A4437
Altenuene from Alternaria sp.
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关于此项目
经验公式（希尔记法）:
C15H16O6
化学文摘社编号:
分子量:
292.28
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
storage temp.
2-8°C
SMILES string
COc1cc(O)c2C(=O)O[C@]3(C)C[C@@H](O)[C@H](O)C=C3c2c1
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Erika Pfeiffer et al.
Molecular nutrition & food research, 53(4), 452-459 (2008-12-10)
The mycotoxins altenuene (ALT) and isoaltenuene (iALT) frequently occur in food and feed items infested by fungi of the genus Alternaria, but nothing is known about their oxidative metabolism in mammals. We have therefore incubated ALT and iALT with microsomes
G F Griffin et al.
Applied and environmental microbiology, 46(6), 1420-1422 (1983-12-01)
The effects in the chicken embryo assay of four Alternaria metabolites (alternariol [AOH], alternariol methyl ether [AME], altenuene [ALT], and tenuazonic acid [TA]) were investigated. Administered to 7-day-old chicken embryos by yolk sac injection, AOH, AME, and ALT caused no
N Magan et al.
Applied and environmental microbiology, 47(5), 1113-1117 (1984-05-01)
Both water activity (aW) and temperature affected the production of altenuene (AE), alternariol (AOH), and alternariol monomethyl ether (AME) by Alternaria alternata on wheat extract agar and wheat grain. Greatest production of all three mycotoxins occurred at 0.98 aW and
P Ren et al.
Journal of industrial microbiology & biotechnology, 20(1), 53-54 (1998-04-02)
The production of mycotoxins by Alternaria alternata in cellulosic ceiling tiles was examined with thin-layer chromatography and high-performance liquid chromatography procedures. Alternariol and alternariol monomethyl ether were found in ceiling tile extracts, whereas extracts of control rice cultures of all
Martina Altemöller et al.
Journal of natural products, 72(7), 1288-1290 (2009-07-04)
Total synthesis of alternaria toxins starting from previously synthesized altenuene (3) and isoaltenuene (4) is described. Dihydroaltenuene B (9) was prepared by hydrogenation of 3, and the non-natural epimer 3-epi-dihydroaltenuene A was obtained analogously from 4. Inspection of the spectroscopic
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