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CAS No 59277-89-3 , 2-amino-9-(2-hydroxyethoxymethyl)-3H-purin-6-one Search by region : Canada

  • Name: 2-amino-9-(2-hydroxyethoxymethyl)-3H-purin-6-one
  • Synonyms: Aciclovir; 59277-89-3;2-amino-9-(2-hydroxyethoxymethyl)-3H-purin-6-one; Zovirax; Avirax; Virorax;Acycloguanosine; Zovir; Vipral; Wellcome-248U;
  • CAS Registry Number:
  • Transport: OTH
  • Density: 1.77
  • Water Solubility: Water solubility: 0.7 mg/mL
  • Safety Statements: S22;S24/25;S36;S26
  • Hazard Symbols: Xi
  • EINECS: 261-685-1
  • Molecular Weight: 225.20464
  • InchiKey: MKUXAQIIEYXACX-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H11N5O3/c9-8-11-6-5(7(15)12-8)10-3-13(6)4-16-2-1-14/h3,14H,
    1-2,4H2,(H3,9,11,12,15)
  • Risk Statements: 36/37/38
  • Molecular Formula: C8H11N5O3
  • Molecular Structure:CAS No:59277-89-3 2-amino-9-(2-hydroxyethoxymethyl)-3H-purin-6-one

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59277-89-3 Acyclovir

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  • Canada Toronto Research Chemicals [Manufacturers]
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59277-89-3 ACYCLOVIR-D4

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59277-89-3 ACYCLOVIR

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References of 2-amino-9-(2-hydroxyethoxymethyl)-3H-purin-6-one
Title: Acyclovir
CAS Registry Number: 59277-89-3
CAS Name: 2-Amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6H-purin-6-one
Synonyms: acycloguanosine; 9-[(2-hydroxyethoxy)methyl]guanine
Manufacturers' Codes: BW-248U; Wellcome 248U
Trademarks: Acicloftal (Bruschettini); Avirase (Lampugnani); Cycloviran (Sigma-Tau); Maynar (Ferrer); Virmen (Menarini); Viruseen (Hommel); Zoliparin (Mann); Zovir (GSK); Zovirax (GSK)
Molecular Formula: C8H11N5O3
Molecular Weight: 225.20
Percent Composition: C 42.67%, H 4.92%, N 31.10%, O 21.31%
Literature References: Orally active acyclic nucleoside with inhibitory activity towards several herpes viruses. Prepn: H. J. Schaeffer, DE 2539963; idem, US 4199574 (1976, 1980 to Wellcome). Convenient synthesis from guanine: H. Matsumoto et al., Chem. Pharm. Bull. 36, 1153 (1988). Selectivity of action: G. B. Elion et al., Proc. Natl. Acad. Sci. USA 74, 5716 (1977). Chemistry, antiviral activity, metabolism: H. J. Schaeffer et al., Nature 272, 583 (1978). In vitro activity: P. Collins, D. J. Bauer, J. Antimicrob. Chemother. 5, 431 (1979). Effect on herpes simplex infections in mice: H. J. Field et al., Antimicrob. Agents Chemother. 15, 554 (1979); on herpes zoster in immunocompromised patients: H. H. Balfour et al., N. Engl. J. Med. 308, 1448 (1983). Treatment of primary episodes of genital herpes simplex infection: Y. J. Bryson et al., ibid. 916; of recurrent genital herpes: S. E. Straus et al., ibid. 310, 1545 (1984); J. M. Douglas et al., ibid. 1551. HPLC determn in serum and clinical pharmacokinetics: G. Bahrami et al., J. Chromatogr. B 816, 327 (2005). Symposia on pharmacology and clinical studies: Am. J. Med. 73, Suppl. 1A, 1-392 (1982); J. Antimicrob. Chemother. 12, Suppl. B, 1-202 (1983); Scand. J. Infect. Dis. Suppl. 47, 1-176 (1985). Review: R. J. Whitley, J. W. Gnann, Jr., N. Engl. J. Med. 327, 782-789 (1992).
Properties: Crystals from methanol, mp 256.5-257°. LD50 in mice (mg/kg): >10,000 orally; 1000 i.p. (Schaeffer).
Melting point: mp 256.5-257°
Toxicity data: LD50 in mice (mg/kg): >10,000 orally; 1000 i.p. (Schaeffer)
Therap-Cat: Antiviral.
Keywords: Antiviral; Purines/Pyrimidinones.