ES2297030T3 - Inhibidores del transportador glyt1 y usos de los mismos en el tratamiento de trastornos neurologicos y neuropsiquiatricos. - Google Patents
Inhibidores del transportador glyt1 y usos de los mismos en el tratamiento de trastornos neurologicos y neuropsiquiatricos. Download PDFInfo
- Publication number
- ES2297030T3 ES2297030T3 ES02788198T ES02788198T ES2297030T3 ES 2297030 T3 ES2297030 T3 ES 2297030T3 ES 02788198 T ES02788198 T ES 02788198T ES 02788198 T ES02788198 T ES 02788198T ES 2297030 T3 ES2297030 T3 ES 2297030T3
- Authority
- ES
- Spain
- Prior art keywords
- hydroxypropyl
- sulfonic
- group
- amide
- acid
- 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.)
- Expired - Lifetime
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- 238000011282 treatment Methods 0.000 title description 8
- 230000000926 neurological effect Effects 0.000 title description 6
- 239000003112 inhibitor Substances 0.000 title description 5
- 102100022622 Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Human genes 0.000 title 1
- 101000972916 Homo sapiens Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Proteins 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 227
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 46
- 125000003118 aryl group Chemical group 0.000 claims abstract description 37
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 33
- 150000003839 salts Chemical class 0.000 claims abstract description 33
- 101710083171 Sodium- and chloride-dependent glycine transporter 1 Proteins 0.000 claims abstract description 29
- 102100023145 Sodium- and chloride-dependent glycine transporter 1 Human genes 0.000 claims abstract description 24
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 23
- 125000004429 atom Chemical group 0.000 claims abstract description 21
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 20
- 150000001408 amides Chemical class 0.000 claims abstract description 19
- 230000014509 gene expression Effects 0.000 claims abstract description 18
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 17
- 230000001404 mediated effect Effects 0.000 claims abstract description 17
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 17
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 17
- 239000003814 drug Substances 0.000 claims abstract description 15
- 239000012453 solvate Substances 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- 150000002148 esters Chemical class 0.000 claims abstract description 13
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 13
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 11
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 10
- 125000002723 alicyclic group Chemical group 0.000 claims abstract description 8
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- 125000004450 alkenylene group Chemical group 0.000 claims abstract description 6
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 6
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 6
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
- 125000002950 monocyclic group Chemical group 0.000 claims abstract description 5
- 125000004419 alkynylene group Chemical group 0.000 claims abstract description 4
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 3
- 239000002253 acid Substances 0.000 claims description 162
- -1 R 21 Chemical compound 0.000 claims description 48
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 239000004480 active ingredient Substances 0.000 claims description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 9
