NCBI Taxonomy: 53828

Apuleia (ncbi_taxid: 53828)

found 40 associated metabolites at genus taxonomy rank level.

Ancestor: Dialioideae

Child Taxonomies: Apuleia leiocarpa

D-Pinitol

(1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol

C7H14O6 (194.079)


Widely distributed in plants. Pinitol is a cyclitol, a cyclic polyol. It is a known anti-diabetic agent isolated from Sutherlandia frutescens leaves. D-Pinitol is a biomarker for the consumption of soy beans and other soy products. D-Pinitol is found in many foods, some of which are ginkgo nuts, carob, soy bean, and common pea. D-Pinitol is found in carob. D-Pinitol is widely distributed in plants.Pinitol is a cyclitol, a cyclic polyol. It is a known anti-diabetic agent isolated from Sutherlandia frutescens leaves. (Wikipedia). D-Pinitol is a biomarker for the consumption of soy beans and other soy products. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3]. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3].

   

Ayanin

4H-1-BENZOPYRAN-4-ONE, 5-HYDROXY-2-(3-HYDROXY-4-METHOXYPHENYL)-3,7-DIMETHOXY-

C18H16O7 (344.0896)


3,5-dihydroxy-3,4,7-trimethoxyflavone is a trimethoxyflavone that is quercetin in which the hydroxy groups at positions 3, 4 and 7 have been replaced by methoxy groups. It has a role as a plant metabolite. It is a dihydroxyflavone and a trimethoxyflavone. It is functionally related to a quercetin. It is a conjugate acid of a 3,5-dihydroxy-3,4,7-trimethoxyflavone(1-). Ayanin is a natural product found in Psiadia viscosa, Solanum pubescens, and other organisms with data available. A trimethoxyflavone that is quercetin in which the hydroxy groups at positions 3, 4 and 7 have been replaced by methoxy groups.

   

Oxyanin A

Oxyayanin A

C18H16O8 (360.0845)


A trihydroxyflavone that is flavone substituted by hydroxy groups at positioms 5, 2 and 5 and methoxy groups at positions 3, 7 and 4 respectively.

   

Oxyanin B

Oxyayanin-B

C18H16O8 (360.0845)


   

Pinitol

(1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentaol

C7H14O6 (194.079)


D-pinitol is the D-enantiomer of pinitol. It has a role as a geroprotector and a member of compatible osmolytes. It is functionally related to a 1D-chiro-inositol. It is an enantiomer of a L-pinitol. Methylinositol has been used in trials studying the treatment of Dementia and Alzheimers Disease. D-Pinitol is a natural product found in Aegialitis annulata, Senna macranthera var. micans, and other organisms with data available. A member of the class of methyl myo-inositols that is cyclohexane-1,2,3,4,5-pentol substituted by a methoxy group at position 6 (the 1R,2S,3S,4S,5S,6S-isomer). D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3]. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3].

   

5-O-Demethylapulein

5-O-Demethylapulein

C19H18O9 (390.0951)


   

leiocarpin

(6aS) -6abeta,12abeta-Dihydro-2,2-dimethyl-2H,6H- [ 1,3 ] dioxolo [ 5,6 ] benzofuro [ 3,2-c ] pyrano [ 2,3-h ] [ 1 ] benzopyran

C21H18O5 (350.1154)


   

5-O-Methyloxyayanin-A

2,5-Dihydroxy-3,4,5,7-tetramethoxyflavone

C19H18O8 (374.1002)


   

5-O-Demethylapulein

5-O-Demethylapulein

C19H18O9 (390.0951)


   

Apuleidin

2- (2,3-Dihydroxy-4-methoxyphenyl) -5-hydroxy-3,7-dimethoxy-4H-1-benzopyran-4-one

C18H16O8 (360.0845)


   

Apulein

2- (2,5-Dihydroxy-4-methoxyphenyl) -3,5,6,7-tetramethoxy-4H-1-benzopyran-4-one

C20H20O9 (404.1107)


   

Apuleirin

6-Hydroxy-2- (3-hydroxy-4,5-dimethoxyphenyl) -3,5,7-trimethoxy-4H-1-benzopyran-4-one

C20H20O9 (404.1107)


   

Apuleisin

2- (2,3-Dihydroxy-4-methoxyphenyl) -5,6-dihydroxy-3,7-dimethoxy-4H-1-benzopyran-4-one

C18H16O9 (376.0794)


   

Apuleitrin

5,6-Dihydroxy-2- (3-hydroxy-4,5-dimethoxyphenyl) -3,7-dimethoxy-4H-1-benzopyran-4-one

C19H18O9 (390.0951)


   

Benthamitin

3,5,6,7,2,4,5-Heptamethoxyflavone

C22H24O9 (432.142)


   

Oxyayanin A

2- (2,5-Dihydroxy-4-methoxyphenyl) -5-hydroxy-3,7-dimethoxy-4H-1-benzopyran-4-one

C18H16O8 (360.0845)


   

pinitol

(1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol

C7H14O6 (194.079)


D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3]. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3].

   

Oxyanin B

Oxyayanin B

C18H16O8 (360.0845)


A trihydroxyflavone that is flavone substituted by hydroxy groups at positioms 5, 6 and 3 and methoxy groups at positions 3, 7 and 4 respectively.

