JP2016534998A - Rorγtのヘテロアリール結合キノリニルモジュレーター - Google Patents
Rorγtのヘテロアリール結合キノリニルモジュレーター Download PDFInfo
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- JP2016534998A JP2016534998A JP2016523254A JP2016523254A JP2016534998A JP 2016534998 A JP2016534998 A JP 2016534998A JP 2016523254 A JP2016523254 A JP 2016523254A JP 2016523254 A JP2016523254 A JP 2016523254A JP 2016534998 A JP2016534998 A JP 2016534998A
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- alkyl
- disease
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- pyridyl
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- 125000001072 heteroaryl group Chemical group 0.000 title description 2
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- 125000004076 pyridyl group Chemical group 0.000 claims description 25
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 108090000629 orphan nuclear receptors Proteins 0.000 description 1
- 102000004164 orphan nuclear receptors Human genes 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 229940014662 pantothenate Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 235000019371 penicillin G benzathine Nutrition 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 208000028169 periodontal disease Diseases 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000009521 phase II clinical trial Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 238000001126 phototherapy Methods 0.000 description 1
- 229950010765 pivalate Drugs 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000029279 positive regulation of transcription, DNA-dependent Effects 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004237 preparative chromatography Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- 230000000770 proinflammatory effect Effects 0.000 description 1
- 208000005069 pulmonary fibrosis Diseases 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 229960000948 quinine Drugs 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 125000004548 quinolin-3-yl group Chemical group N1=CC(=CC2=CC=CC=C12)* 0.000 description 1
