NCBI Taxonomy: 2759664

Arivela (ncbi_taxid: 2759664)

found 6 associated metabolites at genus taxonomy rank level.

Ancestor: Cleomaceae

Child Taxonomies: Arivela bundeica, Arivela uncifera, Arivela tetrandra, Arivela cleomoides, Arivela kenneallyi, Arivela linophylla, Arivela arenitensis, Arivela microphylla, Arivela microaustralica

Fraxetin

7,8-dihydroxy-6-methoxychromen-2-one

C10H8O5 (208.0371718)


Fraxetin is a hydroxycoumarin that is 6-methoxycoumarin in which the hydrogens at positions 7 and 8 have been replaced by hydroxy groups. It has a role as an Arabidopsis thaliana metabolite, an antimicrobial agent, an apoptosis inhibitor, an apoptosis inducer, an antioxidant, an anti-inflammatory agent, a hepatoprotective agent, an antibacterial agent and a hypoglycemic agent. It is a hydroxycoumarin and an aromatic ether. Fraxetin is a natural product found in Santolina pinnata, Campanula dolomitica, and other organisms with data available. A hydroxycoumarin that is 6-methoxycoumarin in which the hydrogens at positions 7 and 8 have been replaced by hydroxy groups. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.550 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.543 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.542 Fraxetin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=574-84-5 (retrieved 2024-06-28) (CAS RN: 574-84-5). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Fraxetin is isolated from Fraxinus rhynchophylla Hance. Fraxetin has antitumor, anti-oxidation effects and anti-inflammory effects. Fraxetin induces apoptosis[1]. Fraxetin is isolated from Fraxinus rhynchophylla Hance. Fraxetin has antitumor, anti-oxidation effects and anti-inflammory effects. Fraxetin induces apoptosis[1].

   

(2r,3r)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2h,3h-[1,4]dioxino[2,3-h]chromen-9-one

(2r,3r)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2h,3h-[1,4]dioxino[2,3-h]chromen-9-one

C21H20O9 (416.110727)


   

11-formyl-5-methyl-8-(prop-1-en-2-yl)cyclotetradeca-1,5,11-triene-1-carboxylic acid

11-formyl-5-methyl-8-(prop-1-en-2-yl)cyclotetradeca-1,5,11-triene-1-carboxylic acid

C20H28O3 (316.2038338)


   

(2r,3r,4r,5r,6s)-2-{[(1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5z)-5-isopropylhept-5-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-methyloxane-3,4,5-triol

(2r,3r,4r,5r,6s)-2-{[(1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5z)-5-isopropylhept-5-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-methyloxane-3,4,5-triol

C35H58O5 (558.4284018)


   

(2s,3s)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2h,3h-[1,4]dioxino[2,3-h]chromen-9-one

(2s,3s)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2h,3h-[1,4]dioxino[2,3-h]chromen-9-one

C21H20O9 (416.110727)


   

2-hydroxy-1,7,8-trimethyl-17-methylidene-15-oxatricyclo[9.3.2.1⁴,⁸]heptadec-11-en-16-one

2-hydroxy-1,7,8-trimethyl-17-methylidene-15-oxatricyclo[9.3.2.1⁴,⁸]heptadec-11-en-16-one

C20H30O3 (318.21948299999997)