AR061570A1 - Compuesto de glicina sustituido en el n heteroaromatico composicion farmaceutica que lo comprende, su uso para preparar un medicamento, procedimientos para preparar dicha composicion farmaceutica y para preparar el compuesto - Google Patents
Compuesto de glicina sustituido en el n heteroaromatico composicion farmaceutica que lo comprende, su uso para preparar un medicamento, procedimientos para preparar dicha composicion farmaceutica y para preparar el compuestoInfo
- Publication number
- AR061570A1 AR061570A1 ARP070102741A ARP070102741A AR061570A1 AR 061570 A1 AR061570 A1 AR 061570A1 AR P070102741 A ARP070102741 A AR P070102741A AR P070102741 A ARP070102741 A AR P070102741A AR 061570 A1 AR061570 A1 AR 061570A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heteroaryl
- aryl
- heterocycloalkyl
- cycloalkyl
- Prior art date
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Classifications
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- 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
- C07D487/08—Bridged systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
- A61K31/515—Barbituric acids; Derivatives thereof, e.g. sodium pentobarbital
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/60—Three or more oxygen or sulfur atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/60—Three or more oxygen or sulfur atoms
- C07D239/62—Barbituric acids
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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
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/10—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 carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—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 only aliphatic carbon atoms
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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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
Un compuesto de glicina sustituido en el N heteroaromático de la formula (1): en la que: R1 y R4 cada uno se selecciona independientemente del grupo que consiste en hidrogeno, -NR5R6, alquilo C1-10, alquenilo C2-10, alquinilo C2-C10, cicloalquilo C3- 8, cicloalquil C3-8-alquilo C1-10, cicloalquenilo C5-8, cicloalquenil C5-8-alquilo C1-10, heterocicloalquilo C3-8, heterocicloalquil C3-8-alquilo C1-10, arilo, aril-alquilo C1-10, heteroarilo y heteroaril-alquilo C1-10; R2 es -NR7R8 o -OR9; R3 es H o alquilo C1-4 en la que R5 y R6 cada uno se selecciona independientemente del grupo que consiste en hidrogeno, alquilo C1-C10, cicloalquilo C3-8, cicloalquil C3-8-alquilo C1-10, heterocicloalquilo C3-8, heterocicloalquil C3-8-alquilo C1-C10, arilo, aril-alquilo C1-10, heteroarilo, heteroaril-alquilo C1-10, -C(O) alquil C1-4, -C(O)cicloalquil C3-6, -C(O)heterocicloalquil C3-6, -C(O)aril, -C(O)heteroaril y -S(O)2alquil C1-4, o, cuando R5 y R6 están unidos al mismo nitrogeno, R5 y R6 tomados juntos con el nitrogeno al que están unidos