AR046166A1 - Inhibidores macrociclicos de la serina proteasa ns3 del virus de la hepatitis c - Google Patents
Inhibidores macrociclicos de la serina proteasa ns3 del virus de la hepatitis cInfo
- Publication number
- AR046166A1 AR046166A1 ARP040103438A ARP040103438A AR046166A1 AR 046166 A1 AR046166 A1 AR 046166A1 AR P040103438 A ARP040103438 A AR P040103438A AR P040103438 A ARP040103438 A AR P040103438A AR 046166 A1 AR046166 A1 AR 046166A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- present
- absent
- aryl
- cycloalkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D245/00—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms
- C07D245/04—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
- A61K38/212—IFN-alpha
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
-
- 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
- A61P31/14—Antivirals for RNA viruses
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
-
- 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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0217—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -C(=O)-C-N-C(=O)-N-C-C(=O)-
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Virology (AREA)
- Inorganic Chemistry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se revelan compuestos que poseen actividad inhibidora de la proteasa del VHC al igual que composiciones farmacéuticas que comprenden dichos compuestos y métodos para usarlos para tratar trastornos asociados con la proteasa del VHC. Reivindicación 1: Un compuesto que posee la estructura general que se muestra en la fórmula (1), o sales, solvatos o ésteres aceptables para uso farmacéutico de dicho compuesto en el cual (1) R' es -C(O)R5 o -B(OR)2; (2) R5 es H, -OH, -OR8, -NR9R10, -C(O)OR8, - C(O)NR9R10, -CF3, -C2F5, -C3F7, -CF2R6, -R6, -C(O)R7 o NR7SO2R8; (3) R7 es H, -OH, -OR8, o -CHR9R10; (4) R6, R8, R9 y R10 pueden ser iguales o diferentes, seleccionándose cada uno independientemente del grupo que consiste en H, alquilo, alquenilo, arilo, heteroalquilo, heteroarilo, cicloalquilo, arilalquilo, heteroarilalquilo, R14, -CH(R1')CH(R1')C(O)OR11, -[CH(R1')]pC(O)OR11, -[CH(R1')]pC(O)NR12R13, -[CH(R1')]pS(O2)R11, -[CH(R1')]pC(O)R11, -[CH(R1')]pS(O2)NR12R13, - CH(R1')C(O)N(H)CH(R2')(R'), -CH(R1')CH(R1')C(O)NR12R13, -CH(R1')CH(R1')S(O2)R11, -CH(R1')CH(R1')S(O2)NR12R13, -CH(R1')CH(R1')C(O)R11, -[CH(R1')]pCH(OH)R11, -CH(R1')C(O)N(H)CH(R2')C(O)OR11, -C(O)N(H)CH(R2')C(O)OR11, -C(O)N(H)CH(R2')C(O)R11, - CH(R1')C(O)N(H)CH(R2')C(O)NR12R13, -CH(R1')C(O)N(H)CH(R2')R', -CH(R1')C(O)N(H)CH(R2')C(O)N(H)CH(R3')C(O)OR11, -CH(R1')C(O)N(H)CH(R2')C(O)CH(R3')NR12R13, -CH(R1')C(O)N(H)CH(R2')C(O)N(H)CH(R3')C(O)NR12R13, - CH(R1')C(O)N(H)CH(R2')C(O)N(H)CH(R3')C(O)N(H)CH(R4')C(O)OR11, -CH(R1')C(O)N(H)CH(R2')C(O)N(H)CH(R3')C(O)N(H)CH(R4')C(O)NR12R13, -CH(R1')C(O)N(H)CH(R2')C(O)N(H)CH(R3')C(O)N(H)CH(R4')C(O)N(H)CH(R5')C(O)OR11, y - CH(R1')C(O)N(H)CH(R2')C(O)N(H)CH(R3')C(O)N(H)CH(R4')C(O)N(H)CH(R5')C(O)NR12R13; en los cuales R1', R2', R3', R4', R5', R11, R12 y R13 pueden ser iguales o diferentes, seleccionándose cada uno independientemente del grupo que consiste en H, halógeno, alquilo, arilo, heteroalquilo, heteroarilo, cicloalquilo, alcoxi, ariloxi, alquenilo, alquinilo, alquil-arilo, alquil-heteroarilo, heterocicloalquilo, aril-alquilo y heteroaralquilo; o R12 y R13 se juntan de forma tal que la combinación es cicloalquilo, heterocicloalquilo, arilo o heteroarilo; R14 se encuentra presente o no y si se encuentra presente se selecciona del grupo conformado por H, alquilo, arilo, heteroalquilo, heteroarilo, cicloalquilo, alquil-arilo, alilo, alquil- heteroarilo, alcoxi, aril-alquilo, alquenilo, alquinilo y heteroaralquilo; (5) R y R' se encuentran presentes o no y si se encuentran presentes pueden ser iguales o diferentes, seleccionándose cada uno independientemente del grupo conformado por H, OH, alquilo C1-10, alquenilo C2-10, cicloalquilo C3-8, heterocicloalquilo C3-8, alcoxi, ariloxi, alquiltio, ariltio, alquilamino, arilamino, amino, amido, ariltioamino, arilcarbonilamino, arilaminocarboxi, alquilaminocarboxi, heteroalquilo, alquenilo, alquinilo, (aril)alquilo, heteroarilalquilo, éster, ácido carboxílico, carbamato, urea, cetone, aldehido, ciano, nitro, halógeno, (cicloalquil)alquilo, arilo, heteroarilo, (alquil)arilo, alquilheteroarilo, alquil-heterociclilo y (heterocicloalquil)alquilo, donde dicho cicloalquilo está compuesto por tres a ocho átomos de carbono, y cero a seis átomos de oxígeno, nitrógeno, azufre, o fósforo, y dicho alquilo es de uno a seis átomos de carbono; (6) L' es H, OH, alquilo, heteroalquilo, arilo, heteroarilo, cicloalquilo, o heterociclilo; (7) M' es H, alquilo, heteroalquilo, arilo, heteroarilo, cicloalquilo, arilalquilo, heterociclilo o una cadena lateral de aminoácido; o L' y M' se unen para formar una estructura anular tal que la porción de la fórmula estructural (1) representada por la fórmula (2) (habiéndose agregado los números 1 y 2 para mostrar la ubicación de un cierto átomo de carbono y de cierto átomo de nitrógeno respectivamente) se representa mediante la fórmula estructural (3), donde E está presente o ausente y si se encuentra presente es C, CH, N o C(R); J está presente o ausente y cuando J se encuentra presente, J es (CH2)p, (CHR-CHR')p, (CHR)p, (CRR')p, S(O2), N(H), N(R) u O; cuando J está ausente y G se encuentra presente, L está unido directamente al átomo de nitrógeno marcado como posición 2; p es un número de 0 a 6; L está presente o ausente, y cuando L se encuentra presente, L es C(H) o C(R); cuando L está ausente, M está presente o ausente; si M se encuentra presente estando L ausente, entonces M está directa e independientemente unido a E, y J está directa e independientemente unido a E; G está presente o ausente y cuando G se encuentra presente, G es (CH2)p, (CHR)p, (CHR-CHR')p o (CRR')p; cuando G está ausente, J se encuentra presente y E está conectado directamente al átomo de carbono marcado como posición 1; Q está presente o ausente y cuando Q se encuentra presente, Q es NR, PR, (CR=CR), (CH2)p, (CHR)p, (CRR')p, (CHR-CHR')p, O, NR, S, SO, o SO2; cuando Q se encuentra ausente, M está (i) ya sea directamente unido a A o (ii) un substituyente independiente sobre L, seleccionándose dicho substituyente independiente de -OR, -CH(R)(R'), S(O)0-2R o -NRR' o (iii) ausente; cuando ambos Q y M están ausentes, A está ya sea directamente unido a L, o A es un substituyente independiente sobre E, seleccionándose dicho substituyente independiente de -OR, -CH(R)(R'), S(O)0-2R o -NRR' o A se encuentra ausente; A está presente o ausente y si se encuentra presente A es O, O(R), (CH2)p, (CHR)p, (CHR-CHR')p, (CRR')p, N(R), NRR', S, S(O2), -OR, CH(R)(R') o NRR'; o A está unido a M para formar un puente cicloalquilo, alifático o heterocíclico; M está presente o ausente y cuando M se encuentra presente, M es halógeno, O, OR, N(R), S, S(O2), (CH2)p, (CHR)p, (CHR-CHR')p, o (CRR')p; o M está unido a A para formar un puente cicloalquilo, alifático o heterocicloalquilo; (8) Z' está representado por cualquiera de (i), (ii), (iii), (iv) o (v) que se muestran a continuación, (i) un compuesto de fórmula (4) en la cual R44 se selecciona del grupo de fórmulas (5) y R77 se selecciona del grupo de fórmulas (6), en los