NCBI Taxonomy: 119950
Eugenia (ncbi_taxid: 119950)
found 36 associated metabolites at genus taxonomy rank level.
Ancestor: Eugenia group
Child Taxonomies: Eugenia cati, Eugenia rara, Eugenia simii, Eugenia regia, Eugenia varia, Eugenia hirta, Eugenia rosea, Eugenia unana, Eugenia virens, Eugenia gregii, Eugenia lucida, Eugenia yumana, Eugenia cuprea, Eugenia woodii, Eugenia nutans, Eugenia patens, Eugenia aurata, Eugenia cereja, Eugenia crassa, Eugenia excisa, Eugenia wentii, Eugenia lucens, Eugenia selloi, Eugenia whytei, Eugenia feijoi, Eugenia capuli, Eugenia binata, Eugenia bojeri, Eugenia laevis, Eugenia abunan, Eugenia rotula, Eugenia sparsa, Eugenia ramboi, Eugenia foetida, Eugenia acutata, Eugenia bullata, Eugenia biflora, Eugenia kalamii, Eugenia excelsa, Eugenia zeyheri, Eugenia modesta, Eugenia stahlii, Eugenia incerta, Eugenia pitanga, Eugenia cordata, Eugenia prasina, Eugenia repanda, Eugenia mosenii, Eugenia umbrosa, Eugenia expansa, Eugenia lineata, Eugenia naguana, Eugenia florida, Eugenia sulcata, Eugenia egensis, Eugenia inversa, Eugenia confusa, Eugenia pisonis, Eugenia rhombea, Eugenia costata, Eugenia arenosa, Eugenia humilis, Eugenia handroi, Eugenia truncata, Eugenia moschata, Eugenia kanakana, Eugenia pacifica, Eugenia capensis, Eugenia walkerae, Eugenia paludosa, Eugenia mooniana, Eugenia cupulata, Eugenia calycina, Eugenia hiemalis, Eugenia eggersii, Eugenia coronata, Eugenia pruinosa, Eugenia linearis, Eugenia lomensis, Eugenia puberula, Eugenia picardae, Eugenia websteri, Eugenia pohliana, Eugenia uniflora, Eugenia pyxidata, Eugenia patrisii, Eugenia exaltata, Eugenia talbotii, Eugenia padronii, Eugenia protenta, Eugenia bacopari, Eugenia hyemalis, Eugenia mattosii, Eugenia speciosa, Eugenia monticola, Eugenia buxifolia, Eugenia axillaris, Eugenia cucullata, Eugenia azurensis, Eugenia natalitia, Eugenia tinifolia, Eugenia tetramera, Eugenia oblongata, Eugenia moraviana, Eugenia stipitata, Eugenia subavenia, Eugenia platysema, Eugenia crenulata, Eugenia cycloidea, Eugenia lineolata, Eugenia leonensis, Eugenia ruschiana, Eugenia pubicalyx, Eugenia umbellata, Eugenia pollicina, Eugenia latifolia, Eugenia neibensis, Eugenia handroana, Eugenia aggregata, Eugenia bahiensis, Eugenia lindahlii, Eugenia caloneura, Eugenia nesiotica, Eugenia fissurata, Eugenia zuluensis, Eugenia splendens, Eugenia spruceana, Eugenia lagoensis, Eugenia vaughanii, Eugenia percincta, Eugenia boliviana, Eugenia hypargyrea, Eugenia salamensis, Eugenia wynadensis, Eugenia albanensis, Eugenia cocosensis, Eugenia macrocalyx, Eugenia stigmatosa, Eugenia adenocalyx, Eugenia pyriformis, Eugenia astringens, Eugenia sintenisii, Eugenia orbiculata, Eugenia mabaeoides, Eugenia brevistyla, Eugenia melanogyna, Eugenia orbignyana, Eugenia pisiformis, Eugenia pluriflora, Eugenia xiriricana, Eugenia glandulosa, Eugenia goiapabana, Eugenia gabonensis, Eugenia pobeguinii, Eugenia victoriana, Eugenia stenoxipha, Eugenia victorinii, Eugenia sonderiana, Eugenia gracillima, Eugenia petaloidea, Eugenia flavescens, Eugenia intermedia, Eugenia leptoclada, Eugenia comorensis, Eugenia ligustrina, Eugenia vattimoana, Eugenia zuccarinii, Eugenia hamiltonii, Eugenia calcadensis, Eugenia mespiloides, Eugenia myrcianthes, Eugenia cerasiflora, Eugenia coffeifolia, Eugenia dysenterica, Eugenia