RU2016140338A - Азаспиро производные в качестве антагонистов trpm8 - Google Patents
Азаспиро производные в качестве антагонистов trpm8 Download PDFInfo
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- RU2016140338A RU2016140338A RU2016140338A RU2016140338A RU2016140338A RU 2016140338 A RU2016140338 A RU 2016140338A RU 2016140338 A RU2016140338 A RU 2016140338A RU 2016140338 A RU2016140338 A RU 2016140338A RU 2016140338 A RU2016140338 A RU 2016140338A
- Authority
- RU
- Russia
- Prior art keywords
- difluoro
- diazaspiro
- decan
- dione
- oxoethyl
- Prior art date
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- 102000003610 TRPM8 Human genes 0.000 title claims 4
- 101150111302 Trpm8 gene Proteins 0.000 title claims 4
- 239000005557 antagonist Substances 0.000 title 1
- -1 (2-oxo-2- (4- (quinolin-2-yl) phenyl) ethyl) -1,3-diazaspiro [4.5] decan-2,4-dione Chemical compound 0.000 claims 24
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 14
- 229910052736 halogen Inorganic materials 0.000 claims 14
- 150000002367 halogens Chemical class 0.000 claims 14
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 12
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000001188 haloalkyl group Chemical group 0.000 claims 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 10
- 125000004438 haloalkoxy group Chemical group 0.000 claims 10
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 9
- 208000035475 disorder Diseases 0.000 claims 9
- 239000000651 prodrug Substances 0.000 claims 9
- 229940002612 prodrug Drugs 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 9
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 8
- WTVNFKVGGUWHQC-UHFFFAOYSA-N decane-2,4-dione Chemical compound CCCCCCC(=O)CC(C)=O WTVNFKVGGUWHQC-UHFFFAOYSA-N 0.000 claims 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 239000001301 oxygen Substances 0.000 claims 7
- 229910052717 sulfur Inorganic materials 0.000 claims 7
- 239000011593 sulfur Substances 0.000 claims 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 208000013403 hyperactivity Diseases 0.000 claims 6
- 229910052757 nitrogen Chemical group 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 208000014001 urinary system disease Diseases 0.000 claims 6
- 239000004305 biphenyl Substances 0.000 claims 5
- 208000019901 Anxiety disease Diseases 0.000 claims 4
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 4
- 206010020853 Hypertonic bladder Diseases 0.000 claims 4
- 208000002193 Pain Diseases 0.000 claims 4
- 208000012931 Urologic disease Diseases 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 230000036506 anxiety Effects 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 208000027866 inflammatory disease Diseases 0.000 claims 4
- 208000004296 neuralgia Diseases 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- 230000003042 antagnostic effect Effects 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 3
- 230000001404 mediated effect Effects 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 239000010802 sludge Substances 0.000 claims 3
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 2
- 206010058019 Cancer Pain Diseases 0.000 claims 2
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
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- 241000124008 Mammalia Species 0.000 claims 2
