MRS-1706

MRS-1706
Names
	IUPAC name N-(4-Acetylphenyl)-2-[4-(2,3,6,7-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]acetamide
	Other names MRS 1706
Identifiers
CAS Number	264622-53-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	4313008 ;
IUPHAR/BPS	3287;
MeSH	C496145
PubChem CID	5139184;
UNII	YEE5LME5K5 ;
	InChI InChI=1S/C27H29N5O5/c1-4-14-31-25-23(26(35)32(15-5-2)27(31)36)29-24(30-25)19-8-12-21(13-9-19)37-16-22(34)28-20-10-6-18(7-11-20)17(3)33/h6-13H,4-5,14-16H2,1-3H3,(H,28,34)(H,29,30) Key: ZKUCFFYOQOJLGT-UHFFFAOYSA-N ; InChI=1/C27H29N5O5/c1-4-14-31-25-23(26(35)32(15-5-2)27(31)36)29-24(30-25)19-8-12-21(13-9-19)37-16-22(34)28-20-10-6-18(7-11-20)17(3)33/h6-13H,4-5,14-16H2,1-3H3,(H,28,34)(H,29,30) Key: ZKUCFFYOQOJLGT-UHFFFAOYAX;
	SMILES CCCN1C2=C(C(=O)N(C1=O)CCC)NC(=N2)C3=CC=C(C=C3)OCC(=O)NC4=CC=C(C=C4)C(=O)C;
Properties
Chemical formula	C27H29N5O5
Molar mass	503.56
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

MRS-1706 is a selective inverse agonist for the adenosine A_2B receptor.^[1] It inhibits release of interleukins and has an antiinflammatory effect.^[2]^[3]

References

↑ "ZM241385, DPCPX, MRS1706 are inverse agonists with different relative intrinsic efficacies on constitutively active mutants of the human adenosine A2B receptor". The Journal of Pharmacology and Experimental Therapeutics 320 (2): 637–45. February 2007. doi:10.1124/jpet.106.111203. PMID 17077318.
↑ "Local stimulation of the adenosine A2B receptors induces an increased release of IL-6 in mouse striatum: an in vivo microdialysis study". Journal of Neurochemistry 105 (3): 904–9. May 2008. doi:10.1111/j.1471-4159.2007.05191.x. PMID 18088370.
↑ "Effect of A2B adenosine receptor gene ablation on proinflammatory adenosine signaling in mast cells". Journal of Immunology 180 (11): 7212–20. June 2008. doi:10.4049/jimmunol.180.11.7212. PMID 18490720.

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