CA2287255A1 - Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof - Google Patents
Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof Download PDFInfo
- Publication number
- CA2287255A1 CA2287255A1 CA002287255A CA2287255A CA2287255A1 CA 2287255 A1 CA2287255 A1 CA 2287255A1 CA 002287255 A CA002287255 A CA 002287255A CA 2287255 A CA2287255 A CA 2287255A CA 2287255 A1 CA2287255 A1 CA 2287255A1
- Authority
- CA
- Canada
- Prior art keywords
- semicarbazone
- benzaldehyde
- alkyl
- hydrogen
- aryl
- 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.)
- Abandoned
Links
- 125000000623 heterocyclic group Chemical group 0.000 title claims abstract description 45
- 150000007659 semicarbazones Chemical class 0.000 title claims abstract description 44
- 229940042396 direct acting antivirals thiosemicarbazones Drugs 0.000 title abstract description 13
- 150000003584 thiosemicarbazones Chemical class 0.000 title abstract description 12
- 125000002837 carbocyclic group Chemical group 0.000 title abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 87
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 78
- 239000001257 hydrogen Substances 0.000 claims abstract description 77
- 125000003118 aryl group Chemical group 0.000 claims abstract description 71
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 53
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 53
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 41
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 38
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 36
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 35
- 125000004103 aminoalkyl group Chemical group 0.000 claims abstract description 34
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 34
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 32
- 125000004181 carboxyalkyl group Chemical group 0.000 claims abstract description 31
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 30
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 26
- 229910052717 sulfur Chemical group 0.000 claims abstract description 25
- 150000003839 salts Chemical class 0.000 claims abstract description 23
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000001301 oxygen Substances 0.000 claims abstract description 18
- 208000002193 Pain Diseases 0.000 claims abstract description 15
- 229940002612 prodrug Drugs 0.000 claims abstract description 15
- 239000000651 prodrug Substances 0.000 claims abstract description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000011593 sulfur Chemical group 0.000 claims abstract description 11
- 208000028867 ischemia Diseases 0.000 claims abstract description 10
- 230000036407 pain Effects 0.000 claims abstract description 10
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims abstract description 5
- 208000030533 eye disease Diseases 0.000 claims abstract description 5
- 229930195712 glutamate Natural products 0.000 claims abstract description 5
- 231100000419 toxicity Toxicity 0.000 claims abstract description 5
- 230000001988 toxicity Effects 0.000 claims abstract description 5
- 230000000626 neurodegenerative effect Effects 0.000 claims abstract description 4
- 206010046543 Urinary incontinence Diseases 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 189
- -1 is defined as above Chemical compound 0.000 claims description 86
- 238000000034 method Methods 0.000 claims description 48
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 38
- YUPBWHURNLRZQL-UHFFFAOYSA-N 4-(4-fluorophenoxy)benzaldehyde Chemical compound C1=CC(F)=CC=C1OC1=CC=C(C=O)C=C1 YUPBWHURNLRZQL-UHFFFAOYSA-N 0.000 claims description 30
- 229910052757 nitrogen Inorganic materials 0.000 claims description 29
- 125000003545 alkoxy group Chemical group 0.000 claims description 26
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 24
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 22
