Exact Mass: 414.3133782
Exact Mass Matches: 414.3133782
Found 500 metabolites which its exact mass value is equals to given mass value 414.3133782,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Diosgenin
Diosgenin is a sapogenin that is spirostan which is substituted by a hydroxy group at the 3beta position, contains a double bond at the 5-6 position, and has R- configuration at position 25. A natural product found in Dioscorea (wild yam) species, it is used as the starting point for the commercial synthesis of a number of steroids, including cortisone, pregnenolone and progesterone. It has a role as an apoptosis inducer, an antiviral agent, an antineoplastic agent and a metabolite. It is a 3beta-sterol, a spiroketal, a hexacyclic triterpenoid and a sapogenin. It derives from a hydride of a spirostan. Diosgenin is a natural product found in Ophiopogon intermedius, Dracaena draco, and other organisms with data available. A spirostan found in DIOSCOREA and other plants. The 25S isomer is called yamogenin. Solasodine is a natural derivative formed by replacing the spiro-ring with a nitrogen, which can rearrange to SOLANINE. See also: Fenugreek seed (part of); Dioscorea polystachya tuber (part of). A sapogenin that is spirostan which is substituted by a hydroxy group at the 3beta position, contains a double bond at the 5-6 position, and has R- configuration at position 25. A natural product found in Dioscorea (wild yam) species, it is used as the starting point for the commercial synthesis of a number of steroids, including cortisone, pregnenolone and progesterone. Diosgenin is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Diosgenin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Diosgenin can be found in a number of food items such as carrot, wild carrot, yam, and bitter gourd, which makes diosgenin a potential biomarker for the consumption of these food products. Diosgenin, a phytosteroid sapogenin, is the product of hydrolysis by acids, strong bases, or enzymes of saponins, extracted from the tubers of Dioscorea wild yam, such as the Kokoro. The sugar-free (aglycone) product of such hydrolysis, diosgenin is used for the commercial synthesis of cortisone, pregnenolone, progesterone, and other steroid products . Bottle Name:Diosgenin; Origin: Plant; Formula(Parent): C27H42O3; PRIME Parent Name:Diosgenin; PRIME in-house No.:T0108; SubCategory_DNP: The sterols, Cholestanes Origin: Plant; Formula(Parent): C27H42O3; Bottle Name:Diosgenin; PRIME Parent Name:Diosgenin; PRIME in-house No.:T0108; SubCategory_DNP: The sterols, Cholestanes CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2260 Diosgenin, a steroidal saponin, can inhibit STAT3 signaling pathway[1]. Diosgenin is an exogenous activator of Pdia3/ERp57[2]. Diosgenin inhibits aortic atherosclerosis progression by suppressing macrophage miR-19b expression[5]. Diosgenin, a steroidal saponin, can inhibit STAT3 signaling pathway[1]. Diosgenin is an exogenous activator of Pdia3/ERp57[2]. Diosgenin inhibits aortic atherosclerosis progression by suppressing macrophage miR-19b expression[5].
Yamogenin
Yamogenin is a triterpenoid. Yamogenin is a natural product found in Cordyline australis, Solanum spirale, and other organisms with data available. See also: Dioscorea polystachya tuber (part of). Diosgenin, a steroidal saponin, can inhibit STAT3 signaling pathway[1]. Diosgenin is an exogenous activator of Pdia3/ERp57[2]. Diosgenin inhibits aortic atherosclerosis progression by suppressing macrophage miR-19b expression[5]. Diosgenin, a steroidal saponin, can inhibit STAT3 signaling pathway[1]. Diosgenin is an exogenous activator of Pdia3/ERp57[2]. Diosgenin inhibits aortic atherosclerosis progression by suppressing macrophage miR-19b expression[5].
delta4-Dafachronic acid
CONFIDENCE standard compound; INTERNAL_ID 107
Lupulone
Lupulone is found in alcoholic beverages. Lupulone is a constituent of hops
3-Methoxy-16-octylestra-1,3,5(10)-triene-16beta,17beta-diol
SCHEMBL16431292
(25S)-Delta(4)-dafachronic acid
A Delta(4)-dafachronic acid that has S configuration at position 25 (the carbon attached to the carboxy group). Found in Caenorhabditis elegans.
Smilagenone
Smilagenone is found in root vegetables. Smilagenone is a constituent of the wild yam Dioscorea deltoidea. Constituent of the wild yam Dioscorea deltoidea. Smilagenone is found in root vegetables.
Adlupulone
Adlupulone is found in alcoholic beverages. Adlupulone is a constituent of hops
11'-Carboxy-alpha-tocotrienol
11-Carboxy-alpha-tocotrienol is a dehydrogenation carboxylate product of 11-hydroxy-a-tocotrienol by an unidentified microsomal enzyme(s) probably via an aldehyde intermediate. Tocotrienols are members of the vitamin E family. An essential nutrient for the body, vitamin E is made up of four tocopherols (alpha, beta, gamma, delta) and four tocotrienols (alpha, beta, gamma, delta).Chemically, vitamin E is an antioxidant. One model for the function of vitamin E in the body is that it protects cell membranes, active enzyme sites, and DNA from free radical damage. Tocotrienols are natural compounds found in select vegetable oils, wheat germ, barley, saw palmetto, and certain types of nuts and grains. This variant of vitamin E only occur at very low levels in nature. While the majority of research on vitamin E has focused on alpha-tocopherol, studies into tocotrienols account for less than 1\\% of all research into vitamin E. 11-Carboxy-alpha-tocotrienol is a dehydrogenation carboxylate product of 11-hydroxy-a-tocotrienol by an unidentified microsomal enzyme(s) probably via an aldehyde intermediate
Setariol
Setariol is found in cereals and cereal products. Setariol is a constituent of the leaves of Setaria italica (foxtail millet). Constituent of the leaves of Setaria italica (foxtail millet). Setariol is found in cereals and cereal products.
DG(8:0/13:0/0:0)
DG(8:0/13:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(8:0/13:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/13:0)
DG(8:0/0:0/13:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(8:0/i-13:0/0:0)
DG(8:0/i-13:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(8:0/i-13:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/i-13:0)
DG(8:0/0:0/i-13:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(8:0/a-13:0/0:0)
DG(8:0/a-13:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(8:0/a-13:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/a-13:0)
DG(8:0/0:0/a-13:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(13:0/8:0/0:0)
DG(13:0/8:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(13:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(13:0/0:0/8:0)
DG(13:0/0:0/8:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(i-13:0/8:0/0:0)
DG(i-13:0/8:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(i-13:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(a-13:0/8:0/0:0)
DG(a-13:0/8:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(a-13:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(a-13:0/0:0/8:0)
DG(a-13:0/0:0/8:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
Docosahexaenoylcholine
Docosahexaenoylcholine, also known as choline docosahexaenoic acid, belongs to the class of organic compounds known as acyl cholines. These are acylated derivatives of choline. Choline or 2-hydroxy-N,N,N-trimethylethanaminium is a quaternary ammonium salt with the chemical formula (CH3)3N+(CH2)2OH. Docosahexaenoylcholine has been identified in blood (PMID: 31396400).
N-Myristoyl Tryptophan
C25H38N2O3 (414.28822779999996)
N-myristoyl tryptophan belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Myristic acid amide of Tryptophan. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Myristoyl Tryptophan is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Myristoyl Tryptophan is therefore classified as a long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.
((1R,2R,5R)-2-(2,6-Dimethoxy-4-(2-methyloctan-2-yl)phenyl)-7,7-dimethyl-4-bicyclo(3.1.1)hept-3-enyl) methanol
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D063385 - Cannabinoid Receptor Modulators D018377 - Neurotransmitter Agents > D063385 - Cannabinoid Receptor Modulators > D063386 - Cannabinoid Receptor Agonists
Diosgenin
Diosgenin, a steroidal saponin, can inhibit STAT3 signaling pathway[1]. Diosgenin is an exogenous activator of Pdia3/ERp57[2]. Diosgenin inhibits aortic atherosclerosis progression by suppressing macrophage miR-19b expression[5]. Diosgenin, a steroidal saponin, can inhibit STAT3 signaling pathway[1]. Diosgenin is an exogenous activator of Pdia3/ERp57[2]. Diosgenin inhibits aortic atherosclerosis progression by suppressing macrophage miR-19b expression[5].
1,25-Dihydroxy-16-ene-vitamin D3
25-Hydroxy-24-oxocholecalciferol
Desoxycorticosterone pivalate
Kuguacin C
Kuguacin c is a member of the class of compounds known as oxosteroids. Oxosteroids are steroid derivatives carrying a C=O group attached to steroid skeleton. Kuguacin c is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Kuguacin c can be found in bitter gourd, which makes kuguacin c a potential biomarker for the consumption of this food product.
22-Hydroxy-24-methylsedn-16-en-24-one-12beta,25beta-olide
Cabralealactone
A tetracyclic triterpenoid isolated from the stems of Aglaia abbreviata.
