NCBI Taxonomy: 911345
Gaillardiinae (ncbi_taxid: 911345)
found 429 associated metabolites at subtribe taxonomy rank level.
Ancestor: Helenieae
Child Taxonomies: Helenium, Gaillardia, Balduina, Plateilema
Luteolin
Luteolin is a naturally occurring flavonoid. (PMID:17168665). The flavonoids are polyphenolic compounds found as integral components of the human diet. They are universally present as constituents of flowering plants, particularly of food plants. The flavonoids are phenyl substituted chromones (benzopyran derivatives) consisting of a 15-carbon basic skeleton (C6-C3-C6), composed of a chroman (C6-C3) nucleus (the benzo ring A and the heterocyclic ring C), also shared by the tocopherols, with a phenyl (the aromatic ring B) substitution usually at the 2-position. Different substitutions can typically occur in the rings, A and B. Several plants and spices containing flavonoid derivatives have found application as disease preventive and therapeutic agents in traditional medicine in Asia for thousands of years. The selection of a particular food plant, plant tissue or herb for its potential health benefits appears to mirror its flavonoid composition. The much lower risk of colon, prostate and breast cancers in Asians, who consume more vegetables, fruits and tea than populations in the Western hemisphere do, raises the question of whether flavonoid components mediate the protective effects of diets rich in these foodstuffs by acting as natural chemopreventive and anticancer agents. An impressive body of information exists on the antitumoral action of plant flavonoids. In vitro work has concentrated on the direct and indirect actions of flavonoids on tumor cells, and has found a variety of anticancer effects such as cell growth and kinase activity inhibition, apoptosis induction, suppression of the secretion of matrix metalloproteinases and of tumor invasive behavior. Furthermore, some studies have reported the impairment of in vivo angiogenesis by dietary flavonoids. Experimental animal studies indicate that certain dietary flavonoids possess antitumoral activity. The hydroxylation pattern of the B ring of the flavones and flavonols, such as luteolin seems to critically influence their activities, especially the inhibition of protein kinase activity and antiproliferation. The different mechanisms underlying the potential anticancer action of plant flavonoids await further elucidation. Certain dietary flavonols and flavones targeting cell surface signal transduction enzymes, such as protein tyrosine and focal adhesion kinases, and the processes of angiogenesis appear to be promising candidates as anticancer agents. Further in vivo studies of these bioactive constituents is deemed necessary in order to develop flavonoid-based anticancer strategies. In view of the increasing interest in the association between dietary flavonoids and cancer initiation and progression, this important field is likely to witness expanded effort and to attract and stimulate further vigorous investigations (PMID:16097445). Luteolin is a tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 4, 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. It has a role as an EC 2.3.1.85 (fatty acid synthase) inhibitor, an antineoplastic agent, a vascular endothelial growth factor receptor antagonist, a plant metabolite, a nephroprotective agent, an angiogenesis inhibitor, a c-Jun N-terminal kinase inhibitor, an anti-inflammatory agent, an apoptosis inducer, a radical scavenger and an immunomodulator. It is a 3-hydroxyflavonoid and a tetrahydroxyflavone. It is a conjugate acid of a luteolin-7-olate. Luteolin is a natural product found in Verbascum lychnitis, Carex fraseriana, and other organisms with data available. Luteolin is a naturally-occurring flavonoid, with potential anti-oxidant, anti-inflammatory, apoptosis-inducing and chemopreventive activities. Upon administration, luteolin scavenges free radicals, protects cells from reactive oxygen species (ROS)-induced damage and induces direct cell cycle arrest and apoptosis in tumor cells. This inhibits tumor cell proliferation and suppresses metastasis. 5,7,3,4-tetrahydroxy-flavone, one of the FLAVONES. See also: Chamomile (part of); Cannabis sativa subsp. indica top (part of); Fenugreek seed (part of). A tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 4, 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. Flavone v. widespread in plant world; found especies in celery, peppermint, rosemary, thyme and Queen Annes Lace leaves (wild carrot). Potential nutriceutical. Luteolin is found in many foods, some of which are soy bean, ginger, abalone, and swiss chard. Acquisition and generation of the data is financially supported in part by CREST/JST. IPB_RECORD: 361; CONFIDENCE confident structure CONFIDENCE standard compound; INTERNAL_ID 48 Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3]. Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3].
Isovitexin
Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of an isovitexin-7-olate. Isovitexin is a natural product found in Carex fraseriana, Rauhiella, and other organisms with data available. See also: Fenugreek seed (part of); Acai (part of); Crataegus monogyna flowering top (part of). [Raw Data] CBA25_Isovitexin_neg_20eV_1-7_01_1425.txt [Raw Data] CBA25_Isovitexin_neg_10eV_1-7_01_1369.txt [Raw Data] CBA25_Isovitexin_pos_30eV_1-7_01_1399.txt [Raw Data] CBA25_Isovitexin_neg_40eV_1-7_01_1427.txt [Raw Data] CBA25_Isovitexin_neg_30eV_1-7_01_1426.txt [Raw Data] CBA25_Isovitexin_neg_50eV_1-7_01_1428.txt [Raw Data] CBA25_Isovitexin_pos_20eV_1-7_01_1398.txt [Raw Data] CBA25_Isovitexin_pos_10eV_1-7_01_1358.txt [Raw Data] CBA25_Isovitexin_pos_40eV_1-7_01_1400.txt [Raw Data] CBA25_Isovitexin_pos_50eV_1-7_01_1401.txt Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.
Vitexin 6'-O-malonyl 2'-O-xyloside
Vitexin 6-o-malonyl 2-o-xyloside, also known as apigenin 8-C-glucoside or 8-glycosyl-apigenin, is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin 6-o-malonyl 2-o-xyloside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin 6-o-malonyl 2-o-xyloside can be synthesized from apigenin. Vitexin 6-o-malonyl 2-o-xyloside is also a parent compound for other transformation products, including but not limited to, vitexin 2-O-beta-L-rhamnoside, 7-O-methylvitexin 2-O-beta-L-rhamnoside, and vitexin 2-O-beta-D-glucoside. Vitexin 6-o-malonyl 2-o-xyloside can be found in common beet, which makes vitexin 6-o-malonyl 2-o-xyloside a potential biomarker for the consumption of this food product. Vitexin, also known as apigenin 8-C-glucoside or 8-glycosylapigenin, belongs to the class of organic compounds known as flavonoid 8-C-glycosides. Flavonoid 8-C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin is also described as an apigenin flavone glucoside. Vitexin has been found in passion flower, chasteberry, bamboo leaves, millet and Hawthorn. Vitexin has shown a wide range of pharmacological effects, such as antioxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects (PMID: 27693342). Vitexin has also been shown to directly inhibit thyroid peroxidase and potentially contributes to goiter (PMID: 1696490). It is sometimes called a goitrogen. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA68_Vitexin_neg_10eV.txt [Raw Data] CBA68_Vitexin_neg_30eV.txt [Raw Data] CBA68_Vitexin_pos_20eV.txt [Raw Data] CBA68_Vitexin_neg_50eV.txt [Raw Data] CBA68_Vitexin_neg_40eV.txt [Raw Data] CBA68_Vitexin_pos_40eV.txt [Raw Data] CBA68_Vitexin_pos_30eV.txt [Raw Data] CBA68_Vitexin_pos_10eV.txt [Raw Data] CBA68_Vitexin_neg_20eV.txt Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].
Eriodictyol
Eriodictyol, also known as 3,4,5,7-tetrahydroxyflavanone or 2,3-dihydroluteolin, belongs to the class of organic compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Thus, eriodictyol is considered to be a flavonoid lipid molecule. Outside of the human body, eriodictyol has been detected, but not quantified in, several different foods, such as common oregano, common thymes, parsley, sweet basils, and tarragons. This could make eriodictyol a potential biomarker for the consumption of these foods. Eriodictyol is a compound isolated from Eriodictyon californicum and can be used in medicine as an expectorant. BioTransformer predicts that eriodictiol is a product of luteolin metabolism via a flavonoid-c-ring-reduction reaction catalyzed by an unspecified-gut microbiota enzyme (PMID: 30612223). Eriodictyol, also known as 5735-tetrahydroxyflavanone, is a member of the class of compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Eriodictyol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Eriodictyol can be found in a number of food items such as rowal, grape, cardamom, and lemon balm, which makes eriodictyol a potential biomarker for the consumption of these food products. Eriodictyol is a bitter-masking flavanone, a flavonoid extracted from yerba santa (Eriodictyon californicum), a plant native to North America. Eriodictyol is one of the four flavanones identified in this plant as having taste-modifying properties, the other three being homoeriodictyol, its sodium salt, and sterubin . Eriodictyol is a tetrahydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 7, 3 and 4 respectively. It is a tetrahydroxyflavanone and a member of 3-hydroxyflavanones. Eriodictyol is a natural product found in Eupatorium album, Eupatorium hyssopifolium, and other organisms with data available. A tetrahydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 7, 3 and 4 respectively. Acquisition and generation of the data is financially supported in part by CREST/JST. Eriodictyol is a flavonoid isolated from the Chinese herb, with antioxidant and anti-inflammatory activity. Eriodictyol induces Nrf2 signaling pathway. Eriodictyol is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 18 nM. Eriodictyol is a flavonoid isolated from the Chinese herb, with antioxidant and anti-inflammatory activity. Eriodictyol induces Nrf2 signaling pathway. Eriodictyol is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 18 nM.
