AR080709A1 - Derivados de triazina disustituidos farmaceuticamente activos - Google Patents
Derivados de triazina disustituidos farmaceuticamente activosInfo
- Publication number
- AR080709A1 AR080709A1 ARP110100926A ARP110100926A AR080709A1 AR 080709 A1 AR080709 A1 AR 080709A1 AR P110100926 A ARP110100926 A AR P110100926A AR P110100926 A ARP110100926 A AR P110100926A AR 080709 A1 AR080709 A1 AR 080709A1
- Authority
- AR
- Argentina
- Prior art keywords
- cr62r63
- cycle
- nhco
- cr49r50
- cr86r87
- Prior art date
Links
- 150000003918 triazines Chemical class 0.000 title abstract 4
- -1 -Ph Chemical group 0.000 abstract 23
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 20
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 14
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 201000010099 disease Diseases 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 125000004917 3-methyl-2-butyl group Chemical group CC(C(C)*)C 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- KDDQRKBRJSGMQE-UHFFFAOYSA-N 4-thiazolyl Chemical group [C]1=CSC=N1 KDDQRKBRJSGMQE-UHFFFAOYSA-N 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 208000035473 Communicable disease Diseases 0.000 abstract 1
- 208000010228 Erectile Dysfunction Diseases 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 102000001253 Protein Kinase Human genes 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 208000006011 Stroke Diseases 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 230000001363 autoimmune Effects 0.000 abstract 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 208000026278 immune system disease Diseases 0.000 abstract 1
- 201000001881 impotence Diseases 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 108060006633 protein kinase Proteins 0.000 abstract 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 abstract 1
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 abstract 1
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 abstract 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 abstract 1
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 abstract 1
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 238000011282 treatment Methods 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
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
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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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
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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
- A61P17/06—Antipsoriatics
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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
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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
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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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
