Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives

B Su, C Cai, M Deng, D Liang, L Wang… - Bioorganic & Medicinal …, 2014 - Elsevier
On the basis of our previous structure–activity relationship (SAR) and antiviral mechanism
studies, a series of 13a-substituted phenanthroindolizidine alkaloid analogues (3a–16a, 3b …
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Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives.

B Su, C Cai, M Deng, D Liang, L Wang… - Bioorganic & Medicinal …, 2014 - europepmc.org
On the basis of our previous structure-activity relationship (SAR) and antiviral mechanism
studies, a series of 13a-substituted phenanthroindolizidine alkaloid analogues (3a-16a, 3b …

Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives.

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studies, a series of 13a-substituted phenanthroindolizidine alkaloid analogues (3a-16a, 3b …

Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives

B Su, C Cai, M Deng, D Liang… - Bioorganic & …, 2014 - pubmed.ncbi.nlm.nih.gov
On the basis of our previous structure-activity relationship (SAR) and antiviral mechanism
studies, a series of 13a-substituted phenanthroindolizidine alkaloid analogues (3a-16a, 3b …

Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives

B Su, C Cai, M Deng, D Liang, L Wang… - Bioorganic & Medicinal …, 2014 - infona.pl
On the basis of our previous structure–activity relationship (SAR) and antiviral mechanism
studies, a series of 13a-substituted phenanthroindolizidine alkaloid analogues (3a–16a, 3b …