Publication | Open Access
New Cholinesterase Inhibiting Steroidal Alkaloids from the Leaves of Sarcococca coriacea of Nepalese Origin.
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Citations
14
References
2002
Year
Medicinal ChemistryBioorganic ChemistryBiochemistryNepalese OriginCholinesterase Inhibitory ActivityNatural SciencesNew Steroidal AlkaloidsMedicineSecondary MetabolitePhytochemistryPharmacologyElectric Eel AcetylcholinesterasePharmaceutical ChemistrySarcococca CoriaceaDrug DiscoveryNatural Product Synthesis
From the leaves of Sarcococca coriacea two new steroidal alkaloids, epoxynepapakistamine-A [(20S)-20-(N-methylamino)-3beta-(tigloylamino)-5alpha-pregna-16alpha,17alpha-epoxy-2beta,4beta-di-O-acetate] (1), and epoxysarcovagenine-D [(20S)-20-(N-methylamino)-3beta-(tigloylamino)-5alpha-pregna-2-en-16alpha,17alpha-epoxy-4-one] (2), and two known compounds funtumafrine C [(20S)-20-(N,N-dimethylamino)-5alpha-pregna-3-one] (3) and N-methylfuntumine (4) were isolated. Their structures were elucidated on the basis of their spectral properties. The compounds 1, 3 and 4 were found to have cholinesterase inhibitory activity when tested for the inhibition of electric eel acetylcholinesterase and horse serum butyrylcholinesterase. They inhibited both enzymes in a concentration dependent fashion.
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