- A61P9/00—Drugs for disorders of the cardiovascular system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/22—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to two ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 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
- C07D413/02—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
- C07D413/10—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 linked by a carbon chain containing aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Gynecology & Obstetrics (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente se refiere a derivados de triazina disustituidos y/o sales farmacéuticamente aceptables de ellos, el uso de estos derivados como agentes farmacéuticamente activos, en especial para la profilaxis y/o el tratamiento de enfermedades infecciosas, incluyendo enfermedades oportunistas, enfermedades inmunologicas, enfermedades autoinmunes, enfermedades cardiovasculares, enfermedades celulares proliferativas, inflamacion, disfuncion eréctil y apoplejía, y a composiciones farmacéuticas conteniendo al menos uno de dichos derivados de triazina disustituidos y/o las sales farmacéuticamente aceptables de ellos. Además la presente se refiere al uso de dichos derivados de triazina disustituidos como inhibidores de una proteína quinasa. Reivindicacion 1: Compuestos de la formula general (1) en que R1 es como en las formulas (2), L es un enlace o -CR5R6-, -CR5R6-CR7R8-, -CR5R6-CR7R8-CR9R10-, CR5R6-CR7R8-CR9R10-CR11 R12-; R5-R12 representan independientemente uno del otro -H, -CH3, -C2H5, -C3H7, -F, -CI, -Br, I; R3 está seleccionado de -H, -NO2, -NH2, -CN, -F, -CI, -Br, -I, -CH3, -C2H5, -Ph, -C3H7, -CH(CH3)2, -C4H9, -CH2-CH(CH3)2, -CH(CH3)-C2H5, -C(CH3)3, -O-CH3, -O-C2H5, -O-C3H7, -O-CH(CH3)2, -O-C4H9, -O-CH2-CH(CH3)2, -O-CH(CH3)-C2H5, -O-C(CH3)3, -CR13R14R21, -CR13R14-CR15R16R21, -O-CR13R14R21, -CR13R14-CR15R16-CR17R18R21, -CR13R14-CR15R16-CR17R18-CR19R20R21, -O-CR13R14-CR15R16R21, -O-CR13R14-CR15R16-CR17R18R21, -SO2R22, -CONR23R24, -NR25COR22, -O-CR13R14-CR15R16-CR17R18-CR19R20R21, -NR25SO2NR23R24, -NR25SO2R22, -NR25CONR23R24, -SO2NR23R24, -SO(NR26)R27, -NH-CO-NH-Ph; R13-R21, R29-R32 y R33-R48 representan independientemente uno del otro -H, -F, -CI, -Br, -I; R26 es -H, -CH3, -C2H5, -C3H7, -CH(CH3)2, -C4H9, -CH2-CH(CH3)2, -CH(CH3)-C2H5, -C(CH3)3, -C5H11, -CH(CH3)-C3H7, -CH2-CH(CH3)-C2H5, -CH(CH3)-CH(CH3)2, -C(CH3)2-C2H5, -CH2-C(CH3)3, -CH(C2H5)2, -C2H4-CH(CH3)2, -C6H13, -C3H6-CH(CH3)2, -C2H4-CH(CH3)-C2H5, -CH(CH3)-C4H9, -CH2-CH(CH3)-C3H7, -CH(CH3)-CH2-CH(CH3)2, -CH(CH3)-CH(CH3)-C2H5, -CH2-CH(CH3)-CH(CH3)2, -CH2-C(CH3)2-C2H5, -C(CH3)2-C3H7, -C(CH3)2-CH(CH3)2, -C2H4-C(CH3)3, -CH(CH3)-C(CH3)3, -CR13R14R21, -COR28, -CR13R14-CR15R16R21, -CR13R14-CR15R16-CR17R18-CR19R20-CR29R30R21, -CR13R14-CR15R16-CR17R18R21, -CR13R14-CR15R16-CR17R18-CR19R20R21, -CR13R14-CR15R16-CR17R18-CR19R20-CR29R30-CR31R32R21, -COOR28, formulas (3) estos grupos cicloalquílicos