forman un anillo saturado de 5 o 6 o 7 miembros que opcionalmente contienen otro heteroátomo seleccionado de oxígeno, nitrogeno y azufre, R7 y R8 cada uno se selecciona independientemente del grupo que consiste en hidrogeno, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-8, heterocicloalquilo C3-8, arilo y heteroarilo, y R9 es H o un cation, o alquilo C1-10 que está sin sustituir o sustituido con uno o más sustituyentes seleccionados independientemente entre el grupo que consiste en cicloalquilo C3-6, heterocicloalquilo, arilo y heteroarilo; X es O o S; e Y es O o S; en la que cualquier carbono o heteroátomo de R1, R2, R3, R4, R5, R6, R7, R8, R9 está sin sustituir o está sustituido con uno o más sustituyentes seleccionados independientemente de alquilo C1-6, haloalquilo C1-6, halogeno, -OR10, -NR5R6, oxo, ciano, nitro, -C(O)R10, - C(O)OR10, -SR10, -S(O)R10, -S(O)2R10, -NR5R6, -CONR5R6, -N(R5)C(O)R10, - N(R5)C(O)OR10, -OC(0)NR5R6, -N(R5)C(O)NR5R6, -SO2NR5R6, -N(R5)SO2R10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-6, heterocicloalquilo C3-6, arilo, alquil C1-6-arilo, heteroarilo y alquil C1-6-heteroarilo, donde R5 y R6 son igual a como se han definido más arriba y R10 se selecciona de hidrogeno, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, -C(O)alquil C1-4, -C(O)aril, -C(O)heteroaril, -C(O)cicloalquil C3-6, -C(O)heterocicloalquil C3-6, -S(O)2aIquil C1-4, cicloalquilo C3-8, heterocicloalquilo C3-8, arilo C6-14, aril-alquilo C1-10, heteroarilo y heteroaril-alquilo C1-10 y/o una sal farmacéuticamente aceptable o solvato del mismo. Composicion farmacéutica que lo comprende. Uso de dicho compuesto para preparar un medicamento util para tratar la anemia, para inhibir HIF prolil hidroxilasas, para tratar la isquemia, infarto de miocardio y su uso junto con EPO o un derivado de la misma para preparar un medicamento util para tratar enfermedades del sistema hematopoyético. Procedimiento para preparar una composicion farmacéutica que comprende dicho compuesto. Procedimientos para preparar dicho compuesto.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US80560206P | 2006-06-23 | 2006-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR061570A1 true AR061570A1 (es) | 2008-09-03 |
Family
ID=38834409
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070102741A AR061570A1 (es) | 2006-06-23 | 2007-06-21 | Compuesto de glicina sustituido en el n heteroaromatico composicion farmaceutica que lo comprende, su uso para preparar un medicamento, procedimientos para preparar dicha composicion farmaceutica y para preparar el compuesto |
Country Status (31)
Country | Link |
---|---|
US (10) | US8324208B2 (es) |
EP (1) | EP2037922B9 (es) |
JP (1) | JP5203361B2 (es) |
KR (1) | KR101411816B1 (es) |
CN (1) | CN101505752B (es) |
AR (1) | AR061570A1 (es) |
AU (1) | AU2007260837B2 (es) |
BR (1) | BRPI0713446B8 (es) |
CA (1) | CA2655491C (es) |
CR (1) | CR10534A (es) |
DK (1) | DK2037922T3 (es) |
