Exact Mass: 400.3372537999999
Exact Mass Matches: 400.3372537999999
Found 500 metabolites which its exact mass value is equals to given mass value 400.3372537999999,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Campesterol
Campesterol is a phytosterol, meaning it is a steroid derived from plants. As a food additive, phytosterols have cholesterol-lowering properties (reducing cholesterol absorption in intestines), and may act in cancer prevention. Phytosterols naturally occur in small amount in vegetable oils, especially soybean oil. One such phytosterol complex, isolated from vegetable oil, is cholestatin, composed of campesterol, stigmasterol, and brassicasterol, and is marketed as a dietary supplement. Sterols can reduce cholesterol in human subjects by up to 15\\\\\%. The mechanism behind phytosterols and the lowering of cholesterol occurs as follows : the incorporation of cholesterol into micelles in the gastrointestinal tract is inhibited, decreasing the overall amount of cholesterol absorbed. This may in turn help to control body total cholesterol levels, as well as modify HDL, LDL and TAG levels. Many margarines, butters, breakfast cereals and spreads are now enriched with phytosterols and marketed towards people with high cholesterol and a wish to lower it. -- Wikipedia. Campesterol is a member of phytosterols, a 3beta-sterol, a 3beta-hydroxy-Delta(5)-steroid and a C28-steroid. It has a role as a mouse metabolite. It derives from a hydride of a campestane. Campesterol is a natural product found in Haplophyllum bucharicum, Bugula neritina, and other organisms with data available. Campesterol is a steroid derivative that is the simplest sterol, characterized by the hydroxyl group in position C-3 of the steroid skeleton, and saturated bonds throughout the sterol structure, with the exception of the 5-6 double bond in the B ring. Campesterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=474-62-4 (retrieved 2024-07-01) (CAS RN: 474-62-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.
5alpha-Campestan-3-one
5alpha-Campestan-3-one, also known as 3-dehydro-campestanol or methylcholestanone, 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, 5alpha-campestan-3-one is considered to be a sterol lipid molecule. 5alpha-Campestan-3-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 5alpha-Campestan-3-one is involved in the brassinosteroid biosynthesis pathway. 5alpha-Campestan-3-one is produced from campest-4-en-3-one by the action of DET2 (EC 1.3.99.-), a probable steroid reductase. 5alpha-Campestan-3-one is then converted into campestanol or 22alpha-hydroxy-5alpha-campestan-3-one. The conversion to 22alpha-hydroxy-5alpha-campestan-3-one is catalyzed by DWF4, a steroid 22-alpha-hydroxylase (EC 1.14.13.-).
Calcidiol
Calfcifediol is a prehormone that is produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase. Calcifediol is then converted in the kidneys into calcitriol (1,25-(OH)2D3), a secosteroid hormone that is the active form of vitamin D. It can also be converted into 24-hydroxycalcidiol in the kidneys via 24-hydroxylation. [Wikipedia]. 25-Hydroxycholecalciferol is found in many foods, some of which are green zucchini, green bell pepper, red bell pepper, and other animal fat. The major circulating metabolite of vitamin D3 (calciferon). It is produced in the liver and is the best indicator of the bodys vitamin D stores. It is effective in the treatment of rickets and osteomalacia, both in azotemic and non-azotemic patients. Calcifediol also has mineralizing properties. A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CC - Vitamin d and analogues H - Systemic hormonal preparations, excl. sex hormones and insulins > H05 - Calcium homeostasis > H05B - Anti-parathyroid agents D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D050071 - Bone Density Conservation Agents Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
DG(10:0/10:0/0:0)
DG(10:0/10:0/0:0) 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(10:0/10:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
4α-methyl-cholesta-8-enol
4α-methyl-cholesta-8-enol, also known as Methost-8-enol, is classified as a cholesterol or a Cholesterol derivative. Cholesterols are compounds containing a 3-hydroxylated cholestane core. 4α-methyl-cholesta-8-enol is considered to be practically insoluble (in water) and basic. 4α-methyl-cholesta-8-enol is a sterol lipid molecule
7a-Hydroxy-cholestene-3-one
7a-Hydroxy-cholestene-3-one is a metabolite in bile acid synthesis. It is derived from 7a-hydroxy-cholesterol and can be further metabolized to 7a,12a,-dihydroxy-cholest-4-en-3-one. Analysis of 7a-Hydroxycholestene-3-one (HCO) in serum may serve as a novel, simple, and sensitive method for the detection of bile acid malabsorption in patients with chronic diarrhea of unknown origin (PMID 9952217) [HMDB] 7a-Hydroxy-cholestene-3-one is a metabolite in bile acid synthesis. It is derived from 7a-hydroxy-cholesterol and can be further metabolized to 7a,12a,-dihydroxy-cholest-4-en-3-one. Analysis of 7a-Hydroxycholestene-3-one (HCO) in serum may serve as a novel, simple, and sensitive method for the detection of bile acid malabsorption in patients with chronic diarrhea of unknown origin (PMID 9952217).
Pollinastanol
Pollinastanol is found in dandelion. Pollinastanol is isolated from Smilax medica (Sarsaparilla
ST 28:1;O
A brassinosteroid that is 5alpha-campestane bearing an oxo substituent at position 3.
(3beta,5alpha,24S)-Ergost-8(14)-en-3-ol
(3beta,5alpha,24R)-Ergost-8(14)-en-3-ol is found in root vegetables. (3beta,5alpha,24R)-Ergost-8(14)-en-3-ol is a constituent of Dioscorea batatas (Chinese yam).
