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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 21. Отображено 21.
13-07-2017 дата публикации

BENZOTHIADIAZOLAMINES

Номер: US20170197979A1
Принадлежит: Bayer Pharma AG

The present invention relates to substituted benzothiadiazolamine compounds of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative and/or angiogenesis disorder, as a sole agent or in combination with other active ingredients.

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27-04-2017 дата публикации

INHIBITORS OF THE WNT SIGNALLING PATHWAYS

Номер: US20170114070A1
Принадлежит:

The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper-proliferative disorder, as a sole agent or in combination with other active ingredients. 4. A compound according to , or , wherein Rrepresents a hydrogen atom.5. A compound according to , , or , wherein Rrepresents a hydrogen atom.6. A compound according to , , , or , wherein Rrepresents a group selected from: C-C-alkyl- , C-C-alkoxy- , C-C-cycloalkoxy- , halo- , hydroxy- , fluoro-C-C-alkyl- , fluoro-C-C-alkoxy- , phenyl- , 5- to 6-membered heteroaryl- , cyano- , —C(═O)—O—C-C-alkyl , —C(═O)—N(R)(R) , R—S— , R—S(═O)— , R—S(═O)—; said C-C-alkyl- or C-C-alkoxy- group being optionally substituted , one or more times , identically or differently , with a substituent selected from: C-C-alkyl- , C-C-alkoxy- , halo-C-C-alkoxy- , hydroxy-C-C-alkoxy- , C-C-alkoxy-C-C-alkoxy- , C-C-cycloalkyl- , 3- to 10-membered heterocycloalkyl- , aryl- , heteroaryl- , —C(═O)R , —C(═O)O—(C-C-alkyl) , —OC(═O)—R , —N(H)C(═O)R , —N(R)C(═O)R , —N(H)C(═O)NRR , —N(R)C(═O)NRR , —N(H)R , —NRR , —C(═O)N(H)R , —C(═O)NRR.7. A compound according to , , , , or , wherein Lrepresents *N(H)—C(═O)**;{'sup': '2', 'wherein “*” indicates the point of attachment to R, and “**” indicates the point of attachment to the phenyl group.'}9. A compound of general formula (I) , or a stereoisomer , a tautomer , an N oxide , a hydrate , a solvate , or a salt thereof , particularly a pharmaceutically acceptable salt thereof , or a mixture of same , according to any one of to , for use in the treatment or prophylaxis of a disease.10. A pharmaceutical composition comprising ...

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20-04-2017 дата публикации

NOVEL COMPOUNDS

Номер: US20170107212A1
Принадлежит:

The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper-proliferative disorder, as a sole agent or in combination with other active ingredients. 5. A compound according to claim 1 , wherein:{'sup': '4', 'Rrepresents a hydrogen atom, and'}{'sup': '5', 'Rrepresents a hydrogen atom.'}6. A compound according to claim 1 , wherein:{'sup': '6', 'Rrepresents a group selected from{'sub': 1', '6', '1', '6', '3', '6', '1', '6', '1', '6', '1', '4', '2, 'sup': 9', '10', '9', '9, 'C-C-alkyl-, C-C-alkoxy-, C-C-cycloalkoxy-, halo-, hydroxy-, fluoro-C-C-alkyl-, fluoro-C-C-alkoxy-, phenyl-, 5- to 6-membered heteroaryl-, cyano-, —C(═O)—O—C-C-alkyl, —C(═O)—N(R)(R), R—S(═O)—, R—S(═O)—;'}{'sub': 1', '6', '1', '6', '1', '3', '1', '3', '1', '3', '1', '3', '1', '3', '2', '3', '3', '7', '1', '4, 'sup': 9', '9', '9', '10', '9', '10', '9', '11', '10', '9', '9', '10', '9', '9', '10', '9, 'said C-C-alkyl- or C-C-alkoxy- group being optionally substituted, one or more times, identically or differently, with a substituent selected from: C-C-alkyl-, C-C-alkoxy-, halo-C-C-alkoxy-, hydroxy-C-C-alkoxy-, C-C-alkoxy-C-C-alkoxy-, C-C-cycloalkyl-, 3- to 10-membered heterocycloalkyl-, aryl-, heteroaryl-, —C(═O)R, —C(═O)O—(C-C-alkyl), —OC(═O)—R, —N(H)C(═O)R, —N(R)C(═O)R, —N(H)C(═O)NRR, —N(R)C(═O)NRR, —N(H)R, —NRR, —C(═O)N(H)R, —C(═O)NRR.'}7. A compound according to claim 1 , wherein:{'sup': '6', 'Rrepresents a group selected from{'sub': 1', '6', '1', '6', '3', '6', '1', '4', '2, 'sup': 9', '10', '9', '9', '9, 'CCalkyl , C-C-alkoxy-, C-C-cycloalkoxy-, halo-, hydroxy-, cyano-, —C(═O)—O—C-C-alkyl, —C(═O)—N(R)(R), ...

