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About This Item
Empirical Formula (Hill Notation):
C32H41N5O5
CAS Number:
Molecular Weight:
575.70
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
208-121-2
MDL number:
solubility
45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.3 mg/mL, ethanol: 3.2 mg/mL, H2O: insoluble
storage temp.
−20°C
SMILES string
CC(C)C[C@@H]1N2C(=O)[C@](NC(=O)[C@H]3CN(C)[C@@H]4Cc5c[nH]c6cccc(C4=C3)c56)(O[C@@]2(O)[C@@H]7CCCN7C1=O)C(C)C
Biochem/physiol Actions
Ergot alkaloid
signalword
Warning
hcodes
pcodes
Hazard Classifications
Repr. 2
Storage Class
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, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
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Silvio Uhlig et al.
Rapid communications in mass spectrometry : RCM, 21(10), 1651-1660 (2007-04-28)
Ergot alkaloids are mycotoxins which are produced among fungi in the family Clavicipitaceae. Poisoning with ergot alkaloids is an important veterinary problem in animal husbandry and has recently also been recognised in wild animals. While the poisoning syndrome observed in
P Zhu et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 32(8), 629-632 (1997-08-01)
The stimulation of sodium deoxycholate (SDC) on alpha-ergocryptine production of Claviceps purpurea strain 94002 (EKPN94002) was investigated. Preliminary results indicated that SDC, as a stimulator and at appropriate concentrations, could obviously increase the extracellular and the total production levels of
B T Larson et al.
Journal of animal science, 77(4), 942-947 (1999-05-18)
Ergot and pyrrolizidine alkaloids, either extracted from endophyte-infected tall fescue, synthesized, or purchased commercially, were evaluated in cultured cells to estimate their binding to the D2 dopamine receptor and subsequent effects on cyclic AMP production in GH4ZR7 cells, transfected with
