Identification of angiotensin II receptor subtypes

AT Chiu, WF Herblin, DE McCall, RJ Ardecky… - Biochemical and …, 1989 - Elsevier
We have demonstrated the existence of two distinct subtypes of the angiotensin II receptor
in the rat adrenal gland using radioligand binding and tissue section autoradiography. The …

Activity of a novel 4-quinolinecarboxylic acid, NSC 368390 [6-fluoro-2-(2′-fluoro-1, 1′-biphenyl-4-yl)-3-methyl-4-quinolinecarboxylic acid sodium salt], against …

DL Dexter, DP Hesson, RJ Ardecky, GV Rao… - Cancer research, 1985 - AACR
A novel, substituted 4-quinolinecarboxylic acid (NSC 339768) demonstrated antitumor
activity against L1210 leukemia and B16 melanoma in the National Cancer Institute's …

Diabetes reversal by inhibition of the low-molecular-weight tyrosine phosphatase

…, V Zhang, RJ Ardecky, MP Hedrick, J Zou… - Nature chemical …, 2017 - nature.com
Obesity-associated insulin resistance plays a central role in type 2 diabetes. As such, tyrosine
phosphatases that dephosphorylate the insulin receptor (IR) are potential therapeutic …

[PDF][PDF] TGR5 contributes to hepatic cystogenesis in rodents with polycystic liver diseases through cyclic adenosine monophosphate/Gαs signaling

…, PY Lee, X Fung, E Sergienko, RJ Ardecky… - …, 2017 - Wiley Online Library
Hepatic cystogenesis in polycystic liver disease is associated with increased levels of cyclic
adenosine monophosphate (cAMP) in cholangiocytes lining liver cysts. Takeda G protein …

Small-molecule IAP antagonists sensitize cancer cells to TRAIL-induced apoptosis: roles of XIAP and cIAPs

…, M Vamos, M González-López, RJ Ardecky… - Molecular cancer …, 2014 - AACR
TNF-related apoptosis-inducing ligand (TRAIL) is a promising anticancer agent because it
shows apoptosis-inducing activity in transformed, but not in normal, cells. As with most …

Expedient synthesis of highly potent antagonists of inhibitor of apoptosis proteins (IAPs) with unique selectivity for ML-IAP

…, ML Gonzalez, SR Ganji, RJ Ardecky… - ACS chemical …, 2013 - ACS Publications
A series of novel, potent antagonists of the inhibitor of apoptosis proteins (IAPs) were
synthesized in a highly convergent and rapid fashion (≤6 steps) using the Ugi four-component …

Biological characterization of a heterodimer-selective retinoid X receptor modulator: potential benefits for the treatment of type 2 diabetes

MD Leibowitz, RJ Ardecky, MF Boehm… - …, 2006 - academic.oup.com
Specific retinoid X receptor (RXR) agonists, such as LG100268 (LG268), and the thiazolidinedione
(TZD) PPARγ agonists, such as rosiglitazone, produce insulin sensitization in rodent …

A tailored therapy for the metabolic syndrome: the dual peroxisome proliferator-activated receptor-α/γ agonist LY465608 ameliorates insulin resistance and diabetic …

…, AJ Shuker, CJ Rito, JR McCarthy, RJ Ardecky… - Diabetes, 2002 - Am Diabetes Assoc
A novel nonthiazolidinedione dual peroxisome proliferator- activated receptor (PPAR)-α/γ
agonist, LY465608, was designed to address the major metabolic disturbances of type 2 …

Discovery of β-arrestin biased, orally bioavailable, and CNS penetrant neurotensin receptor 1 (NTR1) allosteric modulators

…, MP Hedrick, B Falter, RJ Ardecky… - Journal of medicinal …, 2019 - ACS Publications
Neurotensin receptor 1 (NTR1) is a G protein coupled receptor that is widely expressed
throughout the central nervous system where it acts as a neuromodulator. Neurotensin receptors …

LGD-5552, an Antiinflammatory Glucocorticoid Receptor Ligand with Reduced Side Effects, in Vivo

FJ López, RJ Ardecky, B Bebo, K Benbatoul… - …, 2008 - academic.oup.com
Treatment of inflammation is often accomplished through the use of glucocorticoids. However,
their use is limited by side effects. We have examined the activity of a novel glucocorticoid …