Mingfeng Yu

Dr Mingfeng Yu

School of Pharmacy and Biomedical Science

College of Health

Eligible to supervise Masters and PhD - email supervisor to discuss availability.

Available For Media Comment.


Mingfeng Yu completed his PhD in organic chemistry at the University of Sydney under the supervision of Professors Matthew H. Todd and Peter J. Rutledge in 2013. His PhD research entailed the design, synthesis and evaluation of novel scorpionand metal-cyclam complexes appended with biologically-active motifs. He was appointed as a Research Fellow (Medicinal Chemistry) at the University of South Australia upon completion of his PhD, and was promoted to a Senior Research Fellow in 2020. Under the guidance of Professor Shudong Wang, he is currently involved in the discovery and development of patentable, highly potent and selective, and orally active enzyme inhibitors for targeted cancer therapy.

Year Citation
2023 Islam, S., Rahaman, M. H., Yu, M., Noll, B., Martin, J. H., Wang, S., & Head, R. (2023). Anti-Leukaemic Activity of Rilpivirine Is Mediated by Aurora A Kinase Inhibition. Cancers, 15(4), 21 pages.
DOI Scopus5 WoS4 Europe PMC5
2023 Fanta, B. S., Lenjisa, J., Teo, T., Kou, L., Mekonnen, L., Yang, Y., . . . Wang, S. (2023). Discovery of N,4-Di(1H-pyrazol-4-yl)pyrimidin-2-amine-Derived CDK2 Inhibitors as Potential Anticancer Agents: Design, Synthesis, and Evaluation. Molecules, 28(7), 2951.
DOI Scopus7 WoS6 Europe PMC4
2023 Fanta, B. S., Mekonnen, L., Basnet, S. K. C., Teo, T., Lenjisa, J., Khair, N. Z., . . . Wang, S. (2023). 2-Anilino-4-(1-methyl-1H-pyrazol-4-yl)pyrimidine-derived CDK2 inhibitors as anticancer agents: Design, synthesis & evaluation. Bioorganic and Medicinal Chemistry, 80(117158), 117158.
DOI Scopus15 WoS15 Europe PMC10
2022 Chen, R., Hassankhani, R., Long, Y., Basnet, S. K. C., Teo, T., Yang, Y., . . . Wang, S. (2022). Discovery of Potent Inhibitors of Cyclin-Dependent Kinases 7 and 9: Design, Synthesis, Structure-Activity Relationship Analysis and Biological Evaluation. Chemmedchem, 18(3), e202200582.
DOI Scopus5 WoS5 Europe PMC5
2022 Yu, M., Yang, Y., Sykes, M., & Wang, S. (2022). Small-molecule inhibitors of tankyrases as prospective therapeutics for cancer. Journal of Medicinal Chemistry, 65(7), 5244-5273.
DOI Scopus28 Europe PMC27
2021 Yu, M., Long, Y., Yang, Y., Li, M., Teo, T., Noll, B., . . . Wang, S. (2021). Discovery of a potent, highly selective, and orally bioavailable inhibitor of CDK8 through a structure-based optimisation. European Journal of Medicinal Chemistry, 218(113391), 23 pages.
DOI Scopus9 WoS8 Europe PMC8
2021 Long, Y., Yu, M., Ochnik, A. M., Karanjia, J. D., Basnet, S. K., Kebede, A. A., . . . Wang, S. (2021). Discovery of novel 4-azaaryl-N-phenylpyrimidin-2-amine derivatives as potent and selective FLT3 inhibitors for acute myeloid leukaemia with FLT3 mutations. European Journal of Medicinal Chemistry, 213(113215), 113215.
DOI Scopus13 WoS12 Europe PMC9
2021 Yu, M., Teo, T., Yang, Y., Li, M., Long, Y., Philip, S., . . . Wang, S. (2021). Potent and orally bioavailable CDK8 inhibitors: design, synthesis, structure-activity relationship analysis and biological evaluation. European Journal of Medicinal Chemistry, 214, 1-22.
DOI Scopus14 WoS13 Europe PMC11
2021 Bantie, L., Tadesse, S., Likisa, J., Yu, M., Noll, B., Heinemann, G., . . . Wang, S. (2021). Erratum to “A first-in-class CDK4 inhibitor demonstrates in vitro, ex-vivo and in vivo efficacy against ovarian cancer” (Gynecologic Oncology (2020) 159(3) (827–838), (S0090825820339056), (10.1016/j.ygyno.2020.09.012)). Gynecologic Oncology, 163(1), 215.
DOI
2021 Counsell, A. J., Yu, M., Shi, M., Jones, A. T., Batten, J. M., Turner, P., . . . Rutledge, P. J. (2021). Copper(ii) complexes of N-propargyl cyclam ligands reveal a range of coordination modes and colours, and unexpected reactivity. Dalton Transactions, 50(11), 3931-3942.
DOI
2021 Abdelaziz, A. M., Yu, M., & Wang, S. (2021). Mnk inhibitors: a patent review. Pharmaceutical Patent Analyst, 10(1), 25-35.
DOI Scopus9 WoS10 Europe PMC9
2020 Diab, S., Yu, M., & Wang, S. (2020). CDK7 inhibitors in cancer therapy: the sweet smell of success?. Journal of Medicinal Chemistry, 63(14), 7458-7474.
DOI Europe PMC60
2020 Bantie, L., Tadesse, S., Likisa, J., Yu, M., Noll, B., Heinemann, G., . . . Wang, S. (2020). A first-in-class CDK4 inhibitor demonstrates in vitro, ex-vivo and in vivo efficacy against ovarian cancer.. Gynecol Oncol, 159(3), 827-838.
DOI Scopus16 WoS18 Europe PMC16
2019 Abdelaziz, A. M., Diab, S., Islam, S., KC Basnet, S., Noll, B., Li, P., . . . Wang, S. (2019). Discovery of n-phenyl-4-(1h-pyrrol-3-yl)pyrimidin-2-amine derivatives as potent mnk2 inhibitors: design, synthesis, sar analysis, and evaluation of in vitro anti-leukaemic activity. Medicinal chemistry, 15(6), 600-621.
DOI Scopus6 WoS5 Europe PMC5
2019 Abdelaziz, A. M., Basnet, S. K. C., Islam, S., Li, M., Tadesse, S., Albrecht, H., . . . Wang, S. (2019). Synthesis and evaluation of 2'H-spiro[cyclohexane-1,3'-imidazo[1,5-a]pyridine]-1',5'-dione derivatives as Mnk inhibitors. Bioorganic & medicinal chemistry letters, 29(18), 2650-2654.
DOI Scopus10 WoS10 Europe PMC7
2019 Rahaman, M. H., Lam, F., Zhong, L., Teo, T., Adams, J., Yu, M., . . . Wang, S. (2019). Targeting CDK9 for treatment of colorectal cancer. Molecular Oncology, 13(10), 16 pages.
DOI Scopus45 WoS43 Europe PMC40
2018 Tadesse, S., Bantie, L., Tomusange, K., Yu, M., Islam, S., Bykovska, N., . . . Wang, S. (2018). Discovery and pharmacological characterisation of a novel series of highly selective inhibitors of cyclin-dependent kinases 4 and 6 as anticancer agents. British journal of pharmacology, 175(12), 2399-2413.
DOI Scopus23 WoS22 Europe PMC18
2018 Philip, S., Kumarasiri, M., Teo, T., Yu, M., & Wang, S. (2018). Cyclin-Dependent Kinase 8: A New Hope in Targeted Cancer Therapy?. Journal of Medicinal Chemistry, 61(12), 5073-5092.
DOI Scopus93 WoS90 Europe PMC77
2017 Diab, S., Abdelaziz, A. M., Li, P., Teo, T., Basnet, S. K. C., Noll, B., . . . Wang, S. (2017). Dual inhibition of Mnk2 and FLT3 for potential treatment of acute myeloid leukaemia. European journal of medicinal chemistry, 139, 762-772.
DOI Scopus23 WoS22 Europe PMC19
2017 Tadesse, S., Yu, M., Mekonnen, L. B., Lam, F., Islam, S., Tomusange, K., . . . Wang, S. (2017). Highly potent, selective, and orally bioavailable 4-Thiazol-N-(pyridin-2-yl)pyrimidin-2-amine cyclin-dependent kinases 4 and 6 inhibitors as anticancer drug candidates: design, synthesis, and evaluation. Journal of medicinal chemistry, 60(5), 1892-1915.
DOI Scopus72 WoS65 Europe PMC40
2017 Kumarasiri, M., Teo, T., Yu, M., Philip, S., Basnet, S. K. C., Albrecht, H., . . . Wang, S. (2017). In search of novel CDK8 inhibitors by virtual screening. Journal of chemical information and modeling, 57(3), 413-416.
DOI Scopus15 WoS16 Europe PMC10
2017 Tadesse, S., Zhu, G., Mekonnen, L. B., Lenjisa, J. L., Yu, M., Brown, M. P., & Wang, S. (2017). A novel series of N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amines as highly potent CDK4/6 inhibitors. Future Medicinal Chemistry, 9(13), 1495-1506.
DOI Scopus16 WoS16 Europe PMC11
2017 Lenjisa, J. L., Tadesse, S., Khair, N. Z., Kumarasiri, M., Yu, M., Albrecht, H., . . . Wang, S. (2017). CDK5 in oncology: recent advances and future prospects.. Future medicinal chemistry, 9(16), 1939-1962.
DOI Scopus36 WoS35 Europe PMC32
2016 Wong, J. K. H., Ast, S., Yu, M., Flehr, R., Counsell, A. J., Turner, P., . . . Rutledge, P. J. (2016). Synthesis and evaluation of 1,8-disubstituted-cyclam/naphthalimide conjugates as probes for metal ions. ChemistryOpen, 5(4), 375-385.
DOI
2016 Yu, M., Nagalingam, G., Ellis, S., Martinez, E., Sintchenko, V., Spain, M., . . . Triccas, J. A. (2016). Nontoxic metal-cyclam complexes, a new class of compounds with potency against drug-resistant mycobacterium tuberculosis. Journal of medicinal chemistry, 59(12), 5917-5921.
DOI
2016 Diab, S., Li, P., Basnet, S. K. C., Lu, J., Yu, M., Albrecht, H., . . . Wang, S. (2016). Unveiling new chemical scaffolds as Mnk inhibitors. Future Medicinal Chemistry, 8(3), 271-285.
DOI Scopus22 WoS20 Europe PMC15
2016 Li, P., Diab, S., Yu, M., Adams, J., Islam, S., Basnet, S. K. C., . . . Wang, S. (2016). Inhibition of Mnk enhances apoptotic activity of cytarabine in acute myeloid leukemia cells. Oncotarget, 7(35), 1-15.
DOI Scopus23 WoS23 Europe PMC22
2016 Long, Y., Yu, M., Li, P., Islam, S., Goh, A. W., Kumarasiri, M., & Wang, S. (2016). Synthesis and biological evaluation of heteroaryl styryl sulfone derivatives as anticancer agents. Bioorganic & medicinal chemistry letters, 26(23), 5674-5678.
DOI Scopus16 WoS16 Europe PMC7
2016 Rahaman, M. H., Kumarasiri, M., Mekonnen, L. B., Yu, M., Diab, S., Albrecht, H., . . . Wang, S. (2016). Targeting CDK9: A promising therapeutic opportunity in prostate cancer. Endocrine Related Cancer, 23(12), T211-T226.
DOI Scopus63 WoS58 Europe PMC53
2015 Teo, T., Yu, M., Yang, Y., Gillam, T., Lam, F., Sykes, M. J., & Wang, S. (2015). Pharmacologic co-inhibition of Mnks and mTORC1 synergistically suppresses proliferation and perturbs cell cycle progression in blast crisis-chronic myeloid leukemia cells. Cancer Letters, 357(2), 612-623.
DOI Scopus43 WoS39 Europe PMC36
2015 Yu, M., Li, P., K c Basnet, S., Kumarasiri, M., Diab, S., Teo, T., . . . Wang, S. (2015). Discovery of 4-(dihydropyridinon-3-yl)amino-5-methylthieno[2,3-d[pyrimidine derivatives as potent Mnk inhibitors: Synthesis, structure-activity relationship analysis and biological evaluation. European Journal of Medicinal Chemistry, 95, 116-126.
DOI Scopus37 WoS37 Europe PMC20
2015 Teo, T., Lam, F., Yu, M., Yang, Y., Basnet, S., Albrecht, H., . . . Wang, S. (2015). Pharmacologic inhibition of MNKs in acute myeloid leukemia. Molecular Pharmacology, 88(2), 380-389.
DOI Scopus31 WoS28 Europe PMC23
2015 Teo, T., Yang, Y., Yu, M., Basnet, S., Gillam, T., Hou, J., . . . Wang, S. (2015). An integrated approach for discovery of highly potent and selective Mnk inhibitors: Screening, synthesis and SAR analysis. European Journal of Medicinal Chemistry, 103, 539-550.
DOI Scopus31 WoS27 Europe PMC17
2015 Basnet, S., Diab, S., Schmid, R., Yu, M., Yang, Y., Gillam, T., . . . Wang, S. (2015). Identification of a highly conserved allosteric binding site on Mnk1 and Mnk2 s. Molecular Pharmacology, 88(5), 935-948.
DOI Scopus15 WoS15 Europe PMC10
