AR054627A1 - GLICINAMIDAS SUSTITUíDAS COMO INHIBIDORES DE LA SERINA PROTEASAS Y DEL FACTOR XA Y SU USO EN LA PREPARACIoN DE MEDICAMENTOS PARA EL TRATAMIENTO DE ENFERMEDADES TROMBoTICAS. - Google Patents
GLICINAMIDAS SUSTITUíDAS COMO INHIBIDORES DE LA SERINA PROTEASAS Y DEL FACTOR XA Y SU USO EN LA PREPARACIoN DE MEDICAMENTOS PARA EL TRATAMIENTO DE ENFERMEDADES TROMBoTICAS.Info
- Publication number
- AR054627A1 AR054627A1 ARP060102825A ARP060102825A AR054627A1 AR 054627 A1 AR054627 A1 AR 054627A1 AR P060102825 A ARP060102825 A AR P060102825A AR P060102825 A ARP060102825 A AR P060102825A AR 054627 A1 AR054627 A1 AR 054627A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- amino
- alkyloxy
- substituted
- Prior art date
Links
- 108010022999 Serine Proteases Proteins 0.000 title abstract 2
- 102000012479 Serine Proteases Human genes 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title abstract 2
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 34
- -1 nitro, amino, hydroxy, methoxy Chemical group 0.000 abstract 16
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 12
- 125000003545 alkoxy group Chemical group 0.000 abstract 10
- 125000001153 fluoro group Chemical group F* 0.000 abstract 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 6
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 5
- 150000003254 radicals Chemical class 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 abstract 4
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 3
- 229910052731 fluorine Inorganic materials 0.000 abstract 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- 125000006560 (C1-C5)alkylcarbonylamino group Chemical group 0.000 abstract 2
- NQPJDJVGBDHCAD-UHFFFAOYSA-N 1,3-diazinan-2-one Chemical compound OC1=NCCCN1 NQPJDJVGBDHCAD-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 2
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical group C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 abstract 2
- YPWFISCTZQNZAU-UHFFFAOYSA-N Thiane Chemical compound C1CCSCC1 YPWFISCTZQNZAU-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- HTFFABIIOAKIBH-UHFFFAOYSA-N diazinane Chemical compound C1CCNNC1 HTFFABIIOAKIBH-UHFFFAOYSA-N 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 239000012634 fragment Substances 0.000 abstract 2
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 abstract 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000001174 sulfone group Chemical group 0.000 abstract 2
- 150000003462 sulfoxides Chemical class 0.000 abstract 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 2
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 abstract 2
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 abstract 1
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 abstract 1
- 125000006562 (C1-C5) alkyloxycarbonylamino group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 abstract 1
- OYELEBBISJGNHJ-UHFFFAOYSA-N 1,3-oxazinan-2-one Chemical compound O=C1NCCCO1 OYELEBBISJGNHJ-UHFFFAOYSA-N 0.000 abstract 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 abstract 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- 229940123583 Factor Xa inhibitor Drugs 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 abstract 1
- 229940122055 Serine protease inhibitor Drugs 0.000 abstract 1
- 208000007536 Thrombosis Diseases 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005336 allyloxy group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 abstract 1
- 229940050390 benzoate Drugs 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 229940001468 citrate Drugs 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 1
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 abstract 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 230000004770 neurodegeneration Effects 0.000 abstract 1