EA (1) | EA018220B1 (es) |
ES (1) | ES2453100T3 (es) |
HK (1) | HK1130671A1 (es) |
HR (1) | HRP20140306T1 (es) |
IL (1) | IL196070A (es) |
JO (1) | JO2934B1 (es) |
MA (1) | MA30526B1 (es) |
MX (1) | MX2009000165A (es) |
MY (1) | MY149861A (es) |
NO (1) | NO342019B1 (es) |
NZ (1) | NZ573698A (es) |
PE (1) | PE20080209A1 (es) |
PL (1) | PL2037922T3 (es) |
PT (1) | PT2037922E (es) |
SG (1) | SG174775A1 (es) |
SI (1) | SI2037922T1 (es) |
TW (1) | TWI394747B (es) |
UA (1) | UA100225C2 (es) |
WO (1) | WO2007150011A2 (es) |
ZA (1) | ZA200810602B (es) |
Families Citing this family (85)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090299063A1 (en) * | 2005-03-29 | 2009-12-03 | Paul Shapiro | Inhibitors for Extracellular Signal-Regulated Kinase Docking Domains and Uses Therefor |
US7588924B2 (en) | 2006-03-07 | 2009-09-15 | Procter & Gamble Company | Crystal of hypoxia inducible factor 1 alpha prolyl hydroxylase |
AR061570A1 (es) | 2006-06-23 | 2008-09-03 | Smithkline Beecham Corp | Compuesto de glicina sustituido en el n heteroaromatico composicion farmaceutica que lo comprende, su uso para preparar un medicamento, procedimientos para preparar dicha composicion farmaceutica y para preparar el compuesto |
PL2044005T3 (pl) | 2006-06-26 | 2011-04-29 | Akebia Therapeutics Inc | Inhibitory hydroksylazy prolilowej oraz metody ich wykorzystania |
GB0622472D0 (en) * | 2006-11-10 | 2006-12-20 | Addex Pharmaceuticals Sa | Novel heterocyclic derivatives |
US7635715B2 (en) | 2006-12-18 | 2009-12-22 | Amgen Inc. | Naphthalenone compounds exhibiting prolyl hydroxylase inhibitory activity, compositions, and uses thereof |
CA2672652C (en) | 2006-12-18 | 2012-04-17 | Amgen Inc. | Azaquinolone based compounds exhibiting prolyl hydroxylase inhibitory activity, compositions, and uses thereof |
AU2008241577B2 (en) | 2007-04-18 | 2011-04-07 | Amgen Inc. | Indanone derivatives that inhibit prolyl hydroxylase |
US8048894B2 (en) | 2007-04-18 | 2011-11-01 | Amgen Inc. | Quinolones and azaquinolones that inhibit prolyl hydroxylase |
EP2150251B9 (en) | 2007-05-04 | 2013-02-27 | Amgen, Inc | Thienopyridine and thiazolopyridine derivatives that inhibit prolyl hydroxylase activity |
US8097620B2 (en) | 2007-05-04 | 2012-01-17 | Amgen Inc. | Diazaquinolones that inhibit prolyl hydroxylase activity |
KR101552474B1 (ko) * | 2007-09-17 | 2015-09-11 | 애브비 바하마스 리미티드 | C형 간염 치료용 우라실 또는 티민 유도체 |
WO2009089547A1 (en) | 2008-01-11 | 2009-07-16 | Fibrogen, Inc. | Isothiazole-pyridine derivatives as modulators of hif (hypoxia inducible factor) activity |
US8324405B2 (en) | 2008-02-05 | 2012-12-04 | Fibrogen, Inc. | Chromene derivatives and use thereof as HIF hydroxylase activity inhibitors |
WO2009117269A1 (en) * | 2008-03-18 | 2009-09-24 | Merck & Co., Inc. | Substituted 4-hydroxypyrimidine-5-carboxamides |
PT2294066E (pt) | 2008-04-28 | 2014-11-21 | Janssen Pharmaceutica Nv | Benzoimidazoles como inibidores da prolil-hidroxilase |