- WPYJKGWLDJECQD-UHFFFAOYSA-N quinoline-2-carbaldehyde Chemical compound C1=CC=CC2=NC(C=O)=CC=C21 WPYJKGWLDJECQD-UHFFFAOYSA-N 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 208000037803 restenosis Diseases 0.000 description 1
- 229930002330 retinoic acid Natural products 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 201000000306 sarcoidosis Diseases 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229960004540 secukinumab Drugs 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 238000002741 site-directed mutagenesis Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000036262 stenosis Effects 0.000 description 1
- 208000037804 stenosis Diseases 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 201000011549 stomach cancer Diseases 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 238000009121 systemic therapy Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- 229960001727 tretinoin Drugs 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 201000008827 tuberculosis Diseases 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 201000005112 urinary bladder cancer Diseases 0.000 description 1
- 229960003824 ustekinumab Drugs 0.000 description 1
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
Abstract
Description
R1は、アゼチジニル、ピロリル、ピラゾリル、イミダゾリル、トリアゾリル、チアゾリル、ピリジル、ピリジルN−オキシド、ピラジニル、ピリミジニル、ピリダジル、ピペリジニル、テトラヒドロピラニル、フェニル、オキサゾリル、イソオキサゾリル、チオフェニル、ベンゾオキサゾリル、又はキノリニルであり、このとき、前記ピペリジニル、ピリジル、ピリジルN−オキシド、イミダゾリル、フェニル、チオフェニル、ベンゾオキサゾリル、及びピラゾリルは、SO2CH3、C(O)CH3、C(O)NH2、CH3、CH2CH3、CF3、Cl、F、−CN、OCH3、N(CH3)2、−(CH2)3OCH3、SCH3、OH、CO2H、CO2C(CH3)3、又はOCH2OCH3で任意に置換されており、かつCl、OCH3、及びCH3からなる群から独立して選択される最大2つの追加の置換基で任意に置換されており、このとき、前記トリアゾリル、オキサゾリル、イソオキサゾリル、及びチアゾリルは、1つ又は2つのCH3基で任意に置換されており、このとき、前記アゼチジニルは、CO2C(CH3)3、C(O)NH2、CH3、SO2CH3、又はC(O)CH3で任意に置換されており、