9-Octadecenoic acid (9Z)-, 2-[2-(2-hydroxyethoxy)ethoxy]ethyl ester
Lupulone
Lupulone is a beta-bitter acid in which the acyl group is specified as 3-methylbutanoyl. It has a role as an antimicrobial agent, an apoptosis inducer, an angiogenesis inhibitor and an antineoplastic agent. It is a conjugate acid of a lupulone(1-). Lupulone is a natural product found in Humulus lupulus with data available. A beta-bitter acid in which the acyl group is specified as 3-methylbutanoyl.
(6??, 24?鈥?-form-24, 25-Epoxy-6, hydroxycholest-4-en-3-one
(5S)-5-methyl-5-[(5R,8R,9R,10R,13R,14R,17S)-4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-one
22-hydroxy-24-methyl-12,24-dioxoscalar-16-en-25-al
(3S,5Z,7E)-3,25-Dihydroxy-9,10-secocholesta-5,7,10(19)-trien-23-one
(3S,5Z,7E)-3,25-Dihydroxy-9,10-secocholesta-5,7,10(19)-trien-24-one
rel-2R,3R,5S-trihydroxy-6R-nonadecyltetrahydropyran-4-one
25,26,27-trisnor-3-oxo-lanost-9(11)-en-24-oic acid
(3beta,5alpha,6alpha)-3,6-Dihydroxycholesta-9(11),20(22)-dien-23-one
(8alphaOH)-8,25-Dihydroxy-9,10-secocholesta-4,6,10(19)-trien-3-one
(2aS,3S,6R,7aR,8bR,14aR,14bR,14cR)-icosahydro-3,8b,12,12,14,14b-hexamethyl-11H-3,6-epoxynaphtho[2,1:4,5]indeno[7,1-bc]oxocin-11-one|cylindrictone D
5alpha,8alpha-Epidioxycholesta-6,22-dien-3beta-ol|ergosterol-5,8-endoperoxide
cholest-9(11)-en-3alpha-ol-18(21)-olide|sylvestristerol B
cholest-5-en-3alpha-ol-18(21)-olide|sylvestristerol A
3-Oxo-24.25.26.27-tetranor-9alpha-tirucall-7-en-23-saeure-methylester
25,26,27-trisnor-3-ketocycloartan-24-oic acid|3-Oxo-25.26.27-trinor-cycloartansaeure-(24)|3-Oxo-9beta.19-cyclo-25.26.27-trinor-lanostansaeure-(24)|4,4,14-trimethyl-3-oxo-9beta,19-cyclo-5alpha-cholan-24-oic acid|4,4,14-Trimethyl-3-oxo-9beta,19-cyclo-5alpha-cholan-24-saeure
(4R,5S,8S,9S,10S,13S,14R,17R,19E)-22,29,30-trinorshion-19-en-3-one-21-acid|astershionone E
3alpha-hydroxy-25,26,27-trinordammar-22(23)-en-24,20alpha-olide
(22E,24S),5alpha,8alpha-epidioxy-24-methylchlolesta-6,22-dien-3beta-ol
5,8alpha-Epidioxy-5alpha-cholesta-6,9(11)-dien-3beta-ol|5alpha,8alpha-Epidioxycholesta-6,9(11)-dien-3beta-ol
3beta,6alpha-Dihydroxy-5alpha-cholesta-9(11),24-dien-23-on|Marthasteron|Marthasterone
(22Z)-5alpha,8alpha-epidioxy-24xi-methyl-27-nor-cholesta-6,22-dien-3beta-ol
ADLUPULONE
A beta-bitter acid in which the acyl group is specified as 2-methylbutanoyl.
