TIC10

CAS No. 1616632-77-9

TIC10( ONC-201 )

Catalog No. M18091 CAS No. 1616632-77-9

TIC10 inactivates Akt and ERK to induce TRAIL through Foxo3a, possesses superior drug properties: delivery across the blood-brain barrier, superior stability and improved pharmacokinetics. Phase 1/2.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 45 In Stock
10MG 55 In Stock
25MG 84 In Stock
50MG 105 In Stock
100MG 164 In Stock
200MG 259 In Stock
500MG 437 In Stock
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Biological Information

  • Product Name
    TIC10
  • Note
    Research use only, not for human use.
  • Brief Description
    TIC10 inactivates Akt and ERK to induce TRAIL through Foxo3a, possesses superior drug properties: delivery across the blood-brain barrier, superior stability and improved pharmacokinetics. Phase 1/2.
  • Description
    TIC10 inactivates Akt and ERK to induce TRAIL through Foxo3a, possesses superior drug properties: delivery across the blood-brain barrier, superior stability and improved pharmacokinetics. Phase 1/2.(In Vitro):Dordaviprone transcriptionally induces TRAIL in a p53-independent manner and crosses the blood-brain barrier.Dordaviprone induces a sustained up-regulation of TRAIL in tumors and normal cells that may contribute to the demonstrable antitumor activity of Dordaviprone.Dordaviprone inactivates kinases Akt and extracellular signal-regulated kinase (ERK), leading to the translocation of Foxo3a into the nucleus, where it binds to the TRAIL promoter to up-regulate gene transcription.Dordaviprone is an efficacious antitumor therapeutic agent that acts on tumor cells and their micro-environment to enhance the concentrations of the endogenous tumor suppressor TRAIL.Dordaviprone also causes a down-regulation of the total expression of ERK. (In Vivo):In DLD-1 colon cancer xenografts, Dordaviprone induces tumor stasis at 1 week after treatment, whereas TRAIL-treated tumors progress after a single dose. A single dose of Dordaviprone also induces a sustained regression of the SW480 xenograft and is equally effective when delivered by intraperitoneal or oral route, suggesting favorable oral bioavailability for Dordaviprone. Titration of a single oral dose of Dordaviprone in the HCT116 xenograft model reveals sustained antitumor efficacy at 25 mg/kg. Exposure to oral Dordaviprone at 25 mg/kg weekly for 4 weeks in immunocompetent mice does not cause any changes in selected serum chemistry markers. The same oral dosing schedule is applied to Eμ-myc transgenic mice, which spontaneously develop meta-static lymphoma from weeks 9 to 12 of age, and Dordaviprone significantly (P=0.00789) prolongs the survival of these mice by 4 weeks.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ONC-201
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    TRAIL
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1616632-77-9
  • Formula Weight
    386.49
  • Molecular Formula
    C24H26N4O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 33.33 mg/mL 86.24 mM
  • SMILES
    CC1=CC=CC=C1CN1C2=NCCN2C2=C(CN(CC3=CC=CC=C3)CC2)C1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
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