Current progress in the chemistry and pharmacology of akuammiline alkaloids

A Ramirez, S García-Rubio - Current medicinal chemistry, 2003 - ingentaconnect.com
Akuammiline alkaloids are a family of monoterpene indole alkaloids of renewed medicinal
interest. These bases act as ligands for a heterogeneous group of molecular targets and …

Alkaloids of the Calabar bean

S Takano, K Ogasawara - The Alkaloids: Chemistry and Pharmacology, 1990 - Elsevier
Publisher Summary This chapter describes the structures of the alkaloids, synthesis of
alkaloids, and pharmacology of alkaloids of the Calabar bean (Physostigmu uenenosum) …

Synthesis and antinociceptive activity of chimonanthines and pyrrolidinoindoline-type alkaloids

L Verotta, F Orsini, M Sbacchi, MA Scheildler… - Bioorganic & medicinal …, 2002 - Elsevier
Hodgkinsine, a trimeric pyrrolidinoindoline type alkaloid, present as a major constituent of
Psychotria spp.(Rubiaceae), has shown to produce dose-dependent, naloxone reversible …

Fifteen years of research of bioactive alkaloids

A Brossi - Medicinal research reviews, 1992 - Wiley Online Library
The study of bioactive molecules with asymmetric carbon atoms, molecular asymmetry, or
both, requires the preparation of optically pure enantiomers, and the determination of the …

Asymmetric synthesis of indolines bearing a benzylic quaternary stereocenter through intramolecular arylcyanation of alkenes

JC Hsieh, S Ebata, Y Nakao, T Hiyama - Synlett, 2010 - thieme-connect.com
Thieme E-Journals - Synlett / Full Text DE EN Home Products Journals Books Book Series
Service Library Service Help Contact Portal SYNLETT Full-text search Full-text search Author …

Hexahydrochromeno[4,3-b]pyrrole Derivatives as Acetylcholinesterase Inhibitors

ML Bolognesi, V Andrisano, M Bartolini… - Journal of medicinal …, 2001 - ACS Publications
In a search for less flexible analogues of caproctamine (1), a diamine diamide endowed with
an interesting AChE affinity profile, we discovered compound 2, in which the terminal 2 …

Syntheses and Anticholinesterase Activities of (3aS)-N,N8-Bisnorphenserine, (3aS)-N1,N8-Bisnorphysostigmine, Their Antipodal Isomers, and Other …

Q Yu, NH Greig, HW Holloway… - Journal of medicinal …, 1998 - ACS Publications
Hydrolysis of the carbamate side chains in phenserine [(−) 1] and physostigmine [(−) 2]
yields the metabolite (−)-eseroline (3), and the red dye rubreserine (4) on air oxidation of the …

Enantiomer (+) physostigmine prevents organophosphate‐induced subjunctional damage at the neuromuscular synapse by a mechanism not related to …

M Kawabuchi, AF Boyne, SS Deshpande, WM Cintra… - Synapse, 1988 - Wiley Online Library
The natural alkaloid (‐) PHY is a reversible anticholinesterase carbamate, but in contrast, its
optical isomer (+) PHY, is a very weak anticholinesterase. We have shown that treatment of …

Opioid receptors and their ligands: recent developments

AF CASY - Advances in Drug Research, 1989 - Elsevier
The following abbreviations are used in this article (only the abbreviated name and
reference to formula number are given for complex structures): ACE, angiotensin-converting …

Biological Activities of the Alkaloids of the Calabar Bean

B Robinson - The Calabar Bean and its Alkaloids: From Magic, via …, 2023 - Springer
Ach (180) is the cationic neurotransmitter that in the central and peripheral nervous systems
effects the transmission of action potentials across nerve-nerve and neuromuscular …