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New Cholinesterase-Inhibiting Steroidal Alkaloids from Sarcococca saligna

✍ Scribed by Atta-ur-Rahman; Zaheer-ul-Haq; Fareeda Feroz; Asaad Khalid; Sarfraz Ahmad Nawaz; M. Riaz Khan; M. Iqbal Choudhary


Publisher
John Wiley and Sons
Year
2004
Tongue
German
Weight
144 KB
Volume
87
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

Seven new steroidal alkaloids, 2‐hydroxysalignarine‐E (=(2′E,20__S__)‐20‐(dimethylamino)‐2__β__‐hydroxy‐3__β__‐(tigloylamino)pregn‐4‐ene; 1), 5,6‐dihydrosarconidine (=(20__S__)‐20‐(dimethylamino)‐3__β__‐(methylamino)‐5__α__‐pregn‐16‐ene; 2), salignamine (=(20__S__)‐20‐(methylamino)‐3__β__‐methoxypregna‐5,16‐diene; 3), 2‐hydroxysalignamine (=(20__S__)‐20‐(dimethylamino)‐2__β__‐hydroxy‐3__β__‐methoxypregna‐5,16‐diene; 4), salignarine‐F (=(2′E, 20__S__)‐20‐(dimethylamino)‐4__β__‐hydroxy‐3__β__‐(tigloylamino)pregn‐5‐ene; 5), salonine‐C (=(2′E,20__S__)‐20‐(dimethylamino)‐3__β__‐(tigloylamino)pregna‐4,14‐diene; 6), and N‐[formyl(methyl)amino]salonine‐B (=(20__S__)‐20‐[formyl(methyl)amino]‐3__β__‐methoxypregna‐5,16‐diene; 7) have been isolated from the MeOH extract of Sarcococca saligna, along with the six known alkaloids dictyophlebine (8), epipachysamine‐D (9), saracosine (10), iso‐N‐formylchonemorphine (11), sarcodinine (12), and alkaloid‐C (13). The structures of 17 were deduced from spectral data. Compounds 113 demonstrated significant activity against acetyl‐ and butyrylcholinesterase.


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