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
solubility
45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.3 mg/mL, ethanol: 3.2 mg/mL, H2O: insoluble
storage temp.
−20°C
Biochem/physiol Actions
Ergot alkaloid
signalword
Warning
hcodes
pcodes
Hazard Classifications
Repr. 2
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, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
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
Thomas Haarmann et al.
Fungal genetics and biology : FG & B, 45(1), 35-44 (2007-06-15)
The ergot fungus Claviceps purpurea uses mainly the nonhomologous-end-joining (NHEJ) system for integration of exogenous DNA, leading to a low frequency of homologous integration (1-2%). To improve gene targeting efficiency we deleted the C. purpurea ku70 gene in two different
C Szántay et al.
Acta pharmaceutica Hungarica, 64(3), 105-108 (1994-05-01)
Two novel natural derivatives (2 and 3) of the ergot alkaloid alpha-ergokryptine (1), as well as their synthetically brominated analogues (5 and 6) were isolated and identified by NMR and MS methods. Compounds 2 and 5 contain what appears to
I Mahmood
International journal of clinical pharmacology and therapeutics, 36(10), 540-544 (1998-11-03)
The objective of this study was to demonstrate the impact of the sum of parent compound and metabolite in bioequivalence assessment. Four drugs with active metabolite were selected to assess bioequivalence. Bioequivalence criteria of 80 - 125% were applied to
M A Peyronneau et al.
European journal of biochemistry, 223(3), 947-956 (1994-08-01)
The interaction between rat and human liver cytochromes P450 with a series of lysergic acid derivatives and ergopeptide alkaloids was studied by difference visible spectroscopy. Ergopeptides, like bromocriptine, ergocryptine and dihydroergotamine, strongly interacted with rat liver microsomes with the appearance
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