Youxuan Li, Ph.D.
Affiliations: | 2014 | Medical University of South Carolina, Charleston, SC, United States |
Area:
Medicinal ChemistryGoogle:
"Youxuan Li"Mean distance: 10.55 | S | N | B | C | P |
Parents
Sign in to add mentor| Patrick M. Woster | grad student | 2014 | MUSC | |
| (Discovery of histone deacetylase inhibitors with new zinc binding groups.) | ||||
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Publications
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| Nowotarski SL, Pachaiyappan B, Holshouser SL, et al. (2018) Corrigendum to "Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures" [Bioorg. Med. Chem. 23 (2015) 1601-1612]. Bioorganic & Medicinal Chemistry |
| Chen NH, Zhang YB, Huang XJ, et al. (2016) Drychampones A‒C: Three Meroterpenoids from Dryopteris championii. The Journal of Organic Chemistry |
| Luo W, Zhao T, Li Y, et al. (2016) A Micelle Fusion-Aggregation Assembly Approach to Mesoporous Carbon Materials with Rich Active Sites for Ultra-Sensitive Ammo-nia Sensing. Journal of the American Chemical Society |
| Zhang Y, Liu XH, Zhan YZ, et al. (2016) Synthesis and biological activities of novel 5-substituted-1,3,4-oxadiazole Mannich bases and bis-Mannich bases as ketol-acid reductoisomerase inhibitors. Bioorganic & Medicinal Chemistry Letters |
| Li Y, Woster PM. (2015) Discovery of a new class of histone deacetylase inhibitors with a novel zinc binding group. Medchemcomm. 6: 613-618 |
| Nowotarski SL, Pachaiyappan B, Holshouser SL, et al. (2015) Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures. Bioorganic & Medicinal Chemistry. 23: 1601-12 |
| Li Y, Woster PM. (2015) Discovery of a new class of histone deacetylase inhibitors with a novel zinc binding group Medchemcomm. 6: 613-618 |