Synthesis, structure–activity relationships and biological evaluation of dehydroandrographolide and andrographolide derivatives as novel anti-hepatitis B virus agents

• Published in: Bioorganic & medicinal chemistry letters Vol. 24; no. 10; pp. 2353 - 2359
• Main Authors: Chen, Hao, Ma, Yun-Bao, Huang, Xiao-Yan, Geng, Chang-An, Zhao, Yong, Wang, Li-Jun, Guo, Rui-Hua, Liang, Wen-Juan, Zhang, Xue-Mei, Chen, Ji-Jun
• Format: Journal Article
• Language: English
• Published: OXFORD Elsevier Ltd 15.05.2014; Elsevier
• Subjects: Andrographis paniculata; Anti-HBV activity; Antiviral Agents - chemical synthesis; Antiviral Agents - chemistry; Antiviral Agents - pharmacology; Biological Products; Chemistry; Chemistry, Medicinal; Chemistry, Organic; Dehydroandrographolide and andrographolide derivatives; Diterpenes - chemical synthesis; Diterpenes - chemistry; Diterpenes - pharmacology; DNA Replication - drug effects; DNA, Viral - biosynthesis; DNA, Viral - genetics; Hepatitis B virus; Hepatitis B virus - drug effects; Hepatitis B virus - genetics; Hepatitis B virus - physiology; Life Sciences & Biomedicine; Octanol–water partition coefficients; Pharmacology & Pharmacy; Physical Sciences; Science & Technology; Structure-Activity Relationship; Structure–activity relationships; Virus Replication - drug effects; Dehydroandrographolide and andrographolide derivatives; Anti-HBV activity; Octanol–water partition coefficients; Structure–activity relationships; Dehydroandrographolide and; DESIGN; PARTITION-COEFFICIENTS; VIVO; ANALOGS; DRUG DISCOVERY; Octanol-water partition coefficients; Structure-activity relationships; IN-VITRO; andrographolide derivatives; INHIBITORS; CONSTITUENTS
• ISSN: 0960-894X; 1464-3405; 1464-3405
• DOI: 10.1016/j.bmcl.2014.03.060

Dehydroandrographolide and andrographolide, two natural diterpenoids isolated from Andrographis paniculata possessed activity against HBV DNA replication with IC50 values of 22.58 and 54.07μM and low SI values of 8.7 and 3.7 in our random assay. Consequently, 48 derivatives of dehydroandrographolide and andrographolide were synthesized and evaluated for their anti-HBV properties to yield a series of active derivatives with lower cytotoxicity, including 14 derivatives against HBsAg secretion, 19 derivatives against HBeAg secretion and 38 derivatives against HBV DNA replication. Interestingly, compound 4e could inhibit not only HBsAg and HBeAg secretions but also HBV DNA replication with SI values of 20.3, 125.0 and 104.9. Furthermore, the most active compound 2c with SI value higher than 165.1 inhibiting HBV DNA replication was revealed with the optimal logP value of 1.78 and logD values. Structure–activity relationships (SARs) of the derivatives were disclosed for guiding the future research toward the discovery of new anti-HBV drugs. Dehydroandrographolide and andrographolide, two natural diterpenoids isolated from Andrographis paniculata possessed activity against HBV DNA replication with IC50 values of 22.58 and 54.07μM and low SI values of 8.7 and 3.7 in our random assay. Consequently, 48 derivatives of dehydroandrographolide and andrographolide were synthesized and evaluated for their anti-HBV properties to yield a series of active derivatives with lower cytotoxicity, including 14 derivatives against HBsAg secretion, 19 derivatives against HBeAg secretion and 38 derivatives against HBV DNA replication. Interestingly, compound 4e could inhibit not only HBsAg and HBeAg secretions but also HBV DNA replication with SI values of 20.3, 125.0 and 104.9. Furthermore, the most active compound 2c with SI value higher than 165.1 inhibiting HBV DNA replication was revealed with the optimal logP value of 1.78 and logD values. Structure–activity relationships (SARs) of the derivatives were disclosed for guiding the future research toward the discovery of new anti-HBV drugs.