TDI-10229 is a potent and orally bioavailable inhibitor of soluble adenylyl cyclase (sAC, ADCY10) . TDI-10229 displays nanomolar inhibition of sAC in both biochemical and cellular assays ( IC 50 of 195 nM) and exhibits mouse pharmacokinetic properties sufficient to warrant its use as an in vivo tool compound In Vitro TDI-10229 exhibits good permeability with an IC 50 of 92 nM for human 4-4 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo TDI-10229 (5 mg/kg; p.o.) treatment shows the C max , AUC and MRT were 15.5 μM, 94 μg h/mL and 3.95 hours, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: MouseDosage: 20 mg/kg Administration: P.o.(Pharmacokinetic Analysis) Result: The C max , AUC and MRT were 15.5 μM, 94 μg h/mL and 3.95 hours, respectively. IC50& Target:IC 50 : 195 nM (sAC)
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TDI-10229
CAS number:2810887-45-5(DMSO) molecular formula:C16H16ClN5
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| Chinese alias | - | ||
| English alias | - | ||
| CAS number | 2810887-45-5(DMSO) | molecular formula | C16H16ClN5 |
| molecular weight | 313.78 g/mol | Exact mass | 10mM in DMSO |
| PSA | - | logp | - |
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