ES2381452T3 - PIPERIDINO-DIHIDROTIENOPIRIMIDINAS sustituidas - Google Patents
PIPERIDINO-DIHIDROTIENOPIRIMIDINAS sustituidas Download PDFInfo
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- ES2381452T3 ES2381452T3 ES08839793T ES08839793T ES2381452T3 ES 2381452 T3 ES2381452 T3 ES 2381452T3 ES 08839793 T ES08839793 T ES 08839793T ES 08839793 T ES08839793 T ES 08839793T ES 2381452 T3 ES2381452 T3 ES 2381452T3
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- alkyl
- alkylene
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- het
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- 150000003254 radicals Chemical class 0.000 abstract 29
- 125000002947 alkylene group Chemical group 0.000 abstract 25
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 24
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 21
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 15
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 150000002367 halogens Chemical class 0.000 abstract 13
- 125000001072 heteroaryl group Chemical group 0.000 abstract 13
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 10
- 125000004043 oxo group Chemical group O=* 0.000 abstract 10
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 10
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 8
- 108010081348 HRT1 protein Hairy Proteins 0.000 abstract 8
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 abstract 8
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 6
- 229920006395 saturated elastomer Polymers 0.000 abstract 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 5
- -1 -Het Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 229910052794 bromium Inorganic materials 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 4
- 239000000460 chlorine Substances 0.000 abstract 4
- 229920001577 copolymer Chemical group 0.000 abstract 4
- 229910052731 fluorine Inorganic materials 0.000 abstract 4
- 125000005842 heteroatom Chemical group 0.000 abstract 4
- 125000002950 monocyclic group Chemical group 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- 125000003367 polycyclic group Chemical group 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- BSFODEXXVBBYOC-UHFFFAOYSA-N 8-[4-(dimethylamino)butan-2-ylamino]quinolin-6-ol Chemical compound C1=CN=C2C(NC(CCN(C)C)C)=CC(O)=CC2=C1 BSFODEXXVBBYOC-UHFFFAOYSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005549 heteroarylene group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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Abstract
Compuestos de fórmula 1, R3 en la cual X es SO o SO2; R1 es H, alquilo C1-6, R2 es H o un radical seleccionado del grupo consistente en alquilo C1-10 y alquenilo C2-6, que eventualmente puede estar sustituido con uno o varios radicales seleccionados de halógeno y fluoroalquilo C1-3 o que eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo que consiste en OROR2.1 SR2.1 SO2-R2.1, COOR2.1 , CONR2.2R2.3 , , SO-R2.1 , , arilo C6-10, -Het, Hetarilo, un cicloalquilo C3-10 monocíclico o bicíclico, CH2-NR2.2R2.3 y NR2.2R2.3 , que, de nuevo, puede estar eventualmente sustitudo con uno o varios radicales seleccionados del grupo consistente en OH, halógeno, OR2.1, oxo, CF3, CHF2, CH2F, alquilo C1-6, alcanol C1-6, arilo C6-10, COOR2.1 , CH2-NR2.2R2.3 y NR2.2R2.3 , en donde Het es un heterociclo de uno a once miembros, mono-o bi-cíclico, saturado o parcialmente saturado, eventualmente condensado o eventualmente puenteado, que contiene 1, 2, 3 ó 4 heteroátomos elegidos, independientemente uno de otro, del grupo consistente en N, S u O, y en donde Hetarilo es un heteroarilo de cinco a diez miembros, mono-o bi-cíclico, eventualmente condensado, que contiene 1, 2, 3 ó 4 heteroátomos seleccionados, independientemente uno de otro, del grupo consistente en N, S u O, y en donde cicloalquilo puede estar saturado o parcialmente saturado, en donde R2.1 es H o un radical seleccionado del grupo consistente en alquilo C1-6-, alcanol C1-6, haloalquilo C1-3, cicloalquilo C3-10 mono-o bi-cíclico, aril C6-10-alquileno C1-6, hetaril-alquileno C1-6, Het-alquileno C1-6, cicloalquil C3-10-alquileno C1-6, un arilo C6-10 mono-o bi-cíclico, heteroarilo y un -Het, que eventualmente puede estar sustituido con uno varios radicales seleccionados del grupo consistente en OH, O- (alquilo C1-3) , halógeno, alquilo C1-6 y arilo C6-10, y R2.3 en donde R2.2 son, de modo independiente entre sí, H o un radical que está seleccionado del grupo compuesto por alquilo C1-6, cicloalquilo C3-10 mono-o bicíclico, aril C6-10-alquileno C1-6, hetarilalquileno C1-6, arilo C6-10 mono-o bicíclico, Het, Hetarilo, CO-NH2, CO-NHCH3, CO-N (CH3) 2, SO2 (alquilo C1-C2) , CO-R2.1 y COOR2.1 , que eventualmente puede estar sustituido con uno o más radicales seleccionados del grupo consistente en OH, halógeno, alquilo C1-6, arilo C6-10 y COOR2.1 , o R2 es un cicloalquilo C3-10 mono-o policíclico que eventualmente puede estar puenteado una o varias veces a través de grupos alquilo C1-3 y que eventualmente puede estar sustituido con un radical seleccionado del grupo compuesto por alcanol C1-6 ramificado o no ramificado, fluoroalquilo C1-3, alquilen C1-3-OR2.1, OR2.1 , COOR2.1 , - SO2-NR2.2R2.3, Het, -NH-CO-O- (alquilo C1-6) , -NH-CO- (alquilo C1-6) , -NH-CO-O- (arilo C6-10) , -NH-CO- (arilo C6-10) , -NH-CO-O-Hetarilo, -NH-CO-Hetarilo, -NH-CO-O- (alquilen C1-3) - (arilo C6-10) , -NH-CO- (alquilen C1-3) (arilo C6-10) , -N (alquil C1-3) -CO- (alquilo C1-6) , -N (alquil C1-3) -CO-O- (arilo C6-10) , -N (alquil C1-3) -CO- (arilo C6-10) , - N (alquil C1-3) -CO-O-Hetarilo, -N (alquil C1-3) -CO-hetarilo, -N (alquil C1-3) -CO-O- (alquilen C1-3) - (arilo C6-10) , N (alquil C1-3) -CO- (alquilen C1-3) - (arilo C6-10) , arilo C6-10, alquilo C1-6, aril C6-10-alquileno C1-6, Hetaril-alquileno C1-6, cicloalquilo C3-10 mono-o bi-cíclcico y NR2.2R2.3 , que eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo compuesto por OH, OR2.1, oxo, halógeno, CF3, CHF2, CH2F, alquilo C1-6, arilo C6-10 y NR2.2R2.3 , o R2 es un arilo C6-10 mono-o poli-cíclico, que eventualmente puede estar sustituido con OH, SH o halógeno o OR2.1 NR2.2R2.3 con uno o varios radicales seleccionados del grupo consistente en , COOR2.1 , , CH2NR2.2R2.3, cicloalquilo C3-10, Het, alquilo C1-6, fluoroalquilo C1-3, CF3, CHF2, CH2F, aril C6-10-alquileno C1-6, Het-alquileno C1-6, Hetaril-alquileno C1-6, arilo C6-10, SO2-CH3, SO2-CH2CH3 y SO2-NR2.2R2.3 , que, de nuevo, puede estar eventualmente sustituido con uno o varios radicales seleccionados del grupo consistente en OH, OR2.1, CF3, CHF2, CH2F, oxo, halógeno, CF3, CHF2, CH2F, alquilo