Ala Ile Ile Val
Ala Ile Leu Val
Ala Ile Val Ile
Ala Ile Val Leu
Ala Leu Ile Val
Ala Leu Leu Val
Ala Leu Val Ile
Ala Leu Val Leu
Ala Val Ile Ile
Ala Val Ile Leu
Ala Val Leu Ile
Ala Val Leu Leu
Gly Ile Ile Ile
Gly Ile Ile Leu
Gly Ile Leu Ile
Gly Ile Leu Leu
Gly Leu Ile Ile
Gly Leu Ile Leu
Gly Leu Leu Ile
Gly Leu Leu Leu
Ile Ala Ile Val
Ile Ala Leu Val
Ile Ala Val Ile
Ile Ala Val Leu
Ile Gly Ile Ile
Ile Gly Ile Leu
Ile Gly Leu Ile
Ile Gly Leu Leu
Ile Ile Ala Val
Ile Ile Gly Ile
Ile Ile Gly Leu
Ile Ile Ile Gly
Ile Ile Leu Gly
Ile Ile Val Ala
Ile Leu Ala Val
Ile Leu Gly Ile
Ile Leu Gly Leu
Ile Leu Ile Gly
Ile Leu Leu Gly
Ile Leu Val Ala
Ile Val Ala Ile
Ile Val Ala Leu
Ile Val Ile Ala
Ile Val Leu Ala
Leu Ala Ile Val
Leu Ala Leu Val
Leu Ala Val Ile
Leu Ala Val Leu
Leu Gly Ile Ile
Leu Gly Ile Leu
Leu Gly Leu Ile
Leu Gly Leu Leu
Leu Ile Ala Val
Leu Ile Gly Ile
Leu Ile Gly Leu
Leu Ile Ile Gly
Leu Ile Leu Gly
Leu Ile Val Ala
Leu Leu Ala Val
Leu Leu Gly Ile
Leu Leu Gly Leu
Leu Leu Ile Gly
Leu Leu Leu Gly
Leu Leu Val Ala
Leu Val Ala Ile
Leu Val Ala Leu
Leu Val Ile Ala
Leu Val Leu Ala
Val Ala Ile Ile
Val Ala Ile Leu
Val Ala Leu Ile
Val Ala Leu Leu
Val Ile Ala Ile
Val Ile Ala Leu
Val Ile Ile Ala
Val Ile Leu Ala
Val Leu Ala Ile
Val Leu Ala Leu
Val Leu Ile Ala
Val Leu Leu Ala
Val Val Val Val
1α-hydroxy-22-oxovitamin D3 / 1α-hydroxy-22-oxocholecalciferol
24,25-epoxy-1α-hydroxyvitamin D3 / 24,25-epoxy-1α-hydroxycholecalciferol
25,26-epoxy-1α-hydroxyvitamin D3 / 25,26-epoxy-1α-hydroxycholecalciferol
(5Z,7E)-(1S,3R)-24,25-epoxy-23,23-dimethyl-26,27-dinor-9,10-seco-5,7,10(19)-cholestatriene-1,3-diol
25-hydroxy-23-oxovitamin D3 / 25-hydroxy-23-oxocholecalciferol
25-hydroxy-24-oxovitamin D3 / 25-hydroxy-24-oxocholecalciferol
25-hydroxy-1-oxo-3-epiprevitamin D3 / 25-hydroxy-1-oxo-3-epiprecholecalciferol
(5Z,7E)-(1S,3R,23S)-9,10-seco-5,7,10(19),25-cholestatetraene-1,3,23-triol
(5Z,7E,22E)-(1S,3R,24R)-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,24-triol
(5Z,7E,22E)-(1S,3R,24S)-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,24-triol
1α,25-dihydroxy-9,11-didehydrovitamin D3 / 1α,25-dihydroxy-9,11-didehydrocholecalciferol
1α,25-dihydroxy-16,17-didehydrovitamin D3 / 1α,25-dihydroxy-16,17-didehydrocholecalciferol
1α,25-dihydroxy-22,23-didehydrovitamin D3 / 1α,25-dihydroxy-22,23-didehydrocholecalciferol
(5Z,7E,23E)-(1S,3R)-9,10-seco-5,7,10(19),23-cholestatetraene-1,3,25-triol
(1S,3R)-9,10-seco-5(10),8-cholestadien-6-yne-1,3,25-triol
(1R,3S)-9,10-seco-5(10),8-cholestadien-6-yne-1,3,25-triol
(5Z,7E)-(1S,3R,17S,20S)-17,20-methano-21-nor-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,17S,20R)-17,20-methano-21-nor-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E,22E)-(3S,24R)-9,10-seco-5,7,10(19),22-cholestatetraene-3,24,25-triol
(5Z,7E,22E)-(3S,24S)-9,10-seco-5,7,10(19),22-cholestatetraene-3,24,25-triol
18-(3-Hydroxy-3-methylbutyl)-20-methyl-9,10-secopregna-5,7,10(19),20-tetraene-1,3-diol
6-keto Testosterone Enanthate
HU-308
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D063385 - Cannabinoid Receptor Modulators D018377 - Neurotransmitter Agents > D063385 - Cannabinoid Receptor Modulators > D063386 - Cannabinoid Receptor Agonists C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent
Smilagenone
Setariol
ascr#29
An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (2E,16R)-16-hydroxyheptadec-2-enoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.
oscr#29
An omega-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (2E)-17-hydroxyheptadec-2-enoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.
