JPWO2020161216A5 - - Google Patents
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- JPWO2020161216A5 JPWO2020161216A5 JP2021545905A JP2021545905A JPWO2020161216A5 JP WO2020161216 A5 JPWO2020161216 A5 JP WO2020161216A5 JP 2021545905 A JP2021545905 A JP 2021545905A JP 2021545905 A JP2021545905 A JP 2021545905A JP WO2020161216 A5 JPWO2020161216 A5 JP WO2020161216A5
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- Prior art keywords
- disease
- liver
- constipation
- cholestasis
- syndrome
- Prior art date
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- 206010010774 Constipation Diseases 0.000 claims 16
- 210000004185 Liver Anatomy 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 206010008635 Cholestasis Diseases 0.000 claims 7
- 239000003613 bile acid Substances 0.000 claims 7
- 239000003814 drug Substances 0.000 claims 7
- 231100000359 cholestasis Toxicity 0.000 claims 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 6
- 201000001493 benign recurrent intrahepatic cholestasis Diseases 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 5
- 201000009673 liver disease Diseases 0.000 claims 5
- 208000004624 progressive familial intrahepatic 1 Cholestasis Diseases 0.000 claims 5
- 201000002150 progressive familial intrahepatic cholestasis Diseases 0.000 claims 5
- 206010012601 Diabetes mellitus Diseases 0.000 claims 4
- 208000002551 Irritable Bowel Syndrome Diseases 0.000 claims 4
- 208000004622 Abetalipoproteinemia Diseases 0.000 claims 3
- 210000000941 Bile Anatomy 0.000 claims 3
- 206010010356 Congenital anomaly Diseases 0.000 claims 3
- 206010016654 Fibrosis Diseases 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 230000015572 biosynthetic process Effects 0.000 claims 3
- 201000011510 cancer Diseases 0.000 claims 3
- 230000004761 fibrosis Effects 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 230000002265 prevention Effects 0.000 claims 3
- 201000010874 syndrome Diseases 0.000 claims 3
- 238000003786 synthesis reaction Methods 0.000 claims 3
- 230000002194 synthesizing Effects 0.000 claims 3
- 206010003210 Arteriosclerosis Diseases 0.000 claims 2
- 210000000013 Bile Ducts Anatomy 0.000 claims 2
- 206010007554 Cardiac failure Diseases 0.000 claims 2
- 208000008787 Cardiovascular Disease Diseases 0.000 claims 2
- 208000003167 Cholangitis Diseases 0.000 claims 2
- 206010008609 Cholangitis sclerosing Diseases 0.000 claims 2
- 206010072268 Drug-induced liver injury Diseases 0.000 claims 2
- 208000010008 Familial Hypobetalipoproteinemia Diseases 0.000 claims 2
- 208000008665 Gastrointestinal Disease Diseases 0.000 claims 2
- 206010019280 Heart failure Diseases 0.000 claims 2
- 206010019708 Hepatic steatosis Diseases 0.000 claims 2
- 206010020772 Hypertension Diseases 0.000 claims 2
