NCBI Taxonomy: 40678
Alcyoniidae (ncbi_taxid: 40678)
found 360 associated metabolites at family taxonomy rank level.
Ancestor: Malacalcyonacea
Child Taxonomies: Alcyonium, Bellonella, Anthothela, Dampia, Hedera, Sarcophyton, Kotatea, Lohowia, Protodendron, Rhytisma, Ushanaia, Elbeenus, Lobophytum, Lateothela, Anthomastus, Iciligorgia, Paraminabea, Anastromvos, Bathyalcyon, Eleutherobia, Solenocaulon, Alertigorgia, Erythropodium, Thrombophyton, Heteropolypus, Notodysiferus, Sphaerasclera, Pseudoanthomastus, unclassified Alcyoniidae
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].
Pregnenolone
Pregnenolone is a derivative of cholesterol, the product of cytochrome P450 side-chain cleavage (EC 1.14.15.6, CYP11A1. This reaction consists of three consecutive monooxygenations, a 22-hydroxylation, a 20-hydroxylation, and the cleavage of the C20-C22 bond, yielding pregnenolone. Pregnenolone is the precursor to gonadal steroid hormones and the adrenal corticosteroids. This reaction occurs in steroid hormone-producing tissues such as the adrenal cortex, corpus luteum, and placenta. The most notable difference between the placenta and other steroidogenic tissues is that electron supply to CYP11A1 limits the rate at which cholesterol is converted into pregnenolone in the placenta. The limiting component for electron delivery to CYP11A1 is the concentration of adrenodoxin reductase in the mitochondrial matrix which is insufficient to maintain the adrenodoxin pool in a fully reduced state. Pregnenolone is also a neurosteroid, and is produced in the spinal cord; CYP11A1 is the key enzyme catalyzing the conversion of cholesterol into pregnenolone, the rate-limiting step in the biosynthesis of all classes of steroids, and has been localized in sensory networks of the spinal cord dorsal horn. In the adrenal glomerulosa cell, angiotensin II, one of the major physiological regulators of mineralocorticoid synthesis, appears to affect most of the cholesterol transfer to the mitochondrial outer membrane and many steps in the transport to the inner membrane. Thus, it exerts a powerful control over the use of cholesterol for aldosterone production (PMID: 17222962, 15823613, 16632873, 15134809). C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Pregnenolone (3β-Hydroxy-5-pregnen-20-one) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone can protect the brain from cannabis intoxication[1][2]. Pregnenolone is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels[3]. Pregnenolone (3β-Hydroxy-5-pregnen-20-one) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone can protect the brain from cannabis intoxication[1][2]. Pregnenolone is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels[3].
Cholesterol
Cholesterol is a sterol (a combination steroid and alcohol) and a lipid found in the cell membranes of all body tissues and transported in the blood plasma of all animals. The name originates from the Greek chole- (bile) and stereos (solid), and the chemical suffix -ol for an alcohol. This is because researchers first identified cholesterol in solid form in gallstones in 1784. In the body, cholesterol can exist in either the free form or as an ester with a single fatty acid (of 10-20 carbons in length) covalently attached to the hydroxyl group at position 3 of the cholesterol ring. Due to the mechanism of synthesis, plasma cholesterol esters tend to contain relatively high proportions of polyunsaturated fatty acids. Most of the cholesterol consumed as a dietary lipid exists as cholesterol esters. Cholesterol esters have a lower solubility in water than cholesterol and are more hydrophobic. They are hydrolyzed by the pancreatic enzyme cholesterol esterase to produce cholesterol and free fatty acids. Cholesterol has vital structural roles in membranes and in lipid metabolism in general. It is a biosynthetic precursor of bile acids, vitamin D, and steroid hormones (glucocorticoids, estrogens, progesterones, androgens and aldosterone). In addition, it contributes to the development and functioning of the central nervous system, and it has major functions in signal transduction and sperm development. Cholesterol is a ubiquitous component of all animal tissues where much of it is located in the membranes, although it is not evenly distributed. The highest proportion of unesterified cholesterol is in the plasma membrane (roughly 30-50\\\\% of the lipid in the membrane or 60-80\\\\% of the cholesterol in the cell), while mitochondria and the endoplasmic reticulum have very low cholesterol contents. Cholesterol is also enriched in early and recycling endosomes, but not in late endosomes. The brain contains more cholesterol than any other organ where it comprises roughly a quarter of the total free cholesterol in the human body. Of all the organic constituents of blood, only glucose is present in a higher molar concentration than cholesterol. Cholesterol esters appear to be the preferred form for transport in plasma and as a biologically inert storage (de-toxified) form. They do not contribute to membranes but are packed into intracellular lipid particles. Cholesterol molecules (i.e. cholesterol esters) are transported throughout the body via lipoprotein particles. The largest lipoproteins, which primarily transport fats from the intestinal mucosa to the liver, are called chylomicrons. They carry mostly triglyceride fats and cholesterol that are from food, especially internal cholesterol secreted by the liver into the bile. In the liver, chylomicron particles give up triglycerides and some cholesterol. They are then converted into low-density lipoprotein (LDL) particles, which carry triglycerides and cholesterol on to other body cells. In healthy individuals, the LDL particles are large and relatively few in number. In contrast, large numbers of small LDL particles are strongly associated with promoting atheromatous disease within the arteries. (Lack of information on LDL particle number and size is one of the major problems of conventional lipid tests.). In conditions with elevated concentrations of oxidized LDL particles, especially small LDL particles, cholesterol promotes atheroma plaque deposits in the walls of arteries, a condition known as atherosclerosis, which is a major contributor to coronary heart disease and other forms of cardiovascular disease. There is a worldwide trend to believe that lower total cholesterol levels tend to correlate with lower atherosclerosis event rates (though some studies refute this idea). As a result, cholesterol has become a very large focus for the scientific community trying to determine the proper amount of cholesterol needed in a healthy diet. However, the primary association of atherosclerosis with c... Constituent either free or as esters, of fish liver oils, lard, dairy fats, egg yolk and bran Cholesterol is the major sterol in mammals. It is making up 20-25\\% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins[1][2]. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist[3]. Cholesterol is the major sterol in mammals. It is making up 20-25\% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins[1][2]. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist[3].