R2は、1−メチル−1,2,3−トリアゾリル、ピリジル、ピリジル−N−オキシド、1−メチルピラゾール−4−イル、ピリミジン−5−イル、ピリダジル、ピラジン−2−イル、オキサゾリル、イソオキサゾリル、N−アセチル−アゼチジン−3−イル、N−メチルスルホニル−アゼチジン−3−イル、N−Boc−アゼチジン−3−イル、N−メチル−アゼチジン−3−イル、N−アセタミジル−アゼチジン−3−イル、N−アセチルピペリジニル、1−H−ピペリジニル、N−Boc−ピペリジニル、N−C(1〜2)アルキル−ピペリジニル、チアゾール−5−イル、1−(3−メトキシプロピル)−イミダゾール−5−イル、又は1−C(1〜2)アルキルイミダゾール−5−イルであり、このとき、前記1−C(1〜2)アルキルイミダゾール−5−イルは、最大2つの追加のCH3基、又は、SCH3及びClからなる群から選択される1つの置換基で任意に置換されており、前記ピリジル及びピリジル−N−オキシドは、C(O)NH2、−CN、OCH3、CF3、Cl、及びCH3からなる群から独立して選択される最大2つの置換基で任意に置換されており、前記チアゾール−5−イル、オキサゾリル、及びイソオキサゾリルは、最大2つのCH3基で任意に置換されており、前記1−メチルピラゾール−4−イルは、最大2つの追加のCH3基で任意に置換されており、
R3は、H、OH、OCH3、NHCH3、N(CH3)2、又はNH2であり、
R4は、H又はFであり、
R5は、H、Cl、−CN、CF3、SCH3、OC(1〜3)アルキル、OH、C(1〜4)アルキル、N(CH3)OCH3、NH(C(1〜2)アルキル)、N(C(1〜2)アルキル)2、NH−シクロプロピル、OCHF2、4−ヒドロキシ−ピペリジニル、アゼチジン−1−イル、又はフル−2−イルであり、
R6は、−O−フェニル、−NHフェニル、−N(C(1〜3)アルキル)フェニル、−N(CO2C(CH3)3)フェニル、−O−ピリジル、−NHピリジル、−N(C(1〜3)アルキル)ピリジル、又は−N(CO2C(CH3)3)ピリジルであり、このとき、これらの前記フェニル部分又はこれらの前記ピリジル部分は、OCF3、SO2CH3、CF3、CHF2、イミダゾール−1−イル、ピラゾール−1−イル、1,2,4−トリアゾール−1−イル、CH3、OCH3、Cl、F、又は−CNで任意に置換されており、
R7は、H、Cl、−CN、C(1〜4)アルキル、OCH2CF3、OCH2CH2OCH3、CF3、SCH3、SO2CH3、OCHF2、NA1A2、C(O)NHCH3、N(CH3)CH2CH2NA1A2、OCH2CH2NA1A2、OC(1〜3)アルキル、OCH2−(1−メチル)−イミダゾール−2−イル、イミダゾール−2−イル、フル−2−イル、ピラゾール−4−イル、ピリド−3−イル、又はピリミジン−5−イル、チオフェン−3−イル、1−メチル−インダゾール−5−イル、1−メチル−インダゾール−6−イル、フェニル、又は
A1は、H又はC(1〜4)アルキルであり、
A2は、H、C(1〜4)アルキル、シクロプロピル、C(1〜4)アルキルOC(1〜4)アルキル、C(1〜4)アルキルOH、C(O)C(1〜2)アルキル、又はOCH3であり、あるいは、A1及びA2は、それらに結合した窒素と一緒になって、
R1は、アゼチジニル、ピロリル、ピラゾリル、イミダゾリル、トリアゾリル、チアゾリル、ピリジル、ピリジルN−オキシド、ピラジニル、ピリミジニル、ピリダジル、ピペリジニル、テトラヒドロピラニル、フェニル、オキサゾリル、イソオキサゾリル、チオフェニル、ベンゾオキサゾリル、又はキノリニルであり、このとき、前記ピペリジニル、ピリジル、ピリジルN−オキシド、イミダゾリル、フェニル、チオフェニル、ベンゾオキサゾリル、及びピラゾリルは、SO2CH3、C(O)CH3、C(O)NH2、CH3、CH2CH3、CF3、Cl、F、−CN、OCH3、N(CH3)2、−(CH2)3OCH3、SCH3、OH、CO2H、CO2C(CH3)3、又はOCH2OCH3で任意に置換されており、かつCl、OCH3、及びCH3からなる群から独立して選択される最大2つの追加の置換基で任意に置換されており、このとき、前記トリアゾリル、オキサゾリル、イソオキサゾリル、及びチアゾリルは、1つ又は2つのCH3基で任意に置換されており、このとき、前記アゼチジニルは、CO2C(CH3)3、C(O)NH2、CH3、SO2CH3、又はC(O)CH3で任意に置換されており、
