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AB142808

T0901317, LXR agonist

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(2 Publications)

MW 481.3 Da, Purity >99%. Potent, non-selective LXR agonist (EC50 = 50 nM). Increases ABCA1 expression associated with cholesterol efflux regulation and HDL metabolism. Increases muscle expression of PPAR-δ. Shows antiobesogenic effects in vivo. .

View Alternative Names

AIS, ANDR_HUMAN, AR, AR8, AW107337, Androgen nuclear receptor variant 2, Androgen receptor, Androgen receptor (dihydrotestosterone receptor; testicular feminization; spinal and bulbar muscular atrophy; Kennedy disease), BAR, BXR, Bile acid receptor, DHTR, Dihydro testosterone receptor, Dihydrotestosterone receptor (DHTR), FLJ00280, FLJ00318, FLJ16020, FLJ16733, Farnesoid X-activated receptor, Farnesol receptor HRR-1, G-6-Pase, G6PC_HUMAN, G6PT, G6Pase-alpha, GCCR, GCRST, GCR_HUMAN, GR, GSD1, GSD1a, Glucocorticoid receptor, Glucose-6-phosphatase, Glucose-6-phosphatase alpha, Grl1, HRR 1, HUMARA, HYSP1, IMD42, KD, Kennedy disease (KD), LX receptor beta, LXR a, LXR b, LXR beta, Liver X nuclear receptor beta, Liver X receptor alpha, Liver X receptor beta, MGC102720, MGC129539, MGC163350, MGC93613, NER I, NER1, NR1F1, NR1F3, NR1H2_HUMAN, NR1H3_HUMAN, NR1I2_HUMAN, NR2B1, NR3C4, Nuclear orphan receptor LXR beta, Nuclear receptor NER, Nuclear receptor ROR-alpha, Nuclear receptor ROR-gamma, Nuclear receptor RZR-alpha, Nuclear receptor RZR-gamma, Nuclear receptor subfamily 1 group F member 1, Nuclear receptor subfamily 1 group F member 3, Nuclear receptor subfamily 1 group H member 2, Nuclear receptor subfamily 1 group H member 3, Nuclear receptor subfamily 1 group I member 2, Nuclear receptor subfamily 2 group B member 1, Nuclear receptor subfamily 3 group C member 1, Nuclear receptor subfamily 3 group C member 4, Nuclear receptor subfamily 3 group C member 4 (NR3C4), ONR 1, OR-1, OTTHUMP00000022510, OTTHUMP00000215173, OTTHUMP00000215174, OTTHUMP00000215175, Orphan nuclear receptor PAR 1, Orphan nuclear receptor PXR, Oxysterols receptor LXR-alpha, Oxysterols receptor LXR-beta, PAR, PAR q, PRR, Pregnane X receptor, RAR related orphan nuclear receptor variant 2, RAR related orphan receptor C, isoform a, RAR related orphan receptor alpha, RAR related orphan receptor gamma, RAR-related orphan receptor A, RAR-related orphan receptor C, RIP 14, RIP15, RLD 1, RORA_HUMAN, RORG_HUMAN, RP23-281C18.19, RXR alpha1, RXR-interacting protein 14, RXRA_HUMAN, RZR GAMMA, RZR-ALPHA, RZRA, RZRG, Retinoic acid binding receptor gamma, Retinoic acid receptor RXR-alpha, Retinoid X nuclear receptor alpha, Retinoid X receptor alpha, Retinoid X receptor-interacting protein 14, Retinoid-related orphan receptor-alpha, Retinoid-related orphan receptor-gamma, Rorc, SBMA, SMAX1, SXR, Spinal and bulbar muscular atrophy, Spinal and bulbar muscular atrophy (SBMA), Steroid and xenobiotic receptor, Steroid hormone nuclear receptor NER, TFM, TOR, Testicular Feminization (TFM), Transcription factor RZR alpha, UNR, Ubiquitously-expressed nuclear receptor, androgen receptor splice variant 4b, fhl2a, g6pc, glucocorticoid nuclear receptor variant 1, glucose-6-phosphatase, catalytic subunit, nr3c1, nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor), pregnane X nuclear receptor variant 2

1 Images
Chemical Structure - T0901317, LXR agonist (AB142808)
  • Chemical Structure

Lab

Chemical Structure - T0901317, LXR agonist (AB142808)

2D chemical structure image of ab142808, T0901317, LXR agonist

Key facts

CAS number

293754-55-9

Purity

>99%

Form

Solid

form

Molecular weight

481.3 Da

Molecular formula

C<sub>1</sub><sub>7</sub>H<sub>1</sub><sub>2</sub>F<sub>9</sub>NO<sub>3</sub>S

PubChem

447912

Nature

Synthetic

Solubility

Soluble in DMSO to 100 mM

Soluble in ethanol to 100mM

Biochemical name

N-(2,2,2-Trifluoroethyl)-N-{4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}benzenesulfonamide

Biological description

Potent, non-selective LXR agonist (EC50 = 50 nM). Increases ABCA1 expression associated with cholesterol efflux regulation and HDL metabolism. Increases muscle expression of PPAR-δ. Shows antiobesogenic effects in vivo.