Batyl alcohol
C26170 - Protective Agent > C797 - Radioprotective Agent 3-(Octadecyloxy)propane-1,2-diol is an endogenous metabolite.
6-Hydroxyluteolin
Isolated from Valerianella eriocarpa (Italian corn salad). 6-Hydroxyluteolin is found in many foods, some of which are common thyme, mexican oregano, green vegetables, and lemon verbena. 6-Hydroxyluteolin is found in common thyme. 6-Hydroxyluteolin is isolated from Valerianella eriocarpa (Italian corn salad).
24-Methylenecholesterol
24-Methylenecholesterol, also known as chalinasterol or ostreasterol, belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, 24-methylenecholesterol is considered to be a sterol lipid molecule. 24-Methylenecholesterol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 24-Methylenecholesterol is involved in the biosynthesis of steroids. 24-Methylenecholesterol is converted from 5-dehydroepisterol by 7-dehydrocholesterol reductase (EC 1.3.1.21). 24-Methylenecholesterol is converted into campesterol by delta24-sterol reductase (EC 1.3.1.72). 24-methylenecholesterol is a 3beta-sterol having the structure of cholesterol with a methylene group at C-24. It has a role as a mouse metabolite. It is a 3beta-sterol and a 3beta-hydroxy-Delta(5)-steroid. It is functionally related to a cholesterol. 24-Methylenecholesterol is a natural product found in Echinometra lucunter, Ulva fasciata, and other organisms with data available. A 3beta-sterol having the structure of cholesterol with a methylene group at C-24. Constituent of clams and oysters 24-Methylenecholesterol (Ostreasterol), a natural marine sterol, stimulates cholesterol acyltransferase in human macrophages. 24-Methylenecholesterol possess anti-aging effects in yeast. 24-methylenecholesterol enhances honey bee longevity and improves nurse bee physiology[1][2][3].
8(R)-HETE
A HETE having an (8R)-hydroxy group and (5Z)-, (9E)-, (11Z)- and (14Z)-double bonds.
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).
Sinularolide D
A cembrane diterpenoid isolated from Sinularia gibberosa and has been shown to exhibit antineoplastic activity.
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].
Spathulenol
Constituent of Salvia sclarea (clary sage). Spathulenol is found in many foods, some of which are tarragon, spearmint, common sage, and tea.
michaolide A
A cembrane diterpenoid with cytotoxic activity isolated from the soft coral Lobophytum michaelae.
Cholesterol
A cholestanoid consisting of cholestane having a double bond at the 5,6-position as well as a 3beta-hydroxy group. Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong. Cholesterol is the major sterol in mammals. It is making up 20-25\\% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins[1][2]. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist[3]. Cholesterol is the major sterol in mammals. It is making up 20-25\% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins[1][2]. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist[3].
Pregnenolone
A 20-oxo steroid that is pregn-5-ene substituted by a beta-hydroxy group at position 3 and an oxo group at position 20. C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Pregnenolone is a derivative of cholesterol, the product of Cytochrome P450 side-chain cleavage (EC 1.14.15.6, CYP11A1); this reaction consists of three consecutive monooxygenations; a 22-hydroxylation, 20-hydroxylation and the cleavage of the C20-C22 bond, yielding pregnenolone. Pregnenolone is the precursor to gonadal steroid hormones and the adrenal corticosteroids. This reaction occurs in steroid hormone-producing tissues such as the adrenal cortex, corpus luteum and placenta. The most notable difference between the placenta and other steroidogenic tissues is that electron supply to CYP11A1 limits the rate at which cholesterol is converted to pregnenolone in the placenta. The limiting component for electron delivery to CYP11A1 is the concentration of adrenodoxin reductase in the mitochondrial matrix which is insufficient to maintain the adrenodoxin pool in a fully reduced state. Pregnenolone is also a neurosteroid, and is produced in the spinal cord; CYP11A1 is the key enzyme catalyzing the conversion of cholesterol into pregnenolone, the rate-limiting step in the biosynthesis of all classes of steroids, and has been localized in sensory networks of the spinal cord dorsal horn. In the adrenal glomerulosa cell angiotensin II, one of the major physiological regulators of mineralocorticoid synthesis, appears to affect most of the cholesterol transfer to the mitochondrial outer membrane and transport to the inner membrane steps and thus to exerts a powerful control over the use of cholesterol for aldosterone production. (PMID: 17222962, 15823613, 16632873, 15134809) [HMDB]. Pregnenolone is found in many foods, some of which are common wheat, yellow bell pepper, oval-leaf huckleberry, and fenugreek. Pregnenolone (3β-Hydroxy-5-pregnen-20-one) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone can protect the brain from cannabis intoxication[1][2]. Pregnenolone is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels[3]. Pregnenolone (3β-Hydroxy-5-pregnen-20-one) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors. Pregnenolone can protect the brain from cannabis intoxication[1][2]. Pregnenolone is also a TRPM3 channel activator, and also can weakly activate TRPM1 channels[3].