Quercetin
Quercetin appears as yellow needles or yellow powder. Converts to anhydrous form at 203-207 °F. Alcoholic solutions taste very bitter. (NTP, 1992) Quercetin is a pentahydroxyflavone having the five hydroxy groups placed at the 3-, 3-, 4-, 5- and 7-positions. It is one of the most abundant flavonoids in edible vegetables, fruit and wine. It has a role as an antibacterial agent, an antioxidant, a protein kinase inhibitor, an antineoplastic agent, an EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor, a plant metabolite, a phytoestrogen, a radical scavenger, a chelator, an Aurora kinase inhibitor and a geroprotector. It is a pentahydroxyflavone and a 7-hydroxyflavonol. It is a conjugate acid of a quercetin-7-olate. Quercetin is a flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin. Quercetin is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Quercetin is a flavonoid found in many foods and herbs and is a regular component of a normal diet. Extracts of quercetin have been used to treat or prevent diverse conditions including cardiovascular disease, hypercholesterolemia, rheumatic diseases, infections and cancer but have not been shown to be effective in clinical trials for any medical condition. Quercetin as a nutritional supplement is well tolerated and has not been linked to serum enzyme elevations or to episodes of clinically apparent liver injury. Quercetin is a natural product found in Lotus ucrainicus, Visnea mocanera, and other organisms with data available. Quercetin is a polyphenolic flavonoid with potential chemopreventive activity. Quercetin, ubiquitous in plant food sources and a major bioflavonoid in the human diet, may produce antiproliferative effects resulting from the modulation of either EGFR or estrogen-receptor mediated signal transduction pathways. Although the mechanism of action of action is not fully known, the following effects have been described with this agent in vitro: decreased expression of mutant p53 protein and p21-ras oncogene, induction of cell cycle arrest at the G1 phase and inhibition of heat shock protein synthesis. This compound also demonstrates synergy and reversal of the multidrug resistance phenotype, when combined with chemotherapeutic drugs, in vitro. Quercetin also produces anti-inflammatory and anti-allergy effects mediated through the inhibition of the lipoxygenase and cyclooxygenase pathways, thereby preventing the production of pro-inflammatory mediators. Quercetin is a flavonoid widely distributed in many plants and fruits including red grapes, citrus fruit, tomato, broccoli and other leafy green vegetables, and a number of berries, including raspberries and cranberries. Quercetin itself (aglycone quercetin), as opposed to quercetin glycosides, is not a normal dietary component. Quercitin glycosides are converted to phenolic acids as they pass through the gastrointestinal tract. Quercetin has neither been confirmed scientifically as a specific therapeutic for any condition nor been approved by any regulatory agency. The U.S. Food and Drug Administration has not approved any health claims for quercetin. Nevertheless, the interest in dietary flavonoids has grown after the publication of several epidemiological studies showing an inverse correlation between dietary consumption of flavonols and flavones and reduced incidence and mortality from cardiovascular disease and cancer. In recent years, a large amount of experimental and some clinical data have accumulated regarding the effects of flavonoids on the endothelium under physiological and pathological conditions. The meta-analysis of seven prospective cohort studies concluded that the individuals in the top third of dietary flavonol intake are associated with a reduced risk of mortality from coronary heart disease as compared with those in the bottom third, after adju... Quercetin is a flavonoid widely distributed in many plants and fruits including red grapes, citrus fruit, tomato, broccoli and other leafy green vegetables, and a number of berries, including raspberries and cranberries. Quercetin itself (aglycone quercetin), as opposed to quercetin glycosides, is not a normal dietary component. Quercetin glycosides are converted to phenolic acids as they pass through the gastrointestinal tract. Quercetin has neither been confirmed scientifically as a specific therapeutic for any condition nor been approved by any regulatory agency. The U.S. Food and Drug Administration has not approved any health claims for quercetin. Nevertheless, the interest in dietary flavonoids has grown after the publication of several epidemiological studies showing an inverse correlation between dietary consumption of flavonols and flavones and reduced incidence and mortality from cardiovascular disease and cancer. In recent years, a large amount of experimental and some clinical data have accumulated regarding the effects of flavonoids on the endothelium under physiological and pathological conditions. The meta-analysis of seven prospective cohort studies concluded that the individuals in the top third of dietary flavonol intake are associated with a reduced risk of mortality from coronary heart disease as compared with those in the bottom third, after adjustment for known risk factors and other dietary components. A limited number of intervention studies with flavonoids and flavonoid containing foods and extracts has been performed in several pathological conditions (PMID:17015250). Quercetin is isolated from many plants, especially fruits, such as Helichrysum, Euphorbia and Karwinskia spp. Present in the Solanaceae, Rhamnaceae, Passifloraceae and many other families. For example detected in almost all studied Umbelliferae. Nutriceutical with antiinflammatory props. and a positive influence on the blood lipid profile. Found in a wide variety of foods especially apples, bee pollen, blackcurrants, capers, cocoa, cranberries, dock leaves, elderberries, fennel, lovage, red onions, ancho peppers, dill weed and tarragon. A pentahydroxyflavone having the five hydroxy groups placed at the 3-, 3-, 4-, 5- and 7-positions. It is one of the most abundant flavonoids in edible vegetables, fruit and wine. COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 298; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4014; ORIGINAL_PRECURSOR_SCAN_NO 4012 INTERNAL_ID 298; CONFIDENCE standard compound; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4011; ORIGINAL_PRECURSOR_SCAN_NO 4010 CONFIDENCE standard compound; INTERNAL_ID 298; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4019; ORIGINAL_PRECURSOR_SCAN_NO 4018 CONFIDENCE standard compound; INTERNAL_ID 298; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4017; ORIGINAL_PRECURSOR_SCAN_NO 4016 CONFIDENCE standard compound; INTERNAL_ID 298; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4011; ORIGINAL_PRECURSOR_SCAN_NO 4010 CONFIDENCE standard compound; INTERNAL_ID 298; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4096; ORIGINAL_PRECURSOR_SCAN_NO 4094 CONFIDENCE standard compound; INTERNAL_ID 298; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4024; ORIGINAL_PRECURSOR_SCAN_NO 4023 Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CB109_Quercetin_pos_30eV_CB000041.txt IPB_RECORD: 1761; CONFIDENCE confident structure [Raw Data] CB109_Quercetin_pos_10eV_CB000041.txt [Raw Data] CB109_Quercetin_pos_20eV_CB000041.txt [Raw Data] CB109_Quercetin_pos_40eV_CB000041.txt [Raw Data] CB109_Quercetin_pos_50eV_CB000041.txt IPB_RECORD: 161; CONFIDENCE confident structure [Raw Data] CB109_Quercetin_neg_40eV_000027.txt [Raw Data] CB109_Quercetin_neg_50eV_000027.txt [Raw Data] CB109_Quercetin_neg_20eV_000027.txt [Raw Data] CB109_Quercetin_neg_30eV_000027.txt [Raw Data] CB109_Quercetin_neg_10eV_000027.txt CONFIDENCE standard compound; INTERNAL_ID 124 CONFIDENCE standard compound; ML_ID 54 Quercetin, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively[1]. Quercetin, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively[1].
