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Cholinergic enhancers with improved blood-brain barrier permeability for the treatment of diseases accompanied by cognitive impairment

a blood-brain barrier and enhancer technology, applied in the field of cholinergic enhancers with improved blood-brain barrier permeability for the treatment of diseases accompanied by cognitive impairment, can solve the problems of limited bioavailability, poor pharmacodynamic effects, and a small amount of galantamine in the brain, and achieve low peripheral side effects and high pharmacodynamic effects

Inactive Publication Date: 2009-10-08
GALANTOS PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0025]Some embodiments provide compounds usable as pro-drugs or as a medicament having high pharmacodynamic effects in the brain's central nervous system and low peripheral side effects.
[0045]In this way the therapeutic effect-to-dose ratio can be increased and adverse side-effects can be reduced when the drugs are administered as medicaments for the diseases mentioned in the present application. This object is particularly met e.g., by site-specific chemical modification (derivatization) of said compounds.

Problems solved by technology

However, much higher log P values are also of disadvantage, as high lipophilicity is often associated with toxicity, non-specific binding, insufficient oral absorption and limited bioavailability.
The rather low levels of accumulation of galantamine in the brain, when administered as the unmodified drug, are a serious disadvantage with respect to the drug's therapeutic use, i.e., for the treatment of cognitive disorders, such as AD.
In addition to their therapeutic benefits, these drugs induce adverse peripheral and central side effects; the muscarinic ones including nausea, vomiting and diarrhea, and the nicotinic ones including tremors and muscle cramps.
The comparatively low levels of accumulation of Galantamine in the brain are a serious disadvantage with respect to the drug's therapeutic use, i.e., for the treatment of cognitive disorders, such as AD.
However, selective chemical modification for the purpose of increasing penetration through the blood-brain barrier is not considered.
However, selective chemical modifications or other means of improving blood-brain barrier penetration are not considered.
However, selective chemical modifications or other means of improving blood-brain barrier penetration are not considered.
However, it does not deal with other derivatives of Galantamine, or their use as medicaments, or chemical modifications aimed at enhancing blood-barrier penetration of said compounds.
However, no concept is provided in this application for increasing the penetration of compounds through the blood-brain barrier.

Method used

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  • Cholinergic enhancers with improved blood-brain barrier permeability for the treatment of diseases accompanied by cognitive impairment
  • Cholinergic enhancers with improved blood-brain barrier permeability for the treatment of diseases accompanied by cognitive impairment
  • Cholinergic enhancers with improved blood-brain barrier permeability for the treatment of diseases accompanied by cognitive impairment

Examples

Experimental program
Comparison scheme
Effect test

example 1

N-Methoxymethyl-galanthaminiumchloride(=(4aS,6R,8aS)-4a,5,9,10,11,12-Hexahydro-11-methoxymethyl-11-methyl-6H-6-hydroxy-3-methoxy-benzofuro[3a,3,2-ef][2]benzaze-pinium, chloride)

[0204]N-Methoxymethyl-galanthaminiumchloride is obtained from Galantamine via alkylation using chloromethylmethylether:

[0205]To a solution of (−)-Galantamine (5.00 g, 17.4 mmol) in dry dimethylformamide (12 mL) chloromethylmethylether (1.12 g, 13.9 mmol) is added at −5 bis 0° C. in the course of 15 min and stirred for 4 hrs. at room temperature. The reaction mixture is poured on ethyl acetatet (500 mL) and the precipitate obtained is filtered and washed using ethyl acetate (3×50 mL).

[0206]The crude product (4.20 g, 82%) has a purity of 96% (HPLC). For further purification the crude product is dissolved in dry ethanol, stirred after the addition of activated charcoal, filtered and added to ethyl acetate (500 mL). The precipitate is filtered and washed using ethyl acetate (3×50 mL) and dry diethylether (1×50 mL...

example 2

Tert-Butoxycarbonylamino-acetic acid (N-norgalanthaminyl)-methyl ester

[0211]

[0212]To a solution of N-Boc-glycine chloromethylester (1.0 mmol) and norgalantamine (1.0 mmol) in dry DMF (2.0 mL) triethylamine (3 mmol) was added dropwise and the reaction stirred under nitrogen for 3 days. The triethylammonium chloride formed was filtered and washed with dry ether and the filtrate rotoevaporated to dryness. The residue was redissolved in dry acetone (2 ml) upon heating and left to stand overnight at 4° C. for additional precipitation of the triethylammonium salt. After renewed filtration and rotoevaporation the mixture was chromatographed on silica using ethyl acetate / petrol ether. The target product was isolated as an oil.

[0213]13H NMR (DMSO-d6) δ 28.5, 33.9, 37.9, 42.0, 48.2, 51.2, 56.2, 56.9, 61.9, 79.5, 79.9, 88.8, 111.8, 121.3, 126.6, 129.8, 130.8, 133.6, 145.8, 148.2, 156.3, 169.6.

example 3

2-tert-Butoxycarbonylamino-3-phenylpropionic acetic acid (N-norgalantha-minyl)-methyl ester

[0214]

[0215]This compound was prepared using the procedure of example 2 with N-Boc-phenylalanine chloromethylester.

[0216]13H NMR (DMSO-d6) δ 28.5, 33.9, 36.9, 37.9, 48.2, 51.2, 54.6, 56.2, 56.9, 61.9, 79.5, 80.2, 88.8, 111.8, 121.3, 126.0, 126.6, 127.8, 128.7, 129.8, 130.8, 133.6, 139.5, 145.8, 148.2, 4156.0, 171.6.

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Abstract

The present invention refers to compounds that, in addition to enhancing the sensitivity to acetylcholine and choline, and their exogenous agonists, of neuronal cholinergic receptors and / or acting as cholinesterase inhibitors and / or neuroprotective agents, have enhanced blood-brain barrier permeability in comparison to their parent compounds. The compounds are derived (either formally by their chemical structure or directly by chemical synthesis) from natural compounds belonging to the class of amaryllidaceae alkaloids e.g., galantamine, narwedine and lycoramine, or from metabolites of said compounds. The compounds of the present invention can either interact as such with their target molecules, or they can act as “pro-drugs”, in the sense that after reaching their target regions in the body they are converted by hydrolysis or enzymatic attack to the original parent compound and react as such with their target molecules, or both. The compounds of this invention may be used as medicaments.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation-in-part of application Ser. No. 12 / 067,799, filed Jul. 2, 2008, which is U.S. National phase of International Application No. PCT / EP2006 / 009220, filed Sep. 22, 2006, which claims priority to European Patent Application No. EP05020721.6, filed Sep. 22, 2005 and U.S. Provisional Application No. 60 / 780,243, filed Mar. 7, 2006. This application also claims the benefit of U.S. application Ser. No. 11 / 683,148, filed Mar. 7, 2007, which claims priority to U.S. Provisional Application No. 60 / 780,243, filed Mar. 7, 2006. This application also claims the benefit of U.S. provisional application No. 61 / 046,683, filed Apr. 21, 2008. The entire contents of all these applications are hereby incorporated by reference herein in their entireties, as if fully disclosed herein.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The disclosure refers to compounds that, in addition to enhancing the sensitivity to ...

Claims

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Application Information

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IPC IPC(8): A61K31/675C07D223/14A61K31/55C07F9/553
CPCC07D307/91C07D405/12A61K31/55C07F9/6561C07D491/06Y02A50/30
Inventor MAELICKE, ALFRED
Owner GALANTOS PHARMA
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