Exact Mass: 446.37597500000004
Exact Mass Matches: 446.37597500000004
Found 85 metabolites which its exact mass value is equals to given mass value 446.37597500000004,
within given mass tolerance error 1.6E-6 dalton. Try search metabolite list with more accurate mass tolerance error
3.2E-7 dalton.
Stigmastentriol
Stigmastentriol is found in nuts. Stigmastentriol is isolated from Corylus avellana (filbert Isolated from Corylus avellana (filbert). Stigmastentriol is found in nuts.
Schleicherastatin 3
Schleicherastatin 4 is found in fruits. Schleicherastatin 4 is a constituent of the famine food Schleichera oleosa
alpha-Tocopherolquinone
Isolated from spinach (Spinacia oleracea) chloroplasts and many other plant sources. alpha-Tocopherolquinone is found in many foods, some of which are brassicas, spinach, barley, and anise. alpha-Tocopherolquinone is found in anise. alpha-Tocopherolquinone is isolated from spinach (Spinacia oleracea) chloroplasts and many other plant source D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D006401 - Hematologic Agents > D000925 - Anticoagulants D020011 - Protective Agents > D000975 - Antioxidants D-α-Tocopherylquinone (α-Tocopherylquinone) is a quinone, can be isolated from Phaeodactylum tricornutum. D-α-Tocopherylquinone is a oxidation product of α-Tocopherol (vitamin E). D-α-Tocopherylquinone can act as an anticoagulant and as an antioxidant[1][2].
13'-Hydroxy-alpha-tocopherol
13-hydroxy-alpha-tocopherol is the precursor in dehydrogenation to 13-carboxy-alpha-tocopherol by an unidentified microsomal enzyme(s) probably via an aldehyde intermediate. The tocopherols ( a-tocopherol , b-tocopherol ,r-tocopherol and d-tocopherol ) and their corresponding tocotrienols are synthesized by plants and have vitamin E antixoidant activity (see pathway vitamin E biosynthesis ). They differ in the number and location of methyl groups on the chromanol ring. The naturally occurring form of a-tocopherol is (2R,4R,8R)-a-tocopherol (synonym (R,R,R)-a-tocopherol). Synthetic a-tocopherols are a racemic mixture of eight different R and S stereoisomers. Only the 2R forms are recognized as meeting human requirements. The in vivo function of vitamin E is to scavenge peroxyl radicals via its phenolic (chromanol) hydroxyl group, thus protecting lipids against free radical-catalyzed peroxidation. The tocopheryl radical formed can then be reduced by reductants such as L-ascorbate. Other major products of a-tocopherol oxidation include α-tocopherylquinone and epoxy-a-tocopherols. The metabolites a-tocopheronic acid and its lactone, known as the Simon metabolites, are generally believed to be artefacts. In addition to these oxidation products, the other major class of tocopherol metabolites is the carboxyethyl-hydroxychromans.These metabolites are produced in significant amounts in response to excess vitamin E ingestion. Vitamin E is fat-soluble and its utilization requires intestinal fat absorption mechanisms. It is secreted from the intestine into the lymphatic system in chylomicrons which subsequently enter the plasma. Lipolysis of these chylomicrons can result in delivery of vitamin E to tissues, transfer to high-density lipoproteins (and subsequently to other lipoproteins via the phospholipid exchange protein), or retention in chylomicron remnants. These remnants are taken up by the liver. Natural (R,R,R)-α-tocopherol and synthetic 2R-α-tocopherols are then preferentially secreted from the liver into plasma as a result of the specificity of the α-tocopherol transfer protein. This protein, along with the metabolism of excess vitamin E in the liver and excretion into urine and bile, mediate the supply of a-tocopherol in plasma and tissues. 13-hydroxy-alpha-tocopherol is the precursor in dehydrogenation to 13-carboxy-alpha-tocopherol by an unidentified microsomal enzyme(s) probably via an aldehyde intermediate
alpha-tocopherylquinone
D-α-Tocopherylquinone (α-Tocopherylquinone) is a quinone, can be isolated from Phaeodactylum tricornutum. D-α-Tocopherylquinone is a oxidation product of α-Tocopherol (vitamin E). D-α-Tocopherylquinone can act as an anticoagulant and as an antioxidant[1][2].
(24R)-24-ethyl-5alpha-cholestan-3beta,5-diol-6-one|(24R)-3beta,5-dihydroxy-5alpha-stigmastan-6-one|(24R)-3beta,5alpha-dihydroxy-24-ethyl-5alpha-cholestan-6-one|(24R)-3beta,5alpha-dihydroxystigmastan-6-one|3beta,5-dihydroxy-5alpha-stigmastan-6-one|3beta,5alpha-Dihydroxy-6-stigmastanon|stigmastan-3beta,5alpha-diol-6-on
(24S)-29-nor-cycloartane-3beta,24,25-triol|(24S)-29-norcycloartane-3beta,24,25-triol|4alpha,14-dimethyl-9,19-cyclocholestan-3beta,24xi,25-triol
(3S,4S,5R,7S,9R,14R)-3,7-dihydroxy-4,14-dimethyl-7[8->9]-abeo-cholestan-8-one
(2beta,3beta,4alpha,5alpha,8beta)-4-methylergost-24(28)-ene-2,3,8-triol
(3beta,4alpha,5alpha,8beta,11beta)-4-methylergost-24(28)-ene-3,8,11-triol
(20S,24S)-20,24-epoxydammarane-3beta,25-diol|3-epicabraleadiol
24-methylene-27-methylcholestane-3beta,5alpha,6beta-triol
(24Z)-stigmast-24(28)-ene-3beta,5alpha,6beta-triol
(24R)-ethylcholest-5-ene-1alpha,3beta,22alpha(22R)-triol|haloxysterol A
stigmastentriol
Trimina
D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D006401 - Hematologic Agents > D000925 - Anticoagulants D020011 - Protective Agents > D000975 - Antioxidants D-α-Tocopherylquinone (α-Tocopherylquinone) is a quinone, can be isolated from Phaeodactylum tricornutum. D-α-Tocopherylquinone is a oxidation product of α-Tocopherol (vitamin E). D-α-Tocopherylquinone can act as an anticoagulant and as an antioxidant[1][2].
SCHLEICHERASTATIN 3
alpha-Tocopherolquinone
C26170 - Protective Agent > C275 - Antioxidant > C942 - Vitamin E Compound D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D006401 - Hematologic Agents > D000925 - Anticoagulants D020011 - Protective Agents > D000975 - Antioxidants D-α-Tocopherylquinone (α-Tocopherylquinone) is a quinone, can be isolated from Phaeodactylum tricornutum. D-α-Tocopherylquinone is a oxidation product of α-Tocopherol (vitamin E). D-α-Tocopherylquinone can act as an anticoagulant and as an antioxidant[1][2].
13-hydroxy-alpha-tocopherol
A member of the class of chromanols that is (+)-alpha-tocopherol bearing an additional hydroxy substituent at position 13.