Orientin
Orientin is a C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8. It has a role as an antioxidant and a metabolite. It is a C-glycosyl compound, a tetrahydroxyflavone and a 3-hydroxyflavonoid. It is functionally related to a luteolin. Orientin is a natural product found in Itea chinensis, Vellozia epidendroides, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Fenugreek seed (part of); Acai fruit pulp (part of). Orientin is found in barley. Orientin is isolated from Hordeum vulgare (barley) and Passiflora incarnata (maypops).Orientin is a flavone, a chemical flavonoid-like compound found in the passion flower, the palm and Anadenanthera peregrina. Orientin is also reported in millets and in the Phyllostachys nigra bamboo leaves Isolated from Hordeum vulgare (barley) and Passiflora incarnata (maypops) [Raw Data] CBA20_Orientin_pos_40eV_1-2_01_1380.txt [Raw Data] CBA20_Orientin_neg_20eV_1-2_01_1405.txt [Raw Data] CBA20_Orientin_neg_50eV_1-2_01_1408.txt [Raw Data] CBA20_Orientin_neg_40eV_1-2_01_1407.txt [Raw Data] CBA20_Orientin_pos_50eV_1-2_01_1381.txt [Raw Data] CBA20_Orientin_neg_30eV_1-2_01_1406.txt [Raw Data] CBA20_Orientin_pos_20eV_1-2_01_1378.txt [Raw Data] CBA20_Orientin_pos_30eV_1-2_01_1379.txt [Raw Data] CBA20_Orientin_pos_10eV_1-2_01_1353.txt [Raw Data] CBA20_Orientin_neg_10eV_1-2_01_1364.txt Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2]. Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2].
beta-Elemene
(-)-beta-elemene is the (-)-enantiomer of beta-elemene that has (1S,2S,4R)-configuration. It has a role as an antineoplastic agent. beta-Elemene is a natural product found in Xylopia sericea, Eupatorium cannabinum, and other organisms with data available. Beta-elemene is one of the isomers of elemene, a lipid soluble sesquiterpene and the active component isolated from the Chinese medicinal herb Rhizoma zedoariae with potential antineoplastic and chemopreventive activities. Although the exact mechanism of action through which beta-elemene exerts its effect has yet to be fully elucidated, this agent appears to induce apoptosis through different mechanisms of action and induces cell cycle arrest at different stages based on the tumor cell type involved. Beta-elemene may sensitize cancer cells to other chemotherapeutic agents. See also: Cannabis sativa subsp. indica top (part of). Beta-elemene, also known as B-elemen or 2,4-diisopropenyl-1-methyl-1-vinylcyclohexane, is a member of the class of compounds known as elemane sesquiterpenoids. Elemane sesquiterpenoids are sesquiterpenoids with a structure based on the elemane skeleton. Elemane is a monocyclic compound consisting of a cyclohexane ring substituted with a methyl group, an ethyl group, and two 1-methylethyl groups at the 1-, 1-, 2-, and 4-position, respectively. Beta-elemene is a fresh, herbal, and waxy tasting compound and can be found in a number of food items such as lovage, anise, spearmint, and orange mint, which makes beta-elemene a potential biomarker for the consumption of these food products. Beta-elemene can be found primarily in saliva. beta-Elemene belongs to the class of organic compounds known as elemane sesquiterpenoids. These are sesquiterpenoids with a structure based on the elemane skeleton. Elemane is a monocyclic compound consisting of a cyclohexane ring substituted with a methyl group, an ethyl group, and two 1-methylethyl groups at the 1-, 1-, 2-, and 4-position, respectively. beta-Elemene can be found in herbs, spices, and root vegetables, which makes beta-elemene a potential biomarker for the consumption of these food products. It is a constituent of sweet flag, juniper oils, and Mentha species. β-Elemene ((-)-β-Elemene; Levo-β-elemene) is isolated from natural plant Curcuma aromatica with an antitumor activity. β-Elemene can induce cell apoptosis. β-Elemene ((-)-β-Elemene; Levo-β-elemene) is isolated from natural plant Curcuma aromatica with an antitumor activity. β-Elemene can induce cell apoptosis.
Helenalin
Helenalin is a sesquiterpene lactone that is 3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione substituted by a hydroxy group at position 4, methyl groups at positions 4a and 8 and a methylidene group at position 3 (the 3aS,4S,4aR,7aR,8R,9aR stereoisomer). It has a role as an anti-inflammatory agent, an antineoplastic agent, a plant metabolite and a metabolite. It is a gamma-lactone, a cyclic ketone, an organic heterotricyclic compound, a sesquiterpene lactone and a secondary alcohol. Helenalin is a natural product found in Pentanema britannicum, Psilostrophe cooperi, and other organisms with data available. A sesquiterpene lactone that is 3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione substituted by a hydroxy group at position 4, methyl groups at positions 4a and 8 and a methylidene group at position 3 (the 3aS,4S,4aR,7aR,8R,9aR stereoisomer). D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D002316 - Cardiotonic Agents D000893 - Anti-Inflammatory Agents D000970 - Antineoplastic Agents D002317 - Cardiovascular Agents D018501 - Antirheumatic Agents
Tenulin
Tenulin is a sesquiterpene lactone. Tenulin is a natural product found in Helenium quadridentatum, Helenium donianum, and Helenium amarum with data available.
Amyrin
Beta-amyrin is a pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. It has a role as a plant metabolite and an Aspergillus metabolite. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an oleanane. beta-Amyrin is a natural product found in Ficus pertusa, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Centaurium erythraea whole (part of). A pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].
Florilenalin
Florilenalin is a sesquiterpene lactone. Florilenalin is a natural product found in Gaillardia pulchella, Hymenoxys odorata, and other organisms with data available.
Methyl caffeate
Methyl caffeate, an antimicrobial agent, shows moderate antimicrobial and prominent antimycobacterial activities. Methyl caffeate also exhibits α-glucosidase inhibition activity, oxidative stress inhibiting activity, anti-platelet activity, antiproliferative activity in cervix adenocarcinoma and anticancer activity in lung and leukmia cell lines[1]. Methyl caffeate, an antimicrobial agent, shows moderate antimicrobial and prominent antimycobacterial activities. Methyl caffeate also exhibits α-glucosidase inhibition activity, oxidative stress inhibiting activity, anti-platelet activity, antiproliferative activity in cervix adenocarcinoma and anticancer activity in lung and leukmia cell lines[1].
Amaralin
An azulenofuran that is decahydrooxireno[1,2]azuleno[6,5-b]furan-5(1aH)-one substituted by a hydroxy group at position 8, methyl groups at positions 2 and 7a and a methylidene group at position 6.
aromaticin
A sesquiterpene lactone that is 3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione substituted by methyl groups at positions 4a and 8 and a methylidene group at position 3. Isolated from the aerial parts of Inula hupehensis, it exhibits anti-inflammatory activity.
Fastigilin B
Gaillardin
Plenolin
Vitexin
Vitexin is an apigenin flavone glycoside, which is found in the passion flower, bamboo leaves and pearl millet It has a role as a platelet aggregation inhibitor, an EC 3.2.1.20 (alpha-glucosidase) inhibitor, an antineoplastic agent and a plant metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of a vitexin-7-olate. Vitexin is a natural product found in Itea chinensis, Salacia chinensis, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Cytisus scoparius flowering top (part of); Fenugreek seed (part of) ... View More ... An apigenin flavone glycoside, which is found in the passion flower, bamboo leaves and pearl millet Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].
Vitexin
Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].
4-Epiisoinuviscolide
4-Epiisoinuviscolide is found in herbs and spices. 4-Epiisoinuviscolide is a constituent of Inula helenium (elecampane) Constituent of Inula helenium (elecampane). 4-Epiisoinuviscolide is found in herbs and spices.
4',5-Dihydroxy-3',7-dimethoxyisoflavone
4,5-Dihydroxy-3,7-dimethoxyisoflavone is found in green vegetables. 4,5-Dihydroxy-3,7-dimethoxyisoflavone is a constituent of Pterocarpus soyauxii. Constituent of Pterocarpus soyauxii. 4,5-Dihydroxy-3,7-dimethoxyisoflavone is found in green vegetables.
7-Glucosyl-luteolin
C21H20O12 (464.09547200000003)
alpha-Amyrin
Epi-alpha-amyrin, also known as epi-α-amyrin, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Epi-alpha-amyrin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Epi-alpha-amyrin can be found in herbs and spices, pomes, and rosemary, which makes epi-alpha-amyrin a potential biomarker for the consumption of these food products.
Arctiin
D-Iditol
Permitted bulk sweetener for foods. Sweetening agent. Food additive, used as anticaking agent, lubricant, for stabiliser and thickener, and for other uses in food processing
Helenalin
Isovitexin
7-O-Methylapigenin 6-C-beta-D-glucopyranoside
Vitexin
Vitexin is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin can be found in a number of food items such as flaxseed, prairie turnip, mung bean, and tree fern, which makes vitexin a potential biomarker for the consumption of these food products. Vitexin is an apigenin flavone glucoside, a chemical compound found in the passion flower, Vitex agnus-castus (chaste tree or chasteberry), in the Phyllostachys nigra bamboo leaves, in the pearl millet (Pennisetum millet), and in Hawthorn . Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].
