Songchun Jiang
Genomics Institute of the Novartis Research Foundation(US)
Publications by Year
Research Areas
Synthesis of Organic Compounds, Synthesis and biological activity, Synthesis and Biological Activity, Synthetic Organic Chemistry Methods, Quinazolinone synthesis and applications
Most-Cited Works
- → Discovery of 4-Aryl-4H-chromenes as a New Series of Apoptosis Inducers Using a Cell- and Caspase-based High-Throughput Screening Assay. 1. Structure−Activity Relationships of the 4-Aryl Group(2004)279 cited
- → Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure–activity relationships of the 7- and 5-, 6-, 8-positions(2005)270 cited
- → Structural basis of indisulam-mediated RBM39 recruitment to DCAF15 E3 ligase complex(2019)249 cited
- → A role for transferrin receptor in triggering apoptosis when targeted with gambogic acid(2005)211 cited
- → Discovery of 4-Aryl-4H-chromenes as a New Series of Apoptosis Inducers Using a Cell- and Caspase-Based High Throughput Screening Assay. 4. Structure–Activity Relationships of N-Alkyl Substituted Pyrrole Fused at the 7,8-Positions(2008)205 cited
- → Discovery of 4-Aryl-4H-chromenes as a New Series of Apoptosis Inducers Using a Cell- and Caspase-Based High-Throughput Screening Assay. 3. Structure−Activity Relationships of Fused Rings at the 7,8-Positions(2007)194 cited
- → Discovery of N-(4-Methoxyphenyl)-N,2-dimethylquinazolin-4-amine, a Potent Apoptosis Inducer and Efficacious Anticancer Agent with High Blood Brain Barrier Penetration(2009)122 cited
- → Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based HTS assay. Part 5: Modifications of the 2- and 3-positions(2007)103 cited
- → Rates of cooling and denudation of the Early Penglai Orogeny, Taiwan, as assessed by fission-track constraints(2000)97 cited
- → Discovery of 1-benzoyl-3-cyanopyrrolo[1,2-a]quinolines as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. Part 1: Structure–activity relationships of the 1- and 3-positions(2008)82 cited