Description
SR144528 is a selective CB2 antagonist. It is used to study the role of cannabinoid receptor 2 in immunology, neuroscience and cancer. Recent research shows SR144528 to reduce immunoglobulin human SKW 6.4 cells.
| Product Unit Size | Cost | Quantity | Stock |
|---|
SR144528 is a selective CB2 antagonist. It is used to study the role of cannabinoid receptor 2 in immunology, neuroscience and cancer. Recent research shows SR144528 to reduce immunoglobulin human SKW 6.4 cells.
| Cas No. | 192703-06-3 |
|---|---|
| Purity | ≥98% |
| Formula | C29H34ClN3O |
| Formula Wt. | 476.06 |
| Chemical Name | 5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)methyl]-N-[(1R,3S,4S)-2,2,4-trimethyl-3-bicyclo[2.2.1]heptanyl]pyrazole-3-carboxamide |
| IUPAC Name | 5-(4-Chloro-3-methylphenyl)-1-[(4-methylphenyl)methyl]-N-[(1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl]-1H-pyrazole-3-carboxamide |
| Solubility | Soluble in ethanol (~20 mg/ml), DMSO (~20 mg/ml), DMF (~20 mg/ml), and 1: 1 ethanol: PBS (pH 7.2) (~0.5 mg/ml). |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Feng R, Milcarek CA, Xie XQ. Antagonism of cannabinoid receptor 2 pathway suppresses IL-6-induced immunoglobulin IgM secretion. BMC Pharmacol Toxicol. 2014 Jun 9;15:30. PMID: 24913620.
Krylatov AV, Maslov LN, Lasukova OV and Pertwee RG. Cannabinoid receptor antagonists SR141716 and SR144528 exhibit properties of partial agonists in experiments on isolated perfused rat heart. Bull Exp Biol Med. 2005 May;139(5):558-61. PMID: 16224548.
Peptide, GLP-1 analog found in Heloderma; GLP-1...
CD73 inhibitor
Triterpene saponin found in species of Panax.
Polymer precursor
HDM2 inhibitor
Flavonoid found in fruits, vegetables, and grai...
Synthetic steroid; glucocorticoid agonist.
Endogenous peptide hormone inolved in gastric e...
CDK inhibitor.
Nitroimidazole, binds DNA; nucleic acid synthes...
Apoptosis inducing agent.
Non-depolarizing NMJ blocker; AChR antagonist.<...
Terpene lactone found in Ginkgo.
Taxane synthesis intermediate.
Thiazide diuretic; NCCT inhibitor, carbonic anh...
μOR and δOR agonist, D2/D3 DA potentiator.
5-HT1A partial agonist, SERT inhibitor.
Laminin-derived peptapeptide.
Zinc chelator
Ca2+-sensing receptor antagonist.