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xl413

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  • Inhibitors & Agonists
    4
    TargetMol | Inhibitors_Agonists
XL413
T33521169558-38-6In house
XL-413 is an orally bioavailable cell division cycle 7 homolog (CDC7) kinase inhibitor with potential antineoplastic activity. XL-413 binds to and inhibits the activity of CDC7, which may result in the inhibition of DNA replication and mitosis, the induct
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4-6 weeks
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TargetMol | Citations Cited
AJ-108235
T713371170321-78-4
AJ-108235 is a novel inhibitor of long chain fatty acid elongase 6 (ELOVL6).
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6-8 weeks
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XL413 hydrochloride
BMS-863233 Hydrochloride
T67352062200-97-7
XL413 hydrochloride (BMS-863233 Hydrochloride) is a potent, selective and ATP competitive inhibitor of Cdc7, with an IC 50 of 3.4 nM. XL413 hydrochloride also exhibits potent effect with IC 50 s of 215, 42 nM on CK2, PIM1, respectively, and an EC 50 of 118 nM on pMCM.
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6-8 weeks
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TargetMol | Inhibitor Sale
XL413 xHCl
XL-413 Hydrochloride, BMS-863233 HCl, BMS-863233 xHCl
T713391169562-71-3
XL413 HCl is an ATP-competitive Cdc7 inhibitor (IC50: 3.4 nM) that is potent and selective.XL413 HCl inhibited CK2 and PIM1 with IC50 values of 215 and 42 nM, respectively.XL413 HCl showed an EC50 value of 118 against pMCM.
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6-8 weeks
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