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RP-6306

Cat. No. M13388

All AbMole products are for research use only, cannot be used for human consumption.

RP-6306 Structure
Synonym:

Lunresertib; RP6306

Size Price Availability Quantity
1mg USD 240 In stock
5mg USD 560 In stock
10mg USD 760 In stock
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Quality Control & Documentation
Biological Activity

RP-6306 (Lunresertib) is the first-in-class, highly potent and selective PKMYT1 inhibitor that preferentially kills tumor cells overexpressing CCNE1 and was shown to inhibit the growth of a broad range of CCNE1-amplified tumors in xenograft/PDX preclinical models, both as a single agent and in combination therapy settings. RP-6306 inhibition of Thr14 phosphorylation of CDK1 in HCC1569.

In vivo, RP-6306 (15, 50, and 300 ppm; oral; daily; for 21 days) results in a statistically significant and dose-dependent reduction in OVCAR3 tumor growth in CCNE1-amplified ovarian xenograft model (OVCAR3).

Chemical Information
Molecular Weight 324.38
Formula C18H20N4O2
CAS Number 2719793-90-3
Form Solid
Solubility (25°C) DMSO 50 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Janek Szychowski, et al. J Med Chem. Discovery of an Orally Bioavailable and Selective PKMYT1 Inhibitor, RP-6306

[2] David Gallo, et al. Nature. CCNE1 amplification is synthetic lethal with PKMYT1 kinase inhibition

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Keywords: RP-6306, Lunresertib; RP6306 supplier, Wee1, inhibitors, activators

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