NCBI Taxonomy: 180071

Morina chinensis (ncbi_taxid: 180071)

found 64 associated metabolites at species taxonomy rank level.

Ancestor: Morina

Child Taxonomies: none taxonomy data.

Pinoresinol

PHENOL, 4,4-(TETRAHYDRO-1H,3H-FURO(3,4-C)FURAN-1,4-DIYL)BIS(2-METHOXY-, (1S-(1.ALPHA.,3A.ALPHA.,4.BETA.,6A.ALPHA.))-

C20H22O6 (358.1416312)


Epipinoresinol is an enantiomer of pinoresinol having (+)-(1R,3aR,4S,6aR)-configuration. It has a role as a plant metabolite and a marine metabolite. Epipinoresinol is a natural product found in Pandanus utilis, Abeliophyllum distichum, and other organisms with data available. An enantiomer of pinoresinol having (+)-(1R,3aR,4S,6aR)-configuration. (+)-pinoresinol is an enantiomer of pinoresinol having (+)-1S,3aR,4S,6aR-configuration. It has a role as a hypoglycemic agent, a plant metabolite and a phytoestrogen. Pinoresinol is a natural product found in Pandanus utilis, Zanthoxylum beecheyanum, and other organisms with data available. See also: Acai fruit pulp (part of). An enantiomer of pinoresinol having (+)-1S,3aR,4S,6aR-configuration. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.907 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.905 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.897 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.895 Pinoresinol is a lignol of plant origin serving for defense in a caterpillar. Pinoresinol drastically sensitizes cancer cells against TNF-related apoptosis-inducing ligand (TRAIL) -induced apoptosis[1][2]. Pinoresinol is a lignol of plant origin serving for defense in a caterpillar. Pinoresinol drastically sensitizes cancer cells against TNF-related apoptosis-inducing ligand (TRAIL) -induced apoptosis[1][2].

   

3-(4-Methoxyphenyl)-2-propenal

2-Propenal,3-(4-methoxyphenyl)-, (2E)-

C10H10O2 (162.06807600000002)


Isolated from oil of tarragon (Artemisia dracunculus) and other oils. Flavouring ingredient. 3-(4-Methoxyphenyl)-2-propenal is found in many foods, some of which are tarragon, star anise, potato, and sweet basil. 3-(4-Methoxyphenyl)-2-propenal is found in potato. 3-(4-Methoxyphenyl)-2-propenal is isolated from oil of tarragon (Artemisia dracunculus) and other oils. 3-(4-Methoxyphenyl)-2-propenal is a flavouring ingredien 4-Methoxycinnamaldehyde (p-Methoxycinnamaldehyde), an active constituent of Agastache rugosa, exhibits cytoprotective activity against respiratory syncytial virus (RSV) in human larynx carcinoma cell line. 4-Methoxycinnamaldehyde effectively inhibits cytopathic effect of RSV with an estimated IC50 of 0.055 μg/mL[1]. 4-Methoxycinnamaldehyde (p-Methoxycinnamaldehyde), an active constituent of Agastache rugosa, exhibits cytoprotective activity against respiratory syncytial virus (RSV) in human larynx carcinoma cell line. 4-Methoxycinnamaldehyde effectively inhibits cytopathic effect of RSV with an estimated IC50 of 0.055 μg/mL[1].

   

(+)-lariciresinol

4-[(2S,3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol

C20H24O6 (360.1572804)


(+)-Lariciresinol belongs to the class of organic compounds known as 7,9-epoxylignans. These are lignans that contain the 7,9-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at positons 2, 3 and 4, respectively. (+)-Lariciresinol has been detected in several different foods, such as parsnips, white mustards, narrowleaf cattails, turnips, and common sages. This could make (+)-Lariciresinol a potential biomarker for the consumption of these foods. Lariciresinol is also found in sesame seeds, Brassica vegetables, in the bark and wood of white fir (Abies alba). (+)-lariciresinol is a member of the class of compounds known as 7,9-epoxylignans. 7,9-epoxylignans are lignans that contain the 7,9-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at the 2-, 3-, 4-position, respectively (+)-lariciresinol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (+)-lariciresinol can be found in a number of food items such as pili nut, lemon balm, root vegetables, and parsley, which makes (+)-lariciresinol a potential biomarker for the consumption of these food products.

   

Pinoresinol

Phenol,4-(tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl)bis[2-methoxy-, [1S-(1.alpha.,3a.alpha.,4.alpha.,6a.alpha.)]-

C20H22O6 (358.1416312)


4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol is a natural product found in Zanthoxylum riedelianum, Forsythia suspensa, and other organisms with data available. Pinoresinol is a lignol of plant origin serving for defense in a caterpillar. Pinoresinol drastically sensitizes cancer cells against TNF-related apoptosis-inducing ligand (TRAIL) -induced apoptosis[1][2]. Pinoresinol is a lignol of plant origin serving for defense in a caterpillar. Pinoresinol drastically sensitizes cancer cells against TNF-related apoptosis-inducing ligand (TRAIL) -induced apoptosis[1][2].

   

Lariciresinol

4-{4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl}-2-methoxyphenol

C20H24O6 (360.1572804)


(-)-lariciresinol is a member of the class of compounds known as 7,9-epoxylignans. 7,9-epoxylignans are lignans that contain the 7,9-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at the 2-, 3-, 4-position, respectively (-)-lariciresinol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (-)-lariciresinol can be found in a number of food items such as cassava, acorn, celeriac, and banana, which makes (-)-lariciresinol a potential biomarker for the consumption of these food products.

