Toceranib Phosphate
CAS No. 874819-74-6
Toceranib Phosphate( PHA 291639 phosphate | SU11654 phosphate )
Catalog No. M20763 CAS No. 874819-74-6
Toceranib phosphate is a selective inhibitor of the tyrosine kinase activity of several members of the split kinase RTK family including Flk-1/KDR PDGFR.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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| 25MG | 61 | In Stock |
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| 50MG | 77 | In Stock |
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| 100MG | 99 | In Stock |
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Biological Information
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Product NameToceranib Phosphate
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NoteResearch use only, not for human use.
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Brief DescriptionToceranib phosphate is a selective inhibitor of the tyrosine kinase activity of several members of the split kinase RTK family including Flk-1/KDR PDGFR.
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DescriptionToceranib phosphate is a selective inhibitor of the tyrosine kinase activity of several members of the split kinase RTK family including Flk-1/KDR PDGFR.
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In VitroToceranib phosphate (PHA 291639 phosphate) is a selective inhibitor of the tyrosine kinase activity of several members of the split kinase RTK family, including PDGFR and Flk-1/KDR, with Kis of 5 and 6 nM, respectively.To explore mechanisms of acquired Toceranib (TOC) resistance in canine MCT, three resistant sublines are generated from the Toceranib-sensitive exon 11 ITD c-kit mutant C2 cell line designated TR1, TR2, and TR3. Growth of the parental C2 cells is inhibited by Toceranib in a dose-dependent manner with an IC50 of <10 nM. In contrast, TR1, TR2, and TR3 sublines are resistant to inhibition by Toceranib (IC50>?1,000 nM). Sensitivity to three other KIT RTK inhibitors is similar to the observed resistance to Toceranib. The parental line as well as all three sublines retains sensitivity to the cytotoxic agents vinblastine (VBL) and CCNU. Following 72 hr culture in the presence of increasing concentrations of Toceranib, treatment na?ve, parental C2 cells detach from the culture flask and become rounded, shrunken, and clumped with increased exposure to Toceranib. In contrast, Toceranib-induced morphologic differences are not identified in the resistant sublines.
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In VivoAdministration of Toceranib phosphate (PHA 291639 phosphate) significantly decreases the number and percentage of Treg in the peripheral blood of dogs with cancer. Dogs receiving Toceranib phosphate (PHA 291639 phosphate) and cyclophosphamide (CYC) demonstrate a significant increase in serum concentrations of IFN-γ, which is inversely correlated with Treg numbers after 6 weeks of combination treatment.
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SynonymsPHA 291639 phosphate | SU11654 phosphate
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PathwayOthers
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TargetOther Targets
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RecptorProtein-tyrosine kinase 2
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Research Area——
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Indication——
Chemical Information
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CAS Number874819-74-6
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Formula Weight494.45
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Molecular FormulaC22H28FN4O6P
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Purity>98% (HPLC)
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SolubilityDMSO:2.46 mg/mL (4.98 mM)
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SMILESOP(O)(O)=O.Cc1[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c(C)c1C(=O)NCCN1CCCC1
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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
1.Tjostheim S S Stepien R L Markovic L E et al. Effects of Toceranib Phosphate on Systolic Blood Pressure and Proteinuria in Dogs[J]. Journal of Veterinary Internal Medicine 2016 30(4):951-957.
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