Canonical smiles

C1=CC=C(C=C1)S(=O)(=O)N(CC(F)(F)F)C2=CC=C(C=C2)C(C(F)(F)F)(C(F)(F)F)O

InChi

InChI=1S/C17H12F9NO3S/c18-14(19,20)10-27(31(29,30)13-4-2-1-3-5-13)12-8-6-11(7-9-12)15(28,16(21,22)23)17(24,25)26/h1-9,28H,10H2

InChiKey

SGIWFELWJPNFDH-UHFFFAOYSA-N

IUPAC Name

N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-N-(2,2,2-trifluoroethyl)benzenesulfonamide

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The Glucocorticoid Receptor (GR) LXR alpha Androgen Receptor (AR) PXR Retinoid X Receptor alpha (RXRA) ROR alpha (RORA) ROR gamma LXR beta (NER) and G-6-Pase form a diverse group of nuclear receptors and enzymes. These proteins often share a function in regulating gene expression in response to ligands. Glucocorticoid Receptor Androgen Receptor and Retinoid X Receptor alpha are prominent members in steroid and xenobiotic sensing. Masses for these proteins vary with Glucocorticoid Receptor typically around 97 kDa. These targets express in various tissues; GRs in liver musculoskeletal and immune tissues ARs commonly in reproductive tissues while LXRs and RXRAs are seen in liver and adipose tissue. Together they serve as sensors and regulators in numerous physiological processes.
Biological function summary

These receptors control pathways related to lipid metabolism immune regulation and homeostasis. GRs engage in the stress response by modulating anti-inflammatory effects. The Liver X Receptors (LXR alpha and beta) activate genes involved in cholesterol efflux and lipogenesis. Retinoid X Receptor alpha plays a partnering role forming heterodimers with other receptor types enhancing their transcriptional activity. The Glucose-6-Phosphatase (G-6-Pase) is key in glucose homeostasis integral to gluconeogenesis and glycogenolysis processes. These proteins act both independently and as part of larger complexes intertwined in regulating metabolic health.

Pathways

Each target integrates into broader networks essential for maintaining cellular equilibrium. GR activity links to the hypothalamic-pituitary-adrenal (HPA) axis impacting stress hormone secretion and skin and bone health. LXR signaling pathway involves cholesterol homeostasis and inflammation closely associated with RXRA and its ability to form heterodimers. The Androgen Receptor functions in pathways related to reproductive organ development and is also tied to Prostate Specific Antigen regulation. RORs contribute to circadian rhythm modulation interlinked with genes mediating immune function and energy homeostasis weaving together different physiological threads.

These targets play significant roles in various conditions. Dysregulation of Glucocorticoid Receptor has links to conditions like Cushing's syndrome and autoimmune diseases due to disrupted immune response. Defective LXR signaling can contribute to atherosclerosis as impaired cholesterol transport and inflammation occur. Mutations or alterations in the Androgen Receptor often connect to prostate cancer development. In glucose metabolism impaired G-6-Pase function leads to glycogen storage disease (Von Gierke disease) emphasizing its importance in metabolic disorders. Understanding their roles at a molecular level offers potential for targeted therapies across a spectrum of diseases.

Product protocols

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Frontiers in aging neuroscience 13:634948 PubMed34045954

2021

Dichlorodiphenyltrichloroethane Impairs Amyloid Beta Clearance by Decreasing Liver X Receptor α Expression.

Applications

Unspecified application

Species

Unspecified reactive species

Dongmei Wu,Yang Hu,Min Song,Gongbo Li

Acta pharmacologica Sinica 42:1472-1485 PubMed33303989

2020

Celastrol induces lipophagy via the LXRα/ABCA1 pathway in clear cell renal cell carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Chan-Juan Zhang,Neng Zhu,Jia Long,Hong-Tao Wu,Yu-Xiang Wang,Bi-Yuan Liu,Duan-Fang Liao,Li Qin
View all publications

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