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3-MeO-PCMo is a dissociative anesthetic drug which is similar in structure to phencyclidine and been sold online as a designer drug. The inhibitory effect of 3-MeO-PCMo on the reduction in the density of the drebrin clusters by NMDAR stimulation with glutamic acid is lower than that of PCP or 3-MeO-PCP, with half maximal inhibitory concentration (IC50) values of 26.67 μM (3-MeO-PCMo), 2.02 μM (PCP) and 1.51 μM (3-MeO-PCP).

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  • 3-MeO-PCMo (en)
  • 3-MeO-PCMo (es)
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  • 3-MeO-PCMo is a dissociative anesthetic drug which is similar in structure to phencyclidine and been sold online as a designer drug. The inhibitory effect of 3-MeO-PCMo on the reduction in the density of the drebrin clusters by NMDAR stimulation with glutamic acid is lower than that of PCP or 3-MeO-PCP, with half maximal inhibitory concentration (IC50) values of 26.67 μM (3-MeO-PCMo), 2.02 μM (PCP) and 1.51 μM (3-MeO-PCP). (en)
  • 3-MEO-PCMo es un fármaco anestésico disoactivo que tiene una estructura similar a la fenciclidina​​ y se vende en línea como fármaco de diseñado.​​ El efecto inhibidor de 3-MeO-PCMo sobre la reducción de la densidad de los clústeres de drebrin por estimulación NMDAR con ácido glutámico es menor que el de PCP o 3-MeO-PCP, con valores de concentración inhibitoria media máxima (IC50) 26.67 μM (3-MeO-PCMo), 2.02 μM (PCP) y 1.51 μM (3-MeO-PCP).​ (es)
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  • 3-MeO-PCMo is a dissociative anesthetic drug which is similar in structure to phencyclidine and been sold online as a designer drug. The inhibitory effect of 3-MeO-PCMo on the reduction in the density of the drebrin clusters by NMDAR stimulation with glutamic acid is lower than that of PCP or 3-MeO-PCP, with half maximal inhibitory concentration (IC50) values of 26.67 μM (3-MeO-PCMo), 2.02 μM (PCP) and 1.51 μM (3-MeO-PCP). (en)
  • 3-MEO-PCMo es un fármaco anestésico disoactivo que tiene una estructura similar a la fenciclidina​​ y se vende en línea como fármaco de diseñado.​​ El efecto inhibidor de 3-MeO-PCMo sobre la reducción de la densidad de los clústeres de drebrin por estimulación NMDAR con ácido glutámico es menor que el de PCP o 3-MeO-PCP, con valores de concentración inhibitoria media máxima (IC50) 26.67 μM (3-MeO-PCMo), 2.02 μM (PCP) y 1.51 μM (3-MeO-PCP).​ (es)
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  • Schedule I (en)
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  • 138873-80-0
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  • 96QW73BA62
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  • 132605908
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