Charged ion channel blockers and methods for use

a technology of ion channel blockers and ion channels, applied in the direction of heterocyclic compound active ingredients, organic chemistry, drug compositions, etc., can solve the problems of non-productive dry cough, inappropriate cough reflexes, and unproductive local anesthetic administration

Inactive Publication Date: 2021-05-06
NOCION THERAPEUTICS INC
View PDF1 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Thus, while the goal of topical or regional anesthesia is to block transmission of signals in nociceptors to prevent pain, administration of local anesthetics also produces unwanted or deleterious effects such as general numbness from block of low threshold pressure and touch receptors, motor deficits and / or paralysis from block of motor axons and other complications from block of autonomic fibers.
This reflex, however, can became aberrant in a number of diseases leading to a non-productive dry cough where hyper- or allo-tussive states exist.
In addition, inappropriate cough reflexes can be manifested acutely and chronically following viral infection.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Charged ion channel blockers and methods for use
  • Charged ion channel blockers and methods for use
  • Charged ion channel blockers and methods for use

Examples

Experimental program
Comparison scheme
Effect test

example 1

Syntheses

General Abbreviation Definitions

[0193]ACN acetonitrile

aq. aqueous

° C. degrees Celsius

δ chemical shift (ppm)

DCM dichloromethane

DMSO dimethyl sulfoxide

ESI electrospray ionization

Et2O diethyl ether

EtOAc ethyl acetate

h hour

MeOH methanol

mHz megahertz

min min

ml milliliter

MS mass spectrometry

m / z mass to charge ratio

NMR nuclear magnetic resonance

RT room temperature

TLC thin layer chromatography

UV ultraviolet light

Synthesis of 1-benzyl-1-(2-((2-(methoxycarbonyl)-4-methylthiophen-3-yl)amino)-2-oxoethyl)azepan-1-ium bromide

[0194]

Synthesis of intermediate methyl 3-(2-bromoacetamido)-4-methylthiophene-2-carboxylate

[0195]A stirred suspension of methyl 3-amino-4-methylthiophene-2-carboxylate (5 g, 29.20 mmol) in water (50.0 mL) was cooled to 0° C. and 2-bromoacetyl bromide (12 mL, 137.74 mmol) was added drop wise. The resulting mixture was allowed to stir at RT for 16 h as progress of the reaction was monitored by TLC (10% EtOAc in petroleum ether, visualization by UV). The reaction mixture...

example 2

n of Nav1.7 Current

[0200]Representative compounds of the invention were synthesized according to the described methods and tested for the ability to inhibit voltage-gated sodium channels.

Cell Culture

[0201]NaV1.7 was expressed upon induction with tetracycline. Cells were cultured in DVEM containing 10% dialyzed Fetal Bovine Serum (VWR, Radnor, Pa.),1% Glutamax (VWR, Radnor, Pa.), 1% Penicillin-Streptomycin (VWR, Radnor, Pa.), 100 mg / L Hygromycin (Thermo Fisher Scientific, Waltham, Mass. and 5 mg / L Blasticidin (Alfa Aesar, Haverhill, Mass.). Cells were grown and maintained at 37° C. in a humidified environment containing 10% CO2 in air. Cells were detached from the culture flask for passage and harvested using 0.05% Trypsin-EDTA (Thermo Fisher Scientific, Waltham, Mass.). To induce NaV1.7, cells were induced with tetracycline (0.1-1 μg / mL, IBI Scientific, Peosta, Iowa) the day before recording and plated onto 24-well plates. Cells were washed with DPBS (VWR, Radnor, Pa.), trypsinized ...

example 3

Permeability

[0213]The PAMPA assay (pION, Inc., Woburn Mass.) was used to determine the ability of compounds of the invention to cross an artificial lipid membrane by passive diffusion. Test compounds were dissolved in DMSO (10 mM) and diluted 200-fold in buffer (pION Inc., pH 7.4) to provide 50 uM stock solutions. Buffer (150 μL) was added to a UV blank plate and stock solutions (150 μL) were transferred to a UV reference plate. The blank and reference spectrum were read using a spectrophotometer. Stock solutions (200 μL) were added to the donor plate of the PAMPA sandwich plate and an accept plate painted with GIT lipid (pION Inc, 5 μL) was placed on top. Buffer (200 μL) was added to the acceptor plate and the PAMPA sandwich plate was incubated for 4 hours. Aliquots (150 μL) from the acceptor plate were added to a UV plate and read as acceptor spectrum. Aliquots (150 μL) of the donor solutions were added to a UV analysis plate and read as donor spectrum. The permeability coefficien...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
enantiomeric excessaaaaaaaaaa
enantiomeric excessaaaaaaaaaa
enantiomeric excessaaaaaaaaaa
Login to view more

Abstract

The invention provides compounds of Formula (I), or pharmaceutically acceptable salts thereof:The compounds, compositions, methods and kits of the invention are useful for the treatment of pain, itch, and neurogenic inflammation.

Description

RELATED APPLICATIONS[0001]This application is a continuation of application Ser. No. 16 / 815,325 filed on Mar. 11, 2020, which claims the benefit of U.S. Provisional Application Ser. No. 62 / 931,444 filed Nov. 6, 2019. The entire contents of the above applications are incorporated by reference herein.BACKGROUND OF THE INVENTION[0002]The invention features compounds, compositions and methods for the selective inhibition of sensory neurons (nociceptors, cough receptors and pruriceptors) and the treatment of neurogenic inflammation by targeting nociceptors with a small molecule drug, while minimizing effects on non-nociceptive-sensing neurons or other types of cells. According to the method of the invention, small, cationic drug molecules gain access to the intracellular compartment of sensory neurons via entry through large pore receptor / ion channels that are present in pain- cough- and itch-sensing neurons but to a lesser extent or not at all in other types of neurons or in other types...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/55C07D409/12A61K45/06A61K31/4436A61K31/4025
CPCA61K31/55C07D409/12A61K31/4025A61K31/4436A61K45/06A61P25/00C07D333/38A61K31/381A61K31/452
Inventor COLE, BRIDGET MCCARTHYELLIS, JAMES LAMOND
Owner NOCION THERAPEUTICS INC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap