JP2010524893A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010524893A5 JP2010524893A5 JP2010503510A JP2010503510A JP2010524893A5 JP 2010524893 A5 JP2010524893 A5 JP 2010524893A5 JP 2010503510 A JP2010503510 A JP 2010503510A JP 2010503510 A JP2010503510 A JP 2010503510A JP 2010524893 A5 JP2010524893 A5 JP 2010524893A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- methyl
- nitrovinyl
- imidazol
- propylamino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 33
- 150000001875 compounds Chemical class 0.000 claims 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 13
- 125000001072 heteroaryl group Chemical group 0.000 claims 8
- 125000004452 carbocyclyl group Chemical group 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 239000003112 inhibitor Substances 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 6
- 201000010099 disease Diseases 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 206010019375 Helicobacter infections Diseases 0.000 claims 4
- 206010028980 Neoplasm Diseases 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 230000001771 impaired effect Effects 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 125000002950 monocyclic group Chemical group 0.000 claims 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 3
- LZCDAPDGXCYOEH-UHFFFAOYSA-N adapalene Chemical compound C1=C(C(O)=O)C=CC2=CC(C3=CC=C(C(=C3)C34CC5CC(CC(C5)C3)C4)OC)=CC=C21 LZCDAPDGXCYOEH-UHFFFAOYSA-N 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- -1 cyano, hydroxyl Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 230000002757 inflammatory effect Effects 0.000 claims 3
- 201000006417 multiple sclerosis Diseases 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- JUISCZDVYAJMBT-UHFFFAOYSA-N 1-n'-(1,3-benzodioxol-5-yl)-1-n-[3-(5-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound CC1=CN=CN1CCCNC(=C[N+]([O-])=O)NC1=CC=C(OCO2)C2=C1 JUISCZDVYAJMBT-UHFFFAOYSA-N 0.000 claims 2
- KJDYILRPNDWKLG-UHFFFAOYSA-N 1-n'-cyclohexyl-1-n-[4-(5-methylimidazol-1-yl)butyl]-2-nitroethene-1,1-diamine Chemical compound CC1=CN=CN1CCCCNC(=C[N+]([O-])=O)NC1CCCCC1 KJDYILRPNDWKLG-UHFFFAOYSA-N 0.000 claims 2
- MSYGAHOHLUJIKV-UHFFFAOYSA-N 3,5-dimethyl-1-(3-nitrophenyl)-1h-pyrazole-4-carboxylic acid ethyl ester Chemical compound CC1=C(C(=O)OCC)C(C)=NN1C1=CC=CC([N+]([O-])=O)=C1 MSYGAHOHLUJIKV-UHFFFAOYSA-N 0.000 claims 2
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 claims 2
- 208000023697 ABri amyloidosis Diseases 0.000 claims 2
- 208000017227 ADan amyloidosis Diseases 0.000 claims 2
- 102000012440 Acetylcholinesterase Human genes 0.000 claims 2
- 108010022752 Acetylcholinesterase Proteins 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 201000001320 Atherosclerosis Diseases 0.000 claims 2
- 208000012639 Balance disease Diseases 0.000 claims 2
- 206010068597 Bulbospinal muscular atrophy congenital Diseases 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 2
- 201000010374 Down Syndrome Diseases 0.000 claims 2
- 206010061825 Duodenal neoplasm Diseases 0.000 claims 2
- 208000030814 Eating disease Diseases 0.000 claims 2
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 2
- 208000035895 Guillain-Barré syndrome Diseases 0.000 claims 2
- 208000023105 Huntington disease Diseases 0.000 claims 2
- 201000000162 ITM2B-related cerebral amyloid angiopathy 1 Diseases 0.000 claims 2
- 201000000194 ITM2B-related cerebral amyloid angiopathy 2 Diseases 0.000 claims 2
- 208000027747 Kennedy disease Diseases 0.000 claims 2
- 206010027476 Metastases Diseases 0.000 claims 2
- 206010049567 Miller Fisher syndrome Diseases 0.000 claims 2
- 206010033645 Pancreatitis Diseases 0.000 claims 2
- 208000018737 Parkinson disease Diseases 0.000 claims 2
- 201000004681 Psoriasis Diseases 0.000 claims 2
- 206010037779 Radiculopathy Diseases 0.000 claims 2
- 206010054184 Small intestine carcinoma Diseases 0.000 claims 2
- 208000005718 Stomach Neoplasms Diseases 0.000 claims 2
- 230000024932 T cell mediated immunity Effects 0.000 claims 2
- 102000011017 Type 4 Cyclic Nucleotide Phosphodiesterases Human genes 0.000 claims 2
- 108010037584 Type 4 Cyclic Nucleotide Phosphodiesterases Proteins 0.000 claims 2
- 208000006269 X-Linked Bulbo-Spinal Atrophy Diseases 0.000 claims 2
- 201000008629 Zollinger-Ellison syndrome Diseases 0.000 claims 2
- 229940022698 acetylcholinesterase Drugs 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims 2
- 230000033228 biological regulation Effects 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 230000001684 chronic effect Effects 0.000 claims 2
- 230000003210 demyelinating effect Effects 0.000 claims 2
- 235000014632 disordered eating Nutrition 0.000 claims 2
- 201000000312 duodenum cancer Diseases 0.000 claims 2
- 230000008482 dysregulation Effects 0.000 claims 2
- 230000037149 energy metabolism Effects 0.000 claims 2
- 206010017758 gastric cancer Diseases 0.000 claims 2
- 201000000052 gastrinoma Diseases 0.000 claims 2
- 230000013632 homeostatic process Effects 0.000 claims 2
- 230000003054 hormonal effect Effects 0.000 claims 2
- 230000028996 humoral immune response Effects 0.000 claims 2
- 208000000509 infertility Diseases 0.000 claims 2
- 230000036512 infertility Effects 0.000 claims 2
- 231100000535 infertility Toxicity 0.000 claims 2
- 230000023404 leukocyte cell-cell adhesion Effects 0.000 claims 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims 2
- 230000003211 malignant effect Effects 0.000 claims 2
- 201000001441 melanoma Diseases 0.000 claims 2
- 230000009401 metastasis Effects 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 230000005012 migration Effects 0.000 claims 2
- 238000013508 migration Methods 0.000 claims 2
- AMQXTNLKQTXNJU-UHFFFAOYSA-N n'-[3-(5-methylimidazol-1-yl)propyl]-n-naphthalen-1-yl-2-nitroethanimidamide Chemical compound CC1=CN=CN1CCCN=C(C[N+]([O-])=O)NC1=CC=CC2=CC=CC=C12 AMQXTNLKQTXNJU-UHFFFAOYSA-N 0.000 claims 2
- 230000004770 neurodegeneration Effects 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 208000006473 polyradiculopathy Diseases 0.000 claims 2
- 208000037803 restenosis Diseases 0.000 claims 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 201000000980 schizophrenia Diseases 0.000 claims 2
- 208000020685 sleep-wake disease Diseases 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- 201000011549 stomach cancer Diseases 0.000 claims 2
- 125000004001 thioalkyl group Chemical group 0.000 claims 2