- 206010021972 Inflammatory bowel disease Diseases 0.000 claims 2
- 208000001024 Intrahepatic Cholestasis Diseases 0.000 claims 2
- 201000005099 Langerhans-cell histiocytosis Diseases 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 208000008338 Non-alcoholic Fatty Liver Disease Diseases 0.000 claims 2
- 206010053219 Non-alcoholic steatohepatitis Diseases 0.000 claims 2
- 108009000135 Nonalcoholic fatty liver disease Proteins 0.000 claims 2
- 206010033645 Pancreatitis Diseases 0.000 claims 2
- 206010074151 Parenteral nutrition associated liver disease Diseases 0.000 claims 2
- 208000003251 Pruritus Diseases 0.000 claims 2
- 210000002966 Serum Anatomy 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 201000001883 cholelithiasis Diseases 0.000 claims 2
- 230000001684 chronic Effects 0.000 claims 2
- 201000003662 chylomicron retention disease Diseases 0.000 claims 2
- -1 cyano, nitro, amino Chemical group 0.000 claims 2
- 231100000595 drug-induced hepatitis Toxicity 0.000 claims 2
- 229940079593 drugs Drugs 0.000 claims 2
- 230000004129 fatty acid metabolism Effects 0.000 claims 2
- 201000002146 gastrointestinal system disease Diseases 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 201000004408 hypobetalipoproteinemia Diseases 0.000 claims 2
- 230000035935 pregnancy Effects 0.000 claims 2
- 201000000742 primary sclerosing cholangitis Diseases 0.000 claims 2
- 231100000240 steatosis hepatitis Toxicity 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- 102100006243 ABCB11 Human genes 0.000 claims 1
- 101710025669 ABCB11 Proteins 0.000 claims 1
- 102100014002 ABCB4 Human genes 0.000 claims 1
- 101700085131 ABCB4 Proteins 0.000 claims 1
- 201000001563 Aagenaes syndrome Diseases 0.000 claims 1
- 208000004476 Acute Coronary Syndrome Diseases 0.000 claims 1
- 208000002353 Alcoholic Hepatitis Diseases 0.000 claims 1
- 206010002022 Amyloidosis Diseases 0.000 claims 1
- 206010002023 Amyloidosis Diseases 0.000 claims 1
- 206010002388 Angina unstable Diseases 0.000 claims 1
- 206010003658 Atrial fibrillation Diseases 0.000 claims 1
- 206010003827 Autoimmune hepatitis Diseases 0.000 claims 1
- 201000011497 Barrett's esophagus Diseases 0.000 claims 1
- 206010004137 Barrett's oesophagus Diseases 0.000 claims 1
- 208000006766 Bile Reflux Diseases 0.000 claims 1
- 206010004637 Bile duct stone Diseases 0.000 claims 1
- 210000003445 Biliary Tract Anatomy 0.000 claims 1
- 230000035639 Blood Levels Effects 0.000 claims 1
- 102100009546 CYP27A1 Human genes 0.000 claims 1
- 101710036518 CYP27A1 Proteins 0.000 claims 1
- 208000005846 Cardiomyopathy Diseases 0.000 claims 1
- 208000002177 Cataract Diseases 0.000 claims 1
- 206010053684 Cerebrohepatorenal syndrome Diseases 0.000 claims 1
