Exact Mass: 460.3916242
Exact Mass Matches: 460.3916242
Found 271 metabolites which its exact mass value is equals to given mass value 460.3916242,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Betulafolienetriol
Protopanaxadiol is found in tea. Sapogenin of Ginsenosides Rb1, Rb2 and Re from Panax ginseng (ginseng) Protopanaxadiol (PPD) is an organic coumpound characterizing a group of ginsenosides. It is a dammarane-type tetracyclic terpene sapogenin found in ginseng (Panax ginseng) and in notoginseng (Panax pseudoginseng) (20S)-protopanaxadiol is a diastereomer of protopanaxadiol in which the 20-hydroxy substituent has been introduced at the pro-S position. (20S)-Protopanaxadiol is a natural product found in Gynostemma pentaphyllum, Panax ginseng, and Aralia elata with data available. 20S-protopanaxadiol (aPPD) is a metabolite of ginseng saponins, inhibits Akt activity and induces apoptosis in various tumor cells[1]. 20S-protopanaxadiol (aPPD) is a metabolite of ginseng saponins, inhibits Akt activity and induces apoptosis in various tumor cells[1].
5-Pentacosyl-1,3-benzenediol
Constituent of cereal grains. 5-Pentacosyl-1,3-benzenediol is found in many foods, some of which are barley, common wheat, pasta, and breakfast cereal. 5-Pentacosyl-1,3-benzenediol is found in barley. 5-Pentacosyl-1,3-benzenediol is a constituent of cereal grains.
(3beta,5alpha,6beta,9alpha,22E,24R)-23-Methylergosta-7,22-diene-3,5,6,9-tetrol
(3beta,5alpha,6beta,9alpha,22E,24R)-23-Methylergosta-7,22-diene-3,5,6,9-tetrol is found in mushrooms. (3beta,5alpha,6beta,9alpha,22E,24R)-23-Methylergosta-7,22-diene-3,5,6,9-tetrol is a constituent of Lentinula edodes (shiitake). Constituent of Lentinula edodes (shiitake). (3beta,5alpha,6beta,9alpha,22E,24R)-23-Methylergosta-7,22-diene-3,5,6,9-tetrol is found in mushrooms.
(3beta,24xi)-Cycloartane-3,24,25-triol
(3beta,24xi)-Cycloartane-3,24,25-triol is found in fruits. (3beta,24xi)-Cycloartane-3,24,25-triol is a constituent of Mangifera indica (mango) Constituent of Mangifera indica (mango). (3b,24x)-Cycloartane-3,24,25-triol is found in fruits.
(3beta,11alpha,13beta)-3,11,13-Oleananetriol
(3beta,11alpha,13beta)-3,11,13-Oleananetriol is found in nuts. (3beta,11alpha,13beta)-3,11,13-Oleananetriol is a constituent of Pistacia vera (pistachio) Constituent of Pistacia vera (pistachio). (3beta,11alpha,13beta)-3,11,13-Oleananetriol is found in nuts.
Panaxadiol
Panaxadiol is found in tea. Panaxadiol is present in ginsen Present in ginseng. Panaxadiol is found in tea. Panaxadiol (20(R)-Panaxadiol) is an orally active HIF-1α/STAT3 inhibitor. Panaxadiol can suppress HIF-1α and STAT3 then lead to downregulation of programmed cell death-ligand 1 (PD-L1) expression. Panaxadiol shows anticancer, cardioprotective, anti-arrhythmic, and antioxidative activities[1][2]. Panaxadiol (20(R)-Panaxadiol) is an orally active HIF-1α/STAT3 inhibitor. Panaxadiol can suppress HIF-1α and STAT3 then lead to downregulation of programmed cell death-ligand 1 (PD-L1) expression. Panaxadiol shows anticancer, cardioprotective, anti-arrhythmic, and antioxidative activities[1][2]. Panaxadiol (20(R)-Panaxadiol) is an orally active HIF-1α/STAT3 inhibitor. Panaxadiol can suppress HIF-1α and STAT3 then lead to downregulation of programmed cell death-ligand 1 (PD-L1) expression. Panaxadiol shows anticancer, cardioprotective, anti-arrhythmic, and antioxidative activities[1][2].
Schleicherastatin 2
Schleicherastatin 1 is found in fruits. Schleicherastatin 1 is a constituent of the famine food Schleichera oleosa Constituent of the famine food Schleichera oleosa. Schleicherastatin 2 is found in fruits.
13'-Carboxy-alpha-tocopherol
13-carboxy-alpha-tocopherol is a dehydrogenation carboxylate product of 13-hydroxy-a-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-carboxy-alpha-tocopherol is a dehydrogenation carboxylate product of 13-hydroxy-a-tocopherol by an unidentified microsomal enzyme(s) probably via an aldehyde intermediate
N,N,N',N'-Tetracyclohexyl-3-oxapentanediamide
Lexacalcitol
Nephrin
Ocotillol
2-Deoxy-25-Methyldolichosterone
2-deoxy-25-methyldolichosterone belongs to trihydroxy bile acids, alcohols and derivatives class of compounds. Those are prenol lipids structurally characterized by a bile acid or alcohol which bears three hydroxyl groups. 2-deoxy-25-methyldolichosterone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 2-deoxy-25-methyldolichosterone can be found in common bean, green bean, and yellow wax bean, which makes 2-deoxy-25-methyldolichosterone a potential biomarker for the consumption of these food products.
3-epi-2-Deoxy-25-methyldolichosterone
3-epi-2-deoxy-25-methyldolichosterone belongs to trihydroxy bile acids, alcohols and derivatives class of compounds. Those are prenol lipids structurally characterized by a bile acid or alcohol which bears three hydroxyl groups. 3-epi-2-deoxy-25-methyldolichosterone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 3-epi-2-deoxy-25-methyldolichosterone can be found in common bean, green bean, and yellow wax bean, which makes 3-epi-2-deoxy-25-methyldolichosterone a potential biomarker for the consumption of these food products.
25-Hydroxy-24-methoxycycloartanol
25-hydroxy-24-methoxycycloartanol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 25-hydroxy-24-methoxycycloartanol can be found in rice, which makes 25-hydroxy-24-methoxycycloartanol a potential biomarker for the consumption of this food product.
Protopanaxadiol
(20R)-protopanaxadiol is a diastereomer of protopanaxadiol in which the 20-hydroxy substituent has been introduced at the pro-R position. 20(R)-Protopanaxadiol is a natural product found in Panax ginseng with data available. A diastereomer of protopanaxadiol in which the 20-hydroxy substituent has been introduced at the pro-R position. (20S)-protopanaxadiol is a diastereomer of protopanaxadiol in which the 20-hydroxy substituent has been introduced at the pro-S position. (20S)-Protopanaxadiol is a natural product found in Gynostemma pentaphyllum, Panax ginseng, and Aralia elata with data available. A diastereomer of protopanaxadiol in which the 20-hydroxy substituent has been introduced at the pro-S position. (20R)-Protopanaxadiol is a triterpenoid saponin metabolite of 20(R)-ginsenoside Rg3 in black ginseng. (20R)-Protopanaxadiol exhibits anti-tumor activity and cytotoxicity, and potently inhibits the growth of Helicobacter pylori[1][2][3]. (20R)-Protopanaxadiol is a triterpenoid saponin metabolite of 20(R)-ginsenoside Rg3 in black ginseng. (20R)-Protopanaxadiol exhibits anti-tumor activity and cytotoxicity, and potently inhibits the growth of Helicobacter pylori[1][2][3]. 20S-protopanaxadiol (aPPD) is a metabolite of ginseng saponins, inhibits Akt activity and induces apoptosis in various tumor cells[1]. 20S-protopanaxadiol (aPPD) is a metabolite of ginseng saponins, inhibits Akt activity and induces apoptosis in various tumor cells[1].
Panaxadiol
Panaxadiol is a triterpenoid saponin. Panaxadiol is a natural product found in Panax ginseng with data available. Panaxadiol (20(R)-Panaxadiol) is an orally active HIF-1α/STAT3 inhibitor. Panaxadiol can suppress HIF-1α and STAT3 then lead to downregulation of programmed cell death-ligand 1 (PD-L1) expression. Panaxadiol shows anticancer, cardioprotective, anti-arrhythmic, and antioxidative activities[1][2]. Panaxadiol (20(R)-Panaxadiol) is an orally active HIF-1α/STAT3 inhibitor. Panaxadiol can suppress HIF-1α and STAT3 then lead to downregulation of programmed cell death-ligand 1 (PD-L1) expression. Panaxadiol shows anticancer, cardioprotective, anti-arrhythmic, and antioxidative activities[1][2]. Panaxadiol (20(R)-Panaxadiol) is an orally active HIF-1α/STAT3 inhibitor. Panaxadiol can suppress HIF-1α and STAT3 then lead to downregulation of programmed cell death-ligand 1 (PD-L1) expression. Panaxadiol shows anticancer, cardioprotective, anti-arrhythmic, and antioxidative activities[1][2].
