NCBI Taxonomy: 1284867

Ozothamnus stirlingii (ncbi_taxid: 1284867)

found 90 associated metabolites at species taxonomy rank level.

Ancestor: Ozothamnus

Child Taxonomies: none taxonomy data.

Pinocembrin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (S)-(-)-

C15H12O4 (256.0735552)


Pinocembrin is a dihydroxyflavanone in which the two hydroxy groups are located at positions 5 and 7. A natural product found in Piper sarmentosum and Cryptocarya chartacea. It has a role as an antioxidant, an antineoplastic agent, a vasodilator agent, a neuroprotective agent and a metabolite. It is a dihydroxyflavanone and a (2S)-flavan-4-one. Pinocembrin is a natural product found in Prunus leveilleana, Alpinia rafflesiana, and other organisms with data available. Pinocembrin is found in mexican oregano and is isolated from many plants including food plants. Pinocembrin belongs to the family of flavanones. These are compounds containing a flavan-3-one moiety, which structure is characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. A dihydroxyflavanone in which the two hydroxy groups are located at positions 5 and 7. A natural product found in Piper sarmentosum and Cryptocarya chartacea. Isolated from many plants including food plants. (S)-Pinocembrin is found in mexican oregano and pine nut. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1].

   

Pinobanksin

4H-1-BENZOPYRAN-4-ONE, 2,3-DIHYDRO-3,5,7-TRIHYDROXY-2-PHENYL-, (2R,3R)-

C15H12O5 (272.0684702)


Pinobanksin is a trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7. It has a role as an antimutagen, an antioxidant and a metabolite. It is a trihydroxyflavanone and a secondary alpha-hydroxy ketone. Pinobanksin is a natural product found in Populus koreana, Ozothamnus stirlingii, and other organisms with data available. Pinobanksin has apoptotic induction in a B-cell lymphoma cell line[1].

   

(E)-3-(2,3-Dihydroxyphenyl)-2-propenoic acid

(E)-3-(2,3-Dihydroxyphenyl)-2-propenoic acid

C9H8O4 (180.0422568)


(2e)-3-(2,3-dihydroxyphenyl)prop-2-enoic acid, also known as trans-2,3-dihydroxycinnamate or (2e)-3-(2,3-dihydroxyphenyl)acrylate, is a member of the class of compounds known as hydroxycinnamic acids. Hydroxycinnamic acids are compounds containing an cinnamic acid where the benzene ring is hydroxylated (2e)-3-(2,3-dihydroxyphenyl)prop-2-enoic acid is slightly soluble (in water) and a weakly acidic compound (based on its pKa). (2e)-3-(2,3-dihydroxyphenyl)prop-2-enoic acid exists in all living organisms, ranging from bacteria to humans. Identified in Anthemis nobilis (Roman chamomile

   

Pinobanksin acetate

4H-1-Benzopyran-4-one, 3-(acetyloxy)-2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R-trans)-

C17H14O6 (314.0790344)


Pinobanksin 3-O-acetate is a member of dihydroflavonols. 3-O-Acetylpinobanksin is a natural product found in Populus koreana, Ozothamnus stirlingii, and other organisms with data available. Pinobanksin 3-acetate is a one of Pinobanksin ester derivatives that can be isolated from Sonoran propolis[1].

   

2-Phenylethyl 3-phenyl-2-propenoate

2-Propenoic acid, 3-phenyl-, 2-phenylethyl ester

C17H16O2 (252.1150236)


2-Phenylethyl 3-phenyl-2-propenoate is a food flavour. It is isolated from the buds of Populus balsamifera (balsam poplar Food flavour. Isolated from the buds of Populus balsamifera (balsam poplar)

   

Liquidambaric

(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxidanylidene-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid

C30H46O3 (454.34467659999996)


Betulonic acid is a triterpenoid. It has a role as an anticoronaviral agent. Betulonic acid is a natural product found in Lantana camara, Ozothamnus stirlingii, and other organisms with data available. See also: Jujube fruit (part of). Betulonic acid (Betunolic acid), a naturally occurring triterpene, is found in many plants. Betulonic acid has anti-tumor, anti-inflammatory, antiparasitic and anti-viral (HSV-1) activities[2][1][3][4]. Betulonic acid (Betunolic acid), a naturally occurring triterpene, is found in many plants. Betulonic acid has anti-tumor, anti-inflammatory, antiparasitic and anti-viral (HSV-1) activities[2][1][3][4].