- 208000001088 Cerebrotendinous Xanthomatosis Diseases 0.000 claims 1
- 208000006990 Cholangiocarcinoma Diseases 0.000 claims 1
- 206010010317 Congenital absence of bile ducts Diseases 0.000 claims 1
- OMFXVFTZEKFJBZ-HJTSIMOOSA-N Corticosterone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@H](CC4)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OMFXVFTZEKFJBZ-HJTSIMOOSA-N 0.000 claims 1
- 206010011401 Crohn's disease Diseases 0.000 claims 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
- 208000008960 Diabetic Foot Diseases 0.000 claims 1
- 201000010374 Down syndrome Diseases 0.000 claims 1
- 206010058108 Dyslipidaemia Diseases 0.000 claims 1
- 208000006881 Esophagitis Diseases 0.000 claims 1
- 208000009866 Extrahepatic Cholestasis Diseases 0.000 claims 1
- 208000004930 Fatty Liver Diseases 0.000 claims 1
- 108060003412 GRP Proteins 0.000 claims 1
- 208000001130 Gallstone Diseases 0.000 claims 1
- 108009000020 Glucose Homeostasis Proteins 0.000 claims 1
- 102000015779 HDL Lipoproteins Human genes 0.000 claims 1
- 206010003820 Hepatic autoimmune disease Diseases 0.000 claims 1
- 208000006454 Hepatitis Diseases 0.000 claims 1
- 208000005252 Hepatitis A Diseases 0.000 claims 1
- 208000002672 Hepatitis B Diseases 0.000 claims 1
- 208000005176 Hepatitis C Diseases 0.000 claims 1
- 208000005331 Hepatitis D Diseases 0.000 claims 1
- 206010019728 Hepatitis alcoholic Diseases 0.000 claims 1
- 206010019799 Hepatitis viral Diseases 0.000 claims 1
- 208000009576 Hypercholesterolemia Diseases 0.000 claims 1
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 1
- 206010062060 Hyperlipidaemia Diseases 0.000 claims 1
- 208000006575 Hypertriglyceridemia Diseases 0.000 claims 1
- 206010020914 Hypervitaminosis Diseases 0.000 claims 1
- 206010020915 Hypervitaminosis Diseases 0.000 claims 1
- 102000018358 Immunoglobulins Human genes 0.000 claims 1
- 108060003951 Immunoglobulins Proteins 0.000 claims 1
- 206010022489 Insulin resistance Diseases 0.000 claims 1
- 206010061255 Ischaemia Diseases 0.000 claims 1
- 206010023126 Jaundice Diseases 0.000 claims 1
- 208000001083 Kidney Disease Diseases 0.000 claims 1
- 206010061227 Lipid metabolism disease Diseases 0.000 claims 1
- 206010054805 Macroangiopathy Diseases 0.000 claims 1
- 208000008466 Metabolic Disease Diseases 0.000 claims 1
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 1
- 206010028289 Muscle atrophy Diseases 0.000 claims 1
- 210000002027 Muscle, Skeletal Anatomy 0.000 claims 1
- 208000010125 Myocardial Infarction Diseases 0.000 claims 1
- 206010051606 Necrotising colitis Diseases 0.000 claims 1
- 208000004995 Necrotizing Enterocolitis Diseases 0.000 claims 1
- 206010029149 Nephropathy Diseases 0.000 claims 1
- 206010029151 Nephropathy Diseases 0.000 claims 1
