Chemical Formula: C17H12O6
Chemical Formula C17H12O6
Found 115 metabolite its formula value is C17H12O6
Aflatoxin B1
Aflatoxins are naturally occurring mycotoxins that are produced by many species of Aspergillus, a fungus. At least 13 different types of aflatoxin are produced in nature. Aflatoxin B1 is considered the most toxic and is produced by both Aspergillus flavus and Aspergillus parasiticus. The native habitat of Aspergillus is in soil, decaying vegetation, hay, and grains undergoing microbiological deterioration and it invades all types of organic substrates whenever conditions are favourable for its growth. Favourable conditions include high moisture content (at least 7\\\%) and high temperature. Aflatoxins B1 (AFB1) are contaminants of improperly stored foods; they are potent genotoxic and carcinogenic compounds, exerting their effects through damage to DNA. They can also induce mutations that increase oxidative damage (PMID: 17214555). Crops which are frequently affected by Aspergillus contamination include cereals (maize, sorghum, pearl millet, rice, wheat), oilseeds (peanut, soybean, sunflower, cotton), spices (chile peppers, black pepper, coriander, turmeric, ginger), and tree nuts (almond, pistachio, walnut, coconut, brazil nut). Production by Aspergillus flavus and Aspergillus parasiticus. Toxin causing Turkey X disease. One of the most potent carcinogens known in animals. Potential food contaminant especies in grains and nuts D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins Aflatoxin B1 (AFB1) is a Class 1A carcinogen, which is a secondary metabolite of Aspergillus flavus and A. parasiticus. Aflatoxin B1 (AFB1) mainly induces the transversion of G-->T in the third position of codon 249 of the p53 tumor suppressor gene, resulting in mutation[1][2].
Betavulgarin
Betavulgarin, also known as 2-hydroxy-5-methoxy-6,7-methylenedioxyisoflavone, is a member of the class of compounds known as isoflavones. Isoflavones are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom. Thus, betavulgarin is considered to be a flavonoid lipid molecule. Betavulgarin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Betavulgarin can be found in chickpea, common beet, and red beetroot, which makes betavulgarin a potential biomarker for the consumption of these food products.
De-O-methyldihydrosterigmatocystin
De-O-methyldihydrosterigmatocystin is a mycotoxin produced by Aspergillus versicolor. Mycotoxin production by Aspergillus versicolor.
Aloe emodin w-acetate
Aloe emodin w-acetate is found in herbs and spices. Aloe emodin w-acetate is isolated from roots of Rumex acetosa (sorrel). Isolated from roots of Rumex acetosa (sorrel). Aloe emodin w-acetate is found in herbs and spices.
Wairol
Isolated from Medicago sativa (alfalfa) infected with leafspot (Ascochyta imperfecta). Wairol is found in alfalfa and pulses. Wairol is found in alfalfa. Wairol is isolated from Medicago sativa (alfalfa) infected with leafspot (Ascochyta imperfecta).
3',4,4'-Trihydroxypulvinone
3,4,4-Trihydroxypulvinone is found in mushrooms. 3,4,4-Trihydroxypulvinone is a constituent of Suillus grevillei (larch bolete)
3-Hydroxy-8,9-dimethoxycoumestan
3-Hydroxy-8,9-dimethoxycoumestan is found in alfalfa. 3-Hydroxy-8,9-dimethoxycoumestan is isolated from Medicago sativa (alfalfa) and Myroxylon balsamum (Tolu balsam Isolated from Medicago sativa (alfalfa) and Myroxylon balsamum (Tolu balsam). 3-Hydroxy-8,9-dimethoxycoumestan is found in alfalfa and pulses.
(E)-Antibiotic BE 23372M
(E)-Antibiotic BE 23372M is found in fats and oils. (E)-Antibiotic BE 23372M is produced by Rhizoctonia solani found on the bark of Ginkgo biloba (ginkgo). Production by Rhizoctonia solani found on the bark of Ginkgo biloba (ginkgo). (E)-Antibiotic BE 23372M is found in fats and oils.
8-Hydroxy-3-methoxy-1-methylanthraquinone-2-carboxylic acid
8-Hydroxy-3-methoxy-1-methylanthraquinone-2-carboxylic acid is a constituent of Crocus sativus (saffron). Constituent of Crocus sativus (saffron)
3-Carboxy-6,7-dihydroxy-1-(3,4-dihydroxyphenyl)-naphthalene
1-Methoxy-3-hydroxy-2-carbomethoxy-9,10-anthraquinone
(6aR,11aS)-(3,4:8,9)-Bis(methylenedioxy)pterocarpan
4-Methoxy nigricin,5-Hydroxy-4-methoxy-6,7-methylenedioxyisoflavone
5-Hydroxy-7-methoxy-3,4-methylenedioxyflavone
3-Hydroxy-4-methoxy-8,9-methylenedioxypterocarpene
5-Hydroxy-7,4-dimethoxy-5,2-oxido-4-phenylcoumarin
Betavulgarin
A hydroxyisoflavone that is isoflavone substituted by a hydroxy group at position 2, a methoxy group at position 5 and a methylenedioxy group across positions 6 and 7 respectively.
