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
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 50 | In Stock |
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| 5MG | 48 | In Stock |
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| 10MG | 58 | In Stock |
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| 25MG | 88 | In Stock |
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| 50MG | 109 | In Stock |
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| 100MG | 169 | In Stock |
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| 200MG | 268 | In Stock |
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| 500MG | 451 | In Stock |
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| 1G | 644 | In Stock |
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Biological Information
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Product NameTIC10
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NoteResearch use only, not for human use.
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Brief DescriptionTIC10 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.
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DescriptionTIC10 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.
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In Vitro——
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In Vivo——
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SynonymsONC-201
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PathwayOthers
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TargetOther Targets
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RecptorTRAIL
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number1616632-77-9
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Formula Weight386.49
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Molecular FormulaC24H26N4O
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Purity>98% (HPLC)
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SolubilityDMSO : 33.33 mg/mL 86.24 mM
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SMILESCC1=CC=CC=C1CN1C2=NCCN2C2=C(CN(CC3=CC=CC=C3)CC2)C1=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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