MS1943

CAS No. 2225938-17-8

MS1943 ( —— )

Catalog No. M21747 CAS No. 2225938-17-8

MS1943 is a first-in-class, orally bioavailable EZH2 selective degrader, with an IC50 of 120 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    MS1943
  • Note
    Research use only, not for human use.
  • Brief Description
    MS1943 is a first-in-class, orally bioavailable EZH2 selective degrader, with an IC50 of 120 nM.
  • Description
    MS1943 is a first-in-class, orally bioavailable EZH2 selective degrader, with an IC50 of 120 nM. MS1943 significantly reduces EZH2 protein levels in numerous triple-negative breast cancer (TNBC) and other cancer and noncancerous cell lines. MS1943 effectively blocks proliferation of multiple TNBC and other cancer cell lines.
  • In Vitro
    MS1943 (0.625-5 μM; 3 days) inhibits cell growth with an GI50 of 2.2 μM.MS1943 (0.625-5 μM; 4 days) induces cell death in MDA-MB-468 cells. MS1943 effectively reduces EZH2 levels in BT549, HCC70 and MDA-MB-231 TNBC cells, as well as KARPAS-422 and SUDHL8 lymphoma cells and PNT2 non-cancerous prostate cells.MS1943 (1.25-5.0 μM; 2 days) inhibits EZH2 and SUZ12 protein levels in a concentration- and timedependent manner, without affecting EED protein levels, whereas the H3K27me3 mark was also suppressed. Cell Viability Assay Cell Line:MDA-MB-468 cells Concentration:0.625, 1.25, 2.5, 5 μM Incubation Time:3 days Result:Inhibits cell growth with an GI50 of 2.2 μM.Western Blot Analysis Cell Line:MDA-MB-468 cells Concentration:1.25, 2.5, 5.0 μM Incubation Time:2 daysResult:Reduced EZH2 protein levels in a concentration- and time-dependent manner.
  • In Vivo
    MS1943 (150 mg/kg body weight; i.p.; once daily for 36 days) suppresses tumor growth.MS1943 induces apoptosis in the MDA-MB-468 xenograft model.A single i.p. injection of MS1943 at 50 mg/kg body weight achieved a peak plasma concentration (Cmax) of 2.9 μM and resulted in plasma concentrations above its cellular IC50 value for ~2h. A single 150 mg/kg body weight p.o. dose achieved Cmax of 1.1 μM, but plasma concentrations were below the cellular IC50 value. Animal Model:Eight-week-old female BALB/c nude mice (MDA-MB-468 xenografts) Dosage:150 mg/kg body weight Administration:i.p.; once daily for 36 days Result:Suppresses tumor growth.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2225938-17-8
  • Formula Weight
    718.93
  • Molecular Formula
    C??H??N?O?
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 125 mg/mL (173.87 mM; Need ultrasonic)
  • SMILES
    CC(C)N(N=C1)C2=C1C(C(NCC3=C(C)C=C(C)NC3=O)=O)=CC(C4=CC=C(N=C4)N(CC5)CCN5CCNC(CC67C[C@H]8C[C@H](C[C@H](C8)C7)C6)=O)=C2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Ma A, et al. Discovery of a first-in-class EZH2 selective degrader.Nat Chem Biol. 2020 Feb;16(2):214-222.
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