1999-09-17 | 2003-02-21 | Millennium Pharmaceuticals, Inc. | Faktör Xa' nın inhibitörleri. |
EP1216228B1 (en) | 1999-09-17 | 2008-10-29 | Millennium Pharmaceuticals, Inc. | BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa |
JP2001089412A (ja) | 1999-09-22 | 2001-04-03 | Otsuka Pharmaceut Co Ltd | ベンゼン誘導体またはその医薬的に許容される塩 |
GB9926302D0 (en) | 1999-11-05 | 2000-01-12 | Smithkline Beecham Plc | Novel compounds |
EP1255743A1 (en) | 2000-02-01 | 2002-11-13 | Millenium Pharmaceuticals, Inc. | 3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE INHIBITORS OF FACTOR Xa |
WO2001056989A2 (en) | 2000-02-01 | 2001-08-09 | Cor Therapeutics, Inc. | Inhibitors of factor xa |
WO2001057020A1 (en) | 2000-02-01 | 2001-08-09 | Cor Therapeutics, Inc. | INDOLE AND BENZIMIDAZOLE INHIBITORS OF FACTOR Xa |
US20040018192A1 (en) | 2000-02-03 | 2004-01-29 | Toshiaki Wakabayashi | Integrin expression inhibitors |
GB2359078A (en) * | 2000-02-11 | 2001-08-15 | Astrazeneca Uk Ltd | Pharmaceutically active pyrimidine derivatives |
AU783361B2 (en) | 2000-02-18 | 2005-10-20 | Arch Development Corporation | Polyhydroxylated benzene-containing compounds |
WO2001060369A1 (en) | 2000-02-18 | 2001-08-23 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
CO5300399A1 (es) * | 2000-02-25 | 2003-07-31 | Astrazeneca Ab | Heterocicliocs que contienen nitrogeno, proceso para su preparacion y composiciones farmaceuticas que los contienen |
JP3842976B2 (ja) | 2000-03-17 | 2006-11-08 | 富士通株式会社 | 分布帰還型半導体レーザとその製造方法 |
US6653332B2 (en) | 2000-05-03 | 2003-11-25 | Tularik Inc. | Combination therapeutic compositions and method of use |
JP2002031867A (ja) | 2000-05-08 | 2002-01-31 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
GB0011838D0 (en) * | 2000-05-17 | 2000-07-05 | Astrazeneca Ab | Chemical compounds |
US6599926B2 (en) | 2000-06-23 | 2003-07-29 | Bristol-Myers Squibb Company | Heteroaryl-phenyl substituted factor Xa inhibitors |
HUP0301482A3 (en) | 2000-06-28 | 2005-12-28 | Japan Tobacco Inc | Quinolinnyl and benzothiazolyl ppar-gamma modulators pharmaceutical compositions containing them and their use |
EP1314721A1 (en) | 2000-08-31 | 2003-05-28 | Wakunaga Pharmaceutical Co., Ltd. | Novel propenohydroxamic acid derivatives |
EP1578341A4 (en) | 2000-10-11 | 2005-09-28 | Tularik Inc | MODULATION OF THE CCR4 FUNCTION |
US20020147198A1 (en) | 2001-01-12 | 2002-10-10 | Guoqing Chen | Substituted arylamine derivatives and methods of use |
AR032230A1 (es) | 2001-01-16 | 2003-10-29 | Sumitomo Chem Takeda Agro Co | Derivado sulfonamida conteniendo una composicion agricola y horticola |
US6656971B2 (en) | 2001-01-25 | 2003-12-02 | Guilford Pharmaceuticals Inc. | Trisubstituted carbocyclic cyclophilin binding compounds and their use |
WO2003099773A1 (en) * | 2002-05-24 | 2003-12-04 | Millennium Pharmaceuticals, Inc. | Ccr9 inhibitors and methods of use thereof |
US7420055B2 (en) * | 2002-11-18 | 2008-09-02 | Chemocentryx, Inc. | Aryl sulfonamides |
ATE517102T1 (de) * | 2002-11-18 | 2011-08-15 | Chemocentryx Inc | Arylsulfonamide |
ZA200505523B (en) | 2002-12-20 | 2006-09-27 | Amgen Inc | Asthma and allergic inflammation modulators |
US6993400B2 (en) * | 2003-03-07 | 2006-01-31 | Xerox Corporation | System and method for real-time assignment of jobs to production cells |
WO2004099127A1 (en) | 2003-05-07 | 2004-11-18 | Novo Nordisk A/S | Novel compounds as kinase inhibitors |
US7393873B2 (en) | 2003-07-02 | 2008-07-01 | Merck & Co., Inc. | Arylsulfonamide derivatives |
ATE503741T1 (de) | 2005-01-14 | 2011-04-15 | Chemocentryx Inc | Heteroarylsulfonamide und ccr2 |
JP4364168B2 (ja) | 2005-07-11 | 2009-11-11 | アルゼ株式会社 | 遊技機 |
WO2007014054A2 (en) | 2005-07-22 | 2007-02-01 | Glaxo Group Limted | Benzenesulfonamide inhibitor of ccr2 chemokine receptor |
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2003
- 2003-05-21 WO PCT/US2003/016090 patent/WO2003099773A1/en active Application Filing
- 2003-05-21 CA CA2784937A patent/CA2784937A1/en not_active Abandoned
- 2003-05-21 AU AU2003248549A patent/AU2003248549B2/en not_active Ceased
- 2003-05-21 MX MXPA04011465A patent/MXPA04011465A/es active IP Right Grant
- 2003-05-21 EP EP03755422.7A patent/EP1507756B1/en not_active Expired - Lifetime
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- 2003-05-21 NZ NZ566263A patent/NZ566263A/en not_active IP Right Cessation
- 2003-05-21 US US10/443,155 patent/US7238717B2/en not_active Expired - Lifetime
- 2003-05-21 NZ NZ536504A patent/NZ536504A/en not_active IP Right Cessation
- 2003-05-21 EP EP11172253A patent/EP2402309A1/en not_active Withdrawn
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- 2003-05-21 JP JP2004507431A patent/JP4828822B2/ja not_active Expired - Lifetime
- 2003-05-21 EP EP11172255A patent/EP2399903A1/en not_active Withdrawn
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2004
- 2004-11-11 ZA ZA2004/09131A patent/ZA200409131B/en unknown
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2006
- 2006-03-28 US US11/391,633 patent/US7282502B2/en not_active Expired - Lifetime
- 2006-04-27 JP JP2006124437A patent/JP4818798B2/ja not_active Expired - Fee Related
- 2006-11-17 US US11/601,025 patent/US20070066823A1/en not_active Abandoned
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2007
- 2007-10-16 US US11/974,850 patent/US7659272B2/en not_active Expired - Fee Related
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2008
- 2008-10-16 US US12/288,075 patent/US7820717B2/en not_active Expired - Fee Related
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- 2009-10-09 JP JP2009235795A patent/JP2010047584A/ja active Pending
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2010
- 2010-03-19 AU AU2010201073A patent/AU2010201073B2/en not_active Ceased
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- 2010-11-29 JP JP2010265823A patent/JP5544283B2/ja not_active Expired - Fee Related
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2011
- 2011-07-29 JP JP2011167759A patent/JP5432221B2/ja not_active Expired - Fee Related
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- 2013-10-09 US US14/049,452 patent/US9035096B2/en not_active Expired - Lifetime
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- 2014-02-27 JP JP2014036198A patent/JP2014132018A/ja active Pending
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2015
- 2015-04-15 US US14/687,303 patent/US20160068479A1/en not_active Abandoned