- NITUEMISTORFON-PPFXTMJRSA-N (2S)-1-[(2S,3R)-2-[[(2S)-2-[[(2S)-1-[(2S,3R)-2-[[(2S)-2-[[(2S,3S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2R)-2-aminopropanoyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-3-methylbutanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-4-methylpentanoyl]amino]-3-phenylpropanoyl]amino]propanoyl]amino]-4-oxobutanoyl]amino]-3-methylpentanoyl]amino]-3-methylbutanoyl]amino]-3-hydroxybutanoyl]pyrrolidine-2-carbonyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-3-hydroxybutanoyl]pyrrolidine-2-carboxylic acid Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@@H](C)N)C(C)C)C(C)C)C1=CC=CC=C1 NITUEMISTORFON-PPFXTMJRSA-N 0.000 claims 1
- DRDRFTRZLLMRCL-UHFFFAOYSA-N 1-n'-(1,3-benzodioxol-5-yl)-1-n-[3-(4-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound C1=NC(C)=CN1CCCNC(=C[N+]([O-])=O)NC1=CC=C(OCO2)C2=C1 DRDRFTRZLLMRCL-UHFFFAOYSA-N 0.000 claims 1
- HJEWLERUZOGYCA-UHFFFAOYSA-N 1-n'-(2,4-dimethoxyphenyl)-1-n-[3-(4-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound COC1=CC(OC)=CC=C1NC(=C[N+]([O-])=O)NCCCN1C=C(C)N=C1 HJEWLERUZOGYCA-UHFFFAOYSA-N 0.000 claims 1
- PCLRPJYQKLMMKX-UHFFFAOYSA-N 1-n'-(2,4-dimethoxyphenyl)-1-n-[3-(5-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound COC1=CC(OC)=CC=C1NC(=C[N+]([O-])=O)NCCCN1C(C)=CN=C1 PCLRPJYQKLMMKX-UHFFFAOYSA-N 0.000 claims 1
- WEHWOHAOZUUTLE-UHFFFAOYSA-N 1-n'-(3,4-dimethoxyphenyl)-1-n-[3-(4-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound C1=C(OC)C(OC)=CC=C1NC(=C[N+]([O-])=O)NCCCN1C=C(C)N=C1 WEHWOHAOZUUTLE-UHFFFAOYSA-N 0.000 claims 1
- XGSCKLKAQKSJDK-UHFFFAOYSA-N 1-n'-(3,4-dimethoxyphenyl)-1-n-[3-(5-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound C1=C(OC)C(OC)=CC=C1NC(=C[N+]([O-])=O)NCCCN1C(C)=CN=C1 XGSCKLKAQKSJDK-UHFFFAOYSA-N 0.000 claims 1
- HYOMTYOMNXAQKB-UHFFFAOYSA-N 1-n'-(4-chlorophenyl)-1-n-[3-(4-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound C1=NC(C)=CN1CCCNC(=C[N+]([O-])=O)NC1=CC=C(Cl)C=C1 HYOMTYOMNXAQKB-UHFFFAOYSA-N 0.000 claims 1
- ZOWJSWANGDEHQV-UHFFFAOYSA-N 1-n'-cyclohexyl-1-n-[3-(5-methylimidazol-1-yl)propyl]-2-nitroethene-1,1-diamine Chemical compound CC1=CN=CN1CCCNC(=C[N+]([O-])=O)NC1CCCCC1 ZOWJSWANGDEHQV-UHFFFAOYSA-N 0.000 claims 1
- GZQGQPXNGNLMNL-UHFFFAOYSA-N 1-n-[3-(4-methylimidazol-1-yl)propyl]-1-n'-naphthalen-1-yl-2-nitroethene-1,1-diamine Chemical compound C1=NC(C)=CN1CCCNC(=C[N+]([O-])=O)NC1=CC=CC2=CC=CC=C12 GZQGQPXNGNLMNL-UHFFFAOYSA-N 0.000 claims 1
- QXWLNJOMXZMNTB-UHFFFAOYSA-N 1-n-[3-(4-methylimidazol-1-yl)propyl]-2-nitro-1-n'-(3,4,5-trimethoxyphenyl)ethene-1,1-diamine Chemical compound COC1=C(OC)C(OC)=CC(NC(NCCCN2C=C(C)N=C2)=C[N+]([O-])=O)=C1 QXWLNJOMXZMNTB-UHFFFAOYSA-N 0.000 claims 1
- XGCDJSAWMOUHID-UHFFFAOYSA-N 1-n-[3-(4-methylimidazol-1-yl)propyl]-2-nitro-1-n'-[4-(trifluoromethyl)phenyl]ethene-1,1-diamine Chemical compound C1=NC(C)=CN1CCCNC(=C[N+]([O-])=O)NC1=CC=C(C(F)(F)F)C=C1 XGCDJSAWMOUHID-UHFFFAOYSA-N 0.000 claims 1
- DRBBILLFANXMKL-UHFFFAOYSA-N 1-n-[3-(5-methylimidazol-1-yl)propyl]-2-nitro-1-n'-(3,4,5-trimethoxyphenyl)ethene-1,1-diamine Chemical compound COC1=C(OC)C(OC)=CC(NC(NCCCN2C(=CN=C2)C)=C[N+]([O-])=O)=C1 DRBBILLFANXMKL-UHFFFAOYSA-N 0.000 claims 1
- 102000013455 Amyloid beta-Peptides Human genes 0.000 claims 1
- 108010090849 Amyloid beta-Peptides Proteins 0.000 claims 1
