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Results for "

cytidine deaminase

" in MedChemExpress (MCE) Product Catalog:

6

Inhibitors & Agonists

1

Recombinant Proteins

1

Isotope-Labeled Compounds

1

Antibodies

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-109081
    Cedazuridine

    E7727

    		 Others Cancer
    Cedazuridine (E7727) (Compound 7a) is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine can be used for cancer research .
    Cedazuridine
  • HY-15345
    Tetrahydrouridine dihydrate
    1 Publications Verification

    THU dihydrate; NSC-112907 dihydrate

    		 DNA/RNA Synthesis Cancer
    Tetrahydrouridine dihydrate (THU dihydrate) is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine.
    Tetrahydrouridine dihydrate
  • HY-15345A
    Tetrahydrouridine
    1 Publications Verification

    THU; NSC-112907

    		 DNA/RNA Synthesis Cancer
    Tetrahydrouridine dihydrate is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine .
    Tetrahydrouridine
  • HY-13420
    Zebularine
    5 Publications Verification

    NSC309132; 4-Deoxyuridine

    		 DNA Methyltransferase Autophagy Cancer
    Zebularine (NSC309132; 4-Deoxyuridine) is a DNA methyltransferase inhibitor. Zebularine also inhibits cytidine deaminase with a Ki of 0.95 μM.
    Zebularine
  • HY-109081A
    Cedazuridine hydrochloride

    E7727 hydrochloride

    		 Others Cancer
    Cedazuridine (E7727) (Compound 7a) hydrochloride is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine hydrochloride can be used for cancer research .
    Cedazuridine hydrochloride
  • HY-15345AS
    Tetrahydrouridine-d3

    THU-d3; NSC-112907-d3

    		 Isotope-Labeled Compounds Cancer
    Tetrahydrouridine-d3 is the deuterium labeled Tetrahydrouridine[1]. Tetrahydrouridine dihydrate is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine[2][3].
    Tetrahydrouridine-d3

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