Knowledge (XXG)

IMP-1088

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Mousnier, Aurélie; Bell, Andrew S.; Swieboda, Dawid P.; Morales-Sanfrutos, Julia; Pérez-Dorado, Inmaculada; Brannigan, James A.; Newman, Joseph; Ritzefeld, Markus; Hutton, Jennie A.; Guedán, Anabel; Asfor, Amin S.; Robinson, Sean W.; Hopkins-Navratilova, Iva; Wilkinson, Anthony J.; Johnston,
311:. IMP-1088 works to keep cells from generating infectious virus by targeting the cell instead of the rhinovirus itself. It does this by blocking the NMT protein of the host cell which prevents the virus from assembling its 315:, since viral capsid myristoylation by host NMT is essential for assembly. It is thought unlikely that viruses will evolve resistance to such an approach since IMP-1088 works against the human cell and not the virus. 100: 391: 195: 417: 173: 473: 335:"Fragment-derived inhibitors of human N-myristoyltransferase block capsid assembly and replication of the common cold virus" 276: 137: 448: 296: 333:
Sebastian L.; Leatherbarrow, Robin J.; Tuthill, Tobias J.; Solari, Roberto; Tate, Edward W. (14 May 2018).
463: 346: 154: 36: 66: 468: 458: 453: 372: 76: 362: 354: 292: 218: 158: 350: 367: 334: 270: 125: 442: 308: 358: 304: 255: 376: 418:"A team of researchers may have actually found a cure to the common cold" 307:
replication, an area of research relating to potential treatment of the
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Except where otherwise noted, data are given for materials in their
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CC1=NN(C)C(=C1CCOC2=C(C=CC(=C2F)F)C3=CC=C4C(=C3)C(=NN4C)CN(C)C)C
142: 124: 75: 8: 392:"Agent stops common cold virus replication" 157: 15: 366: 324: 200: 178: 153: 41:1-(5-{3,4-Difluoro-2-phenyl}-1-methyl-1 295:of the human N-myristoyltransferases 182:Key: SOXNKJCQBRQUMS-UHFFFAOYSA-N 7: 115: 14: 242: 236: 230: 22: 416:Houser, Kristin (19 May 2018). 396:Chemical & Engineering News 273:(at 25 °C , 100 kPa). 248: 224: 1: 490: 359:10.1038/s41557-018-0039-2 267: 211: 191: 169: 59: 35: 30: 21: 474:Dimethylamino compounds 303:capable of preventing 53:-dimethylmethanamine 37:Preferred IUPAC name 351:2018NatCh..10..599M 263: g·mol 18: 277:Infobox references 16: 449:Enzyme inhibitors 285:Chemical compound 283: 282: 138:CompTox Dashboard 101:Interactive image 481: 433: 432: 430: 428: 422:Business Insider 413: 407: 406: 404: 402: 387: 381: 380: 370: 339:Nature Chemistry 329: 293:enzyme inhibitor 262: 250: 244: 238: 232: 226: 219:Chemical formula 162: 161: 146: 144: 128: 117: 103: 79: 26: 19: 489: 488: 484: 483: 482: 480: 479: 478: 439: 438: 437: 436: 426: 424: 415: 414: 410: 400: 398: 389: 388: 384: 331: 330: 326: 321: 286: 279: 274: 260: 247: 241: 235: 229: 221: 207: 204: 199: 198: 187: 184: 183: 177: 176: 165: 155:DTXSID301336328 147: 140: 131: 118: 106: 93: 82: 69: 55: 54: 45:-indazol-3-yl)- 12: 11: 5: 487: 485: 477: 476: 471: 466: 461: 456: 451: 441: 440: 435: 434: 408: 382: 345:(6): 599–606. 323: 322: 320: 317: 284: 281: 280: 275: 271:standard state 268: 265: 264: 258: 252: 251: 245: 239: 233: 227: 222: 217: 214: 213: 209: 208: 206: 205: 202: 194: 193: 192: 189: 188: 186: 185: 181: 180: 172: 171: 170: 167: 166: 164: 163: 150: 148: 136: 133: 132: 130: 129: 121: 119: 111: 108: 107: 105: 104: 96: 94: 87: 84: 83: 81: 80: 72: 70: 65: 62: 61: 57: 56: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 486: 475: 472: 470: 467: 465: 462: 460: 457: 455: 452: 450: 447: 446: 444: 423: 419: 412: 409: 397: 393: 390:Borman, Stu. 386: 383: 378: 374: 369: 364: 360: 356: 352: 348: 344: 340: 336: 328: 325: 318: 316: 314: 310: 306: 302: 298: 294: 290: 278: 272: 266: 259: 257: 254: 253: 223: 220: 216: 215: 210: 201: 197: 190: 179: 175: 168: 160: 156: 152: 151: 149: 139: 135: 134: 127: 123: 122: 120: 114: 110: 109: 102: 98: 97: 95: 91: 86: 85: 78: 74: 73: 71: 68: 64: 63: 58: 52: 48: 44: 38: 34: 29: 25: 20: 464:Fluoroarenes 425:. Retrieved 421: 411: 399:. Retrieved 395: 385: 342: 338: 327: 288: 287: 77:2059148-82-0 60:Identifiers 50: 46: 42: 309:common cold 212:Properties 443:Categories 319:References 305:rhinoviral 256:Molar mass 88:3D model ( 67:CAS Number 469:Biphenyls 459:Pyrazoles 454:Indazoles 126:132274735 17:IMP-1088 377:29760414 289:IMP-1088 368:6015761 347:Bibcode 261:453.538 113:PubChem 427:20 May 401:20 May 375:  365:  313:capsid 291:is an 196:SMILES 31:Names 174:InChI 90:JSmol 429:2018 403:2018 373:PMID 301:NMT2 299:and 297:NMT1 363:PMC 355:doi 143:EPA 116:CID 445:: 420:. 394:. 371:. 361:. 353:. 343:10 341:. 337:. 234:29 228:25 431:. 405:. 379:. 357:: 349:: 249:O 246:5 243:N 240:2 237:F 231:H 225:C 145:) 141:( 92:) 51:N 49:, 47:N 43:H

Index


Preferred IUPAC name
CAS Number
2059148-82-0
JSmol
Interactive image
PubChem
132274735
CompTox Dashboard
DTXSID301336328
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
enzyme inhibitor
NMT1
NMT2
rhinoviral
common cold
capsid
"Fragment-derived inhibitors of human N-myristoyltransferase block capsid assembly and replication of the common cold virus"
Bibcode
2018NatCh..10..599M
doi
10.1038/s41557-018-0039-2
PMC
6015761

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