Chemical Formula: C17H12O7
Chemical Formula C17H12O7
Found 111 metabolite its formula value is C17H12O7
Aflatoxin M1
Aflatoxin M1 is found in milk and milk products. Minor mycotoxin of Aspergillus flavus, also found in the milk of cows and sheep fed toxic meal. Metab. of Aflatoxin B1
Aflatoxin M1
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
Aflatoxin Q1
Aflatoxin Q1 is a mycotoxin. It is a metabolite of Aflatoxin B. It can be found in Aspergillus flavus and Aspergillus parasiticus (Hugo Vanden Bossche, D.W.R. Mackenzie and G. Cauwenbergh. Aspergillus and Aspergillosis, 1987). D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
2,3-Epoxyaflatoxin B1
2,3-Epoxyaflatoxin B1 is formed due to the metabolism of aflatoxin B1 (AFB1) by CYP2A13, an enzyme predominantly expressed in the human respiratory tract. There is no detectable AFB1 epoxide formation by CYP2A6, which was also reported to be involved in the metabolic activation of AFB1 (PMID: 16385575). 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). BioTransformer predicts that 2,3-epoxyaflatoxin B1 is a product of aflatoxin B1 metabolism via an epoxidation-of-vinyl-ether reaction catalyzed by CYP1A2 and CYP3A4 enzymes (PMID: 30612223). D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins Prob. ultimate carcinogen of Aflatoxin B1 D009676 - Noxae > D002273 - Carcinogens
Aflatoxin b1 epoxide
Aflatoxin G
Aflatoxin G is a mycotoxin produced by Aspergillus flavus and Aspergillus parasiticu D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
Aflatoxin M4
Aflatoxin M4 is a metabolite of Aspergillus flavus and Aspergillus parasiticus (Hugo Vanden Bossche, D.W.R. Mackenzie and G. Cauwenbergh. Aspergillus and Aspergillosis, 1987). Isolated from cultures of Aspergillus parasiticus
3,5-dihydroxy-13,14-dimethoxy-8,17-dioxatetracyclo[8.7.0.0(2),.0(1)(1),(1)]heptadeca-1(10),2,4,6,11,13,15-heptaen-9-one
Rhamnalpinogenin
Rhamnalpinogenin is a constituent of Crocus sativus (saffron)
4,2-Epoxy-5,4-dihydroxy-7,5-dimethoxy-3-phenylcoumarin
4,2-Epoxy-7,4-dihydroxy-5,5-dimethoxy-3-phenylcoumarin
6,7-dihydroxy-3-methoxy-4,5-methylenedioxyisoflavone
5,3-Dihydroxy-2-methoxy-6,7-methylenedioxyisoflavone
1,7-dihydroxy-3,9-dimethoxycoumestan|hedysarimcoumestan F
2-Methoxy-3-hydroxy-5-(4-oxo-5,7-dihydroxy-4H-1-benzopyran-3-yl)benzaldehyde
9,10-Dihydro-3,4,8-trihydroxy-1-methyl-9,10-dioxo-2-anthracenecarboxylic acid methyl ester
2,5,7-Trihydroxyspiro[4H-1-benzopyran-3(2H),5(6H)-cyclobuta[f]-1,3-benzodioxole]-4-one
2-Acetyl-1,5,6,8-tetrahydroxy-3-methylanthraquinone
6-Me ether-3,6,8-Trihydroxy-1-methylanthraquinone-2-carboxylic acid
3,5-Dihydroxy-7-methoxy-3,4-(methylenebisoxy)flavone
(2S)-5,8,4-trihydroxy-6,7-(vinylenedioxy)flavanone
3,8-dihydroxy-6-methoxy-1-methyl-9,10-dioxoanthracene-2-carboxylic acid
5,2-dihydroxy-5-methoxy-6,7-methylenedioxyisoflavone|tetranins B
6,9-dihydroxy-7-(3-methoxyphenyl)-8H-[1,3]dioxolo[4,5-g][1]benzopyran-8-one|loasin B
5-methoxy-3?,4?-dihydroxy-6,7-methylenedioxy-4H-1-benzopyran-4-one|iriskashmirianin A
5,8-dihydroxy-4-methoxy-6,7-methylenedioxyisoflavone|6,7-Methylene,4-Me ether-4,5,6,7,8-Pentahydroxyisoflavone
9,10-Dihydro-3,7,8-trihydroxy-1-methyl-9,10-dioxo-2-anthracenecarboxylic acid methyl ester
3,8-Dimethoxy-1,9-dihydroxy-6H-benzofuro[3,2-c][1]benzopyran-6-one
1,8-Dimethoxy-3,9-dihydroxy-6H-benzofuro[3,2-c][1]benzopyran-6-one
4,9-dihydroxy-3,8-dimethoxy-benzo[4,5]furo[3,2-c]chromen-6-one|buteaspermin B
boeravinoneE
boeravinone E is a natural product found in Mirabilis jalapa with data available.
AFLATOXIN G1
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins CONFIDENCE Reference Standard (Level 1)
AFLATOXIN M1
A member of the class of aflatoxins that is aflatoxin B1 in which the hydrogen at position 9a is replaced by a hydroxy group. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins CONFIDENCE Reference Standard (Level 1)
Rhamnalpinogenin
Aflatoxin M4
2,3,6a,9a-Tetrahydro-3-hydroxy-4-methoxycyclopenta(c)furo(3,2:4,5)furo(2,3-h)(1)benzopyran-1,11-dione
(5Z)-3-(3,4-dihydroxyphenyl)-5-[(3,4-dihydroxyphenyl)methylidene]-4-hydroxyfuran-2-one
Aflatoxin Q1
A member of the class of aflatoxins that is aflatoxin B1 in which the hydrogen at the pro-3S position is replaced by a hydroxy group. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins
2,3-Epoxyaflatoxin B1
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins D009676 - Noxae > D002273 - Carcinogens
aflatoxin B1 endo-8,9-oxide
A member of the class of aflatoxins that is obtained by the formal epoxidation across the 8,9-double bond of aflatoxin B1.
1,3,6-trihydroxy-2-methoxy-10h-5,11-dioxatetraphen-12-one
9-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-2h-[1,3]dioxolo[4,5-g]chromen-8-one
methyl 3,4,8-trihydroxy-1-methyl-9,10-dioxoanthracene-2-carboxylate
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-methoxynaphthalene-1,4-dione
2-(2h-1,3-benzodioxol-5-yl)-3,5-dihydroxy-7-methoxychromen-4-one
1,8-dihydroxy-6-methoxy-3-methyl-9,10-dioxoanthracene-2-carboxylic acid
2,5,7-trihydroxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one
aflatoxin g1
{"Ingredient_id": "HBIN014778","Ingredient_name": "aflatoxin g1","Alias": "NA","Ingredient_formula": "C17H12O7","Ingredient_Smile": "COC1=C2C3=C(C(=O)OCC3)C(=O)OC2=C4C5C=COC5OC4=C1","Ingredient_weight": "328.27 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "673","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "15939117","DrugBank_id": "NA"}
