GLS4 莫非賽定 Morphothiadin

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公司名稱 MedChemExpress LLC
品牌 MedChemExpress (MCE)
型號 GLS4
產(chǎn)地
廠商性質(zhì) 生產(chǎn)廠家
更新時間 2019/6/27 8:50:13
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產(chǎn)品標(biāo)簽

GLS4 morphothiadin

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詳細(xì)信息 在線詢價

供貨周期	現(xiàn)貨	規(guī)格	10 mM * 1 mL；1 mg；5 mg；10 mg；25 mg；50 mg
貨號	HY-108917	應(yīng)用領(lǐng)域	生物產(chǎn)業(yè)

Morphothiadin

產(chǎn)品活性：Morphothiadin 是野生型和阿德福韋耐藥 HBV 復(fù)制的有效抑制劑，其 IC₅₀ 值為 12 nM。

研究領(lǐng)域：Anti-infection

作用靶點：HBV

In Vitro: Morphothiadin is a potent inhibitor on the replication of both wild-type and adefovir-resistant HBV with an IC₅₀ of 12 nM. Morphothiadin (GLS4) shows no toxicity up to 25 μM. The cytotoxic dose whereby 50% of cells die (CC₅₀) for primary hepatocytes is 115 μM for Morphothiadin (P<0.001). The CC₉₀ is 190 μM for Morphothiadin (P<0.01) in HepAD38 cells. Morphothiadin strongly inhibits virus accumulation in the supernatant of HepAD38 cells at 25 nM to 100 nM (P<0.02). Results show a concentration-dependent decrease of core protein in cells treated with Morphothiadin.

In Vivo: The area under the concentration-time curve from 0 to 24 h (AUC_0-24) of Morphothiadin (GLS4) is 556 h?ng/mL. After intravenous administration of 10 mg/kg Morphothiadin, the total plasma clearance and apparent volume distribution are 4.2 liters/h/kg and 7.38 liters/kg, respectively. The bioavailability of Morphothiadin is 25.5%. It is found that virus titers have increased 83.5-fold in mice treated with 3.75 mg/kg per day of Morphothiadin, 28.3-fold among mice treated with 7.5 mg/kg per day, but only 3- to 6-fold among mice treated with the higher doses of Morphothiadin. There is generally an inverse relationship between Morphothiadin dose and virus titer, with the greatest rebound seen in mice treated with 3.75 mg/kg per day of Morphothiadin (540-fold) and the smallest rebound in mice treated with 60 mg/kg per day (23-fold) (P<0.001). The Morphothiadin doses of >7.5 mg/kg per day significantly suppresses the virus replication cycle throughout the treatment period, while Morphothiadin doses of >15 mg/kg per day suppresses virus for up to 2 weeks after the end of treatment.