NCBI Taxonomy: 2707900

Baccharis sect. Thymifoliae (ncbi_taxid: 2707900)

found 75 associated metabolites at section taxonomy rank level.

Ancestor: Baccharis subgen. Molina

Child Taxonomies: Baccharis thymifolia, Baccharis grisebachii

Nevadensin

5,7-Dihydroxy-6,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one

C18H16O7 (344.0895986)


Nevadensin, also known as pedunculin or 5,7-hydroxy-4,6,8-trimethoxyflavone, is a member of the class of compounds known as 8-o-methylated flavonoids. 8-o-methylated flavonoids are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone. Thus, nevadensin is considered to be a flavonoid lipid molecule. Nevadensin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Nevadensin can be found in peppermint and sweet basil, which makes nevadensin a potential biomarker for the consumption of these food products. Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2]. Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2].

   

Gardenin B

5-Hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one

C19H18O7 (358.10524780000003)


Gardenin b, also known as demethyltangeretin or 5-hydroxy-4,6,7,8-tetramethoxyflavone, is a member of the class of compounds known as 8-o-methylated flavonoids. 8-o-methylated flavonoids are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone. Thus, gardenin b is considered to be a flavonoid lipid molecule. Gardenin b is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Gardenin b can be found in mandarin orange (clementine, tangerine), peppermint, sweet basil, and winter savory, which makes gardenin b a potential biomarker for the consumption of these food products. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1]. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1].

   

Demethylnobiletin

4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-

C20H20O8 (388.115812)


Demethylnobiletin is an ether and a member of flavonoids. Demethylnobiletin is a natural product found in Clinopodium dalmaticum, Stachys aegyptiaca, and other organisms with data available. See also: Tangerine peel (part of); Citrus aurantium fruit rind (part of). Isolated from Citrus subspecies, Mentha piperita and Thymus species Demethylnobiletin is found in many foods, some of which are herbs and spices, winter savory, sweet orange, and peppermint. Demethylnobiletin is found in citrus. Demethylnobiletin is isolated from Citrus species, Mentha piperita and Thymus sp. 5-O-Demethylnobiletin (5-Demethylnobiletin), a polymethoxyflavone isolated from Citrus jambhiri Lush., is a direct inhibition of 5-LOX (IC50=0.1 μM), without affecting the expression of COX-2. 5-O-Demethylnobiletin (5-Demethylnobiletin) has anti-inflammatory activity, inhibits leukotriene B (4)(LTB4) formation in rat neutrophils and elastase release in human neutrophils with an IC50 of 0.35 μM[1]. 5-O-Demethylnobiletin (5-Demethylnobiletin), a polymethoxyflavone isolated from Citrus jambhiri Lush., is a direct inhibition of 5-LOX (IC50=0.1 μM), without affecting the expression of COX-2. 5-O-Demethylnobiletin (5-Demethylnobiletin) has anti-inflammatory activity, inhibits leukotriene B (4)(LTB4) formation in rat neutrophils and elastase release in human neutrophils with an IC50 of 0.35 μM[1]. 5-O-Demethylnobiletin (5-Demethylnobiletin), a polymethoxyflavone isolated from Citrus jambhiri Lush., is a direct inhibition of 5-LOX (IC50=0.1 μM), without affecting the expression of COX-2. 5-O-Demethylnobiletin (5-Demethylnobiletin) has anti-inflammatory activity, inhibits leukotriene B (4)(LTB4) formation in rat neutrophils and elastase release in human neutrophils with an IC50 of 0.35 μM[1].

   

Lysionotin

4H-1-Benzopyran-4-one, 5,7-dihydroxy-6,8-dimethoxy-2-(4-methoxyphenyl)-

C18H16O7 (344.0895986)


Nevadensin is a trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 8 and 4 and hydroxy groups at positions 5 and 7 respectively. It has a role as a plant metabolite. It is a trimethoxyflavone and a dihydroxyflavone. It is functionally related to a flavone. It is a conjugate acid of a nevadensin-7-olate. Nevadensin is a natural product found in Calanticaria bicolor, Gardenia resinifera, and other organisms with data available. A trimethoxyflavone that is flavone substituted by methoxy groups at positions 6, 8 and 4 and hydroxy groups at positions 5 and 7 respectively. Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2]. Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2].