C1-6, arilo C6-10 y NR2.2R2.3 , o R2 es un radical seleccionado de un grupo consistente en Het y Hetarilo, que eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo halógeno, OH, oxo, CF3, CHF2 y CH2F o con uno o varios radicales seleccionados del grupo OR2.1, alquilen C1-3-OR2.1, SR2.1, SO-R2.1, SO2-R2.1, COOR2.1 , COR2.1, alcanol C1-6, cicloalqulo C3-10 mono-o bi-cíclico, arilo C6-10, alquilo C1-6, aril C6-10-alquileno C1-6, hetaril-alquileno C1-6, Het, Hetarilo, alquilen C1-3-OR2.1 y NR2.2R2.3 , que, de nuevo, eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo compuesto por OH, OR 2.1, oxo, halógeno, CF3, CHF2, CH2F, alquilo C1-6, arilo C6-10 y NR2.2R2.3 , o en donde NR1R2 son juntos un anillo heterocíclico C4-7 que eventualmente puede estar puentado, que contiene 1, 2 ó 3 heteroátomos seleccionados del grupo consistente en N, O y S y que eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo consistente en OH, OR2.1, alquilen C1-3-OR.1 , oxo, halógeno, alquilo C1-6, arilo C6-10, COOR2.1, CH2-NR2.2-COO-R2.1, CH2-NR2.2-CO-R2.1, CH2-NR2.2-CO-CH2 NR2.2R2.3 CH2-NR2.2-SO2-NR2.2R2.3 , CH2-NR2.2-SO2-alquilo C1-3, , CH2-NR2.2-CO-NR2.2R2.3 , CO-NR2.2R2.3 , CH2-NR2.2R2.3 y NR2.2R2.3 , y en donde R3 es un arilo C6-10, que, eventualmente, puede estar sustituido en posición orto, para o meta con uno, dos o tres radicales seleccionados, independientemente uno de otro, del grupo consistente en flúor, cloro, bromo, hidroxi, CN, alquilo C1-6, fluoroalquilo C1-3, -alquilen C1-3-OR2.1, -alquilen C1-3-NR2.2R2.3, -NR2.2R2.3, O-R2.1; SO-R2.1, SO2R2.1, COOR2.1 , -CO-NH- (alquilen C1-6) -Hetarilo, -CO-NH-Hetarilo, -CO-N (CH3) -Het, -CO-N (CH3) - (alquilen C1-3) -Het, -CO-N (CH3) - (alquilen C1-3) -Hetarilo, -CO-N (cicloalquil C3-7) -Het, -CO-NR2.2R2.3 , -CO-NH (alquilen C1-6) -Het, NR2.2-CO-R2.1, arilo C6-10, aril C6-10-alquileno C1-2, Het-alquileno C1-2, -Het, -CO-Het, CO-N (CH3) -cicloalquilo C3-7, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-2, Hetaril-alquileno C1-2 y Hetarilo, en donde este radical puede estar eventualmente sustituido con uno o varios radicales seleccionados del grupo consistente en OH, halógeno, -fluoroalquilo C1-3, oxo, metilo y fenilo, o en donde R3 es un radical seleccionado del grupo consistente en Het y Hetarilo, que eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo consistente en halógeno, fluoroalquilo C1-3, CN, OH, oxo, -alquilo C1-6, -alquilen C1-3-NR2.2R2.3 , -NR2.2R2.3, SO-R2.1, SO2-R2.1, -O-R2.1 , -COOR2.1, SO2 (CH3) , SO2- (CH2-CH3) , arilo C6-10, Het, cicloalquilo C3-7 y Hetarilo, que, de nuevo, eventualmente puede estar sustituido con uno o varios radicales seleccionados del grupo consistente en OH, halógeno, -fluoroalquilo C1-3, alquilo C1-6, arilo C6-10, -COO (alquilo C1-3) y O- (alquilo C1-3) , o en donde R3 es -O-R3.1 , en donde R3.1 es un radical seleccionado del grupo consistente en -alquilo C1-6, -arilo C6-10, -alquilen C1-3-arilo C6-10, Hetarilo y Het, que, eventualmente puede estar sustituido, en posición orto, para o meta, con uno, dos o tres radicales seleccionados, independientemente uno de otro, del grupo consistente en flúor, cloro, bromo, hidroxi, CN, alquilo C1-6, fluoroalquilo C1-3, CO- (alquilo C1-5) , -CO- (fluoroalquilo C1-3) , -CONH- (alquilen C1-6) -Hetarilo, -CO-N (alquil C1-3) - (alquilen C1-6) -Hetarilo, -CO-N (alquil C1-3) -Het, -CO-N (cicloalquil C3-7) -Het, -alquilen C1-3-OR2.1 , -alquilen C1-3-NR2.2R2.3, -NR2.2R2.3, O-R2.1; SO-R2.1, SO2-R2.1, COOH, COO- (alquilo C1-4) , -O-alquilen C1-3-N (alquilo C1-3) 2, CO-NR2.2R2.3, NR2.2-CO-R2.1 , arilo C6-10, aril C6-10-alquileno C1-2, Het-alquileno C1-2, -CO-Het, Het, -CO-cicloalquilo C3-7, -CO-N (alquil C1-3) -cicloalquilo C3-7, ciloalquilo C3-7, ciloalquil C3-7-alquileno C1-2, Hetaril-alquileno C1-2 y Hetarilo, que, de nuevo, eventualmente puede estar sustituido con 1, 2, 3 ó 4 radicales seleccionados, independientemente uno de otro, del grupo consistente en F, Cl, Br, metilo, O-metilo, etilo, O-etilo, OH, oxo y CF3. y en donde R4 es H, CN, OH, CF3, CHF2, CH2F, F, metilo, etilo, -O- (alquilo C1-3) , -alquilen C1-3-OH, -COO (alquilo C1-3) , -CO-Het, - (alquilen C1-2) -NH-SO2- (alquilo C1-2) , - (alquilen C1-2) -N (alquil C1-3) -SO2- (alquilo C1-2) , - (alquilen C1-2) -O- (alquilen C1-2) -arilo C6-10, -alquilen C1-3-O-alquilo C1-3, - (alquilen C1-2) -N (alquil C1-3) -CO- (alquilo C1-2) , -NH-CO- (alquilen C1-3) -O- (alquilo C1-3) , -alquilen C1-3-NH-CO- (alquilo C1-3) , -alquilen C1-3-NH-CO- (alquilen C1-3) -N (alquilo C1-3) 2, -O- (alquilen C1-2) - (arilo C6-10) , -alquilen C1-3-NH-CO- (alquilen C1-3) -O- (alquilo C1-3) , -CO- (arilo C6-10) , - (alquilen C1-2) -N (alquil C1-3) -CO- (alquilen C1-2) -O- (alquilo C1-3) , en donde el arilo en los radicales anteriores puede estar sustituido, eventualmente de nuevo, con uno o varios otros radicales seleccionados del grupo F, Cl, Br, metilo, etilo, propilo, isopropilo, ciclopropilo, -Ometilo, -O-etilo, -O-propilo, -O-isopropilo, -O-ciclopropilo, -OH y CF3 , o en donde R3 y R4 , en común, forman un heterociclo mono-o bi-cíclico insaturado, saturado o parcialmente saturado, que contiene 1, 2 ó 3 heteroátomos seleccionados del grupo consistente en N, O y S y que, eventualmente, puede estar sustituido con uno o varios radicales seleccionados del grupo consistente en halógeno, OH, oxo, fluoroalquilo C1-3, CN, alquilo C1-6, -O-R2.1 , -COOR2.1, SO-R2.1, SO2-R2.1, -alquilen C1-3-NR2.2R2.3 , NR2.2R2.3, arilo C6-10, cicloalquilo C3-7, Het y Hetarilo, así como sales farmacológicamente compatibles de los mismos.
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| DE1470336A1 (de) * | 1962-07-04 | 1969-03-20 | Thomae Gmbh Dr K | Neue Dihydrothieno-[3,4-d]-pyrimidine und Verfahren zu ihrer Herstellung |
| NL122810C (es) | 1963-06-17 | |||
| DE1470356A1 (de) | 1964-01-15 | 1970-04-30 | Thomae Gmbh Dr K | Neue Thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung |
| NL123139C (es) | 1965-03-31 | |||
| DE2032687A1 (en) | 1970-07-02 | 1972-01-05 | Dr. Karl Thomae Gmbh, 7950 Biberach | Cardiovascular 2-aminoalkylamino-thienopyrimidines - and 4-morpholino derivatives from 4-diethanolamino-compounds by intramolecular cyclisa |
| BE754606A (fr) * | 1969-08-08 | 1971-02-08 | Thomae Gmbh Dr K | Nouvelles 2-aminoalcoylamino-thieno(3,2-d)pyrimidines et leurs procedesde fabrication |
| DE1940572A1 (de) | 1969-08-08 | 1971-02-11 | Thomae Gmbh Dr K | Neue 2-Aminoalkylamino-thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung |
| US3763156A (en) * | 1970-01-28 | 1973-10-02 | Boehringer Sohn Ingelheim | 2-heterocyclic amino-4-morpholinothieno(3,2-d)pyrimidines |