(Z,Z)-1,8,11-Heptadecatriene
(z,z)-1,8,11-heptadecatriene is a member of the class of compounds known as alkatrienes. Alkatrienes are acyclic hydrocarbons that contain exactly three carbon-to-carbon double bonds (z,z)-1,8,11-heptadecatriene can be found in burdock and safflower, which makes (z,z)-1,8,11-heptadecatriene a potential biomarker for the consumption of these food products.
Hispidulin
Hispidulin is a monomethoxyflavone that is scutellarein methylated at position 6. It has a role as an apoptosis inducer, an anti-inflammatory agent, an antioxidant, an anticonvulsant, an antineoplastic agent and a plant metabolite. It is a trihydroxyflavone and a monomethoxyflavone. It is functionally related to a scutellarein. Hispidulin (4,5,7-trihydroxy-6-methoxyflavone) is a potent benzodiazepine (BZD) receptor ligand with positive allosteric properties. Hispidulin is a natural product found in Eupatorium cannabinum, Eupatorium perfoliatum, and other organisms with data available. See also: Arnica montana Flower (part of). A monomethoxyflavone that is scutellarein methylated at position 6. 6-methylscutellarein, also known as 4,5,7-trihydroxy-6-methoxyflavone or dinatin, is a member of the class of compounds known as 6-o-methylated flavonoids. 6-o-methylated flavonoids are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, 6-methylscutellarein is considered to be a flavonoid lipid molecule. 6-methylscutellarein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 6-methylscutellarein can be found in a number of food items such as italian oregano, common sage, sunflower, and common thyme, which makes 6-methylscutellarein a potential biomarker for the consumption of these food products. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM.
nepetin
Eupafolin, also known as 6-methoxy 5 or 734-tetrahydroxyflavone, is a member of the class of compounds known as 6-o-methylated flavonoids. 6-o-methylated flavonoids are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, eupafolin is considered to be a flavonoid lipid molecule. Eupafolin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Eupafolin can be found in common sage, lemon verbena, rosemary, and sesame, which makes eupafolin a potential biomarker for the consumption of these food products. 6-Methoxyluteolin is a natural product found in Eupatorium album, Eupatorium altissimum, and other organisms with data available. See also: Arnica montana Flower (has part). Nepetin (6-Methoxyluteolin) is a natural flavonoid isolated from Eupatorium ballotaefolium HBK with potent anti-inflammatory activities. Nepetin inhibits IL-6, IL-8 and MCP-1 secretion with IC50 values of 4.43 μM, 3.42 μM and 4.17 μM, respectively in ARPE-19 cells[1][2]. Nepetin (6-Methoxyluteolin) is a natural flavonoid isolated from Eupatorium ballotaefolium HBK with potent anti-inflammatory activities. Nepetin inhibits IL-6, IL-8 and MCP-1 secretion with IC50 values of 4.43 μM, 3.42 μM and 4.17 μM, respectively in ARPE-19 cells[1][2].
Jaceosidin
Jaceosidin, also known as 4,5,7-trihydroxy-3,6-dimethoxyflavone, is a member of the class of compounds known as 6-o-methylated flavonoids. 6-o-methylated flavonoids are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, jaceosidin is considered to be a flavonoid lipid molecule. Jaceosidin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Jaceosidin can be found in lemon verbena, which makes jaceosidin a potential biomarker for the consumption of this food product. Jaceosidin is a flavonoid isolated from Artemisia vestita, induces apoptosis in cancer cells, activates Bax and down-regulates Mcl-1 and c-FLIP expression[1]. Jaceosidin exhibits anti-cancer[2], anti-inflammatory activities, decreases leves of inflammatory markers, and suppresses COX-2 expression and NF-κB activation[3]. Jaceosidin is a flavonoid isolated from Artemisia vestita, induces apoptosis in cancer cells, activates Bax and down-regulates Mcl-1 and c-FLIP expression[1]. Jaceosidin exhibits anti-cancer[2], anti-inflammatory activities, decreases leves of inflammatory markers, and suppresses COX-2 expression and NF-κB activation[3].
Vitexin
Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].
Luteolin
Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.976 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.975 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.968 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.971 Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3]. Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3].
Eriodictyol
Constituent of the leaves and branches of Phyllanthus emblica (emblic). Eriodictyol 7-(6-coumaroylglucoside) is found in fruits. Annotation level-1 Eriodictyol is a flavonoid isolated from the Chinese herb, with antioxidant and anti-inflammatory activity. Eriodictyol induces Nrf2 signaling pathway. Eriodictyol is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 18 nM. Eriodictyol is a flavonoid isolated from the Chinese herb, with antioxidant and anti-inflammatory activity. Eriodictyol induces Nrf2 signaling pathway. Eriodictyol is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 18 nM.
Quercetin
Annotation level-1 COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials relative retention time with respect to 9-anthracene Carboxylic Acid is 0.898 D020011 - Protective Agents > D000975 - Antioxidants Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS relative retention time with respect to 9-anthracene Carboxylic Acid is 0.902 Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 1981; CONFIDENCE confident structure IPB_RECORD: 3301; CONFIDENCE confident structure IPB_RECORD: 3283; CONFIDENCE confident structure Quercetin, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively[1]. Quercetin, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively[1].
4-[3,3-dimethyl-2-(3-oxobutyl)cyclobutyl]pent-4-enal
Bigelovin
Bigelovin is a sesquiterpene lactone that is 3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione substituted by methyl groups at positions 4a and 8, a methylidene group at position 3 and an acetoxy group at position 4. Isolated from Inula hupehensis, it exhibits antineoplastic activity. It has a role as an apoptosis inducer, an immunomodulator, an antineoplastic agent and a plant metabolite. It is an acetate ester, an organic heterotricyclic compound, a sesquiterpene lactone, a cyclic ketone and a gamma-lactone. Bigelovin is a natural product found in Dittrichia graveolens, Inula hupehensis, and other organisms with data available. A sesquiterpene lactone that is 3,3a,4,4a,7a,8,9,9a-octahydroazuleno[6,5-b]furan-2,5-dione substituted by methyl groups at positions 4a and 8, a methylidene group at position 3 and an acetoxy group at position 4. Isolated from Inula hupehensis, it exhibits antineoplastic activity. Bigelovin, a sesquiterpene lactone isolated from Inula hupehensis, is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation[1].
Orientin
Orientin is a C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8. It has a role as an antioxidant and a metabolite. It is a C-glycosyl compound, a tetrahydroxyflavone and a 3-hydroxyflavonoid. It is functionally related to a luteolin. Orientin is a natural product found in Itea chinensis, Vellozia epidendroides, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Fenugreek seed (part of); Acai fruit pulp (part of). A C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8. Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2]. Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2].
Isovitexin
Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of an isovitexin-7-olate. Isovitexin is a natural product found in Carex fraseriana, Rauhiella, and other organisms with data available. See also: Fenugreek seed (part of); Acai (part of); Crataegus monogyna flowering top (part of). A C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. Isovitexin is a member of the class of compounds known as flavonoid c-glycosides. Flavonoid c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Isovitexin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Isovitexin can be found in a number of food items such as common salsify, winged bean, flaxseed, and common buckwheat, which makes isovitexin a potential biomarker for the consumption of these food products. Isovitexin (or homovitexin, saponaretin) is a flavone. the apigenin-6-C-glucoside. It can be found in the passion flower, Cannabis, and the açaí palm . Constituent of Cucumis sativus (cucumber). Isovitexin 2-(6-p-coumaroylglucoside) 4-glucoside is found in cucumber and fruits. Constituent of young green barley leaves (Hordeum vulgare variety nudum). Isovitexin 7-(6-sinapoylglucoside) is found in barley and cereals and cereal products. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.
Arctiin
Annotation level-1 Arctiin (NSC 315527) is a plant lignan extracted from burdock seeds and has anti-cancer activity. Arctiin (NSC 315527) is a plant lignan extracted from burdock seeds and has anti-cancer activity.
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one
Annotation level-1
4-Epiisoinuviscolide
A sesquiterpene lactone that is 3a,4,4a,5,6,7,7a,9a-octahydroazuleno[6,5-b]furan-2(3H)-one substituted by a hydroxy group at position 5, methyl groups at positions 5 and 8 and a methylidene group at position 3 (the 3aR,4aR,5S,7aR,9aS stereoisomer). It has been isolated from the aerial parts of Inula hupehensis.
