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. 2022 Nov 22;16:4043–4060. doi: 10.2147/DDDT.S379205

Table 3.

In silico Pharmacokinetic Analysis: Absorption, Distribution, Metabolism, Excretion and Toxicity of FA2 and Acarbose

Properties Compounds Acarbose FA2
Absorption Water solubility Soluble Moderate
P-glycoprotein substrate No No
Log Kp (skin permeation) cm/s -16.29 -6.40
Blood-Brain Barrier No No
Gastro- Intestinal Absorption Low High
Distribution Subcellular localization Mitochondria Mitochondria
Metabolism CYP 3A2 Inhibitor No No
CYP 2C9 Inhibitor No Yes
CYP 2D6 Inhibitor No No
CYP 2C19 Inhibitor No Yes
CYP 3A4 Inhibitor No No
Excretion Renal OCT2 substrate No No
Toxicity Rat acute toxicity (LD50,mol/kg) 1.46 2.515
Oral Toxicity classification VI III
Ames toxicity No No