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Tarloxotinib bromide (TH-4000) is an irreversible EGFR/HER2 inhibitor. Tarloxotinib has the potential to effectively shut down aberrant EGFR signaling in a tumor-selective manner, thus potentially avoiding or reducing the systemic side effects associated with currently available EGFR tyrosine kinase inhibitors.
| Species | Mouse | Rat | Rabbit | Guinea pig | Hamster | Dog |
| Weight (kg) | 0.02 | 0.15 | 1.8 | 0.4 | 0.08 | 10 |
| Body Surface Area (m2) | 0.007 | 0.025 | 0.15 | 0.05 | 0.02 | 0.5 |
| Km factor | 3 | 6 | 12 | 8 | 5 | 20 |
| Animal A (mg/kg) = Animal B (mg/kg) multiplied by | Animal B Km |
| Animal A Km |
For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.
| Molecular Weight | 681.77 |
| Formula | C24H24Br2ClN9O3 |
| CAS Number | 1636180-98-7 |
| Purity | >98% |
| Solubility | DMSO ≥ 28 mg/mL |
| Storage | at -20°C |
[3] Ahmed Salem, et al. Targeting Hypoxia to Improve Non-Small Cell Lung Cancer Outcome
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