   

Betulonic acid

(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-Isopropenyl-5a,5b,8,8,11a-pentamethyl-9-oxo-eicosahydro-cyclopenta[a]chrysene-3a-carboxylic acid

C30H46O3 (454.34467659999996)


Betulonic acid (Betunolic acid), a naturally occurring triterpene, is found in many plants. Betulonic acid has anti-tumor, anti-inflammatory, antiparasitic and anti-viral (HSV-1) activities[2][1][3][4]. Betulonic acid (Betunolic acid), a naturally occurring triterpene, is found in many plants. Betulonic acid has anti-tumor, anti-inflammatory, antiparasitic and anti-viral (HSV-1) activities[2][1][3][4].

   

Pinobanksin

(2R) -2,3-Dihydro-3beta,5,7-trihydroxy-2alpha-phenyl-4H-1-benzopyran-4-one

C15H12O5 (272.0684702)


Pinobanksin is a trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7. It has a role as an antimutagen, an antioxidant and a metabolite. It is a trihydroxyflavanone and a secondary alpha-hydroxy ketone. Pinobanksin is a natural product found in Populus koreana, Ozothamnus stirlingii, and other organisms with data available. A trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7. Pinobanksin has apoptotic induction in a B-cell lymphoma cell line[1].

   

pinocembrine

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)-

C15H12O4 (256.0735552)


4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)- is a natural product found in Alpinia nutans, Alpinia zerumbet, and Boesenbergia rotunda with data available.

   

Pinocembrin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (S)-(-)-

C15H12O4 (256.0735552)


(2s)-pinocembrin, also known as 5,7-dihydroxyflavanone or dihydrochrysin, is a member of the class of compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Thus, (2s)-pinocembrin is considered to be a flavonoid lipid molecule (2s)-pinocembrin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (2s)-pinocembrin can be found in a number of food items such as acorn, lentils, mulberry, and sorghum, which makes (2s)-pinocembrin a potential biomarker for the consumption of these food products. (s)-pinocembrin, also known as 5,7-dihydroxyflavanone or dihydrochrysin, is a member of the class of compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3 (s)-pinocembrin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (s)-pinocembrin is a bitter tasting compound found in mexican oregano and tarragon, which makes (s)-pinocembrin a potential biomarker for the consumption of these food products. relative retention time with respect to 9-anthracene Carboxylic Acid is 1.069 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.067 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.071 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.070 5,7-Dihydroxyflavanone is a natural product found in Pinus contorta var. latifolia, Piper nigrum, and other organisms with data available. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. (±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1]. Pinocembrin ((+)-Pinocoembrin) is a flavonoid found in propolis, acts as a competitive inhibitor of histidine decarboxylase, and is an effective anti-allergic agent, with antioxidant, antimicrobial and anti-inflammatory properties[1].

   

Phenethyl cinnamate

2-Propenoic acid, 3-phenyl-, 2-phenylethyl ester

C17H16O2 (252.1150236)


   

2,3-dihydroxycinnamic acid

(2E)-3-(2,3-Dihydroxyphenyl)prop-2-enoate

C9H8O4 (180.0422568)


   

(2e)-3,7-dimethylocta-2,6-dien-1-yl 3-phenylprop-2-enoate

(2e)-3,7-dimethylocta-2,6-dien-1-yl 3-phenylprop-2-enoate

C19H24O2 (284.17762039999997)


   

(2r,3r)-5-acetyl-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl (2z)-2-methylbut-2-enoate

(2r,3r)-5-acetyl-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl (2z)-2-methylbut-2-enoate

C18H20O5 (316.13106700000003)


   

(2s)-2-(3-hydroxyprop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-2-(3-hydroxyprop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O5 (260.0684702)


   

(2s)-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O4 (244.0735552)


   

5-hydroxy-7-[4-(1-hydroxyethyl)phenoxy]-2-phenyl-2,3-dihydro-1-benzopyran-4-one

5-hydroxy-7-[4-(1-hydroxyethyl)phenoxy]-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C23H20O5 (376.13106700000003)


   

