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124832-26-4 分子结构
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2-[(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate hydrochloride

ChemBase编号:73296
分子式:C13H21ClN6O4
平均质量:360.79664
单一同位素质量:360.13128086
SMILES和InChIs

SMILES:
[nH]1c(nc2c(c1=O)ncn2COCCOC(=O)[C@H](C(C)C)N)N.Cl
Canonical SMILES:
CC([C@@H](C(=O)OCCOCn1cnc2c1nc(N)[nH]c2=O)N)C.Cl
InChI:
InChI=1S/C13H20N6O4.ClH/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20;/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20);1H/t8-;/m0./s1
InChIKey:
ZCDDBUOENGJMLV-QRPNPIFTSA-N

引用这个纪录

CBID:73296 http://www.chembase.cn/molecule-73296.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
2-[(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate hydrochloride
IUPAC传统名
valacyclovir hydrochloride
2-[(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate hydrochloride
别名
Valaciclovir HCl
Valtrex
Zelitrex
Valaciclovir Hydrochloride
(S)-2-((2-amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethyl 2-amino-3-methylbutanoate hydrochloride
CAS号
124832-26-4
124832-27-5
PubChem SID
162038216
PubChem CID
60772

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 60772 external link

理论计算性质

理论计算性质

JChem
Acid pKa 10.160745  质子受体
质子供体 LogD (pH = 5.5) -2.5221028 
LogD (pH = 7.4) -0.91812485  Log P -0.57631254 
摩尔折射率 81.0675 cm3 极化性 30.825937 Å3
极化表面积 146.85 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

安全信息 药理学性质 产品相关信息 生物活性(PubChem)
保存条件
-20°C expand 查看数据来源
生物活性机理
Aciclo-GTP is a very potent inhibitor of viral DNA polymerase expand 查看数据来源
Prodrug of aciclovir. expand 查看数据来源
成盐信息
hcl expand 查看数据来源
HCl expand 查看数据来源
应用领域
Active against herpes simplex and herpes zoster (shingles), Varicella zoster virus (VZV), Epstein-Barr virus (EBV), Cytomegalovirus (CMV) expand 查看数据来源
Antiviral agent expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals
Selleck Chemicals -  S1876 external link
Research Area: Infection
Biological Activity:

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • 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)
  • 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)
  • Eur. Pat., 1989, Wellcome, 308 065; CA, 112, 112048j, (Valaciclovir)
  • 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)
  • Beauchamp, L.M. et al., Antiviral Chem. Chemother., 1992, 3, 157, (Valaciclovir)
  • U.K. Pat., 1993, Norsk Hydro A/S, 2 260 319; CA, 119, 271633g, (acyclovir elaidate)
  • De Miranda, P. et al., Drug Metab. Dispos., 1994, 22, 55, (Valaciclovir)
  • Wagstaff, A.J. et al., Drugs, 1994, 47, 153, (rev)
  • Buck, I.M. et al., Tetrahedron, 1994, 50, 9195-9206, (synth)
  • Shinkai, I. et al., Bioorg. Med. Chem., 1996, 4, 1, (rev, Valaciclovir)
  • 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
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专利

专利

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