您当前所在的位置:首页 > 产品中心 > 产品信息
D-Penicillamine_分子结构_CAS_52-67-5)
点击图片或这里关闭

D-Penicillamine

产品号 Bio-0578 公司名称 InterBioScreen
CAS号 52-67-5 公司网站 http://www.ibscreen.com
分子式 C5H11NO2S 电 话 +7 49652 40091
分子量 149.21134 传 真 +7 49652 40092
纯 度 电子邮件 screen@ibscreen.chg.ru
保 存 Chembase数据库ID: 179831

产品价格信息

请登录

产品别名

标题
D-Penicillamine
IUPAC标准名
(2S)-2-amino-3-methyl-3-sulfanylbutanoic acid
IUPAC传统名
(2S)-2-amino-3-methyl-3-sulfanylbutanoic acid

产品登记号

CAS号 52-67-5

产品性质

应用领域 Antiinflammatory
应用领域 Antirheumatic
应用领域 Chelating agent used in therapy of metal poisoning, and for Wilson's disease, scleroderma and rheumatoid arthritis
生物活性机理 Chelating agent recommended for the removal of excess copper in patients with Wilson's disease.
生物活性机理 From in vitro studies which indicate that one atom of copper combines with two molecules of penicillamine.
生物活性机理 Penicillamine also reduces excess cystine excretion in cystinuria.
生物活性机理 This is done, at least in part, by disulfide interchange between penicillamine and cystine, resulting in formation of penicillamine-cysteine disulfide,
生物活性机理 a substance that is much more soluble than cystine and is excreted readily.
生物活性机理 Penicillamine interferes with the formation of cross-links between tropocollagen molecules and cleaves them when newly formed.
生物活性机理 The mechanism of action of penicillamine in rheumatoid arthritis is unknown although it appears to suppress disease activity.
生物活性机理 Unlike cytotoxic immunosuppressants, penicillamine markedly lowers IgM rheumatoid factor but produces no significant depression in absolute levels of serum immunoglobulins.
生物活性机理 Also unlike cytotoxic immunosuppressants which act on both, penicillamine in vitro depresses T-cell activity but not B-cell activity.

产品详细信息

参考文献

  • ldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 592B; 592C; 592D; 787A, (ir)
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 1, 892B; 1282C, (nmr)
  • Sadtler Standard NMR Spectra, 2305, (pmr)
  • Ss, O., Annalen, 1948, 559, 92, (synth)
  • Ruiz-Torres, Arzneim.-Forsch., 1974, 24, 914, (pharmacol, metab)
  • Rosenfield, R.E. et al., Acta Cryst. B, 1975, 31, 462, (cryst struct, abs config)
  • Weigert, W.M. et al., Angew. Chem., Int. Ed., 1975, 14, 330, (rev)
  • Parrett, D., Proc. R. Soc. Med., 1977, 70, 61, (metab)
  • Jaffe, I.A., Pharmacol. Biochem. Prop. Drug Subst., 1979, 1, 465, (rev, pharmacol)
  • Chiu, C.C. et al., Anal. Profiles Drug Subst., 1981, 10, 601, (rev, synth, prop, tox, pharmacol)
  • Parrett, D. et al., J. Rheumatol. Suppl., 1981, 7, 28, (rev)
  • Scheinberg, I.H. et al., Wilson's Disease, W.B. Saunders, 1984, 126, (use, pharmacol)
  • Busker, E. et al., J. Chromatogr., 1985, 350, 179, (sepn)
  • Nether, P. et al., Clin. Pharmacokinet., 1987, 13, 317, (pharmacol)
  • Wolf-Heuss, E.M., Methods Enzymol., 1987, 143, 186, (rev, detn)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th edn., Akademie-Verlag, 1987, 346
  • Ogawa, T. et al., Chem. Pharm. Bull., 1988, 36, 1957; 1989, 37, 1609, (synth)
  • Van der Korst, J.K. et al., Inflammatory Dis. Ther., 1992, 9, 203, (rev)
  • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 688
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, MCR750; PAP500; PAP550