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盐酸帕洛诺司琼合成路线图解 被引量:4

Graphical Synthetic Routes of Palonosetron Hydrochloride
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摘要 帕洛诺司琼(Palonosetron,1),化学名为(3aS)-2-[(3S)-1-氮杂二环[2.2.2]辛烷.3.基]-2,3,3a,4,5,6-六氢-1-氧代-1H-苯并[de]异喹啉,是由瑞士Helsinn公司研制的5.HT,受体拮抗剂,其盐酸盐于2003年7月首次在美国上市,商品名Aloxi(阿乐喜),临床用于预防中度或高度致吐性化疗引发的急性和迟发性恶心呕吐。本品半衰期长(40h),
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2009年第3期231-233,共3页 Chinese Journal of Pharmaceuticals
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参考文献11

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  • 2NCCN推荐帕洛诺司琼预防化疗后呕吐[J].世界临床药物,2004,25(5):259-259. 被引量:5
  • 3王海凤,王东凯.5-HT_3受体阻滞剂帕洛诺司琼[J].中国新药杂志,2006,15(10):833-835. 被引量:16
  • 4Alois DC, Andrew KB. Process for the preparation of 2- (1 -azabicyclo (2.2.2) oct-3-yl) -2,4,5,6-tetrahydro- IH- benz (de) isoquinolin-l-one and intermediate product: WO, 9601824 [P]. 1996-01-25. (CA 1996, 124: 289284) 被引量:1
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二级参考文献9

  • 1胡凯,丁鼎乐.帕洛诺司琼市场前景看好[J].上海医药,2004,25(11):518-518. 被引量:8
  • 2林清强,叶锦林.新型5-HT3受体拮抗剂帕洛诺司琼[J].中国科技信息,2005(11):157-157. 被引量:12
  • 3Helsinn Healthcare SA.AloxiTM (palonosetron hydrochloride) Injection NDA no.021-372 [ EB/OL].[ 2004-04-15 ].http://www.fda.gov/cder. 被引量:1
  • 4GRALLA R,LICHINITSER M,VAN DER VEGT S,et al.Palonasetron improves prevention of chemotherapy-induced nausea and vomiting following moderately emetogenic chemotherapy:results of a double-blind randomized phase Ⅲ trail comparing single dosed of palonosetron with ondansetron [ J ].Ann Oncol,2003,14 (10):1570-1577. 被引量:1
  • 5STOLTZ R,CYONG JC,SHAH A,et al.Pharmacokinetic and safety evaluation of palonosetron,a 5-hydroxytryptamine-3 receptor antagonist,in U.S.and Japanese healthy subjects [ J].J Clin Pharm,2004,44 (5):520-531. 被引量:1
  • 6STOLTZ R,PARISI S,SHAH A,et al.Pharmacokinetics,metabolism and excretion of intravenous [ 14C ]-palonosetron in healthy human volunteers [ J].Biopharm Drug Dispos,2004,25(8):329-337. 被引量:1
  • 7NAVARI RM.Pathogenesis-based treatment of chemotherapy-induced nausea and vomiting-two new agents[ J].J Support Oncol,2003,1 (2):89-103. 被引量:1
  • 8EISENBERG P,FIGUEROA-VADILLO J,ZAMORA R,et al.Improved prevention of moderately emetogenic chemotherapy-induced nausea and vomiting with palonosetron,a pharmacologically novel 5-HT3 receptor antagonist:results of a phase Ⅲ,single-dose trial versus dolasetron [ J ].Cancer,2003,98 (11):2473-2482. 被引量:1
  • 9SIDDIQUI MA,SCOTT LJ.Palonosetron [ J ].Drugs,2004,64(10):1125-1132;discussion 1133-1134. 被引量:1

共引文献28

同被引文献18

  • 1王海凤,王东凯.5-HT_3受体阻滞剂帕洛诺司琼[J].中国新药杂志,2006,15(10):833-835. 被引量:16
  • 2Alois DC, Andrew KB. Process for the preparation of 2- (1 -azabicyclo (2.2.2) oct-3-yl) -2,4,5,6-tetrahydro- 1H- benz(de) isoquinolin-l-one and intermediate product: WO, 9601824 [P]. 1996-01-25. (CA 1996, 124: 289284) 被引量:1
  • 3Kowalczyk BA. Total synthesis of RS-42358 and analogs using lateral lithiation [J]. Synthesis, 2000, 8:1113-1116. 被引量:1
  • 4Robinson J, Rohloff JC, Kowalczyk BA. Process for preoaring 2- (1-azabicyclo[2.2.2]oct-3-yl)-2,3,3a,4,5,6- hexahydro-lH-benz[de]isoquinolin-1- one: US, 5510486 [P]. 1996-04-23. (CA 1996, 125: 58344) 被引量:1
  • 5Lancelot JC, Rault S, Laduree D, et al. Pyrido[3,2- e]pyrrolo[1,2-a]pyrazines [J]. Chem Pharm Bull, 1985, 33 (7) : 2798-2802. 被引量:1
  • 6Tamura R, Sato M, Oda D. Facile synthesis of allylic nitro compounds by N,N-dimethylethylenediamine-catalyzed condensation of aliphatic and alicyclic ketones with primary nitroalkanes LJ]. J Org Chem, 1986, 51 (23) : 4368-4375. 被引量:1
  • 7沈曦,周慧,王万青,蔡华芳.反相高效液相色谱法检测盐酸帕洛诺司琼及其有关物质[J].中国现代应用药学,2007,24(4):307-308. 被引量:4
  • 8Eisenberg P, Figueroa Vadillo J, Zamora R. Improved prevention of moderately emetogenic chemotherapy-induced nausea and vomiting with palonosetron, a pharmacologically novel 5-HT3 receptor antago- nist[J]. Cancer, 2003,98(11): 2473-2482. 被引量:1
  • 9Ward TJ, Ward KD. Chiral separations: fundamental review 2010 [ J]. Analytical chemistry, 2010,82(12) : 4712-4722. 被引量:1
  • 10Xiao Y, Chung TS. Functionalization of cellulose dialysis membranes for chiral separation using beta-cyclodextrin immobilization [ J ]. Jour- nal ofmembranc science, 2007,290( 1 ) : 78-85. 被引量:1

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