JP2000501707A - グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 - Google Patents
グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置Info
- Publication number
- JP2000501707A JP2000501707A JP09521348A JP52134897A JP2000501707A JP 2000501707 A JP2000501707 A JP 2000501707A JP 09521348 A JP09521348 A JP 09521348A JP 52134897 A JP52134897 A JP 52134897A JP 2000501707 A JP2000501707 A JP 2000501707A
- Authority
- JP
- Japan
- Prior art keywords
- glycine
- treatment
- symptoms
- capture
- gda
- 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.)
- Pending
Links
- 201000000980 schizophrenia Diseases 0.000 title claims abstract description 43
- 238000011282 treatment Methods 0.000 title claims description 78
- 239000005557 antagonist Substances 0.000 title claims description 25
- 208000011580 syndromic disease Diseases 0.000 title description 9
- 230000001149 cognitive effect Effects 0.000 title description 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims abstract description 419
- 239000004471 Glycine Substances 0.000 claims abstract description 210
- 208000028017 Psychotic disease Diseases 0.000 claims abstract description 13
- 102000004868 N-Methyl-D-Aspartate Receptors Human genes 0.000 claims description 27
- 108090001041 N-Methyl-D-Aspartate Receptors Proteins 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 20
- 230000001404 mediated effect Effects 0.000 claims description 19
- 229940079593 drug Drugs 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 14
- 230000005062 synaptic transmission Effects 0.000 claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
- 239000003176 neuroleptic agent Substances 0.000 claims description 8
- 102100022622 Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Human genes 0.000 claims description 6
- 101000972916 Homo sapiens Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Proteins 0.000 claims description 6
- 230000000561 anti-psychotic effect Effects 0.000 claims description 6
- 201000010099 disease Diseases 0.000 claims description 6
- 208000020016 psychiatric disease Diseases 0.000 claims description 6
- 101000856513 Homo sapiens Inactive N-acetyllactosaminide alpha-1,3-galactosyltransferase Proteins 0.000 claims description 5
- 102100025509 Inactive N-acetyllactosaminide alpha-1,3-galactosyltransferase Human genes 0.000 claims description 5
- 241000282412 Homo Species 0.000 claims description 3
- 230000000701 neuroleptic effect Effects 0.000 claims description 3
- 208000024827 Alzheimer disease Diseases 0.000 claims description 2
- 230000005540 biological transmission Effects 0.000 claims description 2
- 208000028683 bipolar I disease Diseases 0.000 claims description 2
- 206010013663 drug dependence Diseases 0.000 claims description 2
- 208000011117 substance-related disease Diseases 0.000 claims description 2
- 208000020925 Bipolar disease Diseases 0.000 claims 1
- 230000003444 anaesthetic effect Effects 0.000 claims 1
- 208000014674 injury Diseases 0.000 claims 1
- 210000005036 nerve Anatomy 0.000 claims 1
- 239000003368 psychostimulant agent Substances 0.000 claims 1
- 230000008733 trauma Effects 0.000 claims 1
- 208000024891 symptom Diseases 0.000 abstract description 74
- 150000001413 amino acids Chemical class 0.000 abstract description 6
- 230000000694 effects Effects 0.000 description 62
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 53
- 208000013403 hyperactivity Diseases 0.000 description 44
- 239000000902 placebo Substances 0.000 description 26
- 229940068196 placebo Drugs 0.000 description 26
- 210000004556 brain Anatomy 0.000 description 21
- 230000006872 improvement Effects 0.000 description 20
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 17
- 230000009467 reduction Effects 0.000 description 16
- 230000000698 schizophrenic effect Effects 0.000 description 16
- 230000001965 increasing effect Effects 0.000 description 14
- 230000002401 inhibitory effect Effects 0.000 description 14
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 14
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 13
- 229940025084 amphetamine Drugs 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 12