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- 208000004550 Postoperative Pain Diseases 0.000 claims 2
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims 2
- 208000003251 Pruritus Diseases 0.000 claims 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
- 208000003782 Raynaud disease Diseases 0.000 claims 2
- 208000012322 Raynaud phenomenon Diseases 0.000 claims 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 2
- 206010046543 Urinary incontinence Diseases 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 208000026935 allergic disease Diseases 0.000 claims 2
- 206010053552 allodynia Diseases 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 2
- 201000002170 dentin sensitivity Diseases 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 231100000869 headache Toxicity 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 230000009610 hypersensitivity Effects 0.000 claims 2
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- 208000002551 irritable bowel syndrome Diseases 0.000 claims 2
- 208000028867 ischemia Diseases 0.000 claims 2
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- 230000007823 neuropathy Effects 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 201000008482 osteoarthritis Diseases 0.000 claims 2
- 208000020629 overactive bladder Diseases 0.000 claims 2
- 208000027753 pain disease Diseases 0.000 claims 2
- 208000033808 peripheral neuropathy Diseases 0.000 claims 2
- 208000020016 psychiatric disease Diseases 0.000 claims 2
- 208000002815 pulmonary hypertension Diseases 0.000 claims 2
- 208000023504 respiratory system disease Diseases 0.000 claims 2
- 210000003932 urinary bladder Anatomy 0.000 claims 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
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- AIUJROUTBQDJAQ-UHFFFAOYSA-N C1(=NC=CC2=CC=NC=C12)C1=CC=C(C=C1)C(CN1C(OC2(C1=O)CCC(CC2)(F)F)=O)=O Chemical compound C1(=NC=CC2=CC=NC=C12)C1=CC=C(C=C1)C(CN1C(OC2(C1=O)CCC(CC2)(F)F)=O)=O AIUJROUTBQDJAQ-UHFFFAOYSA-N 0.000 claims 1
- RNEUBJJKTSCBPM-UHFFFAOYSA-N CC1=NC=2C(=NC(=CC=2)C)N1C1=CC=C(C=C1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O Chemical compound CC1=NC=2C(=NC(=CC=2)C)N1C1=CC=C(C=C1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O RNEUBJJKTSCBPM-UHFFFAOYSA-N 0.000 claims 1
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- XUAVNHKNKZAMJN-UHFFFAOYSA-N N1C=CC=2C1=CN=CC=2C1=CC=C(C=N1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O Chemical compound N1C=CC=2C1=CN=CC=2C1=CC=C(C=N1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O XUAVNHKNKZAMJN-UHFFFAOYSA-N 0.000 claims 1
- XRJQANMYQXUVFN-UHFFFAOYSA-N N1N=CC2=C(C=CC=C12)C1=CC=C(C=C1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O Chemical compound N1N=CC2=C(C=CC=C12)C1=CC=C(C=C1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O XRJQANMYQXUVFN-UHFFFAOYSA-N 0.000 claims 1
- KGJYBHHXHQGMGR-UHFFFAOYSA-N N1N=CC2=C(C=CC=C12)C1=CC=C(C=N1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O Chemical compound N1N=CC2=C(C=CC=C12)C1=CC=C(C=N1)C(CN1C(NC2(C1=O)CCC(CC2)(F)F)=O)=O KGJYBHHXHQGMGR-UHFFFAOYSA-N 0.000 claims 1
- VYKLMURCFPWALC-UHFFFAOYSA-N O=C1NC2(C(N1CC(=O)C1=CC=C(C=C1)C1=CC=CC(=N1)C#N)=O)CCCCC2 Chemical compound O=C1NC2(C(N1CC(=O)C1=CC=C(C=C1)C1=CC=CC(=N1)C#N)=O)CCCCC2 VYKLMURCFPWALC-UHFFFAOYSA-N 0.000 claims 1