R2は、1−メチル−1,2,3−トリアゾリル、ピリジル、ピリジル−N−オキシド、1−メチルピラゾール−4−イル、ピリミジン−5−イル、ピリダジル、ピラジン−2−イル、オキサゾリル、イソオキサゾリル、N−アセチル−アゼチジン−3−イル、N−メチルスルホニル−アゼチジン−3−イル、N−Boc−アゼチジン−3−イル、N−メチル−アゼチジン−3−イル、N−アセタミジル−アゼチジン−3−イル、N−アセチルピペリジニル、1−H−ピペリジニル、N−Boc−ピペリジニル、N−C(1〜2)アルキル−ピペリジニル、チアゾール−5−イル、1−(3−メトキシプロピル)−イミダゾール−5−イル、又は1−C(1〜2)アルキルイミダゾール−5−イル(1−メチルイミダゾール−5−イルを含む)であり、このとき、前記1−C(1〜2)アルキルイミダゾール−5−イルは、最大2つの追加のCH3基、又は、SCH3及びClからなる群から選択される1つの置換基で任意に置換されており、前記ピリジル及びピリジル−N−オキシドは、C(O)NH2、−CN、OCH3、CF3、Cl、及びCH3からなる群から独立して選択される最大2つの置換基で任意に置換されており、前記チアゾール−5−イル、オキサゾリル、及びイソオキサゾリルは、最大2つのCH3基で任意に置換されており、前記1−メチルピラゾール−4−イルは、最大2つの追加のCH3基で任意に置換されており、
R3は、H、OH、OCH3、NHCH3、N(CH3)2、又はNH2であり、
R4は、H、又はFであり、
R5は、H、Cl、−CN、CF3、SCH3、OC(1〜3)アルキル、OH、C(1〜4)アルキル、N(CH3)OCH3、NH(C(1〜2)アルキル)、N(C(1〜2)アルキル)2、NH−シクロプロピル、OCHF2、4−ヒドロキシ−ピペリジニル、アゼチジン−1−イル、又はフル−2−イルであり、
R6は、−O−フェニル、−NHフェニル、−N(C(1〜3)アルキル)フェニル、−N(CO2C(CH3)3)フェニル、−O−ピリジル、−NHピリジル、−N(C(1〜3)アルキル)ピリジル、又は−N(CO2C(CH3)3)ピリジルであり、このとき、これらの前記フェニル部分又はこれらの前記ピリジル部分は、OCF3、SO2CH3、CF3、CHF2、イミダゾール−1−イル、ピラゾール−1−イル、1,2,4−トリアゾール−1−イル、CH3、OCH3、Cl、F、又は−CNで任意に置換されており、
R7は、H、Cl、−CN、C(1〜4)アルキル、OCH2CF3、OCH2CH2OCH3、CF3、SCH3、SO2CH3、OCHF2、NA1A2、C(O)NHCH3、N(CH3)CH2CH2NA1A2、OCH2CH2NA1A2、OC(1〜3)アルキル、OCH2−(1−メチル)−イミダゾール−2−イル、イミダゾール−2−イル、フル−2−イル、ピラゾール−4−イル、ピリド−3−イル、又はピリミジン−5−イル、チオフェン−3−イル、1−メチル−インダゾール−5−イル、1−メチル−インダゾール−6−イル、フェニル、又は
A1は、H又はC(1〜4)アルキル(CH2CH3を含む)であり、
A2は、H、C(1〜4)アルキル(CH2CH3を含む)、シクロプロピル、C(1〜4)アルキルOC(1〜4)アルキル、C(1〜4)アルキルOH、C(O)C(1〜2)アルキル、又はOCH3であり、あるいは、A1及びA2は、それらに結合した窒素と一緒になって、
Raは、H、F、OC(1〜3)アルキル、又はOHであり、
Rbは、CH3、又はフェニルであり、
R8は、H、CH3、OCH3、又はFであり、
R9は、H、又はFである、化合物、
並びにその医薬的に許容される塩を含む。
R1は、6−トリフルオロメチルピリド−3−イル、ピリド−2−イル、4−クロロフェニル、又は3−クロロフェニルであり、
R2は、1−メチルイミダゾール−5−イル、又はピリド−3−イルであり、
R3は、OHであり、
R4は、Hであり、
R5は、Cl、又は−CNであり、
R6は、−O−フェニル、又は−N(CO2C(CH3)3)フェニルであり、このとき前記−O−フェニルは、−CN、又はClで任意に置換されており、
R7は、Cl、NA1A2であり、
A1は、CH2CH3であり、
A2は、CH2CH3であり、あるいは、A1及びA2は、それらに結合した窒素と一緒になって、
本発明の方法に関して用語「投与」は、式Iの化合物又はその形成物、組成物若しくは薬剤を使用することにより、本明細書に記載しているような症候群、障害又は疾患を、治療的又は予防的に、予防、処置又は寛解する方法を意味する。このような方法は、有効量の上記化合物、化合物形成物、組成物若しくは薬剤を、一連の治療の異なる時点で又は組み合わせ形式で同時に、投与することを含む。本発明の方法は、既知の治療学的処置レジメンを全て包含するものとして理解されるものである。
