Novel Partial Retinoid X Receptor Agonists -- additional compounds not disclosed in M15-137L

Peter Jurutka (Inventor), Pamela Marshall (Inventor), Carl Wagner (Inventor)

Research output: Patent

Abstract

The human retinoid X receptors (RXRs) function as transcriptional regulators, often in partnership with members of a larger nuclear receptor family of transcription factors. RXR agonists have been shown to modulate RXR transcription and activate or repress various biological pathways and effect therapeutic results for various conditions. Bexarotene (Targretin) is a synthetic retinoid analog used to treat cutaneous T-cell lymphoma (as well as off label to treat other types of cancer). However, recent research may show significant potential it its use for treatment of Alzheimer's disease. Bexarotene is especially effective because it has specific high affinity for RXRs. HOwever, Bexarotene treatment has some side effects, namely hypothyroidism, hyperlipidemia, and cutaneous toxicity, which may be due to its activation of RXR in several different tissues. Researchers at Arizona State University have developed a portfolio of compounds which are more potent analogs and derivatives of Bexarotene that may provide alternatives to Bexarotene usage. These analogs have a higher selectivity for the retinoid X receptor versus the retinoic acid receptor (RAR) and can be uncoupled from the drastic lipid changes and thyroid axis variations. Additionally, in astrocytes and microglia, these Bexarotene analogs increase expression of ApoE and highly lipidated HDLs, which then promote clearance of amyloid beta in the brain. These new analogs may provide viable and efficacious alternatives to Bexarotene for cancer, Alzheimer's disease (AD), Parkinson's disease (PD), schizophrenia, and other neurodegenerative diseases. Further, animal testing suggests that hte improved PK and triglyceride profiles make these compounds compelling therapeutic candidates. Potential Applications Anti-cancer treatment CTCL, colon, breast, lung, pancreatic and others May be useful in treatment of AD & other neurodegenerative diseases May be useful in treatment of RXR-pathway related diseases May be useful in treatment of diseases associated with dopamine deficiency PD, schizophrenia, depression, and other psychotic disorders May be useful in treatment of non-insulin dependent diabetes mellitus Drug discovery Benefits and Advantages Several analogs demonstrate higher affinity/activation for RXR than Bexarotene Higher efficacies/potency/specificity may allow for lower doses thus alleviating some side effects Improved side effects than parent compound, bexarotene May stimulate gene expression better than Bexarotene Some compounds may be less toxic than bexarotene and produce statistically lower triglyceride levels Improved PK characteristics Dowload Original PDF For more information about the inventor(s) and their research, please see Dr. Wagner's departmental webpage Dr. Jurutka's departmental webpage Dr. Marshall's departmental webpage
Original languageEnglish (US)
StatePublished - Mar 3 2015

Fingerprint

Retinoid X Receptors
Alzheimer Disease
Neurodegenerative Diseases
Parkinson Disease
galantide
bexarotene
Schizophrenia
Triglycerides
Therapeutics
Inventors
Deficiency Diseases
Cutaneous T-Cell Lymphoma
Neoplasms
Retinoic Acid Receptors
Poisons
Retinoids
Microglia
Apolipoproteins E
Therapeutic Uses
Drug Discovery

Cite this

@misc{6349aeb05784424193b0c9f409d75397,
title = "Novel Partial Retinoid X Receptor Agonists -- additional compounds not disclosed in M15-137L",
abstract = "The human retinoid X receptors (RXRs) function as transcriptional regulators, often in partnership with members of a larger nuclear receptor family of transcription factors. RXR agonists have been shown to modulate RXR transcription and activate or repress various biological pathways and effect therapeutic results for various conditions. Bexarotene (Targretin) is a synthetic retinoid analog used to treat cutaneous T-cell lymphoma (as well as off label to treat other types of cancer). However, recent research may show significant potential it its use for treatment of Alzheimer's disease. Bexarotene is especially effective because it has specific high affinity for RXRs. HOwever, Bexarotene treatment has some side effects, namely hypothyroidism, hyperlipidemia, and cutaneous toxicity, which may be due to its activation of RXR in several different tissues. Researchers at Arizona State University have developed a portfolio of compounds which are more potent analogs and derivatives of Bexarotene that may provide alternatives to Bexarotene usage. These analogs have a higher selectivity for the retinoid X receptor versus the retinoic acid receptor (RAR) and can be uncoupled from the drastic lipid changes and thyroid axis variations. Additionally, in astrocytes and microglia, these Bexarotene analogs increase expression of ApoE and highly lipidated HDLs, which then promote clearance of amyloid beta in the brain. These new analogs may provide viable and efficacious alternatives to Bexarotene for cancer, Alzheimer's disease (AD), Parkinson's disease (PD), schizophrenia, and other neurodegenerative diseases. Further, animal testing suggests that hte improved PK and triglyceride profiles make these compounds compelling therapeutic candidates. Potential Applications Anti-cancer treatment CTCL, colon, breast, lung, pancreatic and others May be useful in treatment of AD & other neurodegenerative diseases May be useful in treatment of RXR-pathway related diseases May be useful in treatment of diseases associated with dopamine deficiency PD, schizophrenia, depression, and other psychotic disorders May be useful in treatment of non-insulin dependent diabetes mellitus Drug discovery Benefits and Advantages Several analogs demonstrate higher affinity/activation for RXR than Bexarotene Higher efficacies/potency/specificity may allow for lower doses thus alleviating some side effects Improved side effects than parent compound, bexarotene May stimulate gene expression better than Bexarotene Some compounds may be less toxic than bexarotene and produce statistically lower triglyceride levels Improved PK characteristics Dowload Original PDF For more information about the inventor(s) and their research, please see Dr. Wagner's departmental webpage Dr. Jurutka's departmental webpage Dr. Marshall's departmental webpage",
author = "Peter Jurutka and Pamela Marshall and Carl Wagner",
year = "2015",
month = "3",
day = "3",
language = "English (US)",
type = "Patent",

}

TY - PAT

T1 - Novel Partial Retinoid X Receptor Agonists -- additional compounds not disclosed in M15-137L

AU - Jurutka, Peter

AU - Marshall, Pamela

AU - Wagner, Carl

PY - 2015/3/3

Y1 - 2015/3/3

N2 - The human retinoid X receptors (RXRs) function as transcriptional regulators, often in partnership with members of a larger nuclear receptor family of transcription factors. RXR agonists have been shown to modulate RXR transcription and activate or repress various biological pathways and effect therapeutic results for various conditions. Bexarotene (Targretin) is a synthetic retinoid analog used to treat cutaneous T-cell lymphoma (as well as off label to treat other types of cancer). However, recent research may show significant potential it its use for treatment of Alzheimer's disease. Bexarotene is especially effective because it has specific high affinity for RXRs. HOwever, Bexarotene treatment has some side effects, namely hypothyroidism, hyperlipidemia, and cutaneous toxicity, which may be due to its activation of RXR in several different tissues. Researchers at Arizona State University have developed a portfolio of compounds which are more potent analogs and derivatives of Bexarotene that may provide alternatives to Bexarotene usage. These analogs have a higher selectivity for the retinoid X receptor versus the retinoic acid receptor (RAR) and can be uncoupled from the drastic lipid changes and thyroid axis variations. Additionally, in astrocytes and microglia, these Bexarotene analogs increase expression of ApoE and highly lipidated HDLs, which then promote clearance of amyloid beta in the brain. These new analogs may provide viable and efficacious alternatives to Bexarotene for cancer, Alzheimer's disease (AD), Parkinson's disease (PD), schizophrenia, and other neurodegenerative diseases. Further, animal testing suggests that hte improved PK and triglyceride profiles make these compounds compelling therapeutic candidates. Potential Applications Anti-cancer treatment CTCL, colon, breast, lung, pancreatic and others May be useful in treatment of AD & other neurodegenerative diseases May be useful in treatment of RXR-pathway related diseases May be useful in treatment of diseases associated with dopamine deficiency PD, schizophrenia, depression, and other psychotic disorders May be useful in treatment of non-insulin dependent diabetes mellitus Drug discovery Benefits and Advantages Several analogs demonstrate higher affinity/activation for RXR than Bexarotene Higher efficacies/potency/specificity may allow for lower doses thus alleviating some side effects Improved side effects than parent compound, bexarotene May stimulate gene expression better than Bexarotene Some compounds may be less toxic than bexarotene and produce statistically lower triglyceride levels Improved PK characteristics Dowload Original PDF For more information about the inventor(s) and their research, please see Dr. Wagner's departmental webpage Dr. Jurutka's departmental webpage Dr. Marshall's departmental webpage

AB - The human retinoid X receptors (RXRs) function as transcriptional regulators, often in partnership with members of a larger nuclear receptor family of transcription factors. RXR agonists have been shown to modulate RXR transcription and activate or repress various biological pathways and effect therapeutic results for various conditions. Bexarotene (Targretin) is a synthetic retinoid analog used to treat cutaneous T-cell lymphoma (as well as off label to treat other types of cancer). However, recent research may show significant potential it its use for treatment of Alzheimer's disease. Bexarotene is especially effective because it has specific high affinity for RXRs. HOwever, Bexarotene treatment has some side effects, namely hypothyroidism, hyperlipidemia, and cutaneous toxicity, which may be due to its activation of RXR in several different tissues. Researchers at Arizona State University have developed a portfolio of compounds which are more potent analogs and derivatives of Bexarotene that may provide alternatives to Bexarotene usage. These analogs have a higher selectivity for the retinoid X receptor versus the retinoic acid receptor (RAR) and can be uncoupled from the drastic lipid changes and thyroid axis variations. Additionally, in astrocytes and microglia, these Bexarotene analogs increase expression of ApoE and highly lipidated HDLs, which then promote clearance of amyloid beta in the brain. These new analogs may provide viable and efficacious alternatives to Bexarotene for cancer, Alzheimer's disease (AD), Parkinson's disease (PD), schizophrenia, and other neurodegenerative diseases. Further, animal testing suggests that hte improved PK and triglyceride profiles make these compounds compelling therapeutic candidates. Potential Applications Anti-cancer treatment CTCL, colon, breast, lung, pancreatic and others May be useful in treatment of AD & other neurodegenerative diseases May be useful in treatment of RXR-pathway related diseases May be useful in treatment of diseases associated with dopamine deficiency PD, schizophrenia, depression, and other psychotic disorders May be useful in treatment of non-insulin dependent diabetes mellitus Drug discovery Benefits and Advantages Several analogs demonstrate higher affinity/activation for RXR than Bexarotene Higher efficacies/potency/specificity may allow for lower doses thus alleviating some side effects Improved side effects than parent compound, bexarotene May stimulate gene expression better than Bexarotene Some compounds may be less toxic than bexarotene and produce statistically lower triglyceride levels Improved PK characteristics Dowload Original PDF For more information about the inventor(s) and their research, please see Dr. Wagner's departmental webpage Dr. Jurutka's departmental webpage Dr. Marshall's departmental webpage

M3 - Patent

ER -