| FR2082496A5 (es) | 1970-03-18 | 1971-12-10 | Westinghouse Freins & Signaux | |
| DE2121950A1 (en) | 1971-05-04 | 1972-11-23 | Dr. Karl Thomae Gmbh, 7950 Biberach | Thieno(3,2-d)pyrimidine derivs - with thrombocyte aggregation inhibiting activity |
| DE2750288A1 (de) * | 1977-11-10 | 1979-05-17 | Thomae Gmbh Dr K | Neue 9-(omega-heteroarylamino- alkylamino)-erythromycine, ihre salze, verfahren zu ihrer herstellung und diese enthaltende arzneimittel |
| US4256737A (en) * | 1979-06-11 | 1981-03-17 | Syntex (U.S.A.) Inc. | Long acting depot injectable formulations for LH-RH analogues |
| US5187168A (en) * | 1991-10-24 | 1993-02-16 | American Home Products Corporation | Substituted quinazolines as angiotensin II antagonists |
| US5491201A (en) | 1992-02-06 | 1996-02-13 | The Dow Chemical Company | Mesogenic cyclic imino ether-containing compositions and polymerization products thereof |
| JPH07330777A (ja) | 1994-06-08 | 1995-12-19 | Taisho Pharmaceut Co Ltd | チエノ[3,2−d]ピリミジン−4−オン誘導体 |
| JPH09301958A (ja) | 1996-05-09 | 1997-11-25 | Nippon Shoji Kk | 新規ピリミジン化合物及び抗ロタウイルス剤 |
| US6339089B2 (en) | 1997-08-13 | 2002-01-15 | Fujirebio Inc. | Pyrimidine nucleus-containing compound and a medicament containing the same for a blood oxygen partial pressure amelioration, and a method for preparing the same |
| JP2003520042A (ja) | 2000-01-24 | 2003-07-02 | アイシス・ファーマシューティカルス・インコーポレーテッド | 誘導性一酸化窒素シンターゼ発現のアンチセンスモジュレーション |
| GB0004153D0 (en) | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel use |
| CN100519558C (zh) | 2000-10-12 | 2009-07-29 | 贝林格尔英格海姆法玛两合公司 | 结晶单水合物、其制备方法及其在制备药物组合中的用途 |
| DE10064994A1 (de) * | 2000-12-23 | 2002-07-04 | Merck Patent Gmbh | Sulfamidothienopyrimidine |
| US6849638B2 (en) | 2001-04-30 | 2005-02-01 | Bayer Pharmaceuticals Corporation | 4-amino-5,6-substituted thiopheno [2,3-d] pyrimidines, pharmaceutical compositions containing the same, and their use in the treatment or prevention of pde7b-mediated diseases and conditions |
| AR035700A1 (es) | 2001-05-08 | 2004-06-23 | Astrazeneca Ab | Derivados de arilheteroalquilamina, composicion farmaceutica, usos de estos derivados para la fabricacion de medicamentos, metodos de tratamiento, y proceso para la preparacion de estos derivados |
| CZ302786B6 (cs) | 2001-06-22 | 2011-11-09 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Krystalický bezvodý tiotropiumbromid, zpusob jeho výroby a jeho použití pro výrobu léciva pro lécbu asthmatu |
| US6587548B2 (en) * | 2001-07-17 | 2003-07-01 | Hewlett-Packard Development Co., L.P. | Method and system of using a single telephone number for multiple services |
| WO2003055890A1 (en) | 2001-12-21 | 2003-07-10 | Bayer Pharmaceuticals Corporation | Thienopyrimidine derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents |
| DE60320933D1 (de) | 2002-01-10 | 2008-06-26 | Bayer Healthcare Ag | Rho-kinase inhibitoren |
| SE0203304D0 (sv) | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Coumpounds |
| EA008596B1 (ru) | 2003-04-29 | 2007-06-29 | Пфайзер Инк. | 5,7-ДИАМИНОПИРАЗОЛО[4,3-d]ПИРИМИДИНЫ, ПОЛЕЗНЫЕ ПРИ ЛЕЧЕНИИ ГИПЕРТЕНЗИИ |
| US20050084878A1 (en) | 2003-05-16 | 2005-04-21 | Wisconsin Alumni Research Foundation | Method for isolating and cloning high molecular weight polynucleotide molecules from the environment |