Minabeolide 2
A withanolide that is (22R)-22,26-epoxyergosta-1,4,24-triene substituted by oxo groups at positions 3 and 26 and an acetoxy group at position 18. Isolated from Paraminabea acronocephala, it exhibits anti-inflammatory activity.
Minabeolide 8
A withanolide that is (22R,25S)-22,26-epoxycholest-4-en-26-one substituted by an oxo group at position 3 and an alpha-acetoxy group at position 11. Isolated from Paraminabea acronocephala, it exhibits anti-inflammatory activity.
(2r,3s,6s)-3-methyl-2-(3-oxobutyl)-6-(prop-1-en-2-yl)cycloheptan-1-one
9-(acetyloxy)-12,13-dihydroxy-6-isopropyl-3,9,13-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-3-yl butanoate
1-(4-ethyl-5,6-dimethylheptan-2-yl)-6,9a,11a-trimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
2-[2-(4,6-dihydroxy-8a-methyl-1-oxo-4,4a,5,6,7,8-hexahydronaphthalen-2-yl)-1-methyl-5-(5-methylhex-3-en-2-yl)cyclopentyl]acetaldehyde
(2s,3s,4r,5r)-2-{[(2r)-1-hydroxy-3-(octadecyloxy)propan-2-yl]oxy}oxane-3,4,5-triol
6,10-dimethyl-10-(4-methyl-3-oxopentyl)-2-methylidenebicyclo[7.2.0]undecan-5-one
methyl 2-[2,5-dihydroxy-4-(3,7,11-trimethyl-9-oxododeca-2,6,10-trien-1-yl)phenyl]acetate
(1s,2s,11s,12s)-8-(hydroxymethyl)-1-isopropyl-4,12-dimethyl-15-oxabicyclo[10.2.1]pentadeca-3,7-diene-2,11-diol
ethyl 2-[(1r,3r,4e,7e,12r)-3,12-dihydroxy-4,8,12-trimethyl-11-oxocyclotetradeca-4,7-dien-1-yl]prop-2-enoate
10,14-dihydroxy-3-isopropyl-6,10,14-trimethyl-8-oxo-15-oxatricyclo[9.3.1.0²,⁷]pentadecan-6-yl acetate
[(3ar,15as)-10,14-dimethyl-3-methylidene-2-oxo-3ah,4h,7h,8h,11h,12h,15h,15ah-cyclotetradeca[b]furan-6-yl]methyl acetate
4-isopropyl-1,7,11-trimethylcyclotetradeca-2,7,11-trien-1-ol
{6,14-dimethyl-3-methylidene-2-oxo-3ah,4h,5h,8h,9h,12h,13h,15ah-cyclotetradeca[b]furan-10-yl}methyl acetate
[(1s,2e,4e,8e,12r)-1-isopropyl-8,12-dimethyl-15-oxabicyclo[10.2.1]pentadeca-2,4,8-trien-4-yl]methyl acetate
(1r,2r,5s,8s)-5-hydroxy-2,6,10,10-tetramethyl-12-oxatricyclo[6.3.1.0¹,⁸]dodec-6-en-9-one
2,16-dimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadecane-3,5-diol
7,9-dihydroxy-9a,11a-dimethyl-1-(6-methylhept-5-en-2-yl)-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-10-yl acetate
ethyl 2-[(1r,3s,4e,7e,12r)-3,12-dihydroxy-4,8,12-trimethyl-11-oxocyclotetradeca-4,7-dien-1-yl]prop-2-enoate
(1s,2z,5s,9s,10e,14s,15r)-2,11,15-trimethyl-6-methylidene-7-oxo-8,16,17-trioxatricyclo[13.2.2.0⁵,⁹]nonadeca-2,10-dien-14-yl acetate
(1s,3s,5r,8e,12e,15r,18r)-5-(hydroxymethyl)-18-(methoxymethyl)-9,13-dimethyl-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-17-one
(1s,2e,6e,10e,14s)-14-(3-hydroxyprop-1-en-2-yl)-3,7,11-trimethylcyclotetradeca-2,6,10-trien-1-ol
14-hydroxy-4,8,12-trimethyl-16-methylidene-17-oxo-3,18-dioxatricyclo[13.3.0.0²,⁴]octadeca-7,11-dien-5-yl acetate
9-hydroxy-6-(1-hydroxypropan-2-yl)-3,9,13-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadeca-3,12-dien-10-yl acetate
5a,7,9-trihydroxy-9a,11a-dimethyl-1-(6-methyl-5-methylideneheptan-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-one
methyl (1r,2s,3s,8s,10z,14z,18s,21s,22s,23z,27s,28r)-2,3,28-trihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[25.3.1.0⁵,²².0⁸,²¹]hentriaconta-5,10,14,23-tetraene-21-carboxylate