diapolycopene
4-alpha-Methyl-5-alpha-cholest-7-en-3-beta-ol
4-alpha-Methyl-5-alpha-cholest-7-en-3-beta-ol is involved in the steroid biosynthesis pathway. In this pathway, 4-alpha-methyl-5-alpha-cholest-7-en-3-beta-ol is enzymatically converted to 4-alpha-methyl-5-alpha-cholest-7-en-3-one via the enzyme 3-keto-steroid reductase (EC: 1.1.1.270) and the cofactor NADP(+). This enzyme is responsible for the reduction of the keto group on the C-3 of sterols. (Pathway Commons). Steroid biosynthesis is an anabolic metabolic pathway that produces steroids from simple precursors. This pathway is carried out in different ways in animals than in many other organisms, making the pathway a common target for antibiotics and other anti-infective drugs. In addition, steroid metabolism in humans is the target of cholesterol-lowering drugs such as statins. (Wikipedia). Constituent of potato leaves (Solanum tuberosum)
Gefarnate
A - Alimentary tract and metabolism > A02 - Drugs for acid related disorders > A02B - Drugs for peptic ulcer and gastro-oesophageal reflux disease (gord) C78272 - Agent Affecting Nervous System > C29698 - Antispasmodic Agent D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents
Dihydrobrassicasterol
24-epicampesterol is a 3beta-sterol, a member of phytosterols, an ergostanoid, a 3beta-hydroxy-Delta(5)-steroid and a C28-steroid. 22,23-Dihydrobrassicasterol is a natural product found in Euphorbia fischeriana, Sambucus chinensis, and other organisms with data available. Occurs in Physalis peruviana (Cape gooseberry). Dihydrobrassicasterol is found in many foods, some of which are watermelon, muskmelon, fruits, and cucumber. Dihydrobrassicasterol is found in cucumber. Dihydrobrassicasterol occurs in Physalis peruviana (Cape gooseberry
7-Ketocholesterol
7-Ketocholesterol is a major oxidation product of cholesterol (oxysterol) found in human atherosclerotic plaque and is more atherogenic than cholesterol in some animal studies. Oxysterols (oxygenated forms of cholesterol) are present at low levels in the circulation and accumulate is plasma and tissues in some pathologies. In atherosclerotic lesions, 7-oxygenated oxysterols, predominantly 7-ketocholesterol, accumulate and have been implicated in the pathology of the disease. There is some in vivo and in vitro evidence that sterol 27-hydroxylase acts on 7-ketocholesterol to initiate its degradation to more polar, water-soluble products. Recent studies indicate an alternative mechanism, in which 7-ketocholesterol is reduced to 7 beta-hydroxycholesterol by 11 beta-hydroxysteroid dehydrogenase type 1. 7-Ketocholesterol can inhibit cholesterol 7 alpha-hydroxylase, the rate-limiting step in bile acid biosynthesis, as well as strongly inhibiting HMG-CoA reductase, the rate-limiting enzyme in cholesterol biosynthesis. It has even been suggested that 7-ketocholesterol is formed enzymically as an endogenous regulator of cholesterol biosynthesis. However, when tested as a pharmacological cholesterol-lowering agent, inhibition of HMG-CoA reductase was rapidly overcome and the 7-ketocholesterol metabolised. In vitro, 7-ketocholesterol has wide-ranging and potent effects, most of which have the potential to contribute to atherosclerosis. For example, 7-ketocholesterol can be cytotoxic and can induce apoptosis in vascular cells. These effects, either individually or more likely, in combination, all implicate 7-ketocholesterol in the initiation and development of atherosclerosis, but further work is needed to establish whether or not its role is a direct causal one. 7-Ketocholesterol is the second most abundant oxysterol found in human atherosclerotic plaque, after the enzymically formed 27-hydroxycholesterol (cholest-5-ene-3beta,27-diol). 7-Ketocholesterol differs from cholesterol by a ketone functional group present at the 7-position. It is produced from cholesterol via the epimeric cholesterol 7-hydroperoxides (cholest-5-ene-3beta-ol-7-hydroperoxide) which decompose to the epimeric 7-hydroxycholesterols (cholest-5-ene-3beta,7-diol) and 7-ketocholesterol. 7-Ketocholesterol is a major dietary oxysterol. It has also been widely suggested that 7-ketocholesterol present in atherosclerotic tissue may be derived from the diet. Certainly, 7-ketocholesterol is a major oxysterol found in cholesterol-rich processed foodstuffs. Dietary 7-ketocholesterol is rapidly metabolised by the liver to 7beta-hydroxycholesterol (cholest-5-ene-3beta,7beta-diol), unusual bile acids and perhaps even cholesterol itself. Its conversion to 7beta-hydroxycholesterol is well documented. (PMID: 15798369, 10224662). 7-Ketocholesterol is a major oxidation product of cholesterol (oxysterol) found in human atherosclerotic plaque and is more atherogenic than cholesterol in some animal studies. Oxysterols (oxygenated forms of cholesterol) are present at low levels in the circulation and accumulate is plasma and tissues in some pathologies. In atherosclerotic lesions, 7-oxygenated oxysterols, predominantly 7-ketocholesterol, accumulate and have been implicated in the pathology of the disease. There is some in vivo and in vitro evidence that sterol 27-hydroxylase acts on 7-ketocholesterol to initiate its degradation to more polar, water-soluble products. Recent studies indicate an alternative mechanism, in which 7-ketocholesterol is reduced to 7 beta-hydroxycholesterol by 11 beta-hydroxysteroid dehydrogenase type 1. 7-Ketocholesterol, toxic oxysterol, inhibits the rate-limiting step in bile acid biosynthesis cholesterol 7 alpha-hydroxylase, as well as strongly inhibiting HMG-CoA reductase (the rate-limiting enzyme in cholesterol biosynthesis). 7-Ketocholesterol induces cell apoptosis[1].
5-Methyl-2,4-bis(3-methyl-2-butenyl)-6-(2-methyl-1-oxopropyl)-5-(4-methyl-3-pentenyl)cyclohexanone
5-methyl-2,4-bis(3-methyl-2-butenyl)-6-(2-methyl-1-oxopropyl)-5-(4-methyl-3-pentenyl)cyclohexanone is found in alcoholic beverages. 5-methyl-2,4-bis(3-methyl-2-butenyl)-6-(2-methyl-1-oxopropyl)-5-(4-methyl-3-pentenyl)cyclohexanone is a constituent of Hypericum perforatum (St. Johns Wort) Constituent of Hypericum perforatum (St. Johns Wort). 5-methyl-2,4-bis(3-methyl-2-butenyl)-6-(2-methyl-1-oxopropyl)-5-(4-methyl-3-pentenyl)cyclohexanone is found in tea, alcoholic beverages, and herbs and spices.
(3beta,4alpha,5alpha)-4-Methyl-8(14)-cholesten-3-ol
Constituent of Capsicum annuum seeds. (3beta,4alpha,5alpha)-4-Methyl-8(14)-cholesten-3-ol is found in many foods, some of which are herbs and spices, red bell pepper, yellow bell pepper, and italian sweet red pepper. (3beta,4alpha,5alpha)-4-Methyl-8(14)-cholesten-3-ol is found in herbs and spices. (3beta,4alpha,5alpha)-4-Methyl-8(14)-cholesten-3-ol is a constituent of Capsicum annuum seeds
MG(a-21:0/0:0/0:0)[rac]
MG(a-21:0/0:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(a-21:0/0:0/0:0) is made up of one 18-methyleicosanoyl(R1).
