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Aciclovir

产品号 Bio-0206 公司名称 InterBioScreen
CAS号 59277-89-3 公司网站 http://www.ibscreen.com
分子式 C8H11N5O3 电 话 +7 49652 40091
分子量 225.20464 传 真 +7 49652 40092
纯 度 电子邮件 screen@ibscreen.chg.ru
保 存 Chembase数据库ID: 44444

产品价格信息

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产品别名

标题
Aciclovir
IUPAC标准名
2-amino-9-[(2-hydroxyethoxy)methyl]-6,9-dihydro-1H-purin-6-one
IUPAC传统名
2-amino-9-[(2-hydroxyethoxy)methyl]-6,9-dihydro-1H-purin-6-one
别名
Virasorb
Supraviran
Milavir
Acycloguanosine
Cycloviran
Activir
Avirax
Geavir
Herpetad
Soothelip
Mirolex
Virovir
Zyclir
Zovirax
Acyclovir

产品登记号

CAS号 59277-89-3

产品性质

应用领域 Antiviral agent.
应用领域 Used especially against herpes.
生物活性机理 Guanosine analog that acts as an antimetabolite.
生物活性机理 Viral (HSV-1, HSV-2 and VZV) thymidine kinase converts aciclovir to the aciclovir monophosphate, which is then converted to the diphosphate by cellular guanylate kinase,
生物活性机理 and finally to the triphosphate by phosphoglycerate kinase, phosphoenolpyruvate carboxykinase, and pyruvate kinase.
生物活性机理 Aciclovir triphosphate competitively inhibits viral DNA polymerase and competes with the natural deoxyguanosine triphosphate, for incorporation into viral DNA.
生物活性机理 Once incorporated, aciclovir triphosphate inhibits DNA synthesis by acting as a chain terminator.

产品详细信息

参考文献

  • Ger. Pat., 1976, 2 539 963; CA, 84, 180300p, (synth)
  • Elion, G.B. et al., Proc. Natl. Acad. Sci. U.S.A., 1977, 74, 5716, (pharmacol)
  • Fiddian, A.P., Appl. Virol., 1984, 103, (rev, pharmacol)
  • Birnbaum, G.I. et al., Can. J. Chem., 1984, 62, 2646, (cryst struct)
  • Eur. Pat., 1984, Wellcome, 108 285; CA, 101, 192401e, (Desciclovir, synth, pharmacol)
  • Krenitsky, T.A. et al., Proc. Natl. Acad. Sci. U.S.A., 1984, 81, 3209-3213, (synth, pharmacol)
  • Krasny, H.C. et al., Biochem. Pharmacol., 1986, 35, 4339, (metab)
  • Rees, P.J. et al., J. Antimicrob. Chemother., 1986, 18, 215-222, (pharmacokinet)
  • Kelley, J.L. et al., J. Het. Chem., 1986, 23, 271, (synth)
  • Chu, C.K. et al., J. Het. Chem., 1986, 23, 289, (rev)
  • Radl, S. et al., Cesk. Farm., 1987, 36, 58, (synth)
  • Petty, B.G. et al., Antimicrob. Agents Chemother., 1987, 31, 1317-1322, (pharmacokinet)
  • Matsumoto, H. et al., Chem. Pharm. Bull., 1988, 36, 1153, (synth)
  • Arndt, K.A. et al., J. Am. Acad. Dermatol., 1988, 18, 188, (adverse effects)
  • Stimac, A. et al., Synthesis, 1990, 461-464, (synth)
  • Reardon, J.E. et al., Adv. Pharmacol., 1991, 22, 1, (rev)
  • Alhede, B. et al., J.O.C., 1991, 56, 2139, (synth, cmr)
  • De Miranda, P. et al., Antiviral Chem. Chemother., 1992, 3, 1, (metab, rev)
  • U.K. Pat., 1993, Norsk Hydro A/S, 2 260 319; CA, 119, 271633g, (acyclovir elaidate)
  • Wagstaff, A.J. et al., Drugs, 1994, 47, 153, (rev)
  • Buck, I.M. et al., Tetrahedron, 1994, 50, 9195-9206, (synth)
  • Jennings, R. et al., Antimicrob. Agents Chemother., 1999, 43, 53-61, (acyclovir elaidate)
  • Plass, M. et al., J.C.S. Perkin 2, 1999, 2641-2646, (uv, pmr, ir, Raman)
  • Martindale, The Extra Pharmacopoeia, 32nd edn., Pharmaceutical Press, 1999, 602; 628
  • Ormrod, D. et al., Drugs, 2000, 59, 839-863; 1317-1359
  • Gao, H. et al., Synthesis, 2000, 329-351, (rev)
  • Gao, H. et al., Synth. Commun., 2001, 31, 1399-1419, (synth)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, AEC700; AEC725