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20-04-2017 дата публикации

SUBSTITUTED TETRAHYDROPYRIDOTHIENOPYRIMIDINES

Номер: US20170107229A1
Принадлежит:

The present invention relates to substituted tetrahydropyridothienopyrimidine compounds of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative and/or angiogenesis disorder, as a sole agent or in combination with other active ingredients. 3. The compound according to claim 1 , wherein Rrepresents a hydrogen atom or a group selected from: C-C-alkyl- claim 1 , —(CH)—X—(CH)—R; wherein said C-C-alkyl- group is optionally substituted claim 1 , identically or differently claim 1 , with 1 claim 1 , 2 claim 1 , 3 claim 1 , 4 or 5 Rgroups.4. The compound according to claim 1 , wherein X represents a bond or a bivalent group selected from: —S(═O)— claim 1 , —C(═O)— claim 1 , —N(R)— claim 1 , —C(═O)—O— claim 1 , —C(═O)—N(R)—.5. The compound according to claim 1 , wherein Rrepresents a hydrogen atom or a halogen atom or a group selected from: C-C-alkoxy- claim 1 , —SR.6. The compound according to claim 1 , wherein Rrepresents a methoxy- group.7. The compound according to claim 1 , wherein Rrepresents a group selected from C-C-alkyl- claim 1 , C-C-cycloalkyl- claim 1 , 3- to 10-membered heterocycloalkyl- and heteroaryl-; wherein said C-C-alkyl- claim 1 , C-C-cycloalkyl- claim 1 , 3- to 10-membered heterocycloalkyl- and heteroaryl- group is optionally substituted claim 1 , identically or differently claim 1 , with 1 claim 1 , 2 claim 1 , 3 claim 1 , 4 or 5 Rgroups.8. The compound according to claim 1 , wherein N(R)Rtogether represent a 3- to 10-membered heterocycloalkyl- group claim 1 , said group being optionally substituted claim 1 , identically or differently claim 1 , with 1 claim 1 , 2 claim 1 , 3 claim 1 , 4 or 5 Rgroups.10. The compound ...