hopan-1beta,3beta,22-triol|hopane-1beta,3beta,22-triol
(3aS)-4c,7t-Dihydroxy-5at,5bc,8,8,11ac,13bt-hexamethyl-3t-(alpha-hydroxy-isopropyl)-(3arH,7atH,11btH,13acH)-eicosahydro-1H-cyclopenta[a]chrysen|21betaH-17(22=>21)-Abeo-gammacerantriol-(6alpha,16beta,22)|3alphaH-5(4=>3)-Abeo-gammacerantriol-(4,6alpha,16beta)|A-neo-gammaceranetriol-(6alpha,16beta,22)|A-Neo-gammacerantriol-(6alpha,16beta,22)|A-Neo-gammacerantriol-(6alpha,16beta,22); Leucotylin|leucotylin
cholest-5-ene-1alpha,3beta,11alpha-triol 11-acetate
(24S)-5alpha-lanost-9(11)-ene-3beta,24,25-triol|(24S)-lanost-9(11)-ene-3beta,24,25-triol|lanost-9(11)-ene-3beta,24S,25-triol
12-Ac 鈥樎?2alpha-24,25-Epoxy-20,24-dimethyl-12,24-scalaranediol
17,24-epoxy-20alpha,25-dihydroxy-21-norbaccharan-3-one
A natural product found in Aglaia foveolata.
(24R)-24,25-epoxysunpollenol|(24R)-4-hydroxy-3,4-seco-19(10->9)-abeo-8alpha,9beta,10alpha-tirucallane-3,5beta:24,25-dioxide
(3beta)-lupane-3,20,28-triol|lupane-3beta,20,28-triol
Dammar-24-en-3alpha,17alpha,20-triol|Dammar-24-ene-3,17,20-triol-(3alpha,17alphaOH,20S)-form|dammar-24-ene-3alpha, 17alpha, 20(S)-triol|dammar-24-ene-3alpha,17alpha,20(S)-triol|Triterpen A
(3beta,17(21)E,22R,23R,24R)-23-Methylrgosta-5,17-diene-3,22,23,25-tetrol
7beta,15alpha,22-trihydroxyhopane
A hopanoid that is hopane substituted by hydroxy groups at positions 7, 15 and 22 respectively (the 7beta,15alpha-stereoisomer). It has been isolated from Hypocrella species.
(13alpha,14beta,17alpha,20R)-20,25-dihydroxylanostan-3-one|20alpha,25-dihydroxytirucall-3-one|mesendanin R
(3S,8S,9R,10S,13S,14R,17S,21R)-3,21,22-trihydroxy-D:B-friedobacchar-5-ene|leonatriol
(17R)-19(18?17)-abeo-3alpha,18beta,23,24-tetrahydroxy-28-norolean-12-ene|stewertiisin A
cholesta-5-en-3beta,7beta,19-triol 19-acetate|nebrosteroid N
1-O-Hexadecyl-2-O,3-O-di(trimethylsilyl)glycerol
C25H56O3Si2 (460.37677859999997)
3beta,16(S),20(R)-trihydroxydammar-24-ene|3beta,16beta,20(R),25-trihydroxydammar-24-ene
Serratan-3beta,14beta,21alpha-triol, Tohogenol|Tohogenol
4,4,6a,6b,10,10,12a,14b-Octamethyldocosahydro-2,3,9-picenetriol #
(3beta,4alpha,5alpha,22E,24R)-3,11-Dihydroxy-4,23-dimethyl-9,11-secoergost-22-en-9-one
1α-hydroxy-2β-(2-hydroxyethoxy)vitamin D3 / 1α-hydroxy-2β-(2-hydroxyethoxy)cholecalciferol
(5Z,7E)-(1S,3R,20S)-20-methoxy-24a-homo-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R)-24a,24b,24c-trihomo-22-oxa-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R)-26,27-dimethyl-24a-homo-22-oxa-9,10-seco-5,7,10(19)-cholestatrien-1,3,25-triol
(5Z,7E)-(1S,3R)-20,26,27-trimethyl-23-oxa-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,20R)-26,27-dimethyl-24a-homo-22-oxa-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,11S)-11-(2-hydroxyethyl)-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,11R)-11-(2-hydroxyethyl)-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,20R,22R)-24a,24b-dihomo-9,10-seco-5,7,10(19)-cholestatriene-1,3,22,25-tetrol
(5Z,7E)-(1S,3R,20S)-24a,24b-dihomo-9,10-seco-5,7,10(19)-cholestatriene-1,3,20,25-tetrol
(5Z,7E)-(1S,3R,20S)-26,27-dimethyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,20,25-tetrol
(5Z,7E)-(1S,3R,20R,22R)-26,27-dimethyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,22,25-tetrol
(5Z,7E)-(1S,3R,22S)-26,27-dimethyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,22,25-tetrol
(5Z,7E)-(1S,3R,20S)-26,27-dimethyl-24a-homo-9,10-seco-5,7,10(19)-cholestatriene-1,3,20,25-tetrol
(5Z,7E)-(1S,3R)-18-(5-hydroxy-5-methylhexyloxy)-23,24-dinor-9,10-seco-5,7,10(19)-cholatriene-1,3-diol
protopanaxadiol
A tetracyclic triterpenoid sapogenin (isolated from ginseng) that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 positions and in which a double bond has been introduced at the 24-25 position.
