Exact Mass: 430.38106
Exact Mass Matches: 430.38106
Found 286 metabolites which its exact mass value is equals to given mass value 430.38106
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
alpha-Tocopherol
Alpha-tocopherol is a pale yellow, viscous liquid. (NTP, 1992) (R,R,R)-alpha-tocopherol is an alpha-tocopherol that has R,R,R configuration. The naturally occurring stereoisomer of alpha-tocopherol, it is found particularly in sunflower and olive oils. It has a role as an antioxidant, a nutraceutical, an antiatherogenic agent, an EC 2.7.11.13 (protein kinase C) inhibitor, an anticoagulant, an immunomodulator, an antiviral agent, a micronutrient, an algal metabolite and a plant metabolite. It is an enantiomer of a (S,S,S)-alpha-tocopherol. In 1922, vitamin E was demonstrated to be an essential nutrient. Vitamin E is a term used to describe 8 different fat soluble tocopherols and tocotrienols, alpha-tocopherol being the most biologically active. Vitamin E acts as an antioxidant, protecting cell membranes from oxidative damage. The antioxidant effects are currently being researched for use in the treatment of diseases causing bone loss, cardiovascular diseases, diabetes mellitus and associated comorbidities, eye diseases, inflammatory diseases (including skin conditions), lipid disorders, neurological diseases, and radiation damage. Though this research is so far inconclusive, vitamin E remains a popular supplement and is generally considered safe by the FDA. Vitamin E is a natural product found in Monteverdia ilicifolia, Calea jamaicensis, and other organisms with data available. Alpha-Tocopherol is the orally bioavailable alpha form of the naturally-occurring fat-soluble vitamin E, with potent antioxidant and cytoprotective activities. Upon administration, alpha-tocopherol neutralizes free radicals, thereby protecting tissues and organs from oxidative damage. Alpha-tocopherol gets incorporated into biological membranes, prevents protein oxidation and inhibits lipid peroxidation, thereby maintaining cell membrane integrity and protecting the cell against damage. In addition, alpha-tocopherol inhibits the activity of protein kinase C (PKC) and PKC-mediated pathways. Alpha-tocopherol also modulates the expression of various genes, plays a key role in neurological function, inhibits platelet aggregation and enhances vasodilation. Compared with other forms of tocopherol, alpha-tocopherol is the most biologically active form and is the form that is preferentially absorbed and retained in the body. A generic descriptor for all tocopherols and tocotrienols that exhibit alpha-tocopherol activity. By virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus, these compounds exhibit varying degree of antioxidant activity, depending on the site and number of methyl groups and the type of isoprenoids. See also: Alpha-Tocopherol Acetate (is active moiety of); Tocopherol (related); Vitamin E (related) ... View More ... alpha-Tocopherol is traditionally recognized as the most active form of vitamin E in humans and is a powerful biological antioxidant. The measurement of "vitamin E" activity in international units (IU) was based on fertility enhancement by the prevention of spontaneous abortions in pregnant rats relative to alpha-Tocopherol. Natural vitamin E exists in eight different forms or isomers: four tocopherols and four tocotrienols. In foods, the most abundant sources of vitamin E are vegetable oils such as palm oil, sunflower, corn, soybean, and olive oil. Nuts, sunflower seeds, and wheat germ are also good sources. Constituent of many vegetable oils such as soya and sunflower oils. Dietary supplement and nutrient. Nutriceutical with anticancer and antioxidant props. Added to fats and oils to prevent rancidity. The naturally-occurring tocopherol is a single stereoisomer; synthetic forms are a mixture of all eight possible isomers An alpha-tocopherol that has R,R,R configuration. The naturally occurring stereoisomer of alpha-tocopherol, it is found particularly in sunflower and olive oils. α-Tocopherol (alpha-tocopherol) is a type of vitamin E. Its E number is "E307". Vitamin E exists in eight different forms, four tocopherols and four tocotrienols. All feature a chromane ring, with a hydroxyl group that can donate a hydrogen atom to reduce free radicals and a hydrophobic side chain which allows for penetration into biological membranes. Compared to the others, α-tocopherol is preferentially absorbed and accumulated in humans. Vitamin E is found in a variety of tissues, being lipid-soluble, and taken up by the body in a wide variety of ways. The most prevalent form, α-tocopherol, is involved in molecular, cellular, biochemical processes closely related to overall lipoprotein and lipid homeostasis. Ongoing research is believed to be "critical for manipulation of vitamin E homeostasis in a variety of oxidative stress-related disease conditions in humans."[2] One of these disease conditions is the α-tocopherol role in the use by malaria parasites to protect themselves from the highly oxidative environment in erythrocytes.[3] DL-α-Tocopherol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=16826-11-2 (retrieved 2024-06-29) (CAS RN: 10191-41-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].
4-beta-Hydroxymethyl-4-alpha-methyl-5-alpha-cholest-7-en-3-beta-ol
4-beta-hydroxymethyl-4-alpha-methyl-5-alpha-cholest-7-en-3-beta-ol is part of the Steroid biosynthesis pathway. It is a substrate for: Methylsterol monooxygenase 1, and Methylsterol monooxygenase 1.