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 21
- 229910052736 halogen Inorganic materials 0.000 claims description 20
- 150000002367 halogens Chemical group 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000001624 naphthyl group Chemical group 0.000 claims description 16
- MHUUDVZSPFRUSK-RQZCQDPDSA-N [(e)-[4-(4-fluorophenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(/C=N/NC(=O)N)=CC=C1OC1=CC=C(F)C=C1 MHUUDVZSPFRUSK-RQZCQDPDSA-N 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 12
- 125000004423 acyloxy group Chemical group 0.000 claims description 11
- 125000005843 halogen group Chemical group 0.000 claims description 11
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical group C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 10
- 102000018674 Sodium Channels Human genes 0.000 claims description 10
- 108010052164 Sodium Channels Proteins 0.000 claims description 10
- 125000005018 aryl alkenyl group Chemical group 0.000 claims description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- 125000005015 aryl alkynyl group Chemical group 0.000 claims description 10
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims description 10
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 10
- 125000005312 heteroarylalkynyl group Chemical group 0.000 claims description 10
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 125000003386 piperidinyl group Chemical group 0.000 claims description 10
- 241000124008 Mammalia Species 0.000 claims description 9
- CIRHAKPWVMBBTB-XFXZXTDPSA-N [(z)-1-phenylpropylideneamino]urea Chemical compound NC(=O)N/N=C(/CC)C1=CC=CC=C1 CIRHAKPWVMBBTB-XFXZXTDPSA-N 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 9
- 125000002541 furyl group Chemical group 0.000 claims description 9
- 125000001544 thienyl group Chemical group 0.000 claims description 9
- 206010010904 Convulsion Diseases 0.000 claims description 8
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 8
- 150000001356 alkyl thiols Chemical class 0.000 claims description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 8
- HTXDNWZCBJUCJB-UHFFFAOYSA-N [[4-(1,3-benzodioxol-5-yloxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(OCO2)C2=C1 HTXDNWZCBJUCJB-UHFFFAOYSA-N 0.000 claims description 7
- 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 description 7
- 208000035475 disorder Diseases 0.000 claims description 7
- 230000004770 neurodegeneration Effects 0.000 claims description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 7
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 7
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 7
- 150000003573 thiols Chemical class 0.000 claims description 7
- MICRFRUBLYAXDL-UHFFFAOYSA-N [(4-pyridin-4-yloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=NC=C1 MICRFRUBLYAXDL-UHFFFAOYSA-N 0.000 claims description 6
- CPXYGYOMIMOSCX-YRNVUSSQSA-N [(e)-1-phenylethylideneamino]urea Chemical compound NC(=O)N\N=C(/C)C1=CC=CC=C1 CPXYGYOMIMOSCX-YRNVUSSQSA-N 0.000 claims description 6
- FSNQPMMGABAVRP-UHFFFAOYSA-N [[4-(1-methylpiperidin-4-yl)oxyphenyl]methylideneamino]urea Chemical compound C1CN(C)CCC1OC1=CC=C(C=NNC(N)=O)C=C1 FSNQPMMGABAVRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 6
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 6
- 125000003107 substituted aryl group Chemical group 0.000 claims description 6
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims description 6
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 6
- 125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 claims description 5
- DPHLRUBNDYWFPP-UHFFFAOYSA-N 3-fluoro-4-(4-fluorophenoxy)benzaldehyde Chemical compound C1=CC(F)=CC=C1OC1=CC=C(C=O)C=C1F DPHLRUBNDYWFPP-UHFFFAOYSA-N 0.000 claims description 5
- DHARILAASAAGJJ-UHFFFAOYSA-N 4-benzylbenzaldehyde Chemical compound C1=CC(C=O)=CC=C1CC1=CC=CC=C1 DHARILAASAAGJJ-UHFFFAOYSA-N 0.000 claims description 5
