
CAS 41093-89-4
:Formula:C20H31NO8
InChI:InChI=1S/C20H31NO8/c1-6-12(2)17(23)29-15-8-10-21(27)9-7-14(16(15)21)11-28-18(24)20(26,13(3)22)19(4,5)25/h6-7,13,15-16,22,25-26H,8-11H2,1-5H3/b12-6-/t13-,15+,16+,20-,21?/m0/s1
InChI key:KDJGEXAPDZNXSD-KCFAIRMISA-N
SMILES:C/C=C(/C)\C(=O)O[C@@H]1CC[N+]2([C@@H]1C(=CC2)COC(=O)[C@@]([C@H](C)O)(C(C)(C)O)O)[O-]
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Echimidine N-oxide
CAS:Echimidine N-oxide, a pyrrolizidine alkaloid, exhibits significant inhibitory activity against acetylcholinesterase (AChE) with an IC50 value of 0.347 mM.Formula:C20H31NO8Color and Shape:SolidMolecular weight:413.462Echimidine N-oxide (Standard)
CAS:Echimidine N-oxide (Standard) is a reference standard for research and analysis in studies involving Echimidine N-oxide. Echimidine N-oxide, a pyrrolizidine alkaloid, exhibits significant inhibitory activity against acetylcholinesterase (AChE) with an IC50 value of 0.347 mM.Formula:C20H31NO8Molecular weight:413.462Echimidine-N-oxide 100 µg/mL in Water
CAS:Controlled ProductFormula:C20H31NO8Color and Shape:Single SolutionMolecular weight:413.46Echimidine N-oxide
CAS:Natural alkaloidFormula:C20H31NO8Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:413.46Echimidine N-Oxide-D6
CAS:Controlled ProductApplications (+)-Echimidine N-Oxide-D3 is a labelled analogue of (+)-Echimidine N-Oxide (E325585), a hepatotoxic pyrolizidine alkaloid that is present in honey, pollen, and comfrey tea leaves.
References Cao, Y., et al.: J. Food Comp. Anal., 29, 106 (2013); Hirono, I., et al.: J. Nat. Cancer Inst., 63, 469 (1979); Oberlies, N., et al.: Pub. Health Nut., 7, 919 (2004)Formula:C20D6H25NO8Color and Shape:NeatMolecular weight:416.481Echimidine N-oxide
CAS:Echimidine N-oxide is a natural alkaloid derivative, which is isolated from certain plant species in the Boraginaceae family. It acts as a precursor in the biosynthetic pathway of pyrrolizidine alkaloids. The mode of action involves metabolic conversion within the organism, leading to potential bioactive effects. This compound is primarily used in scientific research to explore its pharmacological properties, particularly its role in influencing various biological pathways. Its applications extend to the study of natural product biosynthesis and investigations into its potential therapeutic benefits, as well as toxicological studies due to its structural relationship to other bioactive alkaloids.Formula:C20H31NO8Purity:Min. 95%Color and Shape:PowderMolecular weight:413.46 g/mol








