NCBI Taxonomy: 72457

Hugonia (ncbi_taxid: 72457)

found 82 associated metabolites at genus taxonomy rank level.

Ancestor: Linaceae

Child Taxonomies: Hugonia mystax, Hugonia spicata, Hugonia longipes, Hugonia busseana, Hugonia jenkinsii, Hugonia orientalis, Hugonia gabunensis, Hugonia obtusifolia, Hugonia platysepala, Hugonia castaneifolia, Hugonia penicillanthemum, Hugonia aff. planchonii McPherson 16804

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].

   

Caryophyllene alpha-oxide

[1R-(1R*,4R*,6R*,10S*)]- Caryophylene oxide Caryophyllene epoxide Caryophyllene oxyde Epoxycaryophyllene [1R-(1R*,4R*,6R*,10S*)]-4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane <>-Caryophyllene epoxide <>-Caryophyllene oxide

C15H24O (220.18270539999997)


Caryophyllene oxide is an epoxide. It has a role as a metabolite. Caryophyllene oxide is a natural product found in Xylopia emarginata, Eupatorium altissimum, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of). Caryophyllene alpha-oxide is a minor produced of epoxidn. of KGV69-V. Minor production of epoxidn. of KGV69-V Caryophyllene oxide, isolated from from Hymenaea courbaril, possesses analgesic and anti-inflammatory activity[1]. Caryophyllene oxide, isolated from from Hymenaea courbaril, possesses analgesic and anti-inflammatory activity[1].

   

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].

   

2-hydroxyhenpentacont-2-enal

2-hydroxyhenpentacont-2-enal

C51H100O2 (744.77229)


   

Caryophyllene oxide

Caryophyllene alpha-oxide

C15H24O (220.18270539999997)


Constituent of oil of cloves (Eugenia caryophyllata)and is) also in oils of Betula alba, Mentha piperita (peppermint) and others. Caryophyllene alpha-oxide is found in many foods, some of which are spearmint, cloves, ceylon cinnamon, and herbs and spices. Caryophyllene beta-oxide is a member of the class of compounds known as sesquiterpenoids. Sesquiterpenoids are terpenes with three consecutive isoprene units. Caryophyllene beta-oxide is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Within the cell, caryophyllene beta-oxide is primarily located in the membrane (predicted from logP). It can also be found in the extracellular space. Caryophyllene oxide, isolated from from Hymenaea courbaril, possesses analgesic and anti-inflammatory activity[1]. Caryophyllene oxide, isolated from from Hymenaea courbaril, possesses analgesic and anti-inflammatory activity[1].

   

epoxide

[1R-(1R*,4R*,6R*,10S*)]- Caryophylene oxide Caryophyllene epoxide Caryophyllene oxyde Epoxycaryophyllene [1R-(1R*,4R*,6R*,10S*)]-4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane <>-Caryophyllene epoxide <>-Caryophyllene oxide

C15H24O (220.18270539999997)


Caryophyllene oxide is an epoxide. It has a role as a metabolite. Caryophyllene oxide is a natural product found in Xylopia emarginata, Eupatorium altissimum, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of). A natural product found in Cupania cinerea. Caryophyllene oxide, isolated from from Hymenaea courbaril, possesses analgesic and anti-inflammatory activity[1]. Caryophyllene oxide, isolated from from Hymenaea courbaril, possesses analgesic and anti-inflammatory activity[1].

   

(1r,4br,7r,8ar,10ar)-7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

(1r,4br,7r,8ar,10ar)-7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

C20H30O2 (302.224568)


   

(2z)-2-hydroxyhenpentacont-2-enal

(2z)-2-hydroxyhenpentacont-2-enal

C51H100O2 (744.77229)


   

(1r,2s,4br,7r,8ar,10ar)-7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthren-2-ol

(1r,2s,4br,7r,8ar,10ar)-7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthren-2-ol

C20H32O2 (304.24021719999996)


   

6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3h-phenanthren-2-one

6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3h-phenanthren-2-one

C18H24O2 (272.17762039999997)


   
   

(1r,2s,7r,8ar,10ar)-7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthren-2-ol

(1r,2s,7r,8ar,10ar)-7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthren-2-ol

C20H32O2 (304.24021719999996)


   

(1s,2r,5r,7r,10s,14r,15r,16r,20r,22s,25s,28r)-7,14,22,28-tetrahydroxy-6,6,10,14,21,21,25,28-octamethylheptacyclo[14.10.2.0²,¹¹.0²,¹⁵.0⁵,¹⁰.0¹⁷,²⁶.0²⁰,²⁵]octacosa-11,17(26)-diene-13,27-dione

(1s,2r,5r,7r,10s,14r,15r,16r,20r,22s,25s,28r)-7,14,22,28-tetrahydroxy-6,6,10,14,21,21,25,28-octamethylheptacyclo[14.10.2.0²,¹¹.0²,¹⁵.0⁵,¹⁰.0¹⁷,²⁶.0²⁰,²⁵]octacosa-11,17(26)-diene-13,27-dione