- ZFFSMUXTPWBHPL-UHFFFAOYSA-N n-[3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C1C(C)CC(C)N1CC(O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 ZFFSMUXTPWBHPL-UHFFFAOYSA-N 0.000 claims description 9
- RDHIMFPEGQJIOF-AMDVSUOASA-N (2r)-1-amino-3-(2,4-dimethylpyrrolidin-1-yl)propan-2-ol Chemical compound CC1CC(C)N(C[C@H](O)CN)C1 RDHIMFPEGQJIOF-AMDVSUOASA-N 0.000 claims description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 239000003981 vehicle Substances 0.000 claims description 7
- USBVRCGGBVULIX-KXUCPTDWSA-N (2r)-1-amino-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]propan-2-ol Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@H](O)CN USBVRCGGBVULIX-KXUCPTDWSA-N 0.000 claims description 6
- HVJAYFJHJZUVBX-UHFFFAOYSA-N n-(2-hydroxy-3-piperidin-1-ylpropyl)naphthalene-1-sulfonamide Chemical compound C=1C=CC2=CC=CC=C2C=1S(=O)(=O)NCC(O)CN1CCCCC1 HVJAYFJHJZUVBX-UHFFFAOYSA-N 0.000 claims description 6
- WFUWCFSYNNOABU-UHFFFAOYSA-N n-(2-hydroxy-3-pyrrolidin-1-ylpropyl)naphthalene-1-sulfonamide Chemical compound C=1C=CC2=CC=CC=C2C=1S(=O)(=O)NCC(O)CN1CCCC1 WFUWCFSYNNOABU-UHFFFAOYSA-N 0.000 claims description 6
- IFCYHVCTAATODB-UHFFFAOYSA-N n-[2-hydroxy-3-(2-methylpiperidin-1-yl)propyl]naphthalene-1-sulfonamide Chemical compound CC1CCCCN1CC(O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 IFCYHVCTAATODB-UHFFFAOYSA-N 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 6
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 5
- 239000008194 pharmaceutical composition Substances 0.000 claims description 5
- BXJSMDGPHQSFCH-QWRGUYRKSA-N 2,5-dichloro-n-[(2r)-3-[(2s)-2-ethylpiperidin-1-yl]-2-hydroxypropyl]thiophene-3-sulfonamide Chemical compound CC[C@H]1CCCCN1C[C@@H](O)CNS(=O)(=O)C1=C(Cl)SC(Cl)=C1 BXJSMDGPHQSFCH-QWRGUYRKSA-N 0.000 claims description 4
- NOZBVIXZASBZPN-AXFHLTTASA-N 2,5-dichloro-n-[(2r)-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]thiophene-3-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=C(Cl)SC(Cl)=C1 NOZBVIXZASBZPN-AXFHLTTASA-N 0.000 claims description 4
- DKKQLDRUDXWMJW-AXFHLTTASA-N 4,5-dibromo-n-[(2r)-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]thiophene-2-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC(Br)=C(Br)S1 DKKQLDRUDXWMJW-AXFHLTTASA-N 0.000 claims description 4
- HZCJPUADBXZCCG-FVJLSDCUSA-N 4-(4-chlorophenyl)-n-[(2r)-3-[(2r,6s)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]benzenesulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=C(C=2C=CC(Cl)=CC=2)C=C1 HZCJPUADBXZCCG-FVJLSDCUSA-N 0.000 claims description 4
- SYVHMARMCXOYJF-AEJSXWLSSA-N 4-bromo-2,5-dichloro-n-[(2r)-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]thiophene-3-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=C(Cl)SC(Cl)=C1Br SYVHMARMCXOYJF-AEJSXWLSSA-N 0.000 claims description 4
- QAVCGAYWPBAKEH-JZXOWHBKSA-N 4-cyano-n-[(2r)-3-[(2r,6s)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=C(C#N)C2=CC=CC=C12 QAVCGAYWPBAKEH-JZXOWHBKSA-N 0.000 claims description 4
- MOLPUSJKGNBHBG-JZXOWHBKSA-N 5-acetyl-n-[(2r)-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=C(C(C)=O)C=CC=C12 MOLPUSJKGNBHBG-JZXOWHBKSA-N 0.000 claims description 4
- MXLFPBSFYGSAAX-XHSDSOJGSA-N 5-chloro-n-[(2r)-3-[(2r,6s)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=C(Cl)C=CC=C12 MXLFPBSFYGSAAX-XHSDSOJGSA-N 0.000 claims description 4
- ZDPSEEDEQGPNBA-HOTGVXAUSA-N 5-chloro-n-[(2r)-3-[(2s)-2-ethylpiperidin-1-yl]-2-hydroxypropyl]-3-methyl-1-benzothiophene-2-sulfonamide Chemical compound CC[C@H]1CCCCN1C[C@@H](O)CNS(=O)(=O)C1=C(C)C2=CC(Cl)=CC=C2S1 ZDPSEEDEQGPNBA-HOTGVXAUSA-N 0.000 claims description 4
