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GW3965 hydrochloride_Molecular_structure_CAS_405911-17-3)
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GW3965 hydrochloride

Catalog No. G6295 Name Sigma Aldrich
CAS Number 405911-17-3 Website http://www.sigmaaldrich.com
M. F. C33H32Cl2F3NO3 Telephone 1-800-521-8956
M. W. 618.5132896 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 73112

SYNONYMS

IUPAC name
2-{3-[3-({[2-chloro-3-(trifluoromethyl)phenyl]methyl}(2,2-diphenylethyl)amino)propoxy]phenyl}acetic acid hydrochloride
IUPAC Traditional name
C33H31ClF3NO3 hydrochloride
Synonyms
3-[3-[N-(2-Chloro-3-trifluoromethylbenzyl)-(2,2-diphenylethyl)amino]propyloxy]phenylacetic acid hydrochloride

DATABASE IDS

PubChem SID 24724494
CAS Number 405911-17-3
MDL Number MFCD08276920

PROPERTIES

Empirical Formula (Hill Notation) C33H31F3ClNO3 · HCl
Purity ≥98% (HPLC)
Apperance white powder
Solubility DMSO: ≥20 mg/mL
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H302-H318-H413
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P280-P305 + P351 + P338
Risk Statements 22-41
Safety Statements 26-39
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
GW3965 is a liver X receptor full agonist on hLXRα and hLXRβ. GW3965 has an EC50 = 125 nM in a cell-free ligand-sensing assay of LXRα and profiles as a full agonist on hLXRα and hLXRβ in cell-based assays with EC50 = 190 nM and 30 nM, respectively. It is orally active in mice. When screened against a panel of nuclear receptors, it cross-reacted with only the pregnane X receptor (PXR). The literature agonist, T0901317 (Tularik), had an EC50 = 60 nM and 85 nM in the cell-free and cell-based assays, respectively.
Description (简体中文)
Biochem/physiol Actions
GW3965 is a liver X receptor full agonist on hLXRα and hLXRβ. GW3965 has an EC50 = 125 nM in a cell-free ligand-sensing assay of LXRα and profiles as a full agonist on hLXRα and hLXRβ in cell-based assays with EC50 = 190 nM and 30 nM, respectively. It is orally active in mice. When screened against a panel of nuclear receptors, it cross-reacted with only the pregnane X receptor (PXR). The literature agonist, T0901317 (Tularik), had an EC50 = 60 nM and 85 nM in the cell-free and cell-based assays, respectively.

REFERENCES