- 206010029331 Neuropathy peripheral Diseases 0.000 claims 1
- 208000010333 North American Indian Childhood Cirrhosis Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 206010030216 Oesophagitis Diseases 0.000 claims 1
- 208000002865 Osteopetrosis Diseases 0.000 claims 1
- 210000000496 Pancreas Anatomy 0.000 claims 1
- 206010061536 Parkinson's disease Diseases 0.000 claims 1
- 206010062585 Peripheral arterial occlusive disease Diseases 0.000 claims 1
- 206010063985 Phytosterolaemia Diseases 0.000 claims 1
- 208000007232 Portal Hypertension Diseases 0.000 claims 1
- 208000000876 Primary Bile Acid Malabsorption Diseases 0.000 claims 1
- 206010057969 Reflux gastritis Diseases 0.000 claims 1
- 206010038435 Renal failure Diseases 0.000 claims 1
- 206010038444 Renal failure chronic Diseases 0.000 claims 1
- 206010061481 Renal injury Diseases 0.000 claims 1
- 206010038923 Retinopathy Diseases 0.000 claims 1
- 206010038932 Retinopathy Diseases 0.000 claims 1
- 101710017705 SUCLG1 Proteins 0.000 claims 1
- 208000002227 Sitosterolemia Diseases 0.000 claims 1
- 208000007718 Stable Angina Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 206010042953 Systemic sclerosis Diseases 0.000 claims 1
- 206010044688 Trisomy 21 Diseases 0.000 claims 1
- 101700075834 UTP4 Proteins 0.000 claims 1
- 102100013268 UTP4 Human genes 0.000 claims 1
- 208000007814 Unstable Angina Diseases 0.000 claims 1
- 201000004525 Zellweger syndrome Diseases 0.000 claims 1
- 230000002159 abnormal effect Effects 0.000 claims 1
- 230000001058 adult Effects 0.000 claims 1
- 201000001320 atherosclerosis Diseases 0.000 claims 1
- 230000003416 augmentation Effects 0.000 claims 1
- 201000001490 benign recurrent intrahepatic cholestasis 1 Diseases 0.000 claims 1
- 201000001488 benign recurrent intrahepatic cholestasis 2 Diseases 0.000 claims 1
- 201000005271 biliary atresia Diseases 0.000 claims 1
- 230000000747 cardiac effect Effects 0.000 claims 1
- 201000008031 cardiomyopathy Diseases 0.000 claims 1
- 201000009331 choledocholithiasis Diseases 0.000 claims 1
- 201000000522 chronic kidney disease Diseases 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 201000003883 cystic fibrosis Diseases 0.000 claims 1
- 230000003111 delayed Effects 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 201000010870 diseases of metabolism Diseases 0.000 claims 1
- 230000004064 dysfunction Effects 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 230000002496 gastric Effects 0.000 claims 1
- 230000001434 glomerular Effects 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- 230000014101 glucose homeostasis Effects 0.000 claims 1
- 230000002440 hepatic Effects 0.000 claims 1
- 231100000283 hepatitis Toxicity 0.000 claims 1
- 201000010284 hepatitis E Diseases 0.000 claims 1