C3-6 pueden ser sustituidos además por uno, dos, tres, cuatro, cinco o más sustituyentes seleccionados del grupo que consiste de R33-R48; R22, R27 y R28 se seleccionan independientemente de -CR49R50R51, -CR49R50-CR52R53R51, -CR49R50-CR52R53-CR54R55-CR56R57-CR58R59R51, -CR49R50-CR52R53-CR54R55R51, -CR49R50-CR52R53-CR54R55-CR56R57R51, -CR49R50-CR52R53-CR54R55-CR56R57-CR58R59-CR60R61R51, -CH2Ph, -CH2Ph cuyo grupo fenil puede ser sustituido además por uno, dos, tres, cuatro, cinco o más sustituyentes seleccionados del grupo que consiste de R5-R12 grupos cicloalquílicos C3-6 listados para R26, que pueden ser sustituidos por uno, dos, tres, cuatro, cinco o más sustituyentes seleccionados del grupo que consiste de R33-R48; R49-R61 representan independientemente uno del otro -H, -CH3, -C2H5, -C3H7, -C4H9, -F, -CI, -Br, -I, -OH, -NO2, -NH2; R23 y R24 se seleccionan independientemente de -H, -CR49R50R51, -CR49R50-CR52R53R51, -CR49R50-CR52R53-CR54R55-CR56R57-CR58R59R51, - CR49R50-CR52R53-CR54R55R51, -CR49R50-CR52R53-CR54R55-CR56R57R51, -CR49R50-CR52R53-CR54R55-CR56R57-CR58R59-CR60R61R51, -CR49R50-CR52R53-O-R51', -CR49R50-CR52R53-CR54R55-O-R51', -CR49R50-CR52R53-NR51'R51ö, -CR49R50-CR52R53-CR54R55-NR51'R51ö, -CR49R50-CR52R53-CR54R55-CR56R57-NR51'R51ö, -CR49R50-CR52R53-CR54R55-CR56R57-CR58R59-NR51'R51ô, fenil, fenil sustituido, bencil, bencil sustituido, o los dos residuos R23 y R24 juntos forman con el átomo de nitrogeno al que están ligados una acetidina, pirrolidina, piperidina, piperazina, azepana o anillo morfolino; R51' y R51ö representan independientemente uno del otro -H, -CH3, -C2H5, -C3H7, -C4H9, -CH2Ph, -COOC(CH3)3, -COOCH3, -COOCH2CH3, -COOCH2CH2CH3, -COOCH(CH3)2, -COOCH2Ph, -COCH3; y R25 es -H, -CH3, -C2H5, -C3H7, -CH(CH3)2, -C4H9, -CH2-CH(CH3)2, -CH(CH3)-C2H5, -C(CH3)3; R4 se selecciona de -H, -NO2, -NH2, -CN, -F, -CI, -Br, -I, -CR62R63R64, grupo de formulas (4), -CONH2, -SO2CH3, -SO2C2H5, -SO2C3H7, -NH-SO2-CH3, -NH-SO2-C2H5, -NH-SO2-C3H7, -NHCO-CH3, -NHCO-C2H5, -NHCO-C3H7, -SO2NR23R24, -CH2-SO2NR23R24, -C2H4-SO2NR23R24, -C3H6-SO2NR23R24, -SO2NH2, -CH2-SO2NH2, -C2H4-SO2NH2, -C3H6-SO2NH2, -O-CR62R63-CR65R66R64, -O- CR62R63-CR65R66-CR67R68R64, -CR62R63-CR65R66-CR67R68-CR69R70R64, -O-CR62R63-CR65R66-CR67R68-CR69R70R64, -CR62R63-CR65R66-CR67R68R64, -O-CR62R63-CR65R66-CR67R68-CR69R70-CR71R72R64, -CR62R63-CR65R66R64, -O-CR62R63-CR65R66-CR67R68-CR69R70-CR71R72-CR73R74R64, -O-CR62R63R64, -CR62R63-CR65R66-CR67R68-CR69R70-CR71R72R64, --CR62R63-CR65R66-CR67R68-CR69R70-CR71R72-CR73R74R64, -OCH2Ph, grupo de formulas (3) y (5) estos grupos cicloalcoxi C3-6 y grupos cicloalquílicos C3-6 pueden estar sustituidos además por uno, dos, tres, cuatro, cinco o más sustituyentes seleccionados del grupo que consiste de R33-R48, R62-R74 representan independientemente uno del otro -H, -ciclo-C3H5, -ciclo-C4H7, -ciclo-C5H9, -CR75R76R77, -CR75R76-CR78R79R77, -CR75R76-CR78R79-CR80R81R77, -CR75R76-CR78R79-CR80R79-CR82R81R77, -F, -CI, -Br, -I, -Ph; R75-R82 