JP2012515209A5 - - Google Patents
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- Publication number
- JP2012515209A5 JP2012515209A5 JP2011546319A JP2011546319A JP2012515209A5 JP 2012515209 A5 JP2012515209 A5 JP 2012515209A5 JP 2011546319 A JP2011546319 A JP 2011546319A JP 2011546319 A JP2011546319 A JP 2011546319A JP 2012515209 A5 JP2012515209 A5 JP 2012515209A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrazin
- hexahydropyrrolo
- ylcarbonyl
- benzenesulfonamide
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 32
- 125000003118 aryl group Chemical group 0.000 claims 26
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 25
- 229910052739 hydrogen Inorganic materials 0.000 claims 22
- 239000001257 hydrogen Substances 0.000 claims 22
- 125000000217 alkyl group Chemical group 0.000 claims 18
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- -1 2,3-difluorophenyl Chemical group 0.000 claims 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 14
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 12
- 125000003545 alkoxy group Chemical group 0.000 claims 11
- 125000001188 haloalkyl group Chemical group 0.000 claims 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 9
- 125000001424 substituent group Chemical group 0.000 claims 9
- 125000001072 heteroaryl group Chemical group 0.000 claims 6
- 208000002193 Pain Diseases 0.000 claims 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 5
- 125000003386 piperidinyl group Chemical group 0.000 claims 5
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 5
- 125000000579 2,2-diphenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])* 0.000 claims 4
- AGPIHNZOZNKRGT-CYBMUJFWSA-N 5-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-4-chloro-2-fluoro-n-(2-fluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC=C1NS(=O)(=O)C1=CC(C(=O)N2C[C@H]3CCCN3CC2)=C(Cl)C=C1F AGPIHNZOZNKRGT-CYBMUJFWSA-N 0.000 claims 4
- 125000003725 azepanyl group Chemical group 0.000 claims 4
- 125000002393 azetidinyl group Chemical group 0.000 claims 4
- 150000002431 hydrogen Chemical group 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 125000002757 morpholinyl group Chemical group 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 239000000651 prodrug Chemical class 0.000 claims 4
- 229940002612 prodrug Drugs 0.000 claims 4
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 4
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 2
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 2
- 208000020925 Bipolar disease Diseases 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 208000019695 Migraine disease Diseases 0.000 claims 2
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 206010027599 migraine Diseases 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- NTGHBMWKKZCQJX-UHFFFAOYSA-N 3-(1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine-2-carbonyl)-n-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound FC(F)(F)C1=CC=CC(NS(=O)(=O)C=2C=C(C=CC=2)C(=O)N2CC3CCCCN3CC2)=C1 NTGHBMWKKZCQJX-UHFFFAOYSA-N 0.000 claims 1
