Synthesis, inverse docking-assisted identification and in vitro biological characterization of Flavonol-based analogs of fisetin as c-Kit, CDK2 and mTOR inhibitors against melanoma and non-melanoma skin cancers

Authors

T. Roy
S.T. Boateng
S. Banang-Mbeumi
P.K. Singh
P. Basnet
R.-C.N. Chamcheu
F. Ladu
I. Chauvin
V.S. Spiegelman
R.A. Hill
K.G. Kousoulas
B.M. Nagalo
A.L. Walker
J. Fotie
S. Murru
M. Sechi
J.C. Chamcheu

Document Type

Article

Publication Date

1-1-2021

Publication Source (Journal or Book title)

Bioorganic Chemistry

Recommended Citation

Roy, T., Boateng, S., Banang-Mbeumi, S., Singh, P., Basnet, P., Chamcheu, R., Ladu, F., Chauvin, I., Spiegelman, V., Hill, R., Kousoulas, K., Nagalo, B., Walker, A., Fotie, J., Murru, S., Sechi, M., & Chamcheu, J. (2021). Synthesis, inverse docking-assisted identification and in vitro biological characterization of Flavonol-based analogs of fisetin as c-Kit, CDK2 and mTOR inhibitors against melanoma and non-melanoma skin cancers. Bioorganic Chemistry, 107 https://doi.org/10.1016/j.bioorg.2020.104595