AR036111A1 - Compuesto de n-[alfa-aminoalcanoil]-3-fluorpirrolidina; composicion farmaceutica formulada con dicho compuesto; su uso en la preparacion de dicha composicion y metodo para el tratamiento de la diabetes tipo 2 utilizando dicho compuesto - Google Patents
Compuesto de n-[alfa-aminoalcanoil]-3-fluorpirrolidina; composicion farmaceutica formulada con dicho compuesto; su uso en la preparacion de dicha composicion y metodo para el tratamiento de la diabetes tipo 2 utilizando dicho compuestoInfo
- Publication number
- AR036111A1 AR036111A1 ARP020102397A ARP020102397A AR036111A1 AR 036111 A1 AR036111 A1 AR 036111A1 AR P020102397 A ARP020102397 A AR P020102397A AR P020102397 A ARP020102397 A AR P020102397A AR 036111 A1 AR036111 A1 AR 036111A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- het
- ring
- substituted phenyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 208000001072 type 2 diabetes mellitus Diseases 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 13
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 3
- 125000003386 piperidinyl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- -1 for example Chemical compound 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 229940124213 Dipeptidyl peptidase 4 (DPP IV) inhibitor Drugs 0.000 abstract 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 150000001413 amino acids Chemical class 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- BJISZDCMBMQNIY-UHFFFAOYSA-N benzene Chemical group [C-]1=CC=CC=C1 BJISZDCMBMQNIY-UHFFFAOYSA-N 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 239000003603 dipeptidyl peptidase IV inhibitor Substances 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- MDQRDWAGHRLBPA-UHFFFAOYSA-N fluoroamine Chemical compound FN MDQRDWAGHRLBPA-UHFFFAOYSA-N 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07D401/06—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 only aliphatic carbon atoms
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
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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
- 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
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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
- C07D417/12—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 chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Engineering & Computer Science (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Compuestos inhibidores de la dipeptidil peptidasa IV y profármacos de los mismos, utilizables en función de sus propiedades inhibitorias de las peptidilpeptidasas (IV) en el tratamiento de la diabetes tipo 2. Dichos compuestos responden a la fórmula (1) donde: A es F ó H; uno de R1A y R1B se selecciona entre H y CN y el otro es H; R2 se selecciona entre H, alquilo C1-8, fenilo opcionalmente sustituido, bencilo opcionalmente sustituido y R5; R3 se selecciona entre H, alquilo C1-8, adamantilo, adamantilmetilo, adamantiletilo y Het-NH(CH2)a; ó R2 y R3 juntos constituyen una cadena de tres o cuatro grupos metileno, de manera de formar, junto con los átomos a los que se encuentran unidos, un anillo de pirrolidina o piperidina, pudiendo dicho anillo, además fusionarse con un anillo bencenoide; R4 se selecciona entre H, R6OCO, H2NCH(R7)CO, H2NCH(R8)CONHCH(R9)CO y un grupo, de acuerdo con la fórmula general (2); R5 se selecciona entre CH2R13, CH2CH2R13 y C(R14)(R15)-X1-R16; R6 se selecciona entre alquilo C1-8, fenilo opcionalmente sustituido, bencilo opcionalmente sustituido y R17CO2C(R18)(R19); R7, R8 y R9 son cada uno independientemente seleccionados entre las cadenas laterales de los aminoácidos proteináceos; R10 se selecciona entre alquilo C1-8, fenilo y O-(alquilo C1-8); R11 se selecciona entre alquilo C1-8; R12 se selecciona entre H, alquilo C1-8 y fenilo; R13 se selecciona entre CO-N(R20)(R21), N(R22)-C(=X2)R23 y N(R22)R24); R14 y R15 se seleccionan en forma independientemente entre H y metilo, o juntos representan -(CH2)z-; R16 se selecciona entre alquilo C1-8, fenilo opcionalmente sustituido, bencilo opcionalmente sustituido y -(CH2)b-R13; R17 se selecciona entre H y alquilo C1-8; R18 y R19 se seleccionan independientemente entre H y alquilo C1-8, o juntos representan -(CH2)y-; R20 y R21 se seleccionan independientemente entre H, alquilo C1-8, fenilo opcionalmente sustituido, fenilalquilo opcionalmente sustituido, Het y -(CH2)cHet, ó R20 y R21 juntos constituyen una cadena de cuatro o cinco grupos metileno de manera de formar junto con el átomo de nitrógeno al que se encuentran unidos, un anillo de pirrolidina o piperidina, pudiendo además dicho anillo fusionarse con un anillo bencenoide; R22 se selecciona entre H y metilo; R23 se selecciona entre R25, O-R25 y N(R26)(R27); R24 se selecciona entre fenilo opcionalmente sustituido, Het y -CH2-Het; R25 se selecciona entre alquilo C1-8, fenilo opcionalmente sustituido, fenilalquilo opcionalmente sustituido, Het y -(CH2)cHet; R26 y R27 se seleccionan independientemente entre H, alquilo C1-8, fenilo opcionalmente sustituido, fenilalquilo opcionalmente sustituido, Het y -(CH2)cHet, ó R26 y R27 juntos forman una cadena de cuatro o cinco grupos metileno de manera de formar, junto con el átomo de nitrógeno al que se encuentran unidos, un anillo de pirrolidina o piperidina, pudiendo además dicho anillo fusionarse con un anillo bencenoide; Het es un heterociclo aromático que contiene nitrógeno seleccionado entre piridilo, piridazinilo, pirimidinilo, pirazinilo, imidazolilo, tiazolilo, isotiazolilo, oxazolilo, isoxazolilo y análogos de éstos fusionados con benceno, como por ejemplo, quinolinilo, isoquinolinilo, quinoxalinilo, bencimidazolilo y similares, pudiendo todos ellos sustituirse opcionalmente en uno o más átomos de carbono, y donde los sustituyentes se seleccionan entre grupos alquilo inferior, hidroxi, alquiloxi inferior, amino, alquilamino inferior, di(alquilo inferior)amino, flúor, cloro, bromo, trifluorometilo, nitro, ciano, carboxi y alquiloxicarbonilo inferior; X1 se selecciona entre -O-, -S- ó -CH2-; X2 se selecciona entre O y S; a representa 2 ó 3; b representa 1, 2 ó 3; c representa 1 ó 2; e y y z representan 2, 3 ó 4. Se describen y reivindican, además, los objetos restantes mencionados en el título.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0115517.5A GB0115517D0 (en) | 2001-06-25 | 2001-06-25 | Novel antidiabetic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR036111A1 true AR036111A1 (es) | 2004-08-11 |
Family
ID=9917321
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020102397A AR036111A1 (es) | 2001-06-25 | 2002-06-26 | Compuesto de n-[alfa-aminoalcanoil]-3-fluorpirrolidina; composicion farmaceutica formulada con dicho compuesto; su uso en la preparacion de dicha composicion y metodo para el tratamiento de la diabetes tipo 2 utilizando dicho compuesto |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US20040235752A1 (es) |
| EP (1) | EP1399154A1 (es) |
| JP (1) | JP2004534815A (es) |
| KR (1) | KR20040010748A (es) |
| CN (1) | CN1520293A (es) |
| AR (1) | AR036111A1 (es) |
| AU (1) | AU2002302857B2 (es) |
| CA (1) | CA2449441A1 (es) |
| CZ (1) | CZ20033413A3 (es) |
| GB (1) | GB0115517D0 (es) |
| HU (1) | HUP0400365A2 (es) |
| IL (1) | IL159152A0 (es) |
| MX (1) | MXPA03011981A (es) |
| NO (1) | NO20035775L (es) |
| NZ (1) | NZ529925A (es) |
| PL (1) | PL364902A1 (es) |
| RU (1) | RU2003136148A (es) |
| UY (1) | UY27357A1 (es) |
| WO (1) | WO2003000250A1 (es) |
| ZA (1) | ZA200309624B (es) |
Families Citing this family (155)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI243162B (en) * | 2000-11-10 | 2005-11-11 | Taisho Pharmaceutical Co Ltd | Cyanopyrrolidine derivatives |