- NHTGKASFJYAJGD-UXLLHSPISA-N 5-chloro-n-[(2r)-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]naphthalene-2-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=C(C(Cl)=CC=C2)C2=C1 NHTGKASFJYAJGD-UXLLHSPISA-N 0.000 claims description 4
- DHIRAKYHVJGYIG-JZXOWHBKSA-N 5-cyano-n-[(2r)-3-[(2r,6s)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=C(C#N)C=CC=C12 DHIRAKYHVJGYIG-JZXOWHBKSA-N 0.000 claims description 4
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 4
- PIOXVFZEJFFVDG-XRZIKPEHSA-N FC(C(=O)O)(F)F.C1(CC1)C1N(CCC1)C[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O Chemical compound FC(C(=O)O)(F)F.C1(CC1)C1N(CCC1)C[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O PIOXVFZEJFFVDG-XRZIKPEHSA-N 0.000 claims description 4
- MUNGBIGXVZYGJQ-FYZYNONXSA-N FC(C(=O)O)(F)F.C1N(CC2=CC=CC=C12)C[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O Chemical compound FC(C(=O)O)(F)F.C1N(CC2=CC=CC=C12)C[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O MUNGBIGXVZYGJQ-FYZYNONXSA-N 0.000 claims description 4
- PEXKCWFDHKYFGG-GCHSOCNYSA-N FC(C(=O)O)(F)F.CC1N(CC(C1)C)C[C@@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O Chemical compound FC(C(=O)O)(F)F.CC1N(CC(C1)C)C[C@@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O PEXKCWFDHKYFGG-GCHSOCNYSA-N 0.000 claims description 4
- HBSSSXSLDXYEHN-OIBOYYEISA-N FC(C(=O)O)(F)F.O[C@@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)CN1C(CCC1)C Chemical compound FC(C(=O)O)(F)F.O[C@@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)CN1C(CCC1)C HBSSSXSLDXYEHN-OIBOYYEISA-N 0.000 claims description 4
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- NJZYOONQSPVLIL-PKESZJFOSA-N FC(C(=O)O)(F)F.O[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)CN1CC(CCC1)C Chemical compound FC(C(=O)O)(F)F.O[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)CN1CC(CCC1)C NJZYOONQSPVLIL-PKESZJFOSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- ANRCWSRLFMGBJL-XRZIKPEHSA-N N-[(2R)-2-hydroxy-3-(2-propan-2-ylpyrrolidin-1-yl)propyl]naphthalene-1-sulfonamide 2,2,2-trifluoroacetic acid Chemical compound FC(C(=O)O)(F)F.O[C@@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)CN1C(CCC1)C(C)C ANRCWSRLFMGBJL-XRZIKPEHSA-N 0.000 claims description 4
- PEXKCWFDHKYFGG-MWVDPUPUSA-N N-[(2R)-3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide 2,2,2-trifluoroacetic acid Chemical compound FC(C(=O)O)(F)F.CC1N(CC(C1)C)C[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O PEXKCWFDHKYFGG-MWVDPUPUSA-N 0.000 claims description 4
- QEYMYCQAAWDSRZ-RTBKNWGFSA-N N-[(2R)-3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]oxadiazole-4-sulfonamide Chemical compound CC1N(CC(C1)C)C[C@H](CNS(=O)(=O)C=1N=NOC=1)O QEYMYCQAAWDSRZ-RTBKNWGFSA-N 0.000 claims description 4
- IPTZVPFJYRFMGA-MWVDPUPUSA-N N-[(2R)-3-(2,5-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide 2,2,2-trifluoroacetic acid Chemical compound FC(C(=O)O)(F)F.CC1N(C(CC1)C)C[C@H](CNS(=O)(=O)C1=CC=CC2=CC=CC=C12)O IPTZVPFJYRFMGA-MWVDPUPUSA-N 0.000 claims description 4
- 125000002619 bicyclic group Chemical group 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 4
- OKVHTTCXTTYJSU-GGYWPGCISA-N n-[(2r)-2-hydroxy-3-[2-(2-methylpropyl)pyrrolidin-1-yl]propyl]naphthalene-1-sulfonamide Chemical compound CC(C)CC1CCCN1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 OKVHTTCXTTYJSU-GGYWPGCISA-N 0.000 claims description 4
- HVJAYFJHJZUVBX-INIZCTEOSA-N n-[(2r)-2-hydroxy-3-piperidin-1-ylpropyl]naphthalene-1-sulfonamide Chemical compound C([C@H](CNS(=O)(=O)C=1C2=CC=CC=C2C=CC=1)O)N1CCCCC1 HVJAYFJHJZUVBX-INIZCTEOSA-N 0.000 claims description 4
- QHFYEUKZQFACOC-CTWPCTMYSA-N n-[(2r)-3-(1,2,3,4,4a,5,6,7-octahydroquinolin-2-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C1CC2CCCC=C2NC1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 QHFYEUKZQFACOC-CTWPCTMYSA-N 0.000 claims description 4
