RP-6306

CAS No. 2719793-90-3

RP-6306( —— )

Catalog No. M35485 CAS No. 2719793-90-3

Lunresertib (RP-6306) is a potent, selective, and orally active PKMYT1 inhibitor with an IC50 of 14 nM. Lunresertib (RP-6306) inhibits the growth of CCNE1-amplified tumor cells in several preclinical xenograft models.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 558 In Stock
5MG 313 In Stock
10MG 464 In Stock
25MG 747 In Stock
50MG 1014 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    RP-6306
  • Note
    Research use only, not for human use.
  • Brief Description
    Lunresertib (RP-6306) is a potent, selective, and orally active PKMYT1 inhibitor with an IC50 of 14 nM. Lunresertib (RP-6306) inhibits the growth of CCNE1-amplified tumor cells in several preclinical xenograft models.
  • Description
    RP-6306((S)-RP-6306) is a potent, selective and orally active PKMYT1 inhibitor with an IC50 of 14 nM. RP-6306 shows a high degree of selectivity over other kinases in cellular binding assays. RP-6306 shows anticancer effects.
  • In Vitro
    ——
  • In Vivo
    Animal Model:OVCAR3-bearing miceDosage:15, 50, and 300 ppm (equivalent to approximately 3, 10, and 60 mg/kg/day) Administration:Oral; daily; for 21 days Result:Resulted in a statistically significant and dose-dependent reduction in OVCAR3 tumor growth.
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Wee1
  • Recptor
    Wee1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2719793-90-3
  • Formula Weight
    324.38
  • Molecular Formula
    C18H20N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (154.14 mM; Ultrasonic )
  • SMILES
    NC=1N(C=2C(C1C(N)=O)=CC(C)=C(C)N2)C3=C(C)C(O)=CC=C3C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Janek Szychowski, et al. Discovery of an Orally Bioavailable and Selective PKMYT1 Inhibitor, RP-6306. J Med Chem. 2022 Aug 11;65(15):10251-10284. ?
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