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6-Substituted Hexamethylene Amiloride (HMA) Derivatives as Potent and Selective Inhibitors of the Human Urokinase Plasminogen Activator for Use in Cancer | Journal of Medicinal Chemistry
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Recent advances in the chemistry of the phosphaethynolate and arsaethynolate anions - Dalton Transactions (RSC Publishing) DOI:10.1039/D1DT03994F
2020-2021 UCLA AAP yearbook - Flipbook by tsewit322 | FlipHTML5
6-Substituted Hexamethylene Amiloride (HMA) Derivatives as Potent and Selective Inhibitors of the Human Urokinase Plasminogen Activator for Use in Cancer | Journal of Medicinal Chemistry
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6-Substituted Hexamethylene Amiloride (HMA) Derivatives as Potent and Selective Inhibitors of the Human Urokinase Plasminogen Activator for Use in Cancer | Journal of Medicinal Chemistry
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2020-2021 UCLA AAP yearbook - Flipbook by tsewit322 | FlipHTML5
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Functional assignment of multiple catabolic pathways for d-apiose | Nature Chemical Biology
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Host casein kinase 1-mediated phosphorylation modulates phase separation of a rhabdovirus phosphoprotein and virus infection | eLife
6-Substituted Hexamethylene Amiloride (HMA) Derivatives as Potent and Selective Inhibitors of the Human Urokinase Plasminogen Activator for Use in Cancer. - Abstract - Europe PMC
6-Substituted Hexamethylene Amiloride (HMA) Derivatives as Potent and Selective Inhibitors of the Human Urokinase Plasminogen Activator for Use in Cancer | Journal of Medicinal Chemistry
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