- DNUPKXDIBVGRIZ-MHJFOBGBSA-N n-[(2r)-3-(2,6-diethylpiperidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound CCC1CCCC(CC)N1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 DNUPKXDIBVGRIZ-MHJFOBGBSA-N 0.000 claims description 4
- ROFWNJGKUBGGMG-AIBWNMTMSA-N n-[(2r)-3-(2-cyclohexylpyrrolidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C([C@H](CNS(=O)(=O)C=1C2=CC=CC=C2C=CC=1)O)N1CCCC1C1CCCCC1 ROFWNJGKUBGGMG-AIBWNMTMSA-N 0.000 claims description 4
- HFCVJZGCTXOFHH-TVPLGVNVSA-N n-[(2r)-3-(5-ethyl-2-methylpiperidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C1C(CC)CCC(C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 HFCVJZGCTXOFHH-TVPLGVNVSA-N 0.000 claims description 4
- ZMYOKSLHZBPNLJ-UEXGIBASSA-N n-[(2r)-3-[(2r,6s)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]-4-phenylbenzenesulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=C(C=2C=CC=CC=2)C=C1 ZMYOKSLHZBPNLJ-UEXGIBASSA-N 0.000 claims description 4
- SAVQSKTYLCBBOS-FCEWJHQRSA-N n-[(2r)-3-[(2r,6s)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]naphthalene-2-sulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=C(C=CC=C2)C2=C1 SAVQSKTYLCBBOS-FCEWJHQRSA-N 0.000 claims description 4
- CKZQTZAWKMRKHE-IRXDYDNUSA-N n-[(2r)-3-[(2s)-2-ethylpiperidin-1-yl]-2-hydroxypropyl]-1-phenylmethanesulfonamide Chemical compound CC[C@H]1CCCCN1C[C@@H](O)CNS(=O)(=O)CC1=CC=CC=C1 CKZQTZAWKMRKHE-IRXDYDNUSA-N 0.000 claims description 4
- KJXJOPDXZUFNRL-IRXDYDNUSA-N n-[(2r)-3-[(2s)-2-ethylpiperidin-1-yl]-2-hydroxypropyl]quinoline-8-sulfonamide Chemical compound CC[C@H]1CCCCN1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=CC=CN=C12 KJXJOPDXZUFNRL-IRXDYDNUSA-N 0.000 claims description 4
- MLTRRNNKHYCISP-OTWHNJEPSA-N n-[(2r)-3-[(2s,6r)-2,6-dimethylpiperidin-1-yl]-2-hydroxypropyl]-4-phenoxybenzenesulfonamide Chemical compound C[C@H]1CCC[C@@H](C)N1C[C@@H](O)CNS(=O)(=O)C(C=C1)=CC=C1OC1=CC=CC=C1 MLTRRNNKHYCISP-OTWHNJEPSA-N 0.000 claims description 4
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- MOIAEDIZRBGTQJ-UHYCVJNDSA-N n-[(2r)-3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]-4-phenylbenzenesulfonamide Chemical compound C1C(C)CC(C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=C(C=2C=CC=CC=2)C=C1 MOIAEDIZRBGTQJ-UHYCVJNDSA-N 0.000 description 1
- RSENPFJXJWAMDD-DQPZFDDXSA-N n-[(2r)-3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]-4-propylbenzenesulfonamide Chemical compound C1=CC(CCC)=CC=C1S(=O)(=O)NC[C@H](O)CN1C(C)CC(C)C1 RSENPFJXJWAMDD-DQPZFDDXSA-N 0.000 description 1
- YDIDSPFFPWAOKC-HGMXIMQMSA-N n-[(2r)-3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]-5-fluoro-2-methylbenzenesulfonamide Chemical compound C1C(C)CC(C)N1C[C@@H](O)CNS(=O)(=O)C1=CC(F)=CC=C1C YDIDSPFFPWAOKC-HGMXIMQMSA-N 0.000 description 1
- ZFFSMUXTPWBHPL-DQPZFDDXSA-N n-[(2r)-3-(2,4-dimethylpyrrolidin-1-yl)-2-hydroxypropyl]naphthalene-1-sulfonamide Chemical compound C1C(C)CC(C)N1C[C@@H](O)CNS(=O)(=O)C1=CC=CC2=CC=CC=C12 ZFFSMUXTPWBHPL-DQPZFDDXSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QYNZYUUXSVZDJO-UHFFFAOYSA-N n-propylbutan-2-amine Chemical compound CCCNC(C)CC QYNZYUUXSVZDJO-UHFFFAOYSA-N 0.000 description 1
- 210000004897 n-terminal region Anatomy 0.000 description 1
- 230000006491 negative regulation of transport Effects 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
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- 230000004770 neurodegeneration Effects 0.000 description 1
- 208000015122 neurodegenerative disease Diseases 0.000 description 1