1alpha-hydroxy-22-oxovitamin D3 / 1alpha-hydroxy-22-oxocholecalciferol
24,25-epoxy-1alpha-hydroxyvitamin D3
25,26-epoxy-1alpha-hydroxyvitamin D3
24,25-epoxy-1alpha-hydroxy-23,23-dimethyl-26,27-dinorvitamin D3
(6E)-(8S)-8,25-dihydroxy-9,10-seco-4,6,10(19)-cholestatrien-3-one
(23S)-1alpha,23-dihydroxy-25,26-didehydrovitamin D3
1alpha,25-dihydroxy-9,11-didehydrovitamin D3 / 1alpha,25-dihydroxy-9,11-didehydrocholecalciferol
1alpha,25-dihydroxy-16,17-didehydrovitamin D3
1alpha,25-dihydroxy-22,23-didehydrovitamin D3 / 1alpha,25-dihydroxy-22,23-didehydrocholecalciferol
(17S,20S)-1alpha,25-dihydroxy-17,20-methano-21-norvitamin D3
4,4-Diapolycopen-4-al
An apo carotenoid triterpenoid that is 4,4-diapolycopene in which one of the terminal methyl groups has been replaced by a formyl group.
Oxabolone cipionate
A - Alimentary tract and metabolism > A14 - Anabolic agents for systemic use > A14A - Anabolic steroids > A14AB - Estren derivatives C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
Desoxycorticosterone pivalate
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
Gestonorone caproate
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone
Methenolone Enanthate
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone
Propidium
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D007364 - Intercalating Agents D004396 - Coloring Agents
7-Nor-Ergosterolide
A steroid lactone that is a derivative of ergostanoid, isolated from the culture extract of Aspergillus ochraceus.
(2E)-17-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]heptadec-2-enoic acid
(2E,16R)-16-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]heptadec-2-enoic acid
seco-plakortolide P
A butan-4-olide that is dihydrofuran-2(3H)-one substituted by a hydroxy group at position 4, a 2-hydroxy-2-methyl-14-phenyltetradeca-11,13-dien-1-yl group at position 5 and a methyl group at position 5 (the 4S,5S stereoisomer). It is isolated from the Australian marine sponge Plakinastrella clathrata.
seco-plakortolide O
A butan-4-olide that is dihydrofuran-2(3H)-one substituted by a hydroxy group at position 4, a 2-hydroxy-2-methyl-14-phenyltetradeca-11,13-dien-1-yl group at position 5 and a methyl group at position 5 (the 4R,5R stereoisomer). It is isolated from the Australian marine sponge Plakinastrella clathrata.
yamogenin
Diosgenin is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Diosgenin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Diosgenin can be found in a number of food items such as bitter gourd, asparagus, carrot, and wild carrot, which makes diosgenin a potential biomarker for the consumption of these food products. Diosgenin, a phytosteroid sapogenin, is the product of hydrolysis by acids, strong bases, or enzymes of saponins, extracted from the tubers of Dioscorea wild yam, such as the Kokoro. The sugar-free (aglycone) product of such hydrolysis, diosgenin is used for the commercial synthesis of cortisone, pregnenolone, progesterone, and other steroid products .
5-Hydroxy-2,2,6-tris(3-methyl-2-buten-1-yl)-4-(2-methyl-1-oxobutyl)-4-cyclohexene-1,3-dione
N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]hexadecanamide
25-Hydroxy-24-oxocalciol
D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols
(22E)-(24R)-24,25-dihydroxy-22,23-didehydrovitamin D3/(22E)-(24R)-24,25-dihydroxy-22,23-didehydrocholecalciferol
Desoxycorticosterone pivalate
Delta(7)-dafachronic acid
A member of the class of dafachronic acids that is (5alpha)-3-oxocholest-7-ene in which the methyl group at position 26 has been oxidised to the correponding carboxylic acid. Found in Caenorhabditis elegans.
