[1]
|
Kastenhuber, E.R. and Lowe, S.W. (2017) Putting p53 in Context, Cell, 170, 1062-1078.
https://doi.org/10.1016/j.cell.2017.08.028
|
[2]
|
Bhatia, N., Khator, R., Kulkarni, S., Singh, Y., Kumar, P. and Tha-reja, S. (2023) Recent Advancements in the Discovery of MDM2/MDM2-p53 Interaction Inhibitors for the Treatment of Cancer. Current Medicinal Chemistry, 30, 3668-3701.
https://doi.org/10.2174/0929867330666221114103924
|
[3]
|
Chahat, Bhatia, R. and Kumar, B. (2023) P53 as a Po-tential Target for treatment of Cancer: A Perspective on Recent Advancements in Small Molecules with Structural In-sights and SAR Studies. European Journal of Medicinal Chemistry, 247, Article ID: 115020. https://doi.org/10.1016/j.ejmech.2022.115020
|
[4]
|
Zhu, H., Gao, H., Ji, Y., Zhou, Q., Du, Z., Tian, L., Jiang, Y., Yao, K. and Zhou, Z. (2022) Targeting p53-MDM2 Interaction by Small-Molecule Inhibitors: Learning from MDM2 In-hibitors in Clinical Trials. Journal of Hematology & Oncology, 15, Article No. 91. https://doi.org/10.1186/s13045-022-01314-3
|
[5]
|
Nishikawa, S. and Iwakuma, T. (2023) Drugs Targeting p53 Mutations with FDA Approval and in Clinical Trials. Cancers, 15, Article No. 429. https://doi.org/10.3390/cancers15020429
|
[6]
|
Afzal, O., Kumar, S., Haider, M.R., Ali, M.R., Kumar, R., Jaggi, M. and Bawa, S. (2015) A Review on Anticancer Potential of Bioactive Heterocycle Quinoline. European Journal of Me-dicinal Chemistry, 97, 871-910.
https://doi.org/10.1016/j.ejmech.2014.07.044
|
[7]
|
Lauria, A., La Monica, G., Bono, A. and Martorana, A. (2021) Quinoline Anticancer Agents Active on DNA and DNA-Interacting Proteins: From Classical to Emerging Therapeutic Targets. European Journal of Medicinal Chemistry, 220, Article ID: 113555. https://doi.org/10.1016/j.ejmech.2021.113555
|
[8]
|
Liu, K., Mo, M., Yu, G., Yu, J., Song, S.M., Cheng, S., Li, H.M., Meng, X.L., Zeng, X.P., Xu, G.C., et al. (2023) Discovery of Novel 2-(Trifluoromethyl)Quinolin-4-Amine De-rivatives as Potent Antitumor Agents with Microtubule Polymerization Inhibitory Activity. Bioorganic Chemistry, 139, Article ID: 106727.
https://doi.org/10.1016/j.bioorg.2023.106727
|
[9]
|
Ilovaisky, A.I., Scherbakov, A.M., Merkulova, V.M., Cherno-burova, E.I., Shchetinina, M.A., Andreeva, O.E., Salnikova, D.I., Zavarzin, I.V. and Terent'ev, A.O. (2023) Secoster-oid-Quinoline Hybrids as New Anticancer Agents. The Journal of Steroid Biochemistry and Molecular Biology, 228, Article ID: 106245.
https://doi.org/10.1016/j.jsbmb.2022.106245
|
[10]
|
Shen, J., Zhang, T., Cheng, Z., Zhu, N., Wang, H., Lin, L., Wang, Z., Yi, H. and Hu, M. (2018) Lycorine Inhibits Glioblastoma Multiforme Growth through EGFR Suppression. Journal of Experimental & Clinical Cancer Research, 37, Article No. 157. https://doi.org/10.1186/s13046-018-0785-4
|
[11]
|
Zhang, Y.-B., Fei, H.-X., Guo, J., Zhang, X.-J., Wu, S.-L. and Zhong, L.-L. (2019) Dauricine Suppresses the Growth of Pancreatic Cancer in Vivo by Modulating the Hedgehog Sig-naling Pathway. Oncology Letters, 18, 4403-4414.
https://doi.org/10.3892/ol.2019.10790
|
[12]
|
Li, S., Zhang, Y., Zhang, J., Yu, B., Wang, W., Jia, B., Chang, J. and Liu, J. (2022) Neferine Exerts Ferroptosis-Inducing Effect and Antitumor Effect on Thyroid Cancer through Nrf2/HO-1/NQO1 Inhibition. Journal of Oncology, 2022, Article ID: 7933775. https://doi.org/10.1155/2022/7933775
|
[13]
|
Sun, Y., Gu, Y., Gao, X., Jin, X., Wink, M., Sharopov, F.S., Yang, L. and Sethi, G. (2023) Lycorine Suppresses the Malignancy of Breast Carcinoma by Modulating Epithelial Mesenchymal Transition and β-Catenin Signaling. Pharmacological Research, 195, Article ID: 106866. https://doi.org/10.1016/j.phrs.2023.106866
|
[14]
|
Wang, K.D., Zhu, M.L., Qin, C.J., Dong, R.F., Xiao, C.M., Lin, Q., Wei, R.Y., He, X.Y., Zang, X., Kong, L.Y., et al. (2023) Sanguinarine Induces Apoptosis in Osteosarcoma by At-tenuating the Binding of STAT3 to the Single-Stranded DNA-Binding Protein 1 (SSBP1) Promoter Region. British Journal of Pharmacology.