cuales R78 se selecciona de metilo, etilo, isopropilo, tert-butilo y fenilo; (ii) un compuesto de fórmula (7), donde R79 se selecciona del grupo de fórmulas (8), (iii) un compuesto de fórmula (9) en la cual el anillo sulfona está substituido opcionalmente con alquilo y cicloalquilo; (iv) un resto del grupo de fórmulas (10); y (v) el resto de fórmula (11), en el cual W es -C(=O)- o -S(O2)-; Z es O ó N; e Y se selecciona del grupo de fórmulas (12), donde Y11 se selecciona del grupo que consiste en H, -C(O)OH, - C(O)OEt, -OMe, -Ph, -OPh, -NHMe, -NHAc, -NHF, -CH(Me)2, 1-triazolilo, 1-imidazolilo y -NHCH2COOH; Y12 se selecciona del grupo que consiste en H, -C(O)OH, -C(O)OMe, -OMe, F, Cl y Br; Y13 se selecciona de los restos del grupo de fórmulas (13); Y14 es MeS(O2)-, -Ac, -Boc, -iBoc, -Cbz, o -Alloc; Y15 e Y16 pueden ser iguales o diferentes y se seleccionan independientemente del grupo que consiste en alquilo, arilo, heteroalquilo y heteroarilo; Y17 es -CF3, -NO2, -C(O)NH2, -OH, -C(O)OCH3, -OCH3, - OC6H5, -C6H5, -C(O)C6H5, -NH2, o -C(O)OH; e Y18 es -C(O)OCH3, -NO2, -N(CH3)2, F, -OCH3, -C(H2)C(O)OH, -C(O)OH, -S(O2)NH2, o -N(H)C(O)CH3; (9) X se representa por la fórmula estructural (14) donde en la fórmula (14), a es 2, 3, 4, 5, 6, 7, 8 ó 9; b, c, d, e y f pueden ser iguales o diferentes, siendo cada uno independientemente 0, 1, 2, 3, 4 ó 5; A es C, N, S u O; R29 y R29' se encuentran presentes o ausentes y si se encuentran presentes pueden ser iguales o diferentes, siendo cada uno independientemente uno o dos substituyentes seleccionados del grupo conformado por H, halo, alquilo, arilo, cicloalquilo, cicloalquilamino, cicloalquilaminocarbonilo, ciano, hidroxi, alcoxi, alquiltio, amino, -NH(alquilo), -NH(cicloalquilo), - N(alquilo)2, carboxilo, -C(O)O-alquilo, heteroarilo, aralquilo, alquilarilo, aralquenilo, heteroaralquilo, alquilheteroarilo, heteroaralquenilo, hidroxialquilo, ariloxi, aralcoxi, acilo, aroilo, nitro, ariloxicarbonilo, aralcoxicarbonilo, alquilsulfonilo, arilsulfonilo, heteroarilsulfonilo, alquilsulfinilo, arilsulfinilo, heteroarilsulfinilo, ariltio, heteroariltio, aralquiltio, heteroaralquiltio, cicloalquenilo, heterociclilo, heterociclenilo, Y1Y2N-alquil-,Y1Y2NC(O)- y Y1Y2NSO2-, en los cuales Y1 e Y2 pueden ser iguales o diferentes y se seleccionan independientemente del grupo que consiste en hidrógeno, alquilo, arilo, y aralquilo; o R29 y R29' están unidos de manera que la combinación es una cadena alifática o heteroalifática de 0 a 6 carbonos; R30 está presente o ausente y si se encuentra presente es uno o dos substituyentes seleccionados independientemente del grupo conformado por H, alquilo, arilo, heteroarilo y cicloalquilo; (10) D en la fórmula (1) se representa por la fórmula estructural (15) donde en la fórmula (15), R32, R33 y R34 se encuentran presentes o ausentes y si se encuentran presentes son independientemente uno o dos substituyentes seleccionados independientemente del grupo que consiste en H, halo, alquilo, arilo, cicloalquilo, cicloalquilamino, espiroalquilo, cicloalquilaminocarbonilo, ciano, hidroxi, alcoxi, alquiltio, amino, -NH(alquilo), -NH(cicloalquilo), -N(alquilo)2, carboxilo, -C(O)O-alquilo, heteroarilo, aralquilo, alquilarilo, aralquenilo, heteroaralquilo, alquilheteroarilo, heteroaralquenilo, hidroxialquilo, ariloxi, aralcoxi, acilo, aroilo, nitro, ariloxicarbonilo, aralcoxicarbonilo, alquilsulfonilo, arilsulfonilo, heteroarilsulfonilo, alquilsulfinilo, arilsulfinilo, heteroarilsulfinilo, ariltio, heteroariltio, aralquiltio, heteroaralquiltio, cicloalquenilo, heterociclilo, heterociclenilo, Y1Y2N-alquil-, Y1Y2NC(O)- y Y1Y2NSO2-, en los cuales Y1 e Y2 pueden ser iguales o diferentes, y se seleccionan independientemente del grupo que consiste en hidrógeno, alquilo, arilo, y aralquilo; o R32 y R34 están unidos de manera que la combinación forma una porción de un grupo cicloalquilo; g es 1, 2, 3, 4, 5, 6, 7, 8 ó 9; h, i, j, k, I y m pueden ser iguales o diferentes, siendo
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50663703P | 2003-09-26 | 2003-09-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR046166A1 true AR046166A1 (es) | 2005-11-30 |
Family
ID=34393181
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040103438A AR046166A1 (es) | 2003-09-26 | 2004-09-23 | Inhibidores macrociclicos de la serina proteasa ns3 del virus de la hepatitis c |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US7592419B2 (es) |
| EP (1) | EP1664092B1 (es) |
| JP (2) | JP4525982B2 (es) |
| KR (1) | KR20060085248A (es) |
| CN (1) | CN1894274A (es) |
| AR (1) | AR046166A1 (es) |
| AT (1) | ATE497505T1 (es) |
| AU (1) | AU2004276281A1 (es) |
| BR (1) | BRPI0414814A (es) |
| CA (1) | CA2540031A1 (es) |
| CO (1) | CO5680449A2 (es) |
| DE (1) | DE602004031298D1 (es) |
| EC (1) | ECSP066456A (es) |
| IL (1) | IL174459A0 (es) |
| MX (1) | MXPA06003455A (es) |
| NO (1) | NO20061822L (es) |
| PE (1) | PE20050953A1 (es) |
| RU (1) | RU2006113880A (es) |
| TW (1) | TWI280964B (es) |
| WO (1) | WO2005030796A1 (es) |
| ZA (1) | ZA200602447B (es) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0932617B1 (en) | 1996-10-18 | 2002-01-16 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| US7176208B2 (en) | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
| US20110150835A1 (en) * | 2003-09-26 | 2011-06-23 | Schering Corporation | Macrocyclic Inhibitors of Hepatitis C Virus NS3 Serine Protease |
| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| WO2006130686A2 (en) | 2005-06-02 | 2006-12-07 | Schering Corporation | Hcv protease inhibitors in combination with food |
| CA2611155A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Pharmaceutical formulations and methods of treatment using the same |
| EP2305695A3 (en) | 2005-07-25 | 2011-07-27 | Intermune, Inc. | Macrocyclic inhibitors of Hepatitis C virus replication |
| DE602006013492D1 (de) * | 2005-08-19 | 2010-05-20 | Vertex Pharma | Verfahren und zwischenprodukte |
| US8399615B2 (en) | 2005-08-19 | 2013-03-19 | Vertex Pharmaceuticals Incorporated | Processes and intermediates |
| AR055395A1 (es) | 2005-08-26 | 2007-08-22 | Vertex Pharma | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c |
| US8119592B2 (en) * | 2005-10-11 | 2012-02-21 | Intermune, Inc. | Compounds and methods for inhibiting hepatitis C viral replication |
| US7705138B2 (en) | 2005-11-11 | 2010-04-27 | Vertex Pharmaceuticals Incorporated | Hepatitis C virus variants |
| EP1951748B1 (en) | 2005-11-11 | 2013-07-24 | Vertex Pharmaceuticals, Inc. | Hepatitis c virus variants |
| US7816348B2 (en) | 2006-02-03 | 2010-10-19 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US9526769B2 (en) * | 2006-06-06 | 2016-12-27 | Enanta Pharmaceuticals, Inc. | Macrocylic oximyl hepatitis C protease inhibitors |
| AR061629A1 (es) * | 2006-06-26 | 2008-09-10 | Enanta Pharm Inc | Quinoxalinil macrociclicos inhibidores de serina proteasa del virus de la hepatitis c. proceso de obtencion y composiciones farmaceuticas |
| CN101674844A (zh) * | 2006-08-04 | 2010-03-17 | 英安塔制药有限公司 | 四唑基大环类c型肝炎丝氨酸蛋白酶抑制剂 |
| US7662779B2 (en) * | 2006-08-11 | 2010-02-16 | Enanta Pharmaceuticals, Inc. | Triazolyl macrocyclic hepatitis C serine protease inhibitors |
| RU2009109355A (ru) | 2006-08-17 | 2010-09-27 | БЕРИНГЕР ИНГЕЛЬХАЙМ ИНТЕРНАЦИОНАЛЬ ГмбХ (DE) | Ингибиторы вырусной полимеразы |
