NCBI Taxonomy: 1209879

Teucrium orientale (ncbi_taxid: 1209879)

found 29 associated metabolites at species taxonomy rank level.

Ancestor: Teucrium

Child Taxonomies: Teucrium orientale var. orientale, Teucrium orientale var. puberulens, Teucrium orientale subsp. glabrescens, Teucrium orientale subsp. gloeotrichum

beta-Sitosterol 3-O-beta-D-galactopyranoside

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.439)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. beta-Sitosterol 3-O-beta-D-galactopyranoside is found in herbs and spices. beta-Sitosterol 3-O-beta-D-galactopyranoside is a constituent of Hibiscus sabdariffa (roselle) leaves. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Cirsilineol

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

C18H16O7 (344.0896)


Cirsilineol, also known as 4,5-dihydroxy-3,6,7-trimethoxy-flavone or anisomelin, is a member of the class of compounds known as 7-o-methylated flavonoids. 7-o-methylated flavonoids are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, cirsilineol is considered to be a flavonoid lipid molecule. Cirsilineol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Cirsilineol can be found in a number of food items such as common thyme, tarragon, common sage, and hyssop, which makes cirsilineol a potential biomarker for the consumption of these food products. Cirsilineol is a bioactive flavone isolated from Artemisia and from Teucrium gnaphalodes . Cirsilineol is a trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7 and 3 and hydroxy groups at positions 5 and 4 respectively. It has a role as a plant metabolite and an antineoplastic agent. It is a trimethoxyflavone and a dihydroxyflavone. It is functionally related to a flavone. Cirsilineol is a natural product found in Thymus herba-barona, Salvia tomentosa, and other organisms with data available. See also: Tangerine peel (part of).

   

Eupatorin

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

C18H16O7 (344.0896)


Eupatorin, also known as 3,5-dihydroxy-4,6,7-trimethoxyflavone, is a member of the class of compounds known as 7-o-methylated flavonoids. 7-o-methylated flavonoids are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, eupatorin is considered to be a flavonoid lipid molecule. Eupatorin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Eupatorin can be found in lemon verbena, mandarin orange (clementine, tangerine), and peppermint, which makes eupatorin a potential biomarker for the consumption of these food products. Eupatorin, a naturally occurring flavone, arrests cells at the G2-M phase of the cell cycle and induces apoptotic cell death involving activation of multiple caspases, mitochondrial release of cytochrome c and poly(ADP-ribose) polymerase cleavage[1]. Eupatorin, a naturally occurring flavone, arrests cells at the G2-M phase of the cell cycle and induces apoptotic cell death involving activation of multiple caspases, mitochondrial release of cytochrome c and poly(ADP-ribose) polymerase cleavage[1].

   

Eupatorin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,7-dimethoxy- (9CI)

C18H16O7 (344.0896)


Eupatorin is a trimethoxyflavone that is 6-hydroxyluteolin in which the phenolic hydogens at positions 4, 6 and 7 have been replaced by methyl groups. It has a role as a Brassica napus metabolite, an apoptosis inducer, a vasodilator agent, a calcium channel blocker, an anti-inflammatory agent, a P450 inhibitor and an antineoplastic agent. It is a dihydroxyflavone, a trimethoxyflavone and a polyphenol. It is functionally related to a 6-hydroxyluteolin. Eupatorin is a natural product found in Eupatorium album, Eupatorium altissimum, and other organisms with data available. A trimethoxyflavone that is 6-hydroxyluteolin in which the phenolic hydogens at positions 4, 6 and 7 have been replaced by methyl groups. Eupatorin, a naturally occurring flavone, arrests cells at the G2-M phase of the cell cycle and induces apoptotic cell death involving activation of multiple caspases, mitochondrial release of cytochrome c and poly(ADP-ribose) polymerase cleavage[1]. Eupatorin, a naturally occurring flavone, arrests cells at the G2-M phase of the cell cycle and induces apoptotic cell death involving activation of multiple caspases, mitochondrial release of cytochrome c and poly(ADP-ribose) polymerase cleavage[1].

   

harpagide

(7S)-4a,5,7-trihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl D-glucopyranoside

C15H24O10 (364.1369)


Origin: Plant; SubCategory_DNP: Monoterpenoids, Harpagide monoterpenoids Harpagide is a class of iridoid glycoside isolated from Scrophularia ningpoensis and has antiparasitic activity, which exhibits good in vitro trypanocidal activities against African trypanosomes (T.b. rhodesiense) with an IC50 of 21 μg/mL. Harpagide exerts significant antileishmanial activity against L. donovani with an IC50 value of 2.0 μg/mL. Harpagide also possess significant anti-inflammatory activities[1][2]. Harpagide is a class of iridoid glycoside isolated from Scrophularia ningpoensis and has antiparasitic activity, which exhibits good in vitro trypanocidal activities against African trypanosomes (T.b. rhodesiense) with an IC50 of 21 μg/mL. Harpagide exerts significant antileishmanial activity against L. donovani with an IC50 value of 2.0 μg/mL. Harpagide also possess significant anti-inflammatory activities[1][2].