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01-02-2018 дата публикации

3-CARBAMOYLPHENYL-4-CARBOXAMIDE AND ISOPHTALAMIDE DERIVATIVES AS INHIBITORS OF THE WNT SIGNALLING PATHWAY

Номер: US20180028507A1
Принадлежит: BAYER PHARMA AKTIENGESELLSCHAFT

The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper-proliferative disorder, as a sole agent or in combination with other active ingredients, in which: Rrepresents a group selected from: C-C-alkoxy-C-C-alkyl-, (A), (B), (C), (D), (E), (F), (G) or (H); wherein * indicates the point of attachment to the rest of the molecule; Rrepresents a group selected from: (I), (J) or (K); wherein * indicates the point of attachment to the rest of the molecule. 2. A compound according to claim 1 , wherein:{'sup': '1', 'sub': 2', '2', '3', '2', '2', '2', '3', '2', '2', '2', '2', '3', '2', '2', '2', '3', '2, 'Rrepresents a group selected from: —CH—CH—O—CH, —CH—CH—CH—O—CH, —CH—CH—CH—O—CH—CH, and —CH—CH—CH—O—C(H)(CH).'}8. A compound according to claim 1 , which is selected from the group consisting of:N-[4-methoxy-3-(pyridin-4-ylcarbamoyl)phenyl]biphenyl-4-carboxamide,N-{4-methoxy-3-[(3-methoxypropyl)carbamoyl]phenyl}biphenyl-4-carboxamide,N-{4-methoxy-3-[(2-methylpyridin-4-yl)carbamoyl]phenyl}biphenyl-4-carboxamide,N-{4-methoxy-3-[(3-methoxypropyl)(methyl)carbamoyl]phenyl}biphenyl-4-carboxamide,N-{3-[(3-ethoxypropyl)carbamoyl]-4-methoxyphenyl}biphenyl-4-carboxamide,N-{3-[(3-isopropoxypropyl)carbamoyl]-4-methoxyphenyl}biphenyl-4-carboxamide,{'sup': 1', '3, 'N-(biphenyl-4-yl)-N-(pyridin-2-ylmethyl)-4-(trifluoromethoxy)isophthalamide,'}N-{3-[(3-fluoropyridin-4-yl)carbamoyl]-4-methoxyphenyl}biphenyl-4-carboxamide,N-{3-[(3-chloropyridin-4-yl)carbamoyl]-4-methoxyphenyl}biphenyl-4-carboxamide,{'sup': 1', '3, 'N-(biphenyl-4-yl)-N-(2-methylpyridin-4-yl)-4-(trifluoromethoxy)isophthalamide,'}{' ...

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15-02-2018 дата публикации

N-PHENYL-(MORPHOLIN-4-YL OR PIPERAZINYL)ACETAMIDE DERIVATIVES AND THEIR USE AS INHIBITORS OF THE WNT SIGNALLING PATHWAYS

Номер: US20180042931A1
Принадлежит: BAYER PHARMA AKTIENGESELLSCHAFT

The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) wherein Lrepresents *CH** or *Δ**; wherein indicates the point of attachment to the carbonyl group, and ** indicates the point of attachment to R; Lrepresents *N(H)—C(═O)** or *C(═O)—N(H)**; wherein * indicates the point of attachment to R, and ** indicates the point of attachment to the phenyl group; Rrepresents a group selected from: (AA); wherein * indicates the point of attachment to L, Rrepresents: (BB) wherein * indicates the point of attachment to R, and ** indicates the point of attachment to LRrepresents a group selected from: (CC); wherein * indicates the point of attachment to R; Rand Rrepresent a hydrogen atom; and Rrepresents a halogen atom or group selected from: —CH, —O—CH, —O—CHF, —O—CF, and —O-cyclopropyl; to methods of preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular, of a hyper-proliferative disorder, as a sole agent or in combination with other active ingredients. 2: The compound according to claim 1 , or a tautomer claim 1 , an N-oxide claim 1 , a hydrate claim 1 , a solvate claim 1 , or a salt thereof claim 1 , or a mixture of any of the foregoing claim 1 , wherein:{'sup': 'A', 'sub': '2', 'Lis *CH**.'}4: The compound according to claim 1 , or a tautomer claim 1 , an N-oxide claim 1 , a hydrate claim 1 , a solvate claim 1 , or a salt thereof claim 1 , or a mixture of any of the foregoing claim 1 , wherein:{'sup': 'B', 'Lis *N(H)—C(═O)**.'}7: The compound according to claim 1 , or a tautomer claim 1 , an N-oxide claim 1 , a hydrate claim 1 , a solvate claim 1 , or a salt thereof claim 1 , or a mixture of any of the foregoing claim 1 , wherein:{'sup': '6', 'sub': 3', '2', '3, 'Ris a group selected from: —O—CH, —O—C(H)(F), and —O—CF.'}8: The compound according to ...