involucrata, Eugenia microphylla, Eugenia bocainensis, Eugenia paracatuana, Eugenia tropophylla, Eugenia verdoorniae, Eugenia domingensis, Eugenia grandissima, Eugenia fajardensis, Eugenia maestrensis, Eugenia mensurensis, Eugenia bimarginata, Eugenia piedraensis, Eugenia retinadenia, Eugenia rigidifolia, Eugenia stirpiflora, Eugenia tuberculata, Eugenia candolleana, Eugenia itacarensis, Eugenia fasciculata, Eugenia punicifolia, Eugenia ellipsoidea, Eugenia hiraeifolia, Eugenia lambertiana, Eugenia platyphylla, Eugenia woodburyana, Eugenia oerstediana, Eugenia guanabarina, Eugenia joseramosii, Eugenia kerianthera, Eugenia burkartiana, Eugenia rostrifolia, Eugenia schuechiana, Eugenia karwinskyana, Eugenia crassipetala, Eugenia angustissima, Eugenia tapacumensis, Eugenia neoglomerata, Eugenia neoverrucosa, Eugenia acapulcensis, Eugenia haematocarpa, Eugenia capitulifera, Eugenia catingiflora, Eugenia sphenophylla, Eugenia verticillata, Eugenia laeteviridis, Eugenia memecyloides, Eugenia stewardsonii, Eugenia cryptocardia, Eugenia langsdorffii, Eugenia stictosepala, Eugenia gongylocarpa, unclassified Eugenia, Eugenia anastomosans, Eugenia dictyophylla, Eugenia klotzschiana, Eugenia anjouanensis, Eugenia borinquensis, Eugenia sessiliflora, Eugenia galalonensis, Eugenia stictopetala, Eugenia brasiliensis, Eugenia multicostata, Eugenia neoaustralis, Eugenia uruguayensis, Eugenia venezuelensis, Eugenia erythrophylla, Eugenia longiracemosa, Eugenia reinwardtiana, Eugenia pseudopsidium, Eugenia convexinervia, Eugenia subterminalis, Eugenia neomyrtifolia, Eugenia luschnathiana, Eugenia membranifolia, Eugenia umbellulifera, Eugenia batingabranca, Eugenia densiracemosa, Eugenia pistaciifolia, Eugenia coloradoensis, Eugenia umtamvunensis, Eugenia neoriedeliana, Eugenia montevidensis, Eugenia singampattiana, Eugenia brongniartiana, Eugenia roseopetiolata, Eugenia capparidifolia, Eugenia bunchosiifolia, Eugenia supraaxillaris, Eugenia longipetiolata, Eugenia calophylloides, Eugenia copacabanensis, Eugenia francavilleana, Eugenia neofasciculata, Eugenia plicatocostata, Eugenia fasciculiflora, Eugenia beaurepairiana, Eugenia neograndifolia, Eugenia longipedunculata, Eugenia magnibracteolata, Eugenia macrobracteolata, Eugenia longohypanthiata, Eugenia agasthiyamalayana, Eugenia cf. rostrata FS393, Eugenia cf. repanda PEEA038, Eugenia cf. eggersii JF-2019, Eugenia cf. sauvallei JF-2019, Eugenia aff. adenocalyx AG-2022, Eugenia cf. tapacumensis HC-2017, Eugenia cf. ligustroides JF-2019, Eugenia cf. orbiculata JJNK-2011, Eugenia cf. verticillata PECB071, Eugenia cf. eggersii Flickinger 77, Eugenia cf. verticillata HUEFS245997, Eugenia cf. pistaciifolia HUEFS246089, Eugenia cf. ligustroides Gomez & al. s.n. 2018-003, Eugenia cf. sauvallei Oviedo & Hernandez s.n. 2017-007
Protocatechuic acid
Protocatechuic acid, also known as protocatechuate or 3,4-dihydroxybenzoate, belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. The enzyme protocatechuate 3,4-dioxygenase uses 3,4-dihydroxybenzoate and O2 to produce 3-carboxy-cis,cis-muconate. Protocatechuic acid is a drug. In the analogous hardening of the cockroach ootheca, the phenolic substance concerned is protocatechuic acid. Protocatechuic acid is a mild, balsamic, and phenolic tasting compound. Outside of the human body, protocatechuic acid is found, on average, in the highest concentration in a few different foods, such as garden onions, cocoa powders, and star anises and in a lower concentration in lentils, liquors, and red raspberries. Protocatechuic acid has also been detected, but not quantified in several different foods, such as cloud ear fungus, american pokeweeds, common mushrooms, fruits, and feijoa. This could make protocatechuic acid a potential biomarker for the consumption of these foods. It is also found in Allium cepa (17,540 ppm). It is a major metabolite of antioxidant polyphenols found in green tea. Similarly, PCA was reported to increase proliferation and inhibit apoptosis of neural stem cells. In vitro testing documented antioxidant and anti-inflammatory activity of PCA, while liver protection in vivo was measured by chemical markers and histological assessment. 3,4-dihydroxybenzoic acid, also known as protocatechuic acid or 4-carboxy-1,2-dihydroxybenzene, belongs to hydroxybenzoic acid derivatives class of compounds. Those are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. 3,4-dihydroxybenzoic acid is soluble (in water) and a weakly acidic compound (based on its pKa). 3,4-dihydroxybenzoic acid can be synthesized from benzoic acid. 3,4-dihydroxybenzoic acid is also a parent compound for other transformation products, including but not limited to, methyl 3,4-dihydroxybenzoate, ethyl 3,4-dihydroxybenzoate, and 1-(3,4-dihydroxybenzoyl)-beta-D-glucopyranose. 3,4-dihydroxybenzoic acid is a mild, balsamic, and phenolic tasting compound and can be found in a number of food items such as white mustard, grape wine, abalone, and asian pear, which makes 3,4-dihydroxybenzoic acid a potential biomarker for the consumption of these food products. 3,4-dihydroxybenzoic acid can be found primarily in blood, feces, and urine, as well as in human fibroblasts and testes tissues. 3,4-dihydroxybenzoic acid exists in all eukaryotes, ranging from yeast to humans. Protocatechuic acid (PCA) is a dihydroxybenzoic acid, a type of phenolic acid. It is a major metabolite of antioxidant polyphenols found in green tea. It has mixed effects on normal and cancer cells in in vitro and in vivo studies . 3,4-dihydroxybenzoic acid is a dihydroxybenzoic acid in which the hydroxy groups are located at positions 3 and 4. It has a role as a human xenobiotic metabolite, a plant metabolite, an antineoplastic agent, an EC 1.1.1.25 (shikimate dehydrogenase) inhibitor and an EC 1.14.11.2 (procollagen-proline dioxygenase) inhibitor. It is a member of catechols and a dihydroxybenzoic acid. It is functionally related to a benzoic acid. It is a conjugate acid of a 3,4-dihydroxybenzoate. 3,4-Dihydroxybenzoic acid is a natural product found in Visnea mocanera, Amomum subulatum, and other organisms with data available. Protocatechuic acid is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Black Cohosh (part of); Vaccinium myrtillus Leaf (part of); Menyanthes trifoliata leaf (part of) ... View More ... A dihydroxybenzoic acid in which the hydroxy groups are located at positions 3 and 4. Protocatechuic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=99-50-3 (retrieved 2024-06-29) (CAS RN: 99-50-3). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect. Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect.
Friedelin
Friedelin is a pentacyclic triterpenoid that is perhydropicene which is substituted by an oxo group at position 3 and by methyl groups at the 4, 4a, 6b, 8a, 11, 11, 12b, and 14a-positions (the 4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS-enantiomer). It is the major triterpenoid constituent of cork. It has a role as an anti-inflammatory drug, a non-narcotic analgesic, an antipyretic and a plant metabolite. It is a pentacyclic triterpenoid and a cyclic terpene ketone. Friedelin is a natural product found in Diospyros eriantha, Salacia chinensis, and other organisms with data available. A pentacyclic triterpenoid that is perhydropicene which is substituted by an oxo group at position 3 and by methyl groups at the 4, 4a, 6b, 8a, 11, 11, 12b, and 14a-positions (the 4R,4aS,6aS,6bR,8aR,12aR,12bS,14aS,14bS-enantiomer). It is the major triterpenoid constituent of cork. Friedelin is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Friedelin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Friedelin can be found in a number of food items such as pomegranate, sugar apple, apple, and mammee apple, which makes friedelin a potential biomarker for the consumption of these food products. Friedelin is a triterpenoid chemical compound found in Azima tetracantha, Orostachys japonica, and Quercus stenophylla. Friedelin is also found in the roots of the Cannabis plant .
Ellagic acid
Ellagic acid appears as cream-colored needles (from pyridine) or yellow powder. Odorless. (NTP, 1992) Ellagic acid is an organic heterotetracyclic compound resulting from the formal dimerisation of gallic acid by oxidative aromatic coupling with intramolecular lactonisation of both carboxylic acid groups of the resulting biaryl. It is found in many fruits and vegetables, including raspberries, strawberries, cranberries, and pomegranates. It has a role as an antioxidant, a food additive, a plant metabolite, an EC 5.99.1.2 (DNA topoisomerase) inhibitor, an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor, an EC 1.14.18.1 (tyrosinase) inhibitor, an EC 2.3.1.5 (arylamine N-acetyltransferase) inhibitor, an EC 2.4.1.1 (glycogen phosphorylase) inhibitor, an EC 2.5.1.18 (glutathione transferase) inhibitor, an EC 2.7.1.127 (inositol-trisphosphate 3-kinase) inhibitor, an EC 2.7.1.151 (inositol-polyphosphate multikinase) inhibitor, an EC 2.7.4.6 (nucleoside-diphosphate kinase) inhibitor, a skin lightening agent, a fungal metabolite, an EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor and a geroprotector. It is an organic heterotetracyclic compound, a cyclic ketone, a lactone, a member of catechols and a polyphenol. It is functionally related to a gallic acid. Ellagic acid is present in several fruits such as cranberries, strawberries, raspberries, and pomegranates. In pomegranates, there are several therapeutic compounds but ellagic acid is the most active and abundant. Ellagic acid is also present in vegetables. Ellagic acid is an investigational drug studied for treatment of Follicular Lymphoma (phase 2 trial), protection from brain injury of intrauterine growth restricted babies (phase 1 and 2 trial), improvement of cardiovascular function in adolescents who are obese (phase 2 trial), and topical treatment of solar lentigines. Ellagic acids therapeutic action mostly involves antioxidant and anti-proliferative effects. Ellagic acid is a natural product found in Fragaria chiloensis, Metrosideros perforata, and other organisms with data available. Ellagic acid is a metabolite found in or produced by Saccharomyces cerevisiae. A fused four ring compound occurring free or combined in galls. Isolated from the kino of Eucalyptus maculata Hook and E. Hemipholia F. Muell. Activates Factor XII of the blood clotting system which also causes kinin release; used in research and as a dye. Ellagic acid is an organic heterotetracyclic compound resulting from the formal dimerisation of gallic acid by oxidative aromatic coupling with intramolecular lactonisation of both carboxylic acid groups of the resulting biaryl. It is found in many fruits and vegetables, including