3-(acetyloxy)-2,2,5,8-tetramethyl-3,3a,3a¹,4,5,5a,6,7,8,9-decahydro-1h-pyren-4-yl acetate
methyl 3-(acetyloxy)-2,28-dihydroxy-18-isopropyl-2,6,7,11,15,24,28-heptamethyl-9,16,19-trioxo-31-oxatetracyclo[25.3.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate
(4r,7z,11r,13s)-11-hydroxy-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]hexadeca-1(16),7-diene-6,9,15-trione
(1r,4s,6s,9e,13s,14r,17s)-13-hydroxy-17-[({[(1r,4s,6s,9e,13s,14r,17s)-13-hydroxy-4,9,13-trimethyl-16-oxo-5,15-dioxatricyclo[12.3.1.0⁴,⁶]octadec-9-en-17-yl]methyl}sulfanyl)methyl]-4,9,13-trimethyl-5,15-dioxatricyclo[12.3.1.0⁴,⁶]octadec-9-en-16-one
(1r,3s,5s,9r,15s)-9-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-7,12-dien-17-one
(1r,2r,4s,8r,10r,13r,16r)-11-methyl-4-(prop-1-en-2-yl)-14,17-dioxapentacyclo[8.5.1.1⁸,¹¹.0²,⁸.0¹³,¹⁶]heptadecane-6,9,15-trione
1-{1-[5-(acetyloxy)-4-(2-hydroxypropan-2-yl)oxolan-2-yl]ethyl}-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate
(5z)-2,6,9-trimethyl-9-(4-methylpent-3-en-1-yl)bicyclo[8.1.0]undec-5-en-2-ol
9a,11a-dimethyl-1-(6-methyl-5-methylidenehept-3-en-2-yl)-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7,9-triol
(1r,7r,8r,11r)-3,3,7,11-tetramethyl-12-oxatricyclo[6.3.1.0¹,⁵]dodec-5-ene-7,8,11-triol
(1s,4s,5r,8e,12r,13r,16r)-4,5,12-trihydroxy-4,8,12,16-tetramethyl-14-oxabicyclo[11.3.1]heptadec-8-en-15-one
methyl (1r,2s,7s,10s,14r,17s,20s,21s,22e,26s,27s,30r)-2-hydroxy-17-isopropyl-1,5,10,14,23,27-hexamethyl-8,15,18-trioxo-31,32-dioxapentacyclo[24.4.1.1²⁷,³⁰.0⁴,²¹.0⁷,²⁰]dotriaconta-4,22-diene-20-carboxylate
(1s,4r,8e,10e,14s)-11-isopropyl-4,8,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-8,10-dien-6-one
(1r,2s,3r,10e,14s)-2-acetyl-4-isopropyl-1,7,11-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-3-yl acetate
(1r,2s,3r,6r,7r,8r,9r,12s)-3-(acetyloxy)-12-hydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-9-yl butanoate
methyl (1s,8s,12r)-1-methyl-3,10,13-trioxo-8-(prop-1-en-2-yl)-15-oxabicyclo[10.2.1]pentadec-5-ene-5-carboxylate
methyl 18-(acetyloxy)-4-methyl-8-oxo-12-(prop-1-en-2-yl)-3,7,17-trioxatetracyclo[12.2.1.1⁶,⁹.0²,⁴]octadeca-1(16),9,14-triene-15-carboxylate
13-hydroxy-4,9,13-trimethyl-17-methylidene-5,15-dioxatricyclo[12.3.1.0⁴,⁶]octadec-9-en-16-one
methyl (1s,8r,11r,14s)-8,14-dihydroxy-11-isopropyl-8,14-dimethyl-15-oxabicyclo[9.3.1]pentadeca-4,9-diene-4-carboxylate
(2r)-5-[(1s,4s,6s,10r,12s)-4,12-dimethyl-9-methylidene-5-oxatricyclo[8.2.0.0⁴,⁶]dodecan-12-yl]-5-oxopentan-2-yl acetate
7-hydroxy-10-(2-hydroxypropan-2-yl)-10-methoxy-3,7,13-trimethylcyclotetradeca-3,8-dien-1-one
[(1as,4as,5s,7ar,7br)-5-hydroxy-3,3,7b-trimethyl-octahydrocyclopropa[e]azulen-5-yl]methyl acetate
9a,11a-dimethyl-1-(6-methyl-5-methylideneheptan-2-yl)-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-7,9,10-triol
(1r,2e,6e,10e,14s)-3,7,11,15,15-pentamethylbicyclo[12.1.0]pentadeca-2,6,10-trien-4-one
9-hydroxy-5,9,13-trimethyl-16-methylidene-15-oxo-4,14-dioxatricyclo[11.3.2.0³,⁵]octadec-7-en-12-yl acetate
(1r,3z,5s,8e,12s,13r)-5,12-dihydroxy-4,8,12-trimethyl-16-methylidene-14-oxabicyclo[11.3.1]heptadeca-3,8-dien-15-one
(1s,3r,9s,13s)-1-methyl-9-(prop-1-en-2-yl)-4,16-dioxatricyclo[11.2.1.1³,⁶]heptadec-6(17)-ene-5,11,14-trione
