NCBI Taxonomy: 61591

Viburnum sieboldii (ncbi_taxid: 61591)

found 32 associated metabolites at species taxonomy rank level.

Ancestor: Viburnum

Child Taxonomies: Viburnum sieboldii var. sieboldii, Viburnum sieboldii var. obovatifolium

Amentoflavone

4H-1-Benzopyran-4-one, 8-(5-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-

C30H18O10 (538.0899928)


Amentoflavone is a biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-3 of the hydroxyphenyl ring and C-8 of the chromene ring. A natural product found particularly in Ginkgo biloba and Hypericum perforatum. It has a role as a cathepsin B inhibitor, an antiviral agent, an angiogenesis inhibitor, a P450 inhibitor and a plant metabolite. It is a biflavonoid, a hydroxyflavone and a ring assembly. Amentoflavone is a natural product found in Podocarpus elongatus, Austrocedrus chilensis, and other organisms with data available. A biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-3 of the hydroxyphenyl ring and C-8 of the chromene ring. A natural product found particularly in Ginkgo biloba and Hypericum perforatum. D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors > D065688 - Cytochrome P-450 CYP2C9 Inhibitors D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors > D065692 - Cytochrome P-450 CYP3A Inhibitors Amentoflavone is found in fruits. Amentoflavone is obtained from Viburnum prunifolium (black haw Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase[1][2][3][4]. Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase[1][2][3][4]. Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase[1][2][3][4].

   

Amentoflavone

4H-1-Benzopyran-4-one, 8-(5-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl)-5,7-dihydroxy-2-(4-hydroxyphenyl)-

C30H18O10 (538.0899928)


D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors > D065688 - Cytochrome P-450 CYP2C9 Inhibitors D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors > D065692 - Cytochrome P-450 CYP3A Inhibitors Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 4341; CONFIDENCE confident structure Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase[1][2][3][4]. Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase[1][2][3][4]. Amentoflavone (Didemethyl-ginkgetin) is a potent and orally active GABA(A) negative modulator. Amentoflavone also shows anti-inflammatory, antioxidative, anti-viral, anti-tumor, anti-radiation, anti-fungal, antibacterial activity. Amentoflavone induces apoptosis and cell cycle arrest at sub-G1 phase[1][2][3][4].

   

2-[8-methyl-2,10-bis(2-oxopropyl)-3,11-dioxatricyclo[6.3.1.0¹,⁵]dodec-5-en-12-yl]ethenyl 3-methylbut-2-enoate

2-[8-methyl-2,10-bis(2-oxopropyl)-3,11-dioxatricyclo[6.3.1.0¹,⁵]dodec-5-en-12-yl]ethenyl 3-methylbut-2-enoate

C24H32O6 (416.2198772)


   

(1z)-2-[(1s,3s,5s,11s,12r)-3-methoxy-11-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

(1z)-2-[(1s,3s,5s,11s,12r)-3-methoxy-11-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C27H40O6 (460.28247400000004)


   

(1e)-2-[(1r,2r,8s,10r,12s)-8-methyl-2,10-bis(2-oxopropyl)-3,11-dioxatricyclo[6.3.1.0¹,⁵]dodec-5-en-12-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1r,2r,8s,10r,12s)-8-methyl-2,10-bis(2-oxopropyl)-3,11-dioxatricyclo[6.3.1.0¹,⁵]dodec-5-en-12-yl]ethenyl 3-methylbut-2-enoate

C24H32O6 (416.2198772)


   

(1e)-2-[(1r,2r,7r)-5-(hydroxymethyl)-2-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1r,2r,7r)-5-(hydroxymethyl)-2-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate

C26H38O6 (446.2668248)


   

2-[3-methoxy-11-(4-methoxy-4-methylpent-2-en-1-yl)-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

2-[3-methoxy-11-(4-methoxy-4-methylpent-2-en-1-yl)-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C27H40O6 (460.28247400000004)


   

(1e)-2-[(1s,3r,5s,11s,12r)-3-methoxy-11-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1s,3r,5s,11s,12r)-3-methoxy-11-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C27H40O6 (460.28247400000004)


   

(1e)-2-[(1s,3s,5s,11s,12r)-3-methoxy-11-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1s,3s,5s,11s,12r)-3-methoxy-11-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-3,11-dimethyl-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C27H40O6 (460.28247400000004)


   

2-[5-(hydroxymethyl)-2-(4-methoxy-4-methylpent-2-en-1-yl)-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate

2-[5-(hydroxymethyl)-2-(4-methoxy-4-methylpent-2-en-1-yl)-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate

C26H38O6 (446.2668248)


   

(1e)-2-[(1s,3s,5s,11s,12r)-3-methoxy-3,11-dimethyl-11-(4-methylpent-3-en-1-yl)-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1s,3s,5s,11s,12r)-3-methoxy-3,11-dimethyl-11-(4-methylpent-3-en-1-yl)-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C26H38O5 (430.2719098)


   

2-[3-methoxy-3,11-dimethyl-11-(4-methylpent-3-en-1-yl)-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

2-[3-methoxy-3,11-dimethyl-11-(4-methylpent-3-en-1-yl)-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C26H38O5 (430.2719098)


   

(1e)-2-[(1s,3r,5s,11s,12r)-3-methoxy-3,11-dimethyl-11-(4-methylpent-3-en-1-yl)-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1s,3r,5s,11s,12r)-3-methoxy-3,11-dimethyl-11-(4-methylpent-3-en-1-yl)-2,6-dioxatricyclo[6.4.0.0¹,⁵]dodec-8-en-12-yl]ethenyl 3-methylbut-2-enoate

C26H38O5 (430.2719098)


   

(1e)-2-[(1r,2r,7s)-5-(hydroxymethyl)-2-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate

(1e)-2-[(1r,2r,7s)-5-(hydroxymethyl)-2-[(2e)-4-methoxy-4-methylpent-2-en-1-yl]-2-methyl-6-oxo-7-(2-oxopropyl)cyclohept-4-en-1-yl]ethenyl 3-methylbut-2-enoate

C26H38O6 (446.2668248)