   

Lariciresinol

3-Furanmethanol, tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-, (2R-(2alpha,3beta,4beta))-

C20H24O6 (360.1572804)


(+)-lariciresinol is a lignan that is tetrahydrofuran substituted at positions 2, 3 and 4 by 4-hydroxy-3-methoxyphenyl, hydroxymethyl and 4-hydroxy-3-methoxybenzyl groups respectively (the 2S,3R,4R-diastereomer). It has a role as an antifungal agent and a plant metabolite. It is a member of oxolanes, a member of phenols, a lignan, a primary alcohol and an aromatic ether. It is an enantiomer of a (-)-lariciresinol. Lariciresinol is a natural product found in Magnolia kachirachirai, Euterpe oleracea, and other organisms with data available. See also: Acai fruit pulp (part of). A lignan that is tetrahydrofuran substituted at positions 2, 3 and 4 by 4-hydroxy-3-methoxyphenyl, hydroxymethyl and 4-hydroxy-3-methoxybenzyl groups respectively (the 2S,3R,4R-diastereomer). (-)-lariciresinol is a member of the class of compounds known as 7,9-epoxylignans. 7,9-epoxylignans are lignans that contain the 7,9-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at the 2-, 3-, 4-position, respectively (-)-lariciresinol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (-)-lariciresinol can be found in a number of food items such as ostrich fern, pepper (c. frutescens), ohelo berry, and guava, which makes (-)-lariciresinol a potential biomarker for the consumption of these food products. Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.823 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.820 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.818 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.812

   

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-methylbut-2-enoate

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-methylbut-2-enoate

C15H18O3 (246.1255878)


   

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)but-2-enoate

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)but-2-enoate

C21H26O6 (374.17292960000003)


   

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-methylbut-2-enoate

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-methylbut-2-enoate

C16H20O4 (276.13615200000004)


   

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-methyl-4-[(3-methylbutanoyl)oxy]but-2-enoate

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-methyl-4-[(3-methylbutanoyl)oxy]but-2-enoate

C20H26O5 (346.17801460000004)


   

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl hexadecanoate

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl hexadecanoate

C31H48O5 (500.3501558)


   

(2z)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z)-octadec-9-enoate

(2z)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z)-octadec-9-enoate

C33H50O5 (526.365805)


   

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-methyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}but-2-enoate

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-methyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}but-2-enoate

C20H24O5 (344.1623654)


   

(2z)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl hexadecanoate

(2z)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl hexadecanoate

C31H48O5 (500.3501558)


   

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z,12z)-octadeca-9,12-dienoate

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z,12z)-octadeca-9,12-dienoate

C33H48O5 (524.3501557999999)


   

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z)-octadec-9-enoate

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z)-octadec-9-enoate

C33H50O5 (526.365805)


   

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-{[(3-methylbutanoyl)oxy]methyl}but-2-enoate

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-{[(3-methylbutanoyl)oxy]methyl}but-2-enoate

C21H28O6 (376.1885788)


   

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-{[(3-methylbut-2-enoyl)oxy]methyl}but-2-enoate

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-{[(3-methylbut-2-enoyl)oxy]methyl}but-2-enoate

C20H24O5 (344.1623654)


   

(2z,4e)-5-(3,4-dimethoxyphenyl)-2-[(3,4-dimethoxyphenyl)methylidene]pent-4-en-1-ol

(2z,4e)-5-(3,4-dimethoxyphenyl)-2-[(3,4-dimethoxyphenyl)methylidene]pent-4-en-1-ol

C22H26O5 (370.17801460000004)


   

(2z)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z,12z)-octadeca-9,12-dienoate

(2z)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z,12z)-octadeca-9,12-dienoate

C33H48O5 (524.3501557999999)


   

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-({[(2z)-2-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)but-2-enoyl]oxy}methyl)but-2-enoate

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-({[(2z)-2-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)but-2-enoyl]oxy}methyl)but-2-enoate

C25H30O7 (442.199143)


   

(3,4-dimethoxyphenyl)[(3r,5r,6r)-6-(3,4-dimethoxyphenyl)-5-[(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl]oxan-3-yl]methanol

(3,4-dimethoxyphenyl)[(3r,5r,6r)-6-(3,4-dimethoxyphenyl)-5-[(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl]oxan-3-yl]methanol

C33H40O8 (564.2723040000001)


   

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-(hydroxymethyl)but-2-enoate

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-(hydroxymethyl)but-2-enoate

C16H20O5 (292.13106700000003)


   

4-[(3ar,6as)-4-(4-hydroxy-3-methoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenol

4-[(3ar,6as)-4-(4-hydroxy-3-methoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenol

C20H22O6 (358.1416312)


   

(3,4-dimethoxyphenyl)[(3s,5r,6r)-6-(3,4-dimethoxyphenyl)-5-[(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl]oxan-3-yl]methanol

(3,4-dimethoxyphenyl)[(3s,5r,6r)-6-(3,4-dimethoxyphenyl)-5-[(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl]oxan-3-yl]methanol

C33H40O8 (564.2723040000001)


   

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-methyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}but-2-enoate

(2e)-3-(3,4-dimethoxyphenyl)prop-2-en-1-yl (2z)-2-methyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}but-2-enoate

C21H26O6 (374.17292960000003)


   

1,2-dimethoxy-4-[(1r)-1-methoxyprop-2-en-1-yl]benzene

1,2-dimethoxy-4-[(1r)-1-methoxyprop-2-en-1-yl]benzene

C12H16O3 (208.1099386)


   

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)but-2-enoate

(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl (2z)-2-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)but-2-enoate

C20H24O5 (344.1623654)


   

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z,12z,15z)-octadeca-9,12,15-trienoate

(2e)-2-ethylidene-3-{[(2e)-3-(4-methoxyphenyl)prop-2-en-1-yl]oxy}-3-oxopropyl (9z,12z,15z)-octadeca-9,12,15-trienoate

C33H46O5 (522.3345065999999)