GB0809262D0 (en) | 2008-05-21 | 2008-06-25 | Isis Innovation | Assay |
JP2011525924A (ja) * | 2008-06-25 | 2011-09-29 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | プロリルヒドロキシラーゼ阻害剤 |
CN102264740B (zh) | 2008-08-20 | 2014-10-15 | 菲布罗根有限公司 | 一种吡咯[1,2-b]哒嗪衍生物及其作为hif调节剂的用途 |
WO2010025087A1 (en) * | 2008-08-25 | 2010-03-04 | Smithkline Beecham Corporation | Prolyl hydroxylase inhibitors |
CN102272117B (zh) | 2008-11-14 | 2015-06-17 | 菲布罗根有限公司 | 作为hif羟化酶抑制剂的苯并噻喃衍生物 |
JP5643233B2 (ja) | 2009-02-10 | 2014-12-17 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプJanssen Pharmaceutica Naamloze Vennootschap | プロリルヒドロキシラーゼ阻害物質としてのキナゾリノン |
JP2012521411A (ja) * | 2009-03-26 | 2012-09-13 | マピ ファーマ リミテッド | アログリプチンの調製プロセス |
EP3144299A1 (en) * | 2009-05-05 | 2017-03-22 | Cambria Pharmaceuticals, Inc. | Pyrimidine-2,4,6-triones for use in the treatment of amyotrophic lateral sclerosis |
KR101706803B1 (ko) * | 2009-07-17 | 2017-02-14 | 니뽄 다바코 산교 가부시키가이샤 | 트리아졸로피리딘 화합물, 그리고 그 프롤릴 수산화효소 저해제 및 에리트로포이에틴 생성 유도제로서의 작용 |
TWI500623B (zh) * | 2009-10-13 | 2015-09-21 | Torrent Pharmaceuticals Ltd | 新穎稠合噻唑及噁唑嘧啶酮 |
HUE026128T2 (en) * | 2009-10-21 | 2016-05-30 | Daiichi Sankyo Co Ltd | 5-Hydroxy-pyrimidine-4-carboxamide derivative |
EP2496082B1 (en) | 2009-11-06 | 2016-10-12 | Aerpio Therapeutics, Inc. | Methods for increasing the stabilization of hypoxia inducible factor-1 alpha |
JP5755741B2 (ja) | 2010-08-13 | 2015-07-29 | ヤンセン ファーマシューティカ エヌ.ベー. | プロリルヒドロキシラーゼインヒビタとしての4−アミノキナゾリン−2−イル−1−ピラゾール−4−カルボン酸化合物 |
WO2012106472A1 (en) | 2011-02-02 | 2012-08-09 | Fibrogen, Inc. | Naphthyridine derivatives as inhibitors of hypoxia inducible factor (hif) hydroxylase |
GB201102659D0 (en) | 2011-02-15 | 2011-03-30 | Isis Innovation | Assay |
AU2012268400C1 (en) | 2011-06-06 | 2016-12-22 | Akebia Therapeutics Inc. | Compounds and compositions for stabilizing hypoxia inducible factor-2 alpha as a method for treating cancer |
NO2686520T3 (es) | 2011-06-06 | 2018-03-17 | ||
GB201113101D0 (en) | 2011-07-28 | 2011-09-14 | Isis Innovation | Assay |
WO2013040789A1 (en) * | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
WO2013040790A1 (en) * | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
WO2013043621A1 (en) | 2011-09-23 | 2013-03-28 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
US9079930B2 (en) | 2011-09-23 | 2015-07-14 | Merck Sharp & Dohme Corp. | Substituted pyrimidines |
CN102432549B (zh) * | 2011-09-28 | 2014-09-03 | 南通市华峰化工有限责任公司 | 一种抑制血管生成、肿瘤发生和增殖疾病的药物中间体1,3-二环己基巴比妥酸的制备方法 |
MX344109B (es) | 2011-10-25 | 2016-12-05 | Janssen Pharmaceutica Nv | Formulaciones de sal de meglumina del ácido 1-(5,6-dicloro-1h-benz o[d]imidazol-2-il)-1h-pirazol-4-carboxílico. |
WO2013070908A1 (en) * | 2011-11-09 | 2013-05-16 | Fibrogen, Inc. | Therapeutic method |
UA112897C2 (uk) * | 2012-05-09 | 2016-11-10 | Байєр Фарма Акцієнгезелльшафт | Біциклічно заміщені урацили та їх застосування для лікування і/або профілактики захворювань |