   

Oxyayanin B

4H-1-Benzopyran-4-one, 5,6-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,7-dimethoxy-

C18H16O8 (360.0845)


   

2-(2,5-diethoxy-4-methoxyphenyl)-3,5,6,7-tetramethoxychromen-4-one

2-(2,5-diethoxy-4-methoxyphenyl)-3,5,6,7-tetramethoxychromen-4-one

C24H28O9 (460.1733)


   

3,5,6,7-tetramethoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one

3,5,6,7-tetramethoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one

C22H24O9 (432.142)


   

3,5,7-trimethoxy-2-(2,4,5-trimethoxyphenyl)chromen-4-one

3,5,7-trimethoxy-2-(2,4,5-trimethoxyphenyl)chromen-4-one

C21H22O8 (402.1315)


   

2-(2,3-diethoxy-4-methoxyphenyl)-5,6-diethoxy-3,7-dimethoxychromen-4-one

2-(2,3-diethoxy-4-methoxyphenyl)-5,6-diethoxy-3,7-dimethoxychromen-4-one

C26H32O9 (488.2046)


   

(1s,2r,4s,5s)-6-methoxycyclohexane-1,2,3,4,5-pentol

(1s,2r,4s,5s)-6-methoxycyclohexane-1,2,3,4,5-pentol

C7H14O6 (194.079)


   

5-[6-(acetyloxy)-3,5,7-trimethoxy-4-oxochromen-2-yl]-2,3-dimethoxyphenyl acetate

5-[6-(acetyloxy)-3,5,7-trimethoxy-4-oxochromen-2-yl]-2,3-dimethoxyphenyl acetate

C24H24O11 (488.1319)


   

5-[5,6-bis(acetyloxy)-3,7-dimethoxy-4-oxochromen-2-yl]-2,3-dimethoxyphenyl acetate

5-[5,6-bis(acetyloxy)-3,7-dimethoxy-4-oxochromen-2-yl]-2,3-dimethoxyphenyl acetate

C25H24O12 (516.1268)


   

2-[2,3-bis(acetyloxy)-4-methoxyphenyl]-3,7-dimethoxy-4-oxochromen-5-yl acetate

2-[2,3-bis(acetyloxy)-4-methoxyphenyl]-3,7-dimethoxy-4-oxochromen-5-yl acetate

C24H22O11 (486.1162)


   

5-hydroxy-3,6,7-trimethoxy-2-(2,3,4-trimethoxyphenyl)chromen-4-one

5-hydroxy-3,6,7-trimethoxy-2-(2,3,4-trimethoxyphenyl)chromen-4-one

C21H22O9 (418.1264)


   

2-(3-hydroxy-4,5-dimethoxyphenyl)-3,5,6,7-tetramethoxychromen-4-one

2-(3-hydroxy-4,5-dimethoxyphenyl)-3,5,6,7-tetramethoxychromen-4-one

C21H22O9 (418.1264)


   

3,5,6,7-tetramethoxy-2-(2,3,4-trimethoxyphenyl)chromen-4-one

3,5,6,7-tetramethoxy-2-(2,3,4-trimethoxyphenyl)chromen-4-one

C22H24O9 (432.142)


   

3,6,7-trimethoxy-4-oxo-2-(2,3,4-trimethoxyphenyl)chromen-5-yl acetate

3,6,7-trimethoxy-4-oxo-2-(2,3,4-trimethoxyphenyl)chromen-5-yl acetate

C23H24O10 (460.1369)


   

2-[2,5-bis(acetyloxy)-4-methoxyphenyl]-3,7-dimethoxy-4-oxochromen-5-yl acetate

2-[2,5-bis(acetyloxy)-4-methoxyphenyl]-3,7-dimethoxy-4-oxochromen-5-yl acetate

C24H22O11 (486.1162)


   

4-(acetyloxy)-2-[5-(acetyloxy)-3,6,7-trimethoxy-4-oxochromen-2-yl]-5-methoxyphenyl acetate

4-(acetyloxy)-2-[5-(acetyloxy)-3,6,7-trimethoxy-4-oxochromen-2-yl]-5-methoxyphenyl acetate

C25H24O12 (516.1268)


   

(1s,3ar,3br,7r,9as,9br,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol

(1s,3ar,3br,7r,9as,9br,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol

C29H50O (414.3861)


   

(1s,14s)-7,7-dimethyl-6,12,18,20,24-pentaoxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²¹]tetracosa-2(11),3,5(10),8,15,17(21),22-heptaene

(1s,14s)-7,7-dimethyl-6,12,18,20,24-pentaoxahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²¹]tetracosa-2(11),3,5(10),8,15,17(21),22-heptaene

C21H18O5 (350.1154)


   

4-(acetyloxy)-2-methoxy-5-(3,5,7-trimethoxy-4-oxochromen-2-yl)phenyl acetate

4-(acetyloxy)-2-methoxy-5-(3,5,7-trimethoxy-4-oxochromen-2-yl)phenyl acetate

C23H22O10 (458.1213)


   

4-(acetyloxy)-5-methoxy-2-(3,5,6,7-tetramethoxy-4-oxochromen-2-yl)phenyl acetate

4-(acetyloxy)-5-methoxy-2-(3,5,6,7-tetramethoxy-4-oxochromen-2-yl)phenyl acetate

C24H24O11 (488.1319)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.3861)


   

5,6-dihydroxy-3,7-dimethoxy-2-(4-methoxy-2,3-diphenoxyphenyl)chromen-4-one

5,6-dihydroxy-3,7-dimethoxy-2-(4-methoxy-2,3-diphenoxyphenyl)chromen-4-one

C30H24O9 (528.142)


   

2-(acetyloxy)-6-[5,6-bis(acetyloxy)-3,7-dimethoxy-4-oxochromen-2-yl]-3-methoxyphenyl acetate

2-(acetyloxy)-6-[5,6-bis(acetyloxy)-3,7-dimethoxy-4-oxochromen-2-yl]-3-methoxyphenyl acetate

C26H24O13 (544.1217)