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| Formula | C16H25NS |
| Molar mass | 263.44 g·mol−1 |
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Gacyclidine (GK-11, OTO-313) is apsychoactive drug which acts as adissociative via functioning as anon-competitiveNMDA receptorantagonist.[3][4][5] It is closely related tophencyclidine (PCP), and specifically, is aderivative oftenocyclidine (TCP).[6][7]
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Gacyclidine is a psychoactive drug that was used for helping with body trauma in humans. While seeing most tests on animals, it was never used commercially to the degree as other painkillers or psychoactive drugs. While gacyclidine has been used in numerous tests dating back to 2012, these tests did not provide fruitful results that would push the future of the drug into a different direction.
The 1,2-addition of 2-methylcyclohexanone (I) with 2-thienyl lithium (II) or 2-thienyl magnesium bromide (III) gives cyclohexanol (IV) as a diastereomeric mixture, which was treated withsodium azide (NaN3) intrichloroacetic acid to yield the azide (V). The reduction of (V) withlithium aluminium hydride (LiAlH4) orRaney nickel inisopropanol affords the corresponding amine (VI), preferentially with thecis-configuration. Finally, this compound is dialkylated with1,5-dibromopentane (VII) by means ofpotassium carbonate (K2CO3) inacetonitrile to provide the target compound as a diastereomeric mixture.[8]
Gacyclidine's original purpose was for helping with human body trauma, specifically spine and brain trauma. Tests were done on animals to see how their bodies would react to the different drugs and see how that information could be applied to humans.[vague] Gacyclidine is used to reduce damage to the brain or spinal cord, hence a treatment for tinnitus, stroke, trauma, and convulsion.[medical citation needed] As a psychoactive drug, alteration of perception is what makes this substance of use.[medical citation needed]
A lipid-based intratympanic formulation of gacyclidine (OTO-313) has been studied as a potential therapy for the treatment oftinnitus.[4][9][10] A randomized, placebo-controlled Phase II trial found that OTO-313 was safe and well-tolerated but did not demonstrate a significant treatment benefit in unilateral tinnitus relative to placebo (believed to be partly due to a high placebo response).[9][10] In 2022, the company developing OTO‑313 announced it would stop developing the drug for tinnitus.[11]
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Testing of gacyclidine was performed on animals in a study. In concluding hours (18-96 h), no necrotic neurons were discovered in animals with dosages of 1, 5, 10, 20 milligrams of gacyclidine. At 20 milligrams the presence of a few cytoplasmic vacuoles were present. In a study conducted to find possible neurotoxicity in dosages, scientists tested the effects of gacyclidine in comparison todizocilpine andCNS-1102, and finalized more positive effects on animals from gacyclidine. When given MK-801 at dosages of 1 or 5 milligrams of gacyclidine, effects were harmless and behaved similarly to untreated animals. At dosages between 5 and 10 milligrams, the animals began to experience behaviors of tremors, sedation and exophthalmos. With CNS-1102, at all doses tested, the animals exhibited some excitation. At the highest doses (10 and 20 milligrams) they suffered from severe akinesia 1 hour after drug administration. Animals that received 1 or 5 milligrams of gacyclidine or its enantiomers behave similarly to untreated animals. At the highest doses (10 and 20 milligrams), the animals began to show some signs of excitation. For all doses, the recovery period was always better with gacyclidine and its enantiomers than with MK-801 or CNS-1102. The days after the testing, labs observed electron microscopy in the 20-milligram group. During observation small lesions were labeled as cytoplasmic or intramitochondrial vacuoles. In addition, no neuronal or glial alterations, such as astrocytic swelling or microglial activation, were seen that could suggest a short-term toxic event had occurred. Further concluding observations, current evidence indicates that the possibility of a short-term toxicity, would be totally reversible. Likewise, any long-term toxicity would become evident after 4 days. But, the evidence in total strongly suggests that gacyclidine and its enantiomers are, at least, far less neurotoxic than MK-801.
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With the use of this drug, motor skills have significantly improved upon use, as it is the antagonist to the NMDA receptor. Gacyclidine is able to reduce calcium getting into cells. While animal test results showed potential in the rats, human tests showed slight improvement to the condition of patients. Outside of results seen in animals like potential trauma assistance and pain relief, there is little to no proof that there will be any clinical benefits in the future of gacyclidine.
