JP2006528980A5 - - Google Patents
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- JP2006528980A5 JP2006528980A5 JP2006532984A JP2006532984A JP2006528980A5 JP 2006528980 A5 JP2006528980 A5 JP 2006528980A5 JP 2006532984 A JP2006532984 A JP 2006532984A JP 2006532984 A JP2006532984 A JP 2006532984A JP 2006528980 A5 JP2006528980 A5 JP 2006528980A5
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- 125000005843 halogen group Chemical group 0.000 claims 15
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- 239000001257 hydrogen Substances 0.000 claims 10
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- 230000008938 immune dysregulation Effects 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- 206010019663 Hepatic failure Diseases 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
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- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
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- 208000009329 Graft vs Host Disease Diseases 0.000 claims 2
- 206010018691 Granuloma Diseases 0.000 claims 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 claims 2
- 206010020751 Hypersensitivity Diseases 0.000 claims 2
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
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- 206010047642 Vitiligo Diseases 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
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- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 2
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- 125000002950 monocyclic group Chemical group 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
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- 125000001715 oxadiazolyl group Chemical group 0.000 claims 2
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- 208000019629 polyneuritis Diseases 0.000 claims 2
- 230000008085 renal dysfunction Effects 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 2
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 claims 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims 1
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- 201000010000 Agranulocytosis Diseases 0.000 claims 1
- 208000035285 Allergic Seasonal Rhinitis Diseases 0.000 claims 1
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- 208000032116 Autoimmune Experimental Encephalomyelitis Diseases 0.000 claims 1
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- 208000010839 B-cell chronic lymphocytic leukemia Diseases 0.000 claims 1