- 210000004498 neuroglial cell Anatomy 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- NXJCBFBQEVOTOW-UHFFFAOYSA-L palladium(2+);dihydroxide Chemical compound O[Pd]O NXJCBFBQEVOTOW-UHFFFAOYSA-L 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 210000001428 peripheral nervous system Anatomy 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068917 polyethylene glycols Drugs 0.000 description 1
- 230000001242 postsynaptic effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 230000003518 presynaptic effect Effects 0.000 description 1
- 210000000063 presynaptic terminal Anatomy 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
- 238000011321 prophylaxis Methods 0.000 description 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- XMIAFAKRAAMSGX-UHFFFAOYSA-N quinolin-5-amine Chemical compound C1=CC=C2C(N)=CC=CC2=N1 XMIAFAKRAAMSGX-UHFFFAOYSA-N 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009103 reabsorption Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- IDAVLHSFLYZTSV-UHFFFAOYSA-N s-quinolin-2-yl n,n-dimethylcarbamothioate Chemical compound C1=CC=CC2=NC(SC(=O)N(C)C)=CC=C21 IDAVLHSFLYZTSV-UHFFFAOYSA-N 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- RMBAVIFYHOYIFM-UHFFFAOYSA-M sodium methanethiolate Chemical compound [Na+].[S-]C RMBAVIFYHOYIFM-UHFFFAOYSA-M 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- LJRGBERXYNQPJI-UHFFFAOYSA-M sodium;3-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC(S([O-])(=O)=O)=C1 LJRGBERXYNQPJI-UHFFFAOYSA-M 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- DHHKPEUQJIEKOA-UHFFFAOYSA-N tert-butyl 2-[6-(nitromethyl)-6-bicyclo[3.2.0]hept-3-enyl]acetate Chemical compound C1C=CC2C(CC(=O)OC(C)(C)C)(C[N+]([O-])=O)CC21 DHHKPEUQJIEKOA-UHFFFAOYSA-N 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- ONCNIMLKGZSAJT-UHFFFAOYSA-N thieno[3,2-b]furan Chemical compound S1C=CC2=C1C=CO2 ONCNIMLKGZSAJT-UHFFFAOYSA-N 0.000 description 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- BSXLLFUSNQCWJP-UHFFFAOYSA-N thiophene-2-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=CS1 BSXLLFUSNQCWJP-UHFFFAOYSA-N 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 150000003852 triazoles Chemical class 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
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
-
- 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
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/06—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with radicals, containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
- C07D215/06—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms having only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/36—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/12—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C07D311/70—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with two hydrocarbon radicals attached in position 2 and elements other than carbon and hydrogen in position 6
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/34—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0130696 | 2001-12-21 | ||
| GBGB0130696.8A GB0130696D0 (en) | 2001-12-21 | 2001-12-21 | Chemical Compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2297030T3 true ES2297030T3 (es) | 2008-05-01 |
Family
ID=9928203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES02788198T Expired - Lifetime ES2297030T3 (es) | 2001-12-21 | 2002-12-19 | Inhibidores del transportador glyt1 y usos de los mismos en el tratamiento de trastornos neurologicos y neuropsiquiatricos. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20050267152A1 (enExample) |
| EP (1) | EP1455777B1 (enExample) |
| JP (1) | JP2005519048A (enExample) |