(1r,2r,3r,4s,5r,6s,7s,8r,10s,11s,14r)-5,11-bis(acetyloxy)-14-(butanoyloxy)-6,10-dihydroxy-3-isopropyl-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate
13-(hydroxymethyl)-2-isopropyl-5,9-dimethylcyclotetradeca-2,4,8,12-tetraen-1-ol
13-isopropyl-2,6,10-trimethyl-15,16-dioxatetracyclo[6.6.1.1²,⁶.0⁹,¹⁴]hexadecan-10-yl acetate
2-{6,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-6,10-dien-3-yl}propan-2-ol
ethyl 2-[2-(acetyloxy)-12-hydroxy-1,5,12-trimethyl-6,16-dioxatricyclo[11.2.1.0⁵,⁷]hexadecan-9-yl]prop-2-enoate
7-hydroperoxy-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-14-yl acetate
1-(1-hydroxyethyl)-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
methyl (1r,4r,6r,8r,9r,10r)-8-hydroxy-6-isopropyl-9-methyl-13-methylidene-5-oxo-15-oxatetracyclo[6.6.1.0¹,¹⁰.0⁴,⁹]pentadec-2-ene-3-carboxylate
(1r,2e,6s,8s,11e)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.0⁶,⁸]octadeca-2,11,15-trien-17-one
[(1s,3s,5s,8e,12e,14s,15r)-14-hydroxy-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate
methyl 2-[(1r,3s,6s,10e,14s)-6-hydroxy-6,10,14-trimethyl-7-oxo-15-oxabicyclo[12.1.0]pentadec-10-en-3-yl]prop-2-enoate
(1s,3as,3bs,9ar,9bs,11as)-1-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,5h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(1r,2e,6e,10e,14r)-3,7,11,15,15-pentamethylbicyclo[12.1.0]pentadeca-2,6,10-trien-4-one
(1s,3r,4e,7e,9r,11r,12s)-3,9-dihydroxy-4,8,12-trimethyl-15-methylidene-14-oxo-13-oxabicyclo[10.3.2]heptadeca-4,7-dien-11-yl acetate
(1s,3s,4e,7e,11r,12s)-3-hydroxy-4,8,12-trimethyl-15-methylidene-14-oxo-13-oxabicyclo[10.3.2]heptadeca-4,7-dien-11-yl acetate
3-hydroxy-4,8,12-trimethyl-15-methylidene-14-oxo-13,18-dioxatricyclo[10.3.2.1⁴,⁷]octadec-8-en-11-yl acetate
1-(6,7-dihydroxy-5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7-triol
(3s)-2-[(1s,3r,4s,4as)-3-(acetyloxy)-4-methyl-7-methylidene-2,3,4,4a,5,6-hexahydro-1h-naphthalen-1-yl]-6-methyl-4-oxohept-5-en-3-yl acetate
(1r,3s,5s,7e,9r,12r,13r)-9-hydroxy-5,9,13-trimethyl-16-methylidene-15-oxo-4,14-dioxatricyclo[11.3.2.0³,⁵]octadec-7-en-12-yl acetate
(2r)-2-[(1e,3e,7e,11e)-4,8,12-trimethylcyclotetradeca-1,3,7,11-tetraen-1-yl]propane-1,2-diol
(1r,4r,6r,9e,13e,15s)-4,9,13-trimethyl-18-methylidene-5,16-dioxatricyclo[13.3.0.0⁴,⁶]octadeca-9,13-diene-3,17-dione
(1r,3ar,5as,6s,7s,9as,9br,11ar)-1-[(2r,5r)-5,6-dimethylheptan-2-yl]-6,9a,11a-trimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
4,12-dimethyl-9-methylidene-5-oxatricyclo[8.2.0.0⁴,⁶]dodecan-12-ol
(4s,5s)-5-[(1e,5e)-2,6-dimethyl-10-oxoundeca-1,5-dien-1-yl]-4-(2-hydroxyethyl)-3-methylideneoxolan-2-one
2-(4,8,12-trimethylcyclotetradeca-1,3,7,11-tetraen-1-yl)propane-1,2-diol
(1r,4s,11s,12s)-8-(hydroxymethyl)-1-isopropyl-4,12-dimethyl-15-oxabicyclo[9.3.1]pentadeca-2,7-diene-4,12-diol
5,9-bis(acetyloxy)-16-(methoxymethyl)-4,8,12-trimethyl-17-oxo-3,18-dioxatricyclo[13.3.0.0²,⁴]octadeca-7,11-dien-14-yl acetate
methyl 1-methyl-3,10,13-trioxo-8-(prop-1-en-2-yl)-15-oxabicyclo[10.2.1]pentadec-5-ene-5-carboxylate
(1r,2r,4r,10s,14s,15s)-10-(acetyloxy)-4,8,12-trimethyl-16-methylidene-17-oxo-3,18-dioxatricyclo[13.3.0.0²,⁴]octadeca-7,11-dien-14-yl acetate
(1e,3z,6e,10z)-14-isopropyl-3,7,11-trimethylcyclotetradeca-1,3,6,10-tetraene
(1e,5s,6e,8r)-1,5-dimethyl-8-(prop-1-en-2-yl)cyclodeca-1,6-diene
