Laychiluh Mekonnen

Dr Laychiluh Mekonnen

Research Fellow

School of Pharmacy and Biomedical Science

College of Health

Eligible to supervise Masters and PhD (as Co-Supervisor) - email supervisor to discuss availability.

Available For Media Comment.


I am a passionate pharmacologist with over five years of experience teaching pharmacology to students in medicine, pharmacy, nursing, and midwifery. During my tenure at Bahir Dar University, Ethiopia, I served as Program Manager of the College of Medicine and Health Sciences and as Head of the Department of Pharmacology, gaining valuable academic leadership and curriculum development experience.
In pursuit of advancing my research career, I was awarded the prestigious Commonwealth RTP/IPRS scholarship and joined the University of South Australia to undertake a PhD in Pharmacology under the supervision of Professor Shudong Wang. My PhD research focused on the preclinical evaluation of novel CDK4/6 inhibitors for cancer treatment. Through this work, I developed broad technical and intellectual expertise in drug discovery, cancer cell biology, pharmacology, and toxicology, bridging both academic and industry research settings. My PhD led to the discovery of two promising drug candidates: AU2-94, a first-in-class CDK4 inhibitor and AU3-14, the most potent dual CDK4/6 inhibitor identified to date. AU3-14 is undergoing Phase I/IIa clinical trial targeting glioblastoma and other advanced solid tumors. I have published over 30 scientific articles and abstracts in reputable peer-reviewed journals. An internship at Aucentra Therapeutics further enriched my understanding of the pharmaceutical industry's expectations and regulatory environment.
Currently, I work as a Research fellow at University of South Australia, where I focus on in vivo combination therapy strategies to support current and future clinical studies. My research interests include drug development, cancer biology, mechanistic studies of drug action, and in vivo pharmacokinetic and pharmacodynamic modeling, with a strong emphasis on translating laboratory findings into clinical impact.

Year Citation
2025 GBD 2019 Acute and Chronic Care Collaborators. (2025). Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019.. Nature Communications, 16(1), 4235-1-4235-36.
DOI WoS11 Europe PMC7
2025 Mekonnen, L. B., Teo, T., Noll, B., Rahaman, M. H., Lenjisa, J., Basnet, S., . . . Wang, S. (2025). A brain-penetrant CDK4/6 inhibitor - AU3-14 shows robust anti-tumor efficacy against glioblastoma.. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 189(118340), 118340.
DOI Europe PMC1
2025 Safaroghli-azar, A., Mekonnen, L. B., Hassankhani, R., Lenjisa, J., Basnet, S. K. C., Batayneh, H., . . . Wang, S. (2025). A novel CDK4 inhibitor for myeloid protection in chemotherapy-treated triple-negative breast Cancer. Investigational New Drugs, 43(3), 728-741.
DOI
2025 Tiruye, T., Duko, B., Mekonnen, L., Ward, P., Nguyen, T. H. H. D., Byrne, S., . . . Beckmann, K. (2025). Cancer Burden Attributable to Potentially Modifiable Risk Factors in Australia. Cancers, 17(19), 1-30.
DOI Scopus1 WoS1
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
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 Safaroghli Azar, A., Emadi, F., Lenjisa, J., Mekonnen, L., & Wang, S. (2023). Kinase inhibitors: opportunities for small molecule anticancer immunotherapies. Drug Discovery Today, 28(5), 1-12.
DOI Scopus3 Europe PMC1
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 Anshabo, A. T., Bantie, L., Diab, S., Lenjisa, J., Kebede, A., Long, Y., . . . Wang, S. (2022). An Orally Bioavailable and Highly Efficacious Inhibitor of CDK9/FLT3 for the Treatment of Acute Myeloid Leukemia. Cancers, 14(5), 1113.
DOI Scopus12 WoS10 Europe PMC10
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
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 Khair, N. Z., Lenjisa, J. L., Tadesse, S., Kumarasiri, M., Basnet, S. K. C., Mekonnen, L. B., . . . Wang, S. (2019). Discovery of CDK5 inhibitors through structure-guided approach. ACS, 10(5), 786-791.
DOI Scopus23 WoS21 Europe PMC18
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
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
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 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
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 Gebeyehu, E., Bantie, L., & Azage, M. (2015). Inappropriate Use of Antibiotics and Its Associated Factors among Urban and Rural Communities of Bahir Dar City Administration, Northwest Ethiopia.. PloS one, 10(9), e0138179.
DOI Europe PMC107
2015 Mekonnen, L. B. (2015). In vivo antimalarial activity of the crude root and fruit extracts of Croton macrostachyus (Euphorbiaceae) against Plasmodium berghei in mice. Journal of Traditional and Complementary Medicine, 5(3), 168-173.
DOI Scopus42 Europe PMC29
2015 Wassie, S. M., Aragie, L. L., Taye, B. W., & Mekonnen, L. B. (2015). Knowledge, Attitude, and Utilization of Traditional Medicine among the Communities of Merawi Town, Northwest Ethiopia: A Cross-Sectional Study. Evidence Based Complementary and Alternative Medicine, 2015, 138073.
DOI Scopus65 Europe PMC43
2014 Bantie, L., Assefa, S., Teklehaimanot, T., & Engidawork, E. (2014). In vivo antimalarial activity of the crude leaf extract and solvent fractions of Croton macrostachyus Hocsht. (Euphorbiaceae) against Plasmodium berghei in mice.. BMC complementary and alternative medicine, 14(1), 79.
DOI Europe PMC79
- Bantie, L., Tadesse, S., Likisa, J., Yu, M., Noll, B., Heinemann, G., . . . Wang, S. (2019). Preclinical development of CDDD3-14, a potent and selective inhibitor of CDK4/6 for the treatment of breast cancer. Oncology Abstracts.
DOI
- Chen, R., Hassankhani, R., Long, Y., Basnet, S. K. C., Teo, T., Yang, Y., . . . Wang, S. (n.d.). Discovery of Novel and Potent Inhibitors of Cyclin-Dependent Kinases 7 and 9: Design, Synthesis, Structure-Activity Relationship Analysis and Biological Evaluation. SSRN Electronic Journal.
DOI

Year Citation
2024 Bantie, L., Likisa, J., Rahaman, M., Teo, T., Safaroghliazar, A., Basnet, S. K. C., . . . Wang, S. (2024). AU2-94: A CDK4-specific inhibitor with the marked anti-tumor efficacy. In CANCER RESEARCH Vol. 84 (pp. 2 pages). CA, San Diego: AMER ASSOC CANCER RESEARCH.
DOI
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

Date Role Research Topic Program Degree Type Student Load Student Name
2025 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Mr Lianmeng Kou
2024 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Mrs Senait Tesfaw
2022 Co-Supervisor - Doctor of Philosophy Doctorate Full Time Miss Ava Safaroghliazar

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