NCBI Taxonomy: 228637

Krameria cytisoides (ncbi_taxid: 228637)

found 10 associated metabolites at species taxonomy rank level.

Ancestor: Krameria

Child Taxonomies: none taxonomy data.

LICARIN A

2-methoxy-4-[(2S,3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C20H22O4 (326.1518)


(-)-Licarin A is a natural product found in Magnolia dodecapetala, Magnolia kachirachirai, and other organisms with data available. Dehydrodiisoeugenol is a natural product found in Myristica fragrans with data available. Dehydrodiisoeugenol is isolated from Myristica fragrans Houtt, shows anti-inflammatory and anti-bacterial actions[1]. Dehydrodiisoeugenol inhibits LPS- stimulated NF-κB activation and cyclooxygenase (COX)-2 gene expression in murine macrophages[2]. Dehydrodiisoeugenol is isolated from Myristica fragrans Houtt, shows anti-inflammatory and anti-bacterial actions[1]. Dehydrodiisoeugenol inhibits LPS- stimulated NF-κB activation and cyclooxygenase (COX)-2 gene expression in murine macrophages[2]. Licarin A ((+)-Licarin A), a neolignan, significantly and dose-dependently reduces TNF-α production (IC50=12.6 μM) in dinitrophenyl-human serum albumin (DNP-HSA)-stimulated RBL-2H3 cells. Anti-allergic effects. Licarin A reduces TNF-α and PGD2 production, and COX-2 expression[1]. Licarin A ((+)-Licarin A), a neolignan, significantly and dose-dependently reduces TNF-α production (IC50=12.6 μM) in dinitrophenyl-human serum albumin (DNP-HSA)-stimulated RBL-2H3 cells. Anti-allergic effects. Licarin A reduces TNF-α and PGD2 production, and COX-2 expression[1].

   

Conocarpan

(+)-Conocarpan

C18H18O2 (266.1307)


   

Rataniaphenol I

Rataniaphenol I

C18H16O3 (280.1099)


A member of the class of benzofurans that is 1-benzofuran substituted by a 2-hydroxy-4-methoxyphenyl group at position 2 and a prop-1-en-1-yl group at position 5. It is a lignan derivative isolated from the roots of Krameria lappacea.

   

rataniaphenol II

rataniaphenol II

C18H16O2 (264.115)


A member of the class of benzofurans that is 1-benzofuran substituted by a 4-hydroxyphenyl group at position 2, a methyl group at position 3 and a prop-1-en-1-yl group at position 5. It is a lignan derivative isolated from the roots of Krameria lappacea.

   

4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C18H18O2 (266.1307)


   

2-(4-hydroxyphenyl)-7-methoxy-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-3-carbaldehyde

2-(4-hydroxyphenyl)-7-methoxy-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-3-carbaldehyde

C19H16O4 (308.1049)


   

4-{7-methoxy-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

4-{7-methoxy-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

C18H16O3 (280.1099)


   

2-methoxy-4-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

2-methoxy-4-[(2r,3r)-7-methoxy-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C20H22O4 (326.1518)


   

4-{5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

4-{5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

C17H14O2 (250.0994)


   

(4s,8r,9r)-8-[(1s)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione

(4s,8r,9r)-8-[(1s)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione

C15H16O8 (324.0845)