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Chemistry (Weinheim an Der Bergstrasse, Germany)|May 20, 2017
N-Aryl Groups Are Ubiquitous in Cross-Dehydrogenative Couplings Because They Stabilize Reactive IntermediatesAlthea S-K Tsang, A Stephen K Hashmi, Peter Comba, et al.Pharmaceuticals (Basel, Switzerland)|July 27, 2024
Identification of Dihydropyrazolo[1,5-a]pyrazin-4(5H)-ones as Cyclic Products of β-Amidomethyl Vinyl Sulfone Alphavirus Cysteine Protease InhibitorsAnirban Ghoshal, Álvaro F Magalhães, Kesatebrhan Haile Asressu, et al.Biochemistry|April 3, 2007
Interactions of isopenicillin N synthase with cyclopropyl-containing substrate analogues reveal new mechanistic insightAnnaleise R Howard-Jones, Jonathan M Elkins, Ian J Clifton, et al.Scientific Reports|October 9, 2019
Bengamides display potent activity against drug-resistant Mycobacterium tuberculosisDiana H Quan, Gayathri Nagalingam, Ian Luck, et al.Frontiers in Pharmacology|October 19, 2018
Experimentally Validated Pharmacoinformatics Approach to Predict hERG Inhibition Potential of New Chemical EntitiesSaba Munawar, Monique J Windley, Edwin G Tse, et al.Chemical Science|June 14, 2021
Correction: Metal complexes as a promising source for new antibioticsAngelo Frei, Johannes Zuegg, Alysha G Elliott, et al.Chemical Science|March 25, 2020
Metal complexes as a promising source for new antibioticsAngelo Frei, Johannes Zuegg, Alysha G Elliott, et al.Journal of Medicinal Chemistry|November 14, 2013
In vitro metabolic profile and in vivo antischistosomal activity studies of (η(6)-praziquantel)Cr(CO)3 derivativesMalay Patra, Katrin Ingram, Anna Leonidova, et al.Plos Medicine|April 19, 2017
An open source pharma roadmapManica Balasegaram, Peter Kolb, John McKew, et al.Journal of Medicinal Chemistry|November 21, 2018
Easy-To-Synthesize Spirocyclic Compounds Possess Remarkable in Vivo Activity against Mycobacterium tuberculosisAna Guardia, Jessica Baiget, Mónica Cacho, et al.Pageof 13