Heptylphysostigmine is in advanced clinical trial as a drug for Alzheimer's disease. 8-Morpholinooctylphysostigmine and 8-(cis-2,6-dimethylmorpholino)octylphysostigmine are currently undergoing pre-clinical evaluation. The mechanism of action of these compounds in the inhibition of acetylcholinesterase has been investigated. All the examined compounds display non competitive-like kinetics of inhibition. There are no reversible components in the observed inhibition: the whole inhibitory effect is due to the time-dependent pseudo-irreversible carbamylation of the active site. Yet the observed time course of the inhibition does not match a simple second order kinetics. An influence of the quaternary structure of the enzyme on the more complex kinetics of carbamylation is hypothesized. Reactivation experiments on the inhibited enzyme show long lasting inhibitory effects for these compounds. The higher duration of the anticholinesterase effect of the morpholino derivatives compared to heptylphysostigmine should provide the basis for their higher therapeutic potential.

Long chain analogs of physostigmine as potential drugs for Alzheimer's disease: new insights into mechanism of action in the inhibition of acetylcholinesterase / Perola, E.; Cellai, L.; Lamba, D.; Filocamo, Luigi; Brufani, Mario. - In: BIOCHIMICA ET BIOPHYSICA ACTA. - ISSN 0006-3002. - STAMPA. - 1347:(1997), pp. 41-50. [10.1016/S0167-4838(97)00133-7]

Long chain analogs of physostigmine as potential drugs for Alzheimer's disease: new insights into mechanism of action in the inhibition of acetylcholinesterase

FILOCAMO, Luigi;BRUFANI, Mario
Supervision
1997

Abstract

Heptylphysostigmine is in advanced clinical trial as a drug for Alzheimer's disease. 8-Morpholinooctylphysostigmine and 8-(cis-2,6-dimethylmorpholino)octylphysostigmine are currently undergoing pre-clinical evaluation. The mechanism of action of these compounds in the inhibition of acetylcholinesterase has been investigated. All the examined compounds display non competitive-like kinetics of inhibition. There are no reversible components in the observed inhibition: the whole inhibitory effect is due to the time-dependent pseudo-irreversible carbamylation of the active site. Yet the observed time course of the inhibition does not match a simple second order kinetics. An influence of the quaternary structure of the enzyme on the more complex kinetics of carbamylation is hypothesized. Reactivation experiments on the inhibited enzyme show long lasting inhibitory effects for these compounds. The higher duration of the anticholinesterase effect of the morpholino derivatives compared to heptylphysostigmine should provide the basis for their higher therapeutic potential.
1997
acetylcholinesterase; inhibition kinetics; physostigmine analog; inhibition mechanism; reactivation time
01 Pubblicazione su rivista::01a Articolo in rivista
Long chain analogs of physostigmine as potential drugs for Alzheimer's disease: new insights into mechanism of action in the inhibition of acetylcholinesterase / Perola, E.; Cellai, L.; Lamba, D.; Filocamo, Luigi; Brufani, Mario. - In: BIOCHIMICA ET BIOPHYSICA ACTA. - ISSN 0006-3002. - STAMPA. - 1347:(1997), pp. 41-50. [10.1016/S0167-4838(97)00133-7]
File allegati a questo prodotto
File Dimensione Formato  
Perola_Long chain_1997.pdf

solo gestori archivio

Tipologia: Documento in Post-print (versione successiva alla peer review e accettata per la pubblicazione)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 784.1 kB
Formato Adobe PDF
784.1 kB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/244126
Citazioni
  • ???jsp.display-item.citation.pmc??? 15
  • Scopus 62
  • ???jsp.display-item.citation.isi??? 55
social impact