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Acetoxycycloheximide

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207: 24: 108: 246: 230:
InChI=1S/C17H25NO6/c1-9-7-17(3,24-10(2)19)8-12(16(9)23)13(20)4-11-5-14(21)18-15(22)6-11/h9,11-13,20H,4-8H2,1-3H3,(H,18,21,22)/t9-,12-,13+,17+/m0/s1
398: 221: 164: 534: 349: 185: 321: 529: 544: 36: 415: 539: 477: 202: 74: 466:"Stages of memory in mice treated with acetoxycycloheximide before or immediately after learning" 446: 505: 438: 394: 390: 549: 495: 485: 430: 337: 269: 173: 128: 206: 84: 481: 414:
Flood, James F.; Bennett, Edward L.; Orme, Ann E.; Rosenzweig, Mark R. (February 1975).
383: 315: 500: 465: 523: 434: 361: 345: 450: 23: 153: 416:"Effects of protein synthesis inhibition on memory for active avoidance training" 341: 300: 119: 509: 490: 442: 140: 314:
Except where otherwise noted, data are given for materials in their
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Flexner, L. B.; Flexner, J. B.; Roberts, R. B. (1 August 1966).
389:(3. ed.). San Diego, Calif. : Academic Press. pp.  352:
in animal cells and can inhibit the formation of memories.
190: 382: 152: 470:Proceedings of the National Academy of Sciences 83: 8: 254:C1C(C(C1=O)(CC2CC(=O)NC(=O)C2)O)(C)OC(=O)C 205: 127: 15: 499: 489: 172: 52:)-3--1,5-dimethyl-4-oxocyclohexyl acetate 373: 251: 226: 201: 340:compound. It can be considered as the 233:Key: UFDHNJJHPSGMFX-SQUSCZTCSA-N 7: 143: 14: 287: 281: 22: 318:(at 25 °C , 100 kPa). 290: 275: 1: 435:10.1016/0031-9384(75)90163-8 350:protein synthesis inhibitor 566: 423:Physiology & Behavior 312: 262: 242: 217: 67: 57: 35: 30: 21: 385:A dictionary of virology 381:Mahy, Brian W J (2001). 60:Acetyloxycycloheximide 491:10.1073/pnas.56.2.730 17:Acetoxycycloheximide 334:Acetoxycycloheximide 482:1966PNAS...56..730F 308: g·mol 18: 535:Secondary alcohols 322:Infobox references 16: 348:. It is a potent 330:Chemical compound 328: 327: 186:CompTox Dashboard 109:Interactive image 557: 514: 513: 503: 493: 461: 455: 454: 420: 411: 405: 404: 388: 378: 338:organic chemical 307: 292: 289: 283: 277: 270:Chemical formula 210: 209: 194: 192: 176: 156: 145: 131: 111: 87: 26: 19: 565: 564: 560: 559: 558: 556: 555: 554: 520: 519: 518: 517: 463: 462: 458: 418: 413: 412: 408: 401: 380: 379: 375: 370: 358: 331: 324: 319: 305: 295: 286: 280: 272: 258: 255: 250: 249: 238: 235: 234: 231: 225: 224: 213: 203:DTXSID001028172 195: 188: 179: 159: 146: 134: 114: 101: 90: 77: 63: 61: 53: 12: 11: 5: 563: 561: 553: 552: 547: 542: 537: 532: 530:Acetate esters 522: 521: 516: 515: 476:(2): 730–735. 456: 429:(2): 177–184. 406: 399: 372: 371: 369: 366: 365: 364: 357: 354: 329: 326: 325: 320: 316:standard state 313: 310: 309: 303: 297: 296: 293: 284: 278: 273: 268: 265: 264: 260: 259: 257: 256: 253: 245: 244: 243: 240: 239: 237: 236: 232: 229: 228: 220: 219: 218: 215: 214: 212: 211: 198: 196: 184: 181: 180: 178: 177: 169: 167: 161: 160: 158: 157: 149: 147: 139: 136: 135: 133: 132: 124: 122: 116: 115: 113: 112: 104: 102: 95: 92: 91: 89: 88: 80: 78: 73: 70: 69: 65: 64: 59: 55: 54: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 562: 551: 548: 546: 543: 541: 538: 536: 533: 531: 528: 527: 525: 511: 507: 502: 497: 492: 487: 483: 479: 475: 471: 467: 460: 457: 452: 448: 444: 440: 436: 432: 428: 424: 417: 410: 407: 402: 400:0-12-465327-8 396: 392: 387: 386: 377: 374: 367: 363: 362:Cycloheximide 360: 359: 355: 353: 351: 347: 346:cycloheximide 343: 339: 335: 323: 317: 311: 304: 302: 299: 298: 274: 271: 267: 266: 261: 252: 248: 241: 227: 223: 216: 208: 204: 200: 199: 197: 187: 183: 182: 175: 171: 170: 168: 166: 163: 162: 155: 151: 150: 148: 142: 138: 137: 130: 126: 125: 123: 121: 118: 117: 110: 106: 105: 103: 99: 94: 93: 86: 82: 81: 79: 76: 72: 71: 66: 56: 51: 47: 43: 38: 34: 29: 25: 20: 545:Glutarimides 473: 469: 459: 426: 422: 409: 384: 376: 344:analogue of 333: 332: 68:Identifiers 58:Other names 49: 45: 41: 540:Antibiotics 263:Properties 524:Categories 368:References 342:acetylated 301:Molar mass 174:UX3Y1I395S 120:ChemSpider 96:3D model ( 75:CAS Number 37:IUPAC name 85:2885-39-4 451:31577844 356:See also 550:Ketones 510:5229991 478:Bibcode 443:1161822 306:339.388 141:PubChem 508:  501:224433 498:  449:  441:  397:  336:is an 247:SMILES 31:Names 447:S2CID 419:(PDF) 222:InChI 154:73396 129:66113 98:JSmol 506:PMID 439:PMID 395:ISBN 165:UNII 62:E-73 496:PMC 486:doi 431:doi 191:EPA 144:CID 526:: 504:. 494:. 484:. 474:56 472:. 468:. 445:. 437:. 427:14 425:. 421:. 393:. 285:25 279:17 48:,5 44:,3 40:(1 512:. 488:: 480:: 453:. 433:: 403:. 391:2 294:6 291:O 288:N 282:H 276:C 193:) 189:( 100:) 50:S 46:S 42:R

Index


IUPAC name
CAS Number
2885-39-4
JSmol
Interactive image
ChemSpider
66113
PubChem
73396
UNII
UX3Y1I395S
CompTox Dashboard
DTXSID001028172
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
organic chemical
acetylated
cycloheximide
protein synthesis inhibitor
Cycloheximide
A dictionary of virology
2
ISBN
0-12-465327-8

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