(22R,23R)-22,23-dihydroxy-campest-4-en-3-one
Ikshusterol
7-Epiikshusterol is a constituent of cane sugar wax
Schleicherastatin 6
Schleicherastatin 7 is found in fruits. Schleicherastatin 7 is a constituent of the famine food Schleichera oleosa
(2beta,3alpha,9alpha,24R)-Ergosta-7,22-diene-2,3,9-triol
(2beta,3alpha,9alpha,24R)-Ergosta-7,22-diene-2,3,9-triol is found in mushrooms. (2beta,3alpha,9alpha,24R)-Ergosta-7,22-diene-2,3,9-triol is a metabolite of Ganoderma lucidum (reishi). Metabolite of Ganoderma lucidum (reishi). (2beta,3alpha,9alpha,24R)-Ergosta-7,22-diene-2,3,9-triol is found in mushrooms.
(3beta,5beta,8beta,22E,24xi)-Ergosta-6,22-diene-3,5,8-triol
(3beta,5beta,8beta,22E,24xi)-Ergosta-6,22-diene-3,5,8-triol is found in mushrooms. (3beta,5beta,8beta,22E,24xi)-Ergosta-6,22-diene-3,5,8-triol is a constituent of Gyroporus castaneus (chestnut bolete). Constituent of Gyroporus castaneus (chestnut bolete). (3beta,5beta,8beta,22E,24xi)-Ergosta-6,22-diene-3,5,8-triol is found in mushrooms.
4alpha-Carboxy-5alpha-cholesta-8-en-3beta-ol
4alpha-carboxy-5alpha-cholesta-8-en-3beta-ol is a 3-beta-hydroxysterol that is an intermediate in cholesterol biosynthesis II (via 24,25-dihydrolanosterol). It is a substrate for NAD(P)-dependent steroid dehydrogenase (H105E3) and it can be generated from the enzymatic carboxylation of 5alpha-cholesta-8-en-3-one. It is also a substrate for C-4 methyl sterol oxidase (SC4MOL) and can be generated from the enzymatic oxidation of 4alpha-formyl-5alpha-cholesta-8-en-3beta-ol. The sequence of reactions and the types of intermediates in cholesterol biosynthesis may vary. Alternate routes exist because reduction of the carbon 24,25 double bond on the hydrocarbon side chain of the sterol ring structure by sterol delta24-reductase can occur at multiple points in the pathway, giving rise to different intermediates. These intermediates, with or without a double bond in the hydrocarbon side chain, can serve as substrates for the other enzymes in the pathway. [HMDB] 4alpha-carboxy-5alpha-cholesta-8-en-3beta-ol is a 3-beta-hydroxysterol that is an intermediate in cholesterol biosynthesis II (via 24,25-dihydrolanosterol). It is a substrate for NAD(P)-dependent steroid dehydrogenase (H105E3) and it can be generated from the enzymatic carboxylation of 5alpha-cholesta-8-en-3-one. It is also a substrate for C-4 methyl sterol oxidase (SC4MOL) and can be generated from the enzymatic oxidation of 4alpha-formyl-5alpha-cholesta-8-en-3beta-ol. The sequence of reactions and the types of intermediates in cholesterol biosynthesis may vary. Alternate routes exist because reduction of the carbon 24,25 double bond on the hydrocarbon side chain of the sterol ring structure by sterol delta24-reductase can occur at multiple points in the pathway, giving rise to different intermediates. These intermediates, with or without a double bond in the hydrocarbon side chain, can serve as substrates for the other enzymes in the pathway.
4alpha-Hydroxymethyl-4beta-methyl-5alpha-cholesta-8-en-3beta-ol
4alpha-hydroxymethyl-4beta-methyl-5alpha-cholesta-8-en-3beta-ol is a 3-beta-hydroxysterol that is an intermediate in cholesterol biosynthesis II (via 24,25-dihydrolanosterol). It is a substrate for C-4 methyl sterol oxidase (SC4MOL) and can be generated from the enzymatic reduction of 4alpha-formyl-4beta-methyl-5alpha-cholesta-8-en-3beta-ol or from the enzymatic oxidation of 4,4-dimethyl-5alpha-cholesta-8-en-3-beta-ol. The sequence of reactions and the types of intermediates in cholesterol biosynthesis may vary. Alternate routes exist because reduction of the carbon 24,25 double bond on the hydrocarbon side chain of the sterol ring structure by sterol delta24-reductase can occur at multiple points in the pathway, giving rise to different intermediates. These intermediates, with or without a double bond in the hydrocarbon side chain, can serve as substrates for the other enzymes in the pathway.
24-Propylcholestan-3-ol
24-Propylcholestan-3-ol is found in mollusks. 24-Propylcholestan-3-ol is a constituent of the edible scallop Trochostoma orientale Constituent of the edible scallop Trochostoma orientale. 24-Propylcholestan-3-ol is found in mollusks.