- 241000283984 Rodentia Species 0.000 description 10
- 238000003556 assay Methods 0.000 description 10
- 230000027455 binding Effects 0.000 description 10
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 10
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 8
- 108010077895 Sarcosine Proteins 0.000 description 7
- 239000000164 antipsychotic agent Substances 0.000 description 7
- 229940005529 antipsychotics Drugs 0.000 description 7
- 230000003542 behavioural effect Effects 0.000 description 7
- 230000008859 change Effects 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 7
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 7
- 238000011534 incubation Methods 0.000 description 7
- 230000004044 response Effects 0.000 description 7
- 229940043230 sarcosine Drugs 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- 210000003169 central nervous system Anatomy 0.000 description 6
- QZUDBNBUXVUHMW-UHFFFAOYSA-N clozapine Chemical compound C1CN(C)CCN1C1=NC2=CC(Cl)=CC=C2NC2=CC=CC=C12 QZUDBNBUXVUHMW-UHFFFAOYSA-N 0.000 description 6
- 230000001629 suppression Effects 0.000 description 6
- UMHNKSKNRHLEEW-UHFFFAOYSA-N 1,14-diaminotetradecan-2-one Chemical compound NCCCCCCCCCCCCC(=O)CN UMHNKSKNRHLEEW-UHFFFAOYSA-N 0.000 description 5
- 102000010726 Glycine Plasma Membrane Transport Proteins Human genes 0.000 description 5
- 108010063380 Glycine Plasma Membrane Transport Proteins Proteins 0.000 description 5
- 241000699670 Mus sp. Species 0.000 description 5
- 229940024606 amino acid Drugs 0.000 description 5
- 235000001014 amino acid Nutrition 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229960004170 clozapine Drugs 0.000 description 5
- 208000035475 disorder Diseases 0.000 description 5
- 229960003638 dopamine Drugs 0.000 description 5
- 229930195712 glutamate Natural products 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 229950010883 phencyclidine Drugs 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 210000002966 serum Anatomy 0.000 description 5
- 108010078791 Carrier Proteins Proteins 0.000 description 4
- 206010054089 Depressive symptom Diseases 0.000 description 4
- HOKKHZGPKSLGJE-GSVOUGTGSA-N N-Methyl-D-aspartic acid Chemical compound CN[C@@H](C(O)=O)CC(O)=O HOKKHZGPKSLGJE-GSVOUGTGSA-N 0.000 description 4
- 208000009668 Neurobehavioral Manifestations Diseases 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- 208000010877 cognitive disease Diseases 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- SEJVQOMVWXKDMS-UHFFFAOYSA-N 1,8-diaminooctan-2-one Chemical compound NCCCCCCC(=O)CN SEJVQOMVWXKDMS-UHFFFAOYSA-N 0.000 description 3
- 208000028698 Cognitive impairment Diseases 0.000 description 3
- 208000027776 Extrapyramidal disease Diseases 0.000 description 3
- 108010063843 Phencyclidine Receptors Proteins 0.000 description 3
- 230000006399 behavior Effects 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 230000036765 blood level Effects 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 230000001684 chronic effect Effects 0.000 description 3
- 238000010367 cloning Methods 0.000 description 3
- 230000004064 dysfunction Effects 0.000 description 3
- NTNZTEQNFHNYBC-UHFFFAOYSA-N ethyl 2-aminoacetate Chemical compound CCOC(=O)CN NTNZTEQNFHNYBC-UHFFFAOYSA-N 0.000 description 3
- 238000000556 factor analysis Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical compound NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 description 3
- 150000002332 glycine derivatives Chemical class 0.000 description 3
- 229960003878 haloperidol Drugs 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- KQSSATDQUYCRGS-UHFFFAOYSA-N methyl glycinate Chemical compound COC(=O)CN KQSSATDQUYCRGS-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001459 mortal effect Effects 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 229960001534 risperidone Drugs 0.000 description 3
- RAPZEAPATHNIPO-UHFFFAOYSA-N risperidone Chemical compound FC1=CC=C2C(C3CCN(CC3)CCC=3C(=O)N4CCCCC4=NC=3C)=NOC2=C1 RAPZEAPATHNIPO-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000007619 statistical method Methods 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- NRSBQSJHFYZIPH-DMTCNVIQSA-N (2s,4r)-pyrrolidine-2,4-dicarboxylic acid Chemical compound OC(=O)[C@H]1CN[C@H](C(O)=O)C1 NRSBQSJHFYZIPH-DMTCNVIQSA-N 0.000 description 2