- UYUPIXPMEDSCQA-UHFFFAOYSA-N OCC=1C(=NC=CN=1)C1=CC=C(C=C1)C(CN1C(NC2(C1=O)CCCCC2)=O)=O Chemical compound OCC=1C(=NC=CN=1)C1=CC=C(C=C1)C(CN1C(NC2(C1=O)CCCCC2)=O)=O UYUPIXPMEDSCQA-UHFFFAOYSA-N 0.000 claims 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000005103 alkyl silyl group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 claims 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229930192474 thiophene Natural products 0.000 claims 1
- 150000003852 triazoles Chemical class 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
-
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- A61K31/4164—1,3-Diazoles
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- A61K31/4164—1,3-Diazoles
- A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
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Claims (162)
1. Соединение следующей формулы (I)
[Хим. 1]
в которой
A обозначает арил и гетероарил;
B обозначает арил и гетероарил;
L независимо выбран из группы, состоящей из химической связи, кислорода, серы, -NR4-, -(CRCRD)t-, -O(CRCRD)t-, -(CRCRD)tO-, -N(R4)(CRCRD)t-, -(CRCRD)tN(R4)-, -N(R4)(CRCRD)tO- и -O(CRCRD)tN(R4)-
X независимо выбран из группы, состоящей из -CH2-, кислорода, серы и NH;
RA и RB независимо выбраны из группы, состоящей из;
(1) водорода, (2) галогена, (3) (C1-C10)алкила, (4) (C3-C10)циклоалкила и (5) (C1-C10)галогеналкила; или RA и RB могут образовывать оксогруппу (=O); или RA и RB могут образовывать 3-8-членное кольцо, которое может содержать один или несколько гетероатомов, независимо выбранных из кислорода, серы и азота; и указанное кольцо необязательно замещено 1-6 заместителями, независимо выбранными из (1) водорода, (2) галогена, (3) гидрокси, (4) (C1-C10)алкила, (5) (C3-C10)циклоалкила, (6) (C1-C10)галогеналкила, (7) (C1-C10)алкокси и (8) (C1-C10)галогеналкокси;
RC и RD независимо выбраны из группы, состоящей из (1) водорода, (2) галогена, (3) (C1-C10)алкила, (4) (C3-C10)циклоалкила и (5) (C1-C10)галогеналкила; или RC и RD могут образовывать 3-8-членное кольцо, которое может содержать один или несколько гетероатомов, независимо выбранных из кислорода, серы и азота; и указанное кольцо необязательно замещено 1-6 заместителями, независимо выбранными из (1) водорода, (2) галогена, (3) гидрокси, (4) (C1-C10)алкила, (5) (C3-C10)циклоалкила, (6) (C1-C10)галогеналкила, (7) (C1-C10)алкокси и (8) (C1-C10)галогеналкокси;
R1 независимо выбран из группы, состоящей из (1) водорода, (2) галогена, (3) амино, (4) циано, (5) гидроксила, (6) (C1-C10)алкила, (7) (C3-C10)циклоалкила, (8) (C1-C10)галогеналкила, (9) (C1-C10)алкокси и (10) (C1-C10)галогеналкокси; два R1 на одном и том же атоме углерода или на разных атомах углерода могут образовывать 3-8-членное кольцо, которое может содержать атом, выбранный из кислорода, серы и азота; и указанное кольцо необязательно замещено 1-6 заместителями, независимо выбранными из (1) водорода, (2) галогена, (3) гидрокси, (4) (C1-C10)алкила, (5) (C3-C10)циклоалкила, (6) (C1-C10)галогеналкила, (7) (C1-C10)алкокси и (8) (C1-C10)галогеналкокси;
R2 независимо выбран из группы, состоящей из (1) водорода, (2) галогена, (3) амино, (4) -NH(C1-C6)алкила, (5) -N[(C1-C6)алкил]2, в котором алкилы являются одинаковыми или разными, (6) циано, (7) гидроксила, (8) нитро, (9) (C1-C6)алкилтио, (10) (C1-C10)алкила, (11) (C3-C10)циклоалкила, (12) (C1-C10)алкокси, (13) (C1-C10)галогеналкила и (14) (C1-C10)галогеналкокси;