- YKRLUOZLOMRDJR-UHFFFAOYSA-N 3-(1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine-2-carbonyl)-n-[4-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound C1=CC(C(F)(F)F)=CC=C1NS(=O)(=O)C1=CC=CC(C(=O)N2CC3CCCCN3CC2)=C1 YKRLUOZLOMRDJR-UHFFFAOYSA-N 0.000 claims 1
- CQXJKNXBJWCGEY-OAHLLOKOSA-N 3-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-(2,6-difluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC(F)=C1NS(=O)(=O)C1=CC=CC(C(=O)N2C[C@H]3CCCN3CC2)=C1 CQXJKNXBJWCGEY-OAHLLOKOSA-N 0.000 claims 1
- KHIZNEYVKZPOBP-MRXNPFEDSA-N 3-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-(2-fluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC=C1NS(=O)(=O)C1=CC=CC(C(=O)N2C[C@H]3CCCN3CC2)=C1 KHIZNEYVKZPOBP-MRXNPFEDSA-N 0.000 claims 1
- PLLFHYFNEYOOHX-TZIWHRDSSA-N 3-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-[(1s)-2-hydroxy-1-phenylethyl]benzenesulfonamide Chemical compound C1([C@H](NS(=O)(=O)C=2C=C(C=CC=2)C(=O)N2C[C@H]3CCCN3CC2)CO)=CC=CC=C1 PLLFHYFNEYOOHX-TZIWHRDSSA-N 0.000 claims 1
- RYXLBQVNMNCNOZ-GOSISDBHSA-N 3-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-[4-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound C1=CC(C(F)(F)F)=CC=C1NS(=O)(=O)C1=CC=CC(C(=O)N2C[C@H]3CCCN3CC2)=C1 RYXLBQVNMNCNOZ-GOSISDBHSA-N 0.000 claims 1
- CQXJKNXBJWCGEY-HNNXBMFYSA-N 3-[(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-(2,6-difluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC(F)=C1NS(=O)(=O)C1=CC=CC(C(=O)N2C[C@@H]3CCCN3CC2)=C1 CQXJKNXBJWCGEY-HNNXBMFYSA-N 0.000 claims 1
- KHIZNEYVKZPOBP-INIZCTEOSA-N 3-[(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-(2-fluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC=C1NS(=O)(=O)C1=CC=CC(C(=O)N2C[C@@H]3CCCN3CC2)=C1 KHIZNEYVKZPOBP-INIZCTEOSA-N 0.000 claims 1
- YBOWDQUKLNJSSM-SFHVURJKSA-N 3-[(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-(3-fluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC(NS(=O)(=O)C=2C=C(C=CC=2)C(=O)N2C[C@@H]3CCCN3CC2)=C1 YBOWDQUKLNJSSM-SFHVURJKSA-N 0.000 claims 1
- KHNAPMIJMHYYJN-TZIWHRDSSA-N 4-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-n-[(1s)-2-hydroxy-1-phenylethyl]benzenesulfonamide Chemical compound C1([C@H](NS(=O)(=O)C=2C=CC(=CC=2)C(=O)N2C[C@H]3CCCN3CC2)CO)=CC=CC=C1 KHNAPMIJMHYYJN-TZIWHRDSSA-N 0.000 claims 1
- IDIMHHNGWGAZGB-CYBMUJFWSA-N 5-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-2,4-dichloro-n-(2-fluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC=C1NS(=O)(=O)C1=CC(C(=O)N2C[C@H]3CCCN3CC2)=C(Cl)C=C1Cl IDIMHHNGWGAZGB-CYBMUJFWSA-N 0.000 claims 1
- AGPIHNZOZNKRGT-ZDUSSCGKSA-N 5-[(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-4-chloro-2-fluoro-n-(2-fluorophenyl)benzenesulfonamide Chemical compound FC1=CC=CC=C1NS(=O)(=O)C1=CC(C(=O)N2C[C@@H]3CCCN3CC2)=C(Cl)C=C1F AGPIHNZOZNKRGT-ZDUSSCGKSA-N 0.000 claims 1
- 206010065040 AIDS dementia complex Diseases 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 206010002388 Angina unstable Diseases 0.000 claims 1
- 208000019901 Anxiety disease Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000008035 Back Pain Diseases 0.000 claims 1
