伏妥昔单抗:修订间差异
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'''伏妥昔单抗''' |
'''伏妥昔单抗'''([[INN]]:futuximab,开发代号:'''992 DS'''),或译'''夫妥昔单抗'''、'''福妥昔单抗''',是一种嵌合[[单克隆抗体]],设计用于治疗[[癌症]]。<ref>[http://www.ama-assn.org/resources/doc/usan/x-pub/futuximab.pdf Statement On A Nonproprietary Name Adopted By The USAN Council - Futuximab] {{Wayback|url=http://www.ama-assn.org/resources/doc/usan/x-pub/futuximab.pdf |date=20160402051807 }}, ''[[American Medical Association]]''.</ref>它充当[[免疫调节剂]]并与[[HER1]]结合。<ref>{{cite journal | author = [[World Health Organization]] | title = International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 107 | journal = WHO Drug Information | volume = 26 | issue = 2 | year = 2012 | url = https://www.who.int/medicines/publications/druginformation/innlists/Final_PL107.pdf | access-date = 2024-03-06 | archive-date = 2016-03-04 | archive-url = https://web.archive.org/web/20160304063336/http://www.who.int/medicines/publications/druginformation/innlists/Final_PL107.pdf | dead-url = no }}</ref><ref>{{cite journal |vauthors=Keir ST, Chandramohan V, Hemphill CD, Grandal MM, Melander MC, Pedersen MW, Horak ID, Kragh M, Desjardins A, Friedman HS, Bigner DD |title=Sym004-induced EGFR elimination is associated with profound anti-tumor activity in EGFRvIII patient-derived glioblastoma models |journal=J. Neurooncol. |volume=138 |issue=3 |pages=489–498 |date=July 2018 |pmid=29564747 |doi=10.1007/s11060-018-2832-6 |pmc=5999169 }}</ref> |
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该药物由 |
该药物由{{le|Symphogen|Symphogen}}开发。 |
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== 参考资料 == |
== 参考资料 == |
2024年6月20日 (四) 12:39的最新版本
单克隆抗体 | |
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种类 | 完整抗体 |
目標 | HER1 |
臨床資料 | |
其他名稱 | 992 DS |
ATC碼 |
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识别信息 | |
CAS号 | 1310460-85-5 |
ChemSpider |
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UNII | |
化学信息 | |
化学式 | C6468H10002N1724O2055S46 |
摩尔质量 | 146,269.94 g·mol−1 |
伏妥昔单抗(INN:futuximab,开发代号:992 DS),或译夫妥昔单抗、福妥昔单抗,是一种嵌合单克隆抗体,设计用于治疗癌症。[1]它充当免疫调节剂并与HER1结合。[2][3]
该药物由Symphogen开发。
参考资料
[编辑]- ^ Statement On A Nonproprietary Name Adopted By The USAN Council - Futuximab (页面存档备份,存于互联网档案馆), American Medical Association.
- ^ World Health Organization. International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 107 (PDF). WHO Drug Information. 2012, 26 (2) [2024-03-06]. (原始内容存档 (PDF)于2016-03-04).
- ^ Keir ST, Chandramohan V, Hemphill CD, Grandal MM, Melander MC, Pedersen MW, Horak ID, Kragh M, Desjardins A, Friedman HS, Bigner DD. Sym004-induced EGFR elimination is associated with profound anti-tumor activity in EGFRvIII patient-derived glioblastoma models. J. Neurooncol. July 2018, 138 (3): 489–498. PMC 5999169 . PMID 29564747. doi:10.1007/s11060-018-2832-6.