representan independientemente uno del otro -H, -F, -CI, -Br, -I, -NH2; R4 junto con R22, R23, R24 o R25 puede formar un grupo -CH2CH2- o -CH2CH2CH2- si R4 está ligado en orto a -L-R3; R2 es como en formulas (6), R83 se selecciona de -H, -OH, -NO2, -CN, -F, -CI, -Br, -I, -CF3, -NR23'R24', -CR62R63R64, -CR62R63-NR23'R24', -CR62R63-CR65R66R64, -CR62R63-CR65R66-NR23'R24', -CR62R63-CR65R66-CR67R68R64, -CR62R63-CR65R66-CR67R68-NR23'R24', -O-CR62R63R64, -O-CR62R63-CR65R66R64, -O-R62R63-CR65R66-CR67R68R64, -CHO, -CH2OH, -CR23'O, -CH2OR23'; R23' y R24' representan independientemente uno del otro -H, -CH3, -C2H5, -C3H7, -CH(CH3)2, -C4H9, -CH2-CH(CH3)2, -CH(CH3)-C2H5, -C(CH3)3; -(ciclo-C3H5); x es un valor entre 0 y 3; B es un enlace, -CR86R87-, -CR86R87-CR88R89-, -CR86R87-CR88R89-CR90R91-, -CR86R87-CR88R89-CR90R91-CR92R93-, -CR86R87-CR88R89-CR90R91-CR92R93-CR94R95-, -CR86R87-CR88R89-CR90R91-CR92R93-CR94R95-CR96R97-; R86-R97 representan independientemente uno del otro -H, -CH3, C2H5, -C3H7, -C4H9, -F, -CI, -Br, -I; Y es un enlace, -O-, -S-, -SO-, -SO2-, -SO2NH-, -NHSO2-, -CO-, -COO-, -OOC-, -CONH-, -NHCO-, -NH-, -N(CH3)-, -NH-CO-NH-, -O-CO-NH-, -NH-CO-O-; R84 se selecciona de un enlace, -CR86R87-, -CR86R87-CR88R89-CR90R91-, -CR86R87-CR88R89-CR90R91-CR92R93-, -CR86R87-CR88R89-CR90R91-CR92R93-CR94R95-, -CR86R87-CR88R89-, -CR86R87-CR88R89-CR90R91-CR92R93-CR94R95-CR96R97-; R85 se selecciona de (i) -H, -OH, -OCH3, -OC2H5, -OC3H7, -O-ciclo-C3H5, -OCH(CH3)2, -OC(CH3)3, -OC4H9, -Ph, -OPh, -OCH2-Ph, -OCPh3, -SH, -SCH3, -SC2H5, -SC3H7, -S-ciclo-C3H5, -SCH(CH3)2, -SC(CH3)3, -SC4H9, -NO2, -F, -CI, -Br, -I, -P(O)(OH)2, -P(O)(OCH3)2, -P(O)(OC2H5)2, -P(O)(OCH(CH3)2)2, -Si(CH3)2(C(CH3)3), -Si(C2H5)3, -Si(CH3)3, -CN, -CHO, -COCH3, -COC2H5, -COC3H7, -CO-ciclo-C3H5, -COCH(CH3)2, -COC(CH3)3, -COC4H9, -COOH, -COOCH3, -COOC2H5, -COOC3H7, -COOC4H9, -COO-ciclo-C3H5, -COOCH(CH3)2, -COOC(CH3)3, -OOC-CH3, -OOC-C2H5, -OOC-C3H7, -OOC-C4H9, -OOC-ciclo-C3H5, -OOC-CH(CH3)2, -OOC-C(CH3)3, -CONR23'R24', -NHCOCH3, -NHCOC2H5, -NHCOC3H7, -NHCO-ciclo-C3H5, -NHCO-CH(CH3)2, -NHCOC4H9, -NHCO-C(CH3)3, -NHCO-OCH3, -NHCO-OC2H5, -NHCO-OC3H7, -NHCO-O-ciclo-C3H5, -NHCO-OC4H9, -NHCO-OCH(CH3)2, -NHCO-OC(CH3)3, -NHCO-OCH2Ph, -NR23R24, -CF3, -SOCH3, -SOC2H5, -SOC3H7, -SO-ciclo-C3H5, -SOCH(CH3)2, -SOC(CH3)3, -SO2CH3, -SO2C2H5, -SO2C3H7, -SO2-ciclo-C3H5, -SO2CH(CH3)2, -SO2C4H9, -SO2C(CH3)3, -SO3H, -SO2NR23'R24', -OCF3, -OC2F5, -O-COOCH3, -O-COOC2H5, -O-COOC3H7, -O-COO-ciclo-C3H5, -O-COOC4H9, -O-COOCH(CH3)2, -O-COOCH2Ph, -O-COOC(CH3)3, -NH-CO-NH2, -NH-CO-NHCH3, -NH-CO-NHC2H5, -NH-CO-NHC3H7, -NH-CO-NHC4H9, -NH-CO-NH-ciclo-C3H5, -OCH2-ciclo-C3H5, -NH-CO-NH[CH(CH3)2], -NH-CO-NH[C(CH3)3], -NH-CO-N(CH3)2, -NH-CO-N(C2H5)2, -NH-CO-N(C3H7)2, -NH-CO-N(C4H9)2, -NH-CO-N(ciclo-C3H5)2, -NH-CO-N[CH(CH3)2]2, -NH-CO-N[C(CH3)3]2, -NH-C(=NH)-NH2, -NH-C(=NH)-NHCH3, -NH-C(=NH)-NHC2H5, -NH-C(=NH)-NHC3H7, -NH-C(=NH)-NHC4H9, -NH-C(=NH)-NH-ciclo-C3H5, -NH-C(=NH)-NH[CH(CH3)2], -NH-C(=NH)-NH[C(CH3)3], -NH-C(=NH)-N(CH3)2, -NH-C(=NH)-N(C2H5)2, -NH-C(=NH)-N(C3H7)2, -NH-C(NH)-N(ciclo-C3H5)2, -NH-C(=NH)-N(C4H9)2, -NH-C(=NH)-N[CH(CH3)2]2, -NH-C(=NH)-N[C(CH3)3]2, -O-CO-N