- 201000001421 hyperglycemia Diseases 0.000 claims 1
- 230000003451 hyperinsulinaemic Effects 0.000 claims 1
- 201000008980 hyperinsulinism Diseases 0.000 claims 1
- 230000001771 impaired Effects 0.000 claims 1
- 201000002450 inherited metabolic disease Diseases 0.000 claims 1
- 201000004332 intermediate coronary syndrome Diseases 0.000 claims 1
- 201000002161 intrahepatic cholestasis of pregnancy Diseases 0.000 claims 1
- 201000006370 kidney failure Diseases 0.000 claims 1
- 201000004044 liver cirrhosis Diseases 0.000 claims 1
- 200000000011 liver disorder Diseases 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- 201000000585 muscular atrophy Diseases 0.000 claims 1
- 201000001119 neuropathy Diseases 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 230000000414 obstructive Effects 0.000 claims 1
- 201000006195 perinatal necrotizing enterocolitis Diseases 0.000 claims 1
- 230000000750 progressive Effects 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 200000000008 restenosis Diseases 0.000 claims 1
- 230000033764 rhythmic process Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 201000000306 sarcoidosis Diseases 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 150000003431 steroids Chemical class 0.000 claims 1
- 201000009594 systemic scleroderma Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 210000001519 tissues Anatomy 0.000 claims 1
- 231100000419 toxicity Toxicity 0.000 claims 1
- 230000001988 toxicity Effects 0.000 claims 1
- 230000002792 vascular Effects 0.000 claims 1
- 201000001862 viral hepatitis Diseases 0.000 claims 1
- 230000029663 wound healing Effects 0.000 claims 1
Claims (5)
- 式(I)の化合物
R1及びR2は各々独立に、C1~4アルキルであり;
R3は独立に、水素、ハロゲン、ヒドロキシ、C1~4アルキル、C1~4ハロアルキル、C1~4アルコキシ、C1~4ハロアルコキシ、シアノ、ニトロ、アミノ、N-(C1~4アルキル)アミノ、N,N-ジ(C1~4アルキル)アミノ、及びN-(アリール-C1~4アルキル)アミノからなる群から選択され;
nは、1、2、又は3の整数であり;
R4は、水素、ハロゲン、ヒドロキシ、シアノ、C1~4アルキル、C3~6シクロアルキル、C1~4アルコキシ、C3~6シクロアルキルオキシ、C1~4アルキルチオ、C3~6シクロアルキルチオ、アミノ、N-(C1~4アルキル)アミノ、及びN,N-ジ(C1~4アルキル)アミノからなる群から選択され;
R5A、R5B、R5C、及びR5Dは各々独立に、水素、ハロゲン、ヒドロキシ、アミノ、C1~4アルキル、及びC1~4アルコキシからなる群から選択される)
又は医薬として許容されるその塩を含む医薬。 - 循環器疾患又は脂肪酸代謝の障害又はグルコース利用障害、例えば、高コレステロール血症;脂肪酸代謝の障害;1型及び2型真性糖尿病;糖尿病の合併症、例えば、白内障、細小及び大血管疾患、網膜症、神経障害、腎症、及び創傷治癒の遅延、組織虚血、糖尿病性足病変、動脈硬化症、心筋梗塞、急性冠症候群、不安定狭心症、安定狭心症、脳卒中、末梢動脈閉塞性疾患、心筋症、心不全、心拍障害、及び血管再狭窄;糖尿病関連疾患、例えば、インスリン抵抗性(グルコース恒常性の障害)、高血糖、高インスリン血症、脂肪酸又はグリセロールの血中レベルの上昇、肥満、脂質異常症、高脂血症、例えば、高トリグリセリド血症、メタボリック症候群(X症候群)、アテローム性動脈硬化症、及び高血圧;並びに高密度リポタンパク質レベルの増加の治療又は予防用の、請求項10に記載の医薬。
- 胃腸疾患又は障害、例えば、便秘(慢性便秘、機能性便秘、慢性特発性便秘(CIC)、断続的/散発性便秘、真性糖尿病に続発する便秘、脳卒中に続発する便秘、慢性腎臓病に続発する便秘、多発性硬化症に続発する便秘、パーキンソン病に続発する便秘、全身性硬化症に続発する便秘、薬物性便秘、便秘型過敏性腸症候群(IBS-C)、混合型過敏性腸症候群(IBS-M)、小児機能性便秘、及びオピオイド誘発性便秘が含まれる);クローン病;一次胆汁酸吸収不良;過敏性腸症候群(IBS);炎症性腸疾患(IBD);回腸の炎症;並びに逆流症及びその合併症、例えば、バレット食道、胆汁逆流食道炎、及び胆汁逆流胃炎の治療又は予防用の、請求項10に記載の医薬。
