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Sitravatinib

Cat. No. M9626

All AbMole products are for research use only, cannot be used for human consumption.

Sitravatinib Structure
Synonym:

MGCD516; MG516

Size Price Availability Quantity
1mg USD 27 In stock
5mg USD 60 In stock
10mg USD 90 In stock
25mg USD 168 In stock
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Quality Control & Documentation
Biological Activity

Sitravatinib (MGCD516) is an orally active receptor tyrosine kinase (RTK) inhibitor. Inhibition of Axl, MER, VEGFR3, VEGFR2, VEGFR1, KIT, FLT3, DDR2, DDR1, TRKA, and TRKB at 1.5 nM, 2 nM, 2 nM, 5 nM, 6 nM, 6 nM, 8 nM, 0.5 nM, respectively. 29 nM, 5 nM and 9 nM. Sitravatinib alone has a potent antitumor effect and enhances pD-1 blockade activity by promoting the antitumor immune microenvironment.


Product Citations
Chemical Information
Molecular Weight 629.68
Formula C33H29F2N5O4S
CAS Number 1123837-84-2
Solubility (25°C) DMSO ≥ 26 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Wenting Du, et al. JCI Insight. Sitravatinib potentiates immune checkpoint blockade in refractory cancer models

[2] Parag P Patwardhan, et al. Oncotarget. Significant blockade of multiple receptor tyrosine kinases by MGCD516 (Sitravatinib), a novel small molecule inhibitor, shows potent anti-tumor activity in preclinical models of sarcoma

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  Catalog
Abmole Inhibitor Catalog




Keywords: Sitravatinib, MGCD516; MG516 supplier, VEGFR/PDGFR, inhibitors, activators

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