BR112015002153B1 (pt) | 2012-07-30 | 2022-09-20 | Taisho Pharmaceutical Co., Ltd | Composto heterocíclico parcialmente saturado contendo nitrogênio e seu uso, medicamento, inibidor de prolil hidroxilase 2 (phd2), promotor de produção de fator hematopoiético eritropoietina (epo) e fármaco |
CN103146720B (zh) * | 2013-03-01 | 2014-12-03 | 河北博伦特药业有限公司 | 一种具有高转化率的反式-4-羟基-l-脯氨酸羟化酶改造基因及其应用 |
CA2914662C (en) | 2013-06-13 | 2022-05-31 | Robert Shalwitz | Compositions and methods for treating anemia |
US9695131B2 (en) | 2013-11-08 | 2017-07-04 | Bayer Pharma Aktiengesellschaft | Substituted uracils as chymase inhibitors |
CN105980381A (zh) * | 2013-11-08 | 2016-09-28 | 拜耳医药股份有限公司 | 取代的尿嘧啶及其用途 |
CR20200220A (es) | 2013-11-15 | 2020-11-18 | Akebia Therapeutics Inc | FORMAS SÓLIDAS DE ÁCIDO {[5-(3-CLOROFENIL)-3-HIDROXIPIRIDIN-2-CARBONIL]AMINO}ACÉTICO, COMPOSICIONES, Y USOS DE LAS MISMAS (Divisional 2016-0222) |
JP5975122B2 (ja) * | 2014-01-29 | 2016-08-23 | 大正製薬株式会社 | [(4−ヒドロキシ−2−オキソ−1,2,5,6−テトラヒドロ−3−ピリジニル)カルボニル]グリシン化合物の結晶形及びそれらの製造方法 |
SG11201606862VA (en) * | 2014-02-19 | 2016-09-29 | Aerpio Therapeutics Inc | Process for preparing n-benzyl-3-hydroxy-4-substituted-pyridin-2-(1h)-ones |
CN104151254A (zh) * | 2014-07-25 | 2014-11-19 | 南通市华峰化工有限责任公司 | 一种制备1,3-双环己基巴比妥酸的方法 |
WO2016034108A1 (zh) | 2014-09-02 | 2016-03-10 | 广东东阳光药业有限公司 | 喹啉酮类化合物及其应用 |
WO2016054805A1 (en) * | 2014-10-10 | 2016-04-14 | Merck Sharp & Dohme Corp. | Substituted pyrimidines as inhibitors of hif prolyl hydroxylase |
WO2016054806A1 (en) * | 2014-10-10 | 2016-04-14 | Merck Sharp & Dohme Corp. | Substittued pyridine inhibitors of hif prolyl hydroxylase |
JP2018039733A (ja) * | 2014-12-22 | 2018-03-15 | 株式会社富士薬品 | 新規複素環誘導体 |
US10150734B2 (en) | 2015-01-23 | 2018-12-11 | Akebia Therapeutics, Inc. | Solid forms of 2-(5-(3-fluorophenyl)-3-hydroxypicolinamido)acetic acid, compositions, and uses thereof |
CN106146395B (zh) | 2015-03-27 | 2019-01-01 | 沈阳三生制药有限责任公司 | 3-羟基吡啶化合物、其制备方法及其制药用途 |
KR20240038132A (ko) | 2015-04-01 | 2024-03-22 | 아케비아 테라퓨틱스 인코포레이티드 | 빈혈 치료용 조성물 및 방법 |
US10401548B2 (en) * | 2015-09-24 | 2019-09-03 | Intel Corporation | Integrated antenna with display uniformity |
CN108347916B (zh) | 2015-10-14 | 2022-02-08 | 先时迈纳米生物科技股份有限公司 | 一种减少冰晶形成的组合物及其方法 |
JP6325139B2 (ja) * | 2016-03-02 | 2018-05-16 | ネルファルマ・エッセ・エッルレ・エッレ | カルムスチンの安全で効率的な製造方法 |
WO2018205928A1 (zh) | 2017-05-09 | 2018-11-15 | 杭州安道药业有限公司 | 吲哚嗪衍生物及其在医药上的应用 |
CN111518038B (zh) * | 2017-05-26 | 2022-04-05 | 深圳市塔吉瑞生物医药有限公司 | 一种取代的嘧啶三酮化合物及包含该化合物的组合物及其用途 |
CA3112277A1 (en) * | 2017-09-15 | 2019-03-21 | Crystal Pharmaceutical (Suzhou) Co., Ltd. | Crystal form of gsk1278863 and preparation method and pharmaceutical use thereof |
CA3097219A1 (en) | 2018-05-09 | 2019-11-14 | Akebia Therapeutics, Inc. | Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid |
CN109134356A (zh) * | 2018-06-18 | 2019-01-04 | 苏州盖德精细材料有限公司 | 一种中间体2-氨基吡啶-4-甲醇的制备方法 |
