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Orphines

Nicknames: benzimidazolones, R6890, SR-17018
Last reviewed: October 2026

History

The piperidine-benzimidazolone group of opioids (orphines) was originally developed during the 1960s through pharmaceutical research associated with Paul Janssen and Janssen Pharmaceutica. This chemistry was significant because it produced opioid activity from a scaffold distinct from those found in morphine, codeine and heroin, which contain phenanthrene frameworks; fentanyl, which belongs to the anilidopiperidine class; and nitazenes, which contain a 2-benzylbenzimidazole scaffold.

Bezitramide was the first marketed medicine based on the piperidine-benzimidazolone scaffold. It was marketed as Burgodin for pain relief in parts of Europe. Its use was later associated with serious safety concerns and fatal overdose reports, and it was ultimately withdrawn from European markets. Bezitramide was internationally controlled in 1969 and remains a Class A drug in the UK.

During the same period, Janssen was also developing fentanyl and related compounds. Fentanyl subsequently proved more commercially and clinically successful, while the orphine programme did not develop into a broad range of marketed medicines. The orphine class also presented practical challenges associated with highly potent synthetic opioids, including difficult dose control, overdose risk, limited safety data for individual analogues and the formulation difficulties involved in handling compounds with high pharmacological activity.

It was after this period that the wider benzimidazolone series became lesser known and used but remained accessible through patents, academic literature and medicinal chemistry databases.

Researchers revisited the scaffold as part of modern opioid-receptor studies in 2018 when brorphine was synthesised as part of a study investigating signalling bias and opioid pharmacology of μ-opioid receptor agonists. In March 2019, brorphine was first mentioned in a post on the forum website Reddit, before the first toxicological identification in the United States in August 2019. The first confirmed brorphine case in Europe occurred in Belgium in February 2020, where the drug was identified at high purity in a powder and in the serum of a patient seeking help for their drug use.

Following a review by the World Health Organization’s Expert Committee on Drug Dependence, the UN Commission on Narcotic Drugs voted in March 2022 to place brorphine under Schedule I of the 1961 Single Convention on Narcotic Drugs. The control subsequently entered into force through the UN notification process. Several countries also introduced national emergency or permanent controls.

As with fentanyl analogues and nitazenes, controlling a single compound did not remove the wider scaffold from circulation. Instead, from approximately 2024 onwards, several structurally related analogues began to be reported, including chlorphine, N-propionitrile chlorphine (cychlorphine), spirochlorphine and 5,6-dichloro desmethylchlorphine. In July 2026, WEDINOS found cyclorphine in a fake nutritional supplement sold as Lion's Mane.

These structural modifications include halogen substitution, cyclisation and changes to the piperidine nitrogen. Such changes can alter μ-opioid-receptor affinity and efficacy, pharmacokinetics, metabolism, duration of action and analytical detectability. However, the effects of each modification cannot be predicted reliably from structure alone, and experimental potency data should not be interpreted as direct human dose-equivalence information.

SR-17018

5,6-dichloro desmethylchlorphine (SR-17018) was developed by Laura Bohn at Scripps Research Institute in 2017, and has been the subject of several laboratory and animal studies due to its unique properties. Recent animal studies suggest SR-17018 may hold promise as a safer pain therapy, with possible utility to help reverse opioid tolerance and reduce withdrawal symptoms. Following this, some individuals including a 27 year old American woman have reported self-medicating with the drug to help come off opioids including kratom (7-OH) and nitazenes.

On 11th June 2026, the UK government enacted a Temporary Class Drug Order (TCDO) on SR-17018 alongside 6 other orphines, with the intention of placing these drugs under Class A of the Missue of Drugs Act 1971. On 1st July 2026, the US Drug Enforcement Agency (DEA) followed suit, issuing a temporary order to place SR-17018 and three other orphines, along with their derivatives, under Schedule I of the Controlled Substances Act. The temporary order quickly faced pushback from civil society: the Rights and Reason project alongside Students for Sensible Drug Policy filed an emergency petition urging the DEA not to ban SR-17018 to enable continued access by scientists studying the drug’s potential for safer pain treatment.

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