(1r,14r)-3,7,11-trimethyl-14-(prop-1-en-2-yl)cyclotetradeca-3,7,11-trien-1-ol
(2z,4e,9s,12e)-2-isopropyl-5,9,13-trimethylcyclotetradeca-2,4,12-triene-1,7-dione
methyl 2-[(1s,3r,6r,7s,10e,14s)-6,7-dihydroxy-6,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadec-10-en-3-yl]prop-2-enoate
(4r,6r,9r,10e,13e,15s)-4,9,13,18-tetramethyl-5,16-dioxatricyclo[13.3.0.0⁴,⁶]octadeca-1(18),10,13-trien-9-ol
(1r,3as,3bs,7r,9s,9ar,9bs,10r,11as)-7,9,10-trihydroxy-9a-methyl-1-[(1r)-1-[(1s,2r)-2-methyl-2-[(2r)-3-methylbutan-2-yl]cyclopropyl]ethyl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-11a-carboxylic acid
2-[(1r,3z,7z,11z)-4,8,12-trimethylcyclotetradeca-3,7,11-trien-1-yl]prop-2-en-1-ol
(1r,4s,13r,16s)-11-methyl-4-(prop-1-en-2-yl)-14-oxatetracyclo[8.5.1.0²,⁸.0¹³,¹⁶]hexadeca-2(8),10-diene-6,9,15-trione
methyl (1e,4z,8z,12s)-12-isopropyl-5,9-dimethyl-3,10,13-trioxocyclotetradeca-1,4,8-triene-1-carboxylate
(1r,4s,6s,10r,13s,14r,17s)-10-hydroperoxy-13-hydroxy-4,13,17-trimethyl-9-methylidene-5,15-dioxatricyclo[12.3.1.0⁴,⁶]octadecan-16-one
7-isopropyl-4,10-dimethyl-11,12-dioxatricyclo[5.3.2.0¹,⁵]dodec-5-en-4-ol
n-(1,3-dihydroxyoctadeca-4,8-dien-2-yl)hexadecanimidic acid
(1s,2s,10e,12s)-5-(hydroxymethyl)-12-isopropyl-1,9-dimethyl-15-oxabicyclo[10.2.1]pentadeca-5,8,10-trien-2-ol
2-[(1r,2r,5r)-2-[(4s,4as,6s,8as)-4,6-dihydroxy-8a-methyl-1-oxo-4,4a,5,6,7,8-hexahydronaphthalen-2-yl]-1-methyl-5-[(2r,3e)-5-methylhex-3-en-2-yl]cyclopentyl]ethyl acetate
7-(acetyloxy)-1-(3,6-dihydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-5-yl acetate
(1s,3s,5s,8e,12e,15r)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-17-one
(3r,5r,8e,13e,15s)-5,9,13,18-tetramethyl-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-1(18),8,13-trien-17-one
(1s,2z,5s,9s,10e,14r,15r)-2,11,15-trimethyl-6-methylidene-7-oxo-8,16,17-trioxatricyclo[13.2.2.0⁵,⁹]nonadeca-2,10-dien-14-yl acetate
(1r,3s,4r,7s,11s,12r)-3,4,7,11-tetrahydroxy-4,12-dimethyl-8,15-dimethylidene-13-oxabicyclo[10.3.2]heptadecan-14-one
(2r)-1-(hexadecanoyloxy)-3-(hexadecyloxy)propan-2-yl hexadecanoate
5-(acetyloxy)-14-(butanoyloxy)-6,11-dihydroxy-3-isopropyl-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadec-9-en-4-yl butanoate
(10e,13e)-9-hydroxy-4,9,13-trimethyl-18-methylidene-17-oxo-5,16-dioxatricyclo[13.3.0.0⁴,⁶]octadeca-10,13-dien-3-yl acetate
3'-(1-hydroxy-2,3,4-trimethylpentyl)-3',9a,11a-trimethyl-2,3,3a,3b,4,6,7,8,9,9b,10,11-dodecahydrospiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-7-ol
(5s,8r)-1-hydroxy-8-isopropyl-4-methoxy-5-methyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde
(1s,2s,3z,5e,9e,13e)-3-isopropyl-6,10,14-trimethylcyclotetradeca-3,5,9,13-tetraene-1,2-diol
methyl (1s,2s,4r,8s,11s,15r,18s,21s,22s,23e,27s,28s)-27-(acetyloxy)-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate
(1s,2s,3s,6s,7s,8s,9s,12r)-12-(acetyloxy)-1,9-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-3-yl butanoate
(1as,3r,4as,7s,8ar)-7-hydroxy-3-[(1s,2r,3r)-2-(2-hydroxyethyl)-2-methyl-3-[(2r)-6-methyl-5-methylideneheptan-2-yl]cyclopentyl]-4a-methyl-hexahydro-1ah-naphtho[1,8a-b]oxiren-4-one
2-[(1s,3r,6e,10e,14r)-6,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-6,10-dien-3-yl]propan-2-ol