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims 1
- 206010058019 Cancer Pain Diseases 0.000 claims 1
- 208000024172 Cardiovascular disease Diseases 0.000 claims 1
- 208000000094 Chronic Pain Diseases 0.000 claims 1
- 206010012289 Dementia Diseases 0.000 claims 1
- 206010012434 Dermatitis allergic Diseases 0.000 claims 1
- 208000001640 Fibromyalgia Diseases 0.000 claims 1
- 206010019196 Head injury Diseases 0.000 claims 1
- 206010019233 Headaches Diseases 0.000 claims 1
- 206010019280 Heart failures Diseases 0.000 claims 1
- 208000004454 Hyperalgesia Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 206010020853 Hypertonic bladder Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 1
- 206010065390 Inflammatory pain Diseases 0.000 claims 1
- 208000005615 Interstitial Cystitis Diseases 0.000 claims 1
- 208000008930 Low Back Pain Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000009722 Overactive Urinary Bladder Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims 1
- 208000003251 Pruritus Diseases 0.000 claims 1
- 208000028017 Psychotic disease Diseases 0.000 claims 1
- 208000008765 Sciatica Diseases 0.000 claims 1
- 201000001880 Sexual dysfunction Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 208000007814 Unstable Angina Diseases 0.000 claims 1
- 208000026723 Urinary tract disease Diseases 0.000 claims 1
- FZLDXPOFLGONMF-LJQANCHMSA-N [(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[2-chloro-4-fluoro-5-[4-(4-fluorophenyl)piperazin-1-yl]sulfonylphenyl]methanone Chemical compound C1=CC(F)=CC=C1N1CCN(S(=O)(=O)C=2C(=CC(Cl)=C(C(=O)N3C[C@H]4CCCN4CC3)C=2)F)CC1 FZLDXPOFLGONMF-LJQANCHMSA-N 0.000 claims 1
- GAGSUTMMGKVUCP-MRXNPFEDSA-N [(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[2-chloro-5-(2,3-dihydroindol-1-ylsulfonyl)-4-fluorophenyl]methanone Chemical compound C1CN2CCC[C@@H]2CN1C(=O)C1=C(Cl)C=C(F)C(S(=O)(=O)N2C3=CC=CC=C3CC2)=C1 GAGSUTMMGKVUCP-MRXNPFEDSA-N 0.000 claims 1
- HRCAYCQDIMSMJS-MUUNZHRXSA-N [(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[3-(4-benzhydrylpiperazin-1-yl)sulfonylphenyl]methanone Chemical compound C([C@H]1CCCN1CC1)N1C(=O)C(C=1)=CC=CC=1S(=O)(=O)N(CC1)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 HRCAYCQDIMSMJS-MUUNZHRXSA-N 0.000 claims 1
- ZDPSZHMSLVWWKX-MUUNZHRXSA-N [(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[3-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]sulfonylphenyl]methanone Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)N1CCN(S(=O)(=O)C=2C=C(C=CC=2)C(=O)N2C[C@H]3CCCN3CC2)CC1 ZDPSZHMSLVWWKX-MUUNZHRXSA-N 0.000 claims 1
- HRCAYCQDIMSMJS-NDEPHWFRSA-N [(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[3-(4-benzhydrylpiperazin-1-yl)sulfonylphenyl]methanone Chemical compound C([C@@H]1CCCN1CC1)N1C(=O)C(C=1)=CC=CC=1S(=O)(=O)N(CC1)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 HRCAYCQDIMSMJS-NDEPHWFRSA-N 0.000 claims 1