(1S,2S,4S,5R,6R,7S,8R,9R,12S,13R,16S)-5,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2-piperidin-1-ium]-16-ol
(1S,2S,4S,5R,7S,9S,12S,13R,16S)-5,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2-oxane]-16-ol
(2S,6E)-6-[(3S,8R,9S,10R,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-ylidene]-2-methylheptanoic acid
2-hydroxy-6-[(4Z)-4-[(2E)-2-(5-hydroxy-2-methylidenecyclohexylidene)ethylidene]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]-2-methylheptan-3-one
D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols
[3-Carboxy-2-(3-oxohexadecanoyloxy)propyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(Z)-3-hydroxyhexadec-9-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[(2S)-3-carboxy-2-[(Z)-3-hydroxyhexadec-9-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-7-hydroxyhexadec-10-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-9-hydroxyhexadec-3-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-9-hydroxyhexadec-6-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-12-hydroxyhexadec-10-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-12-hydroxyhexadec-9-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-4-hydroxyhexadec-2-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[3-carboxy-2-[(E)-10-hydroxyhexadec-8-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
5-[(2E)-2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-3a,5,6,7-tetrahydro-3H-inden-4-ylidene]ethyl]-6-methylidenecyclohex-3-ene-1,3-diol
[(E)-2-(carboxymethyl)-2,18-dihydroxy-3-oxooctadec-4-enyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
(25R)-3beta-hydroxycholest-5-en-7-one-26-al
A 26-oxo steroid resulting from the oxidation of (25R)-3beta,26-dihydroxycholest-5-en-7-one to the corresponding aldehyde.
5-ethyl-2-[(1E,5E,7E,11E)-10-hydroxy-3,7,9,11-tetramethyltrideca-1,5,7,11-tetraenyl]-6-methoxy-3-methylpyran-4-one
N-[2-(dimethylamino)ethyl]-2-[(1s,4s,5s)-5-isopropyl-2-methyl-4-{[(phenylcarbamoyl)amino]methyl}-2-cyclohexen-1-yl]acetamide
C24H38N4O2 (414.29946079999996)
[3-Carboxy-2-(3-hydroxyhexadec-9-enoyloxy)propyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
3beta,6alpha-dihydroxy-5alpha-cholesta-9(11),24-dien-23-one
2-[(1s,4s,5s)-5-Isopropyl-4-{[(isopropylcarbamoyl)amino]methyl}-2-methyl-2-cyclohexen-1-yl]-n-methyl-n-(3-pyridinylmethyl)acetamide
C24H38N4O2 (414.29946079999996)
[(2R)-3-carboxy-2-(3-oxohexadecanoyloxy)propyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
[(2R)-3-carboxy-2-[(Z)-3-hydroxyhexadec-9-enoyl]oxypropyl]-trimethylazanium
C23H44NO5+ (414.32193140000004)
methyl (3R)-6-hydroxy-2,3,5-trimethyl-4-oxo-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]cyclohexa-1,5-diene-1-carboxylate
[(2S)-1-decanoyloxy-3-hydroxypropan-2-yl] undecanoate
(1-Hexanoyloxy-3-hydroxypropan-2-yl) pentadecanoate
(1-Butanoyloxy-3-hydroxypropan-2-yl) heptadecanoate
(1-Hydroxy-3-pentanoyloxypropan-2-yl) hexadecanoate
(1-Heptanoyloxy-3-hydroxypropan-2-yl) tetradecanoate
(1-Hydroxy-3-propanoyloxypropan-2-yl) octadecanoate
(5R,6R,9S,13R)-5,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2-oxane]-16-ol
[1-carboxy-3-[3-[(6E,9E)-dodeca-6,9-dienoyl]oxy-2-hydroxypropoxy]propyl]-trimethylazanium
C22H40NO6+ (414.28554800000006)
(2E,4E,6E,8E,10E,12E,14E,16E,18E,20E)-2,6,10,15,19,23-hexamethyltetracosa-2,4,6,8,10,12,14,16,18,20,22-undecaenal
(25S)-Delta(7)-dafachronic acid
A Delta(7)-dafachronic acid that has S configuration at position 25 (the carbon attached to the carboxy group).
[(2S)-1-hydroxy-3-octanoyloxypropan-2-yl] 10-methyldodecanoate
[(2S)-1-hydroxy-3-octanoyloxypropan-2-yl] tridecanoate
(5Z,7E)-(1S,3R)-1,3-dihydroxy-9,10-seco-5,7,10(19)-cholestatrien-22-one
5alpha,9alpha-Epidioxy-cholesta-6,8(14)-dien-3beta-ol
5alpha,8alpha-epidioxy-24-methyl-27-nor-cholest-6,22Z-dien-3beta-ol
solasodine(1+)
A secondary ammonium ion resulting from the protonation of the amino group of solasodine. The major species at pH 7.3.