- 208000035143 Bacterial infection Diseases 0.000 claims 1
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- 208000033222 Biliary cirrhosis primary Diseases 0.000 claims 1
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- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
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- 208000002177 Cataract Diseases 0.000 claims 1
- 208000002691 Choroiditis Diseases 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 206010009208 Cirrhosis alcoholic Diseases 0.000 claims 1
- 206010009657 Clostridium difficile colitis Diseases 0.000 claims 1
- 206010010741 Conjunctivitis Diseases 0.000 claims 1
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- 206010016654 Fibrosis Diseases 0.000 claims 1
- 208000003084 Graves Ophthalmopathy Diseases 0.000 claims 1
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- 208000001204 Hashimoto Disease Diseases 0.000 claims 1
- 208000030836 Hashimoto thyroiditis Diseases 0.000 claims 1
- 208000035186 Hemolytic Autoimmune Anemia Diseases 0.000 claims 1
- 208000032759 Hemolytic-Uremic Syndrome Diseases 0.000 claims 1
- 206010019786 Hepatitis non-A non-B Diseases 0.000 claims 1
- 206010019799 Hepatitis viral Diseases 0.000 claims 1
- 208000005100 Herpetic Keratitis Diseases 0.000 claims 1
- 206010020850 Hyperthyroidism Diseases 0.000 claims 1
- 206010021074 Hypoplastic anaemia Diseases 0.000 claims 1
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- 201000003838 Idiopathic interstitial pneumonia Diseases 0.000 claims 1
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- 206010062016 Immunosuppression Diseases 0.000 claims 1
- 208000032571 Infant acute respiratory distress syndrome Diseases 0.000 claims 1
- 201000002287 Keratoconus Diseases 0.000 claims 1
- 206010069698 Langerhans' cell histiocytosis Diseases 0.000 claims 1
- GWNVDXQDILPJIG-SHSCPDMUSA-N Leukotriene C4 Natural products CCCCCC=C/CC=C/C=C/C=C/C(SCC(NC(=O)CCC(N)C(=O)O)C(=O)NCC(=O)O)C(O)CCCC(=O)O GWNVDXQDILPJIG-SHSCPDMUSA-N 0.000 claims 1
- 208000012309 Linear IgA disease Diseases 0.000 claims 1
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- 208000031422 Lymphocytic Chronic B-Cell Leukemia Diseases 0.000 claims 1
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- 208000027530 Meniere disease Diseases 0.000 claims 1
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- 208000019695 Migraine disease Diseases 0.000 claims 1
