NCBI Taxonomy: 4197
Pinguicula (ncbi_taxid: 4197)
found 108 associated metabolites at genus taxonomy rank level.
Ancestor: Lentibulariaceae
Child Taxonomies: Pinguicula caerulea, Pinguicula mundi, Pinguicula lutea, Pinguicula agnata, Pinguicula alpina, Pinguicula pumila, Pinguicula pilosa, Pinguicula kondoi, Pinguicula fiorii, Pinguicula algida, Pinguicula albida, Pinguicula bissei, Pinguicula jackii, Pinguicula apuana, Pinguicula mariae, Pinguicula ramosa, Pinguicula laueana, Pinguicula nivalis, Pinguicula zecheri, Pinguicula corsica, Pinguicula sharpii, Pinguicula ibarrae, Pinguicula caudata, Pinguicula villosa, Pinguicula involuta, Pinguicula gracilis, Pinguicula lilacina, Pinguicula medusina, Pinguicula dostalii, Pinguicula gigantea, Pinguicula poldinii, Pinguicula vulgaris, Pinguicula cubensis, Pinguicula elongata, Pinguicula ionantha, Pinguicula mirandae, Pinguicula lavalvae, Pinguicula bohemica, Pinguicula acuminata, Pinguicula conzattii, Pinguicula esseriana, Pinguicula ehlersiae, Pinguicula gypsicola, Pinguicula lignicola, Pinguicula filifolia, Pinguicula benedicta, Pinguicula chilensis, Pinguicula sehuensis, Pinguicula variegata, Pinguicula balcanica, Pinguicula colimensis, Pinguicula cyclosecta, Pinguicula immaculata, Pinguicula lusitanica, Pinguicula moranensis, Pinguicula parvifolia, Pinguicula reticulata, Pinguicula casperiana, Pinguicula tejedensis, Pinguicula longifolia, Pinguicula martinezii, Pinguicula emarginata, Pinguicula leptoceras, Pinguicula macroceras, Pinguicula moctezumae, Pinguicula rectifolia, Pinguicula antarctica, Pinguicula calyptrata, Pinguicula planifolia, Pinguicula christinae, Pinguicula nevadensis, Pinguicula crassifolia, Pinguicula debbertiana, Pinguicula jaumavensis, Pinguicula grandiflora, Pinguicula macrophylla, Pinguicula oblongiloba, Pinguicula potosiensis, Pinguicula calderoniae, Pinguicula saetabensis, Pinguicula mesophytica, Pinguicula crystallina, Pinguicula dertosensis, Pinguicula crenatiloba, Pinguicula heterophylla, Pinguicula orchidioides, Pinguicula elizabethiae, Pinguicula primuliflora, Pinguicula rotundiflora, unclassified Pinguicula, Pinguicula fontiqueriana, Pinguicula vallis-regiae, Pinguicula hemiepiphytica, Pinguicula chuquisacensis, Pinguicula submediterranea, Pinguicula reichenbachiana, Pinguicula vallisneriifolia, Pinguicula cf. apuana ODC-2015, Pinguicula cf. christinae ODC-2015
Catalpol
Catalpol is an organic molecular entity. It has a role as a metabolite. Catalpol is a natural product found in Verbascum lychnitis, Plantago atrata, and other organisms with data available. See also: Rehmannia glutinosa Root (part of). Catalpol (Catalpinoside), an iridoid glycoside found in Rehmannia glutinosa. Catalpol has neuroprotective, hypoglycemic, anti-inflammatory, anti-cancer, anti-spasmodic, anti-oxidant effects and anti-HBV effects[1][2][3]. Catalpol (Catalpinoside), an iridoid glycoside found in Rehmannia glutinosa. Catalpol has neuroprotective, hypoglycemic, anti-inflammatory, anti-cancer, anti-spasmodic, anti-oxidant effects and anti-HBV effects[1][2][3].
Verbascoside
Verbascoside
Acteoside is a glycoside that is the alpha-L-rhamnosyl-(1->3)-beta-D-glucoside of hydroxytyrosol in which the hydroxy group at position 4 of the glucopyranosyl moiety has undergone esterification by formal condensation with trans-caffeic acid. It has a role as a neuroprotective agent, an antileishmanial agent, an anti-inflammatory agent, a plant metabolite and an antibacterial agent. It is a cinnamate ester, a disaccharide derivative, a member of catechols, a polyphenol and a glycoside. It is functionally related to a hydroxytyrosol and a trans-caffeic acid. Acteoside is under investigation in clinical trial NCT02662283 (Validity and Security of Reh-acteoside Therapy for Patients of IgA Nephropathy). Acteoside is a natural product found in Orobanche amethystea, Barleria lupulina, and other organisms with data available. See also: Harpagophytum zeyheri root (part of). A glycoside that is the alpha-L-rhamnosyl-(1->3)-beta-D-glucoside of hydroxytyrosol in which the hydroxy group at position 4 of the glucopyranosyl moiety has undergone esterification by formal condensation with trans-caffeic acid. D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents D064449 - Sequestering Agents > D002614 - Chelating Agents D020011 - Protective Agents > D000975 - Antioxidants D000890 - Anti-Infective Agents D000970 - Antineoplastic Agents Verbascoside is isolated from Acanthus mollis, acts as an ATP-competitive inhibitor of PKC, with an IC50 of 25 μM, and has antitumor, anti-inflammatory and antineuropathic pain activity. Verbascoside is isolated from Acanthus mollis, acts as an ATP-competitive inhibitor of PKC, with an IC50 of 25 μM, and has antitumor, anti-inflammatory and antineuropathic pain activity.
Isoscutellarein
A tetrahydroxyflavone that is apigenin with an extra hydroxy group at position 8.
[(2s,4s,5s,10s)-5-hydroxy-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl benzoate
C22H26O11 (466.14750460000005)
[(1s,2s,4s,5s,6r,10s)-5-hydroxy-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate
[(1s,2r,4r,5s,6r,10s)-5-hydroxy-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl benzoate
C22H26O11 (466.14750460000005)
(5-hydroxy-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl)methyl 3-phenylprop-2-enoate
C24H28O11 (492.16315380000003)
(5-hydroxy-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl)methyl benzoate
C22H26O11 (466.14750460000005)
[(1s,2s,4s,5s,6r,10s)-5-hydroxy-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl (2z)-3-phenylprop-2-enoate
C24H28O11 (492.16315380000003)
[(1s,2s,4s,5s,6r,10s)-5-hydroxy-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl (2e)-3-phenylprop-2-enoate
C24H28O11 (492.16315380000003)
[(1s,2s,4s,5s,6s,10s)-5-hydroxy-10-{[(2s,3s,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl (2z)-3-phenylprop-2-enoate
C24H28O11 (492.16315380000003)
(2s,3r,4s,5s,6r)-2-{[(1s,2r,4r,5s,6r,10s)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
(3r,4r,6r)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-{[(2s,3s,5r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate
[(1s,2s,4s,5s,6s,10s)-5-hydroxy-10-{[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-2-yl]methyl (2e)-3-phenylprop-2-enoate
C24H28O11 (492.16315380000003)