H2, -O-CO-NHCH3, -O-CO-NHC2H5, -O-CO-NHC3H7, -O-CO-NHC4H9, -O-CO-NH-ciclo-C3H5, -O-CO-NH[CH(CH3)2], -O-CO-NH[C(CH3)3], -O-CO-N(CH3)2, -O-CO-N(C2H5)2, -O-CO-N(C3H7)2, -O-CO-N(C4H9)2, -O-CO-N(ciclo-C3H5)2, -O-CO-N[CH(CH3)2]2, -O-CO-N[C(CH3)3]2, (ii) un anillo aromático o heteroaromático mono- o bicíclico seleccionado de 2-tienil, 3-tienil, 2-furanil, 3-furanil, 2-oxazolil, 3-oxazolil, 4-oxazolil, 2-tiazolil, 3-tiazolil, 4-tiazolil, 1-pirazolil, 3-pirazolil, 4-pirazolil, 5-pirazolil, 1-imidazolil, 2-imidazolil, 4-imidazolil, 5-imidazolil, fenil, 1-naftil, 2-naftil, 2-piridil, 3-piridil, 4-piridil, 2-pirimidinil, 4-pirimidinil, 5-pirimidinil, 2-pirazinil, 3-piridazinil, 4-piridazinil, 1,3,5-triazin-2-iI, compuestos de formulas (7) que opcionalmente puede estar sustituido por uno o dos sustituyentes seleccionados de -F, -CI, -Br, -I, -OCH3, -CH3, -NO2, -CN, -CF3; (iii) un anillo saturado seleccionado de ciclopentil, acetidin-1-il, compuestos de formulas (8); R99 representa -H, -CH3, -CH2Ph, -COOC(CH3)3, -COOCH3, -COOCH2CH3, -COOCH2CH2CH3, -COOCH(CH3)2, -COOCH2Ph, -COCH3; el grupo -B-Y-R-R85 junto con un sustituyente R83 puede formar un grupo -OCH2O- si R83 está ligado en posicion orto a -B-Y-R-R85; a condicion de que R83 no sea -H si el grupo -B-Y-R84-R85 es hidrogeno; R98 se selecciona de -NO2, -CN, -F, -CI, -Br, -I, -NH2, -OH, -CR62R63R64, -CR62R63-CR65R66R64, -CR62R63-R65R66-C67R68R64, -CR62R63-CR65R66-CR67R68-CR69R70R64, -O-CR62R63R64, -O-CR62R63-CR65R66R64, -O-CR62R63-CR65R66-CR67R
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| EA202091894A1 (ru) | 2018-02-13 | 2020-12-28 | Байер Акциенгезельшафт | Применение 5-фтор-4-(4-фтор-2-метоксифенил)-n-{4-[(s-метилсульфонимидоил)метил]пиридин-2-ил}пиридин-2-амина для лечения диффузной в-крупноклеточной лимфомы |
| EP3613738A1 (en) * | 2018-08-23 | 2020-02-26 | Lead Discovery Center GmbH | 4-substituted pyrrolo[2,3-b]pyridine as erbb modulators useful for treating cancer |
| CN109776513A (zh) * | 2019-03-18 | 2019-05-21 | 福建省医学科学研究院 | 一类4-苯基-1,3,5-三嗪-2-胺类抗肿瘤化合物及其制备方法 |
| KR102333854B1 (ko) | 2019-10-24 | 2021-12-06 | 한국과학기술연구원 | 단백질 키나아제 저해 활성을 갖는 신규한 피리디닐트리아진 유도체 및 이를 포함하는 암의 예방, 개선 또는 치료용 약학 조성물 |
| CN114787142B (zh) | 2019-12-09 | 2024-08-02 | 石药集团中奇制药技术(石家庄)有限公司 | 作为周期蛋白依赖性激酶9抑制剂的化合物及其应用 |
| CA3172328A1 (en) * | 2020-03-27 | 2021-09-30 | Haruhisa Inoue | Nerve cell degeneration inhibitor |
| WO2022157686A1 (en) * | 2021-01-22 | 2022-07-28 | Ildong Pharmaceutical Co., Ltd. | Inhibitors of anoctamin 6 protein and uses thereof |
| US12109210B2 (en) | 2021-09-29 | 2024-10-08 | Gongwin Biopharm Co., Ltd | Methods for treating mast cell tumors |
| CN115089591B (zh) * | 2022-05-21 | 2024-04-12 | 复旦大学 | 布立尼布在制备抑制肠道病毒71型嗜神经性病毒药物中的应用 |
