Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Uses of histone acetyltransferase activators

a technology of histone acetyltransferase and activator, which is applied in the direction of drug compositions, cardiovascular disorders, organic chemistry, etc., can solve the problems of limited efficacy, untoward side effects, and many of these suffer, so as to reduce pain, anxiety or fear, reduce anxiety or fear, and reduce anxiety.

Inactive Publication Date: 2018-02-22
THE TRUSTEES OF COLUMBIA UNIV IN THE CITY OF NEW YORK
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides a method for improving memory and learning in normal subjects. The methods may reduce pain, anxiety or fear. They may increase neurotransmission and decrease anxiety. The methods may be beneficial for subjects who do not have a neurodegenerative condition or disease.

Problems solved by technology

However, many of these suffer from limited efficacy and / or untoward side effects due to their mechanisms of action.

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
  • Uses of histone acetyltransferase activators
  • Uses of histone acetyltransferase activators
  • Uses of histone acetyltransferase activators

Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis of Compound 1

[0128]

[0129]HAT Activator compound, compound 1 (I) was prepared according to Scheme 1. A solution of commercially available ethyl 6-ethoxy-2-hydroxybenzoate (2.10 g, 10.0 mmol) in EtOH and NaOH 1N (10 mL, 1:1) was heated to reflux for 2 h. The solution was acidified by adding HCl 1N and the resulting precipitate was diluted with CH2Cl2 (50 mL) and washed with HCl 1N (3×50 mL). The organic layer was dried under Na2SO4, filtered and evaporated under reduced pressure. A white solid was obtained as the desired product 3(1.65 g, 91%).

[0130]EDC (2.19 mL, 12.35 mmol) was added dropwise to a solution of 3 (1.5 g, 8.23 mmol) and 3-chloro-4-(trifluoromethyl)aniline (1.61 g, 8.23 mmol) in CH2Cl2 (15 mL) at 0° C. The reaction was stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the final product 4 (2.42 g, 82%) was isolated by precipitation from MeOH as a white needle-like solid.

[0131]To a solution of 4 (170 mg, 0.47 mmol), 2-(d...

example 2

HAT Activator Compound Characteristics

[0132]The preparation of compound 1 was without a column and 2 phases were visible: clear and oily. Compound 1 (50 mg / kg, i.p.) was subsequently administered to mice. The des-ethoxy analog of compound 1, MOM, was also administered via cannula (100 μg / μL per side). Two and four hrs after its administration, the mice were sacrificed and hippocampi were extracted. Interestingly, while MOM did not cross the BBB, YF2 (compound 1) was able to cross the BBB, penetrate the cells and increase AcH3 (lane 1 vs. lanes 9, 10) (FIG. 1). Given that the compound was not 100% clean and needed to be further purified / verified, more compound 1 was synthesized and purified. Purity was verified through Nuclear Magnetic Resonance (NMR) spectroscopy. Mice were administered with compound 1 (i.p. dissolved in saline) at 5, 10, 20 mg / Kg. Hippocampus extraction was made at 3 different time points (0.5, 1 and 2 hrs post treatment). A western blotting for AcH3 was then perfo...

example 3

Compound 1 Increases Histone Acetylation by HAT Activation, Not HDAC Inhibition

[0133]HDAC inhibition causes an increase in histone acetylation. The inventors examined whether histone acetylation occurred via HDAC inhibition. The summary of the results is depicted in Table 1. The mean IC50 values of the compounds (compound 1 and SAHA) are summarized in Table 1.

TABLE 1Inhibitory Effects of the Compounds on HDAC ActivitiesIC50 (nM) or % InhibitionHDACs1SAHAHDAC1>200 μM31HDAC3 / NCOR2>200 μM38HDAC5FL>200 μM>10 μMHDAC6>200 μM30HADC7>200 μM>10 μMHDAC8>200 μM2,236  HDAC10>200 μM65HDAC11>200 μM>10 μMSirtuin 1>200 μM>10 μMSirtuin 2>200 μM>10 μM

[0134]The experiments were done blind, and the studies show that compound 1 has no HDAC inhibition properties. Compound 1 does not inhibit HDACs.

[0135]Materials and Methods

[0136]Materials:

[0137]HDAC Assay Buffer (BPS catalog number 50031)

[0138]HDAC Assay Developer (BPS catalog number 50030)

[0139]HDAC Substrate 1 (BPS number 50032)

[0140]HDAC Substrate 3 (...

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

No PUM Login to View More

Abstract

The invention provides methods for enhancing histone acylation, learning, memory and / or cognition in subjects with compound (I) or compositions comprising compound (I), or a pharmaceutically acceptable salt thereof.

Description

[0001]This application claims priority to U.S. Provisional Application No. 61 / 495,495, filed on Jun. 10, 2011, the entirety of which is incorporated herein by reference.GOVERNMENT SUPPORT[0002]This invention was made with government support under R01-NS049442 awarded by the National Institute of Neurological Disorders and Stroke (NINDS), and under AG034248 awarded by the National Institute of Aging (NIA). The government has certain rights in the invention.[0003]All patents, patent applications and publications cited herein are hereby incorporated by reference in their entirety. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art as known to those skilled therein as of the date of the invention described and claimed herein.[0004]This patent disclosure contains material that is subject to copyright protection. The copyright owner has no objection to the facsimile repro...

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): C07C237/44A61K31/167
CPCC07C237/44A61K31/167A61P25/00A61P25/14A61P25/16A61P25/28A61P25/32A61P31/00A61P31/18A61P43/00A61P9/00A61P9/02
Inventor FRANCIS, YITSHAKARANCIO, OTTAVIOFA, MAURO
Owner THE TRUSTEES OF COLUMBIA UNIV IN THE CITY OF NEW YORK
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com