1. Signaling Pathways
  2. GPCR/G Protein
  3. Prokineticin Receptor

Prokineticin Receptor

Prokineticin Receptors (PKRs) are a class of G protein-coupled receptors comprising two subtypes, PKR1 and PKR2. They bind to endogenous ligands prokineticin (PK1 and PK2) and play pivotal roles in regulating various important physiological and pathological processes. Research has demonstrated that PKRs are critically involved in angiogenesis, neurogenesis, pain perception, reproductive functions, and circadian rhythm regulation[1].
PKR1 is primarily expressed in the cardiovascular system and peripheral tissues, where it participates in angiogenesis and cardioprotection, while PKR2 is predominantly distributed in the central nervous system, modulating neuronal development and synaptic plasticity . Upon activation, PKRs mainly signal through the Gq/11 protein-coupled pathway, stimulating phospholipase C (PLC) activation, which subsequently induces intracellular calcium release and protein kinase C (PKC) activation[2].

Prokineticin Receptor Related Products (3):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-147056
    PKRA83
    Antagonist 98.04%
    PKRA83 (PKRA7) is a potent prokineticin (PK2) antagonist, which can compete for the binding of PK2 to its receptors PKR1 and PKR2. PKRA83 potently inhibits PK2 receptors, with IC50 values of 5.0 nM and 8.2 nM for PKR1 and PKR2, respectively. PKRA83 has anticancer, anti-arthritis and anti-angiogenic activities. PKRA83 can penetrate the blood-brain barrier.
    PKRA83
  • HY-147056B
    PKRA83 hydrochloride
    Antagonist
    PKRA83 (PKRA7) hydrochloride is a potent, blood-brain-penetrating PK2 antagonist that competes for PK2 binding to its receptors, PKR1 and PKR2. PKRA83 hydrochloride potently inhibits PK2 receptors with IC50 values of 5.0 nM and 8.2 nM for PKR1 and PKR2, respectively. PKRA83 hydrochloride exhibits anticancer, antiarthritis, and antiangiogenic activities.
    PKRA83 hydrochloride
  • HY-159972
    PKR1 antagonist 1
    Antagonist
    PKR1 antagonist 1 (PC1) is a potent PKR1 antagonist. PKR1 antagonist 1 reduces hyperalgesia and allodynia in SNI mice.
    PKR1 antagonist 1