Exact Mass: 296.065854
Exact Mass Matches: 296.065854
Found 106 metabolites which its exact mass value is equals to given mass value 296.065854,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Aspulvinone E
A 4-hydroxy-5-(4-hydroxybenzylidene)-3-(4-hydroxyphenyl)furan-2(5H)-one in which the double bond adopts a Z-configuration. It is a marine metabolite isolated from the fungus Aspergillus terreus and exhibits antiviral activity.
N-Methoxyspirobrassinol methyl ether
N-Methoxyspirobrassinol methyl ether is found in brassicas. N-Methoxyspirobrassinol methyl ether is a stress metabolite from Japanese daikon radish inoculated with Pseudomonas cichorii. Stress metabolite from Japanese daikon radish inoculated with Pseudomonas cichorii. N-Methoxyspirobrassinol methyl ether is found in brassicas and radish.
Gyrocyanin
Gyrocyanin is found in mushrooms. Gyrocyanin is a constituent of the mushroom Gyroporus cyanescens (cornflower bolete). Constituent of the mushroom Gyroporus cyanescens (cornflower bolete). Gyrocyanin is found in mushrooms.
Trifluridine
Trifluridine is only found in individuals that have used or taken this drug. It is an antiviral derivative of thymidine used mainly in the treatment of primary keratoconjunctivitis and recurrent epithelial keratitis due to herpes simplex virus. (From Martindale, The Extra Pharmacopoeia, 30th ed, p557)The mechanism of action of trifluridine has not been fully determined, but appears to involve the inhibition of viral replication. Trifluridine does this by incorporating into viral DNA during replication, which leads to the formation of defective proteins and an increased mutation rate. This drug also reversibly inhibits thymidylate synthetase, an enzyme that is necessary for DNA synthesis. C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite S - Sensory organs > S01 - Ophthalmologicals > S01A - Antiinfectives > S01AD - Antivirals D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D009676 - Noxae > D000963 - Antimetabolites Trifluridine (Trifluorothymidine) is an irreversible and orally active thymidylate synthase inhibitor, and thereby suppressing DNA synthesis. Trifluridine is an antiviral molecule used for research of HSV, rhabdovirus and orthopoxvirus infection. Trifluridine induces cell apoptosis and autophagy. Trifluridine is also an anticancer agent used in studies of metastatic colorectal cancer, gastrointestinal tumors[1][2][3][4].
Anhydropisatin
Anhydropisatin is a member of the class of compounds known as pterocarpans. Pterocarpans are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. Thus, anhydropisatin is considered to be a flavonoid lipid molecule. Anhydropisatin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Anhydropisatin can be found in common pea, which makes anhydropisatin a potential biomarker for the consumption of this food product.
2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-carbaldehyde
(2S)-2-[(beta-D-Glucopyranosyl)oxy]butanedioic acid
7-hydroxy-3-[6-hydroxyphenyl-2-oxo-ethyl]chromone|terminalianone
6-O-(1-L-maloyl)-alpha/beta-D-glucopyranose|veracylglucan A
(2-Oxo-2H-chromen-7-yloxy)-phenyl-acetic acid
3-(2,3-Dihydro-1,4-benzodioxin-6-yl)-7-hydroxy-chromen-2-one
Aspulvinone E - Yellow pigment - Found in Aspergillus
Trifluridine
C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite S - Sensory organs > S01 - Ophthalmologicals > S01A - Antiinfectives > S01AD - Antivirals D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D009676 - Noxae > D000963 - Antimetabolites Trifluridine (Trifluorothymidine) is an irreversible and orally active thymidylate synthase inhibitor, and thereby suppressing DNA synthesis. Trifluridine is an antiviral molecule used for research of HSV, rhabdovirus and orthopoxvirus infection. Trifluridine induces cell apoptosis and autophagy. Trifluridine is also an anticancer agent used in studies of metastatic colorectal cancer, gastrointestinal tumors[1][2][3][4].
N-Methoxyspirobrassinol methyl ether
2-(5-bromo-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Octamethylcyclotetrasiloxane
D001697 - Biomedical and Dental Materials D007155 - Immunologic Factors
(6R,7R)-7-Amino-3-[(5-methyl-2H-tetrazol-2-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C10H12N6O3S (296.06915620000007)
2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
1-[4-(3-TRIFLUOROMETHOXY-PHENOXY)-PHENYL]-ETHANONE
1-[4-(4-TRIFLUOROMETHOXY-PHENOXY)-PHENYL]-ETHANONE
3-(4-ACETYL-PHENYL)-2-MERCAPTO-3H-QUINAZOLIN-4-ONE
Benzo[b]thiophene-2-carboximidamide, 6-(benzoyloxy)-
1,1-[Carbonylbis(oxy)]bis(1H-benzotriazole)
C13H8N6O3 (296.06578579999996)
(1-(N,N-DIMETHYLSULFAMOYL)-3-(PYRIDIN-2-YL)-1H-PYRAZOL-4-YL)BORONIC ACID
C10H13BN4O4S (296.07505280000004)
2,2-dimethyl-6,6,7,7,8,8,8-heptafluoro-3,5-octanedione
C10H11F7O2 (296.06472299999996)
2,4,6-Cycloheptatrien-1-one,3-[3-(1,3-benzodioxol-5-yl)-1-oxo-2-propen-1-yl]-2-hydroxy-
ethyl 4-chloro-6,7-dimethoxyquinazoline-2-carboxylate
2,6-Diamino-4-pyrimidinyl p-Toluenesulfonate 3-Oxide
2,3-dimethyl-6-(4-(trifluoromethyl)phenyl)imidazo[2,1-b]thiazole
2-Deoxy-2,2-difluoro-D-erythro-pentofuranose triacetate
C11H14F2O7 (296.07075580000003)
9,10-difluoro-2,3,4,6,7,11b-hexahydro-1H-pyrazino[2,1-a]isoquinoline,dihydrochloride
4-[(3-Mercapto-5-phenyl-[1,2,4]triazol-4-ylimino)-methyl]-phenol
C15H12N4OS (296.07317820000003)
(2S)-2-hydroxy-4-oxo-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoic acid
[(2R,3S,4R,5R)-5-(4-amino-1H-imidazol-3-ium-3-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
C8H15N3O7P+ (296.06475900000004)
N-(3-chloro-4-methoxyphenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine
9-methyl-5H-quinolino[8,7-c][1,2]benzothiazine 6,6-dioxide
Isoaspulvinone E
A 4-hydroxy-5-(4-hydroxybenzylidene)-3-(4-hydroxyphenyl)furan-2(5H)-one in which the double bond adopts an E-configuration. It is a marine metabolite isolated from the fungus Aspergillus terreus and exhibits antiviral activity.
4-[[5-(1-Naphthalenyl)-1,3,4-oxadiazol-2-yl]thio]-2-butyn-1-ol
2-[(4-Oxo-2-phenyl-1-benzopyran-3-yl)oxy]acetic acid
2-tert-butyl-4-[(4-chlorophenyl)thio]-5-methyl-1H-pyrazol-3-one
N-[(E)-(3-phenyl-4-pyrazolylidene)methyl]-2-thiophenecarbohydrazide
C15H12N4OS (296.07317820000003)
Methyl 2-(6-hydroxy-5,7,8-trimethyl-2-oxo-1,4-benzoxathiin-3-yl)acetate
C14H16O5S (296.07184060000003)
[(2R,3S,4R)-5-(4-amino-1H-imidazol-3-ium-3-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
C8H15N3O7P+ (296.06475900000004)