- GQMHURPKRZFOJV-QFIPXVFZSA-N [(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[3-[4-(4-fluorophenyl)piperazin-1-yl]sulfonylphenyl]methanone Chemical compound C1=CC(F)=CC=C1N1CCN(S(=O)(=O)C=2C=C(C=CC=2)C(=O)N2C[C@@H]3CCCN3CC2)CC1 GQMHURPKRZFOJV-QFIPXVFZSA-N 0.000 claims 1
- ZDPSZHMSLVWWKX-NDEPHWFRSA-N [(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]-[3-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]sulfonylphenyl]methanone Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)N1CCN(S(=O)(=O)C=2C=C(C=CC=2)C(=O)N2C[C@@H]3CCCN3CC2)CC1 ZDPSZHMSLVWWKX-NDEPHWFRSA-N 0.000 claims 1
- FMJDPDFOYAFJHW-MUUNZHRXSA-N [3-[[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]sulfonyl]phenyl]-(4-benzhydrylpiperazin-1-yl)methanone Chemical compound C=1C=CC(S(=O)(=O)N2C[C@H]3CCCN3CC2)=CC=1C(=O)N(CC1)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 FMJDPDFOYAFJHW-MUUNZHRXSA-N 0.000 claims 1
- OUYFGDJNIFQCCM-MUUNZHRXSA-N [3-[[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]sulfonyl]phenyl]-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]methanone Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)N1CCN(C(=O)C=2C=C(C=CC=2)S(=O)(=O)N2C[C@H]3CCCN3CC2)CC1 OUYFGDJNIFQCCM-MUUNZHRXSA-N 0.000 claims 1
- FMJDPDFOYAFJHW-NDEPHWFRSA-N [3-[[(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]sulfonyl]phenyl]-(4-benzhydrylpiperazin-1-yl)methanone Chemical compound C=1C=CC(S(=O)(=O)N2C[C@@H]3CCCN3CC2)=CC=1C(=O)N(CC1)CCN1C(C=1C=CC=CC=1)C1=CC=CC=C1 FMJDPDFOYAFJHW-NDEPHWFRSA-N 0.000 claims 1
- OUYFGDJNIFQCCM-NDEPHWFRSA-N [3-[[(8as)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl]sulfonyl]phenyl]-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]methanone Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)N1CCN(C(=O)C=2C=C(C=CC=2)S(=O)(=O)N2C[C@@H]3CCCN3CC2)CC1 OUYFGDJNIFQCCM-NDEPHWFRSA-N 0.000 claims 1
- 208000005298 acute pain Diseases 0.000 claims 1
- 206010053552 allodynia Diseases 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 230000036506 anxiety Effects 0.000 claims 1
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- 201000008937 atopic dermatitis Diseases 0.000 claims 1
- 208000010668 atopic eczema Diseases 0.000 claims 1
- 208000028683 bipolar I disease Diseases 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 210000003169 central nervous system Anatomy 0.000 claims 1
- 208000015114 central nervous system disease Diseases 0.000 claims 1
- 208000026106 cerebrovascular disease Diseases 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
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- 230000004054 inflammatory process Effects 0.000 claims 1
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- 238000000034 method Methods 0.000 claims 1
- PGTKRXNTBSUGKM-UHFFFAOYSA-N n-(4-fluorophenyl)-3-(4-piperidin-1-ylpiperidine-1-carbonyl)benzenesulfonamide Chemical compound C1=CC(F)=CC=C1NS(=O)(=O)C1=CC=CC(C(=O)N2CCC(CC2)N2CCCCC2)=C1 PGTKRXNTBSUGKM-UHFFFAOYSA-N 0.000 claims 1
- TYCVFQIHNMKHJV-UHFFFAOYSA-N n-(4-fluorophenyl)-3-(4-pyrrolidin-1-ylpiperidine-1-carbonyl)benzenesulfonamide Chemical compound C1=CC(F)=CC=C1NS(=O)(=O)C1=CC=CC(C(=O)N2CCC(CC2)N2CCCC2)=C1 TYCVFQIHNMKHJV-UHFFFAOYSA-N 0.000 claims 1
