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Subject Item
dbr:List_of_compounds_with_carbon_number_16
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dbr:Benoxaprofen
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بنوكسابروفين Benoxaprofen Benoxaprofene Benoxaprofen
rdfs:comment
Il benoxaprofene (chiamato anche composto LRCL 3794) è un antinfiammatorio non steroideo dotato di attività antinfiammatoria, analgesica e antipiretica. appartenente alla classe dell'acido arilalcanoico Il farmaco sembra avere la capacità di modulare la fagocitosi e la secrezione di enzimi lisosomiali da parte dei neutrofili polimorfonucleati. Benoxaprofen ist eine chlorhaltige, heterocyclische Verbindung, die sich vom Oxazol und der Propionsäure ableitet. Als Arzneistoff zählt Benoxaprofen wie das ähnliche Ibuprofen zur Gruppe der Nicht-Steroidalen Antirheumatika bzw. Antiphlogistika. Der Arzneistoff wurde in den 1980er Jahren durch Eli Lilly entwickelt und als Analgetikum, Antipyretikum und Antiphlogistikum eingesetzt. Nachdem schwere Nebenwirkungen wie starke allergische Reaktionen (Photosensibilität) auf das Mittel und Leberschäden mit hunderten Toten in Großbritannien auftraten, wurde dem Arzneistoff die Zulassung wieder entzogen. Das frühere Präparat Oraflex® ist nicht mehr erhältlich. بنوكسابروفين (بالإنجليزية: Benoxaprofen)‏ هو مُركب كيميائي، يحمل الصيغة C16H12ClNO3، وهو دواء لاستيرويدي مضاد للالتهاب ويُباع تحت الاسم التجاري أورفليكس في الولايات المتحدة وتحت اسم أوبرين في أوروبا عبر إيلي ليلي وشركاءه. أوقفت شركة إيلي بيع الدواء عام 1982 بعد إبلاغاتٍ من الحكومة البريطانية وإدارة الغذاء والدواء الأمريكية حول الآثار الجانبية والقاتلة للدواء. Benoxaprofen, also known as Benoxaphen, is a chemical compound with the formula C16H12ClNO3. It is a non-steroidal anti-inflammatory drug (NSAID) of the propionic acid class, and was marketed under the brand name Opren in the United Kingdom and Europe by Eli Lilly and Company (commonly referred to as Lilly), and as Oraflex in the United States of America (USA). Lilly suspended sales of Oraflex in 1982 after reports from the British government and the United States Food and Drug Administration (US FDA) of adverse effects and deaths linked to the drug.
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Two-dimensional monochrome diagram showing the structure of the molecule of Benoxaprofen, uing the hexagonal style to depict a chemical compound.
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Benoxaprofen molecule
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dbo:abstract
Benoxaprofen ist eine chlorhaltige, heterocyclische Verbindung, die sich vom Oxazol und der Propionsäure ableitet. Als Arzneistoff zählt Benoxaprofen wie das ähnliche Ibuprofen zur Gruppe der Nicht-Steroidalen Antirheumatika bzw. Antiphlogistika. Der Arzneistoff wurde in den 1980er Jahren durch Eli Lilly entwickelt und als Analgetikum, Antipyretikum und Antiphlogistikum eingesetzt. Nachdem schwere Nebenwirkungen wie starke allergische Reaktionen (Photosensibilität) auf das Mittel und Leberschäden mit hunderten Toten in Großbritannien auftraten, wurde dem Arzneistoff die Zulassung wieder entzogen. Das frühere Präparat Oraflex® ist nicht mehr erhältlich. بنوكسابروفين (بالإنجليزية: Benoxaprofen)‏ هو مُركب كيميائي، يحمل الصيغة C16H12ClNO3، وهو دواء لاستيرويدي مضاد للالتهاب ويُباع تحت الاسم التجاري أورفليكس في الولايات المتحدة وتحت اسم أوبرين في أوروبا عبر إيلي ليلي وشركاءه. أوقفت شركة إيلي بيع الدواء عام 1982 بعد إبلاغاتٍ من الحكومة البريطانية وإدارة الغذاء والدواء الأمريكية حول الآثار الجانبية والقاتلة للدواء. Il benoxaprofene (chiamato anche composto LRCL 3794) è un antinfiammatorio non steroideo dotato di attività antinfiammatoria, analgesica e antipiretica. appartenente alla classe dell'acido arilalcanoico Il farmaco sembra avere la capacità di modulare la fagocitosi e la secrezione di enzimi lisosomiali da parte dei neutrofili polimorfonucleati. Benoxaprofen, also known as Benoxaphen, is a chemical compound with the formula C16H12ClNO3. It is a non-steroidal anti-inflammatory drug (NSAID) of the propionic acid class, and was marketed under the brand name Opren in the United Kingdom and Europe by Eli Lilly and Company (commonly referred to as Lilly), and as Oraflex in the United States of America (USA). Lilly suspended sales of Oraflex in 1982 after reports from the British government and the United States Food and Drug Administration (US FDA) of adverse effects and deaths linked to the drug.
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