[Retracted] A Review of the Phytochemistry, Ethnobotany, Toxicology, and Pharmacological Potentials of Crescentia cujete L. (Bignoniaceae)

Figure 1

Structural representation of selected isolated compounds from C. cujete. [1] (2S, 3S)-3-hydroxy-5,6-dimethoxydehydroiso-α-lapachone; [2] (2R)-5,6-dimethoxydehydroiso-α-lapachone; [3] (2R)-5-methoxydehydroiso-α-lapachone; [4] 2-(l-hydroxyethyl)naphtho[2,3-β]furan-4,9-dione; [5] 5-hydroxy-2-(lhydroxyethyl)naphtho[2,3-β]furan-4,9-dione; [6] 2-isopropenylnaphtho[2,3-β]furan-4,9-dione; [7] 5-hydroxydehydroiso-α-lapachone; [8] Aucubin; [9] Plumieride; [10] Crescentia IV; [11] Agnuside; [12] Trans-cinnamic acid; [13] Crescentin I; [14] Crescentin II; [15] Crescentin III; [16] 6-Epi-aucubin; [17] Epi-eranthemoside; [18] Crescentiol A; [19] Crescentiol B; [20] Acteoside; [21] Sibirioside A; [22] (R)- 1-O-β-D-Glucopyranosyl-(1 ⟶ 6)-β-D-glucopyranosyl-1,3-octanediol; [23] 6-O-p-hydroybenzoyl)-D-glucose; [24] Acanthoside D; [25] β-D- glucopyranosyl benzoate; [26] (R)-1-O-β-D-glucopyranosyl-l,3-octanediol; [27] 1-O-trans-cinamoyl-β-D-glucopyranose; [28] β-D-fructofuranosyl 6-O-(p-hydroxybenzoyl) α-D-glucopyranoside; [29] Hexadecanoic acid.

(a)

(b)