raspberries, strawberries, cranberries, and pomegranates. It has a role as an antioxidant, a food additive, a plant metabolite, an EC 5.99.1.2 (DNA topoisomerase) inhibitor, an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor, an EC 1.14.18.1 (tyrosinase) inhibitor, an EC 2.3.1.5 (arylamine N-acetyltransferase) inhibitor, an EC 2.4.1.1 (glycogen phosphorylase) inhibitor, an EC 2.5.1.18 (glutathione transferase) inhibitor, an EC 2.7.1.127 (inositol-trisphosphate 3-kinase) inhibitor, an EC 2.7.1.151 (inositol-polyphosphate multikinase) inhibitor, an EC 2.7.4.6 (nucleoside-diphosphate kinase) inhibitor, a skin lightening agent, a fungal metabolite and an EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor. It is an organic heterotetracyclic compound, a cyclic ketone, a lactone, a member of catechols and a polyphenol. It derives from a gallic acid. Ellagic acid, also known as ellagate, belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. The antiproliferative and antioxidant properties of ellagic acid have spurred preliminary research into the potential health benefits of ellagic acid consumption. Ellagic acids therapeutic action mostly involves antioxidant and anti-proliferative/anti-cancer effects. Ellagic acid is found, on average, in the highest concentration within a few different foods, such as chestnuts, common walnuts, and japanese walnuts and in a lower concentration in whiskies, arctic blackberries, and cloudberries. Ellagic acid has also been detected, but not quantified in several different foods, such as lowbush blueberries, bilberries, guava, strawberry guava, and bog bilberries. An organic heterotetracyclic compound resulting from the formal dimerisation of gallic acid by oxidative aromatic coupling with intramolecular lactonisation of both carboxylic acid groups of the resulting biaryl. It is found in many fruits and vegetables, including raspberries, strawberries, cranberries, and pomegranates. Widely distributed in higher plants especies dicotyledons. Intestinal astringent, dietary role disputed. Nutriceutical with anticancer and antioxidation props. Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM. Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM.
Nootkatol
Nootkatol (cis or trans) is known to produce during synthetic (+)-nootkatone production from (+)-valencene by oxidation. Nootkatol is also reported as a precursor in several enzymatic oxidation of (+)-valencene to (+)-nootkatone. Nootkatone is an important oxidised sesquiterpene used in flavour and fragrance industry. Natural (+)-nootkatone can be extracted from grapefruit.
Spathulenol
Spathulenol is a tricyclic sesquiterpenoid that is 4-methylidenedecahydro-1H-cyclopropa[e]azulene carrying three methyl substituents at positions 1, 1 and 7 as well as a hydroxy substituent at position 7. It has a role as a volatile oil component, a plant metabolite, an anaesthetic and a vasodilator agent. It is a sesquiterpenoid, a carbotricyclic compound, a tertiary alcohol and an olefinic compound. Spathulenol is a natural product found in Xylopia aromatica, Xylopia emarginata, and other organisms with data available. See also: Chamomile (part of). A tricyclic sesquiterpenoid that is 4-methylidenedecahydro-1H-cyclopropa[e]azulene carrying three methyl substituents at positions 1, 1 and 7 as well as a hydroxy substituent at position 7. Spathulenol is found in alcoholic beverages. Spathulenol is a constituent of Salvia sclarea (clary sage).
Cubenol
Cubenol belongs to the family of Sesquiterpenes. These are terpenes with three consecutive isoprene units
Friedelin
Friedelin is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Friedelin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Friedelin can be found in a number of food items such as apple, pear, mammee apple, and sugar apple, which makes friedelin a potential biomarker for the consumption of these food products. Friedelin is a triterpenoid chemical compound found in Azima tetracantha, Orostachys japonica, and Quercus stenophylla. Friedelin is also found in the roots of the Cannabis plant .
