The benzenesulfoamide T0901317 [N-(2,2,2-trifluoroethyl)-N-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]-benzenesulfonamide] is a novel retinoic acid receptor-related orphan receptor-alpha/gamma inverse agonist.
about
Prospero-related homeobox 1 (Prox1) functions as a novel modulator of retinoic acid-related orphan receptors α- and γ-mediated transactivationRegulation of circadian behaviour and metabolism by synthetic REV-ERB agonistsTargeting Th17 Cells with Small Molecules and Small Interference RNAOrphan nuclear receptors and the regulation of nutrient metabolism: understanding obesityROR nuclear receptors: structures, related diseases, and drug discoveryThe therapeutic potential of RORγ modulators in the treatment of human diseaseChronopharmacology: new insights and therapeutic implicationsCytochrome P450 20A1 in zebrafish: Cloning, regulation and potential involvement in hyperactivity disordersStructural Basis of Digoxin That Antagonizes ROR t Receptor Activity and Suppresses Th17 Cell Differentiation and Interleukin (IL)-17 ProductionBenzoxazepines Achieve Potent Suppression of IL-17 Release in Human T-Helper 17 (TH 17) Cells through an Induced-Fit Binding Mode to the Nuclear Receptor RORγCircadian molecular clock in lung pathophysiologyRegulation of Adaptive Immunity in Health and Disease by Cholesterol MetabolismTherapeutic Effect of a Synthetic RORα/γ Agonist in an Animal Model of AutismAdipogenesis and insulin sensitivity in obesity are regulated by retinoid-related orphan receptor gammaDevelopment of a Topical Treatment for Psoriasis Targeting RORγ: From Bench to SkinRORγ directly regulates the circadian expression of clock genes and downstream targets in vivoMacrophage-independent regulation of reverse cholesterol transport by liver X receptors.Identification of an allosteric binding site for RORγt inhibition.Liver LXRα expression is crucial for whole body cholesterol homeostasis and reverse cholesterol transport in miceHydrogen/deuterium exchange reveals distinct agonist/partial agonist receptor dynamics within vitamin D receptor/retinoid X receptor heterodimerFasting-induced FGF21 is repressed by LXR activation via recruitment of an HDAC3 corepressor complex in miceArtemisia scoparia enhances adipocyte development and endocrine function in vitro and enhances insulin action in vivoRegulation of FGF21 expression and secretion by retinoic acid receptor-related orphan receptor alpha.A second class of nuclear receptors for oxysterols: Regulation of RORalpha and RORgamma activity by 24S-hydroxycholesterol (cerebrosterol)Ligand regulation of retinoic acid receptor-related orphan receptors: implications for development of novel therapeuticsGenome-wide landscape of liver X receptor chromatin binding and gene regulation in human macrophages.Regulation of expression of citrate synthase by the retinoic acid receptor-related orphan receptor α (RORα)Action of RORs and their ligands in (patho)physiology.REV-ERB and ROR nuclear receptors as drug targets.Identification of SR1078, a synthetic agonist for the orphan nuclear receptors RORα and RORγ.LXR-mediated inhibition of CD4+ T helper cells.Crucial roles of mixed-lineage leukemia 3 and 4 as epigenetic switches of the hepatic circadian clock controlling bile acid homeostasis in mice.Small molecule modifiers of circadian clocks.Small molecule amides as potent ROR-γ selective modulators.Liver X receptor (LXR) mediates negative regulation of mouse and human Th17 differentiationNuclear receptors take center stage in Th17 cell-mediated autoimmunity.Identification of SR8278, a synthetic antagonist of the nuclear heme receptor REV-ERB.Homozygous staggerer (sg/sg) mice display improved insulin sensitivity and enhanced glucose uptake in skeletal muscleIdentification of SR3335 (ML-176): a synthetic RORα selective inverse agonistThe identification of naturally occurring neoruscogenin as a bioavailable, potent, and high-affinity agonist of the nuclear receptor RORα (NR1F1).
P2860
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P2860
The benzenesulfoamide T0901317 [N-(2,2,2-trifluoroethyl)-N-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]-benzenesulfonamide] is a novel retinoic acid receptor-related orphan receptor-alpha/gamma inverse agonist.
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
The benzenesulfoamide T0901317 ...... r-alpha/gamma inverse agonist.
@ast
The benzenesulfoamide T0901317 ...... r-alpha/gamma inverse agonist.
@en
type
label
The benzenesulfoamide T0901317 ...... r-alpha/gamma inverse agonist.
@ast
The benzenesulfoamide T0901317 ...... r-alpha/gamma inverse agonist.
@en
prefLabel
The benzenesulfoamide T0901317 ...... r-alpha/gamma inverse agonist.
@ast
The benzenesulfoamide T0901317 ...... r-alpha/gamma inverse agonist.
@en
P2093
P2860
P356
P1476
The benzenesulfoamide T0901317 ...... or-alpha/gamma inverse agonist
@en
P2093
Juliana J Conkright
Laura A Solt
Monica A Istrate
Naresh Kumar
Patrick R Griffin
Ruben D Garcia-Ordonez
Scott A Busby
Yongjun Wang
P2860
P304
P356
10.1124/MOL.109.060905
P50
P577
2009-11-03T00:00:00Z