| US7232924B2 (en) | 2001-06-11 | 2007-06-19 | Xenoport, Inc. | Methods for synthesis of acyloxyalkyl derivatives of GABA analogs |
| US7186855B2 (en) | 2001-06-11 | 2007-03-06 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
| AU2002310409C1 (en) | 2001-06-11 | 2008-04-17 | Xenoport, Inc. | Orally administered dosage forms of GABA analog prodrugs having reduced toxicity |
| US6818787B2 (en) | 2001-06-11 | 2004-11-16 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
| US8048917B2 (en) | 2005-04-06 | 2011-11-01 | Xenoport, Inc. | Prodrugs of GABA analogs, compositions and uses thereof |
| JP3909056B2 (ja) * | 2001-06-27 | 2007-04-25 | スミスクライン ビーチャム コーポレーション | ジペプチジルペプチダーゼ阻害剤としてのフルオロピロリジン類 |
| ATE370943T1 (de) | 2001-06-27 | 2007-09-15 | Smithkline Beecham Corp | Fluoropyrrolidine als dipeptidyl-peptidase inhibitoren |
| ATE380175T1 (de) | 2001-06-27 | 2007-12-15 | Smithkline Beecham Corp | Pyrrolidine als dipeptidyl peptidase inhibitoren |
| CN1939529A (zh) * | 2002-01-29 | 2007-04-04 | Wyeth公司 | 用于调节连接蛋白半通道的组合物和方法 |
| HUP0200849A2 (hu) * | 2002-03-06 | 2004-08-30 | Sanofi-Synthelabo | N-aminoacetil-2-ciano-pirrolidin-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra |
| US7105526B2 (en) | 2002-06-28 | 2006-09-12 | Banyu Pharmaceuticals Co., Ltd. | Benzimidazole derivatives |
| TW200401635A (en) | 2002-07-23 | 2004-02-01 | Yamanouchi Pharma Co Ltd | 2-Cyano-4-fluoropyrrolidine derivative or salt thereof |
| US7407955B2 (en) | 2002-08-21 | 2008-08-05 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions |
| JP2006508975A (ja) | 2002-11-18 | 2006-03-16 | ファイザー・プロダクツ・インク | ジペプチジルペプチダーゼivを阻害するフッ素化環状アミド |
| US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
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-
2001
- 2001-06-25 GB GBGB0115517.5A patent/GB0115517D0/en not_active Ceased
-
2002
- 2002-06-24 JP JP2003506896A patent/JP2004534815A/ja not_active Withdrawn
- 2002-06-24 WO PCT/GB2002/002880 patent/WO2003000250A1/en not_active Ceased
- 2002-06-24 CN CNA028127196A patent/CN1520293A/zh active Pending
- 2002-06-24 HU HU0400365A patent/HUP0400365A2/hu unknown
- 2002-06-24 NZ NZ529925A patent/NZ529925A/en unknown
- 2002-06-24 RU RU2003136148/04A patent/RU2003136148A/ru not_active Application Discontinuation
- 2002-06-24 MX MXPA03011981A patent/MXPA03011981A/es unknown
- 2002-06-24 PL PL02364902A patent/PL364902A1/xx not_active Application Discontinuation
- 2002-06-24 US US10/481,798 patent/US20040235752A1/en not_active Abandoned
- 2002-06-24 CZ CZ20033413A patent/CZ20033413A3/cs unknown
- 2002-06-24 EP EP02730539A patent/EP1399154A1/en not_active Withdrawn
- 2002-06-24 KR KR10-2003-7016581A patent/KR20040010748A/ko not_active Ceased
- 2002-06-24 IL IL15915202A patent/IL159152A0/xx unknown
- 2002-06-24 AU AU2002302857A patent/AU2002302857B2/en not_active Ceased
- 2002-06-24 CA CA002449441A patent/CA2449441A1/en not_active Abandoned
- 2002-06-25 UY UY27357A patent/UY27357A1/es not_active Application Discontinuation
- 2002-06-26 AR ARP020102397A patent/AR036111A1/es not_active Application Discontinuation
-
2003
- 2003-12-11 ZA ZA200309624A patent/ZA200309624B/en unknown
- 2003-12-22 NO NO20035775A patent/NO20035775L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1399154A1 (en) | 2004-03-24 |
| CN1520293A (zh) | 2004-08-11 |
| NZ529925A (en) | 2005-04-29 |
| KR20040010748A (ko) | 2004-01-31 |
| US20040235752A1 (en) | 2004-11-25 |
| RU2003136148A (ru) | 2005-05-20 |
| ZA200309624B (en) | 2004-06-11 |
| UY27357A1 (es) | 2002-09-30 |
| NO20035775L (no) | 2004-02-23 |
| PL364902A1 (en) | 2004-12-27 |
| CA2449441A1 (en) | 2003-01-03 |
| IL159152A0 (en) | 2004-06-01 |
| JP2004534815A (ja) | 2004-11-18 |
| CZ20033413A3 (cs) | 2004-05-12 |
| AU2002302857B2 (en) | 2007-01-25 |
| MXPA03011981A (es) | 2004-06-03 |
| HUP0400365A2 (hu) | 2004-08-30 |
| WO2003000250A1 (en) | 2003-01-03 |
| GB0115517D0 (en) | 2001-08-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |