NCBI Taxonomy: 549416

Galipea (ncbi_taxid: 549416)

found 98 associated metabolites at genus taxonomy rank level.

Ancestor: Zanthoxyloideae

Child Taxonomies: Galipea ciliata, Galipea laxiflora, Galipea dasysperma, Galipea trifoliata, Galipea jasminiflora

Spinosin

6-((2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one

C28H32O15 (608.1741122)


Spinosin is a flavone C-glycoside that is flavone substituted by hydroxy groups at positions 5 and 4, a methoxy group at position 7 and a 2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl residue at position 6 via a C-glycosidic linkage. It has a role as a plant metabolite and an anxiolytic drug. It is a flavone C-glycoside, a dihydroxyflavone and a monomethoxyflavone. It is functionally related to a flavone. Spinosin is a natural product found in Clutia abyssinica, Galipea trifoliata, and other organisms with data available. A flavone C-glycoside that is flavone substituted by hydroxy groups at positions 5 and 4, a methoxy group at position 7 and a 2-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl residue at position 6 via a C-glycosidic linkage. Spinosyn a C-glycoside flavonoid isolated from the seeds of Zizyphus jujube, with neuroprotective effects. Spinosin inhibits Aβ1-42 production and aggregation via activating Nrf2/HO-1 pathway[1][2][3]. Spinosyn a C-glycoside flavonoid isolated from the seeds of Zizyphus jujube, with neuroprotective effects. Spinosin inhibits Aβ1-42 production and aggregation via activating Nrf2/HO-1 pathway[1][2][3].

   

Swertisin

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C22H22O10 (446.1212912)


Swertisin is a flavone C-glycoside that is 7-O-methylapigenin in which the hydrogen at position 6 has been replaced by a beta-D-glucosyl residue. It has a role as a plant metabolite, an adenosine A1 receptor antagonist, an anti-inflammatory agent, an antioxidant and a hypoglycemic agent. It is a flavone C-glycoside, a monosaccharide derivative, a polyphenol, a monomethoxyflavone and a dihydroxyflavone. It is functionally related to an apigenin. Swertisin is a natural product found in Carex fraseriana, Gentiana orbicularis, and other organisms with data available. A flavone C-glycoside that is 7-O-methylapigenin in which the hydrogen at position 6 has been replaced by a beta-D-glucosyl residue. Swertisin, a C-glucosylflavone isolated from Iris tectorum, is known to have antidiabetic, anti-inflammatory and antioxidant effects. Swertisin is an adenosine A1 receptor antagonist[1][2].

   

Vicenin 2

5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C27H30O15 (594.158463)


Constituent of lemons (Citrus limon). Vicenin 2 is found in many foods, some of which are common salsify, fenugreek, sweet orange, and cucumber. Vicenin 2 is found in citrus. Vicenin 2 is a constituent of lemons (Citrus limon) Vicenin 2 is an angiotensin-converting enzyme (ACE) inhibitor (IC50=43.83 μM) from the aerial parts of Desmodium styracifolium[1]. Vicenin 2 is an angiotensin-converting enzyme (ACE) inhibitor (IC50=43.83 μM) from the aerial parts of Desmodium styracifolium[1].

   

isospinosin

Isoswertisin 2-O-glucoside

C28H32O15 (608.1741122)


   

Schaftoside

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-(3,4,5-trihydroxyoxan-2-yl)-4H-chromen-4-one

C26H28O14 (564.1478988)


Apigenin 6-c-glucoside 8-c-riboside is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Apigenin 6-c-glucoside 8-c-riboside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 6-c-glucoside 8-c-riboside can be found in herbs and spices, which makes apigenin 6-c-glucoside 8-c-riboside a potential biomarker for the consumption of this food product. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1]. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1]. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1].

   

8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[(3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C28H32O15 (608.1741122)


8-Galactopyranosyl-6-glucopyranosyl-4,5-dihydroxy-7-methoxyflavone is found in pulses. 8-Galactopyranosyl-6-glucopyranosyl-4,5-dihydroxy-7-methoxyflavone is isolated from roots of Glycine max (soybean). Isolated from roots of Glycine max (soybean). Genkwanin 6-C-glucoside 8-C-galactoside is found in soy bean and pulses.

   

Spinosin

6-[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one

C28H32O15 (608.1741122)


   

7-O-Methylapigenin 6-C-beta-D-glucopyranoside

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C22H22O10 (446.1212912)


   

Vicenin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one

C27H30O15 (594.158463)


Isovitexin 8-C-beta-glucoside is a C-glycosyl compound that is isovitexin in which the hydrogen at position 8 is replaced by a beta-D-glucosyl residue. It has a role as a metabolite. It is a trihydroxyflavone and a C-glycosyl compound. It is functionally related to an isovitexin. Vicenin-2 is a natural product found in Carex fraseriana, Pseudarrhenatherum longifolium, and other organisms with data available. A C-glycosyl compound that is isovitexin in which the hydrogen at position 8 is replaced by a beta-D-glucosyl residue. Vicenin 2 is an angiotensin-converting enzyme (ACE) inhibitor (IC50=43.83 μM) from the aerial parts of Desmodium styracifolium[1]. Vicenin 2 is an angiotensin-converting enzyme (ACE) inhibitor (IC50=43.83 μM) from the aerial parts of Desmodium styracifolium[1].