(5alpha,14alpha)-14-Methylcholestan-3-one
(5alpha,14alpha)-14-Methylcholestan-3-one is found in cereals and cereal products. (5alpha,14alpha)-14-Methylcholestan-3-one is a constituent of mature wheat straw (Triticum aestivum). Constituent of mature wheat straw (Triticum aestivum). (5alpha,14alpha)-14-Methylcholestan-3-one is found in wheat and cereals and cereal products.
(3beta,5alpha,6a)-Cholesta-8,14-diene-3,6-diol
(3beta,5alpha,6a)-Cholesta-8,14-diene-3,6-diol is found in fruits. (3beta,5alpha,6a)-Cholesta-8,14-diene-3,6-diol is a constituent of Stenocereus thurberi (organ pipe cactus) Constituent of Stenocereus thurberi (organ pipe cactus). (3beta,5alpha,6a)-Cholesta-8,14-diene-3,6-diol is found in fruits.
5,6-trans-25-Hydroxyvitamin D3
5,6-trans-25-Hydroxyvitamin D3 is a vitamin D3 derivative, and is found in normal plasma. 5,6-trans-25-Hydroxyvitamin D3 is a 25-hydroxylated metabolite of the secosteroid that is active in inhibiting 3H-thymidine incorporation into cultured normal human keratinocytes. The evidence strongly supports the existence of a heretofore unknown metabolic route in vitamin DS metabolism, namely, the conversion of 5,6-cis compounds to 5,6-trans compounds. The mechanism of this transformation is not clear at present; it could be enzymatic or nonenzymatic. The site of formation of 5,6-trans-25-hydroxyvitamin D3 is unknown. (PMID 6256855, 10876100, 6270082) [HMDB] 5,6-trans-25-Hydroxyvitamin D3 is a vitamin D3 derivative, and is found in normal plasma. 5,6-trans-25-Hydroxyvitamin D3 is a 25-hydroxylated metabolite of the secosteroid that is active in inhibiting 3H-thymidine incorporation into cultured normal human keratinocytes. The evidence strongly supports the existence of a heretofore unknown metabolic route in vitamin DS metabolism, namely, the conversion of 5,6-cis compounds to 5,6-trans compounds. The mechanism of this transformation is not clear at present; it could be enzymatic or nonenzymatic. The site of formation of 5,6-trans-25-hydroxyvitamin D3 is unknown. (PMID 6256855, 10876100, 6270082).
25-Hydroxytachysterol3
25-Hydroxytachysterol3 is a hydroxylated derivative of tachysterol3. 25-hydroxytachysterol is converted to 25-hydroxyprevitamin D3, which is then converted to the hydroxyvitamin D3 through a thermally induced rearrangement. It is now established that, during exposure to sunlight, the cutaneous reservoir of 7-dehydrocholesterol converts to previtamin D3. Once this thermally labile previtamin is formed, it undergoes a temperature-dependent isomerization to vitamin D3 over a period of 3 days. The plasma vitamin-D binding protein preferentially translocates vitamin D3 from the skin into the circulation. During prolonged exposure to the sun, the accumulation of previtamin D3 is limited to about 10 to 15\\% of the original 7-dehydrocholesterol content because the previtamin photoisomerizes to 2 biologically inert photoproducts, lumisterol3 and tachysterol3. (PMID 12617640). 25-Hydroxytachysterol3 is characterized by antirachitic activity and by its ability to elevate serum calcium concentration in conditions of hypoparathyroidism. 25-Hydroxytachysterol3 can be used in the preparation of 25-hydroxydihydrotachysterol 3 (25-OH-DHT3) is considered an effective adjunct in the treatment of hypoparathyroidism, particularly where rapid action in elevating serum calcium concentration is being sought. (25-OH-DHT3) exhibits substantially greater antirachitic activity than DHT 3 [HMDB] 25-Hydroxytachysterol3 is a hydroxylated derivative of tachysterol3. 25-hydroxytachysterol is converted to 25-hydroxyprevitamin D3, which is then converted to the hydroxyvitamin D3 through a thermally induced rearrangement. It is now established that, during exposure to sunlight, the cutaneous reservoir of 7-dehydrocholesterol converts to previtamin D3. Once this thermally labile previtamin is formed, it undergoes a temperature-dependent isomerization to vitamin D3 over a period of 3 days. The plasma vitamin-D binding protein preferentially translocates vitamin D3 from the skin into the circulation. During prolonged exposure to the sun, the accumulation of previtamin D3 is limited to about 10 to 15\\% of the original 7-dehydrocholesterol content because the previtamin photoisomerizes to 2 biologically inert photoproducts, lumisterol3 and tachysterol3. (PMID 12617640). 25-Hydroxytachysterol3 is characterized by antirachitic activity and by its ability to elevate serum calcium concentration in conditions of hypoparathyroidism. 25-Hydroxytachysterol3 can be used in the preparation of 25-hydroxydihydrotachysterol 3 (25-OH-DHT3) is considered an effective adjunct in the treatment of hypoparathyroidism, particularly where rapid action in elevating serum calcium concentration is being sought. (25-OH-DHT3) exhibits substantially greater antirachitic activity than DHT 3.
Alfacalcidol
Alfacalcidol is an active metabolite of Vitamin D, which performs important functions in regulation of the calcium balance and the bone metabolism. Alfacalcidol is Vitamin D-hormone analog which is activated by the enzyme 25-hydroxylase in the liver for systemic and in osteoblasts for local D-hormone actions. It possesses a unique pattern of pleiotropic effects on, e.g. gut, bone, pararthyroids, muscle and brain. Alfacalcidol is superior to plain vitamin D (cholecalciferol) because the final kidney activation of the latter is regulated by a negative feedback mechanism. (PMID:17438884,17668216). A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CC - Vitamin d and analogues D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols D050071 - Bone Density Conservation Agents
1-Phenyl-1,3-heneicosanedione
1-Phenyl-1,3-heneicosanedione is found in fats and oils. 1-Phenyl-1,3-heneicosanedione is a constituent of the pollen of Helianthus annuus (sunflower) Constituent of the pollen of Helianthus annuus (sunflower). 1-Phenyl-1,3-heneicosanedione is found in fats and oils.