4α-carboxy-5α-cholesta-8-en-3β-ol
4α-carboxy-5α-cholesta-8-en-3β-ol is also known as 4alpha-Carboxy-5alpha-cholest-8-en-3beta-ol. 4α-carboxy-5α-cholesta-8-en-3β-ol is considered to be practically insoluble (in water) and acidic. 4α-carboxy-5α-cholesta-8-en-3β-ol is a sterol lipid molecule
4α-hydroxymethyl-4β-methyl-5α-cholesta-8-en-3β-ol
4α-hydroxymethyl-4β-methyl-5α-cholesta-8-en-3β-ol is considered to be practically insoluble (in water) and relatively neutral. 4α-hydroxymethyl-4β-methyl-5α-cholesta-8-en-3β-ol is a sterol lipid molecule
(-)-alpha-Tocopherol
α-tocopherol is a member of the class of compounds known as tocopherols. Tocopherols are vitamin E derivatives containing a saturated trimethyltridecyl chain attached to the carbon C6 atom of a benzopyran ring system. The differ from tocotrienols that contain an unsaturated trimethyltrideca-3,7,11-trien-1-yl chain. α-tocopherol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). α-tocopherol can be found in a number of food items such as lime, rowanberry, horseradish tree, and pineappple sage, which makes α-tocopherol a potential biomarker for the consumption of these food products. α-tocopherol is a form of vitamin E that is preferentially absorbed and accumulated in humans. The measurement of "vitamin E" activity in international units (IU) was based on fertility enhancement by the prevention of spontaneous abortions in pregnant rats relative to α-tocopherol .
Cholesterol carbonate
5-Tricosenylresorcinol
5-tricosenylresorcinol is a member of the class of compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3. 5-tricosenylresorcinol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 5-tricosenylresorcinol can be found in breakfast cereal and common wheat, which makes 5-tricosenylresorcinol a potential biomarker for the consumption of these food products.
5-Stigmastene-3beta,7alpha-diol
5-stigmastene-3beta,7alpha-diol belongs to stigmastanes and derivatives class of compounds. Those are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24. 5-stigmastene-3beta,7alpha-diol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 5-stigmastene-3beta,7alpha-diol can be found in pineapple, which makes 5-stigmastene-3beta,7alpha-diol a potential biomarker for the consumption of this food product.
(22R,23R)-22,23-dihydroxy-campest-4-en-3-one
(22r,23r)-22,23-dihydroxy-campest-4-en-3-one belongs to dihydroxy bile acids, alcohols and derivatives class of compounds. Those are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups (22r,23r)-22,23-dihydroxy-campest-4-en-3-one is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (22r,23r)-22,23-dihydroxy-campest-4-en-3-one can be found in a number of food items such as black radish, chinese water chestnut, arrowroot, and lemon grass, which makes (22r,23r)-22,23-dihydroxy-campest-4-en-3-one a potential biomarker for the consumption of these food products.
(22alpha)-hydroxy-sitosterol
(22alpha)-hydroxy-sitosterol belongs to stigmastanes and derivatives class of compounds. Those are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24 (22alpha)-hydroxy-sitosterol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). (22alpha)-hydroxy-sitosterol can be found in a number of food items such as cottonseed, oil-seed camellia, cloves, and dill, which makes (22alpha)-hydroxy-sitosterol a potential biomarker for the consumption of these food products.
4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol
4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol, also known as 4a-methyl-4b-hydroxymethyl-5a-cholest-7-en-3b-ol, belongs to cholesterols and derivatives class of compounds. Those are compounds containing a 3-hydroxylated cholestane core. Thus, 4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol is considered to be a sterol lipid molecule. 4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol can be found in a number of food items such as broad bean, summer savory, hyssop, and alpine sweetvetch, which makes 4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol a potential biomarker for the consumption of these food products. 4beta-hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol may be a unique S.cerevisiae (yeast) metabolite. 4β-hydroxymethyl-4α-methyl-5α-cholest-7-en-3β-ol, also known as 4a-methyl-4b-hydroxymethyl-5a-cholest-7-en-3b-ol, belongs to cholesterols and derivatives class of compounds. Those are compounds containing a 3-hydroxylated cholestane core. Thus, 4β-hydroxymethyl-4α-methyl-5α-cholest-7-en-3β-ol is considered to be a sterol lipid molecule. 4β-hydroxymethyl-4α-methyl-5α-cholest-7-en-3β-ol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 4β-hydroxymethyl-4α-methyl-5α-cholest-7-en-3β-ol can be found in a number of food items such as broad bean, summer savory, hyssop, and alpine sweetvetch, which makes 4β-hydroxymethyl-4α-methyl-5α-cholest-7-en-3β-ol a potential biomarker for the consumption of these food products. 4β-hydroxymethyl-4α-methyl-5α-cholest-7-en-3β-ol may be a unique S.cerevisiae (yeast) metabolite.