- IZWUORPLOVCIJU-UHFFFAOYSA-N 2-(2-aminoacetyl)undecanamide Chemical compound CCCCCCCCCC(C(N)=O)C(=O)CN IZWUORPLOVCIJU-UHFFFAOYSA-N 0.000 description 2
- MTCFGRXMJLQNBG-UWTATZPHSA-N D-Serine Chemical compound OC[C@@H](N)C(O)=O MTCFGRXMJLQNBG-UWTATZPHSA-N 0.000 description 2
- 229930195711 D-Serine Natural products 0.000 description 2
- PLDUPXSUYLZYBN-UHFFFAOYSA-N Fluphenazine Chemical compound C1CN(CCO)CCN1CCCN1C2=CC(C(F)(F)F)=CC=C2SC2=CC=CC=C21 PLDUPXSUYLZYBN-UHFFFAOYSA-N 0.000 description 2
- YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 description 2
- NRSBQSJHFYZIPH-UHFFFAOYSA-N L-trans-PDC Natural products OC(=O)C1CNC(C(O)=O)C1 NRSBQSJHFYZIPH-UHFFFAOYSA-N 0.000 description 2
- 208000028810 Shared psychotic disease Diseases 0.000 description 2
- 238000000692 Student's t-test Methods 0.000 description 2
- HWHLPVGTWGOCJO-UHFFFAOYSA-N Trihexyphenidyl Chemical group C1CCCCC1C(C=1C=CC=CC=1)(O)CCN1CCCCC1 HWHLPVGTWGOCJO-UHFFFAOYSA-N 0.000 description 2
- 208000003443 Unconsciousness Diseases 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 230000003042 antagnostic effect Effects 0.000 description 2
- 230000008485 antagonism Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000008499 blood brain barrier function Effects 0.000 description 2
- 210000001218 blood-brain barrier Anatomy 0.000 description 2
- 210000000133 brain stem Anatomy 0.000 description 2
- 229960001076 chlorpromazine Drugs 0.000 description 2
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 description 2
- 230000007012 clinical effect Effects 0.000 description 2
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003210 dopamine receptor blocking agent Substances 0.000 description 2
- 230000003291 dopaminomimetic effect Effects 0.000 description 2
- 238000001647 drug administration Methods 0.000 description 2
- 230000008451 emotion Effects 0.000 description 2
- 230000002996 emotional effect Effects 0.000 description 2
- 230000002964 excitative effect Effects 0.000 description 2
- 230000005021 gait Effects 0.000 description 2
- 239000003193 general anesthetic agent Substances 0.000 description 2
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229960003299 ketamine Drugs 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 210000002569 neuron Anatomy 0.000 description 2
- 239000002858 neurotransmitter agent Substances 0.000 description 2
- QKFJKGMPGYROCL-UHFFFAOYSA-N phenyl isothiocyanate Chemical compound S=C=NC1=CC=CC=C1 QKFJKGMPGYROCL-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 210000000278 spinal cord Anatomy 0.000 description 2
- 210000003568 synaptosome Anatomy 0.000 description 2
- 238000012353 t test Methods 0.000 description 2
- 229960001032 trihexyphenidyl Drugs 0.000 description 2
- 238000003828 vacuum filtration Methods 0.000 description 2
- OGNSCSPNOLGXSM-UHFFFAOYSA-N (+/-)-DABA Natural products NCCC(N)C(O)=O OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 description 1
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- XJLSEXAGTJCILF-RXMQYKEDSA-N (R)-nipecotic acid zwitterion Chemical compound OC(=O)[C@@H]1CCCNC1 XJLSEXAGTJCILF-RXMQYKEDSA-N 0.000 description 1
- NHBKXEKEPDILRR-UHFFFAOYSA-N 2,3-bis(butanoylsulfanyl)propyl butanoate Chemical compound CCCC(=O)OCC(SC(=O)CCC)CSC(=O)CCC NHBKXEKEPDILRR-UHFFFAOYSA-N 0.000 description 1
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 206010003805 Autism Diseases 0.000 description 1
- 208000020706 Autistic disease Diseases 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- DYDCUQKUCUHJBH-UWTATZPHSA-N D-Cycloserine Chemical compound N[C@@H]1CONC1=O DYDCUQKUCUHJBH-UWTATZPHSA-N 0.000 description 1
- DYDCUQKUCUHJBH-UHFFFAOYSA-N D-Cycloserine Natural products NC1CONC1=O DYDCUQKUCUHJBH-UHFFFAOYSA-N 0.000 description 1
- 102000015554 Dopamine receptor Human genes 0.000 description 1
- 108050004812 Dopamine receptor Proteins 0.000 description 1
- 229940121891 Dopamine receptor antagonist Drugs 0.000 description 1
- 208000035859 Drug effect increased Diseases 0.000 description 1