Epi-a-amyrin
linoleic
Linolelaidic acid (Linoelaidic acid), an omega-6 trans fatty acid, acts as a source of energy. Linolelaidic acid is an essential nutrient, adding in enteral, parenteral, and infant formulas. Linolelaidic acid can be used for heart diseases research[1]. Linolelaidic acid (Linoelaidic acid), an omega-6 trans fatty acid, acts as a source of energy. Linolelaidic acid is an essential nutrient, adding in enteral, parenteral, and infant formulas. Linolelaidic acid can be used for heart diseases research[1].
(3s,3ar,4ar,5s,6r,7ar,9as)-5,6-dihydroxy-3,5,8-trimethyl-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
9-hydroxy-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
4,9-bis(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(3as,4r,4ar,7as,8r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
7a-hydroxy-8-methyl-3-methylidene-3ah,4h,4ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
9-hydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2r)-5-methyl-4-oxo-2-(prop-1-en-2-yl)hex-5-en-1-yl]oxy}oxan-2-yl]methyl acetate
(3s,3ar,4ar,5s,6r,9ar)-5-hydroxy-3,5,8-trimethyl-2-oxo-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-6-yl (2e)-2-methylbut-2-enoate
(3ar,4ar,5r,7s,7ar,9ar)-5-hydroxy-5,8-dimethyl-3-methylidene-2-oxo-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-7-yl acetate
4,9-dihydroxy-4a-methyl-5-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-7-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
(3s,3ar,4ar,5s,6r,7ar,9ar)-5-hydroxy-3,5,8-trimethyl-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(1r,2s,3s,7r,9r,10s,11s,12r,14s)-11-hydroxy-1,9-dimethyl-4-methylidene-5-oxo-6,13-dioxatetracyclo[8.4.0.0³,⁷.0¹²,¹⁴]tetradecan-2-yl acetate
(3ar,4ar,5r,7ar,9ar)-5-hydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3ar,4ar,5r,7as,9ar)-5,8-dimethyl-3-methylidene-5-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
{7-hydroxy-8-methyl-3-methylidene-2,5-dioxo-octahydroazuleno[6,5-b]furan-4a-yl}methyl 3-methylbutanoate
(2r,9s,13s)-13-hydroxy-2,7,12,13-tetramethyl-10,14-dioxatetracyclo[7.5.1.0²,⁶.0¹²,¹⁵]pentadec-5-ene-3,11-dione
(3as,4ar,5r,8s,9s,9ar)-5,8,9-trihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,9h,9ah-azuleno[6,5-b]furan-2-one
(3ar,4ar,5r,7s,7as,9ar)-5-hydroxy-5-methyl-3,8-dimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-7-yl acetate
2-hydroxy-1,9-dimethyl-4-methylidene-5-oxo-6,12-dioxatetracyclo[8.4.0.0³,⁷.0¹¹,¹³]tetradecan-14-yl 2-methylbut-2-enoate
[(3ar,4as,5s,7s,7as,8r,9as)-5,7-dihydroxy-8-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4a-yl]methyl 3-methylbutanoate
4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 2-methylbut-2-enoate
4,5,7,9-tetrahydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
(3ar,4as,9ar)-5,8-dimethyl-3-methylidene-3ah,4h,4ah,9h,9ah-azuleno[6,5-b]furan-2,7-dione
5,8'a-dimethyl-7-(6-methylhept-5-en-2-yl)-5'-methylidene-3'a,4',4'a,6',7',8',9',9'a-octahydrospiro[bicyclo[2.2.2]octane-2,3'-naphtho[2,3-b]fura]-5-en-2'-one
(3as,4r,4ar,5s,7s,7as,8r,9ar)-7-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl (2e)-2-methylbut-2-enoate
(2s,6e,9r)-9-(hydroxymethyl)-2,6,10-trimethylundeca-6,10-dienoic acid
[5-(acetyloxy)-3,4-dihydroxy-6-[(12-hydroxy-3,7,11-trimethyldodeca-1,6-dien-3-yl)oxy]oxan-2-yl]methyl acetate
(3ar,4as,5r,7s,7as,8r,9ar)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
9-hydroxy-4a,8-dimethyl-7-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 2-methylbut-2-enoate
5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3ar,4as,5r,7r,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3ar,4r,4as,5r,7r,7ar,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
(3ar,4ar,7as,8r,9ar)-7a-hydroxy-8-methyl-3-methylidene-3ah,4h,4ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylpropanoate
5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2s,3e)-5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hex-3-en-1-yl]oxy}oxan-2-yl]methyl acetate
9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate
(1r,2r,6s,7s,9r,12r,13r,15r)-13-hydroxy-2,7,12,13-tetramethyl-10,14-dioxatetracyclo[7.5.1.0²,⁶.0¹²,¹⁵]pentadec-4-ene-3,11-dione
(3ar,4s,4as,5r,7s,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate
5,7-dihydroxy-5-methyl-3,8-dimethylidene-octahydroazuleno[6,5-b]furan-2-one
(3ar,5r,7s,7as,8r,9as)-5,7-dihydroxy-5,8-dimethyl-3-methylidene-3ah,6h,7h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2-one
[5-(acetyloxy)-3,4-dihydroxy-6-[(12-hydroxy-3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methyl acetate
9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
4,5,9-trihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
4-[(1r,2s)-3,3-dimethyl-2-(3-oxobutyl)cyclobutyl]pent-4-enal
4,9-bis(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbutanoate
(3r,3as,4s,4ar,7ar,8r,9as)-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
4,5,9-trihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbutanoate
(3as,4r,4ar,7ar,8r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3as,4r,4as,5r,7s,7as,9r,9ar)-4,5,9-trihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(1r,2r,7r,9s,12r,13s,15r)-13-hydroxy-2,7,12,13-tetramethyl-10,14-dioxatetracyclo[7.5.1.0²,⁶.0¹²,¹⁵]pentadec-5-ene-3,11-dione
5'-[4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]-5,8a-dimethyl-3',4',5,6,7,8,9,9a-octahydro-3ah-spiro[naphtho[2,3-b]furan-3,2'-pyran]-2-one
4,5-dihydroxy-2-({5-methyl-3,8-dimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-5-yl}oxy)oxan-3-yl acetate
(2s,6e,9s)-9-(hydroxymethyl)-2,6,10-trimethylundeca-6,10-dienoic acid
(3s,3as,4s,4ar,7ar,8r,9ar)-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
(3as,4r,4ar,5r,7s,7as,8s,9r,9ar)-5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylpropanoate
(3as,4as,5r,7s,7ar,8s,9ar)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
5,5',8'a-trimethyl-7-(6-methylhept-5-en-2-yl)-5',6',7',8',9',9'a-hexahydro-3'ah-spiro[bicyclo[2.2.2]octane-2,3'-naphtho[2,3-b]fura]-5-en-2'-one
(3as,4r,4ar,5r,7s,7as,8s,9r,9ar)-5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2r)-2-methylbutanoate
4,5,9-trihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,5-bis(acetyloxy)-9-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2r)-2-methylbutanoate
{3,4,5-trihydroxy-6-[(10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl)oxy]oxan-2-yl}methyl acetate
5-hydroxy-2-(4-hydroxyphenyl)-3-methoxy-7-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one
4,6-dihydroxy-4a,8-dimethyl-3-methylidene-octahydroazuleno[6,5-b]furan-2,5-dione
5,6-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3ar,4as,5r,7s,7as,8r,9as)-5-(acetyloxy)-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
(1's,3s,3ar,4s,4'r,4ar,7's,7as,8s,9r,9ar)-9-hydroxy-7'-(2-hydroxypropan-2-yl)-4a,5',8-trimethyl-2,5-dioxo-3a,4,7a,8,9,9a-hexahydrospiro[azuleno[6,5-b]furan-3,2'-bicyclo[2.2.2]octan]-5'-en-4-yl (2z)-2-methylbut-2-enoate
(3as,4r,4as,5r,7s,7as,9r,9ar)-4-(acetyloxy)-5,9-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
14-hydroxy-1,9-dimethyl-4-methylidene-6,12-dioxatetracyclo[8.4.0.0³,⁷.0¹¹,¹³]tetradecan-5-one
(3ar,4ar,5r,7ar,9ar)-5,8-dimethyl-3-methylidene-5-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3r,3as,5s,8ar,9ar)-5'-[(2s,4as,8as)-4a-methyl-8-methylidene-octahydronaphthalen-2-yl]-5,8a-dimethyl-3',4',5,6,7,8,9,9a-octahydro-3ah-spiro[naphtho[2,3-b]furan-3,2'-pyran]-2-one
