ID Name Structure References (top 5) Molecular Target(s)
1ID:5324
RANCINAMYCIN IV


NSC#:22961
Aldrich#:37520
Aldrich#:419370
Aldrich#:D108405
Aldrich#:P4171

Freqency:
in 1 ingredients:

  • 358
  • in 1 recipes:

  • 521

  • Properties
    C7H6O3    138.12





    1:  O'Connor KE, Witholt B, Duetz W.
    p-Hydroxyphenylacetic Acid Metabolism in Pseudomonas putida F6.
    J Bacteriol.    impact factor:   3.712
    2001;  183(3): 928-33

    2:  Napolitano A, Pezzella A, Prota G.
    New reaction pathways of dopamine under oxidative stress conditions: nonenzymatic iron-assisted conversion to norepinephrine and the neurotoxins 6-hydroxydopamine and 6, 7-dihydroxytetrahydroisoquinoline.
    Chem Res Toxicol.    impact factor:   3.47
    1999;  12(11): 1090-7

    3:  Atta M, Fontecave M, Wilkins PC, Dalton H.
    Abduction of iron(III) from the soluble methane monooxygenase hydroxylase and reconstitution of the binuclear site with iron and manganese.
    Eur J Biochem.    impact factor:   3.307
    1993;  217(1): 217-23

    4:  Naoi M, Takahashi T, Kuno N, Nagatsu T.
    L-threo-3,4-dihydroxyphenylserine (DOPS) aldolase: a new enzyme cleaving DOPS into protocatechualdehyde and glycine.
    Biochem Biophys Res Commun.    impact factor:   3.161
    1987;  143(2): 482-8

    5:  Suzuki K, Miyaki M, Umeda M, Nishimura M, Ono T.
    Differential inactivation of DNA polymerases alpha and beta by aldehyde compounds.
    Biochem Biophys Res Commun.    impact factor:   3.161
    1981;  100(4): 1626-33

     
    Time used: 109 milliseconds.

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