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(E)-3,4,5,6,9,10-ヘキサヒドロ-14,16-ジヒドロキシ-3-メチル-1H-2-ベンゾオキサシクロテトラデシン-1,7(8H)-ジオン

Fusarium toxin

HCID 5375083
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
17924-92-4
標準SMILES
CC1CCCC(=O)CCC/C=C/c2cc(O)cc(O)c2C(=O)O1
InChIKey
MBMQEIFVQACCCH-CLTKARDFSA-N
分子式
C18H22O5
平均分子量
318.4 g/mol
単同位体質量
318.1467238

概要

(S,E)-Zearalenone is a macrolide and a member of resorcinols.

名称と識別子

優先名称
Fusarium toxin
IUPAC
(12E)-16,18-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione
現地名
(E)-3,4,5,6,9,10-ヘキサヒドロ-14,16-ジヒドロキシ-3-メチル-1H-2-ベンゾオキサシクロテトラデシン-1,7(8H)-ジオン
英語名
(E)-3,4,5,6,9,10-Hexahydro-14,16-dihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1,7(8H)-dione
分子量
0

名称と別名

7645-23-0RefChem:1085627Fusarium toxin(S,E)-Zearalenone(12E)-16,18-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dioneMycotoxin F-2Toxin, fusarium(E)-3,4,5,6,7,8,9,10-Octahydro-14,16-dihydroxy-3-methyl-7-oxo-1H-2-benzoxacyclotetradecin-1-oneSCHEMBL588841orb12202956-(10-Hydroxy-6-oxo-trans-1-undecenyl)-.beta.-resorcylic acid lactoneCHEMBL1397216
名称をさらに表示
(E)-3,4,5,6,9,10-ヘキサヒドロ-14,16-ジヒドロキシ-3-メチル-1H-2-ベンゾオキサシクロテトラデシン-1,7(8H)-ジオン(11E)-14,16-ジヒドロキシ-3-メチル-3,4,5,6,7,8,9,10-オクタヒドロ-1H-2-ベンゾオキサシクロテトラデシン-1,7-ジオン(E)-3,4,5,6,9,10-Hexahydro-14,16-dihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1,7(8H)-dione
CHEBI:125462CHEBI:175078MBMQEIFVQACCCH-XVNBXDOJSA-N(11S)-11-methyl-15,17-bis(oxidanyl)-12-oxabicyclo[12.4.0]octadeca-1(18),2,14,16-tetraene-7,13-dione(S,E)-14,16-Dihydroxy-3-methyl-3,4,5,6,9,10-hexahydro-1H-benzo[c][1]oxacyclotetradecine-1,7(8H)-dioneNCGC00095344-01NCGC00095344-03AB01209588-01

物性

構造計算による物性

XLogP
3.6
極性表面積
83.8 Ų
水素結合供与体数
2
水素結合受容体数
5
回転可能結合数
0
重原子数
23
形式電荷
0
複雑度
445

実験および物理化学的性質

Melting Point164 - 165 °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

Health Effects · 1 件

Zearalenone is a reproductive toxin and has been shown to cause infertility, abortion or other breeding problems in livestock. In humans it can cause earlier onset of puberty in children, endometrial adenocarcinomas, hyperplasia, and breast cancer in women. Zearalenone is also immunotoxic, genotoxic, and can cause kidney and liver damage. (L1947, A2960)

Exposure RoutesOral, dermal, inhalation, and parenteral (contaminated drugs). (A3101)
Toxicity Summary · 1 件

Zearalenone's genotoxicity results from it's ability to cause DNA fragmentation, chromosome aberrations, and DNA adduct formation. It exerts cytotoxic effects by enhancing lipid peroxidation, increasing oxidative stress, and inducing apoptosis. Zearalenone also has significant estrogenic activity, causing severe reproductive problems in animals. In humans, Zearalenone has been shown to cause an earlier onset of puberty in children, endometrial adenocarcinomas, hyperplasia and breast cancer in women. Mycotoxins are often able to enter the liver and kidney by human organic anion transporters (hOATs) and human organic cation transporters (hOCTs). They can also inhibit uptake of anions and cations by these transporters, interefering with the secretion of endogenous metabolites, drugs, and xenobiotics including themselves. This results in increased cellular accumulation of toxic compounds causing nephro- and hepatotoxicity. (A2960, A3014)

Carcinogen Classification3, not classifiable as to its carcinogenicity to humans. (L135)
Toxicity DataLD50: >2000 mg/kg (Oral, Mouse) (L1912) LD50: >500 mg/kg (Intraperitoneal, Mouse) (L1912)

化学と産業

薬理情報

Metabolism/Metabolites · 1 件

Zearalenone is rapidly absorbed after oral administration. In humans, most of the zearalenone absorbed is not metabolized. The main metabolites include alpha- and beta-zeralenol, and the glucuronide conjugates of both the parent compound and its metabolites. Zearalenone and its metabolites are excreted mainly in the bile. (A741, L1912)

Cellular LocationsMembrane

用途と製造

Uses · 1 件

Zearalenone (ZEA), also known as RAL and F-2 mycotoxin, is a potent estrogenic metabolite produced by some Giberella species. Several Fusarium species also produce zearalenone as their primary toxin. It can be found worldwide in a number of cereal crops, such as maize, barley, oats, wheat, rice, and sorghum, and also in bread. (L1947)

関連反応

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化合物ノート

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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

データベース識別子

CAS
17924-92-4、7645-23-0
PubChem CID
5375083
ChEMBL
CHEMBL1397216
ChEBI
CHEBI:175078
Nikkaji
J108.495J