1443367-20-1

GPR35 agonist 6 Chemical Structure
1443367-20-1

Chemical Structure

GPR35 agonist 6

  • CAS No.: 1443367-20-1
  • Formula:C18H12BrNO6
  • Molecular Weight:418.20

IUPAC Name: 6-bromo-8-(4-methoxybenzamido)-4-oxo-4H-chromene-2-carboxylic acid

InChIKey: TZKQFDIFVZAYER-UHFFFAOYSA-N

SMILES: O=C(O)C=1OC=2C(=CC(Br)=CC2C(=O)C1)NC(=O)C3=CC=C(OC)C=C3

Biological Activity: GPR35 agonist 6 is a potent and selective agonist targeting GPR35, with an EC50 of 12.1 nM against human GPR35. GPR35 agonist 6 activates the human splice variant GPR35b with comparable efficacy, showing an EC50 of 22.1 nM. GPR35 agonist 6 also exhibits weak GPR55 antagonistic activity, with an IC50 of 21.7 μM, and its agonistic activity towards GPR35 is significantly stronger than its antagonistic activity towards GPR55. GPR35 agonist 6 initiates GPR35 downstream signaling by inducing β-arrestin recruitment. GPR35 agonist 6 is used to investigate GPR35-mediated diseases, such as gastrointestinal lesions and gastric cancer[1].

Cat. No. Product Name Purity Description Pricing
HY-W1058476
GPR35 agonist 6 GPR35 agonist 6 is a potent and selective agonist targeting GPR35, with an EC50 of 12.1 nM against human GPR35. GPR35 agonist 6 activates the human splice variant GPR35b with comparable efficacy, showing an EC50 of 22.1 nM. GPR35 agonist 6 also exhibits weak GPR55 antagonistic activity, with an IC50 of 21.7 μM, and its agonistic activity towards GPR35 is significantly stronger than its antagonistic activity towards GPR55. GPR35 agonist 6 initiates GPR35 downstream signaling by inducing β-arrestin recruitment. GPR35 agonist 6 is used to investigate GPR35-mediated diseases, such as gastrointestinal lesions and gastric cancer.
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