AR078408A1 - Derivados de indol como moduladores de los crac - Google Patents
Derivados de indol como moduladores de los cracInfo
- Publication number
- AR078408A1 AR078408A1 ARP100103446A ARP100103446A AR078408A1 AR 078408 A1 AR078408 A1 AR 078408A1 AR P100103446 A ARP100103446 A AR P100103446A AR P100103446 A ARP100103446 A AR P100103446A AR 078408 A1 AR078408 A1 AR 078408A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- optionally substituted
- phenyl
- carbonyl
- Prior art date
Links
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 35
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 26
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000001072 heteroaryl group Chemical group 0.000 abstract 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 7
- 150000002825 nitriles Chemical class 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- -1 -C1-6 alkyl nitrile Chemical class 0.000 abstract 1
- PSOPMMVKRIPMTJ-UHFFFAOYSA-N 1-(sulfonylmethyl)piperazine Chemical compound O=S(=O)=CN1CCNCC1 PSOPMMVKRIPMTJ-UHFFFAOYSA-N 0.000 abstract 1
- OTOIUCLFSQHFOX-UHFFFAOYSA-N 3-sulfonylmorpholine Chemical compound O=S(=O)=C1COCCN1 OTOIUCLFSQHFOX-UHFFFAOYSA-N 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- 108090000312 Calcium Channels Proteins 0.000 abstract 1
- 102000003922 Calcium Channels Human genes 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by 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
- 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
- C07D403/10—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 aromatic rings
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D405/14—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 three or more hetero 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
- 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
-
- 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
- C07D413/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
Se describen también métodos de obtencion de los compuestos y el uso de los compuestos para el tratamiento de enfermedades asociadas con los canales de calcio activados con la liberacion de calcio (CRAC). Reivindicacion 1: Un compuesto de la formula (1): en la que: R1 es: - fenilo sustituido una, dos o tres veces por un grupo o grupo elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; halo-alcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; aminocarbonilo; aminosulfonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; hidroxi; sulfonilmorfolina; sulfonilmetilpiperazina; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - piridinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6 nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - pirimidinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; o - un anillo heteroarilo de cinco eslabones opcionalmente sustituido una, dos o tres veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; cicloalquilo C3-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; y heteroarilo que puede estar opcionalmente sustituido; o dos de dichos sustituyentes junto con los átomos a los que están unidos pueden formar un fenilo fusionado con el anillo heteroarilo de cinco eslabones; es: - cicloalquilo C3-6; - fenilo sustituido una, dos o tres veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; alcoxihidroxi C1-6; halogeno; halo-alquilo C1-6; haloalcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; (alquil C1-6)-carbonilhidroxi; (alcoxi C1-6)-ciano; amino; hidroxi; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - piridinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonil- amino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - pirimidinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; o - un anillo heteroarilo de cinco eslabones opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; cicloalquilo C3-6; halo-alcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; fenilo que puede estar opcionalmente sustituido; y heteroarilo que puede estar opcionalmente sustituido; o dos de dichos sustituyentes junto con los átomos a los que están unidos pueden formar un fenilo fusionado con dicho anillo heteroarilo de cinco eslabones; R3 es hidrogeno; R3' es hidrogeno o alquilo C1-6; es un numero de 0 a 3; cada R4 se elige con independencia entre: hidrogeno; alquilo C1-6; alcoxi C1-6; halogeno; y halo-alquilo C1-6, y dicha línea discontinua es un enlace o está ausente, o una sal farmacéuticamente aceptable de los mismos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24552109P | 2009-09-24 | 2009-09-24 | |
| US37806210P | 2010-08-30 | 2010-08-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078408A1 true AR078408A1 (es) | 2011-11-02 |
Family
ID=43432437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103446A AR078408A1 (es) | 2009-09-24 | 2010-09-22 | Derivados de indol como moduladores de los crac |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20110071150A1 (es) |
| EP (1) | EP2480529A1 (es) |
| JP (2) | JP2013505913A (es) |
| KR (1) | KR20120068947A (es) |
| CN (1) | CN102574788A (es) |
| AR (1) | AR078408A1 (es) |
| BR (1) | BR112012006630A2 (es) |
| CA (1) | CA2771026A1 (es) |
| MX (1) | MX2012003539A (es) |
| RU (1) | RU2012116207A (es) |
| TW (1) | TW201121952A (es) |
| WO (1) | WO2011036130A1 (es) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI423962B (zh) * | 2009-10-07 | 2014-01-21 | Lg Life Sciences Ltd | 有效作為黃嘌呤氧化酶抑制劑之新穎化合物、其製備方法及含該化合物之醫藥組成物 |
| WO2011158108A2 (en) * | 2010-06-16 | 2011-12-22 | Purdue Pharma L.P. | Aryl substituted indoles and the use thereof |
| US20130109720A1 (en) * | 2011-11-01 | 2013-05-02 | Hoffmann-La Roche Inc. | Indole inhibitors of crac |
| WO2013092444A1 (en) * | 2011-12-20 | 2013-06-27 | F. Hoffmann-La Roche Ag | Diazaindole inhibitors of crac |
| US20130158066A1 (en) * | 2011-12-20 | 2013-06-20 | Hoffmann-La Roche Inc. | 4-azaindole inhibitors of crac |
| WO2013092467A1 (en) * | 2011-12-20 | 2013-06-27 | F. Hoffmann-La Roche Ag | 7-azaindole inhibitors of crac |
| EP2909172A1 (en) * | 2012-10-17 | 2015-08-26 | F. Hoffmann-La Roche AG | 6-aminoindole derivatives as trp channel antagonists |
| JP5758864B2 (ja) | 2012-11-08 | 2015-08-05 | ファナック株式会社 | ブレーキの状態を解放状態から締結状態に迅速に変更するブレーキ駆動制御装置 |
| EP2738172A1 (en) | 2012-11-28 | 2014-06-04 | Almirall, S.A. | New bicyclic compounds as crac channel modulators |
| EP2970119B1 (en) * | 2013-03-14 | 2021-11-03 | Merck Sharp & Dohme Corp. | Novel indole derivatives useful as anti-diabetic agents |
| EP2848615A1 (en) | 2013-07-03 | 2015-03-18 | Almirall, S.A. | New pyrazole derivatives as CRAC channel modulators |
| AR097325A1 (es) * | 2013-08-13 | 2016-03-09 | Gruenenthal Gmbh | Pirroles anillados |
| CN105722834B (zh) | 2013-12-13 | 2017-12-22 | 豪夫迈·罗氏有限公司 | 酪氨酸蛋白激酶抑制剂 |
| WO2015086635A1 (en) | 2013-12-13 | 2015-06-18 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
| CN104447490B (zh) * | 2014-11-19 | 2017-06-06 | 连云港恒运医药有限公司 | 一种质子泵抑制剂的晶型、制备中间体及其合成方法和医药用途 |
| MX378998B (es) | 2015-06-03 | 2025-03-11 | Bristol Myers Squibb Co | Agonistas de receptor de apelina (apj) de 4-hidroxi-3-(heteroaril) piridin-2-ona como para uso en el tratamiento de trastornos cardiovasculares. |
| TW201835036A (zh) | 2017-02-27 | 2018-10-01 | 瑞士商隆薩有限公司 | 製備1-甲基-3-(三氟甲基)-1h-吡唑-5-醇的方法 |
| WO2019018562A1 (en) | 2017-07-19 | 2019-01-24 | Ideaya Biosciences, Inc. | AMIDO COMPOUND AS MODULATORS OF AHR |
| EP3710440B1 (en) | 2017-11-14 | 2023-04-05 | Bristol-Myers Squibb Company | Substituted indole compounds |
| SG11202005513TA (en) | 2017-12-15 | 2020-07-29 | Bristol Myers Squibb Co | Substituted indole ether compounds |
| AU2018390820A1 (en) | 2017-12-19 | 2020-08-06 | Bristol-Myers Squibb Company | Substituted indole compounds useful as TLR inhibitors |
| AU2018392316B2 (en) | 2017-12-19 | 2022-05-12 | Bristol-Myers Squibb Company | Amide substituted indole compounds useful as TLR inhibitors |
| CN111699185B (zh) | 2017-12-19 | 2023-06-27 | 百时美施贵宝公司 | 6-氮杂吲哚化合物 |
| KR102714788B1 (ko) | 2017-12-20 | 2024-10-08 | 브리스톨-마이어스 스큅 컴퍼니 | Tlr 억제제로서 유용한 아미노 인돌 화합물 |
| JP7382938B2 (ja) | 2017-12-20 | 2023-11-17 | ブリストル-マイヤーズ スクイブ カンパニー | ジアザインドール化合物 |
| JP7291707B2 (ja) * | 2017-12-20 | 2023-06-15 | ブリストル-マイヤーズ スクイブ カンパニー | アリールおよびヘテロアリール置換されたインドール化合物 |
| EA202190556A1 (ru) | 2018-09-14 | 2021-08-24 | Ризен Фармасьютикалс А Г | Композиции, содержащие ингибитор crac и кортикостероид, и способы их применения |
| EP3628669A1 (en) * | 2018-09-28 | 2020-04-01 | GenKyoTex Suisse SA | Novel compounds as nadph oxidase inhibitors |
| WO2020086503A1 (en) | 2018-10-24 | 2020-04-30 | Bristol-Myers Squibb Company | Substituted indole and indazole compounds |
| JP7597710B2 (ja) | 2018-10-24 | 2024-12-10 | ブリストル-マイヤーズ スクイブ カンパニー | 置換インドール二量体の化合物 |
| ES2987832T3 (es) | 2019-05-09 | 2024-11-18 | Bristol Myers Squibb Co | Compuestos de benzimidazolona sustituidos |
| WO2021067326A1 (en) | 2019-10-01 | 2021-04-08 | Bristol-Myers Squibb Company | Substituted bicyclic heteroaryl compounds |
| US12384760B2 (en) | 2019-10-04 | 2025-08-12 | Bristol-Myers Squibb Company | Substituted carbazole compounds |
| BR112023002737A2 (pt) | 2020-08-19 | 2023-03-14 | Bristol Myers Squibb Co | Derivados de imidazo[1,2-a]piridina e [1,2,4]triazolo[1,5-a]piridina como inibidores de tlr9 para o tratamento de fibrose |
| CN115043770B (zh) * | 2022-07-21 | 2023-09-08 | 南京大学 | 一种吲哚/氮杂吲哚类化合物的光诱导合成方法 |
| CN115124410B (zh) * | 2022-08-13 | 2024-06-04 | 上海珂华生物科技有限公司 | 一种2-氟-4-羟基苯甲醛的制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5785055A (en) * | 1980-11-18 | 1982-05-27 | Konishiroku Photo Ind Co Ltd | Silver halide photographic recording material |
| JP2894617B2 (ja) * | 1989-12-16 | 1999-05-24 | 帝国臓器製薬株式会社 | 2―フエニルインドール誘導体 |
| FR2824827B1 (fr) * | 2001-05-17 | 2004-02-13 | Fournier Lab Sa | Nouveaux derives de 5-phenyl-1h-indole antagoniste des recepteurs de l'interleukine-8 |
| WO2003099206A2 (en) * | 2002-05-21 | 2003-12-04 | Bristol-Myers Squibb Company | Indole compounds useful as impdh inhibitors |
| GB0602768D0 (en) * | 2006-02-10 | 2006-03-22 | Vastox Plc | Treatment of muscular dystrophy |
| SI1986633T1 (sl) * | 2006-02-10 | 2015-03-31 | Summit Corporation Plc | Zdravljenje Duchennove mišične distrofije |
| US20090142832A1 (en) * | 2007-11-29 | 2009-06-04 | James Dalton | Indoles, Derivatives, and Analogs Thereof and Uses Therefor |
| US8785489B2 (en) * | 2008-10-17 | 2014-07-22 | Boehringer Ingelheim International Gmbh | Heteroaryl substituted indole compounds useful as MMP-13 inhibitors |
| KR20100092909A (ko) * | 2009-02-13 | 2010-08-23 | 주식회사 엘지생명과학 | 잔틴 옥시다제 저해제로서 효과적인 신규 화합물, 그 제조방법 및 그를 함유하는 약제학적 조성물 |
| MA33209B1 (fr) * | 2009-03-27 | 2012-04-02 | Merck Sharp & Dohme | Inhibiteurs de la replication du virus de l'hepatite c |
-
2010
- 2010-09-21 WO PCT/EP2010/063838 patent/WO2011036130A1/en not_active Ceased
- 2010-09-21 RU RU2012116207/04A patent/RU2012116207A/ru not_active Application Discontinuation
- 2010-09-21 KR KR1020127010486A patent/KR20120068947A/ko not_active Ceased
- 2010-09-21 BR BR112012006630A patent/BR112012006630A2/pt not_active Application Discontinuation
- 2010-09-21 CA CA2771026A patent/CA2771026A1/en not_active Abandoned
- 2010-09-21 CN CN2010800426038A patent/CN102574788A/zh active Pending
- 2010-09-21 EP EP10754941A patent/EP2480529A1/en not_active Withdrawn
- 2010-09-21 MX MX2012003539A patent/MX2012003539A/es not_active Application Discontinuation
- 2010-09-21 JP JP2012530236A patent/JP2013505913A/ja active Pending
- 2010-09-22 AR ARP100103446A patent/AR078408A1/es unknown
- 2010-09-23 TW TW099132213A patent/TW201121952A/zh unknown
- 2010-09-23 US US12/888,701 patent/US20110071150A1/en not_active Abandoned
-
2012
- 2012-08-15 JP JP2012180132A patent/JP2012246302A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US20110071150A1 (en) | 2011-03-24 |
| CA2771026A1 (en) | 2011-03-31 |
| WO2011036130A1 (en) | 2011-03-31 |
| CN102574788A (zh) | 2012-07-11 |
| KR20120068947A (ko) | 2012-06-27 |
| JP2012246302A (ja) | 2012-12-13 |
| EP2480529A1 (en) | 2012-08-01 |
| TW201121952A (en) | 2011-07-01 |
| RU2012116207A (ru) | 2013-10-27 |
| MX2012003539A (es) | 2012-04-30 |
| BR112012006630A2 (pt) | 2016-05-03 |
| JP2013505913A (ja) | 2013-02-21 |
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