R3 независимо выбран из группы, состоящей из (1) водорода, (2) галогена, (3) циано, (4) нитро, (5) гидроксила, (6) (C1-C6)алкилтио, (7) (C1-C6)алкилсульфинила, (8) (C1-C6)алкилсульфонила, (9) -NR5R6, (10) -C(=O)NR5R6, (11) три(C1-C6)алкилсилила, (12) (C1-C10)алкила, (13) (C3-C10)циклоалкила, (14) (C1-C6)алкокси(C0-C6)алкила, (15) (C3-C10)циклоалкокси, (16) -C(=O)(C1-C6)алкила, (17) -C(=O)O(C1-C6)алкила и (18) -C(=O)ОH; причем указанный (C1-C10)алкил, (C3-C10)циклоалкил, (C1-C6)алкокси(C0-C6)алкил и (C3-C10)циклоалкокси необязательно замещены 1-6 заместителями, независимо выбранными из (1) водорода, (2) галогена, (3) гидроксила, (4) циано, (5) (C3-C10)циклоалкила, (6) (C1-C10)галогеналкила, (7) (C1-C10)алкокси, (8) (C1-C10)галогеналкокси и (9) -NR6R5;
причем R5 и R6, вместе с атомом азота, к которому они присоединены, могут образовывать 3-10-членное кольцо, которое может содержать атом, выбранный из кислорода, серы и азота; и указанное кольцо необязательно замещено 1-6 заместителями, независимо выбранными из (1) водорода, (2) галогена, (3) гидроксила, (4) (C1-C10)алкила, (5) (C3-C10)циклоалкила, (6) (C1-C10)галогеналкила, (7) (C1-C10)алкокси и (8) (C1-C10)галогеналкокси;
R4, R5 и R6 независимо выбраны из группы, состоящей из (1) водорода, (2) (C1-C10)алкила, (3) (C3-C10)циклоалкила, (4) (C1-C10)галогеналкила, (5) гидроксил(C1-C10)алкила, (6) (C1-C10)алкокси(C1-C10)алкила, (7) H2N-(C1-C10)алкила, (8) [(C1-C10)алкил]NH-(C1-C10)алкила, (9) [(C1-C10)алкил]2N-(C1-C10)алкила, (10) (C1-C10)алкилкарбонила и (11) (C1-C10)алкилсульфонила;
p=1, 2, 3 или 4;
q=1, 2, 3 или 4; когда q составляет два или больше, чем два, R1 являются одинаковыми или разными,
r=1, 2, 3 или 4; когда r сосотавляет два или больше, чем два, R2 являются одинаковыми или разными,
s=1, 2, 3, 4, 5, 6 или 7; когда s составляет два или больше, чем два, R3 являются одинаковыми или разными,
t=1, 2 или 3; когда t составляет два или больше, чем два, RC и RD являются одинаковыми или разными,
или его фармацевтически приемлемая соль или пролекарство.
2. Соединение по п.1, в котором
R1 независимо выбран из группы, состоящей из (2) галогена, (3) амино, (4) циано, (5) гидроксила, (8) (C1-C10)галогеналкила, (9) (C1-C10)алкокси и (10) (C1-C10)галогеналкокси; два R1 на одном и том же атоме углерода или на разных атомах углерода могут образовывать 3-8-членное кольцо, которое может содержать атом, выбранный из кислорода, серы и азота; и указанное кольцо необязательно замещено 1-6 заместителями, независимо выбранными из (1) водорода, (2) галогена, (3) гидрокси, (4) (C1-C10)алкила, (5) (C3-C10)циклоалкила, (6) (C1-C10)галогеналкила, (7) (C1-C10)алкокси и (8) (C1-C10)галогеналкокси.
3. Соединение по п.1, в котором
R1 независимо выбран из группы, состоящей из (2) галогена, (3) амино, (4) циано, (5) гидроксила, (8) (C1-C10)галогеналкила, (9) (C1-C10)алкокси и (10) (C1-C10)галогеналкокси.
4. Соединение по п.1, в котором
R1 независимо обозначает (2) галоген.
5. Соединение по любому из пп. 1-4, в котором
A обозначает 6-членный арил или 5-6-членный гетероарил
или его фармацевтически приемлемая соль или пролекарство.
6. Соединение по любому из пп. 1-5, в котором
A независимо выбран из группы, состоящей из бензола, пиридина, пиридазина, пиразина, пиримидина, триазина, тиофена, фурана, пиррола, имидазола, пиразола, тиазола, изотиазола, оксазола, изоксазола и триазола.
или его фармацевтически приемлемая соль или пролекарство.