| AU (1) | AU2002352483A1 (enExample) |
| DE (1) | DE60223715T2 (enExample) |
| ES (1) | ES2297030T3 (enExample) |
| GB (1) | GB0130696D0 (enExample) |
| WO (1) | WO2003055478A1 (enExample) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0314479D0 (en) * | 2003-06-20 | 2003-07-23 | Glaxo Group Ltd | Compounds |
| GB0314478D0 (en) * | 2003-06-20 | 2003-07-23 | Glaxo Group Ltd | Compounds |
| UA86037C2 (ru) * | 2003-10-14 | 2009-03-25 | Пфайзер Продактс Инк. | Бициклические [3.1.0] производные, как ингибиторы переносчика глицина |
| GB0326840D0 (en) * | 2003-11-18 | 2003-12-24 | Glaxo Group Ltd | Compounds |
| GB0329362D0 (en) * | 2003-12-18 | 2004-01-21 | Glaxo Group Ltd | Compounds |
| GB0408777D0 (en) * | 2004-04-20 | 2004-05-26 | Glaxo Group Ltd | Compounds |
| GB0408772D0 (en) * | 2004-04-20 | 2004-05-26 | Glaxo Group Ltd | Compounds |
| RU2387644C2 (ru) * | 2004-09-30 | 2010-04-27 | Мерк Энд Ко., Инк. | Циклопропилпиперидиновые ингибиторы транспортера глицина |
| US20100216837A1 (en) * | 2004-12-23 | 2010-08-26 | Glaxo Group Limited | Glycine transport inhibitors |
| PE20061156A1 (es) * | 2004-12-23 | 2006-12-16 | Glaxo Group Ltd | Derivados de benzamida como agentes inhibidores del transportador de glicina |
| GB0428233D0 (en) * | 2004-12-23 | 2005-01-26 | Glaxo Group Ltd | Compounds |
| GB0428232D0 (en) * | 2004-12-23 | 2005-01-26 | Glaxo Group Ltd | Compounds |
| PE20061330A1 (es) * | 2004-12-23 | 2006-12-27 | Glaxo Group Ltd | Compuestos derivados de benzamida como inhibidores del transportador de glicina |
| JP2009503006A (ja) * | 2005-08-02 | 2009-01-29 | グラクソ グループ リミテッド | GlyT1トランスポーター阻害剤ならびに神経および神経精神障害の治療におけるその使用 |
| EP1994010A1 (en) | 2006-03-16 | 2008-11-26 | Glaxo Group Limited | Compounds which inhibit the glycine transporter and uses thereof |
| GB0612420D0 (en) * | 2006-06-22 | 2006-08-02 | Glaxo Group Ltd | Compounds |
| GB0612425D0 (en) * | 2006-06-22 | 2006-08-02 | Glaxo Group Ltd | Compounds |
| JP5619609B2 (ja) * | 2007-08-22 | 2014-11-05 | アボット ゲーエムベーハーウント カンパニー カーゲー | 4−ベンジルアミノキノリン類、これらを含む医薬組成物およびこれらの使用 |
| WO2009121872A2 (en) | 2008-04-01 | 2009-10-08 | Abbott Gmbh & Co. Kg | Tetrahydroisoquinolines, pharmaceutical compositions containing them, and their use in therapy |
| CA2726610C (en) * | 2008-06-05 | 2015-05-05 | Asahi Kasei Pharma Corporation | Sulfonamide compounds and use thereof |
| AR075442A1 (es) * | 2009-02-16 | 2011-03-30 | Abbott Gmbh & Co Kg | Derivados de aminotetralina, composiciones farmaceuticas que las contienen y sus usos en terapia |
| TW201038569A (en) | 2009-02-16 | 2010-11-01 | Abbott Gmbh & Co Kg | Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy |
| WO2011012622A1 (en) | 2009-07-30 | 2011-02-03 | Glaxo Group Limited | Benzoxazinone derivatives for the treatment of glytl mediated disorders |
| WO2011023753A1 (en) | 2009-08-27 | 2011-03-03 | Glaxo Group Limited | Benzoxazine derivatives as glycine transport inhibitors |
| CN101781244B (zh) * | 2010-02-10 | 2014-04-16 | 中国农业大学 | 化合物4-溴-n-(吡啶-2-甲基)萘-1-磺酰胺的制备方法 |
| US8883839B2 (en) | 2010-08-13 | 2014-11-11 | Abbott Laboratories | Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US8877794B2 (en) | 2010-08-13 | 2014-11-04 | Abbott Laboratories | Phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9051280B2 (en) | 2010-08-13 | 2015-06-09 | AbbVie Deutschland GmbH & Co. KG | Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9045459B2 (en) * | 2010-08-13 | 2015-06-02 | AbbVie Deutschland GmbH & Co. KG | Phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US8846743B2 (en) | 2010-08-13 | 2014-09-30 | Abbott Laboratories | Aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9309200B2 (en) | 2011-05-12 | 2016-04-12 | AbbVie Deutschland GmbH & Co. KG | Benzazepine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| JP2014521682A (ja) | 2011-08-05 | 2014-08-28 | アッヴィ・ドイチュラント・ゲー・エム・ベー・ハー・ウント・コー・カー・ゲー | アミノクロマン、アミノチオクロマンおよびアミノ−1,2,3,4−テトラヒドロキノリン誘導体、これらを含有する医薬組成物、ならびに治療におけるこれらの使用 |