(3ar,4as,5s,7s,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3s,3ar,4ar,5s,6r,9as)-5-hydroxy-3,5,8-trimethyl-2,9-dioxo-3h,3ah,4h,4ah,6h,7h,9ah-azuleno[6,5-b]furan-6-yl (2z)-2-methylbut-2-enoate
(3as,4ar,5s,8r,9r,9ar)-5,8,9-trihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,9h,9ah-azuleno[6,5-b]furan-2-one
4-(acetyloxy)-7-hydroxy-4a,7a,8-trimethyl-3-methylidene-2-oxo-octahydroazuleno[6,5-b]furan-5-yl 2-methylbut-2-enoate
(3ar,4r,4as,5r,7s,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
(3as,4s,4as,5r,7s,8r,9ar)-4,5,7-trihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-9-(acetyloxy)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
(3ar,4s,4as,5r,7s,7as,8r,9as)-7-hydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,9-bis(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
4-(acetyloxy)-5,9-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
(4s,4ar,7ar,8r,9ar)-4-hydroxy-3,4a,8-trimethyl-4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
2-hydroxy-2-(2-hydroxy-4-{[(2-methylpropanoyl)oxy]methyl}phenyl)propyl 2-methylpropanoate
(3ar,4r,4as,5r,7s,7as,8r,9as)-7-hydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
4,5-bis(acetyloxy)-9-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
[(2r,3s,4s,5r,6s)-5-(acetyloxy)-3,4-dihydroxy-6-{[(3s,6e,11s)-12-hydroxy-3,7,11-trimethyldodeca-1,6-dien-3-yl]oxy}oxan-2-yl]methyl acetate
(3ar,4as,5r,7s,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
5,8-dimethyl-3-methylidene-3ah,4h,4ah,9h,9ah-azuleno[6,5-b]furan-2,7-dione
[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2r,3e)-5-methyl-2-(prop-1-en-2-yl)hexa-3,5-dien-1-yl]oxy}oxan-2-yl]methyl acetate
[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(4s,6e,10s)-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl]oxy}oxan-2-yl]methyl acetate
5-hydroxy-3,5,8-trimethyl-2,9-dioxo-3h,3ah,4h,4ah,6h,7h,9ah-azuleno[6,5-b]furan-6-yl 2-methylbut-2-enoate
[(2r,3s,4s,5r,6s)-6-{[(3ar,4ar,5r,7ar,9ar)-5,8-dimethyl-3-methylidene-2-oxo-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-5-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl acetate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,5-bis(acetyloxy)-9-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(3ar,4ar,5s,6r,7ar,9as)-5,6-dihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3as,4r,4ar,5r,7s,7as,8r,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
(2s,3r,4s,5s)-2-{[(3ar,4ar,5r,7as,9ar)-5-methyl-3,8-dimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-5-yl]oxy}-4,5-dihydroxyoxan-3-yl acetate
(3s,3ar,4ar,5r,7s,7as,9ar)-5,7-dihydroxy-3,5-dimethyl-8-methylidene-octahydro-3h-azuleno[6,5-b]furan-2-one
3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
(3ar,4s,4ar,8r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-3ah,4h,6h,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
5'-(4a-methyl-8-methylidene-octahydronaphthalen-2-yl)-5,8a-dimethyl-3',4',5,6,7,8,9,9a-octahydro-3ah-spiro[naphtho[2,3-b]furan-3,2'-pyran]-2-one
4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
(1r,3ar,5as,6s,7s,9ar,9bs,11as)-6,9a,11a-trimethyl-1-[(2r)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one
C21H20O12 (464.09547200000003)
(3as,4r,4ar,5r,7s,7as,8s,9r,9ar)-4,9-dihydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(3s)-3-[(3ar,6s,7r,8ar)-5,7-dimethyl-3-methylidene-2-oxo-3ah,6h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-3-hydroxypropyl acetate
{4-[(2r)-2-methyloxiran-2-yl]-3-[(2-methylpropanoyl)oxy]phenyl}methyl (2s)-2-methylbutanoate
(3ar,4ar,5s,6r,9as)-5,6-dihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3as,4s,4ar,5r,7s,7as,8r,9as)-4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl (2z)-2-methylbut-2-enoate
(3r,3as,4s,4ar,7ar,8r,9ar)-4-hydroxy-3-(methanesulfonylmethyl)-4a,8-dimethyl-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
C16H22O6S (342.11370320000003)
4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 3-methylbutanoate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-9-(acetyloxy)-5,7-dihydroxy-4a,7a,8-trimethyl-3-methylidene-2-oxo-octahydroazuleno[6,5-b]furan-4-yl acetate
5-hydroxy-5,8-dimethyl-3-methylidene-2-oxo-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-7-yl acetate
(1r,2r,4s,5r,6r,8r,11r,12s)-2-hydroxy-11-(hydroxymethyl)-2,6-dimethyl-10-oxo-9,14-dioxatetracyclo[9.2.1.0¹,⁵.0⁸,¹²]tetradecan-4-yl (2z)-2-methylbut-2-enoate
5-(acetyloxy)-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
(3ar,4r,4as,5r,7s,7as,8r,9as)-4-(acetyloxy)-7-hydroxy-4a,7a,8-trimethyl-3-methylidene-2-oxo-octahydroazuleno[6,5-b]furan-5-yl (2z)-2-methylbut-2-enoate
(1s,2s,7s,9r,12s,13r,15s)-13-hydroxy-2,7,12,13-tetramethyl-10,14-dioxatetracyclo[7.5.1.0²,⁶.0¹²,¹⁵]pentadec-5-ene-3,11-dione
(2r)-2-hydroxy-2-(2-hydroxy-4-{[(2-methylpropanoyl)oxy]methyl}phenyl)propyl 2-methylpropanoate
(3as,4r,4ar,5r,7s,7as,9r,9ar)-5-(acetyloxy)-4,9-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
[(3ar,4as,7s,7as,8r,9as)-7-hydroxy-8-methyl-3-methylidene-2,5-dioxo-octahydroazuleno[6,5-b]furan-4a-yl]methyl 3-methylbutanoate
9,13-dimethyl-4-methylidene-5-oxo-6,14-dioxatetracyclo[8.4.0.0¹,¹³.0³,⁷]tetradecan-11-yl acetate
8,9'-dimethyl-4'-methylidene-4,4a,7a,8,9,9a-hexahydro-3ah-6'-oxaspiro[azuleno[6,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0³,⁷]pentadecane]-2,5,5',14'-tetrone
4-(acetyloxy)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-9-yl acetate
4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 2-methylbut-2-enoate
4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(3,4,5-trihydroxy-6-{[5-methyl-4-oxo-2-(prop-1-en-2-yl)hex-5-en-1-yl]oxy}oxan-2-yl)methyl acetate
(3s,3ar,4ar,5s,6r,9r,9as)-5,6,9-trihydroxy-3,5,8-trimethyl-3h,3ah,4h,4ah,6h,7h,9h,9ah-azuleno[6,5-b]furan-2-one
5,8-dimethyl-3-methylidene-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3as,4r,4as,5r,7s,7as,8r,9as)-4,5,7-trihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3ar,4as,5s,7s,7as,8r,9as)-7-hydroxy-4a-(hydroxymethyl)-8-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 3-methylbutanoate
(3ar,4r,4as,8r,9ar)-4-hydroxy-7,8-dimethyl-3-methylidene-3ah,4h,4ah,5h,8h,9h,9ah-azuleno[6,5-b]furan-2,6-dione
4,5-bis(acetyloxy)-9-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbutanoate
2-{4-methyl-2-[(2-methylpropanoyl)oxy]phenyl}propyl 2-methylpropanoate
5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylpropanoate
4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 2-methylbutanoate
(3as,4r,4as,5r,7r,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
7-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-6-yl acetate
(3as,4s,4as,5r,7s,7as,8r,9ar)-4,5,7-trihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
7-[(3,4-dihydroxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-2-(4-hydroxyphenyl)-5-[(3,4,5,6-tetrahydroxyoxan-2-yl)methyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
4,9-dihydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
(1's,3r,3'r,3ar,4ar,7'r,7ar,8r,9'r,9ar,10'r,11's)-8,9'-dimethyl-4'-methylidene-4,4a,7a,8,9,9a-hexahydro-3ah-6'-oxaspiro[azuleno[6,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0³,⁷]pentadecane]-2,5,5',14'-tetrone
(3ar,4s,4as,7as,8r,9r,9ar)-9-hydroxy-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