7. Соединение, выбранное из группы, состоящей из следующих соединений:
3-(2-(2,5-диметил-1-(5-метилизоксазол-3-ил)-1H-пиррол-3-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(2,5-диметил-1-фенил-1H-имидазол-4-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
6-(4-(2-(2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)пиколинонитрил;
3-(2-(1-(3-хлорфенил)-2,5-диметил-1H-имидазол-4-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(1-(3-фторфенил)-2,5-диметил-1H-имидазол-4-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(1,4-диметил-5-фенил-1H-пиразол-3-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(6-метилпиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
6-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)пиколинонитрил;
8,8-дифтор-3-(2-(2ʹ-(гидроксиметил)-[1,1ʹ-бифенил]-4-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(3-метилпиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(2,5-диметил-1-фенил-1H-имидазол-4-ил)-2-оксоэтил)-8,8-дифтор-1-окса-3-азаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(2-(гидроксиметил)пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(4-(гидроксиметил)пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(2,5-диметил-1-(5-метилизоксазол-3-ил)-1H-пиррол-3-ил)-2-оксоэтил)-8,8-дифтор-1-окса-3-азаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(2-(гидроксиметил)фенил)-4-метилтиофен-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(3-(гидроксиметил)пиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(1,4-диметил-5-фенил-1H-пиразол-3-ил)-2-оксоэтил)-8,8-дифтор-1-окса-3-азаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(4-метилпиридазин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)пиразин-2-карбонитрил;
3-(2-(1,4-диметил-5-фенил-1H-пиррол-2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(3-(гидроксиметил)пиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(6-(метил(пиридин-2-ил)амино)пиридин-3-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)пиколинонитрил;
8,8-дифтор-3-(2-оксо-2-(4-(хинолин-8-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-индол-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(хинолин-2-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(изохинолин-8-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(изохинолин-1-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(фуро[3,2-c]пиридин-4-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(6-(метил(пиридин-2-ил)амино)пиридин-3-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(6-(метил(фенил)амино)пиридин-3-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(3-фторпиридин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)изоникотинонитрил;
8,8-дифтор-3-(2-(4-(2-метоксипиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(4-метоксипиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(2-оксоиндолин-4-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(7H-пирроло[2,3-d]пиримидин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-пирроло[3,2-c]пиридин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-пирроло[2,3-b]пиридин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(3-хлорпиридин-2-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(2-метил-1H-бензо[d]имидазол-1-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-индазол-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(6-(1H-индазол-4-ил)пиридин-3-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-бензо[d]имидазол-1-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(5-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-1,3-диметил-1H-пиррол-2-ил)бензонитрил;
3-(2-(4-(1H-пирроло[2,3-c]пиридин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(3-фтор-4-(хинолин-8-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(5-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-1-метил-1H-пиррол-2-ил)бензонитрил;
3-(5-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-3-метилтиофен-2-ил)бензонитрил;
8,8-дифтор-3-(2-(4-(2-(2-гидроксиэтокси)пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(3-фторфенил)-1,4-диметил-1H-пиррол-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(5-(3-хлорфенил)-1,4-диметил-1H-пиррол-2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(5-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-1,3-диметил-1H-пиррол-2-ил)бензамид;
8,8-дифтор-3-(2-(5-(2-фторфенил)-1,4-диметил-1H-пиррол-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-пиразолo[3,4-b]пиридин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-пиразолo[4,3-c]пиридин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-индазол-1-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(3-фторфенил)-1-метил-1H-имидазол-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(2-метил-3H-имидазо-[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(пиридин-2-илокси)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(5-(3,5-дифторфенил)-1,4-диметил-1H-пиррол-2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(2ʹ-метил-[3,3ʹ-бипиридин]-6-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(1H-пиразолo[3,4-d]пиримидин-4-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(6-(1H-пирроло[2,3-c]пиридин-4-ил)пиридин-3-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(3-(2-гидроксиэтокси)пиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(фталазин-1-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(3H-имидазо[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-4-метилтиазол-5-ил)бензонитрил;