Cerevisterol
An ergostanoid that is (22E)-ergosta-7,22-diene substituted by hydroxy groups at positions 3, 5 and 6 (the 3beta,5alpha,6beta stereoisomer). It has been isolated from the fungus, Xylaria species. Cerevisterol is a steroid isolated from the fruiting bodies of Agaricus blazei[1]. Cerevisterol is a steroid isolated from the fruiting bodies of Agaricus blazei[1].
24-Propylcholestan-3-ol
Cyclomicrophyllin B|Cyclomicrophyllin-B|Cyclomicrophylline-B
C27H46N2O2 (430.35590959999996)
(3beta,5beta,6beta)-5,6-epoxyergost-24(28)-ene-3,19-diol|(3beta,5beta,6beta)-5,6-epoxyergost-24(28)-ene-3beta,19-diol|5,6-epoxylitosterol|5beta,6beta-Epoxide-Ergosta-5,24(28)-diene-3,19-diol
(24R)-24-ethyl-5beta-cholest-9-ene-6beta,12alpha-diol|opuntisterol
(24R)-5alpha,6alpha-epoxy-24-ethylcholestane-3beta-ol|5,6alpha-epoxy-5alpha-sitostan-3beta-ol|5,6alpha-epoxy-5alpha-stigmastan-3beta-ol|5,6alpha-epoxysitosterol|5alpha,6alpha-epoxysitostan-3beta-ol|alpha-epoxysitosterol|beta-sitostan-5alpha,6alpha-epoxy-3beta-ol
(3beta,5alpha,24R)-Stigmast-6-ene-3,5-diol|24-ethylcholest-6-ene-3,5-diol
(22E,24S)-24-methylcholesta-7,22-diene-3beta,5alpha,6beta,9alpha-tetrol
6beta-Hydroxy-5alpha-stigmastan-3-on|6beta-hydroxy-5alpha-stigmastan-3-one|6beta-hydroxy-beta-sitosterone
24-Methylcholesta-9(11),24(28)-diene-3??,12??,19-triol
(20R,23S,24R)-5alpha-Dinosterane|(23S,24R)-4alpha,23,24-Trimethyl-5alpha-cholestan-3beta-ol|4alpha,23S,24R-trimethyl-5alpha(H)-cholest-3beta-ol
24-methylenecholest-7-en-3beta,5alpha,6beta-triol|ergosta-7,24(28)-diene-3beta,5alpha,6beta-triol
4alpha,14-dimethyl-9,19-cyclocholestan-3beta,24xi-diol
5beta,6beta-epoxyergost-24(28)-ene-3beta,7beta-diol
(3beta,4alpha,5alpha,22xi,24xi)-4-Methylergost-7-ene-3,22-diol|4alpha,24xi-Dimethyl-cholest-7-en-3beta,22xi-diol
3beta,5-Dihydroxy-5alpha-ergost-7-en-6-on|3beta,5-dihydroxy-5alpha-ergost-7-en-6-one|3beta,5alpha-dihydroxyergost-7-en-6-one|3??,5??-Dihydroxyergost-7-en-6-one
(3beta,4alpha,5alpha,8beta)-4-methylergost-24(28)-ene-3,8-diol|4alpha-methyl-24-methylene-5alpha-cholestan-3beta,8beta-diol
(24S)-24-methyl-5alpha-stigmastan-3beta-ol|24(S)-Methyl-24-ethyl-5alpha-cholestan-3beta-ol
Cyclomicophyllin-C|Cyclomicrophyllin C|Cyclomicrophyllin-C|Cyclomicrophylline-C
C27H46N2O2 (430.35590959999996)
3beta,11-dihydroxy-24-methylene-9,11-secocholest-5-en-9-one|3beta,11-dihydroxy-24-methylene-9,11-secocholestan-5-en-9-one|3beta-3,11-Dihydroxy-9,11-secoergosta-5,24(28)-dien-9-one|8betaH-3beta,11-dihydroxy-24-methylene-9,11-secocholest-5-en-9-one
25,26,27-trisnor-3alpha-methoxy-lanost-9(11)-en-24-oic acid
(3beta,4beta,22R)-ergosta-5,24(24)-diene-3,4,22-triol
5,8-epidioxy-5alpha,8alpha-ergost-22t-en-3beta-ol|5alpha,6alpha-epidioxyergost-6-en-3beta-ol|5alpha,8alpha-epidioxy-24(R)-methylcholesta-6,22-dien-3beta-ol|ergosterol peroxide
24-methylcholesta-5,24(28)-diene-3beta,15beta,19-triol
(24R)-3beta,11-dihydroxy-24-methyl-9,11-secocholest-5,22E-dien-9-one|leptosterol A
25,26,27-trinor-3alpha-methoxycycloartan-24-oic acid
24,25,26,27-tetranor-3beta-acetoxycycloartan-23-ol
(24S,22E)-3beta,5alpha-dihydroxyergost-22-en-6-one
(3beta,4beta,7alpha)-ergosta-5,24(28)-diene-3,4,7-triol|(3S,4R,7S,8S,9S,10R,13R,14S,17R)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-10,13-dimethyl-17-[ (2R)-6-methyl-5-methylideneheptan-2-yl]-1H-cyclopenta[a]phenanthrene-3,4,7-triol
(24R)-5alpha,8alpha-epidioxyergosta-6-en-3beta-ol|5,8-epidioxy-24-methylcholesta-6-en-3beta-ol|5,8-epidioxy-5alpha,8alpha-ergost-6-en-3beta-ol|5alpha,8alpha-epi-dioxy-(24S)-ergost-6-en-3beta-ol|5alpha,8alpha-epidioxy-(24S)-ergost-6-en-3beta-ol|5alpha,8alpha-epidioxy-24(S)-methylcholest-6-en-3beta-ol
24-ethyl-25-hydroxycholesterol|24xi-Delta5-Stigmasten-3beta,25-diol