- 208000015122 neurodegenerative disease Diseases 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 abstract 1
- 125000003566 oxetanyl group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 abstract 1
- 229960001860 salicylate Drugs 0.000 abstract 1
- 229940086735 succinate Drugs 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 abstract 1
- 150000003457 sulfones Chemical class 0.000 abstract 1
- 229940095064 tartrate Drugs 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 1
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 abstract 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 abstract 1
- 230000001732 thrombotic effect Effects 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
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- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
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- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Immunology (AREA)
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Abstract
Compuestos inhibidores de la serina proteasas y del factor Xa y su utilizacion en medicamentos para tratar enfermedades tromboticas y neurodegenerativas Reivindicacion 1: Compuestos de la formula general (1), en la que D representa un sistema de anillo bicíclico sustituido de la formula (2), en el que K1y K4, en cada caso independientemente uno de otro, significan un grupo -CH2, -CHR7a, -CR7bR7c- o un grupo -C(O), y en donde R7a/R7b/R7c, en cada caso independientemente uno de otro, significan un átomo de fluor, un grupo hidroxi, alquiloxi C1-5, tetrahidrofuranilo, oxetanilo, amino, alquil C1-5-amino, di-(alquil C1-5)-amino, cicloalquilen C3-5-imino o alquil C1-5-carbonilamino, un grupo alquilo C1-5, que puede estar sustituido con 1-3 átomos de fluor, un grupo hidroxi-alquilo C1-5, alquiloxi C1-5-alquilo C1-5, amino-alquilo C1-5, alquil C1-5-amino-alquilo C1-5, di-(alquil C1-5)-amino-alquilo C1-5, cicloalquilen C4-7-imino-alquilo C1-5, carboxi-alquilo C0-5, alquiloxi C1-5- carbonil-alquilo C0-5, aminocarbonil-alquilo C0-5, alquil C1-5-aminocarbonil-alquilo C0-5, di-(alquil C1-5)-aminocarbonil-alquilo C0-5, cicloalquilen C4-7-iminocarbonil-alquilo C0-5, un grupo fenilo o un grupo heteroarilo de 5 a 6 miembros, que puede estar sustituido con 1-2 sustituyentes seleccionados de un grupo nitro, amino, hidroxi, metoxi, ciano, alquilo C1-5 o un átomo de fluor, cloro o bromo, en donde al mismo tiempo los dos radicales R7b/R7c no pueden estar unidos al átomo de carbono del anillo a través de un heteroátomo, a excepcion de que -C(R7bR7c)- corresponda a un grupo -CF2, o dos radicales R7b/R7c, junto con el átomo de carbono del anillo, pueden formar un carbociclo saturado de 3, 4, 5, 6 o 7 miembros, o un anillo de ciclopenteno, ciclohexeno, oxetano, azetidina, tietano, tetrahidrofurano, pirrolidina, tetrahidrotiofeno, tetrahidropirano, piperidina, sulfuro de pentametileno, hexametilenimina, 1,3-dioxolano, 1,4-dioxano, hexahidropiridazina, piperazina, tiomorfolina, morfolina, 2-imidazolidinona, 2-oxazolidinona, tetrahidro-2(1H)pirimidinona, [1,3]oxazinan-2-ona, en donde sus grupos metileno pueden estar sustituidos con 1-2 grupos alquilo C1-3 o CF3, y/o sus grupos metileno, en la medida en que no estén unidos a un heteroátomo, pueden estar sustituidos con 1-2 átomos de fluor, y/o en el que un grupo -CH2, junto a un átomo de N, puede estar reemplazado por un grupo -CO, y/o sus grupos imino pueden estar sustituidos en cada caso con un grupo alquilo C1-3 o alquil C1-3-carbonilo, y/o en el que el átomo de azufre puede estar oxidado en un sulfoxido o grupo sulfona; K2 y K3, en cada caso independientemente uno de otro, significan un grupo - CH2-, CHR8a., .CR8bR8c o un grupo -C(O), y en donde R8a/R8b/R8c, en cada caso independientemente uno de otro, significa un grupo alquilo C1-5, que puede estar sustituido con 1-3 átomos de fluor, un grupo hidroxi-alquilo C1-5, alquiloxi