| JP2005003345A (ja) | 2003-05-21 | 2005-01-06 | Showa Denko Kk | 換気兼熱交換装置および空調システム |
| KR20140119198A (ko) * | 2003-10-02 | 2014-10-08 | 디에스엠 아이피 어셋츠 비.브이. | 변형량의 염소 및 칼륨을 사용하는 미세조류 중에 고농도 디에치에이의 생산 |
| MY141220A (en) | 2003-11-17 | 2010-03-31 | Astrazeneca Ab | Pyrazole derivatives as inhibitors of receptor tyrosine kinases |
| US20050137186A1 (en) | 2003-12-18 | 2005-06-23 | Abbott Gmbh & Co. Kg. | Tetrahydrobenzazepines and their use |
| JP4740152B2 (ja) | 2003-12-23 | 2011-08-03 | セロドス アクスイェ セルスカブ | 末梢性5−ht受容体の修飾因子 |
| WO2005082865A1 (ja) | 2004-02-27 | 2005-09-09 | Astellas Pharma Inc. | 縮合二環性ピリミジン誘導体 |
| GB0427403D0 (en) | 2004-12-15 | 2005-01-19 | Astrazeneca Ab | Novel compounds I |
| JP2008540486A (ja) | 2005-05-11 | 2008-11-20 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | Pde4インヒビター及びテトラヒドロビオプテリン誘導体との組合せ物 |
| MX2007012313A (es) * | 2006-04-19 | 2007-11-21 | Boehringer Ingelheim Int | Dihidrotienopirimidinas para el tratamiento de enfermedades inflamatorias. |
| EP1847543A1 (de) * | 2006-04-19 | 2007-10-24 | Boehringer Ingelheim Pharma GmbH & Co. KG | Dihydrothienopyrimidine zur Behandlung von entzündlichen Erkrankungen |
| EA015821B1 (ru) * | 2007-04-20 | 2011-12-30 | Глэксо Груп Лимитед | Трициклические азотсодержащие соединения в качестве антибактериальных агентов |
| US8653282B2 (en) | 2007-10-18 | 2014-02-18 | Boehringer Ingelheim International Gmbh | Preparation of dihydrothieno [3,2-D] pyrimidines and intermediates used therein |
| FR2922550B1 (fr) | 2007-10-19 | 2009-11-27 | Sanofi Aventis | Nouveaux derives de 6-aryl/heteroalkyloxy benzothiazole et benzimidazole, application comme medicaments, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de cmet |
| EP2205609B1 (de) | 2007-10-19 | 2017-03-29 | Boehringer Ingelheim International GmbH | Heterocyclus-substituierte piperazino-dihydrothienopyrimidine |
| US20110028441A1 (en) * | 2007-10-19 | 2011-02-03 | Boehringer Ingelheim International Gmbh | Novel phenyl-substituted piperazino-dihydrothienopyrimidines |
| AR068888A1 (es) | 2007-10-19 | 2009-12-16 | Schering Corp | Derivados de 1, 3, 4 - tiadiazol, una composicion farmaceutica que los comprende y su uso en la preparacion de medicamentos para el tratamiento de enfermedades mediadas por la inhibicion de la quinesina ksp. |
| WO2009050236A1 (de) | 2007-10-19 | 2009-04-23 | Boehringer Ingelheim International Gmbh | Neue piperazino-dihydrothienopyrimidin-derivate |
| PE20090875A1 (es) * | 2007-10-19 | 2009-08-08 | Astrazeneca Ab | Derivados de tetrazol como moduladores de los receptores de glutamato metabotropicos |
| AU2008313660B2 (en) | 2007-10-19 | 2013-11-07 | Boehringer Ingelheim International Gmbh | Substituted piperidino-dihydrothienopyrimidines |
| US9161927B2 (en) * | 2009-02-27 | 2015-10-20 | Boehringer Ingelheim International Gmbh | Drug combinations containing PDE4 inhibitors and NSAIDs |
| CA2753597A1 (en) * | 2009-02-27 | 2010-09-02 | Boehringer Ingelheim International Gmbh | Drug combinations containing pde4-inhibitors and nsaids |
| US20130059866A1 (en) * | 2011-08-24 | 2013-03-07 | Boehringer Ingelheim International Gmbh | Novel piperidino-dihydrothienopyrimidine sulfoxides and their use for treating copd and asthma |
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