17alpha-hydroxy-22,23-epoxy-24-methylcholest-5-en-3beta-ol
(3beta,4beta)-ergosta-5,24(28)-diene-3,4,20-triol|ergosta-5,24(24)-diene-3beta,4beta,20beta-triol
(24S)-5-stigmastene-3beta-24-diol|(24S)-stigmast-5-ene-3beta,24-diol
24-methylenecholest-5-en-1alpha,3beta,11alpha-triol|24-methylenecholest-5-ene-1alpha-3beta,11alpha-triol
(22E)-24-methylcholesta-5,22-diene-1alpha,3beta,7alpha-triol
13-oxo-22-phenyl-docosanoic acid|13-Oxo-22-phenyl-docosansaeure
24(,28-Epoxide-(3beta,7alpha)-Ergosta-5,24(28)-diene-3,7-diol|24xi,28-Epoxide-(3beta,7alpha)-ergosta-5,24(28)-diene-3,7-diol
3beta,7alpha,20beta-Trihydroxyergosta-5,24(24)-diene
24(R)-methylcholesta-5,22-diene-1alpha,3beta,11alpha-triol
24-methylenecholesta-5-en-1alpha,3beta,7beta-triol|sinugrandisterol A
C:D-seco-(8->14),27-nor-urs-12-ene-3beta,20alpha-diol
(22E)-6beta-methoxy-5alpha-cholesta-7,22-diene-3beta,5-diol
Epipachysamin-C-diacetat|N,N-Diacetylepipachysamine C
C27H46N2O2 (430.35590959999996)
3beta-Hydroxy-5alpha-lanostan|3beta-Hydroxy-lanostan|lanostan-3beta-ol|lanostanol|Lanosterol
3beta-(hydroxymethyl)-24xi-n-propyl-A-nor-5alpha-cholestane
Tocopherol
2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-1-benzopyran-6-ol is a tocopherol. Tocopherol exists in four different forms designated as α, β, δ, and γ. They present strong antioxidant activities, and it is determined as the major form of vitamin E. Tocopherol, as a group, is composed of soluble phenolic compounds that consist of a chromanol ring and a 16-carbon phytyl chain. The classification of the tocopherol molecules is designated depending on the number and position of the methyl substituent in the chromanol ring. The different types of tocopherol can be presented trimethylated, dimethylated or methylated in the positions 5-, 7- and 8-. When the carbons at position 5- and 7- are not methylated, they can function as electrophilic centers that can trap reactive oxygen and nitrogen species. Tocopherols can be found in the diet as part of vegetable oil such as corn, soybean, sesame, and cottonseed. It is currently under the list of substances generally recognized as safe (GRAS) in the FDA for the use of human consumption. DL-alpha-Tocopherol is a natural product found in Sida acuta, Tainia latifolia, and other organisms with data available. dl-alpha-Tocopherol is a synthetic form of vitamin E, a fat-soluble vitamin with potent antioxidant properties. Considered essential for the stabilization of biological membranes (especially those with high amounts of polyunsaturated fatty acids), d-alpha-Tocopherol is a potent peroxyl radical scavenger and inhibits noncompetitively cyclooxygenase activity in many tissues, resulting in a decrease in prostaglandin production. Vitamin E also inhibits angiogenesis and tumor dormancy through suppressing vascular endothelial growth factor (VEGF) gene transcription. (NCI04) DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].
VITAMIN E
Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE was 40 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants D018977 - Micronutrients > D014815 - Vitamins Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE was 15 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. Window width to select the precursor ion was 3 Da.; CONE_VOLTAGE was 20 V.; This record was created by the financial support of MEXT/JSPS KAKENHI Grant Number 19HP8024 to the Mass Spectrometry Society of Japan. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. DL-alpha-Tocopherol is a synthetic vitamin E, with antioxidation effect. DL-alpha-Tocopherol protects human skin fibroblasts against the cytotoxic effect of UVB[1]. rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].
1α-hydroxy-25-methoxyvitamin D3 / 1α-hydroxy-25-methoxycholecalciferol
25-methyl-1α,26-dihydroxyvitamin D3 / 25-methyl-1α,26-dihydroxycholecalciferol
(1R)-25-hydroxy-1-(hydroxymethyl)vitamin D3 / (1R)-25-hydroxy-1-(hydroxymethyl)cholecalciferol
(1S)-25-hydroxy-1-(hydroxymethyl)vitamin D3 / (1S)-25-hydroxy-1-(hydroxymethyl)cholecalciferol
(22R)-25-hydroxy-22-methoxyvitamin D3 / (22R)-25-hydroxy-22-methoxycholecalciferol
(22S)-25-hydroxy-22-methoxyvitamin D3 / (22S)-25-hydroxy-22-methoxycholecalciferol
(5Z,7E)-3,3-dimethyl-A-homo-2,4-dioxa-9,10-seco-5,7,10(19)-cholestatrien-25-ol
1α,25-dihydroxy-1β-methylvitamin D3 / 1α,25-dihydroxy-1β-methylcholecalciferol
1β,25-dihydroxy-1α-methylvitamin D3 / 1β,25-dihydroxy-1α-methylcholecalciferol
1α,25-dihydroxy-8(14)a-homovitamin D3 / 1α,25-dihydroxy-8(14)a-homocholecalciferol
2β-methyl-1α,25-dihydroxyvitamin D3 / 2β-methyl-1α,25-dihydroxycholecalciferol
(5Z,7E)-(1S,2S,3S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,2R,3S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
2α-methyl-1β,25-dihydroxyvitamin D3 / 2α-methyl-1β,25-dihydroxycholecalciferol
2β-methyl-1β,25-dihydroxyvitamin D3 / 2β-methyl-1β,25-dihydroxycholecalciferol
(5Z,7E)-(1R,2S,3S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1R,2R,3S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,2S,3R,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,2R,3R,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,2S,3S,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,2R,3S,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1R,2S,3R,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1R,2R,3R,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1R,2S,3S,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1R,2R,3S,20S)-2-methyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
1α,25-dihydroxy-11α-methylvitamin D3 / 1α,25-dihydroxy-11α-methylcholecalciferol
1α,25-dihydroxy-11β-methylvitamin D3 / 1α,25-dihydroxy-11β-methylcholecalciferol
1α,25-dihydroxy-18-methylvitamin D3 / 1α,25-dihydroxy-18-methylcholecalciferol
1α,25-dihydroxy-24a-homovitamin D3 / 1α,25-dihydroxy-24a-homocholecalciferol
(24R)-1α,25-dihydroxy-24-methylvitamin D3 /(24R)-1α,25-dihydroxy-24-methylcholecalciferol
1α,25-dihydroxy-24a-homo-20-epivitamin D3 / 1α,25-dihydroxy-24a-homo-20-epicholecalciferol
1α,25-dihydroxy-26-methylvitamin D3 / 1α,25-dihydroxy-26-methylcholecalciferol
(5E,7E)-(3S,10R)-10-ethoxy-9,10-seco-5,7-cholestadien-3-ol
(5E,7E)-(3S,10S)-10-ethoxy-9,10-seco-5,7-cholestadien-3-ol
(5Z,7E)-(3S,10R)-10-ethoxy-9,10-seco-5,7-cholestadien-3-ol
2α-methyl-1α,25-dihydroxyvitamin D3 / 2α-methyl-1α,25-dihydroxycholecalciferol
1α,25-Dihydroxy-2E-ethylidene-19-norvitamin D3
1α,25-Dihydroxy-2Z-ethylidene-19-norvitamin D3
20(17+mm12β)-abeo-1α,25-Dihydroxy-24-dihomo-21-norvitamin D3
Ikshusterol
SCHLEICHERASTATIN 6
(2beta,3alpha,9alpha,24R)-Ergosta-7,22-diene-2,3,9-triol
(3beta,5beta,8beta,22E,24xi)-Ergosta-6,22-diene-3,5,8-triol
4-beta-Hydroxymethyl-4-alpha-methyl-5-alpha-cholest-7-en-3-beta-ol
ST 29:1;O2
1alpha-hydroxy-25-methoxyvitamin D3
25-methyl-1alpha,26-dihydroxyvitamin D3 / 25-methyl-1alpha,26-dihydroxycholecalciferol
(22R)-25-hydroxy-22-methoxyvitamin D3
(22S)-25-hydroxy-22-methoxyvitamin D3
25-hydroxy-3,3-dimethyl-3-deoxy-A-homo-2,4-dioxavitamin D3
1alpha,25-dihydroxy-1beta-methylvitamin D3 / 1alpha,25-dihydroxy-1beta-methylcholecalciferol
1beta,25-dihydroxy-1alpha-methylvitamin D3 / 1beta,25-dihydroxy-1alpha-methylcholecalciferol
1alpha,25-dihydroxy-8(14)a-homovitamin D3 / 1alpha,25-dihydroxy-8(14)a-homocholecalciferol
2beta-methyl-1alpha,25-dihydroxyvitamin D3 / 2beta-methyl-1alpha,25-dihydroxycholecalciferol
2alpha-methyl-3-epi-1alpha,25-dihydroxyvitamin D3 / 2alpha-methyl-3-epi-1alpha,25-dihydroxycholecalciferol
2beta-methyl-3-epi-1alpha,25-dihydroxyvitamin D3 / 2beta-methyl-3-epi-1alpha,25-dihydroxycholecalciferol
2alpha-methyl-1beta,25-dihydroxyvitamin D3 / 2alpha-methyl-1beta,25-dihydroxycholecalciferol
2beta-methyl-1beta,25-dihydroxyvitamin D3 / 2beta-methyl-1beta,25-dihydroxycholecalciferol
