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1. In vitro and in vivo characterization of a novel, highly potent p53-MDM2 inhibitor. Issue 20 (1st November 2018)

2. NP-MRD: the Natural Products Magnetic Resonance Database. Issue Volume 50:Issue D1(2022) (17th November 2021)

3. HMDB 5.0: the Human Metabolome Database for 2022. Issue Volume 50:Issue D1(2022) (19th November 2021)

4. Structural States of Hdm2 and HdmX: X‐ray Elucidation of Adaptations and Binding Interactions for Different Chemical Compound Classes. (27th May 2019)

5. Front Cover: Structural States of Hdm2 and HdmX: X‐ray Elucidation of Adaptations and Binding Interactions for Different Chemical Compound Classes (ChemMedChem 14/2019). (17th July 2019)

6. Discovery of a novel class of highly potent inhibitors of the p53–MDM2 interaction by structure-based design starting from a conformational argument. Issue 19 (1st October 2016)

7. Identification and optimisation of 4, 5-dihydrobenzo[1, 2-d:3, 4-d]bisthiazole and 4, 5-dihydrothiazolo[4, 5-h]quinazoline series of selective phosphatidylinositol-3 kinase alpha inhibitors. Issue 17 (1st September 2015)

10. ChemFOnt: the chemical functional ontology resource. Issue Volume 51:Issue D1(2023) (28th October 2022)