3,8-dihydroxy-10-methoxyisochromeno[4,3-b]chromen-7(5h)-one
5,6,9,10-Tetrahydroxy-2,3-dihydrophenanthro[9,10-b]furan-2-carbaldehyde
8,10-Dihydroxy-11-methoxy[2]benzopyrano[4,3-b][1]benzopyran-7(5H)-one
8-hydroxy-3-methoxy-7-methyl-1,2-methylenedioxy-anthraquinone
(E)-3-(3,4-dihydroxybenzylidene)-5-(3,4-dihydroxyphenyl)-2(3H)-furanone
6-formyl-2-methoxy-9-methyl-7,8-dihydroxy-1,4-phenanthrenedione
(Z)-5-(2,4-dihydroxybenzylidene)-3-(4-hydroxyphenyl)-4-hydroxyfuran-2(5H)-one|Trihydroxypluvinon
1,5-Dihydroxy-9,10-dioxo-9,10-dihydroanthracene-3-carboxylic acid ethyl ester
3-(3,4-Dihydroxyphenyl)-5-[(alphaE)-alpha,4-dihydroxybenzylidene]furan-2(5H)-one
6,7-dihydrox-3-methoxy-4,5-methyl-enedioxyisoflavone
9,10-Anthracenedione, 2-ethenyl-1,3,6,8-tetrahydroxy-7-methyl-
3,8-Diacetoxy-benzo[c]chromen-6-on|3,8-diacetoxy-benzo[c]chromen-6-one|Urolithin A-diacetat
3-Hydroxy-4,9-dimethoxy-6H-benzofuro[3,2-c][1]benzopyran-6-one
boeravinoneB
boeravinone B is a natural product found in Mirabilis jalapa and Boerhavia diffusa with data available.
Aflatoxin B1
An aflatoxin having a tetrahydrocyclopenta[c]furo[3,2:4,5]furo[2,3-h]chromene skeleton with oxygen functionality at positions 1, 4 and 11. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins CONFIDENCE standard compound; INTERNAL_ID 5962 CONFIDENCE Reference Standard (Level 1) Aflatoxin B1 (AFB1) is a Class 1A carcinogen, which is a secondary metabolite of Aspergillus flavus and A. parasiticus. Aflatoxin B1 (AFB1) mainly induces the transversion of G-->T in the third position of codon 249 of the p53 tumor suppressor gene, resulting in mutation[1][2].
4-(3,4-dihydroxyphenyl)-6,7-dihydroxynaphthalene-2-carboxylic acid
4-(3,4-dihydroxyphenyl)-6,7-dihydroxynaphthalene-2-carboxylic acid
4-(3,4-dihydroxyphenyl)-6,7-dihydroxynaphthalene-2-carboxylic acid_major
3',4,4'-Trihydroxypulvinone
Demethyldihydrosterigmatocystin
8-Hydroxy-3-methoxy-1-methylanthraquinone-2-carboxylic acid
(E)-Antibiotic BE 23372M
2-(5-hydroxy-4-oxo-2-phenylchromen-7-yl)oxyacetic acid
Talosalate
C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic
(3E)-3-(3,4-dihydroxybenzylidene)-5-(3,4-dihydroxyphenyl)furan-2(3H)-one
2H-Pyrano(2,3,4-kl)xanthen-2-one, 10-hydroxy-5,9-dimethoxy-
(Z)-3-(3,4-dihydroxybenzylidene)-5-(3,4-dihydroxyphenyl)-2(3H)-furanone
A butenolide that is furan-2(3H)-one substituted by a 3,4-dihydroxybenzylidene group at position 3 and a 3,4-dihydroxyphenyl group at position 5. It has been isolated from the roots of Scorzonera judaica.
4-(Methyloxy)-2,3,6a,9a-tetrahydrocyclopenta[c]furo[3,2:4,5]furo[2,3-h]chromene-1,11-dione
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins Aflatoxin B1 (AFB1) is a Class 1A carcinogen, which is a secondary metabolite of Aspergillus flavus and A. parasiticus. Aflatoxin B1 (AFB1) mainly induces the transversion of G-->T in the third position of codon 249 of the p53 tumor suppressor gene, resulting in mutation[1][2].
Dihydrodemethylsterigmatocystin
An organic heteropentacyclic compound that is sterigmatocystin in which the methoxy group at position 6 is replaced by a hydroxy group.
BE-23372M
A butenolide that is furan-2(3H)-one substituted by a 3,4-dihydroxybenzylidene group at position 3 and a 3,4-dihydroxyphenyl group at position 5 (the 3E stereoisomer). It is isolated from the fermentation broth of the fungal strain Rhizoctonia solani F23372 and has been found to possess significant tyrosine kinase inhibitory potential. It also inhibits the growth of A431 human epidermoid carcinoma and MKN-7 human stomach cancer cell lines.