Eric Welin Email & Phone Number

San Diego, California, United States

I have worked to develop novel orally bioavailable CELMoD protein degraders and antibody-drug conjugates. I have experience using AI/ML models to optimize drug candidates to improve ADME/PK properties to maximize therapeutic windows to benefit patients.

Richardson, TX

I have established an organic chemistry laboratory at UT Dallas to pursue the total synthesis of natural products, with a focus on biologically active molecules. We have received funding from the Cancer Prevention & Research Institute of Texas (CPRIT) to pursue the total synthesis of a family of natural products and subsequently perform a series of.

Pasadena, CA

I led a team of synthetic chemists that completed the enantioselective total syntheses of jorunnamycin A and jorumycin, two anti-cancer alkaloid natural products. This highly collaborative effort also involved collaboration with medicinal chemists and cancer biologists at the University of California, Los Angeles for the design and testing of non-natural.

I graduated from the lab of David MacMillan working in the field of catalysis and organic methods development. I worked as a team to develop an enantioselective cyanoalkylation reaction, and later I led a team that discovered a novel C–O coupling reaction between aryl bromides and carboxylate nucleophiles mediated by nickel and iridium catalysts. Through.

Doctor Of Philosophy (Ph.D.), Organic Chemistry

Bachelor Of Science (B.S.), Chemistry