医薬的に許容される酸性/陰イオンの塩には、酢酸塩、ベンゼンスルホン酸塩、安息香酸塩、重炭酸塩、酒石酸水素塩、臭化物、エデト酸カルシウム、カンシル酸塩、炭酸塩、塩化物、クエン酸塩、二塩酸塩、エデト酸塩、エジシル酸塩、エストル酸塩、エシル酸塩、フマル酸塩、グルセプト酸塩、グルコン酸塩、グルタミン酸塩、グリコリルアルサニル酸塩、ヘキシルレソルシン酸塩、ヒドラバミン、臭化水素酸塩、塩酸塩、ヒドロキシナフトエ酸塩、ヨウ化物、イセチオン酸塩、乳酸塩、ラクトビオン酸塩、リンゴ酸塩、マレイン酸塩、マンデル酸塩、メシル酸塩、メチル臭化物、メチル硝酸塩、メチル硫酸塩、ムコ酸塩、ナプシル酸塩、硝酸塩、パモ酸塩、パントテン酸塩、リン酸塩/二リン酸塩、ポリガラクツロン酸塩、サリチル酸塩、ステアリン酸塩、塩基性酢酸塩、コハク酸塩、硫酸塩、タンニン酸塩、酒石酸塩、テオクル酸塩、トシル酸塩及びトリエチオジドが挙げられるが、これらに限定されない。有機又は無機の酸としては、ヨウ化水素酸、過塩素酸、硫酸、リン酸、プロピオン酸、グリコール酸、メタンスルホン酸、ヒドロキシエタンスルホン酸、シュウ酸、2−ナフタレンスルホン酸、p−トルエンスルホン酸、シクロヘキサンスルファミン酸、サッカリン酸又はトリフルオロ酢酸が挙げられるが、これらに限定されない。
本発明は、必要がある被験体に、有効量の式Iの化合物、又はその形成物、組成物若しくは薬剤を投与することを含む、RORγt介在性炎症性症候群、障害又は疾患を予防、治療又は寛解する方法を目的とする。
更に、本発明の化合物は、1種又は2種以上の多形体又は非晶質結晶性形態を有してよく、これらの形態も本発明の範囲に含まれるものとする。加えて、化合物は、例えば水(すなわち、水和物)又は一般有機溶媒と共に溶媒和物を形成してよい。本明細書で使用するとき、用語「溶媒和物」は、本発明の化合物と1種又は2種以上の溶媒分子との物理的会合を意味する。この物理的結合には、水素結合を含む、様々な度合のイオン結合及び共有結合を伴う。特定の場合には、溶媒和物は、例えば1種以上の溶媒分子が結晶固形物の結晶格子内に組み込まれた場合に、単離することができる。用語「溶媒和物」は、溶液相及び分離可能な溶媒和物の両方を包含することを意図する。好適な溶媒和物の非限定例としては、エタノレート、メタノレートなどが挙げられる。
本明細書及び本願を通して、以下の略後が使用される。
本発明において、式Iの化合物は、当業者に既知の一般的な合成法に従って合成できる。以下の反応スキームは、本発明の代表的な実施例であるということのみを意味し、すなわち本発明の限定であることは全く意味しない。
4−クロロ−N−メトキシ−N−メチルベンズアミド
(4−クロロフェニル)(1−メチル−1H−イミダゾール−5−イル)メタノン
2−(4−シアノフェノキシ)アセチルクロリド
メチル5−ブロモ−2−(2−(4−シアノフェノキシ)アセトアミド)ベンゾエート
4−((6−ブロモ−4−ヒドロキシ−2−オキソ−1,2−ジヒドロキノリン−3−イル)オキシ)ベンゾニトリル
4−((6−ブロモ−2,4−ジクロロキノリン−3−イル)オキシ)ベンゾニトリル
4−((6−ブロモ−4−クロロ−2−(ピロリジン−1−イル)キノリン−3−イル)オキシ)ベンゾニトリル
6−(トリフルオロメチル)ニコチノイルクロリド
N−メトキシ−N−メチル−6−(トリフルオロメチル)ニコチンアミド
(1−メチル−1H−イミダゾール−5−イル)(6−(トリフルオロメチル)ピリジン−3−イル)メタノン
メチル5−ブロモ−2−(2−フェノキシアセトアミド)ベンゾエート
6−ブロモ−4−ヒドロキシ−3−フェノキシキノリン−2(1H)−オン
6−ブロモ−2,4−ジクロロ−3−フェノキシキノリン
6−ブロモ−4−クロロ−N,N−ジエチル−3−フェノキシキノリン−2−アミン
(1−メチル−1H−イミダゾール−5−イル)(ピリジン−2−イル)メタノール
(1−メチル−1H−イミダゾール−5−イル)(ピリジン−2−イル)メタノン
メチル5−ブロモ−2−(2−(4−クロロフェノキシ)アセトアミド)ベンゾエート
6−ブロモ−3−(4−クロロフェノキシ)−4−ヒドロキシキノリン−2(1H)−オン
6−ブロモ−2,4−ジクロロ−3−(4−クロロフェノキシ)キノリン
6−ブロモ−4−クロロ−3−(4−クロロフェノキシ)−2−(3−イソプロポキシアゼチジン−1−イル)キノリン
6−ブロモ−4−ヒドロキシキノリン−2(1H)−オン
(6−ブロモ−4−ヒドロキシ−2−オキソ−1,2−ジヒドロキノリン−3−イル)(フェニル)ヨードニウムトリフルオロメタンスルホネート
6−ブロモ−4−ヒドロキシ−3−(フェニルアミノ)キノリン−2(1H)−オン
6−ブロモ−2,4−ジクロロ−N−フェニルキノリン−3−アミン
tert−ブチル(6−ブロモ−2,4−ジクロロキノリン−3−イル)(フェニル)カルバメート
4−((4−クロロ−6−(ヒドロキシ(1−メチル−1H−イミダゾール−5−イル)(6−(トリフルオロメチル)ピリジン−3−イル)メチル)−2−(ピロリジン−1−イル)キノリン−3−イル)オキシ)ベンゾニトリル