(3ar,4s,4ar,7ar,8r,9as)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate
(3ar,4s,4ar,7ar,8r,9as)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 2-methylbut-2-enoate
(3as,4s,4ar,5r,7s,7as,8r,9ar)-4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl (2r)-2-methylbutanoate
(3ar,4ar,9ar)-5,8-dimethyl-3-methylidene-3ah,4h,4ah,9h,9ah-azuleno[6,5-b]furan-2,7-dione
4,5-bis(acetyloxy)-9-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
[(2r,3s,4s,5r,6r)-5-(acetyloxy)-3,4-dihydroxy-6-(2-phenylethoxy)oxan-2-yl]methyl acetate
5-(acetyloxy)-4,9-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
[(3ar,4as,5s,7s,7as,8r,9ar)-5,7-dihydroxy-8-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4a-yl]methyl 3-methylbutanoate
4a,8,9'-trimethyl-4'-methylidene-2,5,5',14'-tetraoxo-3a,4,7a,8,9,9a-hexahydro-6'-oxaspiro[azuleno[6,5-b]furan-3,13'-tetracyclo[9.2.2.0¹,¹⁰.0³,⁷]pentadecan]-4-yl acetate
(3ar,4s,4as,5s,7s,7as,8r,9ar)-4,5-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
(3ar,4ar,7ar,8r,9ar)-7a-hydroxy-8-methyl-3-methylidene-3ah,4h,4ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbutanoate
(3ar,4ar,5s,6r,7ar,9ar)-5,6-dihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3as,4s,4ar,7as,8r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3ar,4as,7ar,8r,9ar)-4a-hydroxy-8-methyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3ar,4r,4ar,7ar,8s,9ar)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
4-(acetyloxy)-5,9-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
5,6-dihydroxy-3-(4-hydroxyphenyl)-7-methoxychromen-4-one
4-(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
[(2r,3s,4s,5r,6s)-6-{[(3ar,4ar,5r,9as)-5,8-dimethyl-3-methylidene-2,9-dioxo-3ah,4h,4ah,6h,7h,9ah-azuleno[6,5-b]furan-5-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl acetate
(1r,2s,3'ar,4r,5's,7s,8'ar,9'ar)-5,5',8'a-trimethyl-7-[(2s)-6-methylhept-5-en-2-yl]-5',6',7',8',9',9'a-hexahydro-3'ah-spiro[bicyclo[2.2.2]octane-2,3'-naphtho[2,3-b]fura]-5-en-2'-one
[(2s,3s,4s,5r,6r)-5-(acetyloxy)-3,4-dihydroxy-6-(2-phenylethoxy)oxan-2-yl]methyl acetate
(4r,4ar,8s,9ar)-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,6h,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
[(2r,3s,4s,5r,6s)-5-(acetyloxy)-3,4-dihydroxy-6-{[(3r,6e,10e)-12-hydroxy-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]oxy}oxan-2-yl]methyl acetate
(3as,4r,4ar,5r,7s,7as,8s,9r,9ar)-5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbutanoate
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6,8-bis[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
6,9a,11a-trimethyl-1-(6-methyl-5-methylideneheptan-2-yl)-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,5-bis(acetyloxy)-9-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(3ar,4as,9ar)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3as,4r,4as,5r,7s,7as,9r,9ar)-4,5,9-trihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
1-{5,7-dimethyl-3-methylidene-2-oxo-3ah,6h,7h,8h,8ah-cyclohepta[b]furan-6-yl}-3-hydroxypropyl acetate
6,7-dihydroxy-8a-methyl-3,5-dimethylidene-octahydronaphtho[2,3-b]furan-2-one
7-hydroxy-4a-methyl-3,8-dimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-6-yl acetate
(3s,3ar,4as,5r,7s,7as,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-(piperidin-1-ylmethyl)-decahydroazuleno[6,5-b]furan-2-one
(3r,3as,4ar,8ar,9ar)-5'-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]-8a-methyl-5-methylidene-3',3a,4,4',4a,6,7,8,9,9a-decahydrospiro[naphtho[2,3-b]furan-3,2'-pyran]-2-one
(3as,4s,4ar,7as,8s,9r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl acetate
(3as,4s,4ar,7as,8s,9r,9ar)-9-(acetyloxy)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
(3ar,4as,5s,7s,7as,8r,9ar)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(3ar,4ar,5r,7as,9ar)-5-methyl-3,8-dimethylidene-5-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-octahydroazuleno[6,5-b]furan-2-one
(3s,3ar,4ar,5s,6r,7ar,9ar)-5-hydroxy-3,5,8-trimethyl-2-oxo-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-6-yl (2e)-2-methylbut-2-enoate
(3as,4r,4ar,5r,7s,7as,8s,9r,9ar)-4,9-dihydroxy-4a,8-dimethyl-5-{[(2z)-2-methylbut-2-enoyl]oxy}-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(3as,4s,7as,8r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
3-(acetyloxy)-1-{5,7-dimethyl-3-methylidene-2-oxo-3ah,6h,7h,8h,8ah-cyclohepta[b]furan-6-yl}propyl 2-methylbut-2-enoate
4,9-dihydroxy-4a,8-dimethyl-5-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
(3ar,4r,4ar,7as,8r,9as)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,9-bis(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2r)-2-methylbutanoate
(3ar,4s,4ar,7ar,8r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(1'r,3s,3as,4s,4's,4ar,7's,7as,8s,9r,9ar)-9-hydroxy-7'-(2-hydroxypropan-2-yl)-4a,5',8-trimethyl-2,5-dioxo-3a,4,7a,8,9,9a-hexahydrospiro[azuleno[6,5-b]furan-3,2'-bicyclo[2.2.2]octan]-5'-en-4-yl (2z)-2-methylbut-2-enoate
[6-({5,8-dimethyl-3-methylidene-2,9-dioxo-3ah,4h,4ah,6h,7h,9ah-azuleno[6,5-b]furan-5-yl}oxy)-3,4,5-trihydroxyoxan-2-yl]methyl acetate
4,5-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
4a-hydroxy-8-methyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2e)-2-methylbut-2-enoate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,5,7,9-tetrahydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3as,4r,4ar,5r,7s,7as,9r,9ar)-4,9-dihydroxy-4a-methyl-5-{[(2z)-2-methylbut-2-enoyl]oxy}-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
6,7-dihydroxy-4a-methyl-3,8-dimethylidene-octahydroazuleno[6,5-b]furan-2-one
5,8,9-trihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,9h,9ah-azuleno[6,5-b]furan-2-one
4-hydroxy-3-(methanesulfonylmethyl)-4a,8-dimethyl-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
C16H22O6S (342.11370320000003)
(1s,2r,3r,7s,9r,10s,11r,13s,14r)-14-hydroxy-1,9-dimethyl-4-methylidene-5-oxo-6,12-dioxatetracyclo[8.4.0.0³,⁷.0¹¹,¹³]tetradecan-2-yl acetate
(3as,4r,4as,5s,7s,7as,8s,9r,9ar)-9-(acetyloxy)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
8-methyl-3-methylidene-3ah,4h,4ah,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3s,3ar,4s,4as,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
(3ar,4ar,5r,7as,9ar)-5,8-dimethyl-3-methylidene-5-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3ar,4ar,5s,7ar,9ar)-5,8-dimethyl-3-methylidene-2-oxo-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-5-yl acetate
(3ar,4s,4as,5r,7s,7as,8r,9ar)-7-(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
(3s,3ar,4ar,5s,6r,7ar,9as)-5-hydroxy-3,5,8-trimethyl-2-oxo-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-6-yl (2z)-2-methylbut-2-enoate
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,5,9-trihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2r)-2-methylbutanoate
(1'r,3s,3'r,3ar,4s,4ar,7'r,7ar,8r,9'r,9ar,10'r,11's)-4a,8,9'-trimethyl-4'-methylidene-2,5,5',14'-tetraoxo-3a,4,7a,8,9,9a-hexahydro-6'-oxaspiro[azuleno[6,5-b]furan-3,13'-tetracyclo[9.2.2.0¹,¹⁰.0³,⁷]pentadecan]-4-yl acetate
(3ar,4ar,5r,7s,7as,9ar)-5-hydroxy-5,8-dimethyl-3-methylidene-2-oxo-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-7-yl acetate
(3s,3ar,4ar,5s,6r,9as)-5,6-dihydroxy-3,5,8-trimethyl-3h,3ah,4h,4ah,6h,7h,9ah-azuleno[6,5-b]furan-2,9-dione
(3as,4r,4ar,5r,7s,7as,8r,9as)-4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl (2z)-2-methylbut-2-enoate
