NCBI Taxonomy: 95770

Hymenophytaceae (ncbi_taxid: 95770)

found 34 associated metabolites at family taxonomy rank level.

Ancestor: Pallaviciniineae

Child Taxonomies: Hymenophyton

Eugenin

5-Hydroxy-7-methoxy-2-methyl-4H-1-benzopyran-4-one

C11H10O4 (206.057906)


Constituent of Eugenia aromatica (clove). Eugenin is found in many foods, some of which are wild carrot, carrot, herbs and spices, and java plum. Eugenin is found in carrot. Eugenin is a constituent of Eugenia aromatica (clove). Eugenin is a chromone isolated from Peucedanum japonicum, with potent antiplatelet aggregation activity[1]. Eugenin is a chromone isolated from Peucedanum japonicum, with potent antiplatelet aggregation activity[1].

   

1-(2-hydroxy-4,6-dimethoxyphenyl)but-2-en-1-one

1-(2-hydroxy-4,6-dimethoxyphenyl)but-2-en-1-one

C12H14O4 (222.0892044)


   

1-(2,4,6-TRIMETHOXYPHENYL)BUT-2-EN-1-ONE

1-(2,4,6-TRIMETHOXYPHENYL)BUT-2-EN-1-ONE

C13H16O4 (236.10485359999998)


   

caryophyllene

(-)-beta-Caryophyllene

C15H24 (204.18779039999998)


A beta-caryophyllene in which the stereocentre adjacent to the exocyclic double bond has S configuration while the remaining stereocentre has R configuration. It is the most commonly occurring form of beta-caryophyllene, occurring in many essential oils, particularly oil of cloves. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents β-Caryophyllene is a CB2 receptor agonist. β-Caryophyllene is a CB2 receptor agonist.

   

Eugenin

4H-1-Benzopyran-4-one, 5-hydroxy-7-methoxy-2-methyl-

C11H10O4 (206.057906)


A member of the class of chromones that is chromone substituted by a hydroxy group at position 5, a methoxy group at position 7 and a methyl group at position 2. It has been isolated from Pisonia aculeata. Eugenin is a chromone isolated from Peucedanum japonicum, with potent antiplatelet aggregation activity[1]. Eugenin is a chromone isolated from Peucedanum japonicum, with potent antiplatelet aggregation activity[1].

   

Aldol

3-Butanolal

C4H8O2 (88.0524268)


   

(3r)-3-hydroxy-1-(2-hydroxy-4,6-dimethoxyphenyl)butan-1-one

(3r)-3-hydroxy-1-(2-hydroxy-4,6-dimethoxyphenyl)butan-1-one

C12H16O5 (240.0997686)


   

(2e)-1-(2,4-dihydroxy-6-methoxyphenyl)but-2-en-1-one

(2e)-1-(2,4-dihydroxy-6-methoxyphenyl)but-2-en-1-one

C11H12O4 (208.0735552)


   

(2r)-2,5-dihydroxy-7-methoxy-2-methyl-3h-1-benzopyran-4-one

(2r)-2,5-dihydroxy-7-methoxy-2-methyl-3h-1-benzopyran-4-one

C11H12O5 (224.06847019999998)


   

1-(2,4-dihydroxy-6-methoxyphenyl)but-2-en-1-one

1-(2,4-dihydroxy-6-methoxyphenyl)but-2-en-1-one

C11H12O4 (208.0735552)


   

(2e)-1-(2,4,6-trimethoxyphenyl)but-2-en-1-one

(2e)-1-(2,4,6-trimethoxyphenyl)but-2-en-1-one

C13H16O4 (236.10485359999998)


   

(2e)-1-(2-hydroxy-4,6-dimethoxyphenyl)but-2-en-1-one

(2e)-1-(2-hydroxy-4,6-dimethoxyphenyl)but-2-en-1-one

C12H14O4 (222.0892044)


   

(2z)-1-(2,4,6-trimethoxyphenyl)but-2-en-1-one

(2z)-1-(2,4,6-trimethoxyphenyl)but-2-en-1-one

C13H16O4 (236.10485359999998)


   

5,7-dimethoxy-2-methylchromen-4-one

5,7-dimethoxy-2-methylchromen-4-one

C12H12O4 (220.0735552)


   

2,5-dihydroxy-7-methoxy-2-methyl-3h-1-benzopyran-4-one

2,5-dihydroxy-7-methoxy-2-methyl-3h-1-benzopyran-4-one

C11H12O5 (224.06847019999998)


   

3-hydroxy-1-(2-hydroxy-4,6-dimethoxyphenyl)butan-1-one

3-hydroxy-1-(2-hydroxy-4,6-dimethoxyphenyl)butan-1-one

C12H16O5 (240.0997686)


   

1-(2-hydroxy-4,6-dimethoxyphenyl)butane-1,3-dione

1-(2-hydroxy-4,6-dimethoxyphenyl)butane-1,3-dione

C12H14O5 (238.08411940000002)