- 208000000094 Chronic Pain Diseases 0.000 claims description 5
- IPDRSOSKLXRABX-UHFFFAOYSA-N [(4-cycloheptyloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1CCCCCC1 IPDRSOSKLXRABX-UHFFFAOYSA-N 0.000 claims description 5
- UMVYABDDIMYPPH-UHFFFAOYSA-N [(4-pyridin-2-yloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=CC=N1 UMVYABDDIMYPPH-UHFFFAOYSA-N 0.000 claims description 5
- WJHMQFYNUMSDIR-UHFFFAOYSA-N [(4-pyridin-3-yloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=CN=C1 WJHMQFYNUMSDIR-UHFFFAOYSA-N 0.000 claims description 5
- SVXNZSGCHPATRU-UHFFFAOYSA-N [(6-phenoxypyridin-3-yl)methylideneamino]urea Chemical compound N1=CC(C=NNC(=O)N)=CC=C1OC1=CC=CC=C1 SVXNZSGCHPATRU-UHFFFAOYSA-N 0.000 claims description 5
- XQXULNQXVBBKEB-UHFFFAOYSA-N [[3-fluoro-4-(4-fluorophenoxy)phenyl]methylideneamino]urea Chemical compound FC1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(F)C=C1 XQXULNQXVBBKEB-UHFFFAOYSA-N 0.000 claims description 5
- VYCHOERZTGRWHO-UHFFFAOYSA-N [[4-(4-chloro-2-fluorophenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(Cl)C=C1F VYCHOERZTGRWHO-UHFFFAOYSA-N 0.000 claims description 5
- CDMFRPPPCCUCRP-UHFFFAOYSA-N [[4-(4-nitrophenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C([N+]([O-])=O)C=C1 CDMFRPPPCCUCRP-UHFFFAOYSA-N 0.000 claims description 5
- YFQKNVGPUONCRB-UHFFFAOYSA-N [[4-(oxan-2-yloxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1OCCCC1 YFQKNVGPUONCRB-UHFFFAOYSA-N 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 125000004447 heteroarylalkenyl group Chemical group 0.000 claims description 5
- AACOYOGKHFDXQH-UHFFFAOYSA-N 4-(1,3-benzodioxol-5-yloxy)benzaldehyde Chemical compound C1=CC(C=O)=CC=C1OC1=CC=C(OCO2)C2=C1 AACOYOGKHFDXQH-UHFFFAOYSA-N 0.000 claims description 4
- BCZMLEPHGZNYCE-UHFFFAOYSA-N 4-(2,3-dihydro-1h-inden-5-yloxy)benzaldehyde Chemical compound C1=CC(C=O)=CC=C1OC1=CC=C(CCC2)C2=C1 BCZMLEPHGZNYCE-UHFFFAOYSA-N 0.000 claims description 4
- 208000020925 Bipolar disease Diseases 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- KWHJZTBFOMDTMX-UHFFFAOYSA-N [(4-quinolin-6-yloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(N=CC=C2)C2=C1 KWHJZTBFOMDTMX-UHFFFAOYSA-N 0.000 claims description 4
- RMNIZJBVMFHIGN-QGMBQPNBSA-N [(e)-[4-(3,4-difluorophenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(/C=N/NC(=O)N)=CC=C1OC1=CC=C(F)C(F)=C1 RMNIZJBVMFHIGN-QGMBQPNBSA-N 0.000 claims description 4
- RDSXMWPLZFRVOT-RQZCQDPDSA-N [(e)-[4-(4-chlorophenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(/C=N/NC(=O)N)=CC=C1OC1=CC=C(Cl)C=C1 RDSXMWPLZFRVOT-RQZCQDPDSA-N 0.000 claims description 4
- WTRJFWKBUPJRCB-UHFFFAOYSA-N [[4-(4-chloropyridin-2-yl)oxyphenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC(Cl)=CC=N1 WTRJFWKBUPJRCB-UHFFFAOYSA-N 0.000 claims description 4
- NTHMAJNESPANHH-UHFFFAOYSA-N [[4-(4-fluorophenoxy)cyclohexyl]methylideneamino]urea Chemical compound C1CC(C=NNC(=O)N)CCC1OC1=CC=C(F)C=C1 NTHMAJNESPANHH-UHFFFAOYSA-N 0.000 claims description 4
- JOMLNPAVOCOQIE-UHFFFAOYSA-N [[4-(4-fluorophenyl)sulfanylphenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1SC1=CC=C(F)C=C1 JOMLNPAVOCOQIE-UHFFFAOYSA-N 0.000 claims description 4
- UZHHXLRRUOVIDZ-UHFFFAOYSA-N [[4-[4-(trifluoromethyl)phenoxy]phenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 UZHHXLRRUOVIDZ-UHFFFAOYSA-N 0.000 claims description 4
- QCSQVVDDEIGVBC-UHFFFAOYSA-N [[6-(4-chlorophenoxy)pyridin-3-yl]methylideneamino]urea Chemical compound N1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(Cl)C=C1 QCSQVVDDEIGVBC-UHFFFAOYSA-N 0.000 claims description 4
- 208000028683 bipolar I disease Diseases 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000002757 morpholinyl group Chemical group 0.000 claims description 4
- 208000004296 neuralgia Diseases 0.000 claims description 4
- 208000021722 neuropathic pain Diseases 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 125000005493 quinolyl group Chemical group 0.000 claims description 4
