
Christopher Asquith
@Asquith__Chris
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Medicinal Chemistry PI at @uef_farmasia @UniEastFinland
Kuopio, Finland
Joined September 2022
RT @Nature: Nature research paper: SuFEx-based antitubercular compound irreversibly inhibits Pks13.
nature.com
Nature - A preclinical covalent compound, CMX410, contains a aryl fluorosulfate warhead that targets the acyltransferase domain of Mtb Pks13, an essential enzyme in cell-wall biosynthesis, making...
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RT @FLUORrismo: New paper out. Collaboration with @ATlili1 @MonnereauENSL @LhoussainKz.Strain-Release-Driven Synthesis of Pentafluorosulfan….
pubs.acs.org
Methods to prepare SF5-containing molecules are of significant interest, as the pentafluorosulfanyl (SF5) group imparts unique chemical and physical properties─such as high electronegativity, and...
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RT @Dr_Kevin_Pruitt: Very excited! Please check out our paper @NatureComms. Congrats to @Dali_XIII, @FlaviaSardela, @Geetha_Boligala, @Elli….
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RT @SaitoGroup: Ever since I first came across episulfoxides in the literature, I wondered: could they react with organometallic reagents t….
pubs.acs.org
Reported herein is the application of a sterically hindered episulfoxide for the modular synthesis of sulfoxides and sulfinamides. SO transfer from the episulfoxide to Grignard or organolithium...
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RT @mathiassenge: Check out our new #preprint 📢😀"Bicyclo[1.1.1]pentane Ketones via Friedel-Crafts Acylation" #BCP #isostere @ChemRxiv http….
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Here is our latest publication on a new dual PIP4K2C/PIKfyve inhibitor RMC-113, that blocks SARS-CoV-2 by reversing virus-induced autophagy impairment. @NatureComms @UniEastFinland @Stanford @KU_Leuven @UNC_PHCO @UNC @DruggableGenome - check it out -
nature.com
Nature Communications - The understudied lipid kinase PIP4K2C binds SARS-CoV-2 nonstructural protein 6 and regulates virus-induced autophagic flux impairment, suppressing viral protein degradation....
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RT @ChemistryNews: Regiodivergent hydrophosphination of Bicyclo[1.1.0]-Butanes under catalyst control https://t.co/….
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RT @angew_chem: Photochemical Conversion of Indazoles into Benzimidazoles (Daniele Leonori and co-workers) @LeonoriLab @dbyildiz11 • https:….
onlinelibrary.wiley.com
We present a photochemical strategy for transforming 1H- and 2H-indazoles into benzimidazoles, enabling heteroaromatic interconversion under mild conditions. This approach, grounded in a two-step...
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RT @J_A_C_S: Iron-Catalyzed Enantioconvergent Amination of Alcohols | Journal of the American Chemical Society @TotalSyntheses
https://t.c….
pubs.acs.org
Owing to the prevalence of chiral amines in natural products and pharmaceuticals, we developed an iron-catalyzed borrowing hydrogen enantioconvergent amination of alcohols in the presence of chiral...
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RT @atranscendedman: Singapore researchers outline why antiviral resistance is so common and hard to defeat. Direct-acting antivirals mut….
nature.com
npj Antimicrobials and Resistance - Strategies and efforts in circumventing the emergence of antiviral resistance against conventional antivirals
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RT @ScienceTM: A team has designed a host defense peptide–mimicking prodrug that attacks drug-resistant Gram-negative bacteria at the infec….
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RT @HyperIodine: Site-Selective Nitration of Arene via Hypervalent Iodine-Mediated C–H Functionalization.
pubs.acs.org
We developed a novel nitration method using hypervalent iodine for site-selective C–H functionalization. This technique efficiently synthesizes nitroarenes with high regioselectivity and is scalable,...
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RT @MJKoh87: Our latest invited review article on directing group-free alkene 1,2-dialkylation reactions, in honor of @songlin_chem for the….
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RT @NatRevDrugDisc: FDA new drug approvals in Q1 2025 Only 7 new drugs were approved by the FDA in Q1, but 2 are po….
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RT @NatRevDrugDisc: Trends in the drug target landscape for autoimmune diseases. This new article analyses the evol….
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RT @NatRevDrugDisc: For readers interested in novel antibiotics for Gram-negative bacterial infections, here's a review covering promising….
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RT @Chem_CP: Online now: Strained diradicaloids for σ-bond-insertion reactions: A breakthrough in drug discovery ht….
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RT @neo_papers: Pseudomonas aeruginosa acyl-CoA dehydrogenases and structure-guided inversion of their substrate specificity #neoTwitter ht….
pubmed.ncbi.nlm.nih.gov
Fatty acids are a primary source of carbon for Pseudomonas aeruginosa (PA) in the airways of people with cystic fibrosis (CF). Here, we use tandem mass-tag proteomics to analyse the protein express...
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RT @NatureSynthesis: Now online & open access:. Article by R Güdük, N Kehl, C Stavagna, MJ. Tilby, O Turner, A Ruffoni, HP. Caldora & D Leo….
nature.com
Nature Synthesis - Bioisosteric replacement is vital in drug discovery; however, substituting core ring structures is challenging. Now, a strategy that converts pyridines into benzonitriles, via...
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