5-(12,15-Heneicosadienyl)-1,3-benzenediol
5-(12,15-Heneicosadienyl)-1,3-benzenediol is found in cereals and cereal products. 5-(12,15-Heneicosadienyl)-1,3-benzenediol is a constituent of wheat and rye flour. Constituent of wheat and rye flour. 5-(12,15-Heneicosadienyl)-1,3-benzenediol is found in cereals and cereal products.
3-(Acetyloxy)-2-hydroxypropyl octadecanoate
3-(Acetyloxy)-2-hydroxypropyl octadecanoate belongs to the family of Alk(en)ylacylglycerols. These are Diradyclycerols characterized by one alk(en)yl chain and an acyl chain bound to a glycerol backbone.
3beta-Hydroxy-5-cholestenal
This compound belongs to the family of Monohydroxy Bile Acids, Alcohols and Derivatives. These are bile acids, alcohols or any of their derivatives bearing an hydroxyl group.
27alpha-Hydroxy-8-dehydrocholesterol
This compound belongs to the family of Dihydroxy Bile Acids, Alcohols and Derivatives. These are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups.
MG(0:0/a-21:0/0:0)[rac]
MG(0:0/a-21:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/a-21:0/0:0) is made up of one 18-methyleicosanoyl(R2).
MG(0:0/21:0/0:0)
MG(0:0/21:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/21:0/0:0) is made up of one heneicosanoyl(R2).
MG(21:0/0:0/0:0)
MG(21:0/0:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(21:0/0:0/0:0) is made up of one heneicosanoyl(R1).
MG(0:0/i-21:0/0:0)
MG(0:0/i-21:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/i-21:0/0:0) is made up of one 19-methyleicosanoyl(R2).
DG(8:0/12:0/0:0)
DG(8:0/12:0/0:0) 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(8:0/12:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/12:0)
DG(8:0/0:0/12:0) 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-12:0/0:0)
DG(8:0/i-12:0/0:0) 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-12:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/i-12:0)
DG(8:0/0:0/i-12:0) 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(10:0/0:0/10:0)
DG(10:0/0:0/10:0) 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(12:0/8:0/0:0)
DG(12:0/8:0/0:0) 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(12:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(12:0/0:0/8:0)
DG(12:0/0:0/8:0) 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-12:0/8:0/0:0)
DG(i-12:0/8:0/0:0) 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-12:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(i-12:0/0:0/8:0)
DG(i-12:0/0:0/8:0) 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.
(1R,3Z)-3-[(2E)-2-[(1R,3As,7aR)-1-[(2R)-7-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol
(1R)-3-[2-[(1R,3Ar,7aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol
(1R)-5-[2-[(1R,7Ar)-7a-methyl-1-[(2R)-6-methylheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
(20S)-Hydroxyvitamin D3
22-Oxocholesterol
24-Methylcholesterol
24,25-Epoxycholesterol
3-Hydroxycholest-5-en-7-one
4-Methylcholest-7-en-3-ol
3-Hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-1,2,3,4,5,6,7,9,11,12,16,17-dodecahydrocyclopenta[a]phenanthren-15-one
Cholestane-2,3-dione
hydroxyvitamin d3
ketocholesterol
Sapogenins
Any of the aglycon moieties of saponins; they may be steroids or triterpenes. (ChEBI) Sapogenins are the aglycones, or non-saccharide, portions of the family of natural products known as saponins. Sapogenins contain steroid or other triterpene frameworks as their key organic feature. Sapogenins is found in soft-necked garlic. Any of the aglycon moieties of saponins; they may be steroids or triterpenes. (ChEBI)
24-Methyl-lathosterol
24-methyl-lathosterol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 24-methyl-lathosterol can be found in a number of food items such as tea, cucumber, sunflower, and muskmelon, which makes 24-methyl-lathosterol a potential biomarker for the consumption of these food products.
4alpha-Methyl-5alpha-cholest-8(14)-en-3beta-ol
4alpha-methyl-5alpha-cholest-8(14)-en-3beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 4alpha-methyl-5alpha-cholest-8(14)-en-3beta-ol can be found in a number of food items such as orange bell pepper, green bell pepper, red bell pepper, and pepper (c. annuum), which makes 4alpha-methyl-5alpha-cholest-8(14)-en-3beta-ol a potential biomarker for the consumption of these food products.
24-Methylcholest-7-en-3-beta-ol
24-methylcholest-7-en-3-beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 24-methylcholest-7-en-3-beta-ol can be found in cucumber, which makes 24-methylcholest-7-en-3-beta-ol a potential biomarker for the consumption of this food product.
23-Dehydrocampestanol
23-dehydrocampestanol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 23-dehydrocampestanol can be found in sunflower, which makes 23-dehydrocampestanol a potential biomarker for the consumption of this food product.
delta-7-Campesterol
Delta-7-campesterol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Delta-7-campesterol can be found in common walnut, which makes delta-7-campesterol a potential biomarker for the consumption of this food product.
4alpha-Methylzymostenol
4alpha-methylzymostenol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 4alpha-methylzymostenol can be found in garden onion, which makes 4alpha-methylzymostenol a potential biomarker for the consumption of this food product.
(5alpha)-campestan-3-one
(5alpha)-campestan-3-one belongs to ergosterols and derivatives class of compounds. Those are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton (5alpha)-campestan-3-one is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (5alpha)-campestan-3-one can be found in a number of food items such as macadamia nut (m. tetraphylla), malabar spinach, sourdough, and citrus, which makes (5alpha)-campestan-3-one a potential biomarker for the consumption of these food products.
4alpha-methyl-cholesta-8-enol
4alpha-methyl-cholesta-8-enol belongs to cholesterols and derivatives class of compounds. Those are compounds containing a 3-hydroxylated cholestane core. 4alpha-methyl-cholesta-8-enol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 4alpha-methyl-cholesta-8-enol can be found in a number of food items such as black-eyed pea, swede, saskatoon berry, and chinese chives, which makes 4alpha-methyl-cholesta-8-enol a potential biomarker for the consumption of these food products.
campest-4-en-3beta-ol
Campest-4-en-3beta-ol belongs to ergosterols and derivatives class of compounds. Those are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Campest-4-en-3beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Campest-4-en-3beta-ol can be found in a number of food items such as spirulina, alaska wild rhubarb, avocado, and nanking cherry, which makes campest-4-en-3beta-ol a potential biomarker for the consumption of these food products.