- FMHFQMSHZHILDG-OAQYLSRUSA-N n-[3-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]phenyl]-n-propan-2-yl-3-(trifluoromethyl)benzenesulfonamide Chemical compound C=1C=CC(C(=O)N2C[C@H]3CCCN3CC2)=CC=1N(C(C)C)S(=O)(=O)C1=CC=CC(C(F)(F)F)=C1 FMHFQMSHZHILDG-OAQYLSRUSA-N 0.000 claims 1
- WYKKYPQOAAYHTB-HSZRJFAPSA-N n-[4-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-2-chlorophenyl]-2,2-diphenylacetamide Chemical compound ClC1=CC(C(=O)N2C[C@H]3CCCN3CC2)=CC=C1NC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 WYKKYPQOAAYHTB-HSZRJFAPSA-N 0.000 claims 1
- BBRCLJMUOZNGJS-QGZVFWFLSA-N n-[4-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-2-chlorophenyl]-4-fluorobenzamide Chemical compound C1=CC(F)=CC=C1C(=O)NC1=CC=C(C(=O)N2C[C@H]3CCCN3CC2)C=C1Cl BBRCLJMUOZNGJS-QGZVFWFLSA-N 0.000 claims 1
- MHCUFMBGRRJYKY-OAQYLSRUSA-N n-[4-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-2-chlorophenyl]naphthalene-2-carboxamide Chemical compound C1CN2CCC[C@@H]2CN1C(=O)C1=CC=C(NC(=O)C=2C=C3C=CC=CC3=CC=2)C(Cl)=C1 MHCUFMBGRRJYKY-OAQYLSRUSA-N 0.000 claims 1
- CZWGPXLJPYDHGK-HSZRJFAPSA-N n-[4-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-2-methylphenyl]naphthalene-2-carboxamide Chemical compound C1CN2CCC[C@@H]2CN1C(=O)C1=CC=C(NC(=O)C=2C=C3C=CC=CC3=CC=2)C(C)=C1 CZWGPXLJPYDHGK-HSZRJFAPSA-N 0.000 claims 1
- RAGZMQXBGQELKC-HSZRJFAPSA-N n-[5-[(8ar)-3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazine-2-carbonyl]-2-chlorophenyl]-2,2-diphenylacetamide Chemical compound ClC1=CC=C(C(=O)N2C[C@H]3CCCN3CC2)C=C1NC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 RAGZMQXBGQELKC-HSZRJFAPSA-N 0.000 claims 1
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| CN104352492B (zh) | 2008-04-24 | 2017-12-05 | Msd K.K.公司 | 以芳基磺酰基衍生物作为有效成分的长链脂肪酸延长酶抑制剂 |
| TW201028421A (en) * | 2009-01-15 | 2010-08-01 | Abbott Lab | Novel benzenesulfonamides as calcium channel blockers |
| AU2012308243B2 (en) * | 2011-09-15 | 2017-09-14 | Taipei Medical University | Use of indolyl and indolinyl hydroxamates for treating heart failure of neuronal injury |
| UY34349A (es) | 2011-09-29 | 2013-04-05 | Abb Vie Inc | OCTAHIDROPIRROLO[1,2-a]PIRAZINA SULFONAMIDAS SUSTITUIDAS COMO BLOQUEADORES DE CANALES DE CALCIO |
| WO2013049164A1 (en) | 2011-09-29 | 2013-04-04 | Abbvie Inc. | SUBSTITUTED OCTAHYDROPYRROLO[1,2-a]PYRAZINES AS CALCIUM CHANNEL BLOCKERS |
| US20130178477A1 (en) * | 2012-01-05 | 2013-07-11 | Abbvie Inc. | Methods of treating diabetic neuropathy using benzenesulfonamides |
| AU2013359533A1 (en) * | 2012-12-12 | 2015-05-28 | Abbvie, Inc. | Diazepine derivatives useful as calcium channel blockers in the treatment of pain |
| RU2727516C2 (ru) | 2013-09-10 | 2020-07-22 | Борд Оф Риджентс Оф Дзе Юниверсити Оф Техас Систем | Терапевтические средства, нацеленные на укороченные белки аденоматозного полипоза толстого кишечника (арс) |
| WO2015051336A1 (en) | 2013-10-03 | 2015-04-09 | David Wise | Compositions and methods for treating pelvic pain and other conditions |