(4−クロロ−2−(ジエチルアミノ)−3−フェノキシキノリン−6−イル)(1−メチル−1H−イミダゾール−5−イル)(ピリジン−2−イル)メタノール
4−((2,4−ジクロロ−6−((4−クロロフェニル)(ヒドロキシ)(1−メチル−1H−イミダゾール−5−イル)メチル)キノリン−3−イル)オキシ)ベンゾニトリル
2−(ジエチルアミノ)−6−(ヒドロキシ(1−メチル−1H−イミダゾール−5−イル)(ピリジン−2−イル)メチル)−3−フェノキシキノリン−4−カルボニトリル
(4−クロロ−3−(4−クロロフェノキシ)−2−(3−イソプロポキシアゼチジン−1−イル)キノリン−6−イル)(1−メチル−1H−イミダゾール−5−イル)(6−(トリフルオロメチル)ピリジン−3−イル)メタノール
ThermoFluor(登録商標)アッセイ
ThermoFluor(登録商標)は、タンパク質の熱安定性に対するリガンドの影響を測定することによって、リガンドの結合親和性を推定する蛍光系アッセイである(Pantoliano,M.W.,Petrella,E.C.,Kwasnoski,J.D.,Lobanov,V.S.,Myslik,J.,Graf,E.,Carver,T.,Asel,E.,Springer,B.A.,Lane,P.,and Salemme,F.R.(2001)High−density miniaturized thermal shift assays as a general strategy for drug discovery.J Biomol Screen 6,429〜40,及びMatulis,D.,Kranz,J.K.,Salemme,F.R.,and Todd,M.J.(2005)Thermodynamic stability of carbonic anhydrase:measurements of binding affinity and stoichiometry using ThermoFluor.Biochemistry 44,5258〜66)。この手法は、広範な系に適用することができ、かつ平衡結合定数(KD)を介する理論的な解釈に基づく厳密なものである。
ThermoFluor(登録商標)アッセイに使用されるRORγt構築物において、ヌクレオチド配列の番号は、ヒトRORγt、転写物変異体2、NCBI Accession:NM_001001523.1(配列番号1)の参照配列に基づいていた。野生型ヒトRORγtリガンド結合ドメイン(RORγt LBD)をコードするヌクレオチド850−1635(配列番号2)を、クローニングされた挿入配列の上流に、インフレームのN末端Hisタグ及びTurboTEVプロテアーゼ切断部位(ENLYFQG、配列番号3)を含む、pHIS1ベクター(改変型pET E.coli発現ベクター(Accelagen、San Diego))にクローニングした。Thermofluorアッセイに用いたRORγt構築物のアミノ酸配列を、配列番号4として示す。
0.065mg/mL RORγt
60μM 1,8−ANS
100mM Hepes、pH 7.0
10mM NaCl
2.5mM GSH
0.002% Tween−20
参照RORγt Tm:47.8℃
ΔH(Tm)=115kcal/モル
ΔCp(Tm)=3kcal/モル
RORγtリポーターアッセイ
リポーターアッセイを用いて、RORγt調節性化合物の、RORγt LBDにより促進される転写活性化に対する機能的活性を検査した。このアッセイに用いる細胞は、2つの構築物が同時導入された。第1構築物は、pBIND−RORγt LBDであり、GAL4タンパク質のDNA結合ドメインに融合した野生型ヒトRORγt LBDを含んでいた。第2構築物は、pGL4.31(Promega、カタログ番号C935A)であり、蛍ルシフェラーゼの上流に、複数のGAL4応答性DNA配列を含んでいた。バックグラウンド対照を産生するため、細胞に同様に2つの構築物を同時導入したが、第1構築物では、RORγt LBD中のAF2アミノ酸モチーフを、LYKELF(配列番号5)からLFKELF(配列番号6)に変更した。AF2変異は、RORγt LBDへのコアクチベーターの結合を防ぐことによって、蛍ルシフェラーゼの転写を防ぐことが示されている。変異体構築物を、pBIND−RORγt−AF2と呼んだ。
ヒトTh17アッセイは、Th17の分化に有利である条件下での、RORγt調節性化合物の、CD4T細胞によるIL−17産生への影響を調べる。
