| 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 |
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