Cool to see our paper on GI-restricted PRMT5 inhibitors now incorporated in a JMedChem issue! Particularly as it is on the journal's front cover
@ACSPublications#MyACSCover
Our Discovery Process Research Team at the interface between Medicinal Chemistry and Chemical Process R&D is growing further! Exciting opportunity for creative organic chemists. Check the link below. https://t.co/knhjMwzuTy
@DennisWhom Erik was first to develop an anti-HIV in vitro screening assay and showed that Holy's acyclic NUC analogues have activity. It was the start of Gilead
Sharing our @bioRxivpreprint of “Substrate Binding and Inhibition of the Anion Exchanger 1 Transporter”, in which we reveal how AE1 binds and transports substrates, and how different drugs inhibit the transporter.
@KRHornberger AZT is such an example, and the group of Chris Meier in Hamburg has developed prodrugs of di- and triphosphates...
https://t.co/IVgsy4Ffvn
A very recent example is this JMC paper: https://t.co/TqVqHMgHK5
Check our paper @NeytsVirology@KU Leuven published in @Nature in which we report on a highly potent pan-serotype dengue inhibitor with unprecedented potency in infection models.
https://t.co/whXSPEQi10
Today we report @ChemRxiv a practical method to obtain C–4 alkylated pyridines with exquisite site-selectivity in collaboration with @GodineauEdouard of @Syngenta using simple Minisci decarboxylation: https://t.co/HpZevQpKbk
In 2016, with @EastgateMartin and the @bmsnews team we set out to simplify the way Oligonucleotides therapeutics (OTs) are made. Access to a 3-10-3 LNA/DNA gapmer with 4 different P-linkages had pushed the limits of known chem. Today we report a solution: https://t.co/hSsZXFg3DJ
Today we reveal (https://t.co/y0lSxQ23nU) a new approach to controlling chemoselectivity in synthesis. Imagine, if by simply changing the waveform by which electrical current were delivered one could control the selectivity of reduction of a functionally rich peptide like this?