(3beta,5alpha,6beta,9alpha,22E,24R)-23-Methylergosta-7,22-diene-3,5,6,9-tetrol
(3beta,11alpha,13beta)-3,11,13-Oleananetriol
Betulafolientriol
Schleicherastatin 2
(3beta,24xi)-Cycloartane-3,24,25-triol
Panaxol
1alpha-hydroxy-2beta-(2-hydroxyethoxy)vitamin D3
(20S)-1alpha,25-dihydroxy-20-methoxy-24a-homovitamin D3
1alpha,25-dihydroxy-24a,24b,24c-trihomo-22-oxavitamin D3
1alpha,25-dihydroxy-26,27-dimethyl-24a-homo-22-oxavitamin D3 / 1alpha,25-dihydroxy-26,27-dimethyl-24a-homo-22-oxacholecalciferol
1alpha,25-dihydroxy-20,26,27-trimethyl-23-oxavitamin D3 / 1alpha,25-dihydroxy-20,26,27-trimethyl-23-oxacholecalciferol
1alpha,25-dihydroxy-26,27-dimethyl-24a-homo-22-oxa-20-epivitamin D3
1alpha,25-dihydroxy-11alpha-(2-hydroxyethyl)vitamin D3
1alpha,25-dihydroxy-11beta-(2-hydroxyethyl)vitamin D3
(22R)-1alpha,22,25-trihydroxy-24a,24b-dihomo-20-epivitamin D3
(20S)-1alpha,20,25-trihydroxy-24a,24b-dihomovitamin D3
(20S)-14alpha,20,25-trihydroxy-26,27-dimethylvitamin D3
(20S)-1alpha,20,25-trihydroxy-26,27-dimethyl-24a-homovitamin D3
13-carboxychromanol
Lexacalcitol
D018977 - Micronutrients > D014815 - Vitamins > D004100 - Dihydroxycholecalciferols D018977 - Micronutrients > D014815 - Vitamins > D006887 - Hydroxycholecalciferols D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents D000970 - Antineoplastic Agents
2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl stearate
cabraleadiol
A tetracyclic triterpenoid isolated from Aglaia abbreviata.
1-Hexadecyl-2,3-ditrimethylsilylglycerol
C25H56O3Si2 (460.37677859999997)
(5Z)-5-[(2E)-2-[1-[1-(4-ethyl-4-hydroxyhexoxy)ethyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
Hopane-6Beta,7Beta,22-Triol
A hopanoid that is hopane substituted by hydroxy groups at positions 6, 7 and 22 (the 6beta,7beta-stereoisomer). It has been isolated from Conoideocrella tenuis.
3Beta,15Alpha,22-Trihydroxyhopane
A hopanoid that is hopane substituted by hydroxy groups at positions 3, 15 and 22 respectively (the (3beta,15alpha-stereoisomer). It has been isolated from Hypocrella species.
(1R,2R,5S,8S,10R,11S,14R,15R,20R)-5-hydroxy-8-(2-hydroxypropan-2-yl)-1,2,15,19,19-pentamethyl-9-oxapentacyclo[12.8.0.02,11.05,10.015,20]docosan-18-one
(3R,8R,10R,14R)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
(1-hydroxy-3-octoxypropan-2-yl) (3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoate
[1-hydroxy-3-[(3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoxy]propan-2-yl] octanoate
[1-hydroxy-3-[(9Z,12Z,15Z,18Z,21Z)-tetracosa-9,12,15,18,21-pentaenoxy]propan-2-yl] acetate
[1-hydroxy-3-[(5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenoxy]propan-2-yl] hexanoate
[1-[(7Z,10Z,13Z,16Z,19Z)-docosa-7,10,13,16,19-pentaenoxy]-3-hydroxypropan-2-yl] butanoate
[3-carboxy-2-[(9E,11E,13E,15E,17E)-henicosa-9,11,13,15,17-pentaenoyl]oxypropyl]-trimethylazanium
C28H46NO4+ (460.34266560000003)
[1-Carboxy-3-(2-hydroxy-3-pentadecanoyloxypropoxy)propyl]-trimethylazanium
C25H50NO6+ (460.36379400000004)
DG(26:5)
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WE(31:3)
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