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URACIL Drug Record

  • Summary
  • Interactions
  • Claims
  • URACIL chembl:CHEMBL566

    Alternate Names:

    SQ-6201
    FLUOROURACIL SPECIFIED COMPOUND C
    LAMIVUDINE IMPURITY E
    LAMIVUDINE IMPURITY E RS
    BMS-205603-01
    SQ-7726
    URACIL
    NSC-3970
    SQ-8493

    Drug Info:

    (0 More Sources)

    Publications:

    Milosevic et al., 2006, Uracil nucleotides stimulate human neural precursor cell proliferation and dopaminergic differentiation: involvement of MEK/ERK signalling., J. Neurochem.
    Kotani et al., 1997, Highly selective aldose reductase inhibitors. 3. Structural diversity of 3-(arylmethyl)-2,4,5-trioxoimidazolidine-1-acetic acids., J. Med. Chem.
    Ogawa et al., 2000, Aberrant expression of p27(Kip1) is associated with malignant transformation of the rat urinary bladder epithelium., Carcinogenesis
    Masui et al., 1991, Direct DNA sequencing of the rat neu oncogene transmembrane domain reveals no mutation in urinary bladder carcinomas induced by N-butyl-N-(4-hydroxybutyl)nitrosamine, N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide or N-methyl-N-nitrosourea., Carcinogenesis
  • URACIL   AKR1B1

    Interaction Score: 3.43

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    9057855


    Sources:
    NCI

  • URACIL   CCND1

    Interaction Score: 1.55

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    10607743


    Sources:
    NCI

  • URACIL   ERBB2

    Interaction Score: 0.21

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    1682063


    Sources:
    NCI

  • URACIL   MAPK1

    Interaction Score: 0.19

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    17076658


    Sources:
    NCI

  • NCI: URACIL

    • Version: 14-September-2017

    Alternate Names:
    C917 NCI drug code

    Drug Info:

    Publications:
    Kotani et al., 1997, Highly selective aldose reductase inhibitors. 3. Structural diversity of 3-(arylmethyl)-2,4,5-trioxoimidazolidine-1-acetic acids., J. Med. Chem.
    Masui et al., 1991, Direct DNA sequencing of the rat neu oncogene transmembrane domain reveals no mutation in urinary bladder carcinomas induced by N-butyl-N-(4-hydroxybutyl)nitrosamine, N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide or N-methyl-N-nitrosourea., Carcinogenesis
    Milosevic et al., 2006, Uracil nucleotides stimulate human neural precursor cell proliferation and dopaminergic differentiation: involvement of MEK/ERK signalling., J. Neurochem.

  • ChemblDrugs: chembl:CHEMBL566

    • Version: ChEMBL_27

    Alternate Names:

    Drug Info:

    Publications:

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A finding of a drug-gene interaction or potentially druggable category does not necessarily indicate effectiveness (or lack thereof) of any drug or treatment regimen. A finding of no interaction or no potentially druggable category does not necessarily indicate lack of effectiveness of any drug or treatment regimen. Drug-gene interactions or potentially druggable categories are not presented in ranked order of potential or predicted efficacy.

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DGIdb (v4.2.0 - sha1 afd9f30b) • Last updated 2020-10-21