NCBI Taxonomy: 2858893

Scutellaria caerulea (ncbi_taxid: 2858893)

found 17 associated metabolites at species taxonomy rank level.

Ancestor: Scutellaria

Child Taxonomies: none taxonomy data.

Dihydrooroxylin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-6-methoxy-2-phenyl-, (S)-

C16H14O5 (286.0841194)


Dihydrooroxylin A is a dihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5 and 7 and a methoxy group at position 6. Isolated from Pisonia aculeata, it exhibits antitubercular activity. It has a role as an antitubercular agent and a plant metabolite. It is a dihydroxyflavanone and a monomethoxyflavanone. Dihydrooroxylin A is a natural product found in Scutellaria scandens, Scutellaria caerulea, and other organisms with data available. A dihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5 and 7 and a methoxy group at position 6. Isolated from Pisonia aculeata, it exhibits antitubercular activity. Dihydrooroxylin is found in fruits. Dihydrooroxylin is isolated from Prunus avium (wild cherry) and Piper sp. Isolated from Prunus avium (wild cherry) and Piper species Dihydrooroxylin is found in fruits.

   

Oroxylin A

Oroxylin A

C16H12O5 (284.0684702)


Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis[1][2][3][4][5]. Oroxylin A is an active flavonoid compound with strong anti-cancer effects.

   

Oroxylin_A

4H-1-Benzopyran-4-one, 5,7-dihydroxy-6-methoxy-2-phenyl-

C16H12O5 (284.0684702)


Oroxylin A is a dihydroxy- and monomethoxy-flavone in which the hydroxy groups are positioned at C-5 and C-7 and the methoxy group is at C-6. It has a role as an antineoplastic agent and an EC 1.14.13.39 (nitric oxide synthase) inhibitor. It is a monomethoxyflavone and a dihydroxyflavone. It is a conjugate acid of an oroxylin A(1-). Oroxylin A is a natural product found in Scutellaria likiangensis, Scutellaria amoena, and other organisms with data available. Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis[1][2][3][4][5]. Oroxylin A is an active flavonoid compound with strong anti-cancer effects.

   

Oroxylin A

5,7-dihydroxy-6-methoxy-2-phenyl-4H-1-benzopyran-4-one

C16H12O5 (284.0684702)


Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis[1][2][3][4][5]. Oroxylin A is an active flavonoid compound with strong anti-cancer effects.

   

Dihydrooroxylin A

5,7-Dihydroxy-6-methoxyflavanone

C16H14O5 (286.0841194)


   

Oroxylin

4H-1-Benzopyran-4-one, 5,7-dihydroxy-6-methoxy-2-phenyl-

C16H12O5 (284.0684702)


Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis[1][2][3][4][5]. Oroxylin A is an active flavonoid compound with strong anti-cancer effects.

   

(1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

(1r,2s,3r,4r,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

C26H36O8 (476.2410056)


   

(1r,2s,3r,4s,4as,5r,8ar)-1-(acetyloxy)-4-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-hexahydronaphthalen-2-yl butanoate

(1r,2s,3r,4s,4as,5r,8ar)-1-(acetyloxy)-4-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-hexahydronaphthalen-2-yl butanoate

C28H40O10 (536.2621340000001)


   

(1s,3r,4ar,5s,6r,6ar,10r,10as,10bs)-5,6,10-tris(acetyloxy)-4a,6a,10b-trimethyl-7-methylidene-5'-oxo-octahydrospiro[naphtho[2,1-b]pyran-3,3'-oxolan]-1-yl benzoate

(1s,3r,4ar,5s,6r,6ar,10r,10as,10bs)-5,6,10-tris(acetyloxy)-4a,6a,10b-trimethyl-7-methylidene-5'-oxo-octahydrospiro[naphtho[2,1-b]pyran-3,3'-oxolan]-1-yl benzoate

C33H40O11 (612.257049)


   

(1s)-1-[(1s,2r,3s,4r,4ar,8r,8as)-4-(acetyloxy)-3-(butanoyloxy)-2,8-dihydroxy-1,2,4a-trimethyl-5-methylidene-hexahydronaphthalen-1-yl]-2-(5-oxo-2h-furan-3-yl)ethyl butanoate

(1s)-1-[(1s,2r,3s,4r,4ar,8r,8as)-4-(acetyloxy)-3-(butanoyloxy)-2,8-dihydroxy-1,2,4a-trimethyl-5-methylidene-hexahydronaphthalen-1-yl]-2-(5-oxo-2h-furan-3-yl)ethyl butanoate

C30H44O10 (564.2934324)


   

(1r,2s,3r,4s,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

(1r,2s,3r,4s,4as,5r,8ar)-1-(acetyloxy)-3,5-dihydroxy-3,4,8a-trimethyl-8-methylidene-4-[(1e)-2-(5-oxo-2h-furan-3-yl)ethenyl]-hexahydronaphthalen-2-yl butanoate

C26H36O8 (476.2410056)


   

(1r,2s,3r,4s,4as,5r,8ar)-1,5-bis(acetyloxy)-4-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-3-hydroxy-3,4,8a-trimethyl-8-methylidene-hexahydronaphthalen-2-yl butanoate

(1r,2s,3r,4s,4as,5r,8ar)-1,5-bis(acetyloxy)-4-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-3-hydroxy-3,4,8a-trimethyl-8-methylidene-hexahydronaphthalen-2-yl butanoate

C30H42O11 (578.2726982)