3-(2-(1,4-диметил-5-фенил-1H-имидазол 2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(3-фторфенил)-1,4-диметил-1H-имидазол-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-1,4-диметил-1H-имидазол-5-ил)бензонитрил;
8,8-дифтор-3-(2-(5-(изохинолин-8-ил)-1,4-диметил-1H-имидазол-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(2-(гидроксиметил)фенил)-1,4-диметил-1H-имидазол-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(2-(гидроксиметил)-1H-бензо[d]имидазол-1-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(3-фторфенил)-1,4-диметил-1H-пиррол-3-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-1,3-диметил-1H-пиррол-2-ил)бензонитрил;
3-(2-(5-(1H-бензо[d]имидазол-1-ил)пиразин-2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(2,7-нафтиридин-1-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(2-оксо-2,3-дигидро-1H-бензо[d]имидазол-1-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(2-(гидроксиметил)фенил)пиразин-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(4-метоксипиридин-3-ил)пиразин-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(5-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-2,4-диметилтиофен-3-ил)бензамид;
3-(2-(5-(3,5-дифторфенил)-1,4-диметил-1H-имидазол-2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(пиридазин-3-илокси)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(2-оксо-1H-имидазо[4,5-b]пиридин-3(2H)-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(5-(3,5-дифторфенил)-4-метилтиазол-2-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
4ʹ-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-2ʹ-метокси-[1,1ʹ-бифенил]-2-карбонитрил;
2-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенокси)никотинонитрил;
3-(2-(4-((3-хлорпиридин-2-ил)окси)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(3-(гидроксиметил)пиридин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(2ʹ-(аминометил)-[1,1ʹ-бифенил]-4-ил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(6-(хинолин-8-ил)пиридин-3-ил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(2-метилпиридин-3-ил)пиразин-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(2,7-нафтиридин-1-ил)фенил)-2-оксоэтил)-8,8-дифтор-1-окса-3-азаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)-2-метил-3H-имидазо[4,5-b]пиридин-5-карбонитрил;
8,8-дифтор-3-(2-оксо-2-(4-(2-оксобензо[d]оксазол-3(2H)-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(2,5-диметил-3H-имидазо-[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(5-(2-метил-1H-бензо[d]имидазол-1-ил)пиразин-2-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(2-метокси-5-метил-3H-имидазо-[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(5-метил-2-(трифторметил)-3H-имидазо[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(2-(4-(2-(дифторметил)-5-метил-3H-имидазо[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(5-метил-2-оксо-1H-имидазо[4,5-b]пиридин-3(2H)-ил)фенил)-2-оксоэтил)1,3-диазаспиро[4.5]декан-2,4-дион;
6-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенокси)пиколинонитрил;
8,8-дифтор-3-(2-(4-(5-метил-3H-имидазо-[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(3-метоксипиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-3-фторфенил)пиразин-2-карбонитрил;
8,8-дифтор-3-(2-(4-(имидазо[1,2-b]пиридазин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(2ʹ-(2-гидроксиэтил)-[1,1ʹ-бифенил]-4-ил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
2-(4ʹ-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)-[1,1ʹ-бифенил]-2-ил)ацетонитрил;
3-(2-(4-(1H-имидазо[4,5-b]пиразин-1-ил)фенил)-2-оксоэтил)-8,8-дифтор-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(4-(4-метилпиридазин-3-ил)фенил)-2-оксоэтил)-1-окса-3-азаспиро[4.5]декан-2,4-дион;
3-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенокси)пиридазин-4-карбонитрил;
8,8-дифтор-3-(2-(4-(2-(гидроксиметил)-5-метил-3H-имидазо[4,5-b]пиридин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-оксо-2-(4-(пиразолo[1,5-a]пиримидин-3-ил)фенил)этил)-1,3-диазаспиро[4.5]декан-2,4-дион;
4-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)никотинонитрил;
8,8-дифтор-3-(2-(2-фтор-4-(4-метилпиридазин-3-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион;
8,8-дифтор-3-(2-(2-фтор-4-(3-(гидроксиметил)пиразин-2-ил)фенил)-2-оксоэтил)-1,3-диазаспиро[4.5]декан-2,4-дион; и
2-(4-(2-(8,8-дифтор-2,4-диоксо-1,3-диазаспиро[4.5]декан-3-ил)ацетил)фенил)никотинонитрил
или его фармацевтически приемлемая соль или пролекарство.
8. Применение соединения по любому из пп. 1-7 или его фармацевтически приемлемой соли или пролекарства для получения лекарственного средства для лечения состояния или нарушения, опосредуемого антагонистической активностью по отношению к рецептору TRPM8.