EP3880663A1 (en) | 2018-11-15 | 2021-09-22 | Teva Pharmaceuticals International GmbH | Solid state forms of daprodustat and process for preparation thereof |
CN113811530B (zh) * | 2019-07-03 | 2022-07-19 | 南京明德新药研发有限公司 | 作为糜酶抑制剂的嘧啶酮类化合物及其应用 |
WO2021031102A1 (zh) * | 2019-08-20 | 2021-02-25 | 深圳仁泰医药科技有限公司 | Daprodustat的晶型及其制备方法和用途 |
US11524939B2 (en) | 2019-11-13 | 2022-12-13 | Akebia Therapeutics, Inc. | Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino} acetic acid |
TW202200134A (zh) | 2020-04-20 | 2022-01-01 | 美商阿克比治療有限公司 | 治療病毒感染、器官損傷及相關症狀之方法 |
BR112022024533A2 (pt) | 2020-06-19 | 2022-12-27 | Glaxosmithkline Ip No 2 Ltd | Formulação compreendendo daprodustat |
CN114671878B (zh) * | 2020-12-25 | 2023-08-04 | 广东东阳光药业有限公司 | 取代的含氮双环化合物及其用途 |
WO2022150623A1 (en) | 2021-01-08 | 2022-07-14 | Akebia Therapeutics, Inc. | Compounds and composition for the treatment of anemia |
WO2022179967A1 (en) | 2021-02-23 | 2022-09-01 | Glaxosmithkline Intellectual Property (No.2) Limited | Vadadustat for treating covid-19 in a hospitalized subject |
TW202313072A (zh) | 2021-05-27 | 2023-04-01 | 美商凱立克斯生物製藥股份有限公司 | 檸檬酸鐵之兒科調配物 |
US20240228443A1 (en) | 2021-06-18 | 2024-07-11 | Glaxosmithkline Intellectual Property (No.2) Limited | Novel manufacturing method of daprodustat and precursors thereof |
WO2023006986A1 (en) | 2021-07-30 | 2023-02-02 | Dipharma Francis S.R.L. | Method for preparing and purifying an agent suitable for treating anemia |
IT202200008693A1 (it) | 2022-04-29 | 2023-10-29 | Dipharma Francis Srl | Metodo per la preparazione e la purificazione di un agente per il trattamento dell'anemia |
IT202100020591A1 (it) | 2021-07-30 | 2023-01-30 | Dipharma Francis Srl | Preparazione di un intermedio di un agente per il trattamento dell'anemia |
IT202100020609A1 (it) | 2021-07-30 | 2023-01-30 | Dipharma Francis Srl | Metodo di preparazione di agente adatto per il trattamento dell'anemia |
WO2024022998A1 (en) | 2022-07-26 | 2024-02-01 | Inke, S.A. | Process for preparing daprodustat and cocrystals thereof |
GB202211231D0 (en) | 2022-08-02 | 2022-09-14 | Glaxosmithkline Ip No 2 Ltd | Novel formulation |
GB202301059D0 (en) | 2023-01-25 | 2023-03-08 | Univ Oxford Innovation Ltd | PHD inhibitors |
WO2024256830A1 (en) | 2023-06-14 | 2024-12-19 | Cipla Limited | Daprodustat polymorphs and processes for preparation thereof |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0424064B1 (en) | 1989-10-16 | 1995-02-08 | Chiroscience Limited | Chiral azabicyloheptanone and a process for their preparation |
ES2101420T3 (es) * | 1993-11-02 | 1997-07-01 | Hoechst Ag | Esteres-amidas de acidos carboxilicos heterociclicos sustituidos, su preparacion y su utilizacion como medicamentos. |
AU5316900A (en) * | 1999-06-03 | 2000-12-28 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) |
US6878743B2 (en) * | 2001-09-18 | 2005-04-12 | Sunesis Pharmaceuticals, Inc. | Small molecule inhibitors of caspases |
JP2005524612A (ja) * | 2001-12-06 | 2005-08-18 | ファイブローゲン、インコーポレーテッド | 内因性エリスロポエチン(epo)を増加させる方法 |