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- 206010027910 Mononeuritis Diseases 0.000 claims 1
- 241000907681 Morpho Species 0.000 claims 1
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- 206010051606 Necrotising colitis Diseases 0.000 claims 1
- 206010028974 Neonatal respiratory distress syndrome Diseases 0.000 claims 1
- 206010073938 Ophthalmic herpes simplex Diseases 0.000 claims 1
- 208000001132 Osteoporosis Diseases 0.000 claims 1
- 206010033645 Pancreatitis Diseases 0.000 claims 1
- 208000012896 Peritoneal disease Diseases 0.000 claims 1
- 208000031845 Pernicious anaemia Diseases 0.000 claims 1
- 206010035664 Pneumonia Diseases 0.000 claims 1
- 208000003971 Posterior uveitis Diseases 0.000 claims 1
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 1
- 208000012654 Primary biliary cholangitis Diseases 0.000 claims 1
- 206010036774 Proctitis Diseases 0.000 claims 1
- 208000003100 Pseudomembranous Enterocolitis Diseases 0.000 claims 1
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- 208000006311 Pyoderma Diseases 0.000 claims 1
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- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 1
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Claims (27)
- 下記式Iによって表される化合物または該化合物の製薬上許容される塩。
Aは、C−R3またはNであり;
Dは、C−R4またはNであり;
Eは、C−R6またはNであり;
Gは、C−R7またはNであり;
ただし、A、D、EおよびGのうちの少なくとも一つはNではなく;
X、YおよびZは独立に、NおよびC−R8からなる群から選択され;ただし、X、YおよびZのうちの少なくとも一つはNではなく;
R1およびR2はそれぞれ独立に、
(1)水素および
(2)1〜3個のハロ基で置換されていても良いC1−6アルキル
からなる群から選択されるか、
あるいはR1およびR2は、それらが結合している窒素原子と一体となって、3〜6員の飽和単環式環を形成していても良く;
R3、R4、R6およびR7はそれぞれ独立に、
(1)水素、
(2)ハロ、
(3)シアノおよび
(4)それぞれ1〜3個のハロ基で置換されていても良いC1−4アルキルまたはC1−4アルコキシ
からなる群から選択され;
R5は、
(1)C1−6アルキル、
(2)C2−6アルケニル、
(3)C2−6アルキニル、
(4)C3−6シクロアルキル、
(5)C1−6アルコキシ、
(6)C3−6シクロアルコキシ、
(7)C1−6アシル、
(8)ハロ、
(9)アリールおよび
(10)HET
からなる群から選択され;
上記の基(1)〜(7)は、1個〜最大数の置換可能位置でハロによって置換されていても良く;
上記の基(9)および(10)は、
(a)ハロ、および
(b)それぞれオキソ、ヒドロキシまたは1〜3個のハロ基で置換されていても良いC1−4アルキルまたはC1−4アルコキシ
からなる群から独立に選択される1〜3個の置換基で置換されていても良く;
あるいはR4およびR5は、それらが結合している原子と一体となって、O、SおよびNR8から選択される1〜3個のヘテロ原子を有していても良い5または6員の単環式環を形成していても良く;前記環は、独立に、ハロ、C1−4アルキルおよびC1−4アルコキシからなる群から選択される1〜3個の置換基で置換されていても良く;前記C1−4アルキルまたはC1−4アルコキシは、1〜3個のハロ基で置換されていても良く;
各R8は独立に、水素、ハロおよびC1−4アルキルからなる群から選択され;前記C1−4アルキルは、1〜3個のハロ基で置換されていても良く;
