APA (7th ed.) Citation

TA, E., JR, H., S, M., B, C., K, F., J, B., . . . R, V. (2004). Substituted 3-imidazo[1,2-a]pyridin-3-yl- 4-(1,2,3,4-tetrahydro-[1,4]diazepino-[6,7,1-hi]indol-7-yl)pyrrole-2,5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3. Journal of medicinal chemistry, 47(16), 3934. https://doi.org/10.1021/jm049768a

Chicago Style (17th ed.) Citation

TA, Engler, et al. "Substituted 3-imidazo[1,2-a]pyridin-3-yl- 4-(1,2,3,4-tetrahydro-[1,4]diazepino-[6,7,1-hi]indol-7-yl)pyrrole-2,5-diones as Highly Selective and Potent Inhibitors of Glycogen Synthase Kinase-3." Journal of Medicinal Chemistry 47, no. 16 (2004): 3934. https://doi.org/10.1021/jm049768a.

MLA (9th ed.) Citation

TA, Engler, et al. "Substituted 3-imidazo[1,2-a]pyridin-3-yl- 4-(1,2,3,4-tetrahydro-[1,4]diazepino-[6,7,1-hi]indol-7-yl)pyrrole-2,5-diones as Highly Selective and Potent Inhibitors of Glycogen Synthase Kinase-3." Journal of Medicinal Chemistry, vol. 47, no. 16, 2004, p. 3934, https://doi.org/10.1021/jm049768a.