2alpha-methyl-3-epi-1beta,25-dihydroxyvitamin D3 / 2alpha-methyl-3-epi-1beta,25-dihydroxycholecalciferol
2beta-methyl-3-epi-1beta,25-dihydroxyvitamin D3 / 2beta-methyl-3-epi-1beta,25-dihydroxycholecalciferol
2alpha-methyl-20-epi-1alpha,25-dihydroxyvitamin D3 / 2alpha-methyl-20-epi-1alpha,25-dihydroxycholecalciferol
2beta-methyl-20-epi-1alpha,25-dihydroxyvitamin D3 / 2beta-methyl-20-epi-1alpha,25-dihydroxycholecalciferol
2alpha-methyl-20-epi-1beta,25-dihydroxyvitamin D3
2beta-methyl-20-epi-1beta,25-dihydroxyvitamin D3 / 2beta-methyl-20-epi-1beta,25-dihydroxycholecalciferol
1alpha,25-dihydroxy-11alpha-methylvitamin D3
1alpha,25-dihydroxy-11beta-methylvitamin D3
1alpha,25-dihydroxy-18-methylvitamin D3 / 1alpha,25-dihydroxy-18-methylcholecalciferol
1alpha,25-dihydroxy-24a-homovitamin D3
(24R)-1alpha,25-dihydroxy-24-methylvitamin D3 /(24R)-1alpha,25-dihydroxy-24-methylcholecalciferol
1alpha,25-dihydroxy-24a-homo-20-epivitamin D3
1alpha,25-dihydroxy-26-methylvitamin D3
2alpha-methyl-1alpha,25-dihydroxyvitamin D3 / 2alpha-methyl-1alpha,25-dihydroxycholecalciferol
1alpha,25-Dihydroxy-2E-ethylidene-19-norvitamin D3
1alpha,25-Dihydroxy-2Z-ethylidene-19-norvitamin D3
20(17->12beta)-abeo-1alpha,25-dihydroxy-24-dihomo-21-norvitamin D3
1-(4-pentylcyclohexyl)-4-[4-(4-propylcyclohexyl)phenyl]benzene
2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R)-1,5-dimethylhexyl]-10,13- dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[ a]phenanthren-3-yl]oxy]ethanol
24-homo-1,25-dihydroxyvitamin D3
D018977 - Micronutrients > D014815 - Vitamins > D004100 - Dihydroxycholecalciferols D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols
2,3-Dihydro-2,3,4,6,7-pentamethyl-2-(4,8,12-trimethyltridecyl)-5-benzofuranol
(2s)-2,5,7,8-Tetramethyl-2-[(4r,8s)-4,8,12-trimethyltridecyl]-3,4-dihydro-2h-chromen-6-ol
(2R)-2,5,7,8-tetramethyl-2-[(4R,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol
Ephanyl
COVID info from COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants D018977 - Micronutrients > D014815 - Vitamins Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS rel-α-Vitamin E (rel-D-α-Tocopherol) is a vitamin with antioxidant properties and also a mixture[1]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].
(22alpha)-hydroxy-sitosterol
(22alpha)-hydroxy-sitosterol belongs to stigmastanes and derivatives class of compounds. Those are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24 (22alpha)-hydroxy-sitosterol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). (22alpha)-hydroxy-sitosterol can be found in a number of food items such as cottonseed, oil-seed camellia, cloves, and dill, which makes (22alpha)-hydroxy-sitosterol a potential biomarker for the consumption of these food products. (22α)-hydroxy-sitosterol belongs to stigmastanes and derivatives class of compounds. Those are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24 (22α)-hydroxy-sitosterol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). (22α)-hydroxy-sitosterol can be found in a number of food items such as cottonseed, oil-seed camellia, cloves, and dill, which makes (22α)-hydroxy-sitosterol a potential biomarker for the consumption of these food products.
4alpha-Hydroxymethyl-4beta-methyl-5alpha-cholest-7-en-3beta-ol
4alpha-Hydroxymethyl-14alpha-methyl-cholesta-8-enol
4beta-Hydroxymethyl-4alpha-methyl-5alpha-cholesta-8-en-3beta-ol
[3-Carboxy-2-(3-hydroxyheptadecanoyloxy)propyl]-trimethylazanium
[3-Carboxy-2-(10-hydroxyheptadecanoyloxy)propyl]-trimethylazanium
[3-Carboxy-2-(11-hydroxyheptadecanoyloxy)propyl]-trimethylazanium
[3-Carboxy-2-(12-hydroxyheptadecanoyloxy)propyl]-trimethylazanium
(8S,9S,10R,13S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
(3S,4S,5S,10S,13R,14R,17R)-3-hydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-4-carboxylic acid
3beta-Hydroxy-5alpha-cholest-7-ene-4alpha-carboxylate
(3S,4R,5R,10R,13R,14R,17R)-4-(Hydroxymethyl)-4,10,13-trimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,5,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol
(22S)-hydroxysitosterol
A stigmastane sterol that is sitosterol substituted by a hydroxy group at position 22S.
