APA (7th ed.) Citation

Ghosh, A. K., Williams, J. N., Ho, R. Y., Simpson, H. M., Hattori, S., Hayashi, H., . . . Mitsuya, H. (2018). Design and Synthesis of Potent HIV‑1 Protease Inhibitors Containing Bicyclic Oxazolidinone Scaffold as the P2 Ligands: Structure–Activity Studies and Biological and X‑ray Structural Studies. Journal of medicinal chemistry, 61(21), 9722-9737. https://doi.org/10.1021/acs.jmedchem.8b01227

Chicago Style (17th ed.) Citation

Ghosh, Arun K., et al. "Design and Synthesis of Potent HIV‑1 Protease Inhibitors Containing Bicyclic Oxazolidinone Scaffold as the P2 Ligands: Structure–Activity Studies and Biological and X‑ray Structural Studies." Journal of Medicinal Chemistry 61, no. 21 (2018): 9722-9737. https://doi.org/10.1021/acs.jmedchem.8b01227.

MLA (9th ed.) Citation

Ghosh, Arun K., et al. "Design and Synthesis of Potent HIV‑1 Protease Inhibitors Containing Bicyclic Oxazolidinone Scaffold as the P2 Ligands: Structure–Activity Studies and Biological and X‑ray Structural Studies." Journal of Medicinal Chemistry, vol. 61, no. 21, 2018, pp. 9722-9737, https://doi.org/10.1021/acs.jmedchem.8b01227.