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targeted-therapy / targeted-therapyKinase Inhibitors and PROTACs

Nathanael Gray

纳撒尼尔·格雷

PhD

🏢Stanford University School of Medicine(斯坦福大学医学院)🌐USA

Professor, Department of Chemical and Systems Biology化学与系统生物学系教授

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h-index
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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Nathanael Gray is a world leader in kinase inhibitor design and targeted protein degradation. His laboratory has produced numerous clinical-stage kinase inhibitors and pioneered PROTAC degraders for oncogenic drivers, expanding the druggable proteome in cancer.

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🧪Research Fields 研究领域

Kinase Inhibitor Design激酶抑制剂设计
PROTACs蛋白降解靶向嵌合体
Targeted Protein Degradation靶向蛋白降解
Chemical Biology化学生物学

🎓Key Contributions 主要贡献

Selective Kinase Inhibitor Development

Designed highly selective inhibitors for kinases including CDK8, FGFR, and mutant EGFR variants, several of which have entered clinical trials for solid tumors.

PROTAC-Based Targeted Protein Degradation

Advanced PROTAC technology for degrading oncogenic kinases including BCR-ABL and BTK mutants, offering advantages over conventional inhibitors in overcoming resistance.

Representative Works 代表性著作

[1]

Allosteric inhibition of SHP2 phosphatase inhibits cancers driven by receptor tyrosine kinases

Nature (2016)

Identified allosteric SHP2 inhibitors with potent anti-tumor activity, enabling clinical development of SHP2 inhibitors for RAS-driven cancers.

[2]

PROTAC-induced degradation of mutant EGFR overcomes osimertinib resistance

Cancer Cell (2021)

Demonstrated PROTAC degraders can overcome drug resistance in EGFR-mutant NSCLC, validating degradation as a next-generation therapeutic strategy.

🏆Awards & Recognition 奖项与荣誉

🏆AACR Award for Outstanding Achievement in Chemistry in Cancer Research
🏆American Chemical Society Division of Medicinal Chemistry Award
🏆NIH Director's Pioneer Award

📄Data Sources 数据来源

Last updated: 2026-01-15 | All information from publicly available academic sources

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