- JHJMZCXLJXRCHK-UHFFFAOYSA-N 1,2,3,4,5-pentachloro-6-(3-chlorophenyl)benzene Chemical compound ClC1=CC=CC(C=2C(=C(Cl)C(Cl)=C(Cl)C=2Cl)Cl)=C1 JHJMZCXLJXRCHK-UHFFFAOYSA-N 0.000 claims description 3
- UDHNKKALYSDBQA-UHFFFAOYSA-N 4-(1,3-benzodioxol-5-yloxy)-3-fluorobenzaldehyde Chemical compound FC1=CC(C=O)=CC=C1OC1=CC=C(OCO2)C2=C1 UDHNKKALYSDBQA-UHFFFAOYSA-N 0.000 claims description 3
- OCHOSUFDGPHRJA-UHFFFAOYSA-N 4-(4-nitrophenoxy)benzaldehyde Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(C=O)C=C1 OCHOSUFDGPHRJA-UHFFFAOYSA-N 0.000 claims description 3
- RFPORHXEHBGCCJ-UHFFFAOYSA-N 4-[4-(trifluoromethyl)phenoxy]benzaldehyde Chemical compound C1=CC(C(F)(F)F)=CC=C1OC1=CC=C(C=O)C=C1 RFPORHXEHBGCCJ-UHFFFAOYSA-N 0.000 claims description 3
- COQHVRMZOSMXJQ-UHFFFAOYSA-N 4-benzhydryloxybenzaldehyde Chemical compound C1=CC(C=O)=CC=C1OC(C=1C=CC=CC=1)C1=CC=CC=C1 COQHVRMZOSMXJQ-UHFFFAOYSA-N 0.000 claims description 3
- BJDFSJXBFDJFTB-UHFFFAOYSA-N [(4-benzhydryloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC(C=1C=CC=CC=1)C1=CC=CC=C1 BJDFSJXBFDJFTB-UHFFFAOYSA-N 0.000 claims description 3
- QCRFCHXYIYEZCA-UHFFFAOYSA-N [(4-cyclohexyloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1CCCCC1 QCRFCHXYIYEZCA-UHFFFAOYSA-N 0.000 claims description 3
- GZGFWFKRWZLNPA-UHFFFAOYSA-N [(4-phenylsulfanylphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1SC1=CC=CC=C1 GZGFWFKRWZLNPA-UHFFFAOYSA-N 0.000 claims description 3
- NAPZIDNWXNYCCR-UHFFFAOYSA-N [(4-pyrimidin-2-yloxyphenyl)methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1=NC=CC=N1 NAPZIDNWXNYCCR-UHFFFAOYSA-N 0.000 claims description 3
- CBGLRILSDNCIFX-MHWRWJLKSA-N [(e)-(4-phenoxyphenyl)methylideneamino]urea Chemical compound C1=CC(/C=N/NC(=O)N)=CC=C1OC1=CC=CC=C1 CBGLRILSDNCIFX-MHWRWJLKSA-N 0.000 claims description 3
- SKSVDBVQOMQIQU-LICLKQGHSA-N [(e)-[4-(3-methylphenoxy)phenyl]methylideneamino]urea Chemical compound CC1=CC=CC(OC=2C=CC(\C=N\NC(N)=O)=CC=2)=C1 SKSVDBVQOMQIQU-LICLKQGHSA-N 0.000 claims description 3
- WFKAOJIZWYQQOA-RQZCQDPDSA-N [(e)-[4-(4-bromophenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(/C=N/NC(=O)N)=CC=C1OC1=CC=C(Br)C=C1 WFKAOJIZWYQQOA-RQZCQDPDSA-N 0.000 claims description 3
- HWJCWQZFNRZEFN-LICLKQGHSA-N [(e)-[4-(4-methoxyphenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(OC)=CC=C1OC1=CC=C(\C=N\NC(N)=O)C=C1 HWJCWQZFNRZEFN-LICLKQGHSA-N 0.000 claims description 3
- ACJTZJXCRJAKMZ-XDHOZWIPSA-N [(e)-[4-(4-propylphenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(CCC)=CC=C1OC1=CC=C(\C=N\NC(N)=O)C=C1 ACJTZJXCRJAKMZ-XDHOZWIPSA-N 0.000 claims description 3
- BHVVDWZBFAZXRD-UHFFFAOYSA-N [[2-(4-fluorophenoxy)pyridin-3-yl]methylideneamino]urea Chemical compound NC(=O)NN=CC1=CC=CN=C1OC1=CC=C(F)C=C1 BHVVDWZBFAZXRD-UHFFFAOYSA-N 0.000 claims description 3
- XWCJEYYRESWLGB-UHFFFAOYSA-N [[4-(4-butan-2-ylphenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C(C)CC)=CC=C1OC1=CC=C(C=NNC(N)=O)C=C1 XWCJEYYRESWLGB-UHFFFAOYSA-N 0.000 claims description 3
- KGCLQYJJYBYXOV-UHFFFAOYSA-N [[4-(4-chlorophenyl)sulfanylphenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1SC1=CC=C(Cl)C=C1 KGCLQYJJYBYXOV-UHFFFAOYSA-N 0.000 claims description 3
- SBZXKBVAQSBMJO-UHFFFAOYSA-N [[4-(4-tert-butylphenoxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1=CC=C(C=NNC(N)=O)C=C1 SBZXKBVAQSBMJO-UHFFFAOYSA-N 0.000 claims description 3
- 230000036461 convulsion Effects 0.000 claims description 3
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 3
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims description 2
- 230000006793 arrhythmia Effects 0.000 claims description 2
- 206010003119 arrhythmia Diseases 0.000 claims description 2
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 2
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 238000002690 local anesthesia Methods 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 4
