NCBI Taxonomy: 1854018

Teucrium alyssifolium (ncbi_taxid: 1854018)

found 14 associated metabolites at species taxonomy rank level.

Ancestor: Teucrium

Child Taxonomies: none taxonomy data.

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).

   

Salvigenin

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

C18H16O6 (328.0947)


Salvigenin, also known as psathyrotin or 7-O-methylpectolinarigenin, 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, salvigenin is considered to be a flavonoid lipid molecule. Salvigenin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Salvigenin has been detected, but not quantified in, several different foods, such as rosemaries, mandarin orange (clementine, tangerine), common sages, sweet basils, and peppermints. This could make salvigenin a potential biomarker for the consumption of these foods. BioTransformer predicts that salvigenin is a product of tetramethylscutellarein metabolism via an O-dealkylation reaction catalyzed by CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP2E1, and CYP3A4 enzymes (PMID: 30612223). Salvigenin, also known as 5-hydroxy-6,7,4-trimethoxyflavone or 7-O-methylpectolinarigenin, 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, salvigenin is considered to be a flavonoid lipid molecule. Salvigenin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Salvigenin can be found in a number of food items such as sweet basil, mandarin orange (clementine, tangerine), common sage, and peppermint, which makes salvigenin a potential biomarker for the consumption of these food products. Salvigenin is a trimethoxyflavone that is scutellarein in which the hydroxy groups at positions 4, 6, and 7 are replaced by methoxy groups. It has a role as an autophagy inducer, an apoptosis inhibitor, an antilipemic drug, an immunomodulator, an antineoplastic agent, a neuroprotective agent, a hypoglycemic agent and a plant metabolite. It is a trimethoxyflavone and a monohydroxyflavone. It is functionally related to a scutellarein. Salvigenin is a natural product found in Liatris elegans, Achillea santolina, and other organisms with data available. See also: Tangerine peel (part of). A trimethoxyflavone that is scutellarein in which the hydroxy groups at positions 4, 6, and 7 are replaced by methoxy groups. Salvigenin is a natural polyphenolic compound, with neuroprotective effect. Salvigenin has antitumor cytotoxic and immunomodulatory properties. Salvigenin inhibits H2O2-induced cell apoptosis[1][2]. Salvigenin is a natural polyphenolic compound, with neuroprotective effect. Salvigenin has antitumor cytotoxic and immunomodulatory properties. Salvigenin inhibits H2O2-induced cell apoptosis[1][2].

   

Salvigenin

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

C18H16O6 (328.0947)


Salvigenin is a natural polyphenolic compound, with neuroprotective effect. Salvigenin has antitumor cytotoxic and immunomodulatory properties. Salvigenin inhibits H2O2-induced cell apoptosis[1][2]. Salvigenin is a natural polyphenolic compound, with neuroprotective effect. Salvigenin has antitumor cytotoxic and immunomodulatory properties. Salvigenin inhibits H2O2-induced cell apoptosis[1][2].

   

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.

   

16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

C22H28O7 (404.1835)


   

(2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate

(2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate

C24H30O9 (462.189)


   

(1r,2r,3r,6r,7r,15s,16s,19r)-3-(acetyloxy)-2,16-dihydroxy-2-(hydroxymethyl)-7,15-dimethyl-13,17-dioxapentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadeca-10(14),11-dien-19-yl acetate

(1r,2r,3r,6r,7r,15s,16s,19r)-3-(acetyloxy)-2,16-dihydroxy-2-(hydroxymethyl)-7,15-dimethyl-13,17-dioxapentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadeca-10(14),11-dien-19-yl acetate

C24H32O9 (464.2046)


   

3-(acetyloxy)-2,16-dihydroxy-2-(hydroxymethyl)-7,15-dimethyl-13,17-dioxapentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadeca-10(14),11-dien-19-yl acetate

3-(acetyloxy)-2,16-dihydroxy-2-(hydroxymethyl)-7,15-dimethyl-13,17-dioxapentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadeca-10(14),11-dien-19-yl acetate

C24H32O9 (464.2046)


   

(1'r,2r,3'r,6'r,7'r,15's,16'r,19'r)-16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

(1'r,2r,3'r,6'r,7'r,15's,16'r,19'r)-16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

C22H28O7 (404.1835)


   

(1'r,2r,3'r,6'r,7'r,15's,16's,19'r)-16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

(1'r,2r,3'r,6'r,7'r,15's,16's,19'r)-16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

C22H28O7 (404.1835)


   

(1'r,2r,3'r,6'r,7'r,15's,16's,19's)-16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

(1'r,2r,3'r,6'r,7'r,15's,16's,19's)-16',19'-dihydroxy-7',15'-dimethyl-13',17'-dioxaspiro[oxirane-2,2'-pentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadecane]-10'(14'),11'-dien-3'-yl acetate

C22H28O7 (404.1835)


   

(1r,2r,3r,6r,7r,15s,16s,19s)-3-(acetyloxy)-2,16-dihydroxy-2-(hydroxymethyl)-7,15-dimethyl-13,17-dioxapentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadeca-10(14),11-dien-19-yl acetate

(1r,2r,3r,6r,7r,15s,16s,19s)-3-(acetyloxy)-2,16-dihydroxy-2-(hydroxymethyl)-7,15-dimethyl-13,17-dioxapentacyclo[14.2.1.0¹,⁶.0⁷,¹⁵.0¹⁰,¹⁴]nonadeca-10(14),11-dien-19-yl acetate

C24H32O9 (464.2046)


   

[7-(acetyloxy)-6-[(acetyloxy)methyl]-5,6,9-trihydroxy-3b,9b-dimethyl-4-oxo-5h,7h,8h,9h,9ah,10h,11h-phenanthro[1,2-b]furan-5a-yl]methyl acetate

[7-(acetyloxy)-6-[(acetyloxy)methyl]-5,6,9-trihydroxy-3b,9b-dimethyl-4-oxo-5h,7h,8h,9h,9ah,10h,11h-phenanthro[1,2-b]furan-5a-yl]methyl acetate

C26H34O11 (522.2101)


   

7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate

7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate

C24H30O9 (462.189)