Results 171 to 180 of about 20,091 (201)
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Microbial transformations of galanthamin-precursors

Applied Microbiology and Biotechnology, 1986
Galanthamin is a medical important alkaloid. Its chemical synthesis gives a racemic product in low yields. Starting with a belladinderivative an enzymatic ring closure should lead exclusively to a chiral product possibly with the native structure. Although this reactions type is unknown in preparative biotransformations a large number of microorganisms
G. Spassov   +7 more
openaire   +1 more source

Total Synthesis of (.+‐.)‐Galanthamine (I).

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Xiang‐Dong Hu   +7 more
openaire   +1 more source

Facile synthesis of (±)‐, (+)‐, and (‐)‐galanthamine

Journal of Heterocyclic Chemistry, 1995
AbstractThe Amarylidacea alkaloid galanthamine (1a) is an acetylcholinesterase inhibitor that has been evaluated as a potential agent for the treatment of Alzheimer's disease. We report a very efficent synthesis of (±)‐galanthamine [(±)‐1a] from readily available isovanillin and tyramine.
Jerzy Szewczyk   +3 more
openaire   +1 more source

Galanthamine.

JAMA, 1978
D A, Cozanitis, E, Toivakka
openaire   +3 more sources

Galanthamine in Alzheimer’s Disease

1994
Substantial efforts have been made in neurobiology and molecular biology but we are still far from a causal therapy of Alzheimer’s disease (AD). In the interim, and perhaps ultimately as an adjunct to a progression inhibitor which may not be absolute, symptomatic treatment has to be optimized. Tacrine’s approval by the FDA has stimulated a search for a
Helmut Kewitz   +2 more
openaire   +1 more source

Daffodil production for galanthamine

Galanthamine is a bioactive that has proven effect to reduce the effect of Alzheimer's. A source of natural galanthamine is from daffodils, but only certain varieties grown under specific conditions produce enough galanthamine to make it economically viable to extract for commercial purposes.
Pyke, Nick   +4 more
openaire   +1 more source

GALANTHAMINE

Targets in Heterocyclic Systems. Vol. 20, 2016
Rinner,, Uwe   +2 more
openaire   +1 more source

GALANTHAMINE

1975
Jasjit S. Bindra, Ranjna Bindra
openaire   +1 more source

Galanthamine hydrobromide in mania

The Lancet, 1991
Ernir Snorrason, JónG. Stefánsson
openaire   +1 more source

GALANTHAMINE

1976
Darshan Ranganathan   +1 more
openaire   +1 more source

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