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Fig. 3 | Bulletin of the National Research Centre

Fig. 3

From: Traditional uses, phytochemistry and pharmacology of genus Fritillaria—a review

Fig. 3Fig. 3Fig. 3Fig. 3Fig. 3

Structures of various other chemical compounds of genus Fritillaria: 119. pallidiflosides A, 120. pallidiflosides B, 121. pallidiflosides C, 122. pallidiflosides D, 123. pallidiflosides E, 124. pallidiflosides G, 125. pallidiflosides H, 126. pallidiflosides I, 127. spongipregnoloside A, 128. smilaxchinoside C, 129. timosaponin H1, 130. protobioside, 131. polygonatoside B3, 132. polyphyllin V, 133. deltonin, 134. parispseudoside B, 135. (25R)- 26-[β-D-glucopyranosyl]oxy]-3β-[(O-α-Lrhamnopyranosyl-(1/2)- β-D-glucopyranosyl)oxy]-cholesta-5,17-diene-16,22-dione, 136. (22S,25S)- 26-O-β-D-glucopyranosyl-22, 25-epoxyfurost-5-en-3β, 26-diol-3-O-[α-Lrhamnopyranosyl(1/2)]-β-D-glucopyranoside, 137. 26-O-β-D-glucopyranosyl-3,26-dihydroxy-(25R)- 5β-furost-12-on-20(22)- ene-3-O-α-L rhamnopyranosyl-(1/2)- β-D-glucopyranoside, 138. aspidistrin, 139. gastrodin, 140. 4-(β-D-glucopyranosyloxy) benzoic acid, 141. icariside D2, 142. uridine, 143. adenosine, 144. uracil, 145. (S)- β-L-phenylalanine, 146. arginine, 147. lysine, 148. tryptophan, 149. tyrosine, 150. histidine, 151. isoleucine, 152. glycine, 153. leucine, 154. valine, 155. oxyproline, 156. alanine, 157. glutamate, 158. threonine, 159. proline, 160. methionine, 161. serine, 162. aspartate, 163. cysteine, 164. phenylalanine, 165. ornithine, 166. meristic acid C14:0, 167. pentadecanoic acid C15:0, 168. palmitic acid C16:0, 169. palmitoleic acid C16:1, 170. stearic acid C18:0, 171. oleic acid C18:1, 172. linoleic acid C18:2, 173. linolenic acid C18:3, 174. α -monopalmitin, 175. diosmetin, 176. murrayone, 177. 1-O-β-D-glucopyranosyl-(2S,3R,4E,8Z)-2-[(2-hydroxyoctadecanoyl) amido]-4, 8-octadecadiene-1,3-diol, 178. fritenolide A, 179. fritenolide B, 180. fritenolide C, 181. fritenolide D, 182. fritenolide E

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