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Results for "

STK33+Inhibitors

" in MedChemExpress (MCE) Product Catalog:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-13495
    ML281
    3 Publications Verification

    		 STK33 Cancer
    ML281 is a potent and selective STK33 inhibitor with IC50 of 14 nM.
    ML281
  • HY-13498
    BRD-8899

    		STK33 Cancer
    BRD-8899 is a STK33 inhibitor, with an IC50 of 11 nM .
    BRD-8899
  • HY-13497
    STK33-IN-1

    		STK33 Cancer
    STK33-IN-1 (compound 1) is a STK33 inhibitor, with an IC50 of 7 nM .
    STK33-IN-1
  • HY-176885
    CDD-2211

    		STK33 RET Others
    CDD-2211 is a STK33 inhibitor, with a Kd of 0.018 nM and an IC50 of 5 nM. CDD-2211 has relatively weak inhibitory effects on off-target kinases, with IC50 values of 115 nM for CLK1, 48 nM for CLK2, 187 nM for CLK4, and 78 nM for RET. CDD-2211 can be used for the study of contraception .
    CDD-2211
  • HY-176884
    CDD-2110

    		STK33 RET Others
    CDD-2210 is a STK33 inhibitor, with a Kd of 0.1 nM and an IC50 of 38 nM. CDD-2210 has relatively weak inhibitory effects on off-target kinases, with IC50 values of 1209 nM for CLK1, 917 nM for CLK2, 544 nM for CLK4, and 746 nM for RET. CDD-2210 can be used for the study of contraception .
    CDD-2110
  • HY-176885A
    CDD-2212

    		STK33 RET Others
    CDD-2212 is a STK33 inhibitor, with a Kd of 1.9 nM and an IC50 of 999 nM. CDD-2212 has relatively weak inhibitory effects on off-target kinases, with IC50 values of 3223 nM for CLK1, 1555 nM for CLK2, 5884 nM for CLK4, and 1093 nM for RET. CDD-2212 can be used for the study of contraception .
    CDD-2212

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