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Chemical Communications (Cambridge, England)|October 11, 2016
Benzoxaborole as a new chemotype for carbonic anhydrase inhibitionVincenzo Alterio, Roberta Cadoni, Davide Esposito, et al.ACS Chemical Neuroscience|October 9, 2013
Ceftriaxone blocks the polymerization of α-synuclein and exerts neuroprotective effects in vitroPaolo Ruzza, Giuliano Siligardi, Rohanah Hussain, et al.ACS Medicinal Chemistry Letters|September 27, 2017
Exploring Heteroaryl-pyrazole Carboxylic Acids as Human Carbonic Anhydrase XII InhibitorsRoberta Cadoni, Nicolino Pala, Carrie Lomelino, et al.Antioxidants & Redox Signaling|July 10, 2016
Dual Inhibition of PI3K/Akt and mTOR by the Dietary Antioxidant, Delphinidin, Ameliorates Psoriatic Features In Vitro and in an Imiquimod-Induced Psoriasis-Like Disease in MiceJean Christopher Chamcheu, Vaqar M Adhami, Stephane Esnault, et al.Antiviral Research|December 9, 2019
Discovery of dihydroxyindole-2-carboxylic acid derivatives as dual allosteric HIV-1 Integrase and Reverse Transcriptase associated Ribonuclease H inhibitorsFrancesca Esposito, Mario Sechi, Nicolino Pala, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 1, 2018
Proproliferative function of adaptor protein GRB10 in prostate carcinomaMohammad Imran Khan, Ahmed Al Johani, Abid Hamid, et al.European Journal of Medicinal Chemistry|August 9, 2025
Design, anticancer activity, and mechanistic evaluation of a novel class of selective human carbonic anhydrase IX inhibitors featuring a trifluorodihydroxypropanone pharmacophoreNicolino Pala, Federico Ladu, Wojciech Szlasa, et al.Data in Brief|March 5, 2021
Identification of new fisetin analogs as kinase inhibitors: Data on synthesis and anti-skin cancer activities evaluationTithi Roy, Samuel T Boateng, Sergette Banang-Mbeumi, et al.International Journal of Molecular Sciences|May 11, 2024
EGCG Disrupts the LIN28B/Let-7 Interaction and Reduces Neuroblastoma AggressivenessSimona Cocchi, Valentina Greco, Viktoryia Sidarovich, et al.Bioorganic Chemistry|January 15, 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 cancersTithi Roy, Samuel T Boateng, Sergette Banang-Mbeumi, et al.Pageof 8