Exact Mass: 402.2042
Exact Mass Matches: 402.2042
Found 211 metabolites which its exact mass value is equals to given mass value 402.2042,
within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error
0.0002 dalton.
Citreoviridin A
Citreoviridin A is a metabolite of Penicillium citreo-viride, Penicillium toxicarium, Penicillium ochrosalmoneum and Aspergillus terreus. It is isolated from mouldy rice. Toxin formerly responsible for epidemic-like occurrences of cardiac beriberi in East Asi
Cortisone acetate
Cortisone acetate is a steroid hormone that has both glucocoriticoid and mineral corticoid activities. Corticosteroids are used to provide relief for inflamed areas of the body. They lessen swelling, redness, itching, and allergic reactions. They are often used as part of the treatment for a number of different diseases, such as severe allergies or skin problems, asthma, or arthritis. Endogenous glucocorticoids and some synthetic corticoids have high affinity to the protein transcortin (also called CBG, corticosteroid-binding protein), whereas all of them bind albumin. Glucocorticoids also bind to the cytosolic glucocorticoid receptor. C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones D000893 - Anti-Inflammatory Agents Cortisone acetate (Cortisone 21-acetate), an oxidized metabolite of Cortisol (a Glucocorticoid). Cortisone acetate acts as an immunosuppressant and anti-inflammatory agent. Cortisone acetate can partially intervene in binding of Glucocorticoid to Glucocorticoid-receptor at high concentrations[1][3][4].
Prednisolone Acetate
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid D000893 - Anti-Inflammatory Agents
Virolongin B
Virolongin B is found in herbs and spices. Virolongin B is a constituent of Myristica fragrans (nutmeg). Constituent of Myristica fragrans (nutmeg). Virolongin B is found in herbs and spices.
Melleolide F
Melleolide F is found in mushrooms. Melleolide F is a metabolite of Armillaria mellea (honey mushroom Metabolite of Armillaria mellea (honey mushroom). Melleolide F is found in mushrooms.
Armillyl orsellinate
Armillyl orsellinate is found in mushrooms. Armillyl orsellinate is a metabolite of Armillaria mellea (honey mushroom Metabolite of Armillaria mellea (honey mushroom). Armillyl orsellinate is found in mushrooms.
Citreoviridin C
Citreoviridin C is a mycotoxin produced by the common soil organism Aspergillus terreu
17-Hydroxy-3,11,20-trioxopregn-4-en-21-yl acetate
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones D000893 - Anti-Inflammatory Agents
Citreoviridin
Pred Forte
D000893 - Anti-Inflammatory Agents
Schisanhenol
Schisanhenol is a natural compound solated from Schisandra rubriflora; UGT2B7 UDP-glucuronosyltransferases inhibitor. IC50 value: Target: in vitro: Schisanhenol exhibited strong inhibition toward UGT2B7, with the residual activity to be 7.9\\% of control activity [1]. The BAECs were cultured with ox-LDL (200 microg/ml) in the presence and absence of Sal (10 and 50 micromol L(- 1)) for 24 h. The cytotoxicity of ox-LDL was evaluated by LDH leakage, cell viability and morphological change. Cell apoptosis was estimated by DNA ladder, chromatin condensation, and flow cytometry assay. The intracellular ROS production was detected by using DCF, a ROS probe, with laser confocal microscopy and flow cytometry. Sal was shown to reduce LDH leakage and increase cell viability. Sal also attenuated ox-LDL-induced BAECs apoptosis as indicated in typical internucleosomal DNA degradation (DNA ladder), condensed chromatin, and the sub-G1 peak appearance in flow cytometry assay [2]. in vivo: Sal significantly impeded production of MDA and loss of ATPase activity induced by reoxygenation following anoxia. Oral administration of Sal induced increase of cytosol glutathione-peroxidase of brain in mice under the condition of reoxygenation following anoxia [4]. Schisanhenol is a natural compound solated from Schisandra rubriflora; UGT2B7 UDP-glucuronosyltransferases inhibitor. IC50 value: Target: in vitro: Schisanhenol exhibited strong inhibition toward UGT2B7, with the residual activity to be 7.9\% of control activity [1]. The BAECs were cultured with ox-LDL (200 microg/ml) in the presence and absence of Sal (10 and 50 micromol L(- 1)) for 24 h. The cytotoxicity of ox-LDL was evaluated by LDH leakage, cell viability and morphological change. Cell apoptosis was estimated by DNA ladder, chromatin condensation, and flow cytometry assay. The intracellular ROS production was detected by using DCF, a ROS probe, with laser confocal microscopy and flow cytometry. Sal was shown to reduce LDH leakage and increase cell viability. Sal also attenuated ox-LDL-induced BAECs apoptosis as indicated in typical internucleosomal DNA degradation (DNA ladder), condensed chromatin, and the sub-G1 peak appearance in flow cytometry assay [2]. in vivo: Sal significantly impeded production of MDA and loss of ATPase activity induced by reoxygenation following anoxia. Oral administration of Sal induced increase of cytosol glutathione-peroxidase of brain in mice under the condition of reoxygenation following anoxia [4].