Fungisterol
An ergostanoid that is 5alpha-ergost-7-ene substituted by a beta-hydroxy group at position 3. It has been isolated from the mycelia of Cordyceps sinensis.
(22E,24S)-24-ethyl-19-nor-5alpha-cholest-22-en-3beta-ol
(22E)-3beta,7alpha-dihydroxy-cholest-5,22-diene|(3beta,7alpha,22E)-Cholesta-5,22-diene-3,7-diol
3beta-(hydroxymethyl)-A-nor-5alpha-(24S)-ergost-15-ene
(10S)-3c-Hydroxy-10r.13c-dimethyl-17c-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-(5tH.8cH.9tH.14tH)-hexadecahydro-1H-cyclopenta[a]phenanthren|(22E)-(24xi)-24-methyl-5alpha-cholest-22-en-3beta-ol|(22E,24R)-24-methylcholest-22-en-3beta-ol|24-Methyl-5alpha(H)-cholest-22(E)-en-3beta-ol|24-methyl-5alpha-cholest-22E-en-3beta-ol|24betaF-Methyl-5alpha-cholesten-(22t)-ol-(3beta)|24R-methyl-5alpha-cholest-22E-en-3beta-ol|24xi-methyl-3beta-hydroxy-5alpha-cholest-22-ene|3beta-Hydroxy-10.13-dimethyl-17beta-((1R:4R)-1.4.5-trimethyl-hexen-(2t)-yl)-5alpha-gonan|5alpha-ergost-22E-en-3beta-ol|5alpha-ergosten-(22t)-ol-(3beta)|ergostan-3beta-ol
3beta-(hydroxymethyl)-A-nor-5alpha-ergost-24(28)-ene
24-keto-cholesterol|24-Ketocholesterol|24-oxocholesterol|3beta-hydroxycholest-5-en-24-one|cholest-5-en-3beta-ol-24-one|ZK134306
(3beta,4alpha,5alpha,22Z)-4-Methylcholest-22-en-3-ol
hydroxymethyl-3beta-methyl-24R-nor-A-cholest-5alpha-ene-22-Z
24(R)-cholesta-5,25-diene-3beta,24-diol|cholesta-5,25-diene-3beta,24xi-diol|cholesta-5,25-diene-3beta-24-diol
3beta-Dimethylamino-20alpha(F)-methylacetamido-5-pregnen|saracocine|saracosine
24-methyl-5alpha-cholest-24(28)-en-3beta-ol|24-Methylen-5alpha-cholestan-3beta-ol|24-methylene-5alpha-cholestan-3beta-ol|24-methylenecholestan-3beta-ol|24-methylenecholestanol|5alpha-ergost-24(28)-en-3beta-ol
3beta-26,27-Dinorcycloartan-3-ol|3beta-hydroxy-9,19-cyclo-26,27-norlanostane
4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid
(10R)-3c-Hydroxy-10r.13c-dimethyl-17c-((R)-1-methyl-4-aethyl-hexyl)-(8cH.9tH.14tH)-Delta5-tetradecahydro-1H-cyclopenta[a]phenanthren|24-Ethylcholest-5-en-3beta-ol|24.24-Diaethyl-cholen-(5)-ol-(3beta)|24.24-diethyl-cholen-(5)-ol-(3beta)|3beta-Hydroxy-10.13-dimethyl-17beta-((R)-1-methyl-4-aethyl-hexyl)-gonen-(5)|beta-Sitosterol
25-hydroxy-4-cholesten-3-one|25-hydroxy-4-cholestene-3-one|25-Hydroxy-cholest-4-en-3-on|25-hydroxy-cholest-4-en-3-one|25-Hydroxycholest-4-en-3-one|ZK134308
6beta-Hydroxy-cholest-4-en-3-on|6beta-hydroxy-cholest-4-en-3-one|6beta-hydroxycholest-4-en-3-one|cholest-4-en-6beta-ol-3-one
17-(4-ethyl-1,5-dimethyl-hexyl)-10-methyl-1,2,3,4,7,8,9,11,12,13,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-ol
(24R)-24-methylcholest-20(21)-en-3beta-ol|5,6-dihydro-20,21-dehydrocampesterol|eucanbin
25,26,27-trisnor-3beta-hydroxy-cycloartan-24-al|25,26,27-trisnor-3beta-hydroxycycloartan-24-al|wrightial
3beta-(hydroxymethyl)-22(R),23(R)-methylene-A-nor-5alpha-cholestane
(3beta, 5alpha, 7alpha, 22E)-Cholesta-8(14), 22-diene-3, 7-diol
(3beta,5alpha,22E,24S)-23-Methyl-19-norergost-22-en-3-ol
Campesterol
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. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.
MLS001333092-01!5-Cholesten-3beta-ol-7-one566-28-9
7-KETOCHOLESTEROL
A cholestanoid that consists of cholesterol bearing an oxo substituent at position 7. D004791 - Enzyme Inhibitors 7-Ketocholesterol, toxic oxysterol, inhibits the rate-limiting step in bile acid biosynthesis cholesterol 7 alpha-hydroxylase, as well as strongly inhibiting HMG-CoA reductase (the rate-limiting enzyme in cholesterol biosynthesis). 7-Ketocholesterol induces cell apoptosis[1].
