AR078509A1 - Derivados nitrilo y composiciones farmaceuticas - Google Patents
Derivados nitrilo y composiciones farmaceuticasInfo
- Publication number
- AR078509A1 AR078509A1 ARP100101715A ARP100101715A AR078509A1 AR 078509 A1 AR078509 A1 AR 078509A1 AR P100101715 A ARP100101715 A AR P100101715A AR P100101715 A ARP100101715 A AR P100101715A AR 078509 A1 AR078509 A1 AR 078509A1
- Authority
- AR
- Argentina
- Prior art keywords
- disubstituted
- ring
- rings
- double bonds
- saturated
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 150000002825 nitriles Chemical class 0.000 title 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 10
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 9
- 125000001424 substituent group Chemical group 0.000 abstract 9
- -1 6-cyanomethylpyridin-2-yl Chemical group 0.000 abstract 7
- 229910052757 nitrogen Inorganic materials 0.000 abstract 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- 239000011593 sulfur Substances 0.000 abstract 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Chemical group 0.000 abstract 4
- ABSHJWZFDFHKRH-UHFFFAOYSA-N 2-cyanoethyl carbamimidothioate Chemical compound NC(=N)SCCC#N ABSHJWZFDFHKRH-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- OTRRKMLWFXJTKO-UHFFFAOYSA-N cyanomethyl carbamimidothioate Chemical compound NC(=N)SCC#N OTRRKMLWFXJTKO-UHFFFAOYSA-N 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- GUWGDCBFBSPGKP-UHFFFAOYSA-N (4-cyanophenyl)methyl carbamimidothioate Chemical compound NC(=N)SCC1=CC=C(C#N)C=C1 GUWGDCBFBSPGKP-UHFFFAOYSA-N 0.000 abstract 1
- OEAWSIQIFPMNMW-UHFFFAOYSA-N 1-[4-(2-cyanoethyl)phenyl]-1-ethylthiourea Chemical compound C(#N)CCC1=CC=C(C=C1)N(C(S)=N)CC OEAWSIQIFPMNMW-UHFFFAOYSA-N 0.000 abstract 1
- XJHGAJLIKDAOPE-UHFFFAOYSA-N 2-(4-phenylmethoxyphenyl)acetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1OCC1=CC=CC=C1 XJHGAJLIKDAOPE-UHFFFAOYSA-N 0.000 abstract 1
- YPIIOSFGVPJSFB-UHFFFAOYSA-N 2-cyanoethyl carbamimidothioate;4-methylbenzenesulfonic acid Chemical compound NC(=N)SCCC#N.CC1=CC=C(S(O)(=O)=O)C=C1 YPIIOSFGVPJSFB-UHFFFAOYSA-N 0.000 abstract 1
- PRDJGNVQBVXXEO-UHFFFAOYSA-N 3-cyanopropyl carbamimidothioate Chemical compound NC(=N)SCCCC#N PRDJGNVQBVXXEO-UHFFFAOYSA-N 0.000 abstract 1
- GKCAFDQZKXHYMS-UHFFFAOYSA-N 3-cyanopropyl carbamimidothioate;2,4,6-trinitrophenol Chemical compound NC(=N)SCCCC#N.OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O GKCAFDQZKXHYMS-UHFFFAOYSA-N 0.000 abstract 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 abstract 1
- FURREXICPKHHBX-UHFFFAOYSA-N 4-cyanobutyl carbamimidothioate Chemical compound NC(=N)SCCCCC#N FURREXICPKHHBX-UHFFFAOYSA-N 0.000 abstract 1
- GDMSDVOTQBUXDJ-UHFFFAOYSA-N 5-cyanopentyl carbamimidothioate Chemical compound NC(=N)SCCCCCC#N GDMSDVOTQBUXDJ-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 1
- KQJQICVXLJTWQD-UHFFFAOYSA-N N-Methylthiourea Chemical compound CNC(N)=S KQJQICVXLJTWQD-UHFFFAOYSA-N 0.000 abstract 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract 1
- RZDXIVGFLZZOAA-UHFFFAOYSA-N [2-(cyanomethyl)phenyl] n'-methylcarbamimidothioate Chemical compound CNC(=N)SC1=CC=CC=C1CC#N RZDXIVGFLZZOAA-UHFFFAOYSA-N 0.000 abstract 1
- SOVIHQQCQAGMGK-UHFFFAOYSA-N [3-(cyanomethyl)phenyl] n'-methylcarbamimidothioate Chemical compound CNC(=N)SC1=CC=CC(CC#N)=C1 SOVIHQQCQAGMGK-UHFFFAOYSA-N 0.000 abstract 1
- OVNZBJMYSIFNOO-UHFFFAOYSA-N [4-(cyanomethyl)phenyl] n'-methylcarbamimidothioate Chemical compound CNC(=N)SC1=CC=C(CC#N)C=C1 OVNZBJMYSIFNOO-UHFFFAOYSA-N 0.000 abstract 1
- 125000005577 anthracene group Chemical group 0.000 abstract 1