- 102000009091 Amyloidogenic Proteins Human genes 0.000 claims 1
- 108010048112 Amyloidogenic Proteins Proteins 0.000 claims 1
- 206010003840 Autonomic nervous system imbalance Diseases 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 229940125373 Gamma-Secretase Inhibitor Drugs 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 101710144961 Interferon tau-1 Proteins 0.000 claims 1
- 101710144950 Interferon tau-2 Proteins 0.000 claims 1
- 101710144962 Interferon tau-3 Proteins 0.000 claims 1
- 102000004388 Interleukin-4 Human genes 0.000 claims 1
- 108090000978 Interleukin-4 Proteins 0.000 claims 1
- 229940082332 Muscarinic M1 receptor antagonist Drugs 0.000 claims 1
- 108010008881 NBI 5788 Proteins 0.000 claims 1
- 229940099433 NMDA receptor antagonist Drugs 0.000 claims 1
- 229930012538 Paclitaxel Natural products 0.000 claims 1
- 102100031674 Protein-L-isoaspartate(D-aspartate) O-methyltransferase Human genes 0.000 claims 1
- 102100028656 Sigma non-opioid intracellular receptor 1 Human genes 0.000 claims 1
- 101710104750 Sigma non-opioid intracellular receptor 1 Proteins 0.000 claims 1
- 208000025865 Ulcer Diseases 0.000 claims 1
- 229960000548 alemtuzumab Drugs 0.000 claims 1
- 229940035678 anti-parkinson drug Drugs 0.000 claims 1
- 239000000935 antidepressant agent Substances 0.000 claims 1
- 229940005513 antidepressants Drugs 0.000 claims 1
- 239000000939 antiparkinson agent Substances 0.000 claims 1
- 239000000164 antipsychotic agent Substances 0.000 claims 1
- 229940005529 antipsychotics Drugs 0.000 claims 1
- 239000002249 anxiolytic agent Substances 0.000 claims 1
- 230000000949 anxiolytic effect Effects 0.000 claims 1
- 229940005530 anxiolytics Drugs 0.000 claims 1
- 210000000467 autonomic pathway Anatomy 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 239000002439 beta secretase inhibitor Substances 0.000 claims 1
- 210000001124 body fluid Anatomy 0.000 claims 1
- 239000010839 body fluid Substances 0.000 claims 1
- 208000035269 cancer or benign tumor Diseases 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 208000010877 cognitive disease Diseases 0.000 claims 1
- 230000008021 deposition Effects 0.000 claims 1
- 229940002658 differin Drugs 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 230000004064 dysfunction Effects 0.000 claims 1
- 239000003623 enhancer Substances 0.000 claims 1
- 239000002792 enkephalinase inhibitor Substances 0.000 claims 1
- 229940088598 enzyme Drugs 0.000 claims 1
- 239000002532 enzyme inhibitor Substances 0.000 claims 1
- 229940125532 enzyme inhibitor Drugs 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- 239000003540 gamma secretase inhibitor Substances 0.000 claims 1
- 239000003395 histamine H3 receptor antagonist Substances 0.000 claims 1
- 239000002955 immunomodulating agent Substances 0.000 claims 1
- 229940121354 immunomodulator Drugs 0.000 claims 1
- 230000002584 immunomodulator Effects 0.000 claims 1
- 229960003444 immunosuppressant agent Drugs 0.000 claims 1
- 230000001861 immunosuppressant effect Effects 0.000 claims 1
- 239000003018 immunosuppressive agent Substances 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 108700027921 interferon tau Proteins 0.000 claims 1
- 229940028885 interleukin-4 Drugs 0.000 claims 1