| US8003604B2 (en) * | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20100120716A1 (en) * | 2006-12-06 | 2010-05-13 | Phenomix Corporation | Macrocyclic hepatitis c serine protease inhibitors and uses therefor |
| JP2010512317A (ja) | 2006-12-07 | 2010-04-22 | シェーリング コーポレイション | pH感受性マトリクス処方物 |
| US8143402B2 (en) * | 2007-02-01 | 2012-03-27 | Tibotec Pharmaceuticals Ltd. | Polymorphic forms of a macrocyclic inhibitor of HCV |
| EA200901101A1 (ru) * | 2007-02-20 | 2010-04-30 | Новартис Аг | Макроциклические соединения в качестве ингибиторов протеазы ns3 вгс |
| US20090005387A1 (en) * | 2007-06-26 | 2009-01-01 | Deqiang Niu | Quinoxalinyl macrocyclic hepatitis c virus serine protease inhibitors |
| EP2188274A4 (en) | 2007-08-03 | 2011-05-25 | Boehringer Ingelheim Int | VIRAL POLYMERASE HEMMER |
| US8268777B2 (en) * | 2007-12-05 | 2012-09-18 | Enanta Pharmaceuticals, Inc. | Oximyl macrocyclic derivatives |
| JP2011506472A (ja) * | 2007-12-14 | 2011-03-03 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状オキシミルc型肝炎セリンプロテアーゼ阻害剤 |
| NZ585370A (en) | 2007-12-19 | 2012-09-28 | Boehringer Ingelheim Int | Viral polymerase inhibitors |
| JP5490778B2 (ja) * | 2008-03-20 | 2014-05-14 | エナンタ ファーマシューティカルズ インコーポレイテッド | C型肝炎ウイルス阻害剤としてのフッ素化大環状化合物 |
| CA2720729A1 (en) * | 2008-04-15 | 2009-11-26 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
| US20090285773A1 (en) * | 2008-05-15 | 2009-11-19 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| CN101580535B (zh) * | 2008-05-16 | 2012-10-03 | 太景生物科技股份有限公司 | 丙型肝炎病毒蛋白酶抑制剂 |
| CN102046648A (zh) * | 2008-05-29 | 2011-05-04 | 百时美施贵宝公司 | 丙型肝炎病毒抑制剂 |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| KR20110075019A (ko) * | 2008-10-15 | 2011-07-05 | 인터뮨, 인크. | 치료용 항바이러스성 펩티드 |
| US20100272674A1 (en) * | 2008-12-04 | 2010-10-28 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| CN102271699A (zh) | 2009-01-07 | 2011-12-07 | 西尼克斯公司 | 用于治疗hcv和hiv感染的环孢菌素衍生物 |
| AU2010253791A1 (en) | 2009-05-29 | 2011-11-24 | Merck Sharp & Dohme Corp. | Antiviral compounds composed of three linked Aryl moieties to treat diseases such as Hepatitis C |
| US8232246B2 (en) * | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| SI2477980T1 (sl) * | 2009-09-15 | 2017-01-31 | Taigen Biotechnology Co., Ltd. | Inhibitorji HCV proteaze |
| WO2011041551A1 (en) * | 2009-10-01 | 2011-04-07 | Intermune, Inc. | Therapeutic antiviral peptides |
| CA2782024A1 (en) | 2009-11-25 | 2011-06-03 | Schering Corporation | Fused tricyclic compounds and derivatives thereof useful for the treatment of viral diseases |
| US20130156731A1 (en) | 2009-12-22 | 2013-06-20 | Kevin X. Chen | Fused tricyclic compounds and methods of use thereof for the treatment of viral diseas |
| US20110178107A1 (en) * | 2010-01-20 | 2011-07-21 | Taigen Biotechnology Co., Ltd. | Hcv protease inhibitors |
| ES2558554T3 (es) | 2010-03-09 | 2016-02-05 | Merck Sharp & Dohme Corp. | Compuestos de sililo tricíclicos condensados y métodos de uso de los mismos para el tratamiento de enfermedades víricas |
| AU2011286276A1 (en) | 2010-07-26 | 2013-01-24 | Merck Sharp & Dohme Corp. | Substituted biphenylene compounds and methods of use thereof for the treatment of viral diseases |
| WO2012050848A1 (en) | 2010-09-29 | 2012-04-19 | Schering Corporation | Fused tetracycle derivatives and methods of use thereof for the treatment of viral diseases |
| PE20140039A1 (es) | 2010-12-30 | 2014-03-01 | Enanta Pharm Inc | Inhibidores de serina proteasa de hepatitis c a base de macrociclicos de fenantridina |
| CA2822556A1 (en) | 2010-12-30 | 2012-07-05 | Enanta Pharmaceuticals, Inc | Macrocyclic hepatitis c serine protease inhibitors |
