Knowledge (XXG)

Aflavinine

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Gallagher, Rex T.; McCabe, Terrence; Hirotsu, Ken; Clardy, Jon; Nicholson, Judith; Wilson, Benjamin J. (January 1980). "Aflavinine, a novel indole-mevalonate metabolite from tremorgen-producing species".
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Gloer, James B.; TePaske, Mark R.; Sima, John S.; Wicklow, Donald T.; Dowd, Patrick F. (November 1988). "Antiinsectan aflavinine derivatives from the sclerotia of Aspergillus flavus".
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InChI=1S/C28H39NO/c1-17(2)20-13-15-28-24(30)11-10-19(4)27(28,5)14-12-18(3)26(28)25(20)22-16-29-23-9-7-6-8-21(22)23/h6-9,16-19,24,26,29-30H,10-15H2,1-5H3/t18-,19-,24+,26+,27+,28+/m1/s1
114: 252: 227: 324: 170: 433:"Aflavinines and other antiinsectan metabolites from the ascostromata of Eupenicillium crustaceum and related species" 191: 502: 36: 444: 208: 80: 68:-Indol-3-yl)-4,4a,7-trimethyl-9-propan-2-yl-1,2,3,4,5,6,7,7a,10,11-decahydrobenzonaphthalen-1-ol 478: 460: 413: 378: 134: 468: 452: 405: 370: 340: 275: 179: 90: 212: 448: 318: 473: 432: 374: 496: 456: 159: 303: 125: 464: 417: 382: 482: 409: 146: 23: 317:
Except where otherwise noted, data are given for materials in their
431:
Wang, H. J.; Gloer, J. B.; Wicklow, D. T.; Dowd, P. F. (Dec 1995).
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CC1CCC2(C(CCC(C23C1C(=C(CC3)C(C)C)C4=CNC5=CC=CC=C54)O)C)C
158: 89: 8: 343:compound produced by some plants and fungi. 211: 133: 15: 472: 178: 352: 257: 232: 207: 437:Applied and Environmental Microbiology 239:Key: LXZADDNPPHIYMD-QQVIWQHHSA-N 7: 149: 14: 457:10.1128/aem.61.12.4429-4435.1995 398:The Journal of Organic Chemistry 293: 287: 22: 321:(at 25 °C , 100 kPa). 296: 281: 1: 375:10.1016/s0040-4039(00)71179-8 519: 315: 268: 248: 223: 73: 35: 30: 21: 341:anti-insectan chemical 449:1995ApEnM..61.4429W 410:10.1021/jo00258a011 363:Tetrahedron Letters 311: g·mol 18: 325:Infobox references 16: 443:(12): 4429–4435. 404:(23): 5457–5460. 333:Chemical compound 331: 330: 192:CompTox Dashboard 115:Interactive image 510: 503:Indole alkaloids 487: 486: 476: 428: 422: 421: 393: 387: 386: 357: 310: 298: 295: 289: 283: 276:Chemical formula 216: 215: 200: 198: 182: 162: 151: 137: 117: 93: 26: 19: 518: 517: 513: 512: 511: 509: 508: 507: 493: 492: 491: 490: 430: 429: 425: 395: 394: 390: 359: 358: 354: 349: 334: 327: 322: 308: 292: 286: 278: 264: 261: 256: 255: 244: 241: 240: 237: 231: 230: 219: 201: 194: 185: 165: 152: 140: 120: 107: 96: 83: 69: 12: 11: 5: 516: 514: 506: 505: 495: 494: 489: 488: 423: 388: 369:(3): 243–246. 351: 350: 348: 345: 332: 329: 328: 323: 319:standard state 316: 313: 312: 306: 300: 299: 290: 284: 279: 274: 271: 270: 266: 265: 263: 262: 259: 251: 250: 249: 246: 245: 243: 242: 238: 235: 234: 226: 225: 224: 221: 220: 218: 217: 209:DTXSID40995845 204: 202: 190: 187: 186: 184: 183: 175: 173: 167: 166: 164: 163: 155: 153: 145: 142: 141: 139: 138: 130: 128: 122: 121: 119: 118: 110: 108: 101: 98: 97: 95: 94: 86: 84: 79: 76: 75: 71: 70: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 515: 504: 501: 500: 498: 484: 480: 475: 470: 466: 462: 458: 454: 450: 446: 442: 438: 434: 427: 424: 419: 415: 411: 407: 403: 399: 392: 389: 384: 380: 376: 372: 368: 364: 356: 353: 346: 344: 342: 338: 326: 320: 314: 307: 305: 302: 301: 280: 277: 273: 272: 267: 258: 254: 247: 233: 229: 222: 214: 210: 206: 205: 203: 193: 189: 188: 181: 177: 176: 174: 172: 169: 168: 161: 157: 156: 154: 148: 144: 143: 136: 132: 131: 129: 127: 124: 123: 116: 112: 111: 109: 105: 100: 99: 92: 88: 87: 85: 82: 78: 77: 72: 67: 63: 59: 55: 51: 47: 43: 38: 34: 29: 25: 20: 440: 436: 426: 401: 397: 391: 366: 362: 355: 336: 335: 74:Identifiers 65: 61: 57: 53: 49: 45: 41: 269:Properties 17:Aflavinine 347:References 337:Aflavinine 304:Molar mass 180:42N1443TXV 126:ChemSpider 102:3D model ( 91:74328-59-9 81:CAS Number 37:IUPAC name 465:0099-2240 418:0022-3263 383:0040-4039 497:Category 160:21725958 135:10313765 483:8534106 445:Bibcode 309:405.626 147:PubChem 481:  474:167750 471:  463:  416:  381:  339:is an 253:SMILES 64:)-8-(1 31:Names 228:InChI 104:JSmol 479:PMID 461:ISSN 414:ISSN 379:ISSN 171:UNII 60:,11a 469:PMC 453:doi 406:doi 371:doi 197:EPA 150:CID 56:,7a 48:,4a 499:: 477:. 467:. 459:. 451:. 441:61 439:. 435:. 412:. 402:53 400:. 377:. 367:21 365:. 291:39 285:28 52:,7 44:,4 40:(1 485:. 455:: 447:: 420:. 408:: 385:. 373:: 297:O 294:N 288:H 282:C 199:) 195:( 106:) 66:H 62:S 58:S 54:R 50:S 46:R 42:S

Index


IUPAC name
CAS Number
74328-59-9
JSmol
Interactive image
ChemSpider
10313765
PubChem
21725958
UNII
42N1443TXV
CompTox Dashboard
DTXSID40995845
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
anti-insectan chemical
doi
10.1016/s0040-4039(00)71179-8
ISSN
0040-4039
doi
10.1021/jo00258a011
ISSN
0022-3263

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