NCBI Taxonomy: 229048

Morus wittiorum (ncbi_taxid: 229048)

found 15 associated metabolites at species taxonomy rank level.

Ancestor: Morus

Child Taxonomies: none taxonomy data.

Moracin M

InChI=1/C14H10O4/c15-10-2-1-8-5-13(18-14(8)7-10)9-3-11(16)6-12(17)4-9/h1-7,15-17

C14H10O4 (242.0579)


Moracin M is a member of benzofurans. Moracin M is a natural product found in Morus insignis, Morus mesozygia, and other organisms with data available. Moracin M is found in fruits. Moracin M is isolated from Morus alba (white mulberry) infected with Fusarium solani. Isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin M is found in fruits. Moracin M, a phenolic component in the skin of Morus alba Linn., is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity[1]. Moracin M, a phenolic component in the skin of Morus alba Linn., is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity[1].

   

Moracin C

1,3-Benzenediol, 5-(6-hydroxy-2-benzofuranyl)-2-(3-methyl-2-butenyl)- (9CI); 5-(6-Hydroxy-2-benzofuranyl)-2-(3-methyl-2-buten-1-yl)-1,3-benzenediol

C19H18O4 (310.1205)


Moracin C is a member of benzofurans. Moracin C is a natural product found in Morus mesozygia, Morus alba var. multicaulis, and other organisms with data available. Isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin C is found in mulberry and fruits. Moracin C is found in fruits. Moracin C is isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin C, a natural product, is an anti-inflammatory agent. Moracin C inhibits LPS-activated reactive oxygen species (ROS) and nitric oxide (NO) release from cells[1]. Moracin C, a natural product, is an anti-inflammatory agent. Moracin C inhibits LPS-activated reactive oxygen species (ROS) and nitric oxide (NO) release from cells[1].

   

Wittifuran X

Wittifuran X

C15H12O5 (272.0685)


   

SCHEMBL16362967

SCHEMBL16362967

C40H38O10 (678.2465)


   

Moracin M

InChI=1\C14H10O4\c15-10-2-1-8-5-13(18-14(8)7-10)9-3-11(16)6-12(17)4-9\h1-7,15-17

C14H10O4 (242.0579)


Moracin M, a phenolic component in the skin of Morus alba Linn., is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity[1]. Moracin M, a phenolic component in the skin of Morus alba Linn., is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity[1].

   

Moracin C

5-(6-hydroxy-1-benzofuran-2-yl)-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol

C19H18O4 (310.1205)


Moracin C, a natural product, is an anti-inflammatory agent. Moracin C inhibits LPS-activated reactive oxygen species (ROS) and nitric oxide (NO) release from cells[1]. Moracin C, a natural product, is an anti-inflammatory agent. Moracin C inhibits LPS-activated reactive oxygen species (ROS) and nitric oxide (NO) release from cells[1].

   

(2s,3r,4s,5s,6r)-2-{2-[(2s)-7-hydroxy-8-(2-hydroxyethyl)-3,4-dihydro-2h-1-benzopyran-2-yl]-5-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-{2-[(2s)-7-hydroxy-8-(2-hydroxyethyl)-3,4-dihydro-2h-1-benzopyran-2-yl]-5-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C24H30O10 (478.1839)


   

5-[(11s)-11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5,7-tetraen-5-yl]benzene-1,3-diol

5-[(11s)-11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5,7-tetraen-5-yl]benzene-1,3-diol

C19H18O5 (326.1154)


   

2-{5-hydroxy-2-[8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2h-1-benzopyran-2-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{5-hydroxy-2-[8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2h-1-benzopyran-2-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C24H30O10 (478.1839)


   

(2s,3r,4s,5r)-2-(3-hydroxy-5-{11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5,7-tetraen-5-yl}phenoxy)oxane-3,4,5-triol

(2s,3r,4s,5r)-2-(3-hydroxy-5-{11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5,7-tetraen-5-yl}phenoxy)oxane-3,4,5-triol

C24H26O9 (458.1577)


   

5-{11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5-trien-5-yl}benzene-1,3-diol

5-{11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5-trien-5-yl}benzene-1,3-diol

C19H20O5 (328.1311)


   

2-{2-[7-hydroxy-8-(2-hydroxyethyl)-3,4-dihydro-2h-1-benzopyran-2-yl]-5-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{2-[7-hydroxy-8-(2-hydroxyethyl)-3,4-dihydro-2h-1-benzopyran-2-yl]-5-methoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C24H30O10 (478.1839)


   

(2s,3r,4s,5s,6r)-2-{5-hydroxy-2-[(2r)-8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2h-1-benzopyran-2-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-{5-hydroxy-2-[(2r)-8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2h-1-benzopyran-2-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C24H30O10 (478.1839)


   

(2s,3r,4s,5s,6r)-2-{5-hydroxy-2-[(2s)-8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2h-1-benzopyran-2-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2s,3r,4s,5s,6r)-2-{5-hydroxy-2-[(2s)-8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2h-1-benzopyran-2-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C24H30O10 (478.1839)


   

(3r,4s,5r)-2-(3-hydroxy-5-{11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5,7-tetraen-5-yl}phenoxy)oxane-3,4,5-triol

(3r,4s,5r)-2-(3-hydroxy-5-{11-hydroxy-12,12-dimethyl-4,13-dioxatricyclo[7.4.0.0³,⁷]trideca-1(9),2,5,7-tetraen-5-yl}phenoxy)oxane-3,4,5-triol

C24H26O9 (458.1577)