Design, Synthesis, and Structure–Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-phenyl)acetamides Based on the Reversed Amide Scaffold.

MLA

Rahman, Md Toufiqur, et al. “Design, Synthesis, and Structure–Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-Phenyl)Acetamides Based on the Reversed Amide Scaffold.” ACS Chemical Neuroscience, vol. 15, no. 1, Jan. 2024, pp. 169–92. EBSCOhost, https://doi.org/10.1021/acschemneuro.3c00684.

APA

Rahman, M. T., Guan, D., Chaminda Lakmal, H. H., Decker, A. M., Imler, G. H., Kerr, A. T., Harris, D. L., & Jin, C. (2024). Design, Synthesis, and Structure–Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-phenyl)acetamides Based on the Reversed Amide Scaffold. ACS Chemical Neuroscience, 15(1), 169–192. https://doi.org/10.1021/acschemneuro.3c00684

Chicago

Rahman, Md Toufiqur, Dongliang Guan, Hetti Handi Chaminda Lakmal, Ann M. Decker, Gregory H. Imler, Andrew T. Kerr, Danni L. Harris, and Chunyang Jin. 2024. “Design, Synthesis, and Structure–Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-Phenyl)Acetamides Based on the Reversed Amide Scaffold.” ACS Chemical Neuroscience 15 (1): 169–92. doi:10.1021/acschemneuro.3c00684.