Claims (20)
- 式Iの化合物であって、
R1は、アゼチジニル、ピロリル、ピラゾリル、イミダゾリル、トリアゾリル、チアゾリル、ピリジル、ピリジルN−オキシド、ピラジニル、ピリミジニル、ピリダジル、ピペリジニル、テトラヒドロピラニル、フェニル、オキサゾリル、イソオキサゾリル、チオフェニル、ベンゾオキサゾリル、又はキノリニルであり、前記ピペリジニル、ピリジル、ピリジルN−オキシド、イミダゾリル、フェニル、チオフェニル、ベンゾオキサゾリル、及びピラゾリルは、SO2CH3、C(O)CH3、C(O)NH2、CH3、CH2CH3、CF3、Cl、F、−CN、OCH3、N(CH3)2、−(CH2)3OCH3、SCH3、OH、CO2H、CO2C(CH3)3、又はOCH2OCH3で任意に置換されており、かつCl、OCH3、及びCH3からなる群から独立して選択される最大2つの追加の置換基で任意に置換されており、前記トリアゾリル、オキサゾリル、イソオキサゾリル、及びチアゾリルは、1つ又は2つのCH3基で任意に置換されており、前記アゼチジニルは、CO2C(CH3)3、C(O)NH2、CH3、SO2CH3、又はC(O)CH3で任意に置換されており、
R2は、1−メチル−1,2,3−トリアゾリル、ピリジル、ピリジル−N−オキシド、1−メチルピラゾール−4−イル、ピリミジン−5−イル、ピリダジル、ピラジン−2−イル、オキサゾリル、イソオキサゾリル、N−アセチル−アゼチジン−3−イル、N−メチルスルホニル−アゼチジン−3−イル、N−Boc−アゼチジン−3−イル、N−メチル−アゼチジン−3−イル、N−アセタミジル−アゼチジン−3−イル、N−アセチルピペリジニル、1−H−ピペリジニル、N−Boc−ピペリジニル、N−C(1〜2)アルキル−ピペリジニル、チアゾール−5−イル、1−(3−メトキシプロピル)−イミダゾール−5−イル、又は1−C(1〜2)アルキルイミダゾール−5−イルであり、前記1−C(1〜2)アルキルイミダゾール−5−イルは、最大2つの追加のCH3基、又は、SCH3及びClからなる群から選択される1つの置換基で任意に置換されており、前記ピリジル及びピリジル−N−オキシドは、C(O)NH2、−CN、OCH3、CF3、Cl、及びCH3からなる群から独立して選択される最大2つの置換基で任意に置換されており、前記チアゾール−5−イル、オキサゾリル、及びイソオキサゾリルは、最大2つのCH3基で任意に置換されており、前記1−メチルピラゾール−4−イルは、最大2つの追加のCH3基で任意に置換されており、
R3は、H、OH、OCH3、NHCH3、N(CH3)2、又はNH2であり、
R4は、H又はFであり、
R5は、H、Cl、−CN、CF3、SCH3、OC(1〜3)アルキル、OH、C(1〜4)アルキル、N(CH3)OCH3、NH(C(1〜2)アルキル)、N(C(1〜2)アルキル)2、NH−シクロプロピル、OCHF2、4−ヒドロキシ−ピペリジニル、アゼチジン−1−イル、又はフル−2−イルであり、
R6は、−O−フェニル、−NHフェニル、−N(C(1〜3)アルキル)フェニル、−N(CO2C(CH3)3)フェニル、−O−ピリジル、−NHピリジル、−N(C(1〜3)アルキル)ピリジル、又は−N(CO2C(CH3)3)ピリジルであり、このとき、これらの前記フェニル部分又はこれらの前記ピリジル部分は、OCF3、SO2CH3、CF3、CHF2、イミダゾール−1−イル、ピラゾール−1−イル、1,2,4−トリアゾール−1−イル、CH3、OCH3、Cl、F、又は−CNで任意に置換されており、
R7は、H、Cl、−CN、C(1〜4)アルキル、OCH2CF3、OCH2CH2OCH3、CF3、SCH3、SO2CH3、OCHF2、NA1A2、C(O)NHCH3、N(CH3)CH2CH2NA1A2、OCH2CH2NA1A2、OC(1〜3)アルキル、OCH2−(1−メチル)−イミダゾール−2−イル、イミダゾール−2−イル、フル−2−イル、ピラゾール−4−イル、ピリド−3−イル、又はピリミジン−5−イル、チオフェン−3−イル、1−メチル−インダゾール−5−イル、1−メチル−インダゾール−6−イル、フェニル、又は
A1は、H又はC(1〜4)アルキルであり、
A2は、H、C(1〜4)アルキル、シクロプロピル、C(1〜4)アルキルOC(1〜4)アルキル、C(1〜4)アルキルOH、C(O)C(1〜2)アルキル、又はOCH3であり、あるいは、A1及びA2は、それらに結合した窒素と一緒になって、
Raは、H、F、OC(1〜3)アルキル、又はOHであり、
Rbは、CH3、又はフェニルであり、
R8は、H、CH3、OCH3、又はFであり、