| ES2742299T3 (es) | 2011-03-09 | 2020-02-13 | Jitsubo Co Ltd | Nuevos péptidos entrecruzados que contienen una estructura entrecruzada no peptídica, método para sintetizar péptidos entrecruzados y nuevo compuesto orgánico utilizado en el método |
| WO2012142085A1 (en) | 2011-04-13 | 2012-10-18 | Merck Sharp & Dohme Corp. | 2'-substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
| EP2697242B1 (en) | 2011-04-13 | 2018-10-03 | Merck Sharp & Dohme Corp. | 2'-azido substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| WO2013033899A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for the treatment of viral diseases |
| WO2013033901A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Heterocyclic-substituted benzofuran derivatives and methods of use thereof for the treatment of viral diseases |
| WO2013033900A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases |
| WO2013039876A1 (en) | 2011-09-14 | 2013-03-21 | Merck Sharp & Dohme Corp. | Silyl-containing heterocyclic compounds and methods of use thereof for the treatment of viral diseases |
| CN102617705B (zh) * | 2012-02-16 | 2014-12-31 | 上海纬诺医药科技有限公司 | 抑制丙肝病毒复制的大环类化合物 |
| US9365615B2 (en) | 2013-09-09 | 2016-06-14 | Jitsubo Co., Ltd. | Cross-linked peptides containing non-peptide cross-linked structure, method for synthesizing cross-linked peptides, and novel organic compound used in method |
| US10167298B2 (en) | 2013-10-30 | 2019-01-01 | Merck Sharp & Dohme Corp. | Pseudopolymorphs of an HCV NS5A inhibitor and uses thereof |
| EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
| US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5698390A (en) * | 1987-11-18 | 1997-12-16 | Chiron Corporation | Hepatitis C immunoassays |
| CN1074422C (zh) | 1987-11-18 | 2001-11-07 | 希龙股份有限公司 | 制备含有hcv表位的分离多肽的方法 |
| CA2079105C (en) * | 1990-04-04 | 2000-06-13 | Michael Houghton | Hepatitis c virus protease |
| US5922757A (en) | 1996-09-30 | 1999-07-13 | The Regents Of The University Of California | Treatment and prevention of hepatic disorders |
| EP0932617B1 (en) | 1996-10-18 | 2002-01-16 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly hepatitis c virus ns3 protease |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| PT1012180E (pt) | 1997-08-11 | 2005-04-29 | Boehringer Ingelheim Ca Ltd | Analogos de peptidos inibidores da hepatite c |
| US6323180B1 (en) * | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| AR022061A1 (es) | 1998-08-10 | 2002-09-04 | Boehringer Ingelheim Ca Ltd | Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos. |
| UA74546C2 (en) * | 1999-04-06 | 2006-01-16 | Boehringer Ingelheim Ca Ltd | Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition |
| ATE297946T1 (de) | 2000-04-03 | 2005-07-15 | Vertex Pharma | Inhibitoren von serin proteasen, speziell der hepatitis-c-virus ns3-protease |
| CN1441806A (zh) | 2000-04-05 | 2003-09-10 | 先灵公司 | 包含n-环p2部分的丙型肝炎病毒的大环ns3-丝氨酸蛋白酶抑制剂 |
| NZ521456A (en) * | 2000-04-19 | 2004-07-30 | Schering Corp | Macrocyclic NS3-Serine protease inhibitors of hepatitis C virus comprising alkyl and aryl alanine P2 moieties |
| AR029851A1 (es) | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
| AR034127A1 (es) | 2000-07-21 | 2004-02-04 | Schering Corp | Imidazolidinonas como inhibidores de ns3-serina proteasa del virus de hepatitis c, composicion farmaceutica, un metodo para su preparacion, y el uso de las mismas para la manufactura de un medicamento |
| IL153670A0 (en) | 2000-07-21 | 2003-07-06 | Schering Corp | Novel peptides as ns3-serine protease inhibitors of hepatitis c virus |