(3ar,5s,6r,15as)-6-hydroxy-6,10,14-trimethyl-3-methylidene-2-oxo-3ah,4h,5h,7h,8h,11h,12h,15h,15ah-cyclotetradeca[b]furan-5-yl acetate
methyl 2-(4,8,12-trimethylcyclotetradeca-1,3,7,11-tetraen-1-yl)propanoate
(1s,4r,10s,11r,13s,16s)-11-hydroxy-11-methyl-4-(prop-1-en-2-yl)-14-oxatetracyclo[8.5.1.0²,⁸.0¹³,¹⁶]hexadec-2(8)-ene-6,9,15-trione
6-(5,6-dimethylheptan-2-yl)-5,18-dimethyl-3-oxapentacyclo[8.8.0.0²,⁴.0⁵,⁹.0¹³,¹⁸]octadecane-12,15,17-triol
(1r,3s,5s,7z,9s,12s,13r)-9-hydroperoxy-12-hydroxy-5,9,13-trimethyl-16-methylidene-4,14-dioxatricyclo[11.3.2.0³,⁵]octadec-7-en-15-one
methyl (1r,2s,4r,5s,7s,9s,12r,14s,15r)-5-(chloromethyl)-2,7-dihydroxy-12-methyl-10,17-dioxo-6,16,18,19-tetraoxapentacyclo[12.2.2.1⁴,⁷.1⁹,¹².0¹,¹⁵]icosane-5-carboxylate
(1s,3as,4r,7s)-7-isopropyl-1,4-dimethyl-3,4,5,6-tetrahydro-2h-azulene-1,3a,7-triol
methyl (1r,2r,3s,8s,11s,15r,18s,21s,22s,23e,27s,28r)-3-(acetyloxy)-2,28-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[25.3.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate
3,12-dimethyl (1s,2e,6s,8s,11z,15r)-15-isopropyl-8-methyl-7,16-dioxatricyclo[13.1.0.0⁶,⁸]hexadeca-2,11-diene-3,12-dicarboxylate
methyl 8-hydroxy-6-isopropyl-9,13-dimethyl-5-oxo-15-oxatetracyclo[6.6.1.0¹,¹⁰.0⁴,⁹]pentadec-2-ene-3-carboxylate
methyl (1r,2s,3s,8s,11s,15r,18s,21r,22s,23z,27s,28r)-2,3,28-trihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[25.3.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate
2-hydroxy-n-(3-hydroxy-9-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl)docosanimidic acid
(1r,3as,3bs,7s,9ar,11ar)-1-[(2r,5s)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(1r,2e,4z,7r,8e,12e,14r)-14-(acetyloxy)-7-hydroxy-2-isopropyl-5,9,13-trimethylcyclotetradeca-2,4,8,12-tetraen-1-yl acetate
7-isopropyl-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene
5-hydroxy-2-isopropyl-4a-methyl-8-methylidene-octahydronaphthalen-1-yl acetate
(1r,4s,6s,10s,13s,14r,17s)-10-hydroperoxy-13-hydroxy-4,13,17-trimethyl-9-methylidene-5,15-dioxatricyclo[12.3.1.0⁴,⁶]octadecan-16-one
4,9,13,18-tetramethyl-5,16-dioxatricyclo[13.3.0.0⁴,⁶]octadeca-1(18),9,13-triene
12,13-dihydroxy-6-isopropyl-9,13-dimethyl-3-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-9-yl acetate
3,12-dihydroxy-1,4,8,12-tetramethyl-16-oxatricyclo[11.2.1.1²,⁵]heptadeca-4,8-dien-17-one
6,10,14-trimethyl-3-methylidene-3ah,4h,7h,8h,11h,12h,15h,15ah-cyclotetradeca[b]furan-2-one
(1s,2s,5s,6r)-5,8,8,11-tetramethyltricyclo[4.3.2.0²,⁵]undec-10-en-2-yl acetate
2-[3-(5,6-dimethylheptan-2-yl)-2-(2-hydroxyethyl)-2-methylcyclopentyl]-6-hydroxy-8a-methyl-2,3,5,6,7,8-hexahydronaphthalen-1-one
2-(2,6-dimethylocta-1,5,7-trien-1-yl)-4-methylfuran
methyl 2-[(1s,3r,5e,7s,10e,14s)-7-hydroxy-6,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-5,10-dien-3-yl]prop-2-enoate
10-hydroxy-6,10,14-trimethyl-3-methylidene-3ah,4h,5h,8h,9h,13h,15ah-cyclotetradeca[b]furan-2-one
5-(acetyloxy)-14-(butanoyloxy)-6,10-dihydroxy-3-isopropyl-6,10,14-trimethyl-11-(prop-2-enoyloxy)-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate
7,9,10-trihydroxy-9a-methyl-1-(6-methyl-5-methylideneheptan-2-yl)-tetradecahydro-1h-cyclopenta[a]phenanthrene-11a-carbaldehyde
(1s,2r,5r,6r,9r,10r,13s,15s)-5-[(2r,5s)-5,6-dimethylheptan-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