   

Isoswertisin

8-beta-D-Glucopyranosyl-5-hydroxy-2- (4-hydroxyphenyl) -7-methoxy-4H-1-benzopyran-4-one

C22H22O10 (446.1212912)


   

Phebalosin

7-methoxy-8-(3-prop-1-en-2-yloxiran-2-yl)chromen-2-one

C15H14O4 (258.0892044)


   

Vitexin 2-O-xyloside

Vitexin 2-O-xyloside

C26H28O14 (564.1478988)


   

Swertisin 2-O-xyloside

Swertisin 2-O-xyloside

C27H30O14 (578.163548)


   

Isoschaftoside

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]-6-[(2S,3R,4S,5S)-3,4,5-trihydroxy-2-tetrahydropyranyl]-4-chromenone

C26H28O14 (564.1478988)


Corymboside, also known as 6-arabinopyranosyl-8-galactopyranosylapigenin, is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Corymboside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Corymboside can be found in a number of food items such as red bell pepper, carob, common wheat, and orange bell pepper, which makes corymboside a potential biomarker for the consumption of these food products. [Raw Data] CBA22_Isoschaftoside_neg_50eV_1-4_01_1416.txt [Raw Data] CBA22_Isoschaftoside_neg_40eV_1-4_01_1415.txt [Raw Data] CBA22_Isoschaftoside_neg_30eV_1-4_01_1414.txt [Raw Data] CBA22_Isoschaftoside_neg_20eV_1-4_01_1413.txt [Raw Data] CBA22_Isoschaftoside_neg_10eV_1-4_01_1366.txt [Raw Data] CBA22_Isoschaftoside_pos_50eV_1-4_01_1389.txt [Raw Data] CBA22_Isoschaftoside_pos_40eV_1-4_01_1388.txt [Raw Data] CBA22_Isoschaftoside_pos_30eV_1-4_01_1387.txt [Raw Data] CBA22_Isoschaftoside_pos_20eV_1-4_01_1386.txt [Raw Data] CBA22_Isoschaftoside_pos_10eV_1-4_01_1355.txt Isoschaftoside, a C-glycosylflavonoid from Desmodium uncinatum root exudate, can inhibit growth of germinated S. hermonthica radicles[1][2]. Isoschaftoside, a C-glycosylflavonoid from Desmodium uncinatum root exudate, can inhibit growth of germinated S. hermonthica radicles[1][2].

   

2-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-2-enal

NCGC00381269-01!2-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-2-enal

C15H14O4 (258.0892044)


   

2-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-2-enal

2-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-2-enal

C15H14O4 (258.0892044)


   

Vicenin 2

Vicenin 2

C27H30O15 (594.158463)


Annotation level-1

   

Isoswertisin 2-O-glucoside

Isoswertisin 2-O-glucoside

C28H32O15 (608.1741122)


   

6-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

6-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

C27H30O14 (578.163548)


   

8-[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

8-[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

C28H32O15 (608.1741122)


   

7-{[(2r)-3,3-dimethyloxiran-2-yl]methoxy}-8-[(2r,3r)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

7-{[(2r)-3,3-dimethyloxiran-2-yl]methoxy}-8-[(2r,3r)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

C19H20O5 (328.13106700000003)


   

8-(3-methylbut-2-enoyl)-2-oxochromen-7-yl 3-methylbut-2-enoate

8-(3-methylbut-2-enoyl)-2-oxochromen-7-yl 3-methylbut-2-enoate

C19H18O5 (326.1154178)


   

1,4',5',8,9',10-hexahydroxy-2',6-dimethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-[2,9'-bianthracene]-9,10'-dione

1,4',5',8,9',10-hexahydroxy-2',6-dimethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-[2,9'-bianthracene]-9,10'-dione

C36H32O13 (672.1842822)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

C26H28O14 (564.1478988)


   

7-methoxy-8-[(2s,3s)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

7-methoxy-8-[(2s,3s)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

C15H14O4 (258.0892044)


   

8-[2,2-dimethyl-5-(prop-1-en-2-yl)-1,3-dioxolan-4-yl]-7-methoxychromen-2-one

8-[2,2-dimethyl-5-(prop-1-en-2-yl)-1,3-dioxolan-4-yl]-7-methoxychromen-2-one

C18H20O5 (316.13106700000003)


   

7-[(3-methylbut-2-en-1-yl)oxy]-8-[(2s,3s)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

7-[(3-methylbut-2-en-1-yl)oxy]-8-[(2s,3s)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

C19H20O4 (312.13615200000004)


   

7-methoxy-8-(4-methylfuran-3-yl)chromen-2-one

7-methoxy-8-(4-methylfuran-3-yl)chromen-2-one

C15H12O4 (256.0735552)


   

7-[(3,3-dimethyloxiran-2-yl)methoxy]-8-[3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

7-[(3,3-dimethyloxiran-2-yl)methoxy]-8-[3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

C19H20O5 (328.13106700000003)


   

8-[(4s,5s)-2,2-dimethyl-5-(prop-1-en-2-yl)-1,3-dioxolan-4-yl]-7-methoxychromen-2-one

8-[(4s,5s)-2,2-dimethyl-5-(prop-1-en-2-yl)-1,3-dioxolan-4-yl]-7-methoxychromen-2-one

C18H20O5 (316.13106700000003)


   

6-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

6-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

C27H30O14 (578.163548)


   

8-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

8-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C26H28O14 (564.1478988)


   

7-{[(2s)-3,3-dimethyloxiran-2-yl]methoxy}-8-[(2s,3s)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

7-{[(2s)-3,3-dimethyloxiran-2-yl]methoxy}-8-[(2s,3s)-3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

C19H20O5 (328.13106700000003)


   

7-[(3-methylbut-2-en-1-yl)oxy]-8-[3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

7-[(3-methylbut-2-en-1-yl)oxy]-8-[3-(prop-1-en-2-yl)oxiran-2-yl]chromen-2-one

C19H20O4 (312.13615200000004)


   

8-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

8-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C26H28O14 (564.1478988)


   

8-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

8-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

C28H32O15 (608.1741122)