(2R,3S,4As,7R,8R,8aS)-2,3,4'-trihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-3H-1-benzofuran]-6',7'-dicarbaldehyde
gomisin K3
Schisanhenol is a natural product found in Schisandra rubriflora, Schisandra bicolor, and other organisms with data available. See also: Schisandra chinensis fruit (part of). Schisanhenol is a natural compound solated from Schisandra rubriflora; UGT2B7 UDP-glucuronosyltransferases inhibitor. IC50 value: Target: in vitro: Schisanhenol exhibited strong inhibition toward UGT2B7, with the residual activity to be 7.9\\% of control activity [1]. The BAECs were cultured with ox-LDL (200 microg/ml) in the presence and absence of Sal (10 and 50 micromol L(- 1)) for 24 h. The cytotoxicity of ox-LDL was evaluated by LDH leakage, cell viability and morphological change. Cell apoptosis was estimated by DNA ladder, chromatin condensation, and flow cytometry assay. The intracellular ROS production was detected by using DCF, a ROS probe, with laser confocal microscopy and flow cytometry. Sal was shown to reduce LDH leakage and increase cell viability. Sal also attenuated ox-LDL-induced BAECs apoptosis as indicated in typical internucleosomal DNA degradation (DNA ladder), condensed chromatin, and the sub-G1 peak appearance in flow cytometry assay [2]. in vivo: Sal significantly impeded production of MDA and loss of ATPase activity induced by reoxygenation following anoxia. Oral administration of Sal induced increase of cytosol glutathione-peroxidase of brain in mice under the condition of reoxygenation following anoxia [4]. Schisanhenol is a natural compound solated from Schisandra rubriflora; UGT2B7 UDP-glucuronosyltransferases inhibitor. IC50 value: Target: in vitro: Schisanhenol exhibited strong inhibition toward UGT2B7, with the residual activity to be 7.9\% of control activity [1]. The BAECs were cultured with ox-LDL (200 microg/ml) in the presence and absence of Sal (10 and 50 micromol L(- 1)) for 24 h. The cytotoxicity of ox-LDL was evaluated by LDH leakage, cell viability and morphological change. Cell apoptosis was estimated by DNA ladder, chromatin condensation, and flow cytometry assay. The intracellular ROS production was detected by using DCF, a ROS probe, with laser confocal microscopy and flow cytometry. Sal was shown to reduce LDH leakage and increase cell viability. Sal also attenuated ox-LDL-induced BAECs apoptosis as indicated in typical internucleosomal DNA degradation (DNA ladder), condensed chromatin, and the sub-G1 peak appearance in flow cytometry assay [2]. in vivo: Sal significantly impeded production of MDA and loss of ATPase activity induced by reoxygenation following anoxia. Oral administration of Sal induced increase of cytosol glutathione-peroxidase of brain in mice under the condition of reoxygenation following anoxia [4].