| WO2013072520A1 (en) | 2011-11-18 | 2013-05-23 | AbbVie Deutschland GmbH & Co. KG | N-substituted aminobenzocycloheptene, aminotetraline, aminoindane and phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9365512B2 (en) | 2012-02-13 | 2016-06-14 | AbbVie Deutschland GmbH & Co. KG | Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9656955B2 (en) | 2013-03-15 | 2017-05-23 | Abbvie Inc. | Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9650334B2 (en) | 2013-03-15 | 2017-05-16 | Abbvie Inc. | Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| WO2015055771A1 (en) | 2013-10-17 | 2015-04-23 | AbbVie Deutschland GmbH & Co. KG | Aminotetraline and aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| EP3057960B1 (en) | 2013-10-17 | 2019-02-27 | AbbVie Deutschland GmbH & Co. KG | Aminochromane, aminothiochromane and amino-1,2,3,4-tetrahydroquinoline derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9550754B2 (en) | 2014-09-11 | 2017-01-24 | AbbVie Deutschland GmbH & Co. KG | 4,5-dihydropyrazole derivatives, pharmaceutical compositions containing them, and their use in therapy |
| EP3250209B1 (en) * | 2015-01-30 | 2023-09-13 | Lieber Institute For Brain Development | Comt inhibiting methods and compositions |
| EP3380471B8 (en) | 2015-11-25 | 2022-01-19 | Lieber Institute Inc. DBA Lieber Institute For Brain Development | Tetrahydro-8h-pyrido[1,2-a]pyrazine-8-ones as comt inhibitors for the treatment of neurodegenerative disorders |
| JP7792670B2 (ja) * | 2018-12-18 | 2025-12-26 | 株式会社デ・ウエスタン・セラピテクス研究所 | イソキノリンスルホニルクロリド酸付加塩及びその製造方法 |
| CA3184151A1 (en) * | 2020-06-29 | 2022-01-06 | Chris Murphy | Probenecid compounds for the treatment of inflammasome-mediated lung disease |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0076072B1 (en) * | 1981-09-24 | 1987-05-13 | BEECHAM - WUELFING GmbH & Co. KG | Sulphonamides |
| ZA9610745B (en) * | 1995-12-22 | 1997-06-24 | Warner Lambert Co | 4-Subsituted piperidine analogs and their use as subtype selective nmda receptor antagonists |
| CA2276373C (en) * | 1997-10-31 | 2010-01-12 | Suntory Limited | Arylpiperidinopropanol and arylpiperazinopropanol derivatives and pharmaceuticals containing the same |
| AU2030999A (en) * | 1998-01-09 | 1999-07-26 | Allelix Neuroscience, Inc. | Glycine transport inhibitors |
-
2001
- 2001-12-21 GB GBGB0130696.8A patent/GB0130696D0/en not_active Ceased
-
2002
- 2002-12-19 WO PCT/GB2002/005819 patent/WO2003055478A1/en not_active Ceased
- 2002-12-19 JP JP2003556056A patent/JP2005519048A/ja active Pending
- 2002-12-19 AU AU2002352483A patent/AU2002352483A1/en not_active Abandoned
- 2002-12-19 ES ES02788198T patent/ES2297030T3/es not_active Expired - Lifetime
- 2002-12-19 DE DE60223715T patent/DE60223715T2/de not_active Expired - Fee Related
- 2002-12-19 EP EP02788198A patent/EP1455777B1/en not_active Expired - Lifetime
- 2002-12-19 US US10/499,621 patent/US20050267152A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1455777B1 (en) | 2007-11-21 |
| EP1455777A1 (en) | 2004-09-15 |
| JP2005519048A (ja) | 2005-06-30 |
| DE60223715D1 (de) | 2008-01-03 |
| WO2003055478A1 (en) | 2003-07-10 |
| US20050267152A1 (en) | 2005-12-01 |
| AU2002352483A1 (en) | 2003-07-15 |
| GB0130696D0 (en) | 2002-02-06 |
| DE60223715T2 (de) | 2008-10-30 |
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