9. Применение по п.8, в котором состояние или нарушение представляет собой одно или более воспалительных, болевых и урологических заболеваний или нарушений, включая хроническую боль; нейропатическую боль, включая холодовую аллодинию и диабетическую невропатию; послеоперационную боль; остеоартрит; ревматоидную подагрическую боль; боль при раке; невралгию; невропатии; повышенную чувствительность к боли; гиперчувствительность дентина; повреждение нерва; мигрень; кластерные и тензионные головные боли; ишемию; синдром раздраженной толстой кишки; синдром Рейно; нейродегенерацию; фибромиалгию; инсульт; зуд; психические расстройства, включая тревогу и депрессию; воспалительные заболевания, включая астму, хроническое обструктивное заболевание легких, заболевание дыхательных путей, включая COPD, легочную гипертензию; тревогу, включая другие обусловленные стрессом нарушения; и урологические заболевания или нарушения, включая гиперактивность детрузора или гиперактивный мочевой пузырь, недержание мочи, нейрогенную гиперактивность детрузора или гиперфлексию детрузора, идиопатическую гиперактивность детрузора или нестабильность детрузора, доброкачественную гипертрофию предстательной железы и симптомы нижних мочевыводящих путей; и их комбинации.
10. Способ лечения состояния или нарушения, опосредуемого антагонистической активностью по отношению к рецептору TRPM8, у млекопитающего, включая человека, который включает введение млекопитающему, нуждающемуся в таком лечении, терапевтически эффективного количества соединения по любому из пп. 1-7 или его фармацевтически приемлемой соли или пролекарства.
11. Способ по п.10, в котором состояние или нарушение представляет собой одно или более воспалительных, болевых и урологических заболеваний или нарушений, включая хроническую боль; нейропатическую боль, включая холодовую аллодинию и диабетическую невропатию; послеоперационную боль; остеоартрит; ревматоидную подагрическую боль; боль при раке; невралгию; невропатии; повышенную чувствительность к боли; гиперчувствительность дентина; повреждение нерва; мигрень; кластерные и тензионные головные боли; ишемию; синдром раздраженной толстой кишки; синдром Рейно; нейродегенерацию; фибромиалгию; инсульт; зуд; психические расстройства, включая тревогу и депрессию; воспалительные заболевания, включая астму, хроническое обструктивное заболевание легких, заболевание дыхательных путей, включая COPD, легочную гипертензию; тревогу, включая другие обусловленные стрессом нарушения; и урологические заболевания или нарушения, включая гиперактивность детрузора или гиперактивный мочевой пузырь, недержание мочи, нейрогенную гиперактивность детрузора или гиперфлексию детрузора, идиопатическую гиперактивность детрузора или нестабильность детрузора, доброкачественную гипертрофию предстательной железы и симптомы нижних мочевыводящих путей; и их комбинации.
12. Фармацевтическая композиция, включающая соединение или его фармацевтически приемлемую соль или пролекарство по любому из пп. 1-7 и фармацевтически приемлемый носитель.
13. Фармацевтическая композиция по п.12, дополнительно включающая другое фармакологически активное средство.
14. Соединение по любому из пп. 1-7 или его фармацевтически приемлемая соль или пролекарство для применения в лечении состояния или нарушения, опосредуемого антагонистической активностью по отношению к рецептору TRPM8.
15. Способ получения фармацевтической композиции, включающий смешивание соединения по любому из пп. 1-7, или его фармацевтически приемлемой соли или пролекарства и фармацевтически приемлемого носителя или эксципиента.
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CA2940621A1 (en) | 2015-09-17 |
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KR102425400B1 (ko) | 2022-07-26 |
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EP3116858A4 (en) | 2017-11-22 |
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ES2850999T3 (es) | 2021-09-02 |
CN106103416B (zh) | 2021-03-02 |
EP3116858A1 (en) | 2017-01-18 |
JP6643545B2 (ja) | 2020-02-12 |
US20180339993A1 (en) | 2018-11-29 |
CA2940621C (en) | 2022-03-15 |
EP3116858B1 (en) | 2020-11-11 |
CN106103416A (zh) | 2016-11-09 |
TWI674257B (zh) | 2019-10-11 |
JP2017507981A (ja) | 2017-03-23 |
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