[5-(acetyloxy)-3,4-dihydroxy-6-(2-phenylethoxy)oxan-2-yl]methyl acetate
{5,7-dihydroxy-8-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4a-yl}methyl 3-methylbutanoate
5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
(3r,3as,5s,8ar,9ar)-5'-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]-5,8a-dimethyl-3',4',5,6,7,8,9,9a-octahydro-3ah-spiro[naphtho[2,3-b]furan-3,2'-pyran]-2-one
(3as,4s,4ar,7ar,8s,9r,9as)-9-hydroxy-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
(3as,4s,4ar,8s,9r,9ar)-9-(acetyloxy)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
5'-[4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]-8a-methyl-5-methylidene-3',3a,4,4',4a,6,7,8,9,9a-decahydrospiro[naphtho[2,3-b]furan-3,2'-pyran]-2-one
(3as,4r,4as,5r,7s,7as,8r,9as)-4,5-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate
{4-[(2r)-2-methyloxiran-2-yl]-3-[(2-methylpropanoyl)oxy]phenyl}methyl 2-methylpropanoate
(3ar,4as,7ar,8r,9ar)-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3as,4r,4as,5r,7s,7as,9r,9ar)-9-(acetyloxy)-5,7-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
5,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl 2-methylbut-2-enoate
(1s,3r,7r,9r,10r,11s,13r)-9,13-dimethyl-4-methylidene-5-oxo-6,14-dioxatetracyclo[8.4.0.0¹,¹³.0³,⁷]tetradecan-11-yl acetate
5-(acetyloxy)-4,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(3s,3as,4s,4ar,7as,8s,9r,9as)-9-hydroxy-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
4,5,9-trihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(3ar,4as,7as,8r,9as)-4a,8-dimethyl-3-methylidene-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2,5-dione
(3ar,4s,4as,5r,7s,7as,8r,9as)-4,5,7-trihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3r,3ar,4r,4ar,7as,8r,9as)-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
(3ar,4ar,6r,7r,8as,9ar)-6-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-7-yl acetate
4-[4-(5-hydroxypent-1-en-2-yl)-2,2-dimethylcyclobutyl]butan-2-one
6-{5-[(3,4-dihydroxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl}-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one
14-hydroxy-1,9-dimethyl-4-methylidene-5-oxo-6,12-dioxatetracyclo[8.4.0.0³,⁷.0¹¹,¹³]tetradecan-2-yl acetate
5-hydroxy-3,5,8-trimethyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3as,4r,4as,5r,7s,7as,8s,9r,9ar)-4,5,9-trihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
5,6-dihydroxy-5,8-dimethyl-3-methylidene-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(3as,4r,4ar,8r,9as)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,6h,8h,9h,9ah-azuleno[6,5-b]furan-4-yl acetate
(3ar,4as,5r,7s,7as,8s,9r,9ar)-9-hydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(2s,3r,4s,5s)-2-{[(3ar,4ar,5r,7as,9as)-5-methyl-3,8-dimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-5-yl]oxy}-4,5-dihydroxyoxan-3-yl acetate
(3ar,4as,7s,7as,8r,9as)-7-hydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 3-methylbut-2-enoate
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2r,3s,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
(3as,4as,7ar,8r)-4,5-dihydroxy-8-methyl-3-methylidene-2-oxo-decahydroazuleno[6,5-b]furan-7-yl 2-hydroxypropanoate
(3ar,4as,5r,7s,7as,8s,9r,9ar)-9-hydroxy-4a,8-dimethyl-5-{[(2z)-2-methylbut-2-enoyl]oxy}-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(3ar,4ar,6r,7r,8ar,9ar)-7-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-6-yl acetate
5-methyl-3,8-dimethylidene-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]-octahydroazuleno[6,5-b]furan-2-one
(1r,2r,3s,7r,9r,10s,11r,13r,14r)-2-hydroxy-1,9-dimethyl-4-methylidene-5-oxo-6,12-dioxatetracyclo[8.4.0.0³,⁷.0¹¹,¹³]tetradecan-14-yl (2e)-2-methylbut-2-enoate
(1r,2r,3r,6s,8s,9r)-1,9-dihydroxy-3,8-dimethyltricyclo[4.4.0.0²,⁸]decan-5-one
7-hydroxy-4a-(hydroxymethyl)-8-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 3-methylbutanoate
4,5,9-trihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylbut-2-enoate
3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl 2-methylbutanoate
7-hydroxy-4a,8-dimethyl-5-[(3-methylbutanoyl)oxy]-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl 2-methylbut-2-enoate
3-{5,7-dimethyl-3-methylidene-2-oxo-3ah,6h,7h,8h,8ah-cyclohepta[b]furan-6-yl}-3-hydroxypropyl acetate
(3ar,4ar,5r,7as,9as)-5,8-dimethyl-3-methylidene-5-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(1s,2r,6s,7s,9r,12r,15r)-13-hydroxy-2,7,12,13-tetramethyl-10,14-dioxatetracyclo[7.5.1.0²,⁶.0¹²,¹⁵]pentadec-4-ene-3,11-dione
2-hydroxy-11-(hydroxymethyl)-2,6-dimethyl-10-oxo-9,14-dioxatetracyclo[9.2.1.0¹,⁵.0⁸,¹²]tetradecan-4-yl 2-methylbut-2-enoate
(3as,4r,4as,5r,7s,7as,9r,9ar)-4-(acetyloxy)-5,9-dihydroxy-4a-methyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl (2z)-2-methylbut-2-enoate
(3s,3ar,4ar,5s,6r,9ar)-5-hydroxy-3,5,8-trimethyl-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
5,8-dimethyl-3-methylidene-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
(1s)-1-[(3ar,6s,7r,8ar)-5,7-dimethyl-3-methylidene-2-oxo-3ah,6h,7h,8h,8ah-cyclohepta[b]furan-6-yl]-3-(acetyloxy)propyl (2z)-2-methylbut-2-enoate
(3ar,4ar,6r,7r,8ar,9ar)-6,7-dihydroxy-8a-methyl-3,5-dimethylidene-octahydronaphtho[2,3-b]furan-2-one
[6-({5,8-dimethyl-3-methylidene-2-oxo-3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-5-yl}oxy)-3,4,5-trihydroxyoxan-2-yl]methyl acetate
(3,4,5-trihydroxy-6-{[5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hex-3-en-1-yl]oxy}oxan-2-yl)methyl acetate
(3s,3ar,4s,4ar,7ar,8r,9as)-3,4a,8-trimethyl-2,5-dioxo-3h,3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
4-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 2-methylpropanoate
7-hydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
11-hydroxy-1,9-dimethyl-4-methylidene-5-oxo-6,13-dioxatetracyclo[8.4.0.0³,⁷.0¹²,¹⁴]tetradecan-2-yl acetate
6-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-7-yl acetate
5-hydroxy-5-methyl-3,8-dimethylidene-2-oxo-octahydroazuleno[6,5-b]furan-7-yl acetate
(2r)-2-{4-methyl-2-[(2-methylpropanoyl)oxy]phenyl}propyl 2-methylpropanoate
(3r,3as,4as,7as,8s,9r,9ar)-3-hydroxy-3-(hydroxymethyl)-4a,8-dimethyl-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl acetate
4,5,7-trihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
7-(acetyloxy)-5,9-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-4-yl acetate
(3as,4r,4ar,7as,8s,9r,9ar)-4-hydroxy-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl acetate
(3ar,4ar,5s,6r,7as,9ar)-5,6-dihydroxy-3,5,8-trimethyl-3h,3ah,4h,4ah,6h,7h,7ah,9ah-azuleno[6,5-b]furan-2-one
5,7-dihydroxy-5,8-dimethyl-3-methylidene-3ah,6h,7h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-2-one
(3as,4s,4ar,5r,7s,7as,8r,9ar)-4,7-dihydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-5-yl 3-methylbutanoate
(3,4,5-trihydroxy-6-{[5-methyl-2-(prop-1-en-2-yl)hexa-3,5-dien-1-yl]oxy}oxan-2-yl)methyl acetate
(3ar,4as,5r,7s,8r,9as)-5,7-dihydroxy-4a,8-dimethyl-3-methylidene-octahydro-3ah-azuleno[6,5-b]furan-2-one
(3ar,4s,4ar,7ar,8r,9as)-4a,8-dimethyl-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-4-yl (2z)-2-methylbut-2-enoate
5-[({6-[(acetyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl}oxy)methyl]-2,6-dimethylhepta-1,6-dien-3-yl acetate
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one
C21H20O12 (464.09547200000003)