APA (7th ed.) Citation

Pallavi, P., Pretze, M., Li, Y., Hofmann, B. B., Stamellou, E., Wängler, C., . . . Kälsch, A. (2018). Analyses of synthetic N-acyl dopamine derivatives revealing different structural requirements for their anti-inflammatory and transient-receptor-potential-channel-of-the-vanilloid-receptor-subfamily-subtype-1 (TRPV1)-activating properties. Journal of medicinal chemistry, 61(7), . https://doi.org/10.1021/acs.jmedchem.8b00156

Chicago Style (17th ed.) Citation

Pallavi, Prama, et al. "Analyses of Synthetic N-acyl Dopamine Derivatives Revealing Different Structural Requirements for Their Anti-inflammatory and Transient-receptor-potential-channel-of-the-vanilloid-receptor-subfamily-subtype-1 (TRPV1)-activating Properties." Journal of Medicinal Chemistry 61, no. 7 (2018). https://doi.org/10.1021/acs.jmedchem.8b00156.

MLA (9th ed.) Citation

Pallavi, Prama, et al. "Analyses of Synthetic N-acyl Dopamine Derivatives Revealing Different Structural Requirements for Their Anti-inflammatory and Transient-receptor-potential-channel-of-the-vanilloid-receptor-subfamily-subtype-1 (TRPV1)-activating Properties." Journal of Medicinal Chemistry, vol. 61, no. 7, 2018, https://doi.org/10.1021/acs.jmedchem.8b00156.