ID Name Structure References (top 5) Molecular Target(s)
1ID:7092
CHELERYTHRINE METHANOLATE

Freqency:
in 1 ingredients:

  • 391
  • in 9 recipes:

  • 68
  • 136
  • 199
  • 318
  • 329
  • 332
  • 334
  • 412
  • 483

  • Properties
    C20H18NO6-    368.36





    1:  Exner O, Carsky P.
    Acidity of carboxylic acids: a rebuttal and redefinition.
    J Am Chem Soc.    impact factor:   5.537
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    2:  Pekari K, Tailler D, Weingart R, Schmidt RR.
    Synthesis of the fully phosphorylated GPI anchor pseudohexasaccharide of Toxoplasma gondii.
    J Org Chem.    impact factor:   3.44
    2001;  66(22): 7432-42

    3:  Valerio C, Moulines F, Ruiz J, Blais JC, Astruc D.
    Regioselective chlorocarbonylation of polybenzyl cores and functionalization using dendritic and organometallic nucleophiles
    J Org Chem.    impact factor:   3.44
    2000;  65(7): 1996-2002

    4:  Ofori S, Heikkila RE, Nicklas WJ.
    Attenuation by dopamine uptake blockers of the inhibitory effects of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine and some of its analogs on NADH-linked metabolism in mouse neostriatal slices.
    J Pharmacol Exp Ther.    impact factor:   3.3
    1989;  251(1): 258-66

    5:  Paine TK, Weyhermuller T, Wieghardt K, Chaudhuri P.
    The methanol-methanolate CH(3)OH...OCH3(-) bridging ligand: tuning of exchange coupling by hydrogen bonds in dimethoxo-bridged dichromium(III) complexes.
    Inorg Chem.    impact factor:   2.843
    2002;  41(25): 6538-40

     
    Time used: 140 milliseconds.

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