E5625
Ergocryptin
Sinónimos:
12′-Hydroxy-2′-(1-methylethyl)-5′-α-(2-methylpropyl)ergotaman-3′,6′,18-trione
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Fórmula empírica (notación de Hill):
C32H41N5O5
Número CAS:
Peso molecular:
575.70
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
208-121-2
MDL number:
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Servicio técnico
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Permítanos ayudarlesolubility
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
Clase de almacenamiento
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
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J R Strickland et al.
American journal of veterinary research, 55(5), 716-721 (1994-05-01)
Cultured rat pituitary cells were studied to: determine the effects of ergovaline and loline on in vitro prolactin release; delineate the agonistic activity of these alkaloids at the D2 dopamine receptor, using 2 selective D2 dopamine receptor antagonists; and compare
D J Smith et al.
Journal of animal science, 80(6), 1616-1622 (2002-06-25)
Purified ergopeptine alkaloids are often used in studies related to tall fescue toxicosis without regard to epimerization that occurs when ergopeptines are solvated. The objectives of this study were to measure the rates of alpha-ergocryptine epimerization to alpha-ergocryptinine at room
M S Choudhary et al.
Molecular pharmacology, 47(3), 450-457 (1995-03-01)
In this paper we show that a highly conserved aromatic residue, phenylalanine at the 340-position, is essential for ergoline binding to 5-hydroxytryptamine2A receptors. We hypothesized that F340 was essential for a specific aromatic-aromatic interaction (e.g., pi-pi or hydrophobic) between the