- 206010060891 General symptom Diseases 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 102000018899 Glutamate Receptors Human genes 0.000 description 1
- 108010027915 Glutamate Receptors Proteins 0.000 description 1
- 208000004547 Hallucinations Diseases 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 description 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 208000019022 Mood disease Diseases 0.000 description 1
- 208000016285 Movement disease Diseases 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 229940095474 NMDA agonist Drugs 0.000 description 1
- 206010028813 Nausea Diseases 0.000 description 1
- 206010060860 Neurological symptom Diseases 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- KNTFCRCCPLEUQZ-VKHMYHEASA-N O-methylserine Chemical compound COC[C@H](N)C(O)=O KNTFCRCCPLEUQZ-VKHMYHEASA-N 0.000 description 1
- 108010029485 Protein Isoforms Proteins 0.000 description 1
- 102000001708 Protein Isoforms Human genes 0.000 description 1
- 206010039897 Sedation Diseases 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- KLBQZWRITKRQQV-UHFFFAOYSA-N Thioridazine Chemical compound C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C KLBQZWRITKRQQV-UHFFFAOYSA-N 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000008351 acetate buffer Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000009098 adjuvant therapy Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 229940125516 allosteric modulator Drugs 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940035674 anesthetics Drugs 0.000 description 1
- 230000001090 anti-dopaminergic effect Effects 0.000 description 1
- 230000003063 anti-neuropathic effect Effects 0.000 description 1
- 229940035678 anti-parkinson drug Drugs 0.000 description 1
- 239000000939 antiparkinson agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000037007 arousal Effects 0.000 description 1
- 239000003693 atypical antipsychotic agent Substances 0.000 description 1
- 229940127236 atypical antipsychotics Drugs 0.000 description 1
- 230000009910 autonomic response Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 210000001185 bone marrow Anatomy 0.000 description 1
- 235000021152 breakfast Nutrition 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 210000001638 cerebellum Anatomy 0.000 description 1
- 210000003710 cerebral cortex Anatomy 0.000 description 1
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 1
- 229960002327 chloral hydrate Drugs 0.000 description 1
- 229940068796 clozaril Drugs 0.000 description 1
- 230000008045 co-localization Effects 0.000 description 1
- 229960003920 cocaine Drugs 0.000 description 1
- 230000003920 cognitive function Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 239000012059 conventional drug carrier Substances 0.000 description 1
- 230000001054 cortical effect Effects 0.000 description 1
- 210000003618 cortical neuron Anatomy 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000003001 depressive effect Effects 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 210000002451 diencephalon Anatomy 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 208000037765 diseases and disorders Diseases 0.000 description 1
- 230000008482 dysregulation Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000003492 excitotoxic effect Effects 0.000 description 1
- 231100000063 excitotoxicity Toxicity 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 229960002690 fluphenazine Drugs 0.000 description 1
- -1 for example Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000002306 glutamic acid derivatives Chemical class 0.000 description 1
- 229940095895 haldol Drugs 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 210000001320 hippocampus Anatomy 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000009592 kidney function test Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 238000007449 liver function test Methods 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001095 motoneuron effect Effects 0.000 description 1
- 239000003706 n methyl dextro aspartic acid receptor stimulating agent Substances 0.000 description 1
- 230000008693 nausea Effects 0.000 description 1
- 230000001722 neurochemical effect Effects 0.000 description 1