Calcifediol
A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CC - Vitamin d and analogues H - Systemic hormonal preparations, excl. sex hormones and insulins > H05 - Calcium homeostasis > H05B - Anti-parathyroid agents D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols D050071 - Bone Density Conservation Agents COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
1α-hydroxyvitamin D3 / 1α-hydroxycholecalciferol
1α-hydroxy-3-epivitamin D3 / 1α-hydroxy-3-epicholecalciferol
(5E)-1α-hydroxyvitamin D3 / (5E)-1α-hydroxycholecalciferol
(5E,7E)-(1S,3S)-9,10-seco-5,7,10(19)-cholestatriene-1,3-diol
1β-hydroxyvitamin D3 / 1β-hydroxycholecalciferol
1β-hydroxy-3-epivitamin D3 / 1β-hydroxy-3-epicholecalciferol
(5E)-1β-hydroxyvitamin D3 / (5E)-1β-hydroxycholecalciferol
(5E,7E)-(1R,3S)-9,10-seco-5,7,10(19)-cholestatriene-1,3-diol
2β-hydroxyvitamin D3 / 2β-hydroxycholecalciferol
1α,25-dihydroxy-3-deoxyvitamin D3 / 1α,25-dihydroxy-3-deoxycholecalciferol
(22S)-22-hydroxyvitamin D3 / (22S)-22-hydroxycholecalciferol
(24R)-24-hydroxyvitamin D3 / (24R)-24-hydroxycholecalciferol
(24S)-24-hydroxyvitamin D3 / (24S)-24-hydroxycholecalciferol
25-hydroxy-14-epivitamin D3 / 25-hydroxy-14-epicholecalciferol
5,6-trans-25-Hydroxyvitamin D3
22-Hydroxyvitamin D3
D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols
Alfacalcidol
A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CC - Vitamin d and analogues D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols D050071 - Bone Density Conservation Agents
(3beta,4alpha,5alpha)-4-Methyl-8(14)-cholesten-3-ol
alpha-Ergostenol
Dihydrobrassicasterol
Thurberol
5-Methyl-2,4-bis(3-methyl-2-butenyl)-6-(2-methyl-1-oxopropyl)-5-(4-methyl-3-pentenyl)cyclohexanone
(5alpha,14alpha)-14-Methylcholestan-3-one
Lophenol
1alpha-hydroxyvitamin D3 / 1alpha-hydroxycholecalciferol
1alpha-hydroxy-3-epivitamin D3 / 1alpha-hydroxy-3-epicholecalciferol
(5E)-1alpha-hydroxyvitamin D3 / (5E)-1alpha-hydroxycholecalciferol
(5E)-1alpha-hydroxy-3-epivitamin D3 / (5E)-1alpha-hydroxy-3-epicholecalciferol
1beta-hydroxyvitamin D3 / 1beta-hydroxycholecalciferol
1beta-hydroxy-3-epivitamin D3 / 1beta-hydroxy-3-epicholecalciferol
(5E)-1beta-hydroxyvitamin D3 / (5E)-1beta-hydroxycholecalciferol
(5E)-1beta-hydroxy-3-epivitamin D3 / (5E)-1beta-hydroxy-3-epicholecalciferol
2alpha-hydroxyvitamin D3 / 2alpha-hydroxycholecalciferol
2beta-hydroxyvitamin D3 / 2beta-hydroxycholecalciferol
1alpha,25-dihydroxy-3-deoxyvitamin D3 / 1alpha,25-dihydroxy-3-deoxycholecalciferol
calcidiol
A hydroxycalciol that is calciol in which the hydrogen at position 25 has been replaced by a hydroxy group. A prehormone resulting from the oxidation of calciol in the liver, it is further hydroxylated in the kidney to give calcitriol, the active form of vitamin D3.
Dedrogyl
A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CC - Vitamin d and analogues H - Systemic hormonal preparations, excl. sex hormones and insulins > H05 - Calcium homeostasis > H05B - Anti-parathyroid agents D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols D050071 - Bone Density Conservation Agents
1,7-bis-(tert-Butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane
C20H40N4O4 (400.30494000000004)
Colestolone
D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents > D000924 - Anticholesteremic Agents C78276 - Agent Affecting Digestive System or Metabolism > C29703 - Antilipidemic Agent D009676 - Noxae > D000963 - Antimetabolites
1,3-Propanediyl-bis(tripropylphosphonium) difluoride solution
C21H48F2P2 (400.3199131999999)
3-Hydroxy-2,2-bis(hydroxymethyl)propyl 9-octadecenoate
CHEBI:19809
(5alpha)-campestan-3-one
(5alpha)-campestan-3-one belongs to ergosterols and derivatives class of compounds. Those are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton (5alpha)-campestan-3-one is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (5alpha)-campestan-3-one can be found in a number of food items such as macadamia nut (m. tetraphylla), malabar spinach, sourdough, and citrus, which makes (5alpha)-campestan-3-one a potential biomarker for the consumption of these food products. (5α)-campestan-3-one belongs to ergosterols and derivatives class of compounds. Those are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton (5α)-campestan-3-one is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (5α)-campestan-3-one can be found in a number of food items such as macadamia nut (m. tetraphylla), malabar spinach, sourdough, and citrus, which makes (5α)-campestan-3-one a potential biomarker for the consumption of these food products.
4alpha-methyl-cholesta-8-enol
4alpha-methyl-cholesta-8-enol belongs to cholesterols and derivatives class of compounds. Those are compounds containing a 3-hydroxylated cholestane core. 4alpha-methyl-cholesta-8-enol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 4alpha-methyl-cholesta-8-enol can be found in a number of food items such as black-eyed pea, swede, saskatoon berry, and chinese chives, which makes 4alpha-methyl-cholesta-8-enol a potential biomarker for the consumption of these food products. 4α-methyl-cholesta-8-enol belongs to cholesterols and derivatives class of compounds. Those are compounds containing a 3-hydroxylated cholestane core. 4α-methyl-cholesta-8-enol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 4α-methyl-cholesta-8-enol can be found in a number of food items such as black-eyed pea, swede, saskatoon berry, and chinese chives, which makes 4α-methyl-cholesta-8-enol a potential biomarker for the consumption of these food products.
campest-4-en-3beta-ol
Campest-4-en-3beta-ol belongs to ergosterols and derivatives class of compounds. Those are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Campest-4-en-3beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Campest-4-en-3beta-ol can be found in a number of food items such as spirulina, alaska wild rhubarb, avocado, and nanking cherry, which makes campest-4-en-3beta-ol a potential biomarker for the consumption of these food products. Campest-4-en-3β-ol belongs to ergosterols and derivatives class of compounds. Those are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Campest-4-en-3β-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Campest-4-en-3β-ol can be found in a number of food items such as spirulina, alaska wild rhubarb, avocado, and nanking cherry, which makes campest-4-en-3β-ol a potential biomarker for the consumption of these food products.
.DELTA.8(14)-Ergostenol
Constituent of Dioscorea batatas (Chinese yam). (3beta,5alpha,24R)-Ergost-8(14)-en-3-ol is found in root vegetables.
(22S)-22-hydroxyvitamin D3/(22S)-22-hydroxycholecalciferol
25-Hydroxycholest-4-en-3-one
A cholestanoid that is cholest-4-en-3-one which carries a hydroxy group at position 25.
(25R)-3beta-hydroxycholest-5-en-26-al
A 3beta-hydroxycholest-5-en-26-al in which the stereocentre at position 25 has R-configuration.