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| JP2000229949A (ja) * | 1999-02-10 | 2000-08-22 | Nippon Soda Co Ltd | 含窒素ヘテロ環誘導体 |
| AU770600B2 (en) | 1999-10-07 | 2004-02-26 | Amgen, Inc. | Triazine kinase inhibitors |
| US7291616B2 (en) * | 2001-10-31 | 2007-11-06 | Cell Therapeutics, Inc. | Aryl triazines as LPAAT-β inhibitors and uses thereof |
| CN100412066C (zh) * | 2003-09-30 | 2008-08-20 | Irm责任有限公司 | 用作蛋白激酶抑制剂的化合物和组合物 |
| EP1878726A1 (en) | 2006-07-12 | 2008-01-16 | Bayer Schering Pharma Aktiengesellschaft | Substituted sulphoximines as Tie2 inhibitors and salts thereof, pharmaceutical compositions comprising the same, methods of preparing the same and uses of the same |
| MX2009006536A (es) * | 2006-12-22 | 2009-06-26 | Novartis Ag | Compuestos de heteroaril-heteroarilo como inhibidores de cdk para el tratamiento de cancer, inflamacion e infecciones virales. |
| ES2539518T3 (es) * | 2007-04-24 | 2015-07-01 | Astrazeneca Ab | Inhibidores de proteínas quinasas |
| JP5379787B2 (ja) * | 2007-04-24 | 2013-12-25 | インゲニウム ファーマシューティカルズ ジーエムビーエイチ | プロテインキナーゼの阻害剤 |
| US8507498B2 (en) | 2007-04-24 | 2013-08-13 | Ingenium Pharmaceuticals Gmbh | 4, 6-disubstituted aminopyrimidine derivatives as inhibitors of protein kinases |
| EP2231625A4 (en) | 2007-12-13 | 2010-12-29 | Glaxosmithkline Llc | KINASE INHIBITORS BASED ON THIAZOLE AND OXAZOLE |
| EP2699554B1 (en) * | 2011-04-19 | 2016-11-02 | Bayer Intellectual Property GmbH | Substituted 4-aryl-n-phenyl-1,3,5-triazin-2-amines |
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- 2011-03-20 JP JP2013500385A patent/JP5921525B2/ja not_active Expired - Fee Related
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- 2011-03-20 EP EP11711039.5A patent/EP2550257B1/en not_active Not-in-force
- 2011-03-20 ES ES11711039.5T patent/ES2619585T3/es active Active
- 2011-03-20 MX MX2012010966A patent/MX2012010966A/es active IP Right Grant
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| BR112012024017A2 (pt) | 2016-08-30 |
| CA2789200C (en) | 2020-05-26 |
| BR112012024017B1 (pt) | 2021-12-07 |
| AU2011231975A1 (en) | 2012-08-30 |
| TWI515183B (zh) | 2016-01-01 |
| TW201136901A (en) | 2011-11-01 |
| ES2619585T3 (es) | 2017-06-26 |
| EP2550257B1 (en) | 2016-12-21 |
| UY33286A (es) | 2011-10-31 |
| WO2011116951A1 (en) | 2011-09-29 |
| AU2011231975B2 (en) | 2014-07-03 |
| JP2013522331A (ja) | 2013-06-13 |
| IL221229A0 (en) | 2012-10-31 |
| SA111320281B1 (ar) | 2015-06-04 |
| KR101752519B1 (ko) | 2017-06-29 |
| JP5921525B2 (ja) | 2016-05-24 |
| IL221229A (en) | 2017-05-29 |
| MX2012010966A (es) | 2013-01-29 |
| CN102933561B (zh) | 2016-05-11 |
| CA2789200A1 (en) | 2011-09-29 |
| US20130079345A1 (en) | 2013-03-28 |
| EA201201309A1 (ru) | 2013-04-30 |
| KR20130006632A (ko) | 2013-01-17 |
| HK1181771A1 (zh) | 2013-11-15 |
| EA026917B1 (ru) | 2017-05-31 |
| EP2550257A1 (en) | 2013-01-30 |
| CN102933561A (zh) | 2013-02-13 |
| ZA201206262B (en) | 2013-04-24 |
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