- 肝疾患若しくは障害、例えば、肝臓の遺伝性代謝障害;胆汁酸合成の先天性異常;先天性胆管走行異常;胆道閉鎖;葛西手術後の胆道閉鎖;肝臓移植後の胆道閉鎖;新生児肝炎;新生児胆汁うっ滞;遺伝形式の胆汁うっ滞;脳腱黄色腫症;BA合成の二次的欠陥;ツェルウェガー症候群;嚢胞性線維症に関連する肝疾患;α1アンチトリプシン欠損症;アラジール症候群(ALGS);バイラー症候群;胆汁酸(BA)合成の一次的欠陥;進行性家族性肝内胆汁うっ滞(PFIC)、例えば、PFIC-1、PFIC-2、PFIC-3、及び非特定PFIC、胆汁分流後のPFIC、並びに肝臓移植後のPFIC;良性反復性肝内胆汁うっ滞(BRIC)、例えば、BRIC1、BRIC2、及び非特定BRIC、胆汁分流後のBRIC、並びに肝臓移植後のBRIC;自己免疫性肝炎;原発性胆汁性肝硬変(PBC);肝線維症;非アルコール性脂肪性肝疾患(NAFLD);非アルコール性脂肪性肝炎(NASH);門脈圧亢進症;胆汁うっ滞;ダウン症候群の胆汁うっ滞;薬物性胆汁うっ滞;妊娠の肝内胆汁うっ滞(妊娠中の黄疸);肝内胆汁うっ滞;肝外胆汁うっ滞;経静脈栄養に関連する胆汁うっ滞(PNAC);低リン脂質に関連する胆汁うっ滞;リンパ浮腫胆汁うっ滞症候群1(LSC1);原発性硬化性胆管炎(PSC);免疫グロブリンG4に関連する胆管炎;原発性胆汁性胆管炎;胆石症(胆石);胆道結石症(biliary lithiasis);総胆管結石症;胆石性膵炎;カロリー病;胆管の悪性腫瘍;胆樹の閉塞を引き起こす悪性腫瘍;胆管狭窄;AIDS胆管症;虚血性胆管症;胆汁うっ滞若しくは黄疸によるそう痒;膵臓炎;進行性胆汁うっ滞に至る慢性自己免疫性肝疾患;肝脂肪変性;アルコール性肝炎;急性脂肪肝;妊娠の脂肪肝;薬物性肝炎;鉄過剰症;先天性胆汁酸代謝異常症1型(BAS1型);薬物性肝障害(DILI);肝線維症;先天性肝線維症;肝硬変;ランゲルハンス細胞組織球症(LCH);新生児魚鱗癬硬化性胆管炎(NISCH);骨髄性プロトポルフィリン症(EPP);特発性成人胆管減少(IAD);突発性新生児肝炎(INH);非症候性肝内胆管減少症(NS PILBD);常染色体劣性遺伝性肝内胆汁うっ滞(North American Indian childhood cirrhosis)(NAIC);肝サルコイドーシス;アミロイドーシス;壊死性腸炎;血清中胆汁酸が引き起こす毒性、例えば、異常な血清中胆汁酸プロファイルの状況での心律動障害(例えば、心房細動)、肝硬変に関連する心筋症(「コレカルディア(cholecardia)」)、及び胆汁うっ滞性肝疾患に関連する骨格筋消耗;ウイルス性肝炎(A型肝炎、B型肝炎、C型肝炎、D型肝炎、及びE型肝炎が含まれる);肝細胞癌(肝細胞腫);胆管癌;胆汁酸に関係する胃腸癌;並びに肝臓、胆道、及び膵臓の腫瘍及び新生物によって引き起こされる胆汁うっ滞の治療若しくは予防用の;又は肝疾患におけるコルチコステロイド療法の増強用の、請求項10に記載の医薬。
- 過吸収症候群(無βリポタンパク血症、家族性低βリポタンパク血症(FHBL)、カイロミクロン停滞病(CRD)、及びシトステロール血症が含まれる);ビタミン過剰症及び大理石骨病;高血圧;糸球体過剰濾過;並びに腎不全のそう痒の治療若しくは予防用の;又は肝臓若しくは代謝疾患に関連する腎臓傷害に対する保護用の、請求項10に記載の医薬。
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN201911004690 | 2019-02-06 | ||
IN201911004690 | 2019-02-06 | ||
SE1950463-8 | 2019-04-12 | ||
SE1950463 | 2019-04-12 | ||
IN201911049986 | 2019-12-04 | ||
IN201911049986 | 2019-12-04 | ||
PCT/EP2020/052940 WO2020161216A1 (en) | 2019-02-06 | 2020-02-06 | Benzothiazepine compounds and their use as bile acid modulators |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2022519664A JP2022519664A (ja) | 2022-03-24 |
JPWO2020161216A5 true JPWO2020161216A5 (ja) | 2023-02-02 |
Family
ID=69591607
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2021545905A Pending JP2022519664A (ja) | 2019-02-06 | 2020-02-06 | ベンゾチアゼピン化合物及び胆汁酸モジュレータとしてのそれらの使用 |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP3921027B1 (ja) |
JP (1) | JP2022519664A (ja) |
CN (1) | CN113453753A (ja) |
CA (1) | CA3127408A1 (ja) |
ES (1) | ES2955799T3 (ja) |
WO (1) | WO2020161216A1 (ja) |
Families Citing this family (28)
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2020
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- 2020-02-06 JP JP2021545905A patent/JP2022519664A/ja active Pending
- 2020-02-06 EP EP20705304.2A patent/EP3921027B1/en active Active
- 2020-02-06 CA CA3127408A patent/CA3127408A1/en active Pending
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