NCBI Taxonomy: 1365879

Myrsine umbellata (ncbi_taxid: 1365879)

found 12 associated metabolites at species taxonomy rank level.

Ancestor: Myrsine

Child Taxonomies: none taxonomy data.

Embelin

2,5-dihydroxy-3-undecylcyclohexa-2,5-diene-1,4-dione

C17H26O4 (294.1831)


Embelin (Embelic acid), a potent, nonpeptidic XIAP inhibitor (IC50=4.1 μM), inhibits cell growth, induces apoptosis, and activates caspase-9 in prostate cancer cells with high levels of XIAP. Embelin blocks NF-kappaB signaling pathway leading to suppression of NF-kappaB-regulated antiapoptotic and metastatic gene products. Embelin also induces autophagic and apoptotic cell death in human oral squamous cell carcinoma cells[1][2][3]. Embelin (Embelic acid), a potent, nonpeptidic XIAP inhibitor (IC50=4.1 μM), inhibits cell growth, induces apoptosis, and activates caspase-9 in prostate cancer cells with high levels of XIAP. Embelin blocks NF-kappaB signaling pathway leading to suppression of NF-kappaB-regulated antiapoptotic and metastatic gene products. Embelin also induces autophagic and apoptotic cell death in human oral squamous cell carcinoma cells[1][2][3].

   

Embelin

2,5-Cyclohexadiene-1,4-dione, 2,5-dihydroxy-3-undecyl- (9CI)

C17H26O4 (294.1831)


Embelin is a member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxy-1,4-benzoquinone which is substituted by an undecyl group at position 3. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antimicrobial, antineoplastic and inhibitory activity towards hepatitis C protease. It has a role as a hepatitis C protease inhibitor, an antimicrobial agent, an antineoplastic agent and a plant metabolite. Embelin is a natural product found in Ardisia paniculata, Embelia tsjeriam-cottam, and other organisms with data available. A member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxy-1,4-benzoquinone which is substituted by an undecyl group at position 3. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antimicrobial, antineoplastic and inhibitory activity towards hepatitis C protease. Embelin (Embelic acid), a potent, nonpeptidic XIAP inhibitor (IC50=4.1 μM), inhibits cell growth, induces apoptosis, and activates caspase-9 in prostate cancer cells with high levels of XIAP. Embelin blocks NF-kappaB signaling pathway leading to suppression of NF-kappaB-regulated antiapoptotic and metastatic gene products. Embelin also induces autophagic and apoptotic cell death in human oral squamous cell carcinoma cells[1][2][3]. Embelin (Embelic acid), a potent, nonpeptidic XIAP inhibitor (IC50=4.1 μM), inhibits cell growth, induces apoptosis, and activates caspase-9 in prostate cancer cells with high levels of XIAP. Embelin blocks NF-kappaB signaling pathway leading to suppression of NF-kappaB-regulated antiapoptotic and metastatic gene products. Embelin also induces autophagic and apoptotic cell death in human oral squamous cell carcinoma cells[1][2][3].

   

Myrsinoic acid B

Myrsinoic acid B

C22H30O4 (358.2144)


A member of the class of 1-benzofurans that is 2,3-dihydro-1-benzofuran substituted by a carboxy group at position 5, a 1,5-dimethyl-1-hydroxy-4-hexenyl group at position 2 and a prenyl group at position 7. Isolated from Myrsine seguinii, it exhibits anti-inflammatory activity.

   

(2s)-2-[(2s)-2-hydroxy-6-methylhept-5-en-2-yl]-7-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-5-carboxylic acid

(2s)-2-[(2s)-2-hydroxy-6-methylhept-5-en-2-yl]-7-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-5-carboxylic acid

C22H30O4 (358.2144)


   

3-hydroxy-2-methyl-8-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-1-benzopyran-6-carboxylic acid

3-hydroxy-2-methyl-8-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-1-benzopyran-6-carboxylic acid

C22H30O4 (358.2144)


   

(2e)-6-[(1s,3ar,3br,5ar,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl]-2-methylhepta-2,6-dienal

(2e)-6-[(1s,3ar,3br,5ar,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl]-2-methylhepta-2,6-dienal

C30H46O2 (438.3498)


   

methyl 3-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoate

methyl 3-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoate

C23H32O3 (356.2351)


   

3-(3,7-dimethylocta-2,6-dien-1-yl)-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

3-(3,7-dimethylocta-2,6-dien-1-yl)-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid

C22H30O3 (342.2195)


   

(2r,3s)-3-hydroxy-2-methyl-8-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-1-benzopyran-6-carboxylic acid

(2r,3s)-3-hydroxy-2-methyl-8-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-3,4-dihydro-1-benzopyran-6-carboxylic acid

C22H30O4 (358.2144)


   

6-{3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl}-2-methylhepta-2,6-dienal

6-{3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl}-2-methylhepta-2,6-dienal

C30H46O2 (438.3498)


   

methyl 3-(3,7-dimethylocta-2,6-dien-1-yl)-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoate

methyl 3-(3,7-dimethylocta-2,6-dien-1-yl)-4-hydroxy-5-(3-methylbut-2-en-1-yl)benzoate

C23H32O3 (356.2351)


   

methyl 2-(2-hydroxy-6-methylhept-5-en-2-yl)-7-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-5-carboxylate

methyl 2-(2-hydroxy-6-methylhept-5-en-2-yl)-7-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-5-carboxylate

C23H32O4 (372.23)