- 230000004770 neurodegeneration Effects 0.000 description 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
- 230000009871 nonspecific binding Effects 0.000 description 1
- 210000000956 olfactory bulb Anatomy 0.000 description 1
- 238000011369 optimal treatment Methods 0.000 description 1
- 229940100688 oral solution Drugs 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 208000022821 personality disease Diseases 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229940117953 phenylisothiocyanate Drugs 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 238000001121 post-column derivatisation Methods 0.000 description 1
- 230000003518 presynaptic effect Effects 0.000 description 1
- 230000000506 psychotropic effect Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 238000000611 regression analysis Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 210000001525 retina Anatomy 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 230000036280 sedation Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 210000002182 synaptic membrane Anatomy 0.000 description 1
- 230000015883 synaptic transmission, dopaminergic Effects 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 229960002784 thioridazine Drugs 0.000 description 1
- 238000011277 treatment modality Methods 0.000 description 1
- PIEPQKCYPFFYMG-UHFFFAOYSA-N tris acetate Chemical compound CC(O)=O.OCC(N)(CO)CO PIEPQKCYPFFYMG-UHFFFAOYSA-N 0.000 description 1
- 238000001521 two-tailed test Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Toxicology (AREA)
- Hospice & Palliative Care (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.NMDAレセプター仲介神経伝達を促進するのに十分な量のグリシン捕捉 アンタゴニストをヒトに投与することを含む、ヒトにおけるNMDAレセプター 仲介神経伝達促進法。 2.精神病で患うヒトの患者に、NMDAレセプター仲介神経伝達を促進する のに十分な量のグリシン捕捉アンタゴニストを該患者に投与することを含む該患 者の処置法。 3.精神病が病気と関連する請求項2記載の方法。 4.病気が重度のうつ病、(双極性)躁うつ病、アルツハイマー病または外傷後 ストレス症である請求項2記載の方法。 5.精神病が薬物中毒と関連する請求項2記載の方法。 6.薬物が解離性麻酔薬または精神刺激薬である請求項5記載の方法。 7.精神分裂病で患うヒトの患者にNMDAレセプター仲介神経伝達を促進す るのに十分な量のグリシン捕捉アンタゴニストを投与することを含む精神分裂病 の処置法。 8.抗精神病薬も患者に投与する請求項7記載の方法。 9.抗精神病薬が神経弛緩薬である請求項8記載の方法。 10.GLYT1またはGLYT2仲介グリシン捕捉が抑制される請求項1記 載の方法。 11.GLYT1またはGLYT2仲介グリシン捕捉が抑制される請求項2記 載の方法。 12.GLYT1またはGLYT2仲介グリシン捕捉が抑制される請求項7記 載の方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US836195P | 1995-12-07 | 1995-12-07 | |
US60/008,361 | 1995-12-07 | ||
PCT/US1996/019142 WO1997020553A1 (en) | 1995-12-07 | 1996-12-05 | Treatment of negative and cognitive symptoms of schizophrenia with glycine uptake antagonists |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009066534A Division JP5363152B2 (ja) | 1995-12-07 | 2009-03-18 | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000501707A true JP2000501707A (ja) | 2000-02-15 |
Family
ID=21731199
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP09521348A Pending JP2000501707A (ja) | 1995-12-07 | 1996-12-05 | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 |
JP2009066534A Expired - Fee Related JP5363152B2 (ja) | 1995-12-07 | 2009-03-18 | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 |
JP2012251233A Pending JP2013056918A (ja) | 1995-12-07 | 2012-11-15 | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009066534A Expired - Fee Related JP5363152B2 (ja) | 1995-12-07 | 2009-03-18 | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 |
JP2012251233A Pending JP2013056918A (ja) | 1995-12-07 | 2012-11-15 | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 |
Country Status (10)
Country | Link |
---|---|
US (3) | US5837730A (ja) |
EP (1) | EP0871440B1 (ja) |
JP (3) | JP2000501707A (ja) |
AT (1) | ATE320804T1 (ja) |
DE (1) | DE69635959T2 (ja) |
DK (1) | DK0871440T3 (ja) |
ES (1) | ES2260773T3 (ja) |
IL (1) | IL124536A (ja) |
PT (1) | PT871440E (ja) |
WO (2) | WO1997020553A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003513063A (ja) * | 1999-11-01 | 2003-04-08 | エヌピーエス アレリックス コーポレーション | ジアリール−エニン類 |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6355681B2 (en) * | 1995-12-07 | 2002-03-12 | Glytech, Inc. | Glycine substitutes and precursors for treating a psychosis |
US6361957B1 (en) * | 1999-08-03 | 2002-03-26 | Glytech, Inc. | Assay for D-serine transport antagonist and use for treating psychosis |
