UC2288

CAS No. 1394011-91-6

UC2288( —— )

Catalog No. M28840 CAS No. 1394011-91-6

UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 87 Get Quote
10MG 132 Get Quote
25MG 248 Get Quote
50MG 372 Get Quote
100MG 462 Get Quote
200MG 575 Get Quote
500MG 835 Get Quote
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Biological Information

  • Product Name
    UC2288
  • Note
    Research use only, not for human use.
  • Brief Description
    UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.
  • Description
    UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.(In Vitro):UC2288 (0-10 μM; 24 hours) decreases p21 mRNA expression transcriptionally or post-transcriptionally but independently of p53. UC2288 has no inhibition of VEGFR2 and Raf kinases even at 10 μM.(In Vivo):UC2288 (10 mg/kg; i.p.) attenuates MPTP-induced behavioral impairment, prevents activation of MAPK pathway in the MPTP-treated mice brain. MPTP treatment raises TNF-α, IL-6 and IL-1β levels in MPTP treated mice brain, but UC2288 signicantly decreases MPTP-induced TNF-α, IL-6 levels, but IL-1β is not decreased in brain.UC2888 (15 mg/kg; oral) co-treatment with imetelstat significantly suppresses tumor growth and does not effect mice weight.
  • In Vitro
    Western Blot Analysis Cell Line:HK2 (normal kidney), 786-O (RCC), Caki-1 (RCC), ACHN (RCC) and HEY (ovarian cancer) cells Concentration:0 μM; 1 μM; 3 μM; 10 μM Incubation Time:24 hours Result:Decreased p21 protein expression. RT-PCR Cell Line:p53-mutant?RCC cell line 786-O Concentration:10 μM Incubation Time:24 hours Result:Decreased p21 mRNA independent of p53 expression.
  • In Vivo
    Animal Model:Eight-week old, athymic nude (NCr nu/nu) mice injected subcutaneously with HCT116 and ACHN cancer cells(2.5x106) Dosage:15 mg/kg Administration:Oral gavage; 3 times a week; 4 weeks; co-treatment with imetelstat Result:Combined treatment with imetelstat synergistically inhibited tumor growth in mice.Animal Model:MPTP-induced C57BL6 Parkinson’s disease mice model Dosage:10 mg/kg Administration: Intraperitoneal? injection; 4 times in 7 days Result:Ameliorated MPTP induced PD progression through inhibition of neuroinammation.
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    MDM2-p53
  • Recptor
    mGluR4
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1394011-91-6
  • Formula Weight
    481.82
  • Molecular Formula
    C20H18ClF6N3O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (103.77 mM)
  • SMILES
    FC(F)(F)c1ccc(O[C@H]2CC[C@@H](CC2)NC(=O)Nc2ccc(Cl)c(c2)C(F)(F)F)nc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Niswender CM, et al. Discovery, characterization, and antiparkinsonian effect of novel positiveallosteric modulators of metabotropic glutamate receptor 4. Mol Pharmacol. 2008 Nov;74(5):1345-58.
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