PSB-16671

  Cat. No.:  DC70714   Featured
Chemical Structure
2094630-35-8
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Field of application
PSB-16671 is a novel orthosteric and allosteric activator of GPR84, activates human GPR84 with EC50 of 41.3 nM in cAMP accumulation assays. PSB-16671 is selective versus related fatty acid receptors and the arylhydrocarbon receptor. PSB-16671 shows an EC50 of 5.47 uM in β-Arrestin assays, and allosteric KB value of 634 nM.
Cas No.: 2094630-35-8
Chemical Name: PSB-16671
Synonyms: 3,3′-Methylenebis[5,7-difluoro-1H-indole];PSB-16671;3,3'-Methylenebis[5,7-difluoro-1H-indole]
SMILES: C12=C(C(=CC(=C1)F)F)NC=C2CC1=CNC2C(F)=CC(F)=CC1=2
Formula: C17H10F4N2
M.Wt: 318.268317699432
Purity: >97%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Publication: 1. Sarah J Mancini, et al. Sci Rep. 2019 Feb 12;9(1):1861
Description: PSB-16671 is a novel orthosteric and allosteric activator of GPR84, activates human GPR84 with EC50 of 41.3 nM in cAMP accumulation assays. PSB-16671 is selective versus related fatty acid receptors and the arylhydrocarbon receptor. PSB-16671 shows an EC50 of 5.47 uM in β-Arrestin assays, and allosteric KB value of 634 nM.
References: 1. Sarah J Mancini, et al. Sci Rep. 2019 Feb 12;9(1):1861
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC70714 PSB-16671 PSB-16671 is a novel orthosteric and allosteric activator of GPR84, activates human GPR84 with EC50 of 41.3 nM in cAMP accumulation assays. PSB-16671 is selective versus related fatty acid receptors and the arylhydrocarbon receptor. PSB-16671 shows an EC50 of 5.47 uM in β-Arrestin assays, and allosteric KB value of 634 nM.
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