| US7244721B2 (en) * | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| CZ2003195A3 (cs) * | 2000-07-21 | 2003-04-16 | Schering Corporation | Peptidové inhibitory serinové proteázy NS3 a farmaceutický prostředek |
| WO2002008251A2 (en) | 2000-07-21 | 2002-01-31 | Corvas International, Inc. | Peptides as ns3-serine protease inhibitors of hepatitis c virus |
| AU3659102A (en) * | 2000-12-12 | 2002-06-24 | Schering Corp | Diaryl peptides as ns3-serine protease inhibitors of hepatits c virus |
| MXPA04007163A (es) | 2002-01-23 | 2004-10-29 | Schering Corp | Compuestos de prolina como inhibidores de la proteasa serina ns3 para utilizarse en el tratamiento de la infeccion por el virus de la hepatitis c. |
| KR100940619B1 (ko) * | 2003-02-07 | 2010-02-05 | 이난타 파마슈티칼스, 인코포레이티드 | 마크로사이클릭 씨형 간염 세린 단백효소 억제제 |
| PL1615613T3 (pl) * | 2003-04-18 | 2010-04-30 | Enanta Pharm Inc | Chinoksalinylowe makrocykliczne inhibitory proteazy serynowej zapalenia wątroby typu C |
-
2004
- 2004-09-23 EP EP04784827A patent/EP1664092B1/en not_active Expired - Lifetime
- 2004-09-23 CA CA002540031A patent/CA2540031A1/en not_active Abandoned
- 2004-09-23 US US10/948,367 patent/US7592419B2/en not_active Expired - Fee Related
- 2004-09-23 DE DE602004031298T patent/DE602004031298D1/de not_active Expired - Lifetime
- 2004-09-23 KR KR1020067005941A patent/KR20060085248A/ko not_active Ceased
- 2004-09-23 PE PE2004000928A patent/PE20050953A1/es not_active Application Discontinuation
- 2004-09-23 RU RU2006113880/04A patent/RU2006113880A/ru not_active Application Discontinuation
- 2004-09-23 AU AU2004276281A patent/AU2004276281A1/en not_active Abandoned
- 2004-09-23 CN CNA2004800349233A patent/CN1894274A/zh active Pending
- 2004-09-23 AR ARP040103438A patent/AR046166A1/es unknown
- 2004-09-23 JP JP2006528146A patent/JP4525982B2/ja not_active Expired - Fee Related
- 2004-09-23 WO PCT/US2004/031136 patent/WO2005030796A1/en not_active Ceased
- 2004-09-23 MX MXPA06003455A patent/MXPA06003455A/es unknown
- 2004-09-23 BR BRPI0414814-2A patent/BRPI0414814A/pt not_active IP Right Cessation
- 2004-09-23 AT AT04784827T patent/ATE497505T1/de not_active IP Right Cessation
- 2004-09-23 TW TW093128803A patent/TWI280964B/zh not_active IP Right Cessation
-
2006
- 2006-03-21 IL IL174459A patent/IL174459A0/en unknown
- 2006-03-24 ZA ZA200602447A patent/ZA200602447B/en unknown
- 2006-03-24 EC EC2006006456A patent/ECSP066456A/es unknown
- 2006-03-24 CO CO06029608A patent/CO5680449A2/es not_active Application Discontinuation
- 2006-04-25 NO NO20061822A patent/NO20061822L/no not_active Application Discontinuation
-
2009
- 2009-07-03 JP JP2009159346A patent/JP2009275048A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| ZA200602447B (en) | 2007-09-26 |
| TWI280964B (en) | 2007-05-11 |
| CA2540031A1 (en) | 2005-04-07 |
| JP4525982B2 (ja) | 2010-08-18 |
| JP2009275048A (ja) | 2009-11-26 |
| JP2007534627A (ja) | 2007-11-29 |
| EP1664092A1 (en) | 2006-06-07 |
| WO2005030796A1 (en) | 2005-04-07 |
| US20050119168A1 (en) | 2005-06-02 |
| ECSP066456A (es) | 2006-09-18 |
| PE20050953A1 (es) | 2005-11-19 |
| DE602004031298D1 (de) | 2011-03-17 |
| US7592419B2 (en) | 2009-09-22 |
| BRPI0414814A (pt) | 2006-11-14 |
| CN1894274A (zh) | 2007-01-10 |
| EP1664092B1 (en) | 2011-02-02 |
| NO20061822L (no) | 2006-06-22 |
| RU2006113880A (ru) | 2007-11-20 |
| MXPA06003455A (es) | 2006-05-31 |
| AU2004276281A1 (en) | 2005-04-07 |
| CO5680449A2 (es) | 2006-09-29 |
| IL174459A0 (en) | 2006-08-01 |
| ATE497505T1 (de) | 2011-02-15 |
| KR20060085248A (ko) | 2006-07-26 |
| TW200526687A (en) | 2005-08-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR046166A1 (es) | Inhibidores macrociclicos de la serina proteasa ns3 del virus de la hepatitis c | |
