Knowledge (XXG)

Kanamienamide

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Sumimoto, Shimpei; Iwasaki, Arihiro; Ohno, Osamu; Sueyoshi, Kosuke; Teruya, Toshiaki; Suenaga, Kiyotake (13 September 2016). "Kanamienamide, an Enamide with an Enol Ether from the Marine Cyanobacterium".
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InChI=1S/C28H48N2O5/c1-9-23(34-8)19-26(31)29(6)16-12-10-11-13-24-15-14-21(4)18-22(5)27(32)30(7)25(17-20(2)3)28(33)35-24/h12,16,19-22,24-25H,9-11,13-15,17-18H2,1-8H3/b16-12-,23-19-/t21-,22+,24-,25-/m0/s1
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Prabhakar Reddy, D.; Zhang, Ning; Yu, Zhimei; Wang, Zhen; He, Yun (2017-10-02). "Total Synthesis of Kanamienamide".
517: 464: 326: 444: 331: 152: 36: 306: 522: 413: 377: 369: 98: 448: 527: 405: 361: 219: 512: 156: 268: 123: 491: 301:. The synthesis of kanamienamide consists of several chemical techniques, including 297:
that is currently undergoing research in regards to its inhibitory activity towards
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Except where otherwise noted, data are given for materials in their
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CCC(=CC(=O)N(C)C=CCCCC1CCC(CC(C(=O)N(C(C(=O)O1)CC(C)C)C)C)C)OC
140: 452: 122: 329:. Kanamienamide is a natural product found in 472: 8: 479: 465: 155: 97: 15: 344: 201: 176: 151: 183:Key: MTZDCZNHECVTPF-ZIXRUXROSA-N 7: 433: 431: 113: 498:Heterocyclic compounds with 1 ring 451:. You can help Knowledge (XXG) by 14: 53:)-5-pent-1-en-1-yl}pent-2-enamide 435: 354:The Journal of Organic Chemistry 237: 231: 22: 271:(at 25 °C , 100 kPa). 243: 225: 1: 538:Heterocyclic compound stubs 410:10.1021/acs.orglett.6b02364 335:which is a cyanobacterium. 554: 430: 265: 212: 192: 167: 59: 35: 30: 21: 303:CBS asymmetric reduction 366:10.1021/acs.joc.7b01984 327:ring-closing metathesis 533:Eleven-membered rings 503:Nitrogen heterocycles 445:heterocyclic compound 443:This article about a 37:Preferred IUPAC name 508:Oxygen heterocycles 360:(20): 11262–11268. 321:, Evans asymmetric 261: g·mol 18: 307:Wittig olefination 275:Infobox references 16: 518:Methoxy compounds 460: 459: 404:(19): 4884–4887. 332:Moorea bouillonii 283:Chemical compound 281: 280: 136:CompTox Dashboard 79:Interactive image 545: 481: 474: 467: 439: 432: 422: 421: 392: 386: 385: 349: 260: 245: 239: 233: 227: 220:Chemical formula 160: 159: 144: 142: 126: 115: 101: 81: 26: 19: 553: 552: 548: 547: 546: 544: 543: 542: 488: 487: 486: 485: 428: 426: 425: 398:Organic Letters 394: 393: 389: 351: 350: 346: 341: 284: 277: 272: 258: 248: 242: 236: 230: 222: 208: 205: 200: 199: 188: 185: 184: 181: 175: 174: 163: 153:DTXSID901336314 145: 138: 129: 116: 104: 84: 71: 55: 54: 12: 11: 5: 551: 549: 541: 540: 535: 530: 525: 520: 515: 510: 505: 500: 490: 489: 484: 483: 476: 469: 461: 458: 457: 440: 424: 423: 387: 343: 342: 340: 337: 317:coupling with 287:Kanamienamides 282: 279: 278: 273: 269:standard state 266: 263: 262: 256: 250: 249: 246: 240: 234: 228: 223: 218: 215: 214: 210: 209: 207: 206: 203: 195: 194: 193: 190: 189: 187: 186: 182: 179: 178: 170: 169: 168: 165: 164: 162: 161: 148: 146: 134: 131: 130: 128: 127: 119: 117: 109: 106: 105: 103: 102: 94: 92: 86: 85: 83: 82: 74: 72: 65: 62: 61: 57: 56: 40: 39: 33: 32: 28: 27: 17:Kanamienamide 13: 10: 9: 6: 4: 3: 2: 550: 539: 536: 534: 531: 529: 526: 524: 521: 519: 516: 514: 511: 509: 506: 504: 501: 499: 496: 495: 493: 482: 477: 475: 470: 468: 463: 462: 456: 454: 450: 446: 441: 438: 434: 429: 419: 415: 411: 407: 403: 399: 391: 388: 383: 379: 375: 371: 367: 363: 359: 355: 348: 345: 338: 336: 334: 333: 328: 324: 320: 316: 312: 308: 305:, Stork-Zhao- 304: 300: 296: 292: 289:is a complex 288: 276: 270: 264: 257: 255: 252: 251: 224: 221: 217: 216: 211: 202: 198: 191: 177: 173: 166: 158: 154: 150: 149: 147: 137: 133: 132: 125: 121: 120: 118: 112: 108: 107: 100: 96: 95: 93: 91: 88: 87: 80: 76: 75: 73: 69: 64: 63: 58: 52: 48: 44: 38: 34: 29: 25: 20: 453:expanding it 442: 427: 401: 397: 390: 357: 353: 347: 330: 319:vinyl iodide 299:cancer cells 286: 285: 60:Identifiers 50: 46: 45:)-3-Methoxy- 42: 293:containing 213:Properties 492:Categories 339:References 323:alkylation 313:-mediated 291:enol ether 254:Molar mass 90:ChemSpider 66:3D model ( 374:0022-3263 124:132915918 523:Lactones 418:27623268 382:28944669 99:58197334 528:Lactams 295:enamide 259:492.701 111:PubChem 513:Amides 416:  380:  372:  325:, and 197:SMILES 31:Names 447:is a 315:amide 172:InChI 68:JSmol 449:stub 414:PMID 378:PMID 370:ISSN 49:-{(1 406:doi 362:doi 141:EPA 114:CID 494:: 412:. 402:18 400:. 376:. 368:. 358:82 356:. 311:Cu 309:, 235:48 229:28 41:(2 480:e 473:t 466:v 455:. 420:. 408:: 384:. 364:: 247:5 244:O 241:2 238:N 232:H 226:C 143:) 139:( 70:) 51:Z 47:N 43:E

Index


Preferred IUPAC name
JSmol
Interactive image
ChemSpider
58197334
PubChem
132915918
CompTox Dashboard
DTXSID901336314
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
enol ether
enamide
cancer cells
CBS asymmetric reduction
Wittig olefination
Cu
amide
vinyl iodide
alkylation
ring-closing metathesis
Moorea bouillonii
doi
10.1021/acs.joc.7b01984

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