4-methoxy-5-methyl-6-[(2S,3S)-2-methyl-3-[(2Z,4E)-4-methyl-5-[(1S,2S,4R,5R)-1,2,4-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-4-yl]penta-2,4-dien-2-yl]oxiran-2-yl]pyran-2-one
15beta-hydroxy-5,6-dehydrocalotropin|5,6-dehydrocalotropagenin
(+)-gomisin K2|(-)-gomisin K1|gomisin J|Gomisin K1|Gomisin K2
14alpha-hydroxy-7alpha-ethoxy-11,16-diketo-apian-8-en-(20,6)-olide
(8S,8S)-3,4-methylenedioxy-3,4,9,9-tetramethoxylignan|5-demethoxyniranthin
17-nor-15-oxo-8,11,13-abietatrien-7alpha-hydroxy-18-butanedioic acid|abiesanordine M
3alpha-isovaleryloxyleysseral (2-methylbutyrate)|3alpha-isovaleryloxyleysseral <2-methylbutyrate>
2-(2,5-dimethoxyphenyl) tetrahydro-3,4-dimethyl-5-(3,4,5-trimethoxyphenyl)furan
6,12,14-trihydroxy-9alpha-(2-oxopropyl)abieta-5,8(14),12-triene-7,11-dione
(1S,3R,4S)-1-{2,6-dihydroxy-4-[(1S,2R)-2-hydroxy-1-methylpropyl]-3-methylphenyl}-3,4-dihydro-3,4,5-trimethyl-1H-2-benzopyran-6,8-diol|penidicitrinin B
(1R,2R,4E)-1,5-bis(3,4-dimethoxyphenyl)-2-(methoxymethyl)pent-4-en-1-ol
Cortisone acetate
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones D000893 - Anti-Inflammatory Agents Cortisone acetate (Cortisone 21-acetate), an oxidized metabolite of Cortisol (a Glucocorticoid). Cortisone acetate acts as an immunosuppressant and anti-inflammatory agent. Cortisone acetate can partially intervene in binding of Glucocorticoid to Glucocorticoid-receptor at high concentrations[1][3][4].
6-[(1E,3E,5E,7E)-8-[(2R,3S,4S,5S)-3,4-dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-3-methylpyran-2-one
C23H30O6_2,4,6-Octatrienoic acid, (5aS,9aS,9bS)-1,3,5,5a,6,7,8,9,9a,9b-decahydro-3,9b-dihydroxy-6,6,9a-trimethyl-1-oxonaphtho[1,2-c]furan-5-yl ester, (2E,4E,6E)
C23H30O6_2-Formyl-1-hydroxy-5,5,8a-trimethyl-4-[(2E,4E,6E)-2,4,6-octatrienoyloxy]-1,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid
Citreoviridin
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D001313 - Aurovertins
6-[(1E,3E,5E,7E)-8-[(2R,3S,4S,5S)-3,4-dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-3-methylpyran-2-one [IIN-based on: CCMSLIB00000848362]
6-[(1E,3E,5E,7E)-8-[(2R,3S,4S,5S)-3,4-dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-3-methylpyran-2-one [IIN-based: Match]
Citreoviridin C
melleolide F
A sesquiterpenoid resulting from the formal condensation of the carboxy group of o-orsellinic acid with the 2-hydroxy group of (2R,2aS,4aS,7aS,7bR)-3-(hydroxymethyl)-6,6,7b-trimethyl-1,2,4a,5,6,7,7a,7b-octahydro-2aH-cyclobuta[e]indene-2,2a-diol. It is a metabolite isolated from the fungus Armillaria mellea.
Armillyl orsellinate
ST 23:5;O6
C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C308 - Immunotherapeutic Agent > C574 - Immunosuppressant > C211 - Therapeutic Corticosteroid D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones D000893 - Anti-Inflammatory Agents Cortisone acetate (Cortisone 21-acetate), an oxidized metabolite of Cortisol (a Glucocorticoid). Cortisone acetate acts as an immunosuppressant and anti-inflammatory agent. Cortisone acetate can partially intervene in binding of Glucocorticoid to Glucocorticoid-receptor at high concentrations[1][3][4].