C1-5-alquilo C1-5, amino-alquilo C1-5, alquil C1-5-amino-alquilo C1-5, di-(alquil C1-5)-amino-alquilo C1-5, cicloalquilen C4-7-imino-alquilo C1-5, carboxi-alquilo C0-5, alquiloxi C1-5-carbonil-alquilo C0-5, aminocarbonil-alquilo C0-5, alquil C1-5-aminocarbonil-alquilo C0-5, di-(alquil C1- 5)-aminocarbonil-alquilo C0-5, cicloalquilen C4-7-iminocarbonil-alquilo C0-5, o dos radicales R8b/R8c, junto con el átomo de carbono del anillo, pueden formar un carbociclo saturado de 3, 4, 5, 6 o 7 miembros, o un anillo de ciclopenteno, ciclohexeno, oxetano, azetidina, tietano, tetrahidrofurano, pirrolidina, tetrahidrotiofeno, tetrahidropirano, piperidina, sulfuro de pentametileno, hexametilenimino, hexahidropiridazina, tetrahidro-2(1H)-pirimidinona, [1,3joxazinan-2-ona, en donde sus grupos metileno pueden estar sustituidos con 1-2 grupos alquilo C1-3 o CF3, y/o sus grupos metileno, en la medida en que no estén unidos a un heteroátomo, pueden estar sustituidos con 1-2 átomos de fluor, y/o en el que un grupo -CH2, junto a un átomo de nitrogeno, puede estar reemplazado por un grupo -CO, y/o sus grupos imino pueden estar sustituidos en cada caso con un grupo alquilo C1-3 o alquil C1-3-carbonilo, y/o en el que el átomo de azufre puede estar oxidado en un sulfoxido o grupo sulfona, con la condicion de que un heteroátomo incorporado por R8b o R8c no pueda ser separado por solo un átomo de carbono de X en la formula (1), y en la formula (2) pueden estar presentes en total como máximo cuatro radicales seleccionados de R7a, R7b, R7c, R8a, R8b y R8c, y X significa un átomo de oxigeno o azufre, un grupo sulfeno, sulfona, o un grupo NR1, en el que R1 significa un átomo de hidrogeno o un grupo hidroxi, alquiloxi C1-3, amino, alquil C1-3-amino, di-(alquil C1-3)-amino, un grupo alquilo C1-5, alquenil C2-5-CH2, alquinil C2-5-CH2, cicloalquilo C3-6, cicloalquenilo C4-6, oxetan-3-ilo, tetrahidrofuran-3-ilo, bencilo, alquil C1-5-carbonilo, trifluorometilcarbonilo, cicloalquil C3-6-carbonilo, alquil C1-5-sulfonilo, cicloalquil C3-6-sulfonilo, amino-carbonilo, alquil C1-5-aminocarbonilo, di-(alquil C1-5)-aminocarbonilo, alquiloxi C1-5-carbonilo, cicloalquilen C4-7-iminocarbonilo, en donde los grupos metileno y metilo que se encuentran en los grupos mencionados precedentemente pueden estar adicionalmente sustituidos con un grupo alquilo C1-3, carboxi, alcoxi C1-5-carbonilo o con un grupo hidroxi, alquiloxi C1-5, amino, alquil C1-5-amino, dialquil C1-5-amino o cicloalquilen C4-7-imino, en la medida en que los grupos metileno o metilo no estén unidos directamente a un heteroátomo del grupo O, N o S, y/o uno a tres átomos de hidrogeno pueden estar reemplazados por átomos de fluor, en la medida en que los grupos metileno o metilo no estén unidos directamente a un heteroátomo del grupo O, N o S, y en el que A1 significa N o CR10; A2 significa N o CR11; A3 significa N o CR12; en donde R10, R11 y R12, en cada caso independientemente uno de otro, significan un átomo de hidrogeno, fluor, cloro, bromo o yodo, o un grupo alquilo C1-5, CF3, alquenilo C2-5, alquinilo C2-5, un grupo ciano, carboxi, alquiloxi C1-5-carbonilo, hidroxi, alquiloxi C1-3, CF3O-, CHF2O-, CH2FO-, amino, alquil C1-5-amino, di-(alquil C1-5)-amino o cicloalquilen C4-7- imino, o D representa uno de los cuatro grupos (3), (4), (5) o (6); en la que los radicales A1, A2, A3, K1, K2, K3, K4 están definidos como arriba; y Anion en la formula (5) significa un fluoruro, cloruro, bromuro, yoduro, sulfato, hidrogeno- sulfato, fosfato, hidrogeno-fosfato, benzoato, salicilato, succinato, citrato o tartrato; R3 significa un átomo de hidrogeno o un grupo alquilo C1-3; y R4 y R5, en cada caso independientemente uno de otro, significan un átomo de hidrogeno, un grupo alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 de cadena lineal o ramificada, en donde los átomos de hidrogeno de los