NCBI Taxonomy: 2086458

Myristica castaneifolia (ncbi_taxid: 2086458)

found 10 associated metabolites at species taxonomy rank level.

Ancestor: Myristica

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].

   

Dehydrodiisoeugenol

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

C20H22O4 (326.1518)


   

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

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

C21H24O4 (340.1675)


   

5-hydroxy-2-(8-phenyloctyl)chromen-4-one

5-hydroxy-2-(8-phenyloctyl)chromen-4-one

C23H26O3 (350.1882)


   

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

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

C20H20O4 (324.1362)


   

2-(3,4-dimethoxyphenyl)-7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran

2-(3,4-dimethoxyphenyl)-7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran

C21H24O4 (340.1675)


   

5-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole

5-[7-methoxy-3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]-2h-1,3-benzodioxole

C20H20O4 (324.1362)


   

1-(2,6-dihydroxyphenyl)tetradecan-1-one

1-(2,6-dihydroxyphenyl)tetradecan-1-one

C20H32O3 (320.2351)


   

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)


   

1-(2,6-dihydroxyphenyl)-9-phenylnonan-1-one

1-(2,6-dihydroxyphenyl)-9-phenylnonan-1-one

C21H26O3 (326.1882)