Zhendong Jin, PhD
Introduction
Our research lies at the interface of chemistry and biology of bioactive natural products. Our group (along with our biological collaborators) is the worldwide leader in the study of natural products OSW-1 and superstolide A. Innovative synthetic methodologies and strategies were developed and applied to the syntheses of these natural products and their analogs. Our efficient synthetic approaches have successfully solved their bottleneck of supply and provided biologists a sufficient amount of materials for biological investigation. Our medicinal chemistry study has resulted in defining their minimum pharmacophores and the synthesis of two groups of “patent-protected late stage drug candidates” with improved ADMET profiles that have successfully advanced to preclinical stage and have the potential to be 1st-in-class. Our synthetic approaches can also be modified for the synthesis of innovative molecular probes for the identification of their drug targets and the elucidation of their mechanisms of action. In addition, inspired by these natural products we have successfully designed and developed the new generation of cytotoxic payloads with novel mechanisms of action for antibody-drug conjugates (ADCs), small-molecule drug conjugates (SMDCs) including peptide-drug conjugates (PDCs) and aptamer-drug conjugates (ApDCs) for cancer therapy. Furthermore, our innovative research programs have provided excellent training for graduate students and postdoc fellows who now work either in academia or in the pharmaceutical industry including Merck, Novartis and AstraZeneca.
Current Positions
- Professor of Pharmaceutical Sciences and Experimental Therapeutics
Education
- Ph.D. in Synthetic Organic Chemistry, Department of Chemistry, Purdue University, Lafayette, Indiana
- NIH Postdoctoral Fellow, Department of Chemistry and Chemical Biology, The Scripps Research Institute, La Jolla, California
- NIH Postdoctoral Fellow, Department of Chemistry and Chemical Biology, The Scripps Research Institute, La Jolla, California
Research Interests
- Chemical biology
- Medicinal chemistry
- Organic synthesis
- Novel drug discovery and development
Selected Publications
- Qiu, H., Qian, S., Head, S.A., Sanchez, P.R., Liu, J.O., Jin, Z. (2024). Insights into the Structure-activity Relationship of the Anticancer Compound ZJ-101: a Role Played by the Amide Moiety. Bioorg. Med. Chem. Lett. (105):129741. DOI: 10.1016/j.bmcl.2024.129741
- Ma-Lauer Y., Li P., Niemeyer D., Richter A., Pusl K., von Brunn B., Ru Y., Xiang C., Schwinghammer S., Liu J., Baral P., Berthold E.J., Qiu H., Roy A., Kremmer E., Flaswinkel H., Drosten C., Jin Z., von Brunn A. (2024). Oxysterole-binding protein targeted by SARS-CoV-2 viral proteins regulates coronavirus replication. Front. Cell. Infect. Microbiol. (14):1383917. DOI: 10.3389/fcimb.2024.1383917
- Lu, D., Chen, L., Roy, A. & Jin, Z. (2023). Diastereoselective acyl nitroso Diels-Alder reactions using 1,3-dienes derived from (R)-4-tert-butyldimethylsilyloxy-2-cyclohexen-1-one. TETRAHEDRON LETTERS 117. DOI: 10.1016/j.tetlet.2023.154367.
- Qiu, H., Qian, S., Head, S. A., Liu, J. O. & Jin, Z. (2016). Insights into the structure-activity relationship of the anticancer compound ZJ-101, a derivative of marine natural product superstolide A: A role played by the lactone moiety. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 26 (19) 4702-4704. DOI: 10.1016/j.bmcl.2016.08.046.
- Chen, L., Riaz Ahmed, K. B., Huang, P. & Jin, Z. (2013). Design, synthesis, and biological evaluation of truncated superstolide A. Angewandte Chemie - International Edition 52 (12) 3446-3449. DOI: 10.1002/anie.201209300.
- Garcia-Prieto, C., Begam Riaz Ahmed, K., Chen, Z., Zhou, Y., Hammoudi, N., Kang, Y., Lou, C., Mei, Y., Jin, Z. & Huang, P. (2013). Effective Killing of Leukemia Cells by the Natural Product OSW-1 through Disruption of Cellular Calcium Homeostasis. Journal of Biological Chemistry 288 (5) 3240-3250. DOI: 10.1074/jbc.M112.384776.
- Chen, L., Hua, Z., Li, G. & Jin, Z. (2011). Controlling the Facial Selectivity of Asymmetric [4+2] Cycloadditions: A Concise Synthesis of the cis-Decalin Core Structure of Superstolides A and B. Organic Letters 13 3580. DOI: 10.1021/ol201095b.
- Zhou, Y., Garcia-Prieto, C., Carney, D. A., Xu, R. h., Pelicano, H., Kang, Y., Yu, W., Lou, C., Kondo, S., Liu, J., Harris, D. M., Estrov, Z., Keating, M. J., Jin, Z. & Huang, P. (2005). OSW-1: A natural compound with potent anticancer activity and a novel mechanism of action. Journal of the National Cancer Institute 97 (23) 1781-1785. DOI: 10.1093/jnci/dji404.
- Kang, Y., Mei, Y., Du, Y. & Jin, Z. (2003). Total Synthesis of the Highly Potent Anti-HIV Natural Product Daurichromenic Acid along with Its Two Chromane Derivatives, Rhododaurichromanic Acids A and B. Organic Letters 5 (23) 4481-4484. DOI: 10.1021/ol030109m.
- Yu, W. & Jin, Z. (2002). Total synthesis of the anticancer natural product OSW-1. Journal of the American Chemical Society 124 (23) 6576-6583. DOI: 10.1021/ja012119t.