GLPBio

DNA Damage/DNA Repair

Research Areas

Products Related to DNA Damage/DNA Repair(1968)

  • GC79095 structure
    GC79095Im-GDP
    CAS: 1199264-75-9
    Purity: >91.50%

    Im-GDP is a monomeric raw material that can be used for nucleic acid synthesis.

  • GC79096 structure
    GC790965-F-UTP trisodium
    Purity: >95.00%

    5-F-UTP (5-Fluorouridine-5'-triphosphate) trisodium is a monomeric raw material that can be used for nucleic acid synthesis.

  • GC79097 structure
    GC790975'-O-DMTr-2'-O-Me-rA
    CAS: 103285-23-0
    Purity: >99.50%

    5'-O-DMTr-2'-O-Me-rA is a monomeric raw material that can be used for nucleic acid synthesis.

  • GC79098 structure
    GC790983',5'-UpU TEA
    CAS: 101609-06-7
    Purity: >98.00%

    3',5'-UpU TEA (3',5'-Uridylyluridine TEA) is a 3',5'-linked uridylyluridine dinucleotide.

  • GC79099 structure
    GC790995'-O-DMTr-3'-O-Me-rA(Bz)
    CAS: 127212-38-8
    Purity: >98%

    5'-O-DMTr-3'-O-Me-rA(Bz) is a monomeric raw material that can be used for nucleic acid synthesis.

  • GC79100 structure
    GC79100Morpholino G(PhAc) subunit
    CAS: 1044241-74-8
    Purity: >98%

    Morpholino G(PhAc) subunit is a nucleoside analog that can be used to synthesize phosphorodiamidate morpholino oligonucleotides (PMO) [1] .

  • GC79101 structure
    GC79101Diguanosine 5′-triphosphate triammonium
    Purity: >98.50%

    Diguanosine 5′-triphosphate (Gp3G) triammonium is a dinucleoside triphosphates.

  • GC79102 structure
    GC79102(S)-HPMPA
    CAS: 92999-29-6
    Purity: >99.50%

    (S)-HPMPA is an antiviral agent.

  • GC79103 structure
    GC79103Berzosertib hydrochloride
    CAS: 1428935-04-9
    Purity: >98.50%

    Berzosertib (VE-822) hydrochloride is an orally active, CNS-penetrant, and selective ATR kinase inhibitor.

  • GC79104 structure
    GC79104(Rac)-Chem-0199
    CAS: 122981-77-5
    Purity: >99.50%

    (Rac)-Chem-0199 is the racemic mixture of Chem-0199.

  • GC79105 structure
    GC79105MDOLL-0286
    Purity: >99.50%

    MDOLL-0286 is a selective Poly(ADP-ribose) Glycohydrolase (PARG) ( ARH3 ) inhibitor with an IC 50 of 2.3μM.

  • GC79106 structure
    GC79106FORX-428
    CAS: 2922789-15-7
    Purity: >98.00%

    FORX-428 is an orally active, selective poly (ADP-ribose) glycohydrolase ( PARG ) inhibitor.

  • GC79107 structure
    GC79107iso-ADP ribose TEA
    Purity: >99.50%

    iso-ADP ribose TEA is the small-molecule ligand for protein nucleic acid modification, comprising parts of two consecutive ADP-ribosyl units within the PAR chain.

  • GC79108 structure
    GC79108AP4-43
    Purity: >99.50%

    AP4-43 is an orally active CLK1, CLK4, PI3K, DDR1, EGFR and NEK4 inhibitor.

  • GC79110 structure
    GC79110CK1-IN-5
    CAS: 1000340-33-9
    Purity: >99.00%

    CK1-IN-5 (compound B-AZ) is an inhibitor of CK1.

  • GC79111 structure
    GC79111CK2-TN03
    CAS: 313226-24-3
    Purity: >98.00%

    CK2-TN03 is an ATP-competitive casein kinase 2 ( CK2 ) inhibitor, with an IC 50 of 165 nM and a K i of 20 nM.

  • 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%

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

  • GC79144 structure
    GC79144MC3817 free base
    Purity: >98%

    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).