Spathulenol
Constituent of Salvia sclarea (clary sage). Spathulenol is found in many foods, some of which are tarragon, spearmint, common sage, and tea.
Ellagic Acid
Origin: Plant, Ellagic acids, Benzopyranoids, Pyrans Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM. Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM.
Catechol
Catechin ((+)-Catechin) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Catechin ((+)-Catechin) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.
delta-Cadinene
A member of the cadinene family of sesquiterpenes in which the double bonds are located at the 4-4a and 7-8 positions, and in which the isopropyl group at position 1 is cis to the hydrogen at the adjacent bridgehead carbon (position 8a).
2-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl 3,4,5-trihydroxybenzoate
(1r,3as,5ar,5br,7ar,9s,10r,11ar,11br,13ar,13br)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid
[(2r,3s,4s,5r,6s)-6-{[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate
(2s,3r,4s,5s,6r)-4,5-dihydroxy-3-(3,4,5-trihydroxybenzoyloxy)-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl 3,4,5-trihydroxybenzoate
(4as,6as,6br,8ar,9r,10r,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
4-hydroxy-2-(4-hydroxyphenoxy)-5-(3,4,5-trihydroxybenzoyloxy)-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-3-yl 3,4,5-trihydroxybenzoate
(11r,12r,14r,15r,29r,30r,37r,38r,40r,57r,58s,65s)-4,5,6,12,20,21,22,25,30,31,31,38,46,47,48,51,52-heptadecahydroxy-9,17,32,35,43,55,62-heptaoxo-65-(3,4,5-trihydroxybenzoyloxy)-2,10,13,16,28,36,39,42,56,59,63-undecaoxadodecacyclo[35.15.6.5¹⁴,²⁷.1¹¹,¹⁵.1²⁶,³⁰.0³,⁸.0¹⁸,²³.0²⁹,³⁴.0⁴⁰,⁵⁷.0⁴⁴,⁴⁹.0⁵⁰,⁵⁴.0²⁴,⁶¹]pentahexaconta-1(52),3(8),4,6,18,20,22,24(61),25,27(60),33,44(49),45,47,50,53-hexadecaen-58-yl 3,4,5-trihydroxybenzoate
(1r,3as,5as,5br,9r,10r,11ar)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysene-3a-carboxylic acid
(1r,4r,6s,10s)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.0⁴,⁶]dodecane
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-{[(2s,3s,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium
(11r,12s,14r,15r,37r,38r,40r,57r,58s,64s)-4,5,6,12,20,21,22,30,31,32,38,46,47,48,51,52,59,60-octadecahydroxy-9,17,35,43,55,61-hexaoxo-64-(3,4,5-trihydroxybenzoyloxy)-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.3¹⁴,²⁵.2²⁴,²⁷.1¹¹,¹⁵.0³,⁸.0¹⁸,²³.0²⁹,³⁴.0⁴⁰,⁵⁷.0⁴⁴,⁴⁹.0⁵⁰,⁵⁴]tetrahexaconta-1(53),3,5,7,18(23),19,21,24,26,29,31,33,44(49),45,47,50(54),51,59-octadecaen-58-yl 3,4,5-trihydroxybenzoate
(7ar)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol
3,4,5,13,21,22,23-heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyloxy)-9,14,17-trioxatetracyclo[17.4.0.0²,⁷.0¹⁰,¹⁵]tricosa-1(23),2(7),3,5,19,21-hexaen-12-yl 2-{[3,4,5,12,22,23-hexahydroxy-8,18-dioxo-11,13-bis(3,4,5-trihydroxybenzoyloxy)-9,14,17-trioxatetracyclo[17.4.0.0²,⁷.0¹⁰,¹⁵]tricosa-1(23),2(7),3,5,19,21-hexaen-21-yl]oxy}-3,4,5-trihydroxybenzoate
C68H50O44 (1570.1674899999998)