NCBI Taxonomy: 366643

Senecio scandens var. incisus (ncbi_taxid: 366643)

found 16 associated metabolites at varietas taxonomy rank level.

Ancestor: Senecio scandens

Child Taxonomies: none taxonomy data.

Afzelin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4H-chromen-4-one

C21H20O10 (432.105642)


5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one is a member of the class of compounds known as flavonoid-3-o-glycosides. Flavonoid-3-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one can be found in a number of food items such as endive, linden, peach, and ginkgo nuts, which makes 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one a potential biomarker for the consumption of these food products. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1]. Afzelin (Kaempferol-3-O-rhamnoside)It is a flavonol glycoside that has anti-inflammatory, anti-oxidative stress response, anti-apoptotic, and anti-cardiac cytotoxic effects. AfzelinIt can reduce mitochondrial damage, enhance mitochondrial biosynthesis, and reduce mitochondria-related proteins. Parkinand PTENinduced putative kinase 1 (putative kinase 1)s level. AfzelinCan be improved D-galactosamine(GalN)/LPSSurvival rate of mice treated with doxorubicin prophylaxis (HY-15142A)Induced cardiotoxicity and scopolamine (HY-N0296)-induced neurological injury. AfzelinAlso inhibits asthma and allergies caused by ovalbumin[1][2][3][4]. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1].

   

(2s,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

(2s,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C23H24O11 (476.13185539999995)


   

(2s,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

(2s,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

C23H24O11 (476.13185539999995)


   

[(1s,6r)-1,6-dihydroxy-4-oxocyclohex-2-en-1-yl]acetic acid

[(1s,6r)-1,6-dihydroxy-4-oxocyclohex-2-en-1-yl]acetic acid

C8H10O5 (186.052821)


   

(1,6-dihydroxy-4-oxocyclohex-2-en-1-yl)acetic acid

(1,6-dihydroxy-4-oxocyclohex-2-en-1-yl)acetic acid

C8H10O5 (186.052821)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.105642)


   

(2r,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C23H24O12 (492.1267704)


   

(2r,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3r,4s,5s,6r)-2,4,5-trihydroxy-6-({[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy}methyl)oxan-3-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

C23H24O12 (492.1267704)