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The Journal of Organic Chemistry|June 8, 2022
Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic ScaffoldsDiana Gapanenok, Azat Makhmet, Anatoly A Peshkov, et al.Bioorganic & Medicinal Chemistry|September 14, 2019
Highly hydrophilic 1,3-oxazol-5-yl benzenesulfonamide inhibitors of carbonic anhydrase II for reduction of glaucoma-related intraocular pressureStanislav Kalinin, Annika Valtari, Marika Ruponen, et al.The Journal of Organic Chemistry|July 17, 2023
Substrate-Controlled Three-Component Synthesis of Diverse Fused HeterocyclesAnatoly A Peshkov, Diana Gapanenok, Aleksandra Puzyk, et al.European Journal of Medicinal Chemistry|August 11, 2019
Novel electrophilic amides amenable by the Ugi reaction perturb thioredoxin system via thioredoxin reductase 1 (TrxR1) inhibition: Identification of DVD-445 as a new lead compound for anticancer therapyMirna Jovanović, Daniil Zhukovsky, Ana Podolski-Renić, et al.European Journal of Medicinal Chemistry|October 14, 2025
Extending the chemical space of glutarimide-based cereblon ligands through an efficient Rh(II)-catalyzed X-H insertion reactionEkaterina Levashova, Luca Bischof, Alexander Bunev, et al.European Journal of Medicinal Chemistry|March 28, 2021
Insertion of metal carbenes into the anilinic N-H bond of unprotected aminobenzenesulfonamides delivers low nanomolar inhibitors of human carbonic anhydrase IX and XII isoformsTatiana Sharonova, Polina Paramonova, Stanislav Kalinin, et al.European Journal of Medicinal Chemistry|February 1, 2019
Attachment of a 5-nitrofuroyl moiety to spirocyclic piperidines produces non-toxic nitrofurans that are efficacious in vitro against multidrug-resistant Mycobacterium tuberculosisMikhail Krasavin, Alexei Lukin, Tatiana Vedekhina, et al.Bioorganic & Medicinal Chemistry|April 26, 2018
Design, in silico prioritization and biological profiling of apoptosis-inducing lactams amenable by the Castagnoli-Cushman reactionMikhail Krasavin, Maxim A Gureyev, Dmitry Dar'in, et al.Chemmedchem|June 29, 2021
RhII -Catalyzed De-symmetrization of Ethane-1,2-dithiol and Propane-1,3-dithiol Yields Metallo-β-lactamase InhibitorsMikhail Krasavin, Daniil Zhukovsky, Igor Solovyev, et al.Bioorganic Chemistry|July 31, 2018
Discovery of polar spirocyclic orally bioavailable urea inhibitors of soluble epoxide hydrolaseAlexey Lukin, Jan Kramer, Markus Hartmann, et al.Pageof 8