5HT6-ligand-1

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

5HT6-ligand-1是有效的 5-HT6 受体配体，与其结合的 Ki 值为1.43 nM。

5HT6-ligand-1 is a potent 5-HT6 receptor ligand with a Ki of 1.43 nM.

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5HT6-ligand-1 is extensively metabolized in rat liver microsomes whereas in human liver microsomes, 5HT6-ligand-1 is extensively metabolized (90%). The IC50 values for 5HT6-ligand-1 at CYP 3A4 is 35.97%, whereas the IC50 values at CYP 2D6 enzymes is less than 20 μM. 5HT6-ligand-1 at an oral dose of 10 mg/kg is rapidly absorbed in rats with a good oral half-life of 3.17±0.49 h with an oral bioavailability of 29±5%. The observed oral Cmax is 60±44 ng/mL and occurs at 1.83 h. 5HT6-ligand-1 displays an oral exposure of 217±92 ng h/mL. It has a clearance of 220±92 mL/min/kg with a volume of distribution of 32.6±10.7 L/kg for iv dose. Extensive rat metabolism coupled with high clearance could be the possible reason for moderate oral bioavailability showed by 5HT6-ligand-1. Oral administration of 5HT6-ligand-1 reverses the time delay induced memory deficit and statistically significant effect is observed at a dose of 10 mg/kg indicating cognitive improvement potential of the compound 6a.

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GPCR/G Protein

5-HT Receptor

5-HT Receptor

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1038988-11-2

448.38

C20H22BrN3O2S

>98% (HPLC)

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C(C1=C2C(N(S(=O)(=O)C3=C(Br)C=CC=C3)C=C2)=CC=C1)N4CCN(C)CC4

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(-20℃)

With Ice Pack

≥ 2 years