SP 141

CAS No. 1253491-42-7

SP 141( —— )

Catalog No. M22094 CAS No. 1253491-42-7

SP 141 is a MDM2 inhibitor.SP-141 promotes MDM2 auto-ubiquitination and degradation, with anticancer activity.SP141, which bound directly to MDM2, promoting its auto-ubiquitination and degradation by the proteasome.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 93 In Stock
5MG 81 In Stock
10MG 123 In Stock
25MG 250 In Stock
50MG 398 In Stock
100MG 635 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SP 141
  • Note
    Research use only, not for human use.
  • Brief Description
    SP 141 is a MDM2 inhibitor.SP-141 promotes MDM2 auto-ubiquitination and degradation, with anticancer activity.SP141, which bound directly to MDM2, promoting its auto-ubiquitination and degradation by the proteasome.
  • Description
    SP 141 is a MDM2 inhibitor.SP-141 promotes MDM2 auto-ubiquitination and degradation, with anticancer activity.SP141, which bound directly to MDM2, promoting its auto-ubiquitination and degradation by the proteasome. The compound reduced levels of MDM2 in pancreatic cancer cell lines, as well as their proliferation, with 50% inhibitory concentrations <0.5 μM (0.38-0.50 μM). Increasing concentrations of SP141 induced increasing levels of apoptosis and G2-M-phase arrest of pancreatic cancer cell lines, whether or not they expressed functional P53. Injection of nude mice with SP141 (40 mg/kg/d) inhibited growth of xenograft tumors (by 75% compared with control mice), and led to regression of orthotopic tumors.
  • In Vitro
    Cell Viability Assay Cell Line:HPAC, Panc-1, AsPC-1, and Mia-Paca-2 pancreatic cancer cell lines. Human primary fibroblasts (IMR90)Concentration:0.01, 0.1, 1, and 10 μM Incubation Time:72 hours Result:IC50s of 0.38, 0.50, 0.36, 0.41, and 13.22 μM for HPAC, Panc-1, AsPC-1, Mia-Paca-2, and IMR90, respectively.Western Blot Analysis Cell Line:HPAC and Panc-1 cells Concentration:0.5 μM Incubation Time:120 minutes Result:Reduced the MDM2 protein levels.Increased the degradation rate of the MDM2 protein in the presence of Cycloheximide (15 μg/mL).
  • In Vivo
    Animal Model:Nude mice bearing Panc-1 xenograft tumors Dosage:40 mg/kg Administration:Administered by i.p. injection; 5 d/wk for about three weeks Result:Significantly suppressed the growth of pancreatic xenograft tumors. On Day 18, the tumor volume in the treated group was reduced by 75% compared with that in the control group. There were no significant differences in the body weight compared with the control group.
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    MDM2-p53
  • Recptor
    Mdm2
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1253491-42-7
  • Formula Weight
    324.38
  • Molecular Formula
    C22H16N2O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (385.35 mM)
  • SMILES
    COc1ccc2[nH]c3c(nccc3c2c1)-c1cccc2ccccc12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Wei Wang, et al. The Pyrido[b]indole MDM2 Inhibitor SP-141 Exerts Potent Therapeutic Effects in Breast Cancer Models. Nat Commun. 2014 Oct 1;5:5086.
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