![PDF) Corrigendum to “Pyridine containing M1 positive allosteric modulators with reduced plasma protein binding” [Bioorg. Med. Chem. Lett. 20 (2010) 657] | Lei Ma - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/43569239/mini_magick20190215-11310-1dxjnl5.png?1550292595 "PDF) Corrigendum to “Pyridine containing M1 positive allosteric modulators with reduced plasma protein binding” [Bioorg. Med. Chem. Lett. 20 (2010) 657] | Lei Ma - Academia.edu")
PDF) Corrigendum to “Pyridine containing M1 positive allosteric modulators with reduced plasma protein binding” [Bioorg. Med. Chem. Lett. 20 (2010) 657] | Lei Ma - Academia.edu
Publications_2012
Writing Your Next Medicinal Chemistry Article: Journal Bibliometrics and Guiding Principles for Industrial Authors | Journal of Medicinal Chemistry
Design, Synthesis, and Evaluation of Highly Potent FAK-Targeting PROTACs | ACS Medicinal Chemistry Letters
![PDF) Corrigendum to “Discovery and SAR of 2-amino-5-[(thiomethyl)aryl]thiazoles as potent and selective Itk inhibitors” [Bioorg. Med. Chem. Lett. 16 (2006) 2411–2415] | Tai-An Lin - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/52287160/mini_magick20190123-29662-11w8dly.png?1548247061 "PDF) Corrigendum to “Discovery and SAR of 2-amino-5-[(thiomethyl)aryl]thiazoles as potent and selective Itk inhibitors” [Bioorg. Med. Chem. Lett. 16 (2006) 2411–2415] | Tai-An Lin - Academia.edu")
PDF) Corrigendum to “Discovery and SAR of 2-amino-5-[(thiomethyl)aryl]thiazoles as potent and selective Itk inhibitors” [Bioorg. Med. Chem. Lett. 16 (2006) 2411–2415] | Tai-An Lin - Academia.edu
Bioorganic & Medicinal Chemistry Letters | Vol 21, Issue 21, Pages 6207-6614 (1 November 2011) | ScienceDirect.com by Elsevier
Publications – Santos Lab
Writing Your Next Medicinal Chemistry Article: Journal Bibliometrics and Guiding Principles for Industrial Authors
Corrigendum to “Novel purine-based fluoroaryl-1,2,3-triazoles as neuroprotecting agents: Synthesis, neuronal cell culture
![PDF) Corrigendum to “Synthesis and carbonic anhydrase inhibitory properties of novel chalcone substituted benzenesulfonamides” [Bioorg. Med. Chem. Lett. 26 (2016) 5867–5870]](https://i1.rgstatic.net/publication/318331613_Corrigendum_to_Synthesis_and_carbonic_anhydrase_inhibitory_properties_of_novel_chalcone_substituted_benzenesulfonamides_Bioorg_Med_Chem_Lett_26_2016_5867-5870/links/5e28005b92851c3aadcfb95e/largepreview.png "PDF) Corrigendum to “Synthesis and carbonic anhydrase inhibitory properties of novel chalcone substituted benzenesulfonamides” [Bioorg. Med. Chem. Lett. 26 (2016) 5867–5870]")
PDF) Corrigendum to “Synthesis and carbonic anhydrase inhibitory properties of novel chalcone substituted benzenesulfonamides” [Bioorg. Med. Chem. Lett. 26 (2016) 5867–5870]
Development of Highly Potent and Selective Steroidal Inhibitors and Degraders of CDK8 | ACS Medicinal Chemistry Letters
名古屋大学大学院創薬科学研究科 天然物化学分野
Bioorganic
Bioorganic & Medicinal Chemistry Letters | Vol 26, Issue 1, Pages 1-240 (1 January 2016) | ScienceDirect.com by Elsevier
Writing Your Next Medicinal Chemistry Article: Journal Bibliometrics and Guiding Principles for Industrial Authors | Journal of Medicinal Chemistry
The Dark Side of Fluorine | ACS Medicinal Chemistry Letters
CCHF | Publication
Bioorganic & Medicinal Chemistry Letters | Vol 28, Issue 14, Pages 2343-2576 (1 August 2018) | ScienceDirect.com by Elsevier
Bioorganic & Medicinal Chemistry Letters | Vol 26, Issue 15, Pages 3381-3830 (1 August 2016) | ScienceDirect.com by Elsevier
Portfolio of hits — Laboratory of Medicinal Chemistry — Ghent University
Bioorganic & Medicinal Chemistry Letters | Vol 30, Issue 17, 1 September 2020 | ScienceDirect.com by Elsevier
名古屋大学大学院創薬科学研究科 天然物化学分野
Writing Your Next Medicinal Chemistry Article: Journal Bibliometrics and Guiding Principles for Industrial Authors | Journal of Medicinal Chemistry
Dima Sabbah, Ph.D. PEER REVIEWED SCIENTIFIC ARTICLES (11SUBMITTED/ ACCEPTED/ PUBLISHED PEER REVIEWED ARTICLES) 1. Sweidan K.,
Figure 3, Summary of second generation small molecule 3CLpro inhibitors, some containing reactive warhead groups and known to have a covalent mode of action - Probe Reports from the NIH Molecular Libraries