TG(20:0)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved
(3r,5as,5br,7as,8s,11as,11br,13r,13as)-8-ethyl-13-hydroxy-3,5b,8,11a,13a-pentamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-1-one
(1r,2r,6s,10s,11r,13s,15r)-1-hydroxy-4,8,12,12,15-pentamethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2r)-2,3-dimethylbutanoate
4-(docos-17-en-13,15-diyn-1-yl)-5-(hydroxymethyl)oxolan-2-one
(1r,5s,7r)-4-hydroxy-5,8,8-trimethyl-1,7-bis(3-methylbut-2-en-1-yl)-3-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione
(1s,5s,7r)-4-hydroxy-1,6,6-trimethyl-5,7-bis(3-methylbut-2-en-1-yl)-3-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione
1-hydroxy-4,8,12,12,15-pentamethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl 2,3-dimethylbutanoate
4,6,6-trimethyl-3-(2,6,6-trimethyl-4-{2,6,6-trimethylbicyclo[3.1.1]hepta-1,3-dien-3-yl}bicyclo[3.1.1]hepta-1,3-dien-3-yl)bicyclo[3.1.1]hepta-2,4-dien-2-ol
(2r,5r,9r,13s,15s)-15-hydroxy-6-[(2e,4s,5s)-5-hydroxy-4-methoxyhex-2-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one
(1'r,2r,2's,4's,7's,8'r,9's,12's,13's,16'r,18's)-7',9',13'-trimethyl-5-methylidene-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-ol
(1's,2r,2's,4'r,5r,7'r,8'r,9's,12's,13'r,16's)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol
[3,5-dimethyl-5-(2-methyl-12-phenyldodeca-9,11-dien-1-yl)-1,2-dioxolan-3-yl]acetic acid
(2r,3r,4r)-2,3,4,5-tetrahydroxypentyl octadeca-9,12-dienoate
(1s,3as,3bs,5as,9ar,9bs,11as)-1-[(2s)-2-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,3h,3ah,3bh,4h,5h,5ah,6h,9bh,10h,11h-cyclopenta[a]phenanthrene-2,7-dione
12-(6-hydroxy-5-methoxy-6-methylhept-3-en-2-yl)-1,4-dimethyl-6-oxotricyclo[9.3.0.0³,⁷]tetradeca-4,8-diene-8-carbaldehyde
(1s,2r,5r,6r,9r,10r,13s,15s)-5-[(2e,4s)-4,5-dimethylhex-2-en-1-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
(5s)-5-[(1s,3ar,3br,5ar,9ar,9bs,11ar)-3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl]-5-methyloxolan-2-one
5-hydroxy-1-[(2r,4e)-6-hydroxy-6-methylhept-4-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,5h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-en-16'-ol
(4r)-4-[(1s,3br,4r,5ar,9ar,9br,11as)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,4h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]oxolan-2-one
22-cyclopentyloxil-22-deisopenty-3β-hydroxyl-furostanol
{"Ingredient_id": "HBIN003689","Ingredient_name": "22-cyclopentyloxil-22-deisopenty-3\u03b2-hydroxyl-furostanol","Alias": "NA","Ingredient_formula": "C27H42O3","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "4524","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
22-cyclopentyloxil-22-deisopentyl-3beta-hydroxyl-guranstanol
{"Ingredient_id": "HBIN003690","Ingredient_name": "22-cyclopentyloxil-22-deisopentyl-3beta-hydroxyl-guranstanol","Alias": "NA","Ingredient_formula": "C27H42O3","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "26060","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
methyl 5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate
(1'r,2r,2's,4's,5r,7's,8'r,9's,12's,13's,18's)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-one
3-ethyl-6-[(1e,5e,7e,11e)-10-hydroxy-3,7,9,11-tetramethyltrideca-1,5,7,11-tetraen-1-yl]-2-methoxy-5-methylpyran-4-one
4-[(3e,7e)-4,8-dimethyl-10-(2,6,6-trimethylcyclohex-1-en-1-yl)deca-3,7-dien-1-yl]-5-ethoxy-5h-furan-2-one
(1s,3as,3br,5as,9ar,9bs,11as)-1-hydroxy-1-[(2s,3e)-1-hydroxy-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,5ah,6h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(1's,2r,2's,4's,5r,7's,8'r,9's,12's,13'r,16's)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-en-16'-ol