(1S,2R,7S,10S,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azoniahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-7-ol
(4E)-4-[(2Z)-2-(5-hydroxy-2-methylidenecyclohexylidene)ethylidene]-7a-methyl-1-(6-methylheptan-2-yl)-2,3,3a,5,6,7-hexahydro-1H-inden-2-ol
[(S)-3-Carboxylato-2-(palmitoyloxy)propyl]trimethylaminium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(14-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(12-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(9-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(5-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(6-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(11-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(3-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(8-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(7-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(13-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(4-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
[3-Carboxy-2-(10-methylpentadecanoyloxy)propyl]-trimethylazanium
C23H46NO4+ (400.34266560000003)
(3Z)-3-[(2E)-2-[1-(7-hydroxy-6-methylheptan-2-yl)-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol
(3Z)-3-[(2E)-2-[1-(2-hydroxy-6-methylheptan-2-yl)-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol
(20S)-Hydroxyvitamin D3
A hydroxycalciol that consists of vitamin D3 (calciol) carrying an additional hydroxy group at position 20 with S-configuration. D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols
3beta-Hydroxycholest-5-en-26-al
A 26-oxo steroid resulting from the oxidation of one of the terminal methyl groups of cholesterol to the corresponding aldehyde.
(3S,8S,9S,10R,13R,14S,17R)-3-hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one
2-[(3S)-3-acetyloxyhexadecanoyl]oxyethyl-trimethylazanium
C23H46NO4+ (400.34266560000003)
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
(1-Hexanoyloxy-3-hydroxypropan-2-yl) tetradecanoate
2-(Trimethylsilyloxy)nonadecanoic acid methyl ester
C23H48O3Si (400.3372537999999)
Ethyl (4AS,5S,8AS)-E-(+)-3-methyl-5-((5alpha-(4-methyl-3-pentenyl)-2,5beta,8abeta-trimethyl-3,4,4A,5,6,7,8,8A-octahydronaphthalenyl)-2-pentenoate
(1-Hydroxy-3-propanoyloxypropan-2-yl) heptadecanoate
(1-Heptanoyloxy-3-hydroxypropan-2-yl) tridecanoate
(1-Hydroxy-3-pentanoyloxypropan-2-yl) pentadecanoate
(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-undecaene
(3beta,5E,7E)-9,10-Secocholesta-5,7,10(19)-triene-3,25-diol
cholesta-5,7-dien-3beta,25-diol
A cholestanoid that is 7-dehydrocholesterol carrying an additional hydroxy substituent at position 25.
4alpha-methyl-5alpha-cholest-8(14)-en-3beta-ol
A 3beta-sterol that is 5alpha-cholest-8(14)-en-3beta-ol bearing an alpha-methyl substituent at position 4.
(24Z),26-hydroxydesmosterol
A cholestanoid that is desmosterol carrying an additional hydroxy susbstituent at position 26.
cholesta-5,7-dien-3beta,24S-diol
A cholestanoid that is 7-dehydrocholesterol carrying an additional hydroxy substituent at position 24 (24S-stereoisomer).
4alpha-methyl-5alpha-cholest-8-en-3beta-ol
A 3beta-sterol that is 5alpha-cholest-8-en-3beta-ol carrying an additional methyl substituent at position 4alpha.
7alpha-Hydroxycholest-4-en-3-one
A cholestanoid consisting of a cholesterol core having an oxo group at the 3-position, a C=C bond at the 4,5-position and an alpha-hydroxy group at the 7-position.
WE(27:5)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved
CmE(0:0)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved
(1r,3ar,5as,7s,9as,11ar)-1-[(2r,5s)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol
(1r,3ar,3bs,5r,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-5-hydroxy-1h,2h,3h,3ah,3bh,4h,5h,8h,9h,9ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-7-one
(1r,3as,3br,5as,7s,9as,9bs,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(4e,8e,12e,16e)-4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid
(1s,3ar,5as,7r,9ar,9bs,11as)-1-[(2r,5r)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(1s)-3-{2-[(1r,3as,7ar)-1-[(2r)-6-hydroxy-6-methylheptan-2-yl]-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
(6s,7s,9as,11ar)-6,9a,11a-trimethyl-1-[(2s)-6-methylheptan-2-yl]-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol
(1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5s)-5-hydroxy-6-methylhept-6-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(2s)-2,8-dimethyl-2-[(4r,8r)-4,8,12-trimethyltridecyl]chromen-6-ol
(1r,3as,3br,5as,7s,9as,9bs,11ar)-1-[(2r,4e)-5,6-dimethylhept-4-en-2-yl]-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
6,9a,11a-trimethyl-1-(6-methylheptan-2-yl)-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol
(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
1-(5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-7-one
(1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-hydroxy-6-methylhept-6-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
16-(1-aminoethyl)-6-(dimethylamino)-7,7,13,18-tetramethyltetracyclo[9.7.0.0³,⁸.0¹³,¹⁷]octadeca-1,3-dien-15-ol
1-(5-ethyl-6-methylheptan-2-yl)-7-hydroxy-1h,2h,3h,3ah,3bh,6h,7h,8h,9h,9ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-4-one
n-[(1s)-1-[(1s,3as,3bs,7r,9ar,9bs,11as)-7-(dimethylamino)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]ethyl]-n-methylacetamide
15-hydroxy-n-[2-(1h-indol-3-yl)ethyl]pentadecanimidic acid
(3s,6r)-6-[(1r,3as,3br,9as,9bs,11ar)-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-1-yl]-2,3-dimethylhept-1-en-1-ol
(1r,3as,3br,9as,9bs,11ar)-1-[(2r)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-7-one
(1r,3as,3bs,7r,9ar,9bs,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
2-methyl-6-[(2e,7r,11r)-3,7,11,15-tetramethylhexadec-2-en-1-yl]cyclohexa-2,5-diene-1,4-dione
(1r,5as,6s,7s,9as,9br,11ar)-6,9a,11a-trimethyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,4h,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(1r,7s,9as,11ar)-1-(5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(1s,3ar,3br,7s,9ar,9bs,11ar)-1-[(2r,5r)-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,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,4e)-6-hydroxy-6-methylhept-4-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
n-[(1r)-1-[(1r,3ar,3br,7s,9as,9br,11as)-7-(dimethylamino)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]ethyl]-n-methylacetamide
