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Youseung Shin

Scripps Research Institute

30

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1726

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Structural and Dynamic Elucidation of a Non-acid PPARg Partial Agonist: SR1988

2019
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Defining a conformational ensemble that directs activation of PPARγ

2018 Nature Communications
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베트남 하노이의 주거유형 변화와 고층 아파트단지 형성특성

2017
- Youseung Shin
- Mack-Joong Choi
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SR2067 Reveals a Unique Kinetic and Structural Signature for PPARγ Partial Agonism

2016 ACS Chemical Biology
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Design, Synthesis, and Biological Evaluation of Indole Biphenylcarboxylic Acids as PPARγ Antagonists.

2015 ACS Medicinal Chemistry Letters
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Pharmacological targeting of the mammalian clock regulates sleep architecture and emotional behaviour

2014 Nature Communications
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Synthesis and activity of substituted heteroaromatics as positive allosteric modulators for α4β2α5 nicotinic acetylcholine receptors.

2014 Bioorganic & Medicinal Chemistry Letters
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Design and synthesis of 1-aryl-5-anilinoindazoles as c-Jun N-terminal kinase inhibitors.

2013 Bioorganic & Medicinal Chemistry Letters
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Synthesis and SAR of 2,4-diaminopyrimidines as potent c-jun N-terminal kinase inhibitors

2012 MedChemComm
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Small Molecule Tertiary Amines as Agonists of the Nuclear Hormone Receptor Rev-erbα

2012 Bioorganic & Medicinal Chemistry Letters
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