We shown that, in contrast to classical opioid receptors, ACKR3 would not cause classical G protein signaling and is not modulated with the classical prescription or analgesic opioids, like morphine, fentanyl, or buprenorphine, or by nonselective opioid antagonists such as naloxone. As an alternative, we founded that LIH383, an https://robinsons282kor2.wikimillions.com/user