3beta-hydroxy-5alpha-cholest-8-ene-4alpha-carboxylic acid
A 3beta-sterol that is 5alpha-cholest-8-en-3beta-ol carrying an additional carboxy substituent at position 4alpha.
4alpha-hydroxymethyl-4beta-methyl-5alpha-8-cholesten-3beta-ol
A 3beta-sterol that is 5alpha-cholest-8-en-3beta-ol carrying hydroxymethyl and methyl substituents at position 4.
4beta-Hydroxymethyl-4alpha-methyl-5alpha-cholest-7-en-3beta-ol
14-(5-ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-5,9-diol
Stigmast-5-ene-3beta,7alpha-diol
A 3beta-hydroxy steroid that is sitosterol substituted by an additional alpha-hydroxy group at position 7. It has been isolated from the roots of Breynia fruticosa.
9-oxo-24-methylene-9,11-seco-cholest-5-en-3beta,11-diol
5alpha,6beta-dihydroxy-24-methylenecholestan-3-one
Alpha-tocopherol
α-Tocopherol (alpha-tocopherol) is a type of vitamin E. Its E number is "E307". Vitamin E exists in eight different forms, four tocopherols and four tocotrienols. All feature a chromane ring, with a hydroxyl group that can donate a hydrogen atom to reduce free radicals and a hydrophobic side chain which allows for penetration into biological membranes. Compared to the others, α-tocopherol is preferentially absorbed and accumulated in humans. Vitamin E is found in a variety of tissues, being lipid-soluble, and taken up by the body in a wide variety of ways. The most prevalent form, α-tocopherol, is involved in molecular, cellular, biochemical processes closely related to overall lipoprotein and lipid homeostasis. Ongoing research is believed to be "critical for manipulation of vitamin E homeostasis in a variety of oxidative stress-related disease conditions in humans."[2] One of these disease conditions is the α-tocopherol role in the use by malaria parasites to protect themselves from the highly oxidative environment in erythrocytes.[3] Stereoisomers α-Tocopherol has three stereocenters, so it is a chiral molecule.[4] The eight stereoisomers of α-tocopherol differ in the configuration of these stereocenters. RRR-α-tocopherol is the natural one.[5] The older name of RRR-α-tocopherol is d-α-tocopherol, but this d/l naming should no longer be used, because whether l-α-tocopherol should mean SSS enantiomer or the SRR diastereomer is not clear, from historical reasons. The SRR may be named 2-epi-α-tocopherol, the diastereomeric mixture of RRR-α-tocopherol and 2-epi-α-tocopherol may be called 2-ambo-α-tocopherol (formerly named dl-α-tocopherol). The mixture of all eight diastereomers is called all-rac-α-tocopherol.[6] One IU of tocopherol is defined as 2⁄3 milligram of RRR-α-tocopherol (formerly named d-α-tocopherol). 1 IU is also defined as 0.9 mg of an equal mix of the eight stereoisomers, which is a racemic mixture, all-rac-α-tocopheryl acetate. This mix of stereoisomers is often called dl-α-tocopheryl acetate.[7] Starting with May 2016, the IU unit is made obsolete, such that 1 mg of "Vitamin E" is 1 mg of d-alpha-tocopherol or 2 mg of dl-alpha-tocopherol.[8] α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2]. α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant[1][2].
n-{1-[6-(dimethylamino)-7,7,12,16-tetramethyltetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadecan-15-yl]ethyl}ethanimidic acid
(1r,3as,3bs,4s,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-4,7-diol
(1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-5a,7-diol
2,16-dimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadecane-3,5-diol
7-amino-10,14,16,20-tetramethyl-23-oxa-18-azahexacyclo[12.11.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁴.0¹⁷,²²]pentacosan-22-ol
C27H46N2O2 (430.35590959999996)
9a,11a-dimethyl-1-(6-methyl-5-methylideneheptan-2-yl)-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-7,9,10-triol
1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-diol
(1s,3as,3br,7s,9ar,9bs,11as)-1-[(2r,3s)-3-hydroxy-6-methyl-5-methylideneheptan-2-yl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-1,7-diol
1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-5,7,9b-triol
(1s,2r,5r,6r,9r,10r,13s,15s)-5-[(2r,5s)-5,6-dimethylheptan-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
(1s,2r,5s,7s,10s,11s,14s,15r,16s,17s,20r,22s,24s)-7-amino-10,14,16,20-tetramethyl-23-oxa-18-azahexacyclo[12.11.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁴.0¹⁷,²²]pentacosan-22-ol
C27H46N2O2 (430.35590959999996)