WO1997020553A1 (en) * | 1995-12-07 | 1997-06-12 | Javitt Daniel C | Treatment of negative and cognitive symptoms of schizophrenia with glycine uptake antagonists |
US6191165B1 (en) | 1996-05-31 | 2001-02-20 | Allelix Neuroscience Inc. | Pharmaceutical for treatment of neurological and neuropsychiatric disorders |
US6001854A (en) * | 1996-05-31 | 1999-12-14 | Allelix Neuroscience Inc. | Pharmaceutical for treating of neurological and neuropsychiatric disorders |
PT1073432E (pt) | 1998-04-14 | 2007-10-22 | Gen Hospital Corp | Utilização da d-alanina ou da d-serina para o tratamento da esquizofrenia |
US6416975B1 (en) * | 1998-11-12 | 2002-07-09 | Gliatech, Inc. | Human glycine transporter type 2 |
AU4361500A (en) * | 1999-04-20 | 2000-11-02 | Advocare International Llc | Nutritional composition for improved cognitive performance |
US6551993B1 (en) * | 1999-08-16 | 2003-04-22 | Thomas Jefferson University | Partial agonists at the glycine modulatory site of the NMDA receptor for treating cognitive dysfunction |
TWI243173B (en) | 1999-11-17 | 2005-11-11 | Akzo Nobel Nv | Spiro[2H-1-benzopyran-2,4'-piperidine] derivatives |
KR100900020B1 (ko) | 2001-02-16 | 2009-06-01 | 알레릭스 뉴로사이언스, 인크. | Glyt-1 저해제로서의 티오펜 치환 아민 유도체 |
US20020187544A1 (en) * | 2001-04-05 | 2002-12-12 | Wisconsin Alumni Research Foundation | Uropathogenic E. coli D-serine detoxification operon |
WO2004005935A1 (ja) * | 2002-07-04 | 2004-01-15 | Mitsubishi Pharma Corporation | 統合失調症の検査、診断方法 |
FR2843590B1 (fr) * | 2002-08-14 | 2007-10-05 | Prestwick Scient Capital Inc | Derives de l'acide r(+)-2-amino-3-hydroxypropanoique a action glycinergique |
US7160913B2 (en) * | 2002-09-13 | 2007-01-09 | Thomas Jefferson University | Methods and kit for treating Parkinson's disease |
KR101095939B1 (ko) * | 2003-01-16 | 2011-12-19 | 아카디아 파마슈티칼스 인코포레이티드 | 신경퇴행성 질환에 대한 치료제로서 선택적 세로토닌2a/2c 리셉터 역작용제 |
IL154318A (en) | 2003-02-06 | 2010-05-31 | Sarah Herzog Memorial Hospital | Pharmaceutical compositions for the treatment of movement disorders |
AU2004233942A1 (en) | 2003-04-30 | 2004-11-11 | H. Lundbeck A/S | Aromatic oxyphenyl and aromatic sulfanylphenyl derivatives |
CN1867358A (zh) * | 2003-08-21 | 2006-11-22 | H.隆德贝克有限公司 | 用于治疗抑郁症的5-羟色胺再摄取抑制剂和1型甘氨酸转运蛋白抑制剂的联合药物 |
EP1696857A2 (en) * | 2003-12-04 | 2006-09-06 | The Research Foundation Of the City university of New York | Clozapine and cocaine effects on dopamine and serotonin release in nucleus accumbens during psychostimulant behavior and withdrawal |
US20090017047A1 (en) * | 2004-06-11 | 2009-01-15 | Egon Tech | Preparation for the Prevention and Treatment of Stress Conditions as Well as Functional and Organic Disorders of the Nervous System and Metabolic Disorders |
WO2006000222A2 (en) * | 2004-06-24 | 2006-01-05 | H. Lundbeck A/S | The combination of an antipsychotic and a glycine transporter type i inhibitor for the treatment of schizophrenia |
CA2579962A1 (en) | 2004-08-09 | 2006-06-01 | Enrique Melendez Hevia | Glycine as a diet supplement for the treatment of health problems that result from underlying metabolic disorders |
EP1830833B1 (en) * | 2004-12-16 | 2010-01-27 | Janssen Pharmaceutica N.V. | Combination of a glycine transporter (glyt1) inhibitor and an antipsychotic for the treatment of symptoms of schizophrenia as well as its preparation and use thereof |
TW200820963A (en) * | 2006-07-28 | 2008-05-16 | Xenoport Inc | Acyloxyalkyl carbamate prodrugs of α-amino acids, methods of synthesis and use |
CN101677971A (zh) | 2007-03-19 | 2010-03-24 | 阿卡蒂亚药品公司 | 5-ht2a反向激动剂和拮抗剂与抗精神病药物的组合 |
DK2200610T3 (en) * | 2007-09-21 | 2018-04-23 | Acadia Pharm Inc | ADMINISTRATION OF PIMAVANSERIN WITH OTHER AGENTS |
IL188681A0 (en) * | 2008-01-09 | 2008-12-29 | Amino Acid Solutions Inc | Pharmaceutical compositions and methods utilizing a d-amino acid |
US20110263968A1 (en) * | 2008-11-04 | 2011-10-27 | Mclean Hospital Corporation | Drug-Enhanced Neurofeedback |
US8951968B2 (en) | 2009-10-05 | 2015-02-10 | Northwestern University | Methods of treating depression and other related diseases |
US8624052B2 (en) * | 2010-11-12 | 2014-01-07 | Promentis Pharmaceuticals, Inc. | S-t-butyl protected cysteine di-peptide analogs and related compounds |
US9737531B2 (en) | 2012-07-12 | 2017-08-22 | Glytech, Llc | Composition and method for treatment of depression and psychosis in humans |
SI3325444T1 (sl) | 2015-07-20 | 2021-11-30 | Acadia Pharmaceuticals Inc. | Postopki za pripravo N-(4-fluorobenzil)-N-(1-metilpiperidin-4-il)-N'- (4-(2-metilpropiloksi)fenilmetil)karbamida in njegove tartratne soli in polimorfne oblike C |
US10953000B2 (en) | 2016-03-25 | 2021-03-23 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome P450 modulators |
WO2017165635A1 (en) | 2016-03-25 | 2017-09-28 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome p450 modulators |
WO2018118626A1 (en) | 2016-12-20 | 2018-06-28 | Acadia Pharmaceuticals Inc. | Pimavanserin alone or in combination for use in the treatment of alzheimer's disease psychosis |
US11135211B2 (en) | 2017-04-28 | 2021-10-05 | Acadia Pharmaceuticals Inc. | Pimavanserin for treating impulse control disorder |
CN110996948A (zh) | 2017-06-12 | 2020-04-10 | 格莱泰施有限责任公司 | 用nmda拮抗剂和d2/5ht2a或选择性5ht2a拮抗剂治疗抑郁症 |
EP3675827A1 (en) | 2017-08-30 | 2020-07-08 | Acadia Pharmaceuticals Inc. | Formulations of pimavanserin |
CN111491629A (zh) | 2017-11-22 | 2020-08-04 | 康塞特医药品公司 | D-丝氨酸的氘化类似物及其用途 |
AU2019206950B2 (en) * | 2018-01-10 | 2021-07-01 | XWPharma Ltd. | Prodrugs of ketamine, compositions and uses thereof |
WO2020150698A1 (en) * | 2019-01-18 | 2020-07-23 | The Johns Hopkins University | Prevention of anesthetic-induced neurocognitive dysfunction |
CA3158912A1 (en) * | 2019-11-18 | 2021-05-27 | Societe Des Produits Nestle S.A. | Compositions and methods for glutathione enhancement for use in brain health |
AU2022326513A1 (en) | 2021-08-13 | 2024-02-15 | XWPharma Ltd. | Pharmaceutical compositions and oral dosage forms of ketamine derivatives |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4904681A (en) * | 1987-12-01 | 1990-02-27 | G. D. Searle & Co. | D-cycloserine and its prodrugs as cognitive enhancers |
JPH07103018B2 (ja) * | 1988-09-16 | 1995-11-08 | 武田薬品工業株式会社 | 精神分裂病治療剤 |
JP2757960B2 (ja) * | 1988-10-17 | 1998-05-25 | サントリー株式会社 | (2R,3S,4S)−α−(カルボキシシクロプロピル)グリシン |
US5187171A (en) * | 1989-01-09 | 1993-02-16 | G. D. Searle & Co. | Use of a glycine b partial agonist as an antipsychotic |
US5179085A (en) * | 1989-03-15 | 1993-01-12 | Warner-Lambert Company | N-substituted α-amino acids and derivatives thereof having pharmaceutical activity |
JPH03236315A (ja) * | 1989-12-05 | 1991-10-22 | Nippon Oil & Fats Co Ltd | 抗精神病薬 |
US5260324A (en) * | 1990-02-06 | 1993-11-09 | G. D. Searle & Company | Composition containing D-cycloserine and D-alanine for memory and learning enhancement or treatment of a cognitive or psychotic disorder |
US5086072A (en) * | 1990-06-18 | 1992-02-04 | The United States Of America As Represented By The Department Of Health And Human Services | Treatment of mood disorders with functional antagonists of the glycine/nmda receptor complex |
US5756348A (en) | 1991-11-12 | 1998-05-26 | Synaptic Pharmaceutical Corporation | DNA encoding a glycine transporter and uses thereof |
US5428069A (en) * | 1993-01-11 | 1995-06-27 | The United States Of America As Represented By The Department Of Health & Human Services | Treating cognition with, aminocyclopropanecarboxylic derivatives |
US5656608B1 (en) * | 1995-02-23 | 2000-09-26 | Novartis Nutrition Ltd | Amino acid compositions and methods of treatment using same |
WO1997020553A1 (en) * | 1995-12-07 | 1997-06-12 | Javitt Daniel C | Treatment of negative and cognitive symptoms of schizophrenia with glycine uptake antagonists |
-
1996
- 1996-12-05 WO PCT/US1996/019142 patent/WO1997020553A1/en active IP Right Grant
- 1996-12-05 IL IL12453696A patent/IL124536A/xx not_active IP Right Cessation
- 1996-12-05 DK DK96941518T patent/DK0871440T3/da active
- 1996-12-05 JP JP09521348A patent/JP2000501707A/ja active Pending
- 1996-12-05 DE DE69635959T patent/DE69635959T2/de not_active Expired - Lifetime
- 1996-12-05 ES ES96941518T patent/ES2260773T3/es not_active Expired - Lifetime
- 1996-12-05 PT PT96941518T patent/PT871440E/pt unknown
- 1996-12-05 AT AT96941518T patent/ATE320804T1/de active
- 1996-12-05 EP EP96941518A patent/EP0871440B1/en not_active Revoked