(1s,4e,8r,10s,13e,15s,17r,18s)-4,8,13,18-tetramethyl-9,16,19-trioxatetracyclo[13.4.0.0¹,¹⁸.0⁸,¹⁰]nonadeca-4,13-dien-17-ol
4,4-dimethyl-2-[(2z)-2-methyl-6-oxohept-2-en-1-yl]cyclopent-2-en-1-one
(1e,3e,11e)-4-isopropyl-1,7,11-trimethylcyclotetradeca-1,3,7,11-tetraene
(1s,2e,6s,8r,11e)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.0⁶,⁸]octadeca-2,11,15-trien-17-one
{6-[(acetyloxy)methyl]-5-(2-chloroethyl)-2,2-dimethyl-1,3-dihydroinden-4-yl}methyl acetate
3,4,11-trihydroxy-4,8,12-trimethyl-15-methylidene-13-oxabicyclo[10.3.2]heptadec-7-en-14-one
methyl (1r,2s,3s,8r,10e,14z,18r,21s,22r,23z,27s,28s)-2,3,27-trihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,10,14,23-tetraene-21-carboxylate
6-isopropyl-9-methyl-3,13-dimethylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadecane-9,12-diol
(1r,3as,3bs,5r,5ar,7s,9ar,9bs,11ar)-1-[(2r,5s)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7-triol
[(1r,3r,5s,8e,12e,14r,15r)-14-(acetyloxy)-9,13-dimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.0³,⁵]octadeca-8,12-dien-5-yl]methyl acetate
n-[(2s,3s,4r)-1,3,4-trihydroxyhexacosan-2-yl]icosanimidic acid
methyl (1r,4r,6r,8s,9r,10r)-8-hydroxy-6-isopropyl-9-methyl-13-methylidene-5-oxo-15-oxatetracyclo[6.6.1.0¹,¹⁰.0⁴,⁹]pentadec-2-ene-3-carboxylate
(1r,2r,4s)-1-ethenyl-1-methyl-4-(6-methylhepta-2,6-dien-2-yl)-2-(prop-1-en-2-yl)cyclohexane
(1s,2r,5z,7e,11e)-5-(2-hydroxypropan-2-yl)-2,8,12-trimethylcyclotetradeca-5,7,11-triene-1,2-diol
(5z,7e,12r,13s)-12-isopropyl-5,9-dimethyl-14-oxabicyclo[11.2.1]hexadeca-1(16),5,7-triene-3,10,15-trione
1,1,4,7-tetramethyl-octahydrocyclopropa[e]azulene-4,7-diol
1,5,5-trimethyl-2-(3-oxobutyl)bicyclo[5.1.0]octan-3-one
(1s,3e,7e,11s,12r,16r)-1-hydroxy-11-(hydroxymethyl)-3,7-dimethyl-15-methylidene-13,17-dioxatricyclo[9.5.1.1¹²,¹⁶]octadeca-3,7-dien-14-one
(8e,11r,12r,13r)-12-isopropyl-5,9-dimethyl-3,15-dioxo-14-oxabicyclo[11.2.1]hexadeca-1(16),5,8-trien-11-yl acetate
(1r,2s,4s,6s,13s,14r)-2,11-dimethyl-7-methylidene-14-(prop-1-en-2-yl)-5,16-dioxatricyclo[11.2.1.0⁴,⁶]hexadec-10-en-2-ol
(1r,6r,8r,11s)-11-hydroperoxy-3,8,16-trimethyl-12-methylidene-7,18-dioxatricyclo[13.3.0.0⁶,⁸]octadeca-2,15-dien-17-one
(1s,3r,6z,9s,13s,17r)-17-hydroxy-1-methyl-9-(prop-1-en-2-yl)-4,16-dioxatricyclo[11.2.1.1³,⁶]heptadec-6-ene-5,11,14-trione
(3e,8s,9e,13r)-10-(2-hydroxypropan-2-yl)-3,8,13-trimethylcyclotetradeca-3,9-diene-1,7-dione
(1s,2e,6s,8s,9s,11e)-9-hydroxy-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.0⁶,⁸]octadeca-2,11,15-trien-17-one
1-hydroperoxy-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.0⁶,⁸]octadeca-2,11,15-trien-17-one
methyl (1r,4r,6r,10s,12r)-4,12-dimethyl-9-methylidene-5-oxatricyclo[8.2.0.0⁴,⁶]dodecane-12-carboxylate
(1r,3as,3bs,5as,7s,9s,9as,9bs,11ar)-5a,7,9-trihydroxy-9a,11a-dimethyl-1-[(2r)-6-methyl-5-methylideneheptan-2-yl]-dodecahydro-1h-cyclopenta[a]phenanthren-5-one
14-isopropyl-3,7,11-trimethylcyclotetradeca-2,6,10-trien-1-ol
7-hydroxy-4-isopropyl-1,7,11-trimethyl-15-oxabicyclo[12.1.0]pentadeca-3,5,10-trien-2-yl acetate
(1s,2e,4r,7z,11s,12s)-11-chloro-8-(hydroxymethyl)-1-isopropyl-4,12-dimethyl-15-oxabicyclo[10.2.1]pentadeca-2,7-dien-4-ol
C20H33ClO3 (356.2118098000001)