| US10082496B2 (en) | 2014-09-10 | 2018-09-25 | Board Of Regents Of The University Of Texas System | Targeting emopamil binding protein (EBP) with small molecules that induce an abnormal feedback response by lowering endogenous cholesterol biosynthesis |
| EP3364993B1 (en) | 2015-10-22 | 2022-11-09 | Cavion, Inc. | Methods for treating angelman syndrome |
| CN110545806A (zh) | 2017-02-15 | 2019-12-06 | 卡维昂公司 | 钙通道抑制剂 |
| EP3615521A4 (en) | 2017-04-26 | 2021-02-17 | Cavion, Inc. | METHODS FOR IMPROVING MEMORY AND COGNITION AND TREATING MEMORY AND COGNITIVE DISORDERS |
| AU2019207491A1 (en) | 2018-01-10 | 2020-07-30 | Cura Therapeutics, Llc | Pharmaceutical compositions comprising phenylsulfonamides, and their therapeutic applications |
| US11858910B2 (en) | 2018-08-24 | 2024-01-02 | Sunshine Lake Pharma Co., Ltd. | Pyridinylmethylenepiperidine derivatives and uses thereof |
| JP7480131B2 (ja) | 2018-10-03 | 2024-05-09 | カビオン・インコーポレイテッド | （ｒ）－２－（４－イソプロピルフェニル）－ｎ－（１－（５－（２，２，２－トリフルオロエトキシ）ピリジン－２－イル）エチル）アセトアミドを使用した本態性振戦の処置 |
| US20200131156A1 (en) * | 2018-10-30 | 2020-04-30 | H. Lundbeck A/S | ARYLSULFONYLPYROLECARBOXAMIDE DERIVATIVES AS Kv3 POTASSIUM CHANNEL ACTIVATORS |
| WO2021007478A1 (en) * | 2019-07-11 | 2021-01-14 | Cura Therapeutics, Llc | Sulfone compounds and pharmaceutical compositions thereof, and their therapeutic applications for the treatment of neurodegenerative diseases |
| WO2021007487A1 (en) | 2019-07-11 | 2021-01-14 | Praxis Precision Medicines, Inc. | Formulations of t-type calcium channel modulators and methods of use thereof |
| CN117229257B (zh) * | 2022-06-06 | 2026-01-30 | 中国药科大学 | 间氨磺酰苯甲酰胺类化合物及制法、药物组合物和应用 |
| WO2025255502A1 (en) | 2024-06-07 | 2025-12-11 | Cavion, Inc. | PYRIDYL AMIDE Cav3 CHANNEL MODULATORS |
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| ATE269848T1 (de) | 1999-04-07 | 2004-07-15 | Univ Virginia | Calciumkanalblocker als antikrebsmittel |
| TW200503994A (en) | 2003-01-24 | 2005-02-01 | Novartis Ag | Organic compounds |
| US7223754B2 (en) | 2003-03-10 | 2007-05-29 | Dynogen Pharmaceuticals, Inc. | Thiazolidinone, oxazolidinone, and imidazolone derivatives for treating lower urinary tract and related disorders |
| DE602004027171D1 (de) * | 2003-04-11 | 2010-06-24 | High Point Pharmaceuticals Llc | Verbindungen mit Aktivität an der 11Beta-Hydroxasteroiddehydrogenase |
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| WO2006105127A2 (en) * | 2005-03-31 | 2006-10-05 | Takeda San Diego, Inc. | Hydroxysteroid dehydrogenase inhibitors |
| WO2007052843A1 (ja) * | 2005-11-04 | 2007-05-10 | Takeda Pharmaceutical Company Limited | 複素環アミド化合物およびその用途 |
| EP2074105A4 (en) * | 2006-10-13 | 2010-10-06 | Neuromed Pharmaceuticals Ltd | CYCLOPROPYL-PIPERAZINE COMPOUNDS AS CALCIUM INHIBITORS |
| KR20100033981A (ko) * | 2007-06-03 | 2010-03-31 | 벤더르빌트 유니버시티 | 벤즈아미드 대사성 글루타민산염 수용체5 양성 알로스테릭 조절자 및 이의 제조 및 사용방법 |
| CN104352492B (zh) | 2008-04-24 | 2017-12-05 | Msd K.K.公司 | 以芳基磺酰基衍生物作为有效成分的长链脂肪酸延长酶抑制剂 |
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