- 229940121386 matrix metalloproteinase inhibitor Drugs 0.000 claims 1
- 239000003771 matrix metalloproteinase inhibitor Substances 0.000 claims 1
- 208000027061 mild cognitive impairment Diseases 0.000 claims 1
- 239000000234 muscarinic M1 receptor antagonist Substances 0.000 claims 1
- 239000003703 n methyl dextro aspartic acid receptor blocking agent Substances 0.000 claims 1
- GPQHOIQTHKOAGY-UHFFFAOYSA-N n'-[3-(5-methylimidazol-1-yl)propyl]-2-nitro-n-[4-(trifluoromethyl)phenyl]ethanimidamide Chemical compound CC1=CN=CN1CCCN=C(C[N+]([O-])=O)NC1=CC=C(C(F)(F)F)C=C1 GPQHOIQTHKOAGY-UHFFFAOYSA-N 0.000 claims 1
- KJIVXLFFKWSWIW-UHFFFAOYSA-N n-(2,3-dihydro-1,4-benzodioxin-6-yl)-n'-[3-(4-methylimidazol-1-yl)propyl]-2-nitroethanimidamide Chemical compound C1=NC(C)=CN1CCCN=C(C[N+]([O-])=O)NC1=CC=C(OCCO2)C2=C1 KJIVXLFFKWSWIW-UHFFFAOYSA-N 0.000 claims 1
- MZYLSVFGZFWYEJ-UHFFFAOYSA-N n-(2,3-dihydro-1,4-benzodioxin-6-yl)-n'-[3-(5-methylimidazol-1-yl)propyl]-2-nitroethanimidamide Chemical compound CC1=CN=CN1CCCN=C(C[N+]([O-])=O)NC1=CC=C(OCCO2)C2=C1 MZYLSVFGZFWYEJ-UHFFFAOYSA-N 0.000 claims 1
- OVKWACFPXWSZFC-UHFFFAOYSA-N n-(4-chlorophenyl)-n'-[3-(5-methylimidazol-1-yl)propyl]-2-nitroethanimidamide Chemical compound CC1=CN=CN1CCCN=C(C[N+]([O-])=O)NC1=CC=C(Cl)C=C1 OVKWACFPXWSZFC-UHFFFAOYSA-N 0.000 claims 1
- 229960005027 natalizumab Drugs 0.000 claims 1
- 230000009826 neoplastic cell growth Effects 0.000 claims 1
- 239000004090 neuroprotective agent Substances 0.000 claims 1
- 229960001592 paclitaxel Drugs 0.000 claims 1
- 230000001568 sexual effect Effects 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 claims 1
- 108010018276 trimethylguanosine synthase Proteins 0.000 claims 1
- 229940046728 tumor necrosis factor alpha inhibitor Drugs 0.000 claims 1
- 239000002452 tumor necrosis factor alpha inhibitor Substances 0.000 claims 1
- 0 BN(*)C(N*)=* Chemical compound BN(*)C(N*)=* 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91253707P | 2007-04-18 | 2007-04-18 | |
| US60/912,537 | 2007-04-18 | ||
| PCT/EP2008/054710 WO2008128981A1 (en) | 2007-04-18 | 2008-04-18 | Nitrovinyl-diamine derivatives as glutaminyl cyclase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010524893A JP2010524893A (ja) | 2010-07-22 |
| JP2010524893A5 true JP2010524893A5 (OSRAM) | 2011-05-19 |
| JP5675340B2 JP5675340B2 (ja) | 2015-02-25 |
Family
ID=39639570
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010503510A Expired - Fee Related JP5675340B2 (ja) | 2007-04-18 | 2008-04-18 | 新規阻害剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8772508B2 (OSRAM) |
| EP (1) | EP2142513B1 (OSRAM) |
| JP (1) | JP5675340B2 (OSRAM) |
| DK (1) | DK2142513T3 (OSRAM) |
| ES (1) | ES2468551T3 (OSRAM) |
| WO (1) | WO2008128981A1 (OSRAM) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7732162B2 (en) * | 2003-05-05 | 2010-06-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases |
| EP2142536B1 (en) * | 2007-04-20 | 2015-10-21 | Probiodrug AG | Aminopyrimidine derivatives as glutaminyl cyclase inhibitors |
| JP2011501652A (ja) * | 2007-09-12 | 2011-01-13 | プロビオドルグ エージー | トランスジェニックマウス |
| EP2238252B1 (en) * | 2008-01-14 | 2013-07-31 | Probiodrug AG | Mouse models carrying a knock-out mutation of the glutaminyl cyclase gene |
| AU2009273387B9 (en) | 2008-07-21 | 2015-06-11 | Vivoryon Therapeutics N.V. | Diagnostic antibody assay |
| US9925282B2 (en) | 2009-01-29 | 2018-03-27 | The General Hospital Corporation | Cromolyn derivatives and related methods of imaging and treatment |
| NZ598685A (en) | 2009-09-11 | 2013-05-31 | Probiodrug Ag | Heterocylcic derivatives as inhibitors of glutaminyl cyclase |
| US20110152341A1 (en) | 2009-12-22 | 2011-06-23 | Probiodrug Ag | Cleavage of b-amyloid precursor protein |
| US20110195161A1 (en) | 2010-02-08 | 2011-08-11 | Coca Cola Company | Solubility enhanced terpene glycoside(s) |
| US20110212853A1 (en) | 2010-02-18 | 2011-09-01 | Probiodrug Ag | Novel diagnostic method |
| SG192805A1 (en) | 2011-03-16 | 2013-09-30 | Probiodrug Ag | Diagnostic antibody assay |
| AU2013334874B2 (en) | 2012-10-25 | 2018-04-05 | The General Hospital Corporation | Combination therapies for the treatment of Alzheimer's disease and related disorders |
| US10525005B2 (en) | 2013-05-23 | 2020-01-07 | The General Hospital Corporation | Cromolyn compositions and methods thereof |
| CA2928028A1 (en) | 2013-10-22 | 2015-04-30 | The General Hospital Corporation | Cromolyn derivatives and related methods of imaging and treatment |
| JP2018501482A (ja) | 2014-12-19 | 2018-01-18 | プロビオドルグ エージー | ｐＧｌｕ−Ａｂｅｔａペプチドの検出のための新規の方法 |
| US20180305458A1 (en) * | 2015-10-16 | 2018-10-25 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of autoimmune inflammatory diseases |
| US20190240194A1 (en) | 2016-08-31 | 2019-08-08 | The General Hospital Corporation | Macrophages/microglia in neuro-inflammation associated with neurodegenerative diseases |
| AU2017423862A1 (en) | 2017-07-20 | 2020-02-06 | Aztherapies, Inc. | Powdered formulations of cromolyn sodium and ibuprofen |
| EP3461819B1 (en) | 2017-09-29 | 2020-05-27 | Probiodrug AG | Inhibitors of glutaminyl cyclase |
| EP3521308B1 (en) | 2018-01-31 | 2024-03-13 | Vivoryon Therapeutics N.V. | Humanized and de-immunized antibodies |
| AU2019299347A1 (en) | 2018-07-02 | 2021-01-21 | Aztherapies, Inc. | Powdered formulations of cromolyn sodium and alpha-lactose |
| SG11202106117SA (en) | 2018-12-10 | 2021-07-29 | Massachusetts Gen Hospital | Cromolyn esters and uses thereof |
| US12458622B2 (en) | 2020-04-06 | 2025-11-04 | The General Hospital Corporation | Methods of treatment of coronavirus-induced inflammation conditions |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4277485A (en) * | 1973-05-17 | 1981-07-07 | Smith Kline & French Laboratories Limited | Oxazole or isoxazole alkylamino ethylene compounds as inhibitors of H-2 histamine receptors |
| DE3044566A1 (de) * | 1980-11-26 | 1982-07-15 | Basf Ag, 6700 Ludwigshafen | N-substituierte imidazol-derivate, ihre herstellung, diese enthaltende arzneimittel und ihre verwendung |
| WO2001070696A1 (en) | 2000-03-21 | 2001-09-27 | Ishihara Sangyo Kaisha, Ltd. | Nitroethenamine derivatives or salts thereof and pharmaceutical compositions containing the derivatives or the salts |
| US6948038B2 (en) * | 2001-07-24 | 2005-09-20 | Microsoft Corporation | System and method for backing up and restoring data |
| US8338120B2 (en) * | 2003-05-05 | 2012-12-25 | Probiodrug Ag | Method of treating inflammation with glutaminyl cyclase inhibitors |
| NZ568459A (en) * | 2003-05-05 | 2009-06-26 | Probiodrug Ag | Use of effectors of glutaminyl and glutamate cyclases |
| US7732162B2 (en) * | 2003-05-05 | 2010-06-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases |
| ZA200508439B (en) * | 2003-05-05 | 2007-03-28 | Probiodrug Ag | Medical use of inhibitors of glutaminyl and glutamate cyclases |
| NZ546322A (en) * | 2003-10-15 | 2008-11-28 | Probiodrug Ag | Use of effectors of glutaminyl and glutamate cyclases |
| US20050171112A1 (en) * | 2003-11-03 | 2005-08-04 | Probiodrug Ag | Combinations useful for the treatment of neuronal disorders |
| EP1680120A2 (en) * | 2003-11-03 | 2006-07-19 | Probiodrug AG | Combinations useful for the treatment of neuronal disorders |
| US7667044B2 (en) * | 2003-11-03 | 2010-02-23 | Probiodrug Ag | Compounds for the treatment of neurological disorders |
| CA2554809C (en) * | 2004-02-05 | 2014-04-29 | Probiodrug Ag | Novel n-alkyl thiourea- and thioamide-substituted imidazolyl inhibitors of glutaminyl cyclase |
| EP2082041B1 (en) * | 2006-09-21 | 2018-03-14 | Probiodrug AG | Novel genes related to glutaminyl cyclase |
| US8420684B2 (en) * | 2006-11-09 | 2013-04-16 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| ES2481442T3 (es) * | 2006-11-09 | 2014-07-30 | Probiodrug Ag | Inhibidores novedosos de glutaminil ciclasa |
| US9126987B2 (en) * | 2006-11-30 | 2015-09-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| SI2121944T1 (sl) * | 2007-01-19 | 2011-12-30 | Probiodrug Ag | In vivo presejalni modeli za zdravljenje Alzheimerjeve bolezni in drugih motenj, povezanih s QPCT |
| EP2118101B1 (en) * | 2007-03-09 | 2012-09-26 | Probiodrug AG | Imidazo [1,5-a] pyridine derivatives as inhibitors of glutaminyl cyclase |
-
2008
- 2008-04-18 DK DK08736360.2T patent/DK2142513T3/da active
- 2008-04-18 ES ES08736360.2T patent/ES2468551T3/es active Active
- 2008-04-18 US US12/105,730 patent/US8772508B2/en active Active
- 2008-04-18 JP JP2010503510A patent/JP5675340B2/ja not_active Expired - Fee Related
- 2008-04-18 WO PCT/EP2008/054710 patent/WO2008128981A1/en not_active Ceased
- 2008-04-18 EP EP08736360.2A patent/EP2142513B1/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2010524893A5 (OSRAM) | ||
| JP2010524898A5 (OSRAM) | ||
| JP2010524895A5 (OSRAM) | ||
| JP2010524899A5 (OSRAM) | ||
| JP2010524897A5 (OSRAM) | ||
| JP2010524896A5 (OSRAM) | ||
| JP2010509284A5 (OSRAM) | ||
| JP2010511013A5 (OSRAM) | ||
| JP2013504544A5 (OSRAM) | ||
| JP2010509286A5 (OSRAM) | ||
| JP2010509285A5 (OSRAM) | ||
| JP2010520869A5 (OSRAM) | ||
| JP2013521325A5 (OSRAM) | ||
| JP2020512373A5 (OSRAM) | ||
| JP2013521260A5 (OSRAM) | ||
| JP2012502006A5 (OSRAM) | ||
| JP5191497B2 (ja) | Ｓ１ｐ受容体調節化合物およびその使用 | |
| IL307911A (en) | New inhibitors | |
| EA022420B1 (ru) | Гетероциклические ингибиторы глутаминилциклазы (qc, ec 2.3.2.5) | |
| AU782191B2 (en) | Substituted 1-aminoalkyl-lactams and their use as muscarinic receptor antagonists | |
| JP2013525334A5 (OSRAM) | ||
| JP2014508184A5 (OSRAM) | ||
| KR20130042590A (ko) | 기질 메탈로프로테나제 저해제 | |
| US11479550B2 (en) | EP4 antagonist | |
| JP3555620B2 (ja) | Ｎ−フェニル−アリールスルフォンアミド化合物、その化合物を有効成分として含有する薬剤、その化合物の合成中間体およびその製造方法 |