Toceranib-d8 structure
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Common Name | Toceranib-d8 | ||
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CAS Number | 1795134-78-9 | Molecular Weight | 404.51 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C22H17D8FN4O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Toceranib-d8Toceranib-d8 (SU11654-d8) is the deuterium labeled Toceranib. Toceranib (SU11654) is an orally active receptor tyrosine kinase (RTK) inhibitor, and it potently inhibits PDGFR, VEGFR, and Kit with Kis of 5 and 6 nM for PDGFRβ and Flk-1/KDR, respectively. Toceranib (SU11654) has antitumor and antiangiogenic activity, and used in the treatment of canine mast cell tumors[1][2]. |
Name | Toceranib-d8 |
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Description | Toceranib-d8 (SU11654-d8) is the deuterium labeled Toceranib. Toceranib (SU11654) is an orally active receptor tyrosine kinase (RTK) inhibitor, and it potently inhibits PDGFR, VEGFR, and Kit with Kis of 5 and 6 nM for PDGFRβ and Flk-1/KDR, respectively. Toceranib (SU11654) has antitumor and antiangiogenic activity, and used in the treatment of canine mast cell tumors[1][2]. |
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Related Catalog | |
In Vitro | Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1]. |
References |
Molecular Formula | C22H17D8FN4O2 |
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Molecular Weight | 404.51 |
Hazard Codes | Xi |
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