R9は、H、又はFである、化合物、
並びにこれらの医薬的に許容される塩。 - R1が、6−トリフルオロメチルピリド−3−イル、ピリド−2−イル、4−クロロフェニル、又は3−クロロフェニルであり、
R2が、1−メチルイミダゾール−5−イル、又はピリド−3−イルであり、
R3が、OHであり、
R4が、Hであり、
R5が、Cl、又は−CNであり、
R6が、−O−フェニル、又は−N(CO2C(CH3)3)フェニルであり、このとき前記−O−フェニルは、−CN、又はClで任意に置換されており、
R7が、Cl、NA1A2であり、
A1が、CH2CH3であり、
A2が、CH2CH3であり、あるいは、A1及びA2が、それらに結合した窒素と一緒になって、
並びにこれらの医薬的に許容される塩。 - 請求項1に記載の化合物と、医薬的に許容される担体と、を含む、医薬組成物。
- 請求項1に記載の化合物及び医薬的に許容される担体を混合してなる、医薬組成物。
- 請求項1に記載の化合物及び医薬的に許容される担体を混合することを含む、医薬組成物の製造方法。
- 必要がある被験体に有効量の請求項1に記載の化合物を投与することを含む、RORγt介在性炎症性症候群、障害又は疾患を治療又は寛解する方法。
- 前記疾患が、炎症性腸疾患、関節リウマチ、乾癬、慢性閉塞性肺疾患、乾癬性関節炎、強直性脊椎炎、好中球性喘息、ステロイド耐性喘息、多発性硬化症、及び全身性エリテマトーデスからなる群から選択される、請求項7に記載の方法。
- 前記疾患が乾癬である、請求項7に記載の方法。
- 前記疾患が関節リウマチである、請求項7に記載の方法。
- 前記炎症性腸疾患が潰瘍性大腸炎である、請求項8に記載の方法。
- 前記炎症性腸疾患がクローン病である、請求項8に記載の方法。
- 前記疾患が多発性硬化症である、請求項7に記載の方法。
- 前記疾患が好中球性喘息である、請求項7に記載の方法。
- 前記疾患がステロイド耐性喘息である、請求項7に記載の方法。
- 前記疾患が乾癬性関節炎である、請求項7に記載の方法。
- 前記疾患が強直性脊椎炎である、請求項7に記載の方法。
- 前記疾患が全身性エリテマトーデスである、請求項7に記載の方法。
- 前記疾患が慢性閉塞性肺疾患である、請求項7に記載の方法。
- 必要がある被験体における症候群、障害又は疾患を治療又は寛解する方法であって、1つ又は2つ以上の抗炎症剤、又は免疫抑制剤との併用療法において被験体に有効量の請求項1に記載の化合物又はその組成物若しくは薬剤を投与することを含み、前記症候群、障害又は疾患が、関節リウマチ及び乾癬からなる群から選択される、方法。
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ES2929140T3 (es) | 2018-06-18 | 2022-11-25 | Janssen Pharmaceutica Nv | Imidazoles sustituidos con fenilo y piridinilo como moduladores de RORgammat |
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JP2015534979A (ja) * | 2012-10-16 | 2015-12-07 | ヤンセン ファーマシューティカ エヌ.ベー. | Rorγtのヘテロアリール結合させたキノリニルモジュレータ |
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JP2004500539A (ja) * | 1998-03-20 | 2004-01-08 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフトング | アテローム性動脈硬化症の治療に有用な物質をスクリーニングするためのror受容体の使用 |
WO2004037792A2 (en) * | 2002-09-27 | 2004-05-06 | Karo Bio Ab | Benzo (f) quinolinone variants as nuclear hormone receptor ligands |
JP2015534979A (ja) * | 2012-10-16 | 2015-12-07 | ヤンセン ファーマシューティカ エヌ.ベー. | Rorγtのヘテロアリール結合させたキノリニルモジュレータ |
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