- SISAYUDTHCIGLM-UHFFFAOYSA-N bromine dioxide Inorganic materials O=Br=O SISAYUDTHCIGLM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- OSVXSBDYLRYLIG-UHFFFAOYSA-N chlorine dioxide Inorganic materials O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 abstract 1
- 235000019398 chlorine dioxide Nutrition 0.000 abstract 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052737 gold Inorganic materials 0.000 abstract 1
- 239000010931 gold Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- WXDJHDMIIZKXSK-UHFFFAOYSA-N iodine dioxide Inorganic materials O=I=O WXDJHDMIIZKXSK-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000619 oxo-lambda(3)-bromanyloxy group Chemical group *OBr=O 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/02—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton
- C07C255/03—Mononitriles
-
- 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
- A61K31/275—Nitriles; Isonitriles
-
- 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
- A61K31/275—Nitriles; Isonitriles
- A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
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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]
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- 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
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- 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
-
- 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
- A61P31/12—Antivirals
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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
- A61P35/02—Antineoplastic agents specific for leukemia
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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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
- C07C335/32—Isothioureas having sulfur atoms of isothiourea groups bound to acyclic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
- C07C335/34—Isothioureas having sulfur atoms of isothiourea groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
- C07C335/36—Isothioureas having sulfur atoms of isothiourea groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/57—Nitriles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
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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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Virology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Quinoline Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicacion 8: Una composicion farmacéutica de acuerdo con cualquiera de las reivindicaciones 1 a 4, composicion ésta que incluye un compuesto seleccionado a partir de S-(2-cianoetil)isotiourea, S-(4-cianobutil)isotiourea, S-(5-cianopentil)isotiourea, S-(4-cianometilfenil)metilisotiourea, S-2(4-[2-cianoetil]fenil)etilisotiourea, S-(2-cianometilfenil)metilisotiourea, S-(6-cianometilpiridin-2-il)metilisotiourea, S-(3-cianometilfenil)metilisotiourea, S-(1-cianometilnaft-2-il))metilisotiourea y las sales farmacéuticamente aceptables del mismo y un vehículo farmacéuticamente aceptable. Reivindicacion 32: Un compuesto de la formula (1) donde Z es seleccionado a partir de azufre, cobre, plata, oro y platino o Z es una estructura contentiva de halogenos seleccionada a partir de ClO2, BrO2, e IO2, donde n es igual a cero o es un numero entero comprendido entre 1 y 8 y m es igual a cero o es un numero entero comprendido entre 1 y 8; R1, R2 y R3 son seleccionados de manera independiente a partir de hidrogeno, -CH2-ciclohexilo, alquilo C1-6, alquenilo C2-6 y alquinilo C2-6, donde las estructuras alquilo de dichos grupos alquilo, alquenilo y alquinilo pueden ser lineales, ramificadas y cíclicas y combinaciones de estructuras alquilo, alquenilo y alquinilo, lineales, ramificadas y