HETは、ベンゾイミダゾリル、ベンゾフラニル、ベンゾピラゾリル、ベンゾトリアゾリル、ベンゾチオフェニル、ベンゾオキサゾリル、カルバゾリル、カルボリニル、シンノリニル、フラニル、イミダゾリル、インドリニル、インドリル、インドラジニル、インダゾリル、イソベンゾフラニル、イソインドリル、イソキノリル、イソチアゾリル、イソオキサゾリル、ナフチリジニル、オキサジアゾリル、オキサゾリル、ピラジニル、ピラゾリル、ピリドピリジニル、ピリダジニル、ピリジル、ピリミジル、ピロリル、キナゾリニル、キノリル、キノキサリニル、チアジアゾリル、チアゾリル、チエニル、トリアゾリル、アゼチジニル、1,4−ジオキサニル、ヘキサヒドロアゼピニル、ピペラジニル、ピペリジニル、ピロリジニル、モルホリニル、チオモルホリニル、ジヒドロベンゾイミダゾリル、ジヒドロベンゾフラニル、ジヒドロベンゾチオフェニル、ジヒドロベンゾオキサゾリル、ジヒドロフラニル、ジヒドロイミダゾリル、ジヒドロインドリル、ジヒドロイソオキサゾリル、ジヒドロイソチアゾリル、ジヒドロオキサジアゾリル、ジヒドロオキサゾリル、ジヒドロピラジニル、ジヒドロピラゾリル、ジヒドロピリジニル、ジヒドロピリミジニル、ジヒドロピロリル、ジヒドロキノリニル、ジヒドロテトラゾリル、ジヒドロチアジアゾリル、ジヒドロチアゾリル、ジヒドロチエニル、ジヒドロトリアゾリル、ジヒドロアゼチジニル、メチレンジオキシベンゾイル、テトラヒドロフラニルおよびテトラヒドロチエニルからなる群から選択される。] - AがNであり、
DがC−R4であり、
EがC−R6であり、
GがC−R7である請求項1に記載の化合物。 - AがC−R3であり、
DがC−R4であり、
EがC−R6であり、
GがC−R7である請求項1に記載の化合物。 - X、YおよびZがC−R8である請求項3に記載の化合物。
- R3、R6およびR7が水素である請求項3に記載の化合物。
- R4がトリフルオロメチルまたはシアノである請求項5に記載の化合物。
- R1およびR2がそれぞれ独立に、水素、メチルおよびエチルからなる群から選択される請求項3に記載の化合物。
- R5が
(1)C2−6アルキル、
(2)C3−6シクロアルキル、
(3)C2−6アルコキシ、
(4)C3−6シクロアルコキシおよび
(5)C3−6アシル
からなる群から選択され;
上記の基(1)〜(5)が1〜5個のフルオロ基で置換されていても良い請求項3に記載の化合物。 - R5が1〜5個のフルオロ基で置換されていても良いC2−6アルコキシである請求項8に記載の化合物。
- R5が
(1)独立にハロ、メチル、メトキシおよびヒドロキシメチルからなる群から選択される1〜3個の置換基で置換されていても良いフェニル、
(2)オキサジアゾリル、
(3)オキサゾリル、
(4)フラニルおよび
(5)チエニル
からなる群から選択される請求項3に記載の化合物。 - XがNであり;YおよびZがいずれもC−R8である請求項3に記載の化合物。
- XおよびZがいずれもC−R8であり;YがNである請求項3に記載の化合物。
- R1およびR2がそれぞれ独立に、水素およびメチルからなる群から選択され、
R3、R6およびR7が水素であり、
R4がトリフルオロメチルまたはシアノであり、
R5が1〜5個のフルオロ基で置換されていても良いC2−6アルコキシである請求項3に記載の化合物。 - R5が2,2,2−トリフルオロエトキシおよび2,2,2−トリフルオロ−1−メチルエトキシから選択される請求項13に記載の化合物。
- X、YおよびZがC−R8であり;各R8が独立に水素、メチルおよびハロから選択される請求項14に記載の化合物。
- XがNであり;YおよびZがいずれもC−R8であり;各R8が独立に水素、メチルおよびハロから選択される請求項14に記載の化合物。
- XおよびZがいずれもC−R8であり;YがNであり;各R8が独立に水素、メチルおよびハロから選択される請求項14に記載の化合物。
- 処置を必要とする哺乳動物患者における免疫調節異常の治療方法であって、前記患者に対して、前記免疫調節異常を治療する上で有効な量で請求項1に記載の化合物を投与する段階を有する方法。
- 前記免疫調節異常が、全身紅斑性狼瘡、慢性関節リウマチ、I型糖尿病、炎症性腸疾患、胆汁性肝硬変、ブドウ膜炎、多発性硬化症、クローン病、潰瘍性大腸炎、類天疱瘡、サルコイドーシス、乾癬、自己免疫筋肉炎、ヴェグナー肉芽腫、魚鱗癬、グレーブス眼症および喘息からなる群から選択される自己免疫疾患または慢性炎症性疾患である請求項19に記載の方法。
- 前記免疫調節異常が、骨髄もしくは臓器の移植片拒絶または移植片対宿主病である請求項19に記載の方法。
- 前記免疫調節異常が、臓器もしくは組織の移植、移植によって生じる移植片対宿主病、慢性関節リウマチなどの自己免疫症候群、全身紅斑性狼瘡、橋本甲状腺炎、多発性硬化症、重症筋無力症、I型糖尿病、ブドウ膜炎、後部ブドウ膜炎、アレルギー性脳脊髄炎、糸球体腎炎、リウマチ熱および感染後糸球体腎炎などの感染後自己免疫疾患、炎症性および高増殖性皮膚疾患、乾癬、アトピー性皮膚炎、接触皮膚炎、湿疹性皮膚炎、脂漏性皮膚炎、扁平苔癬、天疱瘡、類天疱瘡、表皮水疱症、蕁麻疹、血管浮腫、脈管炎、紅斑、皮膚好酸球増加症、紅斑性狼瘡、アクネ、円形脱毛症、角結膜炎、春季結膜炎、ベーチェット病に関連するブドウ膜炎、角膜炎、疱疹性角膜炎、円錐角膜、角膜上皮異栄養症、角膜白斑、眼天疱瘡、モーレン潰瘍、強膜炎、グレーブス眼症、フォークト−小柳−原田症候群、サルコイドーシス、花粉アレルギー、可逆的閉塞性気道疾患、気管支喘息、アレルギー性喘息、内因性喘息、外因性喘息、塵埃喘息、慢性もしくは難治性喘息、遅発性喘息および気道過敏症、気管支炎、胃潰瘍、虚血性疾患および血栓症によって生じる血管損傷、虚血性腸疾患、炎症性腸疾患、壊死性小腸大腸炎、熱傷に関連する腸病変、腹腔疾患、直腸炎、好酸球性胃腸炎、肥満細胞症、クローン病、潰瘍性大腸炎、片頭痛、鼻炎、湿疹、間質性腎炎、グッドパスチャー症候群、溶血尿毒症症候群、糖尿病性腎症、多発性筋炎、ギランバレー症候群、メニエール病、多発性神経炎、多発性神経炎、単発神経炎、神経根症、甲状腺機能亢進、バセドー病、純赤血球無形成症、無形成性貧血、形成不全性貧血、特発性血小板減少性紫斑病、自己免疫性溶血性貧血、無顆粒球症、悪性貧血、巨大赤芽球性貧血、赤血球形成不全、骨粗鬆症、サルコイドーシス、肺線維症、特発性間質性肺炎、皮膚筋炎、尋常性白斑、尋常魚鱗癬、光アレルギー性過敏、皮膚T細胞リンパ腫、動脈硬化、アテローム性動脈硬化、大動脈炎症候群、結節性多発動脈炎、心筋症、強皮症、ヴェグナー肉芽腫、シェーグレン症候群、脂肪過多症、好酸球増加症性筋膜炎、歯肉,歯周組織,歯槽骨,歯のセメント質の病変、糸球体腎炎、脱毛防止もしくは毛髪萌芽の提供および/または毛髪発生および毛髪成長の促進による男性型脱毛症もしくは老人性脱毛、筋ジストロフィー、膿皮症およびセザール症候群、アジソン氏病、防腐、移植もしくは虚血疾患時に起こる臓器の虚血−再潅流損傷、内毒素ショック、偽膜性大腸炎、薬剤もしくは放射線照射によって生じる大腸炎、虚血性急性腎機能不全、慢性腎機能不全、肺−酸素もしくは薬剤によって生じる中毒症、肺癌、肺気腫、白内障、鉄肺症、色素性網膜炎、老年斑点性変性、ガラス体瘢痕化、角膜アルカリやけど、多形紅斑性皮膚炎、線状IgA水疱症およびセメント皮膚炎、歯肉炎、歯周炎、敗血症、膵炎、環境汚染,加齢,癌発生,癌の転移および高山病によって生じる疾患、ヒスタミンもしくはロイコトリエン−C4放出によって生じる疾患、ベーチェット病、自己免疫肝炎、原発性胆汁性肝硬変、硬化性胆管炎、部分肝臓切除術、急性肝臓壊死、毒物,ウィルス性肝炎,ショックもしくは無酸素によって生じる壊死、B型ウィルス肝炎、非A非B肝炎、肝硬変、アルコール性肝硬変、肝不全、激症肝不全、遅発性肝不全、「慢性急性化」肝不全、化学療法効果の増強、サイトメガロウイルス感染、HCMV感染、AIDS、癌、老人性痴呆、外傷ならびに慢性細菌感染からなる群から選択される請求項19に記載の方法。
- 前記免疫調節異常が、
1)多発性硬化症、
2)関節リウマチ、
3)全身紅斑性狼瘡、
4)乾癬、
5)移植臓器もしくは組織の拒絶、
6)炎症性腸疾患、
7)リンパを起源とする悪性腫瘍、
8)急性および慢性のリンパ球性白血病およびリンパ腫、
9)インシュリン依存型および非インシュリン依存型の糖尿病
からなる群から選択される請求項19に記載の方法。 - 免疫抑制を必要とする哺乳動物患者での免疫系の抑制方法であって、その患者に対して免疫抑制上有効量の請求項1に記載の化合物を投与する段階を有する方法。
- 製薬上許容される担体との組み合わせで請求項1に記載の化合物からなる医薬組成物。
- 処置を必要とする哺乳動物患者での呼吸器の疾患または状態を治療する方法であって、該患者に対して、前記呼吸器の疾患または状態を治療する上で有効な量の請求項1に記載の化合物を投与する段階を有する方法。
- 前記呼吸器の疾患または状態が、喘息、慢性気管支炎、慢性閉塞性肺疾患、成人呼吸窮迫性症候群、乳児呼吸窮迫性症候群、咳、好酸球性肉芽腫、呼吸器合包体ウィルス細気管支炎、気管支拡張症、特発性肺線維症、急性肺傷害および閉塞性細気管支炎器質化肺炎からなる群から選択される請求項26に記載の方法。
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IL31990A (en) * | 1968-04-26 | 1974-05-16 | Chinoin Gyogyszer Es Vegyeszet | Pyridyl 1,2,4-oxadiazole derivatives,process for the preparation thereof and pharmaceutical compositions containing same |
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EP1549640A4 (en) * | 2002-06-17 | 2008-08-06 | Merck & Co Inc | 1 - ((5-ARYL-1,2,4-OXADIAZOL-3-YL) BENZYL) AZETIDINE-3-CARBOXYLATE AND 1 - ((5-ARYL-1,2,4-OXADIAZOL-3-YL) BENZYL) PYRROLIDIN-3-CARBOXYLATE AS EDG RECEPTOR AGONISTS |
-
2004
- 2004-05-12 CA CA002524867A patent/CA2524867A1/en not_active Abandoned
- 2004-05-12 WO PCT/US2004/014837 patent/WO2004103279A2/en active Application Filing
- 2004-05-12 JP JP2006532984A patent/JP2006528980A/ja not_active Withdrawn
- 2004-05-12 CN CNA2004800129905A patent/CN1788008A/zh active Pending
- 2004-05-12 AU AU2004240586A patent/AU2004240586A1/en not_active Abandoned
- 2004-05-12 EP EP04751981A patent/EP1625123A4/en not_active Withdrawn
- 2004-05-12 US US10/554,665 patent/US20060252741A1/en not_active Abandoned
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