NCBI Taxonomy: 13590
Leucopogon (ncbi_taxid: 13590)
found 27 associated metabolites at genus taxonomy rank level.
Ancestor: Styphelieae
Child Taxonomies: Leucopogon fraseri, Leucopogon muticus, Leucopogon gibbosus, Leucopogon nutans, Leucopogon blakei, Leucopogon distans, Leucopogon elegans, Leucopogon setiger, Leucopogon woodsii, Leucopogon microphyllus, Leucopogon hispidus, Leucopogon allittii, Leucopogon rupicola, Leucopogon bossiaea, Leucopogon cordatus, Leucopogon pendulus, Leucopogon extremus, Leucopogon obtectus, Leucopogon biflorus, Leucopogon strictus, Leucopogon virgatus, Leucopogon collinus, Leucopogon costatus, Leucopogon cymbulae, Leucopogon opponens, Leucopogon compactus, Leucopogon concurvus, Leucopogon pubescens, Leucopogon exolasius, Leucopogon gilbertii, Leucopogon insularis, Leucopogon malayanus, Leucopogon yorkensis, Leucopogon appressus, Leucopogon assimilis, Leucopogon australis, Leucopogon ericoides, Leucopogon fletcheri, Leucopogon glabellus, Leucopogon oxycedrus, Leucopogon concinnus, Leucopogon revolutus, Leucopogon exolacius, Leucopogon carinatus, Leucopogon fimbriatus, Leucopogon mitchellii, Leucopogon apiculatus, Leucopogon leptanthus, Leucopogon marginatus, Leucopogon flavescens, Leucopogon dielsianus, Leucopogon esquamatus, Leucopogon margarodes, Leucopogon acuminatus, Leucopogon propinquus, Leucopogon rubicundus, Leucopogon attenuatus, Leucopogon lavarackii, Leucopogon planifolius, Leucopogon racemulosus, Leucopogon ruscifolius, Leucopogon sonderensis, Leucopogon pimeleoides, Leucopogon cordifolius, Leucopogon cuneifolius, Leucopogon cymbiformis, Leucopogon juniperinus, Leucopogon lanceolatus, Leucopogon neoanglicus, Leucopogon ovalifolius, Leucopogon parviflorus, Leucopogon pogonocalyx, Leucopogon atherolepis, Leucopogon tamminensis, Leucopogon xerampelinus, Leucopogon glaucifolius, unclassified Leucopogon, Leucopogon capitellatus, Leucopogon fasciculatus, Leucopogon corynocarpus, Leucopogon crassiflorus, Leucopogon crassifolius, Leucopogon denticulatus, Leucopogon melaleucoides, Leucopogon rotundifolius, Leucopogon alternifolius, Leucopogon amplexicaulis, Leucopogon blepharolepis, Leucopogon plumuliflorus, Leucopogon gnaphalioides, Leucopogon pluriloculatus, Leucopogon conostephioides, Leucopogon leptospermoides, Leucopogon aff. marginatus CPL047-10, Leucopogon aff. marginatus Brown 97/316
Shikimic acid
Shikimic acid is a cyclohexenecarboxylic acid that is cyclohex-1-ene-1-carboxylic acid substituted by hydroxy groups at positions 3, 4 and 5 (the 3R,4S,5R stereoisomer). It is an intermediate metabolite in plants and microorganisms. It has a role as an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite and a plant metabolite. It is a cyclohexenecarboxylic acid, a hydroxy monocarboxylic acid and an alpha,beta-unsaturated monocarboxylic acid. It is a conjugate acid of a shikimate. Shikimic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Shikimic acid is a natural product found in Quercus mongolica, Populus tremula, and other organisms with data available. Shikimic acid is a metabolite found in or produced by Saccharomyces cerevisiae. A tri-hydroxy cyclohexene carboxylic acid important in biosynthesis of so many compounds that the shikimate pathway is named after it. Shikimic acid, more commonly known as its anionic form shikimate, is a cyclohexene, a cyclitol and a cyclohexanecarboxylic acid. It is an important biochemical intermediate in plants and microorganisms. Its name comes from the Japanese flower shikimi (the Japanese star anise, Illicium anisatum), from which it was first isolated. Shikimic acid is a precursor for: the aromatic amino acids phenylalanine and tyrosine; indole, indole derivatives and tryptophan; many alkaloids and other aromatic metabolites; tannins; and lignin. In pharmaceutical industry, shikimic acid from chinese star anise is used as a base material for production of Tamiflu (oseltamivir). Although shikimic acid is present in most autotrophic organisms, it is a biosynthetic intermediate and generally found in very low concentrations. A cyclohexenecarboxylic acid that is cyclohex-1-ene-1-carboxylic acid substituted by hydroxy groups at positions 3, 4 and 5 (the 3R,4S,5R stereoisomer). It is an intermediate metabolite in plants and microorganisms. Acquisition and generation of the data is financially supported in part by CREST/JST. CONFIDENCE standard compound; INTERNAL_ID 175 KEIO_ID S012 Shikimic acid is a key metabolic intermediate of the aromatic amino acid biosynthesis pathway, found in microbes and plants. Shikimic acid is a key metabolic intermediate of the aromatic amino acid biosynthesis pathway, found in microbes and plants.