- 1996-12-05 WO PCT/US1996/019141 patent/WO1997020552A1/en active Application Filing
- 1996-12-06 US US08/759,681 patent/US5837730A/en not_active Expired - Lifetime
- 1996-12-06 US US08/759,714 patent/US5854286A/en not_active Expired - Lifetime
-
1998
- 1998-12-16 US US09/212,273 patent/US6162827A/en not_active Expired - Lifetime
-
2009
- 2009-03-18 JP JP2009066534A patent/JP5363152B2/ja not_active Expired - Fee Related
-
2012
- 2012-11-15 JP JP2012251233A patent/JP2013056918A/ja active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003513063A (ja) * | 1999-11-01 | 2003-04-08 | エヌピーエス アレリックス コーポレーション | ジアリール−エニン類 |
Also Published As
Publication number | Publication date |
---|---|
JP2009167205A (ja) | 2009-07-30 |
DE69635959T2 (de) | 2006-12-07 |
JP2013056918A (ja) | 2013-03-28 |
US5837730A (en) | 1998-11-17 |
IL124536A (en) | 2001-03-19 |
EP0871440B1 (en) | 2006-03-22 |
EP0871440A1 (en) | 1998-10-21 |
EP0871440A4 (en) | 1999-01-20 |
JP5363152B2 (ja) | 2013-12-11 |
DE69635959D1 (de) | 2006-05-11 |
ATE320804T1 (de) | 2006-04-15 |
WO1997020553A1 (en) | 1997-06-12 |
ES2260773T3 (es) | 2006-11-01 |
WO1997020552A1 (en) | 1997-06-12 |
IL124536A0 (en) | 1998-12-06 |
US5854286A (en) | 1998-12-29 |
US6162827A (en) | 2000-12-19 |
PT871440E (pt) | 2006-07-31 |
DK0871440T3 (da) | 2006-07-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5363152B2 (ja) | グリシン捕捉性アンタゴニストを用いる拒絶性および認知性精神分裂病症候群の処置 | |
Panenka et al. | Methamphetamine use: a comprehensive review of molecular, preclinical and clinical findings | |
AU2018201436B2 (en) | New therapeutic approaches for treating Parkinson's disease | |
JP4846063B2 (ja) | 選択的s1p1レセプターアゴニストの投与法 | |
CA3079259A1 (en) | Ganaxolone for use in treating genetic epileptic disorders | |
JP5900988B2 (ja) | 抗痙攣医薬組成物 | |
KR20100088160A (ko) | Cmt 및 관련 장애를 치료하기 위한 신규 치료적 접근법 | |
JP2014098018A (ja) | Nmdanr2b−サブタイプ選択的アンタゴニストを使用する障害の処置方法 | |
EP1444979A1 (en) | Pharmaceutical compositions comprising an NMDA receptor agonist or partial agonist for the treatment of movement disorders | |
JP2018039817A (ja) | 多発性硬化症を治療するためのPPARγアゴニスト | |
US20180344694A1 (en) | Use of indole compounds to stimulate the immune system | |
JP2013501805A (ja) | 脱髄性および他の神経系疾患を患っている患者における神経認知的および/または神経精神医学的障害を改善するための4−アミノピリジンの使用 | |
US20020161048A1 (en) | Glycine substitutes and precursors for treating a psychosis | |
CN114007607A (zh) | 用于治疗神经变性疾病的材料和方法 | |
Singer et al. | Interactions between the glycine transporter 1 (GlyT1) inhibitor SSR504734 and psychoactive drugs in mouse motor behaviour | |
EP1830833B1 (en) | Combination of a glycine transporter (glyt1) inhibitor and an antipsychotic for the treatment of symptoms of schizophrenia as well as its preparation and use thereof | |
INADA et al. | Antihypertensive action of a new angiotensin converting enzyme inhibitor,(R)-3-[(S)-1-carboxy-5-(4-piperidyl) pentyl] amino-4-oxo-2, 3, 4, 5-tetrahydro-1, 5-benzothiazepine-5-acetic acid (CV-5975), in various hypertensive models | |
CA2239624C (en) | Treatment of negative and cognitive symptoms of schizophrenia with glycine uptake antagonists | |
JP7257091B2 (ja) | 認知症の治療及び予防薬 | |
JP2002220345A (ja) | 脂肪肝改善剤 | |
JPH09500375A (ja) | パーキンソン病の治療を目的とする医薬品の製造のためのエファロキサンおよびその誘導体の使用 | |
JP2021535216A (ja) | セバコイルジナルブフィンとアセトアミノフェンの医薬品製剤及び疼痛を治療する方法 | |
JPH11246408A (ja) | 肝障害治療剤 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20061128 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20070228 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20070416 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070528 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20081118 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20090218 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20090507 |
|
RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20090507 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20090508 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20090907 |
|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20090907 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20110927 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20111005 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20111228 |