Knowledge (XXG)

AT-121

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373: 29: 243:. The interaction with the nociceptin receptor is expected to block the abuse and dependence-related side effects that are typical of opioids. A study in nonhuman primates found that AT-121 has morphine-like analgesic effects, but suppressed the addictive effects. 192: 206: 353: 414: 453: 438: 433: 458: 65: 41: 448: 407: 292:"A bifunctional nociceptin and mu opioid receptor agonist is analgesic without opioid side effects in nonhuman primates" 463: 400: 236: 443: 240: 82: 339: 321: 384: 91: 311: 303: 132: 316: 291: 116: 427: 290:
Ding H, Kiguchi N, Yasuda D, Daga PR, Polgar WE, Lu JJ, et al. (August 2018).
257: 372: 307: 262: 168: 380: 228: 325: 232: 102: 20: 252: 340:"Scientists take big step toward finding non-addictive painkiller" 267: 191: 182: 28: 354:"Study: Non-addictive painkiller is safe, effective in animals" 214:
CC(C)1CC(CC1)N1CCC2(CC1)C(=O)N(CCNS(N)(=O)=O)CC1=CC=CC=C21
388: 231:. It was designed to be bifunctional, acting as an 180: 167: 131: 126: 101: 81: 56: 40: 35: 115: 90: 408: 8: 19: 415: 401: 73:3-oxo-1'-(4-propan-2-ylcyclohexyl)-2-spiro 27: 315: 279: 211: 70: 285: 283: 18: 7: 369: 367: 106: 387:. You can help Knowledge (XXG) by 14: 342:. Science Daily. August 29, 2018. 371: 149: 143: 454:Experimental psychiatric drugs 296:Science Translational Medicine 161: 155: 137: 1: 439:Nociceptin receptor agonists 308:10.1126/scitranslmed.aar3483 434:Mu-opioid receptor agonists 480: 366: 127:Chemical and physical data 202: 61: 26: 459:Tetrahydroisoquinolines 356:. UPI. August 30, 2018. 383:-related article is a 449:4-Phenylpiperidines 241:nociceptin receptor 227:is an experimental 23: 396: 395: 302:(456): eaar3483. 237:μ-opioid receptor 222: 221: 193:Interactive image 16:Chemical compound 471: 417: 410: 403: 375: 368: 358: 357: 350: 344: 343: 336: 330: 329: 319: 287: 195: 175: 163: 157: 151: 145: 139: 119: 109: 108: 94: 31: 24: 22: 479: 478: 474: 473: 472: 470: 469: 468: 464:Analgesic stubs 424: 423: 422: 421: 364: 362: 361: 352: 351: 347: 338: 337: 333: 289: 288: 281: 276: 249: 218: 215: 210: 209: 198: 173: 160: 154: 148: 142: 122: 105: 97: 77: 74: 69: 68: 52: 49:Investigational 17: 12: 11: 5: 477: 475: 467: 466: 461: 456: 451: 446: 441: 436: 426: 425: 420: 419: 412: 405: 397: 394: 393: 376: 360: 359: 345: 331: 278: 277: 275: 272: 271: 270: 265: 260: 255: 248: 245: 220: 219: 217: 216: 213: 205: 204: 203: 200: 199: 197: 196: 188: 186: 178: 177: 171: 165: 164: 158: 152: 146: 140: 135: 129: 128: 124: 123: 121: 120: 112: 110: 99: 98: 96: 95: 87: 85: 79: 78: 76: 75: 72: 64: 63: 62: 59: 58: 54: 53: 51: 50: 46: 44: 38: 37: 33: 32: 15: 13: 10: 9: 6: 4: 3: 2: 476: 465: 462: 460: 457: 455: 452: 450: 447: 445: 442: 440: 437: 435: 432: 431: 429: 418: 413: 411: 406: 404: 399: 398: 392: 390: 386: 382: 377: 374: 370: 365: 355: 349: 346: 341: 335: 332: 327: 323: 318: 313: 309: 305: 301: 297: 293: 286: 284: 280: 273: 269: 266: 264: 261: 259: 256: 254: 251: 250: 246: 244: 242: 238: 234: 230: 226: 212: 208: 201: 194: 190: 189: 187: 184: 179: 172: 170: 166: 136: 134: 130: 125: 118: 114: 113: 111: 104: 100: 93: 89: 88: 86: 84: 80: 71: 67: 60: 55: 48: 47: 45: 43: 39: 34: 30: 25: 389:expanding it 378: 363: 348: 334: 299: 295: 258:Cebranopadol 235:at both the 224: 223: 92:2099681-31-7 42:Legal status 36:Legal status 263:Oliceridine 176: g·mol 57:Identifiers 444:Sulfamides 428:Categories 274:References 181:3D model ( 169:Molar mass 83:CAS Number 66:IUPAC name 381:analgesic 229:analgesic 117:129188444 326:30158150 247:See also 239:and the 317:6295194 233:agonist 133:Formula 103:PubChem 324:  314:  253:AT-076 225:AT-121 207:SMILES 174:462.65 21:AT-121 379:This 268:PZM21 183:JSmol 385:stub 322:PMID 312:PMC 304:doi 107:CID 430:: 320:. 310:. 300:10 298:. 294:. 282:^ 147:38 141:24 416:e 409:t 402:v 391:. 328:. 306:: 185:) 162:S 159:3 156:O 153:4 150:N 144:H 138:C

Index


Legal status
IUPAC name
CAS Number
2099681-31-7
PubChem
129188444
Formula
Molar mass
JSmol
Interactive image
SMILES
analgesic
agonist
μ-opioid receptor
nociceptin receptor
AT-076
Cebranopadol
Oliceridine
PZM21


"A bifunctional nociceptin and mu opioid receptor agonist is analgesic without opioid side effects in nonhuman primates"
doi
10.1126/scitranslmed.aar3483
PMC
6295194
PMID
30158150
"Scientists take big step toward finding non-addictive painkiller"

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