2015 Le, B. T., Kumarasiri, M., Adams, J. R. J., Yu, M., Milne, R. W., Sykes, M. J., & Wang, S. (2015). Targeting Pim kinases for cancer treatment : opportunities and challenges. Future medicinal chemistry, 7(1), 35-53.
DOI Europe PMC33
2015 Tadesse, S., Yu, M., Kumarasiri, M., Le, B. T., & Wang, S. (2015). Targeting CDK6 in cancer: state of the art and new insights. Cell cycle, 14(20), 3220-3230.
DOI Europe PMC101
2015 Abdelaziz, A. M., Yu, M., Li, P., Zhong, L., Singab, A. N. B., Hanna, A. G., . . . Wang, S. (2015). Synthesis and evaluation of 5-chloro-2-methoxy-N-(4-sulphamoylphenyl) benzamide derivatives as anti-cancer agents. Medicinal chemistry, 5(5), 253-260.
DOI
2014 Lu, T., Goh, A. W., Yu, M., Adams, J., Lam, F., Teo, T., . . . Wang, S. (2014). Discovery of (E)-3-((Styrylsulfonyl) methyl) pyridine and (E)-2-((Styrylsulfonyl) methyl) pyridine Derivatives as Anticancer Agents: Synthesis, Structure–Activity Relationships, and Biological Activities. Journal of Medicinal Chemistry, 57(6), 2275-2291.
DOI Scopus33 WoS33 Europe PMC15
2014 Diab, S., Teo, T. H. S., Kumarasiri, M., Li, P., Yu, M., Lam, F., . . . Wang, S. (2014). Discovery of 5-(2-(phenylamino)pyrimidin-4-yl)thiazol-2(3H)-one derivatives as potent Mnk2 inhibitors : synthesis, SAR analysis and biological evaluation. ChemMedChem, 9(5), 962-972.
DOI Scopus80 WoS76 Europe PMC58
2014 Diab, S., Kumarasiri, M., Yu, M., Teo, T., Proud, C., Milne, R., & Wang, S. (2014). MAP kinase-interacting kinases - emerging targets against cancer. Chemistry & Biology, 21(4), 441-452.
DOI Scopus88 WoS84 Europe PMC70
2013 Yu, M., Lim, N. H., Ellis, S., Nagase, H., Triccas, J. A., Rutledge, P. J., & Todd, M. H. (2013). Incorporation of bulky and cationic cyclam-triazole moieties into marimastat can generate potent MMP inhibitory activity without inducing cytotoxicity. Chemistry open, 2(3), 99-105.
DOI
2013 Yu, M., Yu, Q., Rutledge, P. J., & Todd, M. H. (2013). A fluorescent allosteric scorpion and complex visualizes a biological recognition event. ChemBioChem: a European journal of chemical biology, 14(2), 224-229.
DOI
2011 Yu, M., Price, J. R., Jensen, P., Lovitt, C. J., Shelper, T., Duffy, S., . . . Todd, M. H. (2011). Copper, nickel, and zinc cyclam-amino acid and cyclam-peptide complexes may be synthesized with "click" chemistry and are noncytotoxic. Inorganic chemistry, 50(24), 12823-12835.
DOI
2010 Zhang, A., Yu, M., Lan, T., Liu, Z., & Mao, Z. (2010). Novel synthesis of 4-or 6-substituted indirubin derivatives. Synthetic communications, 40(21), 3125-3134.
DOI
2010 Jiang, J., Zhao, M., Zhang, A., Yu, M., Lin, X., Wu, M., . . . Han, W. (2010). Characterization of a GSK-3 inhibitor in culture of human cord blood primitive hematopoietic cells. Biomedicine and pharmacotherapy, 64(7), 482-486.
DOI
2009 Xu, Y., Yu, M., Long, Y., Wu, H., & Mao, Z. (2009). Synthesis of pyrrolo[2,3-d]pyrimidine analogues: 'pyridine ring' analogues of pemetrexed. Heterocycles, 78(9), 2353-2360.
DOI

Year Citation
2017 Tadesse, S., Bantie, L., Tomusange, K., Islam, S., Rahaman, M. H., Noll, B., . . . Wang, S. (2017). CDKI-15, a novel and highly selective CDK4/6 inhibitor: discovery, <i>in vitro</i> and <i>in vivo</i> anticancer efficacy. In CANCER RESEARCH Vol. 77 (pp. 2 pages). DC, Washington: AMER ASSOC CANCER RESEARCH.
DOI

Year Citation
2017 Wang, S., Zeleke, S. T., & Yu, M. (2017). WO2017020065, N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amine derivatives as therapeutic compounds.

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