cíclicas y donde estos grupos pueden ser sustituidos con grupos seleccionados a partir de metilo, etilo, propilo, isopropilo, n-butilo, t-butilo, metoxi, etoxi, O-n-propilo, O-isopropilo, O-n-butilo y O-t-butilo; o R1 y R2, tomados conjuntamente con los nitrogenos a los cuales se encuentran directamente acoplados y con el carbono que está acoplado a los nitrogenos, forman un anillo de cinco o más miembros, donde p es un numero entero comprendido entre 1 y 7, conforme se ilustra en formula (2) donde la línea discontinua representa un enlace doble opcional, siempre que, cuando exista este enlace doble, R3 esté ausente y el grupo CH2 adyacente al enlace doble tenga un hidrogeno en lugar de dos hidrogenos, o R2 y R3, tomados conjuntamente con el nitrogeno al cual se encuentran acoplados, forman un anillo de tres o más miembros, donde p es un numero entero comprendido entre 1 y 7, conforme se ilustra en formula (3); W está ausente o W es seleccionado a partir de -CH2-, -CH2-CH2-, trans - CH=CH-, cis -CH=CH-, -C:::C-, -CHR4-CHR5-, trans -C R4=C R5-, cis -CR4=CR5-, donde R4 y R5 son seleccionados de manera independiente a partir de -CH2-ciclohexilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 y éter alquílico C1-6 (igualmente denominado alquilo C1-6-O-); o W es una estructura disustituida, donde se utiliza el término disustituido para indicar como se acopla W a los grupos (CH2)m y (CH2)n, estructura ésta que es seleccionada a partir del grupo de estructuras disustituidas constituido por (a) un anillo de seis miembros 1,2-, 1,3- o 1,4-disustituido que puede ser saturado o insaturado con uno, dos o tres enlaces dobles; un anillo de cinco miembros 1,2- o 1,3-disustituido que puede ser saturado o insaturado con uno o dos enlaces dobles; un anillo de cuatro miembros 1,2- o 1,3-disustituido que puede ser saturado o insaturado con uno o dos enlaces dobles; o un anillo de tres miembros 1,2-disustituido que puede ser saturado e insaturado con un enlace doble, conforme se ilustra en las formulas (4), donde los sustituyentes de estos anillos disustituidos son los grupos acoplados a W en la formula (1) donde las líneas discontinuas son indicativas de enlaces dobles opcionales; (b) un anillo de seis miembros 1,2-, 1,3- o 1,4-disustituido que puede ser saturado o insaturado con uno, dos o tres enlaces dobles; un anillo de cinco miembros 1,2- o 1,3-disustituido que puede ser saturado o insaturado con uno o dos enlaces dobles; un anillo de cuatro miembros 1,2- o 1,3-disustituido que puede ser saturado o insaturado con uno o dos enlaces dobles; o un anillo de tres miembros 1,2-disustituido que puede ser saturado e insaturado con un enlace doble, conforme se ilustra en las formulas (4), donde los sustituyentes de estos anillos disustituidos son los grupos acoplados a W en la formula (1) y donde los anillos disustituidos pueden incluir sustituyentes adicionales R6, R7, R8, y R9 conforme se ilustra en formulas (5) donde las líneas discontinuas son indicativas de enlaces dobles opcionales; donde R6, R7, R8 y R9 son seleccionados de manera independiente a partir de hidrogeno, -CH2-ciclohexilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o éter alquílico C1-6; donde el anillo de seis miembros pueden ser saturado o disponer de uno, dos o tres enlaces dobles, los anillos de cuatro y cinco miembros pueden ser saturados o incluir uno o dos enlaces dobles y el anillo de tres miembros puede ser saturado o disponer de un enlace doble; donde Y es nitrogeno, oxígeno o azufre; (c) un anillo seleccionado a partir de los anillos de 9 miembros 1,2-, 1,3-, 1,4-, 1,5-, 1,6- o 1,7-disustituidos, saturados e insaturados con uno o más enlaces dobles, con las posiciones