fragmentos metileno y/o metilo del grupo alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 de cadena lineal o ramificada pueden estar reemplazados, eventualmente en su totalidad o en parte, con átomos de fluor, y/o en donde uno o dos átomos de hidrogeno del grupo alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 de cadena lineal o ramificada pueden estar sustituidos en sus fragmentos metileno y/o metilo, eventualmente en cada caso independientemente uno de otro, con un grupo cicloalquilo C3-7, un grupo nitrilo, hidroxi o alquiloxi C1-5, en donde los átomos de hidrogeno del grupo alquiloxi C1-5 pueden estar reemplazados, eventualmente en su totalidad o en parte, por átomos de fluor, un grupo aliloxi, propargiloxi, fenilmetiloxi, fenetiloxi, alquil C1-5-carboniloxi, alquiloxi C1-5-carboniloxi, carboxi-alquiloxi C1-5, alquiloxi C1-5-carbonil-alquiloxi , alquiloxi C1-5- alquiloxi C2-5, mercapto, alquil C1-5-sulfanilo, alquil C1-5-sulfinilo, alquil C1-5-sulfonilo, carboxi, alquiloxi C1-5-carbonilo, aminocarbonilo, alquil C1-5-aminocarbonilo, di-(alquil C1-5)-aminocarbonilo, alquil C1-5-aminocarboniloxi, di-(alquil C1-5)-aminocarboniloxi, cicloalquilen C4-7-iminocarbonilo, aminosulfonilo, alquil C1-5-aminosulfonilo, di(alquil C1-5)-aminosulfonilo, cicloalquilen C4-7-iminosulfonilo, di-(alquil C1-5)-fosforilo, amino, alquil C1-5-amino, di-(alquil C1-5)-amino, alquil C1-5-carbonilamino, trifluoroacetilamino, alquiloxi C1-5-alquil C1-5-carbonilamino, fenilcarbonilamino, alquil C1-5aminocarbonilamino, di-(alquil C1-5)-aminocarbonilamino, alquiloxi C1-5-carbonilamino, fenilmetiloxi-carbonilamino, alquiloxi C1-5-alquiloxi C2-5-alquil- C1-2-carbonilamino, alquil C1-5-sulfonilamino, N-(alquil C1-5-sulfonil)-alquil C0-5-amino, cicloalquil C3-6carbonilamlno, 4-morfolinocarbonilamino, o un grupo morfolinilo, tiomorfolinilo, plrrolidinilo, piperidinilo, piperazinilo, tetrahidrofuranilo, tetrahidropiranilo, en donde los carbociclos y heterociclos en el anillo antes mencionados pueden estar sustituidos en cada caso con 1 a 4 grupos alquilo C1-3 o alquil C1-3-carbonilo, o en cada caso con 1 o 2 grupos oxo, y/o en donde los radicales fenilo y heteroarilo antes mencionados pueden estar reemplazados por 1 o 2 sustituyentes seleccionados de fluoro, cloro, bromo, metilo, metoxi, amino o trifluorometilo, o dos átomos de carbono vecinos de un anillo de fenilo pueden estar sustituidos con un grupo -CH2-O-CH2, y/o en donde los grupos alquilo antes mencionados pueden estar sustituidos con un grupo ciano-alquiloxi C1-5-carbonilo o carboxi, en donde las amidas de ácido carboxílico o sulfonico antes mencionadas pueden estar eventualmente sustituidas en el nitrogeno, adicionalmente, con un grupo alquilo C1-5, y/o en donde los átomos de hidrogeno de los átomos de carbono sp2-hibridados del grupo alquenilo C2-6 de cadena lineal o ramificada pueden estar reemplazados, en su totalidad o en parte, por átomos de fluor, un grupo carboxi, aminocarbonilo, alquil C1-5-aminocarbonilo, cicloalquil 3-6-aminocarbonilo, di-(alquil C1-5)-aminocarbonilo, alquiloxi C1-5-carbonilo, cicloalquilen C4-7- iminocarbonilo, un grupo fenilo, heteroarilo mono- o bi-cíclico, fenil-alquilo C1-5 o heteroaril-alquilo C1-5 mono- o bicíclico, que en la p
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| PE20080145A1 (es) | 2006-03-21 | 2008-02-11 | Janssen Pharmaceutica Nv | Tetrahidro-pirimidoazepinas como moduladores de trpv1 |
| JP2009543812A (ja) * | 2006-07-20 | 2009-12-10 | キャスケイド・セラピューティクス・インコーポレイテッド | 5−HT2Cリガンドとしてのテトラヒドロ−5H−ピリド[2,3−d]アゼピン |
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| WO2005111029A1 (de) * | 2004-05-13 | 2005-11-24 | Boehringer Ingelheim International Gmbh | Neue substituierte thiophencarbonsäureamide, deren herstellung und deren verwendung als arzneimittel |
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