Interesting scientific research on 16588-26-4

Although many compounds look similar to this compound(16588-26-4)Category: alcohols-buliding-blocks, numerous studies have shown that this compound(SMILES:BrC1=C(C=CC(=C1)[N+](=O)[O-])Cl), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Category: alcohols-buliding-blocks. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 3-Bromo-4-chloronitrobenzene, is researched, Molecular C6H3BrClNO2, CAS is 16588-26-4, about 4-Methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide: A Potent and Selective Agonist of S1P1. Author is Pennington, Lewis D.; Sham, Kelvin K. C.; Pickrell, Alexander J.; Harrington, Paul E.; Frohn, Michael J.; Lanman, Brian A.; Reed, Anthony B.; Croghan, Michael D.; Lee, Matthew R.; Xu, Han; McElvain, Michele; Xu, Yang; Zhang, Xuxia; Fiorino, Michael; Horner, Michelle; Morrison, Henry G.; Arnett, Heather A.; Fotsch, Christopher; Wong, Min; Cee, Victor J..

The sphingosine-1-phosphate-1 receptor (S1P1) and its endogenous ligand sphingosine-1-phosphate (S1P) cooperatively regulate lymphocyte trafficking from the lymphatic system. Herein, we disclose 4-methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide (8), an uncommon example of a synthetic S1P1 agonist lacking a polar headgroup, which is shown to effect dramatic reduction of circulating lymphocytes (POC = -78%) in rat 24 h after a single oral dose (1 mg/kg). The excellent potency that 8 exhibits toward S1P1 (EC50 = 0.035 μM, 96% efficacy) and the >100-fold selectivity that it displays against receptor subtypes S1P2-5 suggest that it may serve as a valuable tool to understand the clin. relevance of selective S1P1 agonism.

Although many compounds look similar to this compound(16588-26-4)Category: alcohols-buliding-blocks, numerous studies have shown that this compound(SMILES:BrC1=C(C=CC(=C1)[N+](=O)[O-])Cl), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
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