Pharmacokinetic evaluation of callistemon viminalis derived natural compounds as targeted inhibitors against δ-opioid receptor and farnesyl transferase

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Journal: Lett Drug Design Discovery Year:2017 | Volume:14 | Issue:4 Page(s): 488-499

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Title

Pharmacokinetic evaluation of callistemon viminalis derived natural compounds as targeted inhibitors against δ-opioid receptor and farnesyl transferase

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Abstract

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Efficiency of vanillin in impeding metabolic adaptability and virulence of Candida albicans by inhibiting glyoxylate cycle, morphogenesis, and biofilm formation

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APA: Copy

. (2017). Pharmacokinetic evaluation of callistemon viminalis derived natural compounds as targeted inhibitors against δ-opioid receptor and farnesyl transferase. Lett Drug Design Discovery, 14(4), 488-499. SID. https://sid.ir/paper/783177/en

Vancouver: Copy

. Pharmacokinetic evaluation of callistemon viminalis derived natural compounds as targeted inhibitors against δ-opioid receptor and farnesyl transferase. Lett Drug Design Discovery[Internet]. 2017;14(4):488-499. Available from: https://sid.ir/paper/783177/en

IEEE: Copy

, “Pharmacokinetic evaluation of callistemon viminalis derived natural compounds as targeted inhibitors against δ-opioid receptor and farnesyl transferase,” Lett Drug Design Discovery, vol. 14, no. 4, pp. 488–499, 2017, [Online]. Available: https://sid.ir/paper/783177/en

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