Substance
ID:182178
Names and Identifiers
Synonyms
MLA[1α,4(S),6β,14α,16β]-20-Ethyl-1,6,14,16-tetramethoxy-4-[[[2-(3-methyl-2,5-dioxo-1-pyrrolidinyl)benzoyl]oxy]methyl]aconitane-7,8-diol citrate saltMethyllycaconitine citrate salt hydrate
IUPAC name
2-hydroxypropane-1,2,3-tricarboxylic acid [(1S,2R,3R,4S,5R,6S,8R,9R,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate
IUPAC Traditional name
citro [(1S,2R,3R,4S,5R,6S,8R,9R,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate
Properties
Physical Property
Solubility
H2O: soluble42 mg/mL
Apperance
white
Safety Information
Storage Temperature
-20°C
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Product Information
Purity
≥96% (HPLC)
Biological Source
from Delphinium brownii seeds
Molecule Details
Biochem/physiol Actions
Potent and specific nicotinic receptor antagonist that binds to neuronal α-bungarotoxin sites.
Potent and specific nicotinic receptor antagonist that binds to neuronal α-bungarotoxin sites.
Molecular Spectra
No Data Available
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References
No Data Available
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