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阿扎司琼

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阿扎司琼
临床资料
AHFS/Drugs.com国际药品名称
给药途径口服
ATC码
  • 未分配
药物动力学数据
生物利用度90%
排泄途径60-70%
识别信息
  • N-(1-azabicyclo[2.2.2]octan-8-yl)-6-chloro-4-methyl-3-oxo-1,4-benzoxazine-8-carboxamide
CAS号123040-69-7
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
化学信息
化学式C17H20ClN3O3
摩尔质量349.82 g·mol−1
3D模型(JSmol英语JSmol
  • CN1C(=O)COc2c1cc(Cl)cc2C(=O)NC3CN4CCC3CC4
  • InChI=1S/C17H20ClN3O3/c1-20-14-7-11(18)6-12(16(14)24-9-15(20)22)17(23)19-13-8-21-4-2-10(13)3-5-21/h6-7,10,13H,2-5,8-9H2,1H3,(H,19,23) checkY
  • Key:WUKZPHOXUVCQOR-UHFFFAOYSA-N checkY

阿扎司琼(英语:Azasetron)是一种止吐药,作为5-HT3受体英语5-HT3 receptor拮抗剂英语5-HT3 antagonist,pKi=9.27,[1]用于治疗癌症化疗(如顺铂化疗)引起的恶心和呕吐。盐酸阿扎司琼的常用剂量为10毫克,每日一次,口服或静脉注射。它在日本获准上市,由鸟居制药有限公司独家销售,商品名为“Serotone I.V. Injection 10 mg”和“Serotone Tablets 10 mg”。[2]该药物的药代动力学数据来自冢越茂(Tsukagoshi Shigeru)。[3]

苯磺酸R-阿扎司琼(R-azasetron besylate,SENS-401)已被研究用于预防与突发感音神经性听力损失[4]声创伤英语Acoustic trauma[5]和顺铂引起的耳毒性英语Ototoxicity相关的听力损失。[4][6]

参考资料

[编辑]
  1. ^ Azasetron. drugcentral.org/. UNM School of Medicine. 2016-07-31 [2016-11-11]. (原始内容存档于2020-09-21). 
  2. ^ Torii Pharmaceutical to Solely Market Antiemetic Drugs. Torii Pharmaceutical Co Ltd. 2009-01-13 [2016-11-11]. (原始内容存档于2014-06-13). 
  3. ^ Tsukagoshi S. [Pharmacokinetics of azasetron (Serotone), a selective 5-HT3 receptor antagonist]. Gan to Kagaku Ryoho. Cancer & Chemotherapy. June 1999, 26 (7): 10011008. PMID 10396331. 
  4. ^ 4.0 4.1 Drug and Device News. P & T. October 2017, 42 (10): 608651. PMC 5614410可免费查阅. PMID 29018295. SENS-401 for Platinum-Induced Ototoxicity Sensorion has received the FDAs orphan drug designation for SENS-401 for the prevention of platinum-induced ototoxicity in pediatric patients. As many as 60% of patients develop severe hearing loss due to platinum-based chemo therapies. There is no approved pharmaceutical treatment. SENS-401 (R-azasetron besylate) is designed to protect and preserve inner ear tissue when lesions may cause progressive hearing impairments. The drug (both oral and injectable) is also in development for the treatment of sudden sensorineural hearing loss. Sensorion expects to initiate a phase 2 clinical trial in this indication in the first half of 2018. 
  5. ^ Petremann M, Romanet C, Broussy A, Van Ba CT, Poli S, Dyhrfjeld-Johnsen J. SENS-401 Effectively Reduces Severe Acoustic Trauma-Induced Hearing Loss in Male Rats With Twice Daily Administration Delayed up to 96hours. Otology & Neurotology (Ovid Technologies (Wolters Kluwer Health)). February 2019, 40 (2): 254263. PMID 30570608. doi:10.1097/mao.0000000000002088. 
  6. ^ Petremann M, Tran Van Ba C, Broussy A, Romanet C, Dyhrfjeld-Johnsen J. Oral Administration of Clinical Stage Drug Candidate SENS-401 Effectively Reduces Cisplatin-induced Hearing Loss in Rats. Otology & Neurotology (Ovid Technologies (Wolters Kluwer Health)). October 2017, 38 (9): 13551361. PMID 28796092. doi:10.1097/mao.0000000000001546.