   

GardeninB

4H-1-Benzopyran-4-one, 5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-

C19H18O7 (358.10524780000003)


Gardenin B is a tetramethoxyflavone that is tangeretin in which the methoxy group at position 5 has been replaced by a hydroxy group. It has a role as a plant metabolite. It is a tetramethoxyflavone and a monohydroxyflavone. It is functionally related to a tangeretin. Gardenin B is a natural product found in Citrus tankan, Chromolaena odorata, and other organisms with data available. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1]. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1].

   

Gardenin

4H-1-Benzopyran-4-one, 5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-

C19H18O7 (358.10524780000003)


Gardenin B is a tetramethoxyflavone that is tangeretin in which the methoxy group at position 5 has been replaced by a hydroxy group. It has a role as a plant metabolite. It is a tetramethoxyflavone and a monohydroxyflavone. It is functionally related to a tangeretin. Gardenin B is a natural product found in Citrus tankan, Chromolaena odorata, and other organisms with data available. A tetramethoxyflavone that is tangeretin in which the methoxy group at position 5 has been replaced by a hydroxy group. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1]. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1].

   

Demethylnobiletin

2- (3,4-Dimethoxyphenyl) -5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one

C20H20O8 (388.115812)


5-O-Demethylnobiletin (5-Demethylnobiletin), a polymethoxyflavone isolated from Citrus jambhiri Lush., is a direct inhibition of 5-LOX (IC50=0.1 μM), without affecting the expression of COX-2. 5-O-Demethylnobiletin (5-Demethylnobiletin) has anti-inflammatory activity, inhibits leukotriene B (4)(LTB4) formation in rat neutrophils and elastase release in human neutrophils with an IC50 of 0.35 μM[1]. 5-O-Demethylnobiletin (5-Demethylnobiletin), a polymethoxyflavone isolated from Citrus jambhiri Lush., is a direct inhibition of 5-LOX (IC50=0.1 μM), without affecting the expression of COX-2. 5-O-Demethylnobiletin (5-Demethylnobiletin) has anti-inflammatory activity, inhibits leukotriene B (4)(LTB4) formation in rat neutrophils and elastase release in human neutrophils with an IC50 of 0.35 μM[1]. 5-O-Demethylnobiletin (5-Demethylnobiletin), a polymethoxyflavone isolated from Citrus jambhiri Lush., is a direct inhibition of 5-LOX (IC50=0.1 μM), without affecting the expression of COX-2. 5-O-Demethylnobiletin (5-Demethylnobiletin) has anti-inflammatory activity, inhibits leukotriene B (4)(LTB4) formation in rat neutrophils and elastase release in human neutrophils with an IC50 of 0.35 μM[1].

   

Gardenin B

5-Hydroxy-6,7,8-trimethoxy-2- (4-methoxyphenyl) -4H-1-benzopyran-4-one

C19H18O7 (358.10524780000003)


Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1]. Gardenin B is a flavonoid isolated from Gardenia jasminoides. Gardenin B induces cell death in human leukemia cells involves multiple caspases[1].

   

Nevadensin

2- (4-Methoxyphenyl) -5,7-dihydroxy-6,8-dimethoxy-4H-1-benzopyran-4-one

C18H16O7 (344.0895986)


Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2]. Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2].

   

Lysionotin

4H-1-Benzopyran-4-one, 5,7-dihydroxy-6,8-dimethoxy-2-(4-methoxyphenyl)-

C18H16O7 (344.0895986)


Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2]. Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive[1][2].

   

2-(4-methylpent-3-en-1-yl)-6-[3-(2-oxo-5h-furan-3-yl)propylidene]hept-2-enedioic acid

2-(4-methylpent-3-en-1-yl)-6-[3-(2-oxo-5h-furan-3-yl)propylidene]hept-2-enedioic acid

C20H26O6 (362.17292960000003)


   

methyl (2e)-5-(furan-3-yl)-2-{3-[(3e,6r)-6-(2-hydroxypropan-2-yl)-2-oxooxan-3-ylidene]propyl}pent-2-enoate

methyl (2e)-5-(furan-3-yl)-2-{3-[(3e,6r)-6-(2-hydroxypropan-2-yl)-2-oxooxan-3-ylidene]propyl}pent-2-enoate

C21H28O6 (376.1885788)


   

(2e,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-ene-1,7-diol

(2e,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-ene-1,7-diol

C20H30O3 (318.21948299999997)


   

1,7-dimethyl (2e,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioate

1,7-dimethyl (2e,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioate

C22H30O5 (374.209313)