Pregn-4-en-18-al,21-(acetyloxy)-11-hydroxy-3,20-dioxo-, (11b)-
Pregn-4-ene-3,20-dione,21-(acetyloxy)-9,11-epoxy-17-hydroxy-, (9b,11b)-
(2R,3S,4As,7R,8R,8aS)-2,3,4'-trihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-3H-1-benzofuran]-6',7'-dicarbaldehyde
2H-Pyran-2-one, 4-methoxy-3-methyl-6-[7-methyl-8-(tetrahydro-3,4-dihydroxy-2,4,5-trimethyl-2-furanyl)-1,3,5,7-octatetraenyl]-, [2R-[2alpha(1E,3E,5E,7E),3beta,4alpha,5alpha]]-
6-[(1E,3E,5E,7Z)-8-[(2S,3R,4R,5R)-3,4-dihydroxy-2,4,5-trimethyloxolan-2-yl]-7-methylocta-1,3,5,7-tetraenyl]-4-methoxy-5-methylpyran-2-one
(9s,10r)-3,4,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-5-ol
(3r,3as,4r,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-7-oxo-2,3a,4,8-tetrahydro-1h-azulen-4-yl 4-hydroxy-3-methoxybenzoate
(9s,10r)-4,5,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-3-ol
methyl (1s,2s)-2,10-dimethyl-5-[(2s)-2-methyloctanoyl]-4-oxo-3,11-dioxatricyclo[6.4.0.0²,⁶]dodeca-5,7,9-triene-7-carboxylate
(3r,3as,4s,8r,8as)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-7-oxo-2,3a,4,8-tetrahydro-1h-azulen-4-yl 4-methoxybenzoate
methyl (1s,4as,5s,8ar)-4a-[(acetyloxy)methyl]-5-[2-(furan-3-yl)-2-oxoethyl]-1-methyl-6-methylidene-hexahydro-2h-naphthalene-1-carboxylate
5-(2,5-dihydroxyphenyl)-5-ethoxy-3-[(3e,7z)-9-hydroxy-4,8-dimethylnona-3,7-dien-1-yl]furan-2-one
methyl 5-(acetyloxy)-3,6,14-trimethyl-2-oxo-4h,5h,8h,9h,12h,13h,15ah-cyclotetradeca[b]furan-10-carboxylate
(7r,8r)-7-hydroxy-3,7-dimethyl-6-oxo-8-[(3e)-2-oxoundec-3-en-1-yl]-8h-isochromene-5-carboxylic acid
(1r,3as,3br,7r,8r,9as,9bs,11ar)-3a,7,8-trihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-1h,2h,3h,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-9a-carbaldehyde
4-[(3as,3br,5ar,7s,8s,9as,9bs,11ar)-3a,7,8-trihydroxy-9a,11a-dimethyl-10-oxo-3h,3bh,4h,5h,5ah,6h,7h,8h,9h,9bh,11h-cyclopenta[a]phenanthren-1-yl]-5h-furan-2-one
[(1s,2r,3r)-1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-3-(methoxymethyl)-1,2,3,4-tetrahydronaphthalen-2-yl]methanol
11-(2,6-dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one
(1s,3s,6s,10r,12r,13z)-15-hydroxy-3,10,12,14-tetramethyl-17,19-dioxo-18-oxatricyclo[14.2.1.0¹,⁶]nonadeca-4,13,15-triene-4-carboxylic acid
1,3-dimethoxy-5-(prop-2-en-1-yl)-2-{[(2s)-1-(3,4,5-trimethoxyphenyl)propan-2-yl]oxy}benzene
1-{3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl}ethyl 3-methylbutanoate
(2r,3s)-6-({2,6-dihydroxy-4-[(2s,3r)-3-hydroxybutan-2-yl]-3-methylphenyl}methyl)-2,3,4-trimethyl-2,3-dihydro-1-benzofuran-5,7-diol
16-dehydrostrophanthidin
{"Ingredient_id": "HBIN001849","Ingredient_name": "16-dehydrostrophanthidin","Alias": "NA","Ingredient_formula": "C23H30O6","Ingredient_Smile": "CC12CCC3C(C1(CC=C2C4=CC(=O)OC4)O)CCC5(C3(CCC(C5)O)C=O)O","Ingredient_weight": "402.5 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "4971","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "23417","DrugBank_id": "NA"}
5-demethoxyniranthin
{"Ingredient_id": "HBIN011510","Ingredient_name": "5-demethoxyniranthin","Alias": "NA","Ingredient_formula": "C23H30O6","Ingredient_Smile": "COCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC(=C(C=C3)OC)OC)COC","Ingredient_weight": "402.5 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "5051","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "10971435","DrugBank_id": "NA"}
7,14-dihydroxy-11,16-dioxo-8-apianen-20,6-olide; (6β,7α,14α)-form,7-et ether
{"Ingredient_id": "HBIN012871","Ingredient_name": "7,14-dihydroxy-11,16-dioxo-8-apianen-20,6-olide; (6\u03b2,7\u03b1,14\u03b1)-form,7-et ether","Alias": "NA","Ingredient_formula": "C23H30O6","Ingredient_Smile": "NA","Ingredient_weight": "402.48","OB_score": "NA","CAS_id": "213907-85-8","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "7494","PubChem_id": "NA","DrugBank_id": "NA"}
