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Based on a high throughput screening hit, pyrrolopyrimidine inhibitors of the Akt kinase are explored.
Starting from a screening hit, two new JAK2 inhibitor chemotypes were designed by scaffold morphing.
Furthermore, we detail the optimization of a screening hit using ligand binding efficiency and log D.
A series of pyrimidones has been designed from a screening hit, and nanomolar inhibitors identified.
An orally active GPR4 antagonist 39c was developed, starting from a high throughput screening hit 1.
Herein, we establish structure activity relationships of 51 N-phenylphthalimide analogs of the screening hit 1.
Application of structure-based design to screening hit 1 yielded sub-micromolar inhibitors.
A screening hit 1 against Trypanosoma brucei methionyl-tRNA synthetase was optimized using a structure-guided approach.
Based on screening hit 1, a series of tricyclic quinoxalinones have been designed and evaluated for inhibition of PARP-1.
Beginning with a diaminotriazine screening hit, several series of novel, tricyclic gamma-secretase modulators (GSMs) were designed.
Optimization of an in-house screening hit gave compounds that exhibited potent binding affinity and functional activity at MCH-R1.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com