- MALIONKMKPITBV-UHFFFAOYSA-N 2-(3-chloro-4-hydroxyphenyl)-n-[2-(4-sulfamoylphenyl)ethyl]acetamide Chemical compound C1=CC(S(=O)(=O)N)=CC=C1CCNC(=O)CC1=CC=C(O)C(Cl)=C1 MALIONKMKPITBV-UHFFFAOYSA-N 0.000 claims 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 2
- OYLADQWPEDUQEG-UHFFFAOYSA-N [(4-cyclohexyloxyphenyl)methylideneamino]urea [[4-(2,3-dihydro-1H-inden-5-yloxy)phenyl]methylideneamino]urea Chemical compound C1=CC(C=NNC(=O)N)=CC=C1OC1CCCCC1.C1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(CCC2)C2=C1 OYLADQWPEDUQEG-UHFFFAOYSA-N 0.000 claims 1
- AWQOXJLIZDMMGR-UHFFFAOYSA-N [[6-(4-fluorophenoxy)pyridin-3-yl]methylideneamino]urea Chemical compound N1=CC(C=NNC(=O)N)=CC=C1OC1=CC=C(F)C=C1 AWQOXJLIZDMMGR-UHFFFAOYSA-N 0.000 claims 1
- 239000001961 anticonvulsive agent Substances 0.000 abstract description 12
- 230000002265 prevention Effects 0.000 abstract description 9
- 230000003288 anthiarrhythmic effect Effects 0.000 abstract description 6
- 239000003416 antiarrhythmic agent Substances 0.000 abstract description 6
- 229940125681 anticonvulsant agent Drugs 0.000 abstract description 5
- 239000003589 local anesthetic agent Substances 0.000 abstract description 5
- 229960005015 local anesthetics Drugs 0.000 abstract description 5
- 230000003561 anti-manic effect Effects 0.000 abstract description 4
- 208000032131 Diabetic Neuropathies Diseases 0.000 abstract description 3
- 230000003961 neuronal insult Effects 0.000 abstract description 2
- 201000010901 lateral sclerosis Diseases 0.000 abstract 1
- 208000005264 motor neuron disease Diseases 0.000 abstract 1
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Classifications
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
- C07D213/643—2-Phenoxypyridines; Derivatives thereof
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- A61K31/175—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine having the group, >N—C(O)—N=N— or, e.g. carbonohydrazides, carbazones, semicarbazides, semicarbazones; Thioanalogues thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/06—Compounds containing any of the groups, e.g. semicarbazides
- C07C281/08—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones
- C07C281/12—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones the carbon atom being part of a ring other than a six-membered aromatic ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/06—Compounds containing any of the groups, e.g. semicarbazides
- C07C281/08—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones
- C07C281/14—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones the carbon atom being further bound to a carbon atom of a six-membered aromatic ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 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
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- C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D213/63—One oxygen atom
- C07D213/68—One oxygen atom attached in position 4
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- 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
- C07D215/12—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 substituted hydrocarbon radicals attached to ring carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members 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
- C07D309/10—Oxygen atoms
- C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
-
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- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
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- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
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- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring 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 atoms of the carbocyclic ring
-
