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  • (R)-Mephenytoin
(R)-Mephenytoin的可视化放大

(R)-Mephenytoin

An enantiomer of mephenytoin

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(R)-Mephenytoin的二维码
  • 库存: 现货
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    促销价
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  • 1mg
    ¥450.00
    360.00
    - +
  • 5mg
    ¥1112.00
    890.00
    - +
  • 10mg
    ¥1975.00
    1580.00
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  • 25mg
    ¥4262.00
    3410.00
    - +
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  • 货号: ajci20814
  • CAS: 71140-51-7
  • 别名: 美芬妥英,(–)-Mephenytoin
  • 分子式: C12H14N2O2
  • 分子量: 218.3
  • 纯度: >98%
  • 溶解度: 15mg/mL in ethanol, 25mg/mL in DMSO, or in DMF
  • 储存: Store at -20°C
  • 库存: 现货

Background

(R)-Mephenytoin is the (R) enantiomer of the anticonvulsant mephenytoin.[1] (R)-Mephenytoin can be demethylated by the cytochrome P450 (CYP) isoform CYP2C9 to form the active metabolite 5-ethyl-5-phenylhydantoin (nirvanol). [2][3]The ratio of (S)-mephenytoin to (R)-mephenytoin in urine following administration of the racemic mixture has been used to detect polymorphisms in drug metabolism by CYP2C19, as only (S)-mephenytoin is a substrate of CYP2C19.[4][5][2]


Reference:
[1]. Meier, U.T., Kronbach, T., and Meyer, U.A. Assay of mephenytoin metabolism in human liver microsomes by high-performance liquid chromatography. Anal. Biochem. 151(2), 286-291 (1985).
[2]. Lewis, D.F., Dickins, M., Weaver, R.J., et al. Molecular modelling of human CYP2C subfamily enzymes CYP2C9 and CYP2C19: Rationalization of substrate specificity and site-directed mutagenesis experiments in the CYP2C subfamily. Xenobiotica. 28(3), 235-268 (1998).
[3]. Wong, P.T.H., Tan, S.F., and Lee, H.S. N-demethylation of methyl and dimethyl derivatives of phenytoin and their anticonvulsant activities in mice. Japanese Journal of Pharmacology 48(4), 473-478 (1988).
[4]. Ferguson, R.J., de Morais, S.M., Benhamou, S., et al. A new genetic defect in human CYP2C19: Mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin. Journal of Pharmacology and Experimental Therapeutics 284(1), 356-361 (1998).
[5]. Guttendorf, R.J., Britto, M., Blouin, R.A., et al. Rapid screening for polymorphisms in dextromethorphan and mephenytoin metabolism. British Journal of Clinical Pharmacology 29(4), 373-380 (1990).

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