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15-02-2018 дата публикации

1,3,4-THIADIAZOL-2-YL-BENZAMIDE DERIVATIVES AS INHIBITORS OF THE WNT SIGNALLING PATHWAY

Номер: US20180044306A1
Принадлежит: BAYER PHARMA AKTIENGESELLSCHAFT

The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper-proliferative disorder, as a sole agent or in combination with other active ingredients. 6. (canceled)8. The compound according to claim 1 , which is selected from the group consisting of:3-{[(4-methylpiperazin-1-yl)acetyl]amino}-N-[5-(piperidin-1-yl)-1,3,4-thiadiazol-2-yl]-4-(trifluoromethoxy)benzamide,tert-butyl 4-(5-{[3-{[(4-methylpiperazin-1-yl)acetyl]amino}-4-(trifluoromethoxy)benzoyl]amino}-1,3,4-thiadiazol-2-yl)piperazine-1-carboxylate,{'b': '1', 'tert-butyl 4-[5-({3-[(morpholin-4-ylacetyl)amino]-4-(trifluoromethoxy)benzoyl}amino)-1,3,4-thiadiazol-2-yl]piperazine-1-carboxylate, p 3-{[(4-methylpiperazin-1-yl)acetyl]amino}-N-[5-(pyrrolidin-1-yl)-1,3,4-thiadiazol-2-yl]-4-(trifluoromethoxy)benzamide,'}N-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)-3-{[(4-methylpiperazin-1-yl)acetyl]amino}-4-(trifluoromethoxy)benzamide,methyl 4-(5-{[3-{[(4-methylpiperazin-1-yl)acetyl]amino}-4-(trifluoromethoxy)benzoyl]amino}-1,3,4-thiadiazol-2-yl)piperazine-1-carboxylate,3-{[(4-methylpiperazin-1-yl)acetyl]amino}-N-[5-(4-methylpiperidin-1-yl)-1,3,4-thiadiazol-2-yl]-4-(trifluoromethoxy)benzamide,N-[5-(4-hydroxy-4-methylpiperidin-1-yl)-1,3,4-thiadiazol-2-yl]-3-{[(4-methylpiperazin-1-yl)acetyl]amino}-4-(trifluoromethoxy)benzamide,N-{5-[4-(cyclopropylcarbonyl)piperazin-1-yl]-1,3,4-thiadiazol-2-yl}-3-{[(4-methylpiperazin-1-yl)acetyl]amino}-4-(trifluoromethoxy)benzamide,N-{5-[4-(2-hydroxypropan-2-yl)piperidin-1-yl]-1,3,4-thiadiazol-2-yl}-3-[(morpholin-4-ylacetyl)amino]-4-(trifluoromethoxy)benzamide,N-[5-(4-methoxypiperidin-1-yl)-1,3,4- ...

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20-02-2020 дата публикации

SUBSTITUTED 6-(1H-PYRAZOL-1-YL)PYRIMIDIN-4-AMINE DERIVATIVES AND USES THEREOF

Номер: US20200055842A1
Принадлежит:

The present invention covers substituted 6-(1H-pyrazol-1-yl)pyrimidin-4-amine compounds of general formula (I) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular and renal diseases, as a sole agent or in combination with other active ingredients. 6: A method for treatment or prophylaxis of a disease claim 1 , comprising administering to a patient in need thereof an effective amount of a compound of formula (I) according to .7: A method for treatment or prophylaxis of a disease or condition associated with hyperphosphatemia claim 1 , elevated plasma FGF23 levels claim 1 , disbalanced phosphate homeostasis claim 1 , soft tissue calcification claim 1 , chronic kidney disease (CKD) claim 1 , or soft tissue calcification claim 1 , comprising administering to a patient in need thereof an effective amount of at least one compound of formula (I) according to .8: A pharmaceutical composition comprising a compound of the formula (I) as defined in any of in combination with an inert claim 1 , non-toxic claim 1 , pharmaceutically suitable auxiliary.9: A pharmaceutical combination comprising a compound of the formula (I) as defined in in combination with a further active compound selected from the group consisting of the hypotensive active compounds claim 1 , of the antiinflammatory agents/immunosuppressive agents claim 1 , the phosphate binders claim 1 , the sodium-phosphate co-transporters claim 1 , NHE3 inhibitors claim 1 , antiarrhythmic agents claim 1 , agents that alter lipid metabolism and the active compounds which modulate vitamin D metabolism.10: A method for treatment or prophylaxis of a cardiovascular or renal disorder claim 8 , ...

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14-06-2018 дата публикации

PYRAZOLOPYRIDINAMINES AS MKNK1 AND MKNK2 INHIBITORS

Номер: US20180162877A1
Принадлежит:

The present invention relates to substituted pyrazolopyridinamine compounds of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative and/or angiogenesis disorder, inflammatory disease and disease associated with inflammatory pain, as a sole agent or in combination with other active ingredients. 2. The compound according to claim 1 , wherein{'sup': '1', 'sub': 1', '3', '1', '3', '1', '3', '3', '2', '1', '3, 'Rrepresents a hydrogen atom or a halogen atom or a group selected from the group consisting of: C-C-alkyl-, C-C-alkoxy-, halo-C-C-alkyl-, —N(CH), and —S—(C-C-alkyl) groups.'}3. The compound according to claim 1 , wherein{'sup': '1', 'sub': '3', 'Rrepresents a hydrogen atom or a —O—CHgroup.'}4. The compound according to claim 1 , wherein{'sup': '2', 'Rrepresents a hydrogen atom.'}5. The compound according to claim 1 , wherein{'sup': 3', '5, 'sub': 1', '6', '2', 'q', '2', 'p, 'claim-text': {'sub': 1', '6, 'sup': '4', 'wherein said C-C-alkyl-group is optionally substituted, identically or differently, with 1, 2, 3, 4 or 5 Rgroups.'}, 'Rrepresents C-C-alkyl- or —(CH)—X—(CH)—Rgroup;'}6. The compound according to claim 1 , wherein {'sup': '5a', '—C(═O)—, —C(═O)—O—, and —C(═O)—N(R)-groups.'}, 'X represents a bivalent group selected from the group consisting of7. The compound according to claim 1 , wherein{'sup': '5a', 'X represents a bivalent —C(═O)—N(R)-group.'}8. The compound according to claim 1 , wherein{'sup': 4', '6a', '6b', '6a', '6b', '6a', '6d', '6a', '6b', '6a', '6b, 'sub': 1', '3', '1', '3', '1', '3, 'Rrepresents halo-, hydroxy-, cyano-, C-C-alkyl-, C-C-alkoxy-, —N(R)—C(═O)—O—R, —N(R)R, —N(R)R, —C(═O)—N(R)R, or —(C-C-alkyl)- ...

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28-01-2021 дата публикации

Antibody drug conjugates (adcs) with nampt inhibitors

Номер: WO2021013693A1

Conjugate of a binder having formula (AA) wherein AB stands for a binder, Z' stands for a linker, D stands for an active component which is a NAMPT inhibitor and its use as pharmaceuticals.

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23-06-2016 дата публикации

Pyrazolopyridinamines as mknk1 and mknk2 inhibitors

Номер: CA2971242A1
Принадлежит: Bayer Pharma AG

The present invention relates to substituted pyrazolopyridinamine compounds of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative and/or angiogenesis disorder, inflammatory disease and disease associated with inflammatory pain, as a sole agent or in combination with other active ingredients.

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03-12-2015 дата публикации

Benzothiadiazolamines

Номер: CA2950218A1
Принадлежит: Bayer Pharma AG

The present invention relates to substituted benzothiadiazolamine compounds of general formula(I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative and/or angiogenesis disorder, as a sole agent or in combination with other active ingredients.

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06-12-2016 дата публикации

NEW COMPOUNDS

Номер: CR20160433A
Принадлежит: Bayer Pharma AG

La presente invenciónse refiere a inhibidores de las vías de señalización de Wntde la fórmula general (I) como se describe y se define en la presente,a métodos de preparación de dichos compuestos, a compuestos intermediarios útiles para preparar dichos compuestos, a composiciones farmacéuticas y combinaciones que comprenden dichos compuestos y al uso de dichos compuestospara producir una composición farmacéutica para el tratamiento o la prevención de una enfermedad, en particular de un trastorno hiperproliferativo, como un único agente o en combinación con otros ingredientes activos.

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21-08-2019 дата публикации

Substituted 6-(1h-pyrazol-1-yl)pyrimidin-4-amine derivatives and uses thereof

Номер: EP3526212A1
Принадлежит: Bayer AG, Bayer Pharma AG

The present invention covers substituted 6-(1H-pyrazol-1-yl)pyrimidin-4-amine compounds of general formula (I) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular and renal diseases, as a sole agent or in combination with other active ingredients.

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25-08-2016 дата публикации

N-phenyl-(morpholin-4-yl or piperazinyl)acetamide derivatives and their use as inhibitors of the wnt signalling pathways

Номер: CA2976973A1
Принадлежит: Bayer Pharma AG

The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) wherein LA represents *CH2** or *?**; wherein indicates the point of attachment to the carbonyl group, and ** indicates the point of attachment to R1; LB represents *N(H)-C(=O)** or *C(=O)-N(H)**; wherein * indicates the point of attachment to R2, and ** indicates the point of attachment to the phenyl group; R1 represents a group selected from: (AA); wherein * indicates the point of attachment to LA, R2 represents: (BB) wherein * indicates the point of attachment to R3, and ** indicates the point of attachment to LB R3 represents a group selected from: (CC); wherein * indicates the point of attachment to R2; R4 and R5 represent a hydrogen atom; and R6 represents a halogen atom or group selected from: -CH3, -O-CH3, -O-CHF2, -O-CF3, and -O-cyclopropyl; to methods of preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular, of a hyper-proliferative disorder, as a sole agent or in combination with other active ingredients.

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31-10-2016 дата публикации

WNT SIGNALING ROAD INHIBITORS

Номер: DOP2016000251A
Принадлежит: Bayer Pharma Aktiengesellchaft

La presente invención se refiere a inhibidores de las vías de señalización de Wnt de la fórmula general (I) como se describe y se define en la presente, a métodos de preparación de dichos compuestos, a compuestos intermediarios útiles para preparar dichos compuestos, a composiciones farmacéuticas y combinaciones que comprenden dichos compuestos y al uso de dichos compuestos para producir una composición farmacéutica para el tratamiento o la prevención de una enfermedad, en particular de un trastorno hiperproliferativo, como un único agente o en combinación con otros ingredientes activos.

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20-10-2017 дата публикации

Pyrazolpyridinamines as mknk1 and mknk2 inhibitors

Номер: CO2017005968A2
Принадлежит: Bayer Pharma AG

Compuestos de pirazolpiridinamina sustituida de fórmula general (I) según se los describe y define aquí, métodos para preparar dichos compuestos, compuestos intermediarios útiles para preparar dichos compuestos, composiciones farmacéuticas y combinaciones que comprenden a dichos compuestos y el uso de dichos compuestos para elaborar una composición farmacéutica para el tratamiento o la profilaxis de una enfermedad, en particular de un trastorno hiperproliferativo y/o de angiogénesis, como único agente o en combinación con otros ingredientes activos. Substituted pyrazolpyridinamine compounds of general formula (I) as described and defined herein, methods for preparing said compounds, intermediates useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds and the use of said compounds to make a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular a hyperproliferative disorder and / or angiogenesis, as a single agent or in combination with other active ingredients.

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04-11-2019 дата публикации

SUBSTITUTE DERIVATIVES OF 6- (1H-PIRAZOL-1-IL) PYRIMIDIN-4-AMINE

Номер: CU20190035A7
Принадлежит: Bayer AG, Bayer Pharma AG

<p>La presente invención se refiere a compuestos sustituidos de 6-(1 H-pirazol-1-il)pirimidin-4-amina de la fórmula general (I) tal como se describen y definen en el presente, a procedimientos para preparar dichos compuestos, y a compuestos intermedios útiles para preparar dichos compuestos.</p> <p> The present invention relates to substituted 6- (1 H-pyrazol-1-yl) pyrimidin-4-amine compounds of the general formula (I) as described and defined herein, to processes for preparing said compounds, and useful intermediates to prepare said compounds. </p>

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10-09-2019 дата публикации

substituted 6- (1h-pyrazol-1-yl) pyrimidin-4-amine derivatives and their use

Номер: BR112019007496A2
Принадлежит: Bayer AG, Bayer Pharma AG

derivados de 6-(1h-pirazol-1-il)pirimidin-4-amina substituída e seu uso. a presente invenção abrange compostos de 6-(1h-pirazol-1-il)pirimidin-4-amina substituída da fórmula geral (i) como descrito e definido aqui, métodos de preparação dos referidos compostos, compostos intermediários úteis para preparar esses compostos, composições farmacêuticas e combinações que compreendem esses compostos e o uso de compostos citados para fabricação de composições farmacêuticas para o tratamento ou a profilaxia de doenças, em particular para o tratamento e/ou a profilaxia de doenças cardiovasculares e renais, como um único agente ou em combinação com outros ingredientes ativos. substituted 6- (1h-pyrazol-1-yl) pyrimidin-4-amine derivatives and their use. the present invention encompasses substituted 6- (1h-pyrazol-1-yl) pyrimidin-4-amine compounds of the general formula (i) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing such compounds, pharmaceutical compositions and combinations comprising such compounds and the use of said compounds for the manufacture of pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular for the treatment and / or prophylaxis of cardiovascular and renal diseases, as a single agent or in combination with other active ingredients.

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05-04-2017 дата публикации

BENZAMIDS AND SUBSTITUTES REPLACED IN QUALITY OF INHIBITORS OF THE WNT SIGNALING ROADS, THE COMPOSITIONS AND PHARMACEUTICAL COMBINATIONS THAT UNDERSTAND THEM, AND THE INTERMEDIARY COMPOUNDS TO PREPARE THESE COMPOUNDS

Номер: CU20160139A7
Принадлежит: Bayer Pharma AG

La presente invención se refiere a las benzamidas y anilidas sustituidas de fórmula general (I) en calidad de inhibidores de las vías de señalización de Wnt, ESPACIO PARA LA FÓRMULA a métodos de preparación de dichos compuestos, a compuestos intermediarios útiles para preparar dichos compuestos, a composiciones farmacéuticas y combinaciones que comprenden dichos compuestos y al uso de dichos compuestos para producir una composición farmacéutica para el tratamiento o Ia prevención de una enfermedad, en particular de un trastorno hiperproliferativo, como un único agente o en combinación con otros ingredientes activos. The present invention relates to substituted benzamides and anilides of the general formula (I) as inhibitors of the Wnt signaling pathways, SPACE FOR FORMULA to methods of preparing said compounds, to intermediates useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds to produce a pharmaceutical composition for the treatment or prevention of a disease, in particular of a hyperproliferative disorder, as a single agent or in combination with other active ingredients.

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03-03-2017 дата публикации

Compuestos derivados de benzamida, inhibidores de las vías de señalización de wnt; compuestos intermediarios; composiciones y combinaciones farmacológicas; útiles para la prevención o tratamiento de poliposis coli, síndrome de osteoporosispseudoglioma, vitreorretinopatía exudativa, angiogénesis retinal, enfermedad coronaria temprana, síndrome tetra amelia, diabetes mellitus tipo 2, síndrome de frágil, tumores sólidos, entre otras.

Номер: CL2016002368A1
Принадлежит: Bayer Pharma AG

Compuestos derivados de benzamida, inhibidores de las vías de señalización de WNT; compuestos intermediarios; composiciones y combinaciones farmacológicas; útiles para la prevención o tratamiento de poliposis coli, síndrome de osteoporosispseudoglioma, vitreorretinopatía exudativa, angiogénesis retinal, enfermedad coronaria temprana, síndrome tetra Amelia, diabetes mellitus tipo 2, síndrome de frágil, tumores sólidos, entre otras.

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