   

beta-Sitosterol 3-O-beta-D-galactopyranoside

2-{[14-(5-ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.439)


   

ST 29:1;O;Hex

stigmast-5-en-3beta-yl beta-D-galactopyranoside

C35H60O6 (576.439)


   

Cirsilineol

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

C18H16O7 (344.0896)


Cirsilineol is a trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7 and 3 and hydroxy groups at positions 5 and 4 respectively. It has a role as a plant metabolite and an antineoplastic agent. It is a trimethoxyflavone and a dihydroxyflavone. It is functionally related to a flavone. Cirsilineol is a natural product found in Thymus herba-barona, Salvia tomentosa, and other organisms with data available. See also: Tangerine peel (part of). A trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7 and 3 and hydroxy groups at positions 5 and 4 respectively.

   

(4as,7s,7ar)-4a,5-dihydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate

(4as,7s,7ar)-4a,5-dihydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate

C17H26O11 (406.1475)


   

(1r,2s,4as,5r,6r,8r,8ar)-2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,6,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydrospiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

(1r,2s,4as,5r,6r,8r,8ar)-2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,6,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydrospiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

C24H32O10 (480.1995)


   

(2r,3as,4r,6s,6ar,7r,10as)-6-(acetyloxy)-2-(furan-3-yl)-2-hydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

(2r,3as,4r,6s,6ar,7r,10as)-6-(acetyloxy)-2-(furan-3-yl)-2-hydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

C24H30O9 (462.189)


   

(1's,2r,6'r,7's,9's,11's,13's)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

(1's,2r,6'r,7's,9's,11's,13's)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

C22H26O8 (418.1628)


   

2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,6,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydrospiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,6,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydrospiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

C24H32O10 (480.1995)


   

(1'r,2r,6'r,7's,9's,11'r,13'r)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

(1'r,2r,6'r,7's,9's,11'r,13'r)-11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

C22H26O8 (418.1628)


   

6-(acetyloxy)-2-(furan-3-yl)-2-hydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

6-(acetyloxy)-2-(furan-3-yl)-2-hydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

C24H30O9 (462.189)


   

(1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one

(1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one

C20H28O7 (380.1835)


   

2-(furan-3-yl)-2,6-dihydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

2-(furan-3-yl)-2,6-dihydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

C22H28O8 (420.1784)


   

11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

11'-(furan-3-yl)-7'-hydroxy-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

C22H26O8 (418.1628)


   

(2s,3r,4s,5s,6r)-2-{[(4ar,5s,7r,7ar)-4a,5-dihydroxy-7-methyl-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-{[(4ar,5s,7r,7ar)-4a,5-dihydroxy-7-methyl-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C15H24O9 (348.142)


   

(1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

(1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

C22H30O8 (422.1941)


   

(4as,5s,7s,7as)-4a,5-dihydroxy-7-methyl-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h-cyclopenta[c]pyran-7a-yl acetate

(4as,5s,7s,7as)-4a,5-dihydroxy-7-methyl-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h-cyclopenta[c]pyran-7a-yl acetate

C17H26O11 (406.1475)


   

(1r,2s,4as,5s,6s,8r,8ar)-2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,8-dihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

(1r,2s,4as,5s,6s,8r,8ar)-2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,8-dihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

C24H32O9 (464.2046)


   

5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

C22H30O8 (422.1941)


   

4a,5-dihydroxy-7-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h-cyclopenta[c]pyran-7a-yl acetate

4a,5-dihydroxy-7-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h-cyclopenta[c]pyran-7a-yl acetate

C17H26O11 (406.1475)


   

(2r,3as,4r,6s,6ar,7r,10as)-2-(furan-3-yl)-2,6-dihydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

(2r,3as,4r,6s,6ar,7r,10as)-2-(furan-3-yl)-2,6-dihydroxy-3a,4-dimethyl-8-oxo-hexahydrospiro[naphtho[4a,4-b]furan-7,2'-oxiran]-6a-ylmethyl acetate

C22H28O8 (420.1784)


   

(1's,2r,6'r,7's,9'r,11's,13's)-7'-(acetyloxy)-11'-(furan-3-yl)-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

(1's,2r,6'r,7's,9'r,11's,13's)-7'-(acetyloxy)-11'-(furan-3-yl)-9',13'-dimethyl-4'-oxo-10',14'-dioxaspiro[oxirane-2,5'-tetracyclo[9.2.1.0¹,⁶.0⁹,¹³]tetradecan]-6'-ylmethyl acetate

C24H28O9 (460.1733)


   

2-{[(4as,7s)-4a,5,7-trihydroxy-7-methyl-1h,5h,6h,7ah-cyclopenta[c]pyran-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{[(4as,7s)-4a,5,7-trihydroxy-7-methyl-1h,5h,6h,7ah-cyclopenta[c]pyran-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C15H24O10 (364.1369)


   

2-({4a,5-dihydroxy-7-methyl-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

2-({4a,5-dihydroxy-7-methyl-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C15H24O9 (348.142)


   

2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,8-dihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

2-(acetyloxy)-5-[2-(furan-3-yl)ethyl]-4a,8-dihydroxy-5,6-dimethyl-7-oxo-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-8a-ylmethyl acetate

C24H32O9 (464.2046)