GLPBio

DNA Damage/DNA Repair

Research Areas

Products Related to DNA Damage/DNA Repair(2120)

  • GC79112 structure
    GC79112PF-670462
    CAS: 950980-98-0
    Purity: >99.00%

    PF-670462 is a selective CKI ε/δ inhibitor.

  • GC79113 structure
    GC79113Casein Kinase II Substrate acetate
    Purity: >99.50%

    Casein Kinase II Substrate acetate is a casein kinase II ( CK2 ) peptide substrate that can be selectively phosphorylated by CK2 [1] .

  • GC79114 structure
    GC79114CCK1-specific peptide substrate acetate
    Purity: >98.00%

    CCK1-specific peptide substrate acetate is a biological active peptide.

  • GC79121 structure
    GC79121XL495
    CAS: 3040320-93-9
    Purity: >98.00%

    XL495 is an potent, selective and orally active PKMYT1 inhibitor.

  • GC79144 structure
    GC79144MC3817 free base
    Purity: >98.00%

    MC3817 free base is a selective DNMT1 inhibitor.

  • GC79145 structure
    GC79145MC3817
    Purity: >99.50%

    MC3817 is a selective DNMT1 inhibitor.

  • GC79150 structure
    GC79150NV914
    CAS: 2341941-41-9
    Purity: >98.50%

    NV914 is an inhibitor of FTSJ1 (tryptophan tRNA-specific 2'-O-methyltransferase) that inhibits the methyltransferase activity of FTSJ1, induces translational readthrough of premature termination codons, and enables genes carrying nonsense mutations to synthesize full-length proteins.

  • GC79167 structure
    GC79167METTL1-WDR4-IN-1 TFA
    Purity: >99.50%

    METTL1-WDR4-IN-1 (Compound 1) TFA is a selective competitive inhibitor of the methyltransferase complex METTL1-WDR4 ( IC 50 =144 μM).

  • GC79176 structure
    GC79176ARUK2010489
    Purity: >96.50%

    ARUK2010489 (Compound 23) is a potent, selective and brain-penetrant NUAK1 inhibitor with a pIC 50 of 8.7.

  • GC79354 structure
    GC79354YL0441
    Purity: >98.50%

    YL0441 is an inhibitor of ΔFOSB/JUND heterodimers and ΔFOSB homomultimers, with IC 50 values of 13.7 μM and 12.3 μM, respectively.

  • GC79370 structure
    GC79370PD-L1/HDAC6-IN-1 TFA
    Purity: >99.50%

    PD-L1/HDAC6-IN-1 TFA is an orally active dual inhibitor of PD-L1 and HDAC6, with IC 50 values of 26.8 nM and 78 nM, respectively.

  • GC79451 structure
    GC79451JP-11646
    CAS: 1902983-63-4
    Purity: >98.50%

    JP-11646 is a pan-PIM inhibitor with increased potency against PIM2 ( IC 50 = 0.5 nM).

  • GC79476 structure
    GC79476ETC-501
    CAS: 3094990-88-9
    Purity: >97.00%

    ETC-501 is a blood-brain barrier-permeable, orally active, and selective MNK1 / MNK2 inhibitor, with an IC 50 of 0.033 μM against MNK1 and 0.111 μM against MNK2.

  • GC79488 structure
    GC79488QBS10072S dihydrochloride
    CAS: 1802735-31-4
    Purity: >98.00%

    QBS10072S dihydrochloride is a LAT1 -selective substrate with blood-brain barrier permeability that inhibits tumor growth.

  • GC79577 structure
    GC79577PFKFB4-IN-1
    CAS: 2664831-55-2
    Purity: >99.50%

    PFKFB4-IN-1 is a potent and selective ATP-competitive PFKFB4 inhibitor ( IC 50 = 4.50 μM) that reduces intracellular PFKFB4 protein levels.

  • GC79584 structure
    GC79584UDP-Glucosamine
    CAS: 17479-04-8
    Purity: >98.00%

    UDP-Glucosamine is a sugar nucleotide analog, glycosyl donor, and metabolite of D-galactosamine.

  • GC79816 structure
    GC79816Cryptolepine
    CAS: 480-26-2
    Purity: >98.00%

    Cryptolepine is an orally active multi-potent alkaloid with anti-cancer, anti-bacterial, anti-viral, anti-malarial, anti-inflammatory, anti-hyperglycemic, relieve pain and other properties.

  • GC79866 structure
    GC79866Gem-C12
    CAS: 849139-19-1
    Purity: >99.00%

    Gem-C12 is a prodrug of Gemcitabine.

  • GC79867 structure
    GC79867Prexasertib-d 4
    Purity: >98.00%

    Prexasertib -d 4 (LY2606368-d 4 ) is the deuterium labeled Prexasertib.

  • GC79871 structure
    GC79871CHNQD-00824
    CAS: 2222643-74-3
    Purity: >98.00%

    CHNQD-00824 is a Terphenyllin derivative with potent anticancer effect.

  • GC79988 structure
    GC79988GS-441524-d
    CAS: 2647440-98-8
    Purity: >98.00%

    GS-441524 -d is the deuterium labeled GS-441524.

  • GC79989 structure
    GC79989Irinotecan- 13 C 6
    CAS: 718613-65-1
    Purity: >98.00%

    Irinotecan - 13 C 6 ((+)-Irinotecan- 13 C 6 ) is the 13 C-labeled Irinotecan.

  • GC79990 structure
    GC79990Gemcitabine- 13 C, 15 N 2
    CAS: 1233921-74-8
    Purity: >99.00%

    antimetabolite and an antineoplastic agent.

  • GC79991 structure
    GC79991Im-m7GDP sodium
    CAS: 240137-51-3
    Purity: >89.00%

    Im-m7GDP sodium is a capping reagent and also the P-imidazolide of N7-methylguanosine 5'-diphosphate.