de los anillos enumeradas conforme se ilustra en el primer anillo de formula (6), anillo éste que es seleccionado a partir del anillo de formula (7) a (18), donde los sustituyentes de estos anillos disustituidos son los grupos acoplados a W en la formula (1) y donde los anillos disustituidos pueden incluir sustituyentes adicionales R6, R7, R8, R9 y R10 y donde las líneas discontinuas son indicativas de enlaces dobles opcionales; donde R6, R7, R8, R9 y R10 son seleccionados de manera independiente a partir de hidrogeno, -CH2-ciclohexilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o éter alquílico C1-6 donde Y es nitrogeno, oxígeno o azufre; (d) un anillo seleccionado a partir de los anillos de naftaleno 1,2-, 13-, 1,4-, 1,5-, 1,6-, 1,7- o 1,8-disustituidos, saturados e insaturados con uno o más enlaces dobles, con las posiciones de los anillos enumeradas conforme se ilustra en el anillo de formula (19), anillos éstos que son seleccionados a partir del anillo de formula (20) a (24), donde los sustituyentes de estos anillos disustituidos son los grupos acoplados a W en la formula (1) y donde los anillos disustituidos pueden incluir sustituyentes adicionales R6, R7, R8, R9, R10 y R11 y donde las líneas discontinuas son indicativas de enlaces dobles opcionales; donde R6, R7, R8, R9, R10 y R11 son seleccionados de manera independiente a partir de hidrogeno, -CH2-ciclohexilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, o éter alquílico C1-6 donde Y es nitrogeno, oxígeno o azufre; y (e) un anillo seleccionado a partir de los anillos de antraceno 1,2-, 1,3-, 1,4-, 1,5-, 1,6-, 1,7-, 1,8-, 1,9-, 1,10-, 2,5-, 3,5-, 4,5- o 5,10- disustituidos, saturados e insaturados con uno o más enlaces dobles, con las posiciones de los anillos enumeradas conforme se ilustra en el anillo de formula (25), anillo éste que es seleccionado a partir del anillo de formula (26) a (33), donde los sustituyentes de estos anillos disustituidos son los grupos acoplados a W en la formula (1) y donde los anillos disustituidos pueden incluir sustituyentes adicionales R6, R7, R8, R9, R10, R11, R12 y R13 donde las líneas discontinuas son indicativas de enlaces dobles opcionales; donde R6, R7, R8, R9, R10, R11, R12 y R13 son seleccionados de manera independiente a partir de hidrogeno, -CH2-ciclohexilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o éter alquílico C1-6 donde Y es nitrogeno, oxígeno o azufre; o una sal farmacéuticamente aceptable del mismo, siempre que el compuesto no sea S-(cianometil)isotiourea HCI, S-(cianometil)isotiourea HBr, S-(2-cianoetil)isotiourea HCI, S-(2-cianoetil)isotiourea HBr, p-toluensulfonato de S-(2-cianoetil)isotiourea, S-(3-cianopropil)isotiourea HCI, picrato de S-(3- cianopropil) isotiourea o S-para-cianobencilisotiourea HCI.
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| MY159756A (en) * | 2009-05-20 | 2017-01-31 | Cellceutix Corp | Nitrile derivatives and their pharmaceutical use and compositions |
| CN102464601A (zh) * | 2010-11-17 | 2012-05-23 | 何兰 | 含氰基硫脲类化合物及应用 |
| US9844592B2 (en) * | 2011-07-18 | 2017-12-19 | Icahn School Of Medicine At Mount Sinai | Bacterial RNAs as vaccine adjuvants |
| JP2016516005A (ja) | 2013-02-25 | 2016-06-02 | ノバルティス アーゲー | 新規のアンドロゲンレセプター変異 |
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| WO2007088545A2 (en) | 2006-02-02 | 2007-08-09 | Chemagis Ltd. | Novel process for preparing 1-(mercaptomethyl) cyclopropaneacetic acid, a useful intermediate in the preparation of montelukast and salts thereof |
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| CN101550098B (zh) | 2009-01-14 | 2014-07-09 | 何兰 | 4-异硫尿基丁腈盐酸盐及其衍生物的用途 |
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