3-(4-hydroxy-3-methoxyphenyl)propyl (2e)-3-phenylprop-2-enoate

3-(4-hydroxy-3-methoxyphenyl)propyl (2e)-3-phenylprop-2-enoate

C19H20O4 (312.13615200000004)


   

(1r,3as,5ar,5br,7ar,11ar,11br,13ar,13br)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid

(1r,3as,5ar,5br,7ar,11ar,11br,13ar,13br)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysene-3a-carboxylic acid

C30H46O3 (454.34467659999996)


   

3-(3,4-dihydroxy-5-methoxyphenyl)propyl 3-phenylprop-2-enoate

3-(3,4-dihydroxy-5-methoxyphenyl)propyl 3-phenylprop-2-enoate

C19H20O5 (328.13106700000003)


   

3,7-dimethylocta-2,6-dien-1-yl 3-phenylprop-2-enoate

3,7-dimethylocta-2,6-dien-1-yl 3-phenylprop-2-enoate

C19H24O2 (284.17762039999997)


   

3-(4-hydroxy-3-methoxyphenyl)propyl 3-phenylprop-2-enoate

3-(4-hydroxy-3-methoxyphenyl)propyl 3-phenylprop-2-enoate

C19H20O4 (312.13615200000004)


   

2-(3-hydroxyprop-1-en-2-yl)-10-methoxy-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

2-(3-hydroxyprop-1-en-2-yl)-10-methoxy-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O6 (290.0790344)


   

(2s)-2-(3-hydroxyprop-1-en-2-yl)-10-methoxy-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-2-(3-hydroxyprop-1-en-2-yl)-10-methoxy-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O6 (290.0790344)


   

5-acetyl-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl 2-methylbut-2-enoate

5-acetyl-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl 2-methylbut-2-enoate

C18H20O5 (316.13106700000003)


   

(2e)-3-(4-hydroxy-5-methoxycyclohexa-2,4-dien-1-yl)prop-2-en-1-yl 3-phenylprop-2-enoate

(2e)-3-(4-hydroxy-5-methoxycyclohexa-2,4-dien-1-yl)prop-2-en-1-yl 3-phenylprop-2-enoate

C19H20O4 (312.13615200000004)


   

2-(3-hydroxyprop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

2-(3-hydroxyprop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O5 (260.0684702)


   

2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O4 (244.0735552)


   

3-(3,4-dihydroxy-5-methoxyphenyl)propyl (2e)-3-phenylprop-2-enoate

3-(3,4-dihydroxy-5-methoxyphenyl)propyl (2e)-3-phenylprop-2-enoate

C19H20O5 (328.13106700000003)


   

2-{10-methoxy-7-oxo-2h,3h-[1,4]dioxino[2,3-g]chromen-2-yl}prop-2-enal

2-{10-methoxy-7-oxo-2h,3h-[1,4]dioxino[2,3-g]chromen-2-yl}prop-2-enal

C15H12O6 (288.06338519999997)


   

(2e)-3,7-dimethylocta-2,6-dien-1-yl (2e)-3-phenylprop-2-enoate

(2e)-3,7-dimethylocta-2,6-dien-1-yl (2e)-3-phenylprop-2-enoate

C19H24O2 (284.17762039999997)


   

[5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-3a-yl]acetic acid

[5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-3a-yl]acetic acid

C31H48O3 (468.36032579999994)


   

(2s)-10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O5 (274.0841194)


   

[(1r,3ar,5ar,5br,7ar,11ar,11br,13ar,13br)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-3a-yl]acetic acid

[(1r,3ar,5ar,5br,7ar,11ar,11br,13ar,13br)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-3a-yl]acetic acid

C31H48O3 (468.36032579999994)


   

2-[(2s)-10-methoxy-7-oxo-2h,3h-[1,4]dioxino[2,3-g]chromen-2-yl]prop-2-enal

2-[(2s)-10-methoxy-7-oxo-2h,3h-[1,4]dioxino[2,3-g]chromen-2-yl]prop-2-enal

C15H12O6 (288.06338519999997)


   

(2s)-5-hydroxy-7-{4-[(1s)-1-hydroxyethyl]phenoxy}-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2s)-5-hydroxy-7-{4-[(1s)-1-hydroxyethyl]phenoxy}-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C23H20O5 (376.13106700000003)


   

10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

10-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O5 (274.0841194)