23s- Methylcholest
{"Ingredient_id": "HBIN004175","Ingredient_name": "23s- Methylcholest","Alias": "NA","Ingredient_formula": "C28H48O","Ingredient_Smile": "CC(C)CC(C)CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "38183","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
24-Methylcholest-7-en-3belta-ol
{"Ingredient_id": "HBIN004443","Ingredient_name": "24-Methylcholest-7-en-3belta-ol","Alias": "24-methylcholest-7-en-3belta-ol","Ingredient_formula": "C28H48O","Ingredient_Smile": "CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)O)C)C)C","Ingredient_weight": "400.76","OB_score": "8.790447814","CAS_id": "NA","SymMap_id": "SMIT01025","TCMID_id": "25503","TCMSP_id": "MOL009613","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
(24r-alpha-methyl cholest-8(14)-enol
{"Ingredient_id": "HBIN004503","Ingredient_name": "(24r-alpha-methyl cholest-8(14)-enol","Alias": "NA","Ingredient_formula": "C28H48O","Ingredient_Smile": "CC(C)C(C)CCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "25501","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
(24s)-belta-methyl cholesterol
{"Ingredient_id": "HBIN004533","Ingredient_name": "(24s)-belta-methyl cholesterol","Alias": "NA","Ingredient_formula": "C28H48O","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "31582","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
(2r,3r,4s,6s)-3-methyl-4,6-di(3-methyl-2-butenyl)-2-(2-methyl-1-oxopropyl)-3-(4-meth-yl-3-pentenyl)-cyclohexanone
{"Ingredient_id": "HBIN006443","Ingredient_name": "(2r,3r,4s,6s)-3-methyl-4,6-di(3-methyl-2-butenyl)-2-(2-methyl-1-oxopropyl)-3-(4-meth-yl-3-pentenyl)-cyclohexanone","Alias": "NA","Ingredient_formula": "C27H44O2","Ingredient_Smile": "CC(C)C(=O)C1C(=O)C(CC(C1(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "14315","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
4α-methyl-cholest-7-en-3β-ol
{"Ingredient_id": "HBIN010208","Ingredient_name": "4\u03b1-methyl-cholest-7-en-3\u03b2-ol","Alias": "NA","Ingredient_formula": "C28H48O","Ingredient_Smile": "CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "14228","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
4alpha-methylcholest-8-enol
{"Ingredient_id": "HBIN010210","Ingredient_name": "4alpha-methylcholest-8-enol","Alias": "NA","Ingredient_formula": "C28H48O","Ingredient_Smile": "CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3CCC4C(C)CCCC(C)C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "25504","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
4-methylcholest-7-enol
{"Ingredient_id": "HBIN010688","Ingredient_name": "4-methylcholest-7-enol","Alias": "NA","Ingredient_formula": "C28H48O","Ingredient_Smile": "CC1CCCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)CO)C)C","Ingredient_weight": "400.7 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT18884","TCMID_id": "25505","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "66727514","DrugBank_id": "NA"}
abricin
{"Ingredient_id": "HBIN014233","Ingredient_name": "abricin","Alias": "NA","Ingredient_formula": "C27H44O2","Ingredient_Smile": "NA","Ingredient_weight": "400.64","OB_score": "40.7324","CAS_id": "73030-55-4","SymMap_id": "SMIT09065","TCMID_id": "NA","TCMSP_id": "MOL007682","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
(1s,3r,6s,8r,11s,12r,14r,15s,16r)-6-(dimethylamino)-12,16-dimethyl-15-[(1s)-1-(methylamino)ethyl]-7-methylidenepentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-14-ol
1-(5-ethyl-6-methylhept-3-en-2-yl)-11a-methyl-hexadecahydrocyclopenta[a]phenanthren-7-ol
(1r,3ar,3br,7s,9ar,9br,11ar)-1-[(2r,5r)-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
(5s)-5-[(1s,3ar,3br,5as,9as,9br,11ar)-3a,3b,6,6,9a-pentamethyl-dodecahydro-1h-cyclopenta[a]phenanthren-1-yl]-5-methyloxolan-2-one
(1r,3ar,5as,7s,9ar,9br,11ar)-7-hydroxy-9a,11a-dimethyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one
1-[4-(3,3-dimethyloxiran-2-yl)butan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
1-(5,6-dimethylhept-1-en-2-yl)-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(1r,3ar,5ar,7s,9as,9br,11ar)-1-[(2r,5r)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(1r,3as,3br,5as,7s,9as,9bs,11as)-1-[(5r)-5,6-dimethylhept-1-en-2-yl]-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(1r,3ar,3bs,5as,7s,9as,9bs,11ar)-9a,11a-dimethyl-1-[(2r)-6-methyl-5-methylideneheptan-2-yl]-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
1-[1-(2-isopropylcyclopropyl)propan-2-yl]-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(1r,3as,3br,5ar,7s,9as,9bs,11ar)-1-[(2r,3e,5s)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(3as,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-9-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-tetradecahydro-2h-cyclopenta[a]chrysen-1-one
2,8-dimethyl-2-(4,8,12-trimethyltridec-11-en-1-yl)-3,4-dihydro-1-benzopyran-6-ol
(3r,6r)-6-[(1r,3ar,9as,9br,11ar)-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2,3-dimethylheptan-1-ol
(1r,3as,3bs,9ar,9bs,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,3as,3bs,7s,9bs)-1-[(2r,5r)-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,5as,7s,9as,9bs,11ar)-1-[(2r,5s)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,4h,5h,5ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(2s,3as,3bs,5as,7s,9as,9bs,11ar)-2-[(2s,3e,5s)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-ol
(1s,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-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,3as,3bs,5as,9ar,9bs,11ar)-1-[(2r,5r)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-7-one
6-(dimethylamino)-12,16-dimethyl-15-[1-(methylamino)ethyl]-7-methylidenepentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-14-ol
[13-(5,6-dimethylheptan-2-yl)-2,14-dimethyltetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-11-en-5-yl]methanol
(1s,3as,3bs,7s,9ar,9br,11as)-1-[(2r,5r)-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
1-(6-hydroxy-6-methylhept-4-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
3a,9a,11a-trimethyl-1-(6-methylheptan-2-yl)-1h,2h,3h,3bh,4h,5h,5ah,6h,7h,8h,9h,11h-cyclopenta[a]phenanthren-7-ol
[2,14-dimethyl-13-(6-methyl-5-methylideneheptan-2-yl)tetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadecan-5-yl]methanol
(2-{[(3s)-3-(acetyloxy)hexadecanoyl]oxy}ethyl)trimethylazanium
[C23H46NO4]+ (400.34266560000003)