| AR038183A1 (es) | Peptidos como inhibidores de la proteasa serina ns3 del virus de la hepatitis c | |
| AR030558A1 (es) | COMPUESTOS MACROCICLICOS, QUE INCLUYEN ENANTIOMEROS, ESTEROISOMEROS, ROTAMEROS Y TAUTOMEROS, SALES Y SOLVATOS FARMACEUTICAMENTE ACEPTABLES, COMPOSICIoN FARMACEUTICA, UN METODO PARA SU PREPARACION Y EL USO DE DICHOS COMPUESTOS PARA LA ELABORACION DE UN MEDICAMENTO, INHIBIDORES DE LA SERINA PROTEASA, | |
| PE20030188A1 (es) | Compuesto de anillo fundido como inhibidores de polimerasa del virus de la hepatitis c | |
| AR035854A1 (es) | Compuestos derivados de piridopirimidina y naftiridina, su uso, un procedimiento para prepararlos, una composicion que los comprende, compuestos intermediarios y un proceso para preparar un compuesto sulfuro | |
| HRP20030467B1 (hr) | Tioeterom supstituirani imidazokinolini | |
| AR038214A1 (es) | Compuestos de prolina como inhibidores de la serina proteasa ns3 del virus de la hepatitis c | |
| AR045497A1 (es) | Inhibidores peptidomimeticos de la serina proteasa ns3 del virus de la hepatitis c | |
| AR036093A1 (es) | Compuestos derivados de tiazolidinilo, pirrolidinilo, oxazolidinilo, piperidilo, morfolinilo y tiomorfolinilo, su uso, composiciones farmaceuticas que los comprenden, y compuestos intermediarios | |
| AR048241A1 (es) | Compuestos azufrados como inhibidores de la serina proteasa ns3 del virus de la hepatitis c . | |
| PE20020691A1 (es) | PEPTIDOS DIARILICOS COMO INHIBIDORES DE LA NS3/NS4a SERINA PROTEASA DEL VIRUS DE LA HEPATITIS C | |
| AR029903A1 (es) | Inhibidores macrociclicos de la ns3-serina proteasa, del virus de la hepatitis c, que comprenden partes p2 n-ciclicas, composiciones farmaceuticas y utilizacion de los mismos para la manufactura de un medicamento | |
| AR035933A1 (es) | Un compuesto derivado de fosfonato nucleosido aciclico, uso del mismo, un proceso para su preparacion y un compuesto de fosfonato. | |
| EA200400886A1 (ru) | Макроциклические пептиды, обладающие активностью в отношении вируса гепатита c | |
| AR015512A1 (es) | Derivados ciclicos n-acilo amina, un procedimiento para su preparacion, un intermediario y una composicion farmaceutica | |
| HRP20000896B1 (en) | Adenosine derivatives | |
| AR054327A1 (es) | Fenil-metanonas sustituidas por heterociclos, procesos de preparacion y composiciones farmaceuticas que lo contienen | |
| PE20050940A1 (es) | Nuevos inhibidores de la ns3/ns4a serina proteasa del virus de la hepatitis c | |
| AR033985A1 (es) | Peptidos inhibidores de proteasa serina-ns3 del virus de la hepatitis c, composicion farmaceutica que los comprende, un metodo para su preparacion, uso de los mismos para la fabricacion de un medicamento y un metodo de modulacion de la actividad de la proteasa del virus de la hepatitis c | |
| PE20090630A1 (es) | Derivados de indol 2-carboxi sustituidos y metodos para su utilizacion | |
| AR023152A1 (es) | Compuesto tienopirimidina, procedimiento para producirlo, composicion farmaceutica que lo comprende y uso de dicho compuesto para preparar dichacomposicion | |
| AR056195A1 (es) | Procedimientos para preparar derivados de (etinil-bencil)-benceno sustituidos de glucopiranosilo y compuestos intermedios de los mismos | |
| AR049263A1 (es) | Heterociclos biciclicos inhibidores de quinasa utiles como agentes anticancer | |
| PT1140916E (pt) | Acetais heteroarilo ciclicos | |
| AR021354A1 (es) | Procedimiento para la preparacion de un compuesto derivado de quinolina y un procedimiento para preparar una composicion farmaceutica |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |