AR087755A1 - Derivados de heterociclos biciclicos para el tratamiento de la hipertension arterial pulmonar - Google Patents
Derivados de heterociclos biciclicos para el tratamiento de la hipertension arterial pulmonarInfo
- Publication number
- AR087755A1 AR087755A1 ARP120103226A ARP120103226A AR087755A1 AR 087755 A1 AR087755 A1 AR 087755A1 AR P120103226 A ARP120103226 A AR P120103226A AR P120103226 A ARP120103226 A AR P120103226A AR 087755 A1 AR087755 A1 AR 087755A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- alkoxy
- heterocyclyl
- halogen
- Prior art date
Links
- 206010064911 Pulmonary arterial hypertension Diseases 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 41
- 229910052736 halogen Inorganic materials 0.000 abstract 20
- 150000002367 halogens Chemical class 0.000 abstract 20
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 17
- 125000000623 heterocyclic group Chemical group 0.000 abstract 16
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 13
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 8
- 125000001424 substituent group Chemical group 0.000 abstract 8
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 4
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 4
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004043 oxo group Chemical group O=* 0.000 abstract 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 108091008606 PDGF receptors Proteins 0.000 abstract 1
- 102000011653 Platelet-Derived Growth Factor Receptors Human genes 0.000 abstract 1
- 230000004071 biological effect Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Útiles en la inhibición de la actividad biológica mediada por el receptor PDGF. Reivindicación 1: Un compuesto representado por la fórmula (1) o una sal farmacéuticamente aceptable del mismo, en donde, A es un compuesto de formula (2) ó (3); R¹ es alquilo C₁₋₄; alcoxilo C₁₋₄ opcionalmente sustituido por uno o más átomos de halógeno; CN; ó halógeno; R¹ᵃ es H, halógeno, alquilo C₁₋₄ ó haloalquilo C₁₋₄; X es N ó CH; R² es H; alquilo C₁₋₈ opcionalmente sustituido por uno o más OH, -NR⁹R¹¹ ó alcoxilo C₁₋₄; haloalquilo C₁₋₈; alquinilo C₂₋₈ sustituido por uno o más halógeno, OH, -NR⁹R¹¹ ó alcoxilo C₁₋₄; cicloalquilo C₃₋₁₀; -(alquilo C₁₋₄)-cicloalquilo C₃₋₈; alcoxilo C₁₋₈ opcionalmente sustituido por uno o más halógeno, -NR⁹R¹¹ u OH; OH; CN; halógeno; -(alquilo C₀₋₄)-NR⁹R¹¹; -(alquilo C₀₋₄)-CO₂R¹⁵; -(alquilo C₀₋₄)-C(O)NR⁹R¹¹; -(alquilo C₀₋₄)-arilo C₆₋₁₄; ó -(alquilo C₀₋₄)-heterociclilo de 3 a 14 miembros; en donde el cicloalquilo, -(alquilo C₀₋₄)-arilo C₆₋₁₄ y -(alquilo C₀₋₄)-heterociclilo de 3 a 14 miembros son cada uno opcionalmente sustituidos por uno o más sustituyentes de Zᵃ; R³ es H; alquilo C₁₋₈ opcionalmente sustituido por uno o más OH, -NR⁹R¹¹ ó alcoxilo C₁₋₄; haloalquilo C₁₋₈; alquinilo C₂₋₈ sustituido por uno o más halógeno, OH, -NR⁹R¹¹, ó alcoxilo C₁₋₄; cicloalquilo C₃₋₁₀; -(alquilo C₁₋₄)-cicloalquilo C₃₋₈; alcoxilo C₁₋₈ opcionalmente sustituido por uno o más halógeno, -NR⁹R¹¹ u OH; OH; CN; halógeno; -(alquilo C₀₋₄)-NR⁹R¹¹; -(alquilo C₀₋₄)-CO₂R¹⁵; -(alquilo C₀₋₄)-C(O)NR⁹R¹¹; -(alquilo C₀₋₄)-arilo C₆₋₁₄; ó -(alquilo C₀₋₄)-heterociclilo de 3 a 14 miembros; en donde el cicloalquilo, -(alquilo C₀₋₄)-arilo C₆₋₁₄ y -(alquilo C₀₋₄)-heterociclilo de 3 a 14 miembros son cada uno opcionalmente sustituidos por uno o más sustituyentes de Zᵃ; cada Zᵃ es independientemente OH; (alquilo C₀₋₄)-arilo C₆; O-arilo C₆; alquilo C₁₋₄ opcionalmente sustituido por uno o más OH, CN ó -NR¹⁹ᵃR²¹ᵃ; haloalquilo C₁₋₄; alcoxilo C₁₋₄ opcionalmente sustituido por uno o más OH, -CO₂R¹⁹ᵃ, -NR¹⁹ᵃR²¹ᵃ ó alcoxilo C₁₋₄; -NR¹⁸ᵃC(O)R²¹ᵃ; -C(O)NR¹⁹ᵃR²¹ᵃ; -NR¹⁸ᵃC(O)NR¹⁹ᵃR²¹ᵃ; -NR¹⁹ᵃR²¹ᵃ; -(alquilo C₀₋₄)-C(O)OR¹⁸ᵃ; -(alquilo C₀₋₄)-C(O)R¹⁹ᵃ; oxo; CN; NO₂; halógeno; -(alquilo C₀₋₄)-heterociclilo de 4 a 6 miembros; ó -O-(heterociclilo de 4 a 6 miembros); en donde el (alquilo C₀₋₄)-arilo C₆, O-arilo C₆, -(alquilo C₀₋₄)-heterociclilo de 4 a 6 miembros y -O-(heterociclilo de 4 a 6 miembros) son cada uno opcionalmente sustituidos por OH, halógeno, alquilo C₁₋₄, haloalquilo C₁₋₄ ó alcoxilo C₁₋₄ opcionalmente sustituido por uno o más halógenos; R⁴ es H; R⁵ es H, alquilo C₁₋₄ o haloalquilo C₁₋₄; R⁶ se selecciona a partir de alquilo C₁₋₈ opcionalmente sustituido por uno o más alcoxilo C₁₋₄ ó -NR¹⁹R²¹; haloalquilo C₁₋₈; -(alquilo C₀₋₄)-cicloalquilo C₃₋₈; alcoxilo C₁₋₈ opcionalmente sustituido por uno ó más átomos de halógeno; -NR¹⁹R²¹; -(alquilo C₀₋₄)-arilo C₆₋₁₄; y -(alquilo C₀₋₄)-heterociclilo de 3 a 14 miembros; en donde el -(C₀₋₄alquilo)-cicloalquilo C₃₋₈, -(alquilo C₀₋₄)-arilo C₆₋₁₄ y -(alquilo C₀₋₄)-heterociclilo de 3 a 14 miembros son cada uno opcionalmente sustituidos por uno o más sustituyentes de Z; cada Z se selecciona independientemente a partir de (alquilo C₀₋₄)-arilo C₆; O-arilo C₆; alquilo C₁₋₆ opcionalmente sustituido por uno o más alcoxilo C₁₋₆, CN ó -NR¹⁹R²¹; haloalquilo C₁₋₆; alcoxilo C₁₋₆ opcionalmente sustituido por uno o más -NR¹⁹R²¹ ó alcoxilo C₁₋₄; -NR¹⁹R²¹; (alquilo C₀₋₄)-C(O)R¹⁹; CN; halógeno y (alquilo C₀₋₄)-heterociclilo de 4 a 6 miembros; y en donde el arilo y heterociclilo son cada uno opcionalmente sustituidos por uno o más halógeno, alquilo C₁₋₆, haloalquilo C₁₋₆ y alcoxilo C₁₋₆ opcionalmente sustituido por uno o más halógenos; R⁹ y R¹¹ son cada uno independientemente seleccionados a partir de H; alquilo C₁₋₆ opcionalmente sustituido por uno o más alcoxilo C₁₋₄ u OH; haloalquilo C₁₋₆; -(alquilo C₀₋₄)-cicloalquilo C₃₋₆; (alquilo C₀₋₄)-arilo C₆₋₁₄ opcionalmente sustituido por uno o más grupos seleccionados a partir de: alquilo C₁₋₆, alcoxilo C₁₋₆ y halógeno; y (alquilo C₀₋₄)-heterociclilo de 3- a 14- miembros opcionalmente sustituidos por uno o más grupos seleccionados a partir de: halógeno, oxo, alquilo C₁₋₆ y C(O)alquilo C₁₋₆; ó R⁹ y R¹¹ junto con el átomo de nitrógeno al cual están fijados forman un heterociclilo de 5 a 10 miembros, dicho heterociclilo incluye 0 a 3 heteroátomos adicionales seleccionados a partir de N, O y S, el heterociclilo siendo opcionalmente sustituido por uno o más sustituyentes seleccionados a partir de: OH; halógeno; fenilo, heterociclilo de 5 a 10 miembros; alquilo C₁₋₆; haloalquilo C₁₋₆; alcoxilo C₁₋₆ opcionalmente sustituido por uno o más OH ó alcoxilo C₁₋₄; y C(O)O-alquilo C₁₋₆; en donde los grupos sustituyentes fenilo y heterociclilo son por sí mismos opcionalmente sustituidos por alquilo C₁₋₆, haloalquilo C₁₋₆ ó alcoxilo C₁₋₆; R¹⁵ se selecciona a partir de H; alquilo C₁₋₈; haloalquilo C₁₋₈; cicloalquilo C₃₋₁₀; -(alquilo C₁₋₄)-cicloalquilo C₃₋₈; -(alquilo C₀₋₄)-arilo C₆₋₁₄ y -(alquilo C₀₋₄)-grupo heterociclilo de 3 a 14 miembros; en donde el cicloalquilo C₃₋₁₀, -(alquilo C₁₋₄)-cicloalquilo C₃₋₈, -(alquilo C₀₋₄)-arilo C₆₋₁₄ y -(alquilo C₀₋₄)-grupo heterociclilo de 3 a 14 miembros son cada uno opcionalmente sustituidos por uno o más sustituyentes de Z; R¹⁸ᵃ es independientemente H ó alquilo C₁₋₆; R¹⁹ᵃ y R²¹ᵃ son cada uno independientemente H; alquilo C₁₋₆ opcionalmente sustituido por uno o más alcoxilo C₁₋₄, -NR²²R²³, u OH; haloalquilo C₁₋₆; -(alquilo C₀₋₁)-cicloalquilo C₃₋₆; -(alquilo C₀₋₄)-arilo C₆₋₁₄ opcionalmente sustituido por uno o más grupos seleccionados a partir de: alquilo C₁₋₆, alcoxilo C₁₋₆ y halógeno; ó -(alquilo C₀₋₄)-heterociclilo de 3- a 14- miembros opcionalmente sustituidos por uno o más grupos seleccionados a partir de: halógeno, oxo, alquilo C₁₋₆ y C(O)alquilo C₁₋₆; ó R¹⁹ᵃ y R²¹ᵃ junto con el átomo de nitrógeno al cual están fijados forman un heterociclilo de 5 a 10 miembros, dicho heterociclilo incluye 0 a 3 heteroátomos adicionales seleccionados a partir de N, O y S, el heterociclilo siendo opcionalmente sustituido por uno o más sustituyentes seleccionados a partir de: OH; halógeno; fenilo; heterociclilo de 5 a 10 miembros; alquilo C₁₋₆; haloalquilo C₁₋₆; alcoxilo C₁₋₆ opcionalmente sustituido por uno o más OH ó alcoxilo C₁₋₄; y C(O)O-alquilo C₁₋₆; en donde los grupos sustituyentes fenilo y heterociclilo son por sí mismos opcionalmente sustituidos por alquilo C₁₋₆, haloalquilo C₁₋₆ ó alcoxilo C₁₋₆; R¹⁸ es independientemente H ó alquilo C₁₋₆; R¹⁹ y R²¹ son cada uno independie
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161530049P | 2011-09-01 | 2011-09-01 | |
| US201261680119P | 2012-08-06 | 2012-08-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR087755A1 true AR087755A1 (es) | 2014-04-16 |
Family
ID=47018333
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP120103226A AR087755A1 (es) | 2011-09-01 | 2012-08-31 | Derivados de heterociclos biciclicos para el tratamiento de la hipertension arterial pulmonar |
Country Status (28)
| Country | Link |
|---|---|
| US (2) | US8883819B2 (es) |
| EP (1) | EP2751108B1 (es) |
| JP (1) | JP5815870B2 (es) |
| KR (1) | KR101687082B1 (es) |
| CN (2) | CN105001218B (es) |
| AP (1) | AP3818A (es) |
| AR (1) | AR087755A1 (es) |
| AU (1) | AU2012303674B2 (es) |
| BR (1) | BR112014004631B1 (es) |
| CA (1) | CA2845753C (es) |
| CL (1) | CL2014000459A1 (es) |
| CO (1) | CO6900139A2 (es) |
| CR (1) | CR20140099A (es) |
| EA (1) | EA024068B1 (es) |
| ES (1) | ES2585048T3 (es) |
| IL (1) | IL231228A0 (es) |
| MA (1) | MA35364B1 (es) |
| MX (1) | MX360316B (es) |
| PE (1) | PE20141674A1 (es) |
| PH (1) | PH12014500407A1 (es) |
| PL (1) | PL2751108T3 (es) |
| PT (1) | PT2751108T (es) |
| SG (1) | SG11201400253YA (es) |
| TN (1) | TN2014000067A1 (es) |
| TW (1) | TW201313718A (es) |
| UY (1) | UY34305A (es) |
| WO (1) | WO2013030802A1 (es) |
| ZA (1) | ZA201401294B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2685903B2 (ja) | 1989-07-05 | 1997-12-08 | アルプス電気株式会社 | 磁気ヘッド支持装置 |
| UY34305A (es) * | 2011-09-01 | 2013-04-30 | Novartis Ag | Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar |
| US9073921B2 (en) | 2013-03-01 | 2015-07-07 | Novartis Ag | Salt forms of bicyclic heterocyclic derivatives |
| UA119247C2 (uk) | 2013-09-06 | 2019-05-27 | РОЙВЕНТ САЙЕНСИЗ ҐмбГ | Спіроциклічні сполуки як інгібітори триптофангідроксилази |
| WO2015089137A1 (en) | 2013-12-11 | 2015-06-18 | Karos Pharmaceuticals, Inc. | Acylguanidines as tryptophan hydroxylase inhibitors |
| CN105524058B (zh) * | 2014-10-21 | 2018-03-27 | 广州艾格生物科技有限公司 | 吡唑并[1,5‑a]吡啶类化合物及其应用 |
| WO2016109501A1 (en) | 2014-12-30 | 2016-07-07 | Karos Pharmaceuticals, Inc. | Amide compounds as tryptophan hydroxylase inhibitors |
| US9611201B2 (en) | 2015-03-05 | 2017-04-04 | Karos Pharmaceuticals, Inc. | Processes for preparing (R)-1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanol and 1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanone |
| GB201801355D0 (en) * | 2018-01-26 | 2018-03-14 | Enterprise Therapeutics Ltd | Compounds |
| EP3880680A1 (en) | 2018-11-14 | 2021-09-22 | Altavant Sciences GmbH | A crystalline spirocyclic compound inhibitor of tryptophan hydroxylase 1 (tph1) for treating diseases or disorders associated with peripheral serotonin |
| MX2022007044A (es) * | 2019-12-13 | 2022-06-24 | Nippon Shinyaku Co Ltd | Compuesto y composicion como inhibidor de cinasa del receptor de los factores de crecimiento derivados de las plaquetas (pdgf). |
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