US7180893B1 (en) | 2002-03-22 | 2007-02-20 | Juniper Networks, Inc. | Parallel layer 2 and layer 3 processing components in a network router |
JP2006500351A (ja) * | 2002-08-13 | 2006-01-05 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | マトリックスメタロプロテアーゼ−13阻害剤としてのピリミジン−2,4−ジオン誘導体 |
US8614204B2 (en) * | 2003-06-06 | 2013-12-24 | Fibrogen, Inc. | Enhanced erythropoiesis and iron metabolism |
SI1644336T1 (sl) | 2003-06-06 | 2011-06-30 | Fibrogen Inc | Heteroarilne spojine, ki vsebujejo duĺ ik in njihova uporaba pri zviĺ anju endogenega eritropoetina |
EP1699777B1 (en) * | 2003-09-08 | 2012-12-12 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
EA013427B1 (ru) * | 2004-03-15 | 2010-04-30 | Такеда Фармасьютикал Компани Лимитед | Ингибиторы дипептидилпептидазы |
JP2007277096A (ja) | 2004-07-15 | 2007-10-25 | Astellas Pharma Inc | フェネチルニコチンアミド誘導体含有医薬 |
US7718624B2 (en) * | 2004-09-01 | 2010-05-18 | Sitkovsky Michail V | Modulation of immune response and inflammation by targeting hypoxia inducible factors |
JP5390184B2 (ja) * | 2005-06-06 | 2014-01-15 | ファイブローゲン、インコーポレーテッド | 貧血の改良された治療方法 |
WO2007048042A2 (en) * | 2005-10-21 | 2007-04-26 | University Of Alabama At Birmingham | Small molecule inhibitors of hiv-1 capsid assembly |
US20070293575A1 (en) * | 2006-06-15 | 2007-12-20 | Fibrogen, Inc. | Compounds and methods for treatment of cancer-related anemia |
US7713986B2 (en) * | 2006-06-15 | 2010-05-11 | Fibrogen, Inc. | Compounds and methods for treatment of chemotherapy-induced anemia |
AR061570A1 (es) * | 2006-06-23 | 2008-09-03 | Smithkline Beecham Corp | Compuesto de glicina sustituido en el n heteroaromatico composicion farmaceutica que lo comprende, su uso para preparar un medicamento, procedimientos para preparar dicha composicion farmaceutica y para preparar el compuesto |
PE20080943A1 (es) * | 2006-06-23 | 2008-09-27 | Smithkline Beecham Corp | Sal toluenosulfonato de 4-{[6-cloro-3-({[(2-cloro-3-fluorofenil)amino]carbonil}amino)-2-hidroxifenil]sulfonil}-1-piperazinacarboxilato de 1,1-dimetiletilo como antagonista del receptor de il-8 |
US20090011051A1 (en) | 2006-09-28 | 2009-01-08 | Roth Mark B | Methods, Compositions and Articles of Manufacture for HIF Modulating Compounds |
WO2008073292A2 (en) * | 2006-12-08 | 2008-06-19 | Caritas St. Elizabeth's Medical Center Of Boston, Inc. | Method for protecting renal tubular epithelial cells from radiocontrast nephro parhy (rcn) |
TW200845994A (en) * | 2007-01-12 | 2008-12-01 | Smithkline Beecham Corp | N-substituted glycine derivatives: prolyl hydroxylase inhibitors |
CA3112277A1 (en) | 2017-09-15 | 2019-03-21 | Crystal Pharmaceutical (Suzhou) Co., Ltd. | Crystal form of gsk1278863 and preparation method and pharmaceutical use thereof |
EP3880663A1 (en) | 2018-11-15 | 2021-09-22 | Teva Pharmaceuticals International GmbH | Solid state forms of daprodustat and process for preparation thereof |
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