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Utopioid (drug class)

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427: 407: 365: 600: 580: 564: 506: 486: 345: 544: 525: 385: 466: 447: 110: 616: 277: 301: 636: 236: 656: 130: 258: 216: 196: 174: 154: 90: 63:. Most utopioid derivatives are however selective kappa agonists, which may have limited abuse potential as dissociative hallucinogens, but do not alleviate withdrawal distress in opioid dependent individuals or maintain addiction in a typical sense. Nevertheless, this has not stopped them from being sold as designer drugs, and a number of these compounds are now banned in many jurisdictions alongside U-47700 itself. 323: 50:
and became widely sold around the world for several years before being banned in various jurisdictions from 2016 onwards. Following the prohibition of U-47700, a number of related compounds have continued to appear on illicit drug markets. They are often marketed online or included as components in
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Vandeputte MM, Persson M, Walther D, Vikingsson S, Kronstrand R, Baumann MH, Gréen H, Stove CP (March 2022). "Characterization of recent non-fentanyl synthetic opioids via three different in vitro µ-opioid receptor activation assays".
960:"Investigation of the μ- and κ-opioid receptor activation by eight new synthetic opioids using the [35 S]-GTPγS assay: U-47700, isopropyl U-47700, U-49900, U-47931E, N-methyl U-47931E, U-51754, U-48520, and U-48800" 59:
and N-Ethyl-U-47700 retain similar mu selectivity but with lower potency similar to that of morphine, or have a mixture of mu and kappa mediated effects, such as
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mixtures sold under the guise of "street heroin." U-47700 itself is the most potent mu opioid agonist from this class, around 7-10x the potency of
1115: 773:"The search for the "next" euphoric non-fentanil novel synthetic opioids on the illicit drugs market: current status and horizon scanning" 1076:
Cheney BV. Structure-activity relationships for drugs binding to the agonist and antagonist states of the primary morphine receptor.
34:. However, they were never marketed for medical use. Some compounds from this class have been used for scientific research as model 1030:"In vitro μ-opioid receptor activation potential of U10 and β-U10, positional isomers of the synthetic opioid naphthyl U-47700" 1007: 1120: 681: 686: 1125: 1110: 865:"U-47700 and Its Analogs: Non-Fentanyl Synthetic Opioids Impacting the Recreational Drug Market" 820:
Kyei-Baffour K, Lindsley CW (December 2020). "DARK Classics in Chemical Neuroscience: U-47700".
1130: 35: 1008:"Non-fentanyl opioids and related new psychoactive substances with no known legitimate uses" 8: 1059: 989: 940: 891: 864: 845: 797: 772: 753: 39: 644: 588: 533: 514: 494: 474: 455: 435: 426: 415: 406: 395: 373: 353: 333: 204: 184: 1088: 1063: 1051: 993: 981: 944: 932: 896: 849: 837: 802: 745: 741: 664: 624: 552: 266: 224: 162: 118: 98: 757: 364: 246: 142: 1081: 1041: 971: 924: 886: 876: 863:
Baumann MH, Tocco G, Papsun DM, Mohr AL, Fogarty MF, Krotulski AJ (November 2020).
829: 792: 784: 737: 311: 505: 289: 833: 599: 579: 390: 56: 726:"Fentanyl, fentanyl analogs and novel synthetic opioids: A comprehensive review" 563: 485: 344: 928: 788: 543: 524: 1104: 881: 465: 47: 725: 706: 446: 384: 1055: 985: 936: 900: 841: 806: 749: 1092: 615: 283: 136: 109: 1085: 276: 635: 1046: 1029: 976: 959: 655: 300: 129: 27: 257: 235: 215: 195: 173: 153: 89: 306: 52: 913: 328: 241: 179: 60: 43: 30:
drugs first developed in the 1970s by the pharmaceutical company
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Sharma KK, Hales TG, Rao VJ, NicDaeid N, McKenzie C (2019).
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Otte L, Wilde M, Auwärter V, Grafinger KE (July 2022).
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Armenian P, Vo KT, Barr-Walker J, Lynch KL (May 2018).
862: 770: 819: 1102: 1027: 1021: 951: 907: 856: 813: 764: 717: 1045: 975: 890: 880: 796: 1116:Chemical classes of psychoactive drugs 1103: 711:Cayman Chemical News and Announcements 1028:Vandeputte MM, Stove CP (July 2023). 1015:International Narcotics Control Board 66: 42:selective compound from this class, 13: 14: 1142: 742:10.1016/j.neuropharm.2017.10.016 654: 634: 614: 598: 578: 562: 542: 523: 504: 484: 464: 445: 425: 405: 383: 363: 343: 321: 299: 275: 256: 234: 214: 194: 172: 152: 128: 108: 88: 38:agonists. In the mid-2010s, one 1070: 55:. Some other compounds such as 1000: 699: 1: 692: 682:List of benzimidazole opioids 834:10.1021/acschemneuro.0c00330 7: 675: 23:) are a class of synthetic 10: 1147: 929:10.1007/s00204-021-03207-9 687:List of fentanyl analogues 432:3,4-Ethylenedioxy-U-51574 412:3,4-Ethylenedioxy-U-47700 1080:. 1988 Mar;31(3):521-31. 1034:Drug Testing and Analysis 964:Drug Testing and Analysis 822:ACS Chemical Neuroscience 789:10.1007/s11419-018-0454-5 882:10.3390/brainsci10110895 370:N,N-Didesmethyl-U-47700 1121:Dimethylamino compounds 917:Archives of Toxicology 511:N-Cyclopropyl-U-47700 621:4-TFM-U-48520 (U-04) 605:2,4-Difluoro-U-48800 585:3,4-Difluoro-U-47700 36:kappa opioid receptor 569:3,4-Dibromo-U-47700 491:N-Isopropyl-U-47700 350:N-Desmethyl-U-47700 1086:10.1021/jm00398a007 777:Forensic Toxicology 74:Chemical structure 1017:. 28 January 2022. 549:N-Methyl-U-47931E 530:N-Methoxy-U-47700 67:Table of Utopioids 46:, re-emerged as a 40:mu opioid receptor 828:(23): 3928–3936. 736:(Pt A): 121–132. 730:Neuropharmacology 673: 672: 471:N-Propyl-U-47700 1138: 1126:Cyclohexylamines 1095: 1074: 1068: 1067: 1049: 1047:10.1002/dta.3554 1025: 1019: 1018: 1012: 1004: 998: 997: 979: 977:10.1002/dta.3238 970:(7): 1187–1199. 955: 949: 948: 911: 905: 904: 894: 884: 860: 854: 853: 817: 811: 810: 800: 768: 762: 761: 721: 715: 714: 703: 658: 638: 618: 602: 582: 566: 546: 527: 508: 488: 468: 452:N-Ethyl-U-47700 449: 429: 409: 387: 367: 347: 325: 303: 279: 260: 238: 218: 198: 176: 156: 132: 112: 92: 71: 70: 1146: 1145: 1141: 1140: 1139: 1137: 1136: 1135: 1101: 1100: 1099: 1098: 1075: 1071: 1026: 1022: 1010: 1006: 1005: 1001: 956: 952: 912: 908: 861: 857: 818: 814: 769: 765: 722: 718: 713:. 12 July 2018. 705: 704: 700: 695: 678: 391:3,4-MDO-U-47700 69: 57:3,4-MDO-U-47700 12: 11: 5: 1144: 1134: 1133: 1128: 1123: 1118: 1113: 1111:Lists of drugs 1097: 1096: 1069: 1040:(3): 323–326. 1020: 999: 950: 923:(3): 877–897. 906: 869:Brain Sciences 855: 812: 763: 716: 697: 696: 694: 691: 690: 689: 684: 677: 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167:67579-11-7 137:Bromadoline 123:82657-23-6 103:67579-13-9 83:CAS number 1105:Categories 1078:J Med Chem 693:References 135:U-47931E ( 77:Drug name 1064:260101432 994:246701889 945:246239574 850:220438986 645:165362154 589:165362347 534:155907659 515:165361451 495:137700166 475:137700434 456:155907846 436:137700374 416:137700298 396:139598237 374:129406364 354:129390993 334:117071705 282:U-62066 ( 221:U-50211 205:129392412 185:137700072 28:analgesic 17:Utopioids 1056:37482925 986:35142070 937:35072756 901:33238449 842:32639714 807:30636980 758:21404877 750:29042317 676:See also 665:54524276 625:53720446 553:54482637 267:44269303 263:U-51574 225:13544017 201:U-49900 163:13544026 159:U-48520 119:13544016 115:U-47700 99:44269286 95:U-47109 80:PubChem 53:morphine 1093:2831361 892:7700279 798:6314991 329:U-77891 307:U-69593 247:3036289 242:U-50488 180:U-48800 143:6328449 61:U-48800 44:U-47700 1091:  1062:  1054:  992:  984:  943:  935:  899:  889:  848:  840:  805:  795:  756:  748:  661:β-U10 641:α-U10 312:105104 32:Upjohn 25:opioid 1060:S2CID 1011:(PDF) 990:S2CID 941:S2CID 846:S2CID 754:S2CID 290:55652 1089:PMID 1052:PMID 982:PMID 933:PMID 897:PMID 838:PMID 803:PMID 746:PMID 1082:doi 1042:doi 972:doi 925:doi 887:PMC 877:doi 830:doi 793:PMC 785:doi 738:doi 734:134 1107:: 1058:. 1050:. 1038:16 1036:. 1032:. 1013:. 988:. 980:. 968:14 966:. 962:. 939:. 931:. 921:96 919:. 895:. 885:. 873:10 871:. 867:. 844:. 836:. 826:11 824:. 801:. 791:. 781:37 779:. 775:. 752:. 744:. 732:. 728:. 709:. 286:) 139:) 1084:: 1066:. 1044:: 996:. 974:: 947:. 927:: 903:. 879:: 852:. 832:: 809:. 787:: 760:. 740:: 19:(

Index

opioid
analgesic
Upjohn
kappa opioid receptor
mu opioid receptor
U-47700
designer drug
morphine
3,4-MDO-U-47700
U-48800

44269286

13544016

Bromadoline
6328449

13544026

U-48800
137700072

129392412

13544017

U-50488
3036289

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