Cat. No. Name Size Price Add Cart
KI2515CID1602004610 mg$465.4
CID1602004650 mg$1911

Chemical Characteristic

Product NameCID16020046
SynonymsN/A
CAS No.834903-43-4
Molecular Weight 425.44
FormulaC25H19N3O4
Chemical Name?4-[4,6-Dihydro-4-(3-hydroxyphenyl)-3-(4-methylphenyl)-6-oxopyrrolo[3,4-c]pyrazol-5(1H)-yl]benzoic acid
SmilesC(=O)(c1ccc(cc1)N1C(=O)c2[nH]nc(c2C1c1cc(ccc1)O)c1ccc(cc1)C)O
Chemical Structure

Biological activities

CID16020046 is a selective G protein-coupled receptor 55(GPR55) antagonist. CID16020046 antagonizes agonist-induced receptor activation in yeast cells expressing human GPR55. CID16020046 (40 nM to 10 mM) inhibits GPR55 constitutive activity with an IC50 of 0.15 mM. CID16020046 inhibits LPI-induced activation of nuclear factor of activated T-cells (NFAT), nuclear factor κ of activated B cells (NF-κB) and serum response element, translocation of NFAT and NF-κB, and GPR55 internalization. CID16020046 also reduces LPI-induced wound healing in primary human lung microvascular endothelial cells and reverses LPI-inhibited platelet aggregation.[1]

Protocols

In vitro, CID16020046 is dissolved in DMSO.[1]

References

[1] Kargl J, et al. A selective antagonist reveals a potential role of G protein-coupled receptor 55 in platelet and endothelial cell function. J Pharmacol Exp Ther. 2013, 346(1): 54-66.

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