AZD4694 (NAV4694), a fluorinated β-amyloid (Aβ) plaque neuroimaging PET radioligand, shows high affinity for Aβ fibrils ( K d = 2.3 nM) In Vivo Administration of unlabeled AZD4694 to rat showed that it has a pharmacokinetic profile consistent with good PET radioligands, it quickly entered and rapidly cleared from normal rat brain tissue . AZD4694 (4 mL/kg; intravenous injection) inhibits [ 3 H]AZD2184 binding (1 nM) in a concentration-dependent manner, with a Ki of 23.1 nM, in postmortem brain sections from AD patients . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Sprague–Dawley rats (275-300 g) Dosage: 4 mL/kg Administration: I.v. Result: Inhibited [ 3 H]AZD2184 binding in a concentration-dependent manner, with a Ki of 23.1 nM, in postmortem brain sections from AD patients. Form:Solid IC50& Target:Kd: 2.3 nM (Aβ)
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AZD4694
CAS number:1054629-49-0 molecular formula:C14H11FN2O2
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| Chinese alias | - | ||
| English alias | - | ||
| CAS number | 1054629-49-0 | molecular formula | C14H11FN2O2 |
| molecular weight | 258.25 g/mol | Exact mass | ≥99% |
| PSA | 58.300 Ų | logp | 3.300 |
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