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2,3,6a,8,9,9a-ヘキサヒドロ-4-メトキシシクロペンタ[c]フロ[3′,2′:4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン

Aflatoxin B2 alpha

HCID 23648
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
22040-96-6
標準SMILES
COc1cc2c(c3oc(=O)c4c(c13)CCC4=O)C1CCOC1O2
InChIKey
WWSYXEZEXMQWHT-UHFFFAOYSA-N
分子式
C17H14O6
平均分子量
314.29 g/mol
単同位体質量
314.07903816

概要

Aflatoxin B2 alpha is a member of coumarins.

名称と識別子

優先名称
Aflatoxin B2 alpha
IUPAC
11-methoxy-6,8,19-trioxapentacyclo[10.7.0.02,9.03,7.013,17]nonadeca-1,9,11,13(17)-tetraene-16,18-dione
現地名
2,3,6a,8,9,9a-ヘキサヒドロ-4-メトキシシクロペンタ[c]フロ[3′,2′:4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
英語名
aflatoxin B2
分子式
C17H14O6
分子量
314.28946

名称と別名

Aflatoxin B2 alpha22040-96-611-methoxy-6,8,19-trioxapentacyclo[10.7.0.02,9.03,7.013,17]nonadeca-1,9,11,13(17)-tetraene-16,18-dione11-methoxy-6,8,19-trioxapentacyclo(10.7.0.02,9.03,7.013,17)nonadeca-1,9,11,13(17)-tetraene-16,18-dioneRefChem:915226Dihydroafflatoxin B1orb321388SCHEMBL621001SCHEMBL29838910DTXSID10871940CHEBI:181914WWSYXEZEXMQWHT-UHFFFAOYSA-N
名称をさらに表示
2,3,6a,8,9,9a-ヘキサヒドロ-4-メトキシシクロペンタ[c]フロ[3′,2′:4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン11-メトキシ-6,8,19-トリオキサペンタシクロ[10.7.0.02,9.03,7.013,17]ノナデカ-1,9,11,13(17)-テトラエン-16,18-ジオン
Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione, 2,3,6a.alpha.,8,9,9a.alpha.-hexahydro-4-methoxy-NS000027524-Methoxy-2,3,6a,8,9,9a-hexahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dioneCyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione, 2,3,6a,8,9,9a-hexahydro-4-methoxy-

データベース識別子

CAS

物性

構造計算による物性

XLogP
1.3
極性表面積
71.1 Ų
水素結合供与体数
0
水素結合受容体数
6
回転可能結合数
1
重原子数
23
形式電荷
0
複雑度
610

実験および物理化学的性質

Melting Point310 °C
Physical DescriptionSolid

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

毒性情報

Treatment · 1 件

Administration of phonobarbital enhances hepatic transformation activities and also protects against AFB-induced toxicity, carcinogenicity and DNA binding in vivo. In cases of ingestion, feeding large quantities of an adsorbent such as activated charcoal may be used. Antioxidants such as ellagic acid and inducers of some cytochromes P450, such as indole-3-carbinol, may give a protective effect. (A704, L1879)

Health Effects · 1 件

The main target organ in mammals is the liver so aflatoxicosis is primarily a hepatic disease. Protracted exposure to aflatoxins may cause liver damage and necrosis, cholestasis, and hepatomas. Moreover, protracted exposure to aflatoxins has been associated with hepatocellular carcinoma, acute hepatitis, Reye's syndrome, bile duct cell proliferation, periportal fibrosis, hemorrhages, mucous membrane jaundice, fatty liver changes, cirrhosis in malnourished children, and kwashiorkor. However, aflatoxins accumulate in the presence of liver disease, and the association with hepatic cancer is confounded by the occurrence of hepatitis-B. Thus, it is not clear in these various instances whether aflatoxin is a primary cause of the disease, is an innocent bystander which accumulates secondary to the disease process, or is a contributing cause in conjunction with other factors. It is also mutagenic and teratogenic. Inhaled aflatoxins may produce pulmonary adenomatosis. Aflatoxins modify the immune system by affecting antibody formation, complement, cell-mediated immunity, and phagocytosis. (A704, L1956) Furocoumarins can cause photosensitization dermatitis especially if these compounds come into contact with the skin. Some furocoumarins, especially bifunctional furocoumarins, are known to be carcinogenic (A15105). Furocoumarin photochemotherapy is known to induce a number of side-effects including erythema, edema, hyperpigmentation, and premature aging of skin. All photobiological effects of furocoumarins result from their photochemical reactions. Because many dietary or water soluble furocoumarins are strong inhibitors of cytochrome P450s, they will also cause adverse drug reactions when taken with other drugs. Limited evidence of carcinogenic effect. (L579)

Exposure RoutesOral, dermal, inhalation, and parenteral (contaminated drugs). (A3101)
Toxicity Summary

化学と産業

薬理情報

Metabolism/MetabolitesAflatoxin B2 is metabolized in the liver by microsomal monooxygenases to the less toxic reactive metabolite alfatoxin M2. Aflatoxin B2 is also proposed to be metabolized to B1, which in turn is transformed to M1. (A705, L1956)
Cellular LocationsCytoplasm

用途と製造

Uses · 1 件

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 favorable for its growth. Crops which are frequently affected 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). The toxin can also be found in the milk of animals which are fed contaminated feed. Thus, aflatoxins are usually encountered in thecontext of chronic exposure, via food intake or secondary to the handling of foodstuffs. (L1956)

関連反応

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化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
22040-96-6、7220-81-7
PubChem CID
23648
DTXSID
DTXSID10871940
ChEBI
CHEBI:181914
Nikkaji
J3.035.013H
· 1 件

Aflatoxins produce singlet oxygen upon their exposure to UV (365-nm) light. Singlet oxygen in turn activates them to mutagens and DNA binding species. Aflatoxin metabolites can intercalate into DNA and alkylate the bases through their epoxide moiety, binding particularity to N7-guanine bases. In addition to randomly mutating DNA, this is thought to cause mutations in the p53 gene, an important gene in preventing cell cycle progression when there are DNA mutations, or signaling apoptosis. (L1877, A2859, A2972) The mechanism of action many furocoumarins is based on their ability to form photoadducts with DNA and other cellular components such as RNA, proteins, and several proteins found in the membrane such as phospholipases A2 and C, Ca-dependent and cAMPdependent protein-kinase and epidermal growth factor. Furocoumarins intercalate between base pairs of DNA and after ultraviolet-A irradiation, giving cycloadducts. (L579)

Signs and SymptomsA broad range of symptoms can be found depending upon dosage, including, vomiting, abdominal pain, hemorrhage, and pulmonary edema. (L1879)
Carcinogen Classification1, carcinogenic to humans (L135)