   

1,7-dimethyl (2e,6e)-2-[(3r)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

1,7-dimethyl (2e,6e)-2-[(3r)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

C22H32O7 (408.2147922)


   

(2z,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

(2z,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

C20H26O5 (346.17801460000004)


   

1,7-dimethyl (2e,6e)-2-[(3s)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

1,7-dimethyl (2e,6e)-2-[(3s)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

C22H32O7 (408.2147922)


   

[(2s,3r)-3-{2-[(2s,3r)-3-[2-(furan-3-yl)ethyl]-2-(hydroxymethyl)oxiran-2-yl]ethyl}-2-(4-methylpent-3-en-1-yl)oxiran-2-yl]methanol

[(2s,3r)-3-{2-[(2s,3r)-3-[2-(furan-3-yl)ethyl]-2-(hydroxymethyl)oxiran-2-yl]ethyl}-2-(4-methylpent-3-en-1-yl)oxiran-2-yl]methanol

C20H30O5 (350.209313)


   

(2e,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

(2e,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

C20H26O5 (346.17801460000004)


   

(2z)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

(2z)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

C20H26O5 (346.17801460000004)


   

6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioic acid

C20H26O5 (346.17801460000004)


   

2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioic acid

2-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioic acid

C22H28O7 (404.1834938)


   

1,7-dimethyl (2z,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioate

1,7-dimethyl (2z,6e)-6-[3-(furan-3-yl)propylidene]-2-(4-methylpent-3-en-1-yl)hept-2-enedioate

C22H30O5 (374.209313)


   

(2e,6e)-2-(4-methylpent-3-en-1-yl)-6-[3-(2-oxo-5h-furan-3-yl)propylidene]hept-2-enedioic acid

(2e,6e)-2-(4-methylpent-3-en-1-yl)-6-[3-(2-oxo-5h-furan-3-yl)propylidene]hept-2-enedioic acid

C20H26O6 (362.17292960000003)


   

(2s)-2-[(2r,5e)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

(2s)-2-[(2r,5e)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

C20H30O4 (334.214398)


   

(2r)-2-[(2s,5e)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

(2r)-2-[(2s,5e)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

C20H30O4 (334.214398)


   

1,7-dimethyl (2z,6e)-2-[(3r)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

1,7-dimethyl (2z,6e)-2-[(3r)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

C22H32O7 (408.2147922)


   

(2e,6e)-2-[(3z)-5-(acetyloxy)-4-methylpent-3-en-1-yl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioic acid

(2e,6e)-2-[(3z)-5-(acetyloxy)-4-methylpent-3-en-1-yl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioic acid

C22H28O7 (404.1834938)


   

(2r)-2-[(2s,3r,6s)-2-[2-(furan-3-yl)ethyl]-1,5-dioxaspiro[2.5]octan-6-yl]-6-methylhept-5-ene-1,2-diol

(2r)-2-[(2s,3r,6s)-2-[2-(furan-3-yl)ethyl]-1,5-dioxaspiro[2.5]octan-6-yl]-6-methylhept-5-ene-1,2-diol

C20H30O5 (350.209313)


   

(2e)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-enoic acid

(2e)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-enoic acid

C14H16O3 (232.1099386)


   

(2s)-2-[(2r)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

(2s)-2-[(2r)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

C20H30O4 (334.214398)


   

1,7-dimethyl (2z,6e)-2-[(3s)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

1,7-dimethyl (2z,6e)-2-[(3s)-3,4-dihydroxy-4-methylpentyl]-6-[3-(furan-3-yl)propylidene]hept-2-enedioate

C22H32O7 (408.2147922)


   

(2s)-2-[(2r,3s,6r)-2-[2-(furan-3-yl)ethyl]-1,5-dioxaspiro[2.5]octan-6-yl]-6-methylhept-5-ene-1,2-diol

(2s)-2-[(2r,3s,6r)-2-[2-(furan-3-yl)ethyl]-1,5-dioxaspiro[2.5]octan-6-yl]-6-methylhept-5-ene-1,2-diol

C20H30O5 (350.209313)


   

(2r)-2-[(2s)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

(2r)-2-[(2s)-5-[3-(furan-3-yl)propylidene]oxan-2-yl]-6-methylhept-5-ene-1,2-diol

C20H30O4 (334.214398)