Longqin Hu, Ph.D.
Affiliations: | 1999- | Medicinal Chemistry | Rutgers University, New Brunswick, New Brunswick, NJ, United States |
Area:
Medicinal ChemistryGoogle:
"Longqin Hu"Parents
Sign in to add mentorMichael Doughty | grad student | 1988-1993 | University of Kansas |
Roberta F. Colman | post-doc | 1993-1996 | University of Delaware |
Children
Sign in to add traineeYongying Jiang | grad student | 2005 | Rutgers, New Brunswick |
Xinghua Wu | grad student | 2008 | Rutgers, New Brunswick |
Herve Aloysius | grad student | 2014 | Rutgers, New Brunswick |
Lin Chen | grad student | 2014 | Rutgers, New Brunswick |
Daigo Inoyama | grad student | 2014 | Rutgers, New Brunswick |
Dhulfiqar Ali Abed | grad student | 2018 | Rutgers, New Brunswick |
Haifa Mohammed Albanyan | grad student | 2019 | Rutgers, New Brunswick |
Sumi Lee | grad student | 2019 | Rutgers, New Brunswick |
Ahmed R. Ali | grad student | 2021 | Rutgers, New Brunswick |
Jeffrey Yang | grad student | 2022 | Rutgers, New Brunswick |
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Publications
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Hu L, Albanyan H, Yang J, et al. (2024) Structure-activity relationships and pharmacokinetic evaluation of L-cystine diamides as L-cystine crystallization inhibitors for cystinuria. Medicinal Chemistry Research : An International Journal For Rapid Communications On Design and Mechanisms of Action of Biologically Active Agents. 33: 1384-1407 |
Hu L, Albanyan H, Yang J, et al. (2024) 8-l-Cystinyl Bis(1,8-diazaspiro[4.5]decane) as an Orally Bioavailable l-Cystine Crystallization Inhibitor for Cystinuria. Acs Medicinal Chemistry Letters. 15: 1026-1031 |
Lee S, Ali AR, Abed DA, et al. (2023) Structural modification of C2-substituents on 1,4-bis(arylsulfonamido)benzene or naphthalene-N,N'-diacetic acid derivatives as potent inhibitors of the Keap1-Nrf2 protein-protein interaction. European Journal of Medicinal Chemistry. 265: 116104 |
Yang J, Albanyan H, Wang Y, et al. (2023) Development of convenient crystallization inhibition assays for structure-activity relationship studies in the discovery of crystallization inhibitors. Medicinal Chemistry Research : An International Journal For Rapid Communications On Design and Mechanisms of Action of Biologically Active Agents. 32: 1391-1399 |
Abed DA, Ali AR, Lee S, et al. (2023) Optimization of the C2 substituents on the 1,4-bis(arylsulfonamido)naphthalene-N,N'-diacetic acid scaffold for better inhibition of Keap1-Nrf2 protein-protein interaction. European Journal of Medicinal Chemistry. 252: 115302 |
Xie T, Zahid H, Ali AR, et al. (2023) Inhibitors of Keap1-Nrf2 protein-protein interaction reduce estrogen responsive gene expression and oxidative stress in estrogen receptor-positive breast cancer. Toxicology and Applied Pharmacology. 116375 |
Wang J, Lam D, Yang J, et al. (2022) Discovery of mobocertinib, a new irreversible tyrosine kinase inhibitor indicated for the treatment of non-small-cell lung cancer harboring EGFR exon 20 insertion mutations. Medicinal Chemistry Research : An International Journal For Rapid Communications On Design and Mechanisms of Action of Biologically Active Agents. 1-16 |
Lee S, Abed DA, Nguyen MU, et al. (2022) Structure-activity relationships of 1,4-bis(arylsulfonamido)-benzene or naphthalene-N,N'-diacetic acids with varying C2-substituents as inhibitors of Keap1-Nrf2 protein-protein interaction. European Journal of Medicinal Chemistry. 237: 114380 |
Abed DA, Lee S, Wen X, et al. (2021) Optimization of 1,4-bis(arylsulfonamido)naphthalene-N,N'-diacetic acids as inhibitors of Keap1-Nrf2 protein-protein interaction to suppress neuroinflammation. Bioorganic & Medicinal Chemistry. 44: 116300 |
Lee S, Abed DA, Beamer LJ, et al. (2020) Development of a Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) Assay for the Inhibition of Keap1-Nrf2 Protein-Protein Interaction. Slas Discovery : Advancing Life Sciences R & D. 2472555220935816 |