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- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring 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 atoms of the carbocyclic ring
- C07D317/64—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
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| US6264997P | 1997-10-22 | 1997-10-22 | |
| US60/044,530 | 1997-10-22 | ||
| US60/062,649 | 1997-10-22 | ||
| PCT/US1998/008004 WO1998047869A1 (en) | 1997-04-22 | 1998-04-22 | Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof |
Publications (1)
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| CA2287255A1 true CA2287255A1 (en) | 1998-10-29 |
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| BE622079A (enExample) | 1961-09-11 | |||
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| BE639727A (enExample) | 1962-11-13 | |||
| BE643709A (enExample) | 1963-02-12 | 1900-01-01 | ||
| DE1288086B (enExample) | 1963-12-26 | 1969-01-30 | ||
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| GB9102423D0 (en) | 1991-02-05 | 1991-03-20 | Ciba Geigy Ag | Pryimidinyl-and triazinylsalicyl-and-picolinylaldehyde derivatives |
| WO1994006758A1 (en) * | 1992-09-21 | 1994-03-31 | University Of Saskatchewan | Aryl semicarbazone anticonvulsants |
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| US5741818A (en) * | 1995-06-07 | 1998-04-21 | University Of Saskatchewan | Semicarbazones having CNS activity and pharmaceutical preparations containing same |
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| US5688830A (en) | 1996-01-25 | 1997-11-18 | Syntex (U.S.A.) Inc. | Treatment of neuropathic pain |
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| KR20010020201A (ko) * | 1997-04-22 | 2001-03-15 | 코센시스 인크 | 탄소고리 및 헤테로고리 치환된 세미카르바존 및 티오세미카르바존과 그들의 사용 방법 |
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-
1998
- 1998-04-22 KR KR1019997009780A patent/KR20010020201A/ko not_active Ceased
- 1998-04-22 AT AT98922043T patent/ATE289295T1/de not_active IP Right Cessation
- 1998-04-22 CA CA002287255A patent/CA2287255A1/en not_active Abandoned
- 1998-04-22 WO PCT/US1998/008004 patent/WO1998047869A1/en not_active Ceased
- 1998-04-22 IL IL13252298A patent/IL132522A0/xx unknown
- 1998-04-22 EP EP98922043A patent/EP0986540B1/en not_active Expired - Lifetime
- 1998-04-22 JP JP54626998A patent/JP2001526648A/ja not_active Withdrawn
- 1998-04-22 DE DE69829048T patent/DE69829048T2/de not_active Expired - Fee Related
- 1998-04-22 BR BR9809288-0A patent/BR9809288A/pt not_active IP Right Cessation
- 1998-04-22 AU AU74676/98A patent/AU738197C/en not_active Ceased
- 1998-04-22 NZ NZ500590A patent/NZ500590A/en unknown
-
1999
- 1999-10-19 NO NO995094A patent/NO995094L/no not_active Application Discontinuation
- 1999-10-21 US US09/421,403 patent/US6613803B1/en not_active Expired - Fee Related
-
2001
- 2001-12-06 US US10/003,249 patent/US6638947B2/en not_active Expired - Fee Related
-
2002
- 2002-06-25 US US10/178,477 patent/US6696442B2/en not_active Expired - Fee Related
-
2003
- 2003-06-18 US US10/463,814 patent/US20030225080A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20030225080A1 (en) | 2003-12-04 |
| US6613803B1 (en) | 2003-09-02 |
| US6696442B2 (en) | 2004-02-24 |
| NZ500590A (en) | 2001-11-30 |
| DE69829048T2 (de) | 2006-02-09 |
| WO1998047869A1 (en) | 1998-10-29 |
| KR20010020201A (ko) | 2001-03-15 |
| NO995094L (no) | 1999-12-20 |
| AU7467698A (en) | 1998-11-13 |
| US6638947B2 (en) | 2003-10-28 |
| EP0986540A1 (en) | 2000-03-22 |
| NO995094D0 (no) | 1999-10-19 |
| AU738197B2 (en) | 2001-09-13 |
| US20020061886A1 (en) | 2002-05-23 |
| BR9809288A (pt) | 2001-08-07 |
| EP0986540B1 (en) | 2005-02-16 |
| US20020183321A1 (en) | 2002-12-05 |
| AU738197C (en) | 2002-05-16 |
| JP2001526648A (ja) | 2001-12-18 |
| ATE289295T1 (de) | 2005-03-15 |
| EP0986540A4 (en) | 2001-07-11 |
| DE69829048D1 (de) | 2005-03-24 |
| IL132522A0 (en) | 2001-03-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |