NCBI Taxonomy: 16123
Hypoxis (ncbi_taxid: 16123)
found 149 associated metabolites at genus taxonomy rank level.
Ancestor: Hypoxidaceae
Child Taxonomies: Hypoxis villosa, Hypoxis aurea, Hypoxis leptocarpa, Hypoxis obtusa, Hypoxis juncea, Hypoxis setosa, Hypoxis hirsuta, Hypoxis goetzei, Hypoxis nyasica, Hypoxis parvula, Hypoxis fischeri, Hypoxis rigidula, Hypoxis wrightii, Hypoxis glabella, Hypoxis sessilis, Hypoxis schimperi, Hypoxis curtissii, Hypoxis decumbens, Hypoxis gregoriana, Hypoxis filiformis, Hypoxis polystachya, Hypoxis occidentalis, Hypoxis angustifolia, Hypoxis hygrometrica, unclassified Hypoxis, Hypoxis hemerocallidea
cis-Hinokiresinol
cis-Hinokiresinol, a type of lignan, is a natural compound found in various plants, particularly conifers like cypress. Lignans, including cis-Hinokiresinol, have garnered significant interest in the field of pharmacology and nutrition due to their diverse biological functions: 1. **Antioxidant Activity**: cis-Hinokiresinol exhibits antioxidant properties, which means it can help neutralize harmful free radicals in the body. This activity is important for protecting cells from oxidative stress, which is associated with aging and various diseases. 2. **Anti-Inflammatory Effects**: The compound has been found to possess anti-inflammatory properties. Chronic inflammation is linked to numerous diseases, including heart disease, cancer, and autoimmune disorders. By reducing inflammation, cis-Hinokiresinol may contribute to the prevention or treatment of these conditions. 3. **Anticancer Potential**: Some studies suggest that lignans, including cis-Hinokiresinol, may have anti-cancer properties. They may influence cancer cell growth, apoptosis (cell death), and angiogenesis (formation of new blood vessels in tumors). However, more research is needed to fully understand these effects. 4. **Estrogenic and Anti-Estrogenic Activities**: cis-Hinokiresinol and other lignans can bind to estrogen receptors in the body, exhibiting both estrogenic and anti-estrogenic effects. This dual activity might be beneficial in conditions where estrogen balance is crucial, such as in hormone-related cancers. 5. **Prebiotic Effects**: In the gut, lignans can be metabolized by gut bacteria into compounds with estrogenic or anti-estrogenic properties. This transformation contributes to the overall hormonal balance in the body and may have implications for health.
Acuminoside
Constituent of damask rose (Rosa damascena) and wine grapes (Vitis vinifera). Geranyl apiosyl-glucoside is found in many foods, some of which are green vegetables, alcoholic beverages, herbs and spices, and fruits. Acuminoside is found in alcoholic beverages. Acuminoside is a constituent of damask rose (Rosa damascena) and wine grapes (Vitis vinifera)
Acuminoside
4-[(1Z,3S)-3-(4-hydroxyphenyl)penta-1,4-dienyl]phenol
(2s,3r,4s,5s,6r)-2-{4-[(1z,3s)-3-(4-{[(2s,3r,4s,5s,6r)-6-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}phenyl)penta-1,4-dien-1-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
2-(hydroxymethyl)-6-{4-[3-(4-hydroxyphenyl)penta-1,4-dien-1-yl]phenoxy}oxane-3,4,5-triol
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-{4-[(1e,3s)-3-(4-hydroxyphenyl)penta-1,4-dien-1-yl]phenoxy}oxane-3,4,5-triol
(2r,3s,4r,5r,6s)-2-{2-hydroxy-4-[(4e)-5-(3-hydroxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)pent-4-en-1-yn-1-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-{4-[(1z,3s)-3-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)penta-1,4-dien-1-yl]phenoxy}oxane-3,4,5-triol
4-[(1e)-5-(4-hydroxyphenyl)pent-1-en-4-yn-1-yl]benzene-1,2-diol
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-{4-[(3r,4e)-5-(4-hydroxyphenyl)penta-1,4-dien-3-yl]phenoxy}oxane-3,4,5-triol
(2r,3s,4s,5r,6r)-2-({[(2s,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}oxane-3,4,5-triol
2-(hydroxymethyl)-6-{4-[3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)penta-1,4-dien-1-yl]phenoxy}oxane-3,4,5-triol
[(2r,3s,4s,5r,6r)-6-[(2,5-dihydroxyphenyl)methoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-hydroxy-2,6-dimethoxybenzoate
C22H26O12 (482.14241960000004)
(2r,3s,4s,5r,6r)-2-({[(2r,3s,4s)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-{[(2e)-3,7-dimethylocta-2,6-dien-1-yl]oxy}oxane-3,4,5-triol
4-[5-(4-hydroxyphenyl)pent-1-en-4-yn-1-yl]benzene-1,2-diol
(2s,3r,4s,5s,6r)-2-{2-hydroxy-4-[(4e)-5-(3-hydroxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)pent-4-en-1-yn-1-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
(2r,3r,4s,5s,6r)-2-{[(1r,2r)-1,5-bis(3,4-dihydroxyphenyl)-1-hydroxypent-4-yn-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
C23H26O11 (478.14750460000005)
(2s,3r,4s,5s,6r)-2-{4-[(1e)-5-(3-hydroxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)pent-1-en-4-yn-1-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
2-(hydroxymethyl)-6-{4-[(1e)-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)penta-1,4-dien-1-yl]phenoxy}oxane-3,4,5-triol
4-[5-(3,4-dihydroxyphenyl)pent-4-en-1-yn-1-yl]benzene-1,2-diol
4-[(4e)-5-(3,4-dihydroxyphenyl)pent-4-en-1-yn-1-yl]benzene-1,2-diol
4-[(4e)-5-(4-hydroxyphenyl)pent-4-en-1-yn-1-yl]benzene-1,2-diol
2-{[1,5-bis(3,4-dihydroxyphenyl)-1-hydroxypent-4-yn-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
C23H26O11 (478.14750460000005)
2-{4-[3-(4-{[6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}phenyl)penta-1,4-dien-1-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
{6-[(2,5-dihydroxyphenyl)methoxy]-3,4,5-trihydroxyoxan-2-yl}methyl 3-hydroxy-2,6-dimethoxybenzoate
C22H26O12 (482.14241960000004)