Gardenoside
C17H24O11 (404.13185539999995)
A cyclopentapyran that is 7-deoxyloganin with a methyl and hydrogen replaced by hydroxy and hydroxymethyl groups at position 7. Gardenoside is a natural product found in Gardenia jasminoides, Catunaregam obovata, and other organisms with data available. Gardenoside is a natural compound found in Gardenia fruits, with hepatoprotective properties. Gardenoside suppresses the pain of chronic constriction injury by regulating the P2X3 and P2X7 receptors. Gardenoside has an inhibitory effect on free fatty acids (FFA)-induced cellular steatosis[1][2]. Gardenoside is a natural compound found in Gardenia fruits, with hepatoprotective properties. Gardenoside suppresses the pain of chronic constriction injury by regulating the P2X3 and P2X7 receptors. Gardenoside has an inhibitory effect on free fatty acids (FFA)-induced cellular steatosis[1][2]. Gardenoside is a natural compound found in Gardenia fruits, with hepatoprotective properties. Gardenoside suppresses the pain of chronic constriction injury by regulating the P2X3 and P2X7 receptors. Gardenoside has an inhibitory effect on free fatty acids (FFA)-induced cellular steatosis[1][2].
Gardenoside
C17H24O11 (404.13185539999995)
shikimate
Shikimic acid, also known as shikimate or 3,4,5-trihydroxy-1-cyclohexenecarboxylic acid, is a member of the class of compounds known as shikimic acids and derivatves. Shikimic acids and derivatves are cyclitols containing a cyclohexanecarboxylic acid substituted with three hydroxyl groups at positions 3, 4, and 5. Shikimic acid is soluble (in water) and a weakly acidic compound (based on its pKa). Shikimic acid can be found in a number of food items such as date, rocket salad, redcurrant, and poppy, which makes shikimic acid a potential biomarker for the consumption of these food products. Shikimic acid can be found primarily in blood and urine. Shikimic acid exists in all living species, ranging from bacteria to humans. Shikimic acid, more commonly known as its anionic form shikimate, is a cyclohexene, a cyclitol and a cyclohexanecarboxylic acid. It is an important biochemical metabolite in plants and microorganisms. Its name comes from the Japanese flower shikimi (シキミ, the Japanese star anise, Illicium anisatum), from which it was first isolated in 1885 by Johan Fredrik Eykman. The elucidation of its structure was made nearly 50 years later . Shikimic acid is a key metabolic intermediate of the aromatic amino acid biosynthesis pathway, found in microbes and plants. Shikimic acid is a key metabolic intermediate of the aromatic amino acid biosynthesis pathway, found in microbes and plants.
5,7-dihydroxy-2-(4-hydroxy-3-oxidophenyl)-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-1λ⁴-chromen-1-ylium
(4as,4br,7s,8ar)-7-ethenyl-1,1,4b,7-tetramethyl-3,4,4a,5,6,8,8a,9-octahydro-2h-phenanthrene
5,7-dihydroxy-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-1λ⁴-chromen-1-ylium
[C20H19O11]+ (435.09273240000005)