1-(2-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,3h,3ah,3bh,4h,5h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-2,7-dione
4-formyl-2-methoxyphenyl (9z,12z)-octadeca-9,12-dienoate
1-[(2r)-4-(3,3-dimethyloxiran-2-yl)butan-2-yl]-5-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,5h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(3s,5as,5br,7as,8s,11as,11br,13s,13as)-8-ethyl-13-hydroxy-3,5b,8,11a,13a-pentamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-1-one
3,5-dihydroxy-4,6,6-tris(3-methylbut-2-en-1-yl)-2-[(2r)-2-methylbutanoyl]cyclohexa-2,4-dien-1-one
(4r,5s)-4-[(17z)-docos-17-en-13,15-diyn-1-yl]-5-(hydroxymethyl)oxolan-2-one
(1s,3as,3bs,5as,9ar,9bs,11as)-1-[(2s,3z)-2-hydroxy-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthrene-5,7-dione
(1r,3ar,5ar,7s,9ar,9bs,11ar)-5a,7-dihydroxy-9a,11a-dimethyl-1-[(2r,3e)-6-methylhept-3-en-2-yl]-1h,2h,3h,3ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one
(2s,3s,5r,6s)-2,3,5-trihydroxy-6-nonadecyloxan-4-one
3-ethyl-6-[(2e,5e,7e,11e)-10-hydroxy-3,7,9,11-tetramethyltrideca-2,5,7,11-tetraen-1-yl]-2-methoxy-5-methylpyran-4-one
methyl (1s,4s,5s,9s,10r,13r)-9-methyl-5-({[(2z)-2-methylbut-2-enoyl]oxy}methyl)-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate
methyl (3s)-3-[(1s,3as,5ar,9ar,9br,11as)-3a,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]butanoate
10-hydroxy-4,5,9,9,13-pentamethyl-20-oxahexacyclo[17.2.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tricosan-21-one
[(3r,5r)-3,5-dimethyl-5-[(7e,11z)-2-methyl-12-phenyldodeca-7,11-dien-1-yl]-1,2-dioxolan-3-yl]acetic acid
(1r,4r,5r,8r,10s,13r,14r,17r,18r,19s)-10-hydroxy-4,5,9,9,13-pentamethyl-20-oxahexacyclo[17.2.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tricosan-21-one
7-hydroxy-9a,11a-dimethyl-1-(6-methyl-5-methylideneheptan-2-yl)-1h,2h,3h,3ah,5ah,6h,7h,8h,9h,10h,11h-indeno[4,5-c]isochromen-5-one
15-hydroxy-6-(5-hydroxy-2-methoxyhex-3-en-2-yl)-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one
(2r,5s,9r,13s,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one
(2e)-3-(4-hydroxyphenyl)prop-2-en-1-yl (9z)-octadec-9-enoate
(2r,5r,9r,13s,15s)-15-hydroxy-6-[(2e,4s,5r)-5-hydroxy-4-methoxyhex-2-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one
(1s,2r,5r,6r,9r,10r,13s,15s)-6,10-dimethyl-5-[(2r,3z,5r)-5-methylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
(1's,2s,2's,4's,5r,7's,8's,9's,12's,13'r,16's)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-ol
(4r)-4-[(1r,3as,3bs,5ar,9as,11ar)-3a,6,6,9a,11a-pentamethyl-7-oxo-1h,2h,3h,3bh,4h,5h,5ah,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]pentanoic acid
1-hydroxy-1-(1-hydroxy-6-methylhept-3-en-2-yl)-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,5h,5ah,6h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
2,6,10,15,19,23-hexamethyltetracosa-2,4,6,8,10,12,14,16,18,20,22-undecaenal
(1s,3as,3bs,5as,9ar,9bs,11as)-1-[(2s)-2-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,5h,5ah,6h,7h,9bh,11h-cyclopenta[a]phenanthrene-4,10-dione
(1s,4r,5r,8r,10s,13r,14r,17r,18r,19r)-10-hydroxy-4,5,9,9,13-pentamethyl-20-oxahexacyclo[17.2.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tricosan-21-one
5-(4,5-dimethylhex-2-en-1-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
(1r,2s,3as,4s,7as)-2-hydroxy-4-[2-(5-hydroxy-2-methylphenyl)ethyl]-7a-methyl-1-(6-methylheptan-2-yl)-hexahydro-1h-inden-5-one
5-{3a,3b,6,6,9a-pentamethyl-7-oxo-dodecahydrocyclopenta[a]phenanthren-1-yl}-5-methyloxolan-2-one
6-amino-n-{5-amino-1-[(7-amino-2-oxoheptan-3-yl)-c-hydroxycarbonimidoyl]pentyl}-2-(methylamino)hexanimidic acid
C20H42N6O3 (414.33182220000003)