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  2. Fluoropyrimidine - Wikipedia

    en.wikipedia.org/wiki/Fluoropyrimidine

    Fluorouracil (5-FU) Tegafur; Some metabolites of these drugs, such as 5-fluorodeoxyuridylate monophosphate, also have fluoropyrimidine structures in the general sense of the term, but the more specific meaning is typically reserved for substances used as pharmaceuticals.

  3. Fluorouracil - Wikipedia

    en.wikipedia.org/wiki/Fluorouracil

    Fluorouracil (5-FU, 5-fluorouracil), sold under the brand name Adrucil among others, is a cytotoxic chemotherapy medication used to treat cancer. [3] By intravenous injection it is used for treatment of colorectal cancer , oesophageal cancer , stomach cancer , pancreatic cancer , breast cancer , and cervical cancer . [ 3 ]

  4. Fluorodeoxyuridylate - Wikipedia

    en.wikipedia.org/wiki/Fluorodeoxyuridylate

    Fluorodeoxyuridylate, [1] also known as FdUMP, 5-fluoro-2'-deoxyuridylate, and 5-fluoro-2'-deoxyuridine 5'-monophosphate, is a molecule formed in vivo from 5-fluorouracil and 5-fluorodeoxyuridine. FdUMP acts as a suicide inhibitor of thymidylate synthase (TS). By inhibiting the deoxynucleotide biosynthesis, FdUMP stops the rapidly proliferation ...

  5. 5-Fluoroorotic acid - Wikipedia

    en.wikipedia.org/wiki/5-Fluoroorotic_Acid

    5-Fluoroorotic acid (5FOA) is a fluorinated derivative of the pyrimidine precursor orotic acid. It is used in yeast genetics to select for the absence of the URA3 gene, which encodes the enzyme for the decarboxylation of 5-fluoroorotic acid to 5-fluorouracil , a toxic metabolite. [ 1 ]

  6. 5-fluorouracil - Wikipedia

    en.wikipedia.org/?title=5-fluorouracil&redirect=no

    Download QR code ; Print/export ... In other projects Appearance. move to sidebar hide. From Wikipedia, the free encyclopedia ... Retrieved from "https://en.wikipedia ...

  7. Tegafur - Wikipedia

    en.wikipedia.org/wiki/Tegafur

    Tegafur is a chemotherapeutic prodrug of 5-fluorouracil (5-FU) used in the treatment of cancers. It is a component of the combination drug tegafur/uracil. When metabolised, it becomes 5-FU. [1] It was patented in 1967 and approved for medical use in 1972. [2]

  8. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    A [1,5] shift involves the shift of 1 substituent (hydride, alkyl, or aryl) down 5 atoms of a π system. Hydrogen has been shown to shift in both cyclic and open-chain compounds at temperatures at or above 200 ˚C. [4] These reactions are predicted to proceed suprafacially, via a Hückel-topology transition state. [1,5] hydride shift in a ...

  9. Thymidylate synthase - Wikipedia

    en.wikipedia.org/wiki/Thymidylate_synthase

    Thymidylate synthase (TS) (EC 2.1.1.45) [5] is an enzyme that catalyzes the conversion of deoxyuridine monophosphate (dUMP) to deoxythymidine monophosphate (dTMP). Thymidine is one of the nucleotides in DNA. With inhibition of TS, an imbalance of deoxynucleotides and increased levels of dUMP arise. Both cause DNA damage. [6] [7]

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