https://doi.org/10.1111/bph.16202
|
[15]
|
Chen, Z., Dong, Y., Yan, Q., Li, Q., Yu, C., Lai, Y., Tan, J., Fan, M., Xu, C., Li, L., et al. (2023) Liquid Chromatography-Tandem Mass Spectrometry Analysis of a Ratio-Optimized Drug Pair of Sophora flavescens Aiton and Coptis chinensis Franch and Study on the Mechanism of Anti-Colorectal Cancer Effect of Two Alkaloids Thereof. Frontiers in Oncology, 13, Article 1198467. https://doi.org/10.3389/fonc.2023.1198467
|
[16]
|
Hu, M., Peng, S., He, Y., Qin, M., Cong, X., Xing, Y., Liu, M. and Yi, Z. (2015) Lycorine Is a Novel Inhibitor of the Growth and Metastasis of Hormone-Refractory Prostate Cancer. Oncotarget, 6, 15348-15361.
https://doi.org/10.18632/oncotarget.3610
|
[17]
|
Solomon, V.R. and Lee, H. (2011) Quinoline as a Privileged Scaf-fold in Cancer Drug Discovery. Current Medicinal Chemistry, 18, 1488-1508. https://doi.org/10.2174/092986711795328382
|
[18]
|
Man, R.J., Jeelani, N., Zhou, C. and Yang, Y.S. (2021) Recent Progress in the Development of Quinoline Derivatives for the Exploitation of Anti-Cancer Agents. Anti-Cancer Agents in Medicinal Chemistry, 21, 825-838.
https://doi.org/10.2174/1871520620666200516150345
|
[19]
|
Pradhan, V., Salahuddin, Kumar, R., Mazumder, A., Abdullah, M.M., Shahar Yar, M., Ahsan, M.J. and Ullah, Z. (2023) Molecular Target Interactions of Quinoline Deriva-tives as Anticancer Agents: A Review. Chemical Biology & Drug Design, 101, 977-997. https://doi.org/10.1111/cbdd.14196
|
[20]
|
Sonawane, H.R., Vibhute, B.T., Aghav, B.D., Deore, J.V. and Patil, S.K. (2023) Versatile Applications of Transition Metal Incorporating Quinoline Schiff Base Metal Complexes: An Overview. European Journal of Medicinal Chemistry, 258, Article ID: 115549. https://doi.org/10.1016/j.ejmech.2023.115549
|
[21]
|
Tyagi, S., Salahuddin, Mazumder, A., Kumar, R., Datt, V., Shabana, K., Yar, M.S. and Ahsan, M.J. (2023) Synthesis and SAR of Potential Anti-Cancer Agents of Quinoline Ana-logues: A Review. Medicinal Chemistry, 9, 785-812.
https://doi.org/10.2174/1573406419666230228140619
|
[22]
|
de Araújo, R.S.A., da Silva-Junior, E.F., de Aquino, T.M., Scotti, M.T., Ishiki, H.M., Scotti, L. and Mendonça-Junior, F.J.B. (2020) Computer-Aided Drug Design Applied to Secondary Metabolites as Anticancer Agents. Current Topics in Medicinal Chemistry, 20, 1677-1703. https://doi.org/10.2174/1568026620666200607191838
|
[23]
|
Vemula, D., Jayasurya, P., Sushmitha, V., Kumar, Y.N. and Bhandari, V. (2023) CADD, AI and ML in Drug Discovery: A Comprehensive Review. European Journal of Pharmaceutical Sciences, 181, Article ID: 106324.
https://doi.org/10.1016/j.ejps.2022.106324
|
[24]
|
Abdolmaleki, A., Ghasemi, J.B. and Ghasemi, F. (2017) Computer Aided Drug Design for Multi-Target Drug Design: SAR /QSAR, Molecular Docking and Pharmacophore Methods. Current Drug Targets, 18, 556-575.
https://doi.org/10.2174/1389450117666160101120822
|
[25]
|
Dar, K.B., Bhat, A.H., Amin, S., Hamid, R., Anees, S., Anjum, S., Reshi, B.A., Zargar, M.A., Masood, A. and Ganie, S.A. (2018) Modern Computational Strategies for De-signing Drugs to Curb Human Diseases: A Prospect. Current Topics in Medicinal Chemistry, 18, 2702-2719. https://doi.org/10.2174/1568026619666190119150741
|
[26]
|
Giordano, D., Biancaniello, C., Argenio, M.A. and Facchiano, A. (2022) Drug Design by Pharmacophore and Virtual Screening Approach. Pharmaceuticals, 15, Article No. 646. https://doi.org/10.3390/ph15050646
|
[27]
|
Haronikova, L., Bonczek, O., Zatloukalova, P., Kokas-Zavadil, F., Kucerikova, M., Coates, P.J., Fahraeus, R. and Vojtesek, B. (2021) Resistance Mechanisms to Inhibitors of p53-MDM2 Interactions in Cancer Therapy: Can We Overcome Them? Cellular & Molecular Biology Letters, 26, Article No. 53.
https://doi.org/10.1186/s11658-021-00293-6
|
[28]
|
Mohammed, I., Hampton, S.E., Ashall, L., Hildebrandt, E.R., Kutlik, R.A., Manandhar, S.P., Floyd, B.J., Smith, H.E., Dozier, J.K., Distefano, M.D., et al. (2016) 8-Hydroxyquinoline-Based Inhibitors of the Rce1 Protease Disrupt Ras Membrane Localization in Human Cells. Bioor-ganic & Medicinal Chemistry, 24, 160-178.
https://doi.org/10.1016/j.bmc.2015.11.043
|