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|---|---|---|
| 5mg | $403 | Get quote |
| 10mg | $645 | Get quote |
| 50 mg | Get quote | |
| 100 mg | Get quote | |
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| Cat. No. : | HY-110056 |
| M.Wt: | 437.79 |
| Formula: | C21H23Cl3N4 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
NBI 35965 hydrochloride is a selective, orally active and brain-penetrant corticotropin-releasing factor receptor 1 (CRF1) antagonist with a Ki value of 4 nM and a pKi value of 8.5. NBI 35965 hydrochloride does not inhibit CRF2. NBI 35965 hydrochloride reduces CRF or stress-induced adrenocorticotropic hormone (ACTH) production in vivo with pIC50 values of 7.1 and 6.9, respectively. NBI 35965 hydrochloride shows anxiolytic effects[1][2].
In Vitro:NBI 35965 hydrochloride displays a high affinity for CRF1 while having no binding affinity to CRF2. NBI 35965 hydrochloride also inhibits the stimulation of cAMP induced by Sauvagine in CRF1 transfected cells[2].
In Vivo:NBI 35965 hydrochloride (20 mg/kg; oral gavage; once) reduces stress induced ACTH production in mice[1].
In rats, NBI 35965 hydrochloride (Compound 12a; 10 mg/kg) has a volume of distribution 17.8 L/kg, a plasma clearance of 17 mL/min/kg, and a half-life of 12 h. The estimated oral bioavailability is 34% with a mean maximal plasma concentration at 1 h of 560 ng/mL. NBI 35965 hydrochloride also penetrated the blood-brain barrier, resulting in a mean maximal brain concentration of 700 ng/g[1].
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