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Garlic is a perennial plant of the amaryllis family that produces strong-smelling pungent bulbs from a strong tall stem of 25–70 cm and can be grown in mild climates. Garlic is commonly used as a spice in cooking and and in herbal medicine.
The physicochemical properties for the main five most bioactive phytochemicals in garlic (aliin, allicin, diallylsulfide, z-ajoene and 2-vinyl-4H-1,3-dithiin) were calculated based on the combination of Lipinski’s, Ghose’s, and Veber’s rules (L-Ro5, GF, VR), summarized as follow: molecular weight (160-500 Da); hydrogen bond donors ≤5; hydrogen bond acceptors ≤10; molar refractivity (40-130); lipophilicity (-0.4–5.6); rotatable bonds ≤ 10: polar surface area <140; total number of atoms (20-70) [51],[52],[53],[54]. These are described as an approximation for the pharmacokinetics of a molecule in the body. From garlic’s phytochemicals, 40% (aliin and z-ajoene) comply with all of the “drug-likeness” rules. The 60% (allicin, diallylsulfide, and 2-vinyl-4H-1,3-dithiin) violate the total number of atoms (<20), polar surface area (<40), and MW <160 Da. Accordingly, diallylsulfide is predicted to have the lowest GI, followed by 2-Vinyl-4H-1,3-dithiin and then, allicin.