C36H52O6 (580.3763692)


   

7-ethenyl-1,1,4b,7-tetramethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthrene-2,3-diol

7-ethenyl-1,1,4b,7-tetramethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthrene-2,3-diol

C20H32O2 (304.24021719999996)


   
   

(2r,3s,4br,7r,8ar,10ar)-7-ethenyl-1,1,4b,7-tetramethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthrene-2,3-diol

(2r,3s,4br,7r,8ar,10ar)-7-ethenyl-1,1,4b,7-tetramethyl-3,5,6,8,8a,9,10,10a-octahydro-2h-phenanthrene-2,3-diol

C20H32O2 (304.24021719999996)


   

(2r,4br,7r,8ar,10ar)-7-ethenyl-2-hydroxy-1,1,4b,7-tetramethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

(2r,4br,7r,8ar,10ar)-7-ethenyl-2-hydroxy-1,1,4b,7-tetramethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

C20H30O2 (302.224568)


   
   

7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

7-ethenyl-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

C20H30O2 (302.224568)


   

(10r,11r,15r,16r)-16-hydroxy-2-methoxy-10-(3,4,5-trimethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one

(10r,11r,15r,16r)-16-hydroxy-2-methoxy-10-(3,4,5-trimethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one

C23H24O9 (444.14202539999997)


   

7-ethenyl-2-hydroxy-1,1,4b,7-tetramethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

7-ethenyl-2-hydroxy-1,1,4b,7-tetramethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

C20H30O2 (302.224568)


   

(11r)-2-hydroxy-10-(3,4,5-trimethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one

(11r)-2-hydroxy-10-(3,4,5-trimethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1,3(7),8-trien-12-one

C22H22O8 (414.1314612)


   

(2r,5r,7r,14r,15r,20r,22s,28r)-7,14,22,28-tetrahydroxy-6,6,10,14,21,21,25,28-octamethylheptacyclo[14.10.2.0²,¹¹.0²,¹⁵.0⁵,¹⁰.0¹⁷,²⁶.0²⁰,²⁵]octacosa-11,17(26)-diene-13,27-dione

(2r,5r,7r,14r,15r,20r,22s,28r)-7,14,22,28-tetrahydroxy-6,6,10,14,21,21,25,28-octamethylheptacyclo[14.10.2.0²,¹¹.0²,¹⁵.0⁵,¹⁰.0¹⁷,²⁶.0²⁰,²⁵]octacosa-11,17(26)-diene-13,27-dione

C36H52O6 (580.3763692)


   

(1s,2r,5r,7r,10s,14r,15r,16r,20r,25s,28r)-7,14,28-trihydroxy-6,6,10,14,21,21,25,28-octamethylheptacyclo[14.10.2.0²,¹¹.0²,¹⁵.0⁵,¹⁰.0¹⁷,²⁶.0²⁰,²⁵]octacosa-11,17(26)-diene-13,22,27-trione

(1s,2r,5r,7r,10s,14r,15r,16r,20r,25s,28r)-7,14,28-trihydroxy-6,6,10,14,21,21,25,28-octamethylheptacyclo[14.10.2.0²,¹¹.0²,¹⁵.0⁵,¹⁰.0¹⁷,²⁶.0²⁰,²⁵]octacosa-11,17(26)-diene-13,22,27-trione

C36H50O6 (578.36072)


   

7-ethenyl-2-hydroxy-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

7-ethenyl-2-hydroxy-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

C20H30O3 (318.21948299999997)


   

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)


   

4-methoxy-3,5,5,9-tetramethyl-2,3,4,6,7,8-hexahydro-1h-benzo[7]annulen-4a-ol

4-methoxy-3,5,5,9-tetramethyl-2,3,4,6,7,8-hexahydro-1h-benzo[7]annulen-4a-ol

C16H28O2 (252.20891880000002)


   

(1r,2r,4br,7r,8ar,10ar)-7-ethenyl-2-hydroxy-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

(1r,2r,4br,7r,8ar,10ar)-7-ethenyl-2-hydroxy-1-(hydroxymethyl)-1,4b,7-trimethyl-2,5,6,8,8a,9,10,10a-octahydrophenanthren-3-one

C20H30O3 (318.21948299999997)


   

(3r,4r,4ar)-4-methoxy-3,5,5,9-tetramethyl-2,3,4,6,7,8-hexahydro-1h-benzo[7]annulen-4a-ol

(3r,4r,4ar)-4-methoxy-3,5,5,9-tetramethyl-2,3,4,6,7,8-hexahydro-1h-benzo[7]annulen-4a-ol

C16H28O2 (252.20891880000002)


   

(4as,10ar)-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3h-phenanthren-2-one

(4as,10ar)-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3h-phenanthren-2-one

C18H24O2 (272.17762039999997)


   

(4ar,10ar)-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3h-phenanthren-2-one

(4ar,10ar)-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3h-phenanthren-2-one

C18H24O2 (272.17762039999997)