Knowledge

Suberedamine

Source 📝

440: 37: 24: 75: 67: 200:
B: InChI=1S/C24H32Br3N3O3/c1-28-21(15-16-6-7-22(32-4)18(25)12-16)24(31)29-9-8-17-13-19(26)23(20(27)14-17)33-11-5-10-30(2)3/h6-7,12-14,21,28H,5,8-11,15H2,1-4H3,(H,29,31)/t21-/m0/s1
190:
A: InChI=1S/C23H30Br3N3O3/c1-29(2)9-4-10-32-22-18(25)12-16(13-19(22)26)7-8-28-23(30)20(27)14-15-5-6-21(31-3)17(24)11-15/h5-6,11-13,20H,4,7-10,14,27H2,1-3H3,(H,28,30)/t20-/m0/s1
292:
Kottakota, S. K.; Evangelopoulos, D.; Alnimr, A.; Bhakta, S.; McHugh, T. D.; Gray, M.; Groundwater, P. W.; Marrs, E. C.; Perry, J. D.; Spilling, C. D.; Harburn, J. J. (2012).
362:
Tsuda, Masashi; Sakuma, Yusuke; Kobayashi, Jun'ichi (July 2001). "Suberedamines A and B, New Bromotyrosine Alkaloids from a Sponge Suberea Species".
294:"Synthesis and biological evaluation of purpurealidin E-derived marine sponge metabolites: aplysamine-2, aplyzanzine A, and suberedamines A and B" 481: 216: 422: 342: 474: 181: 246: 525: 467: 104: 96: 510: 515: 500: 332: 412: 133: 125: 505: 392: 8: 455: 418: 379: 338: 313: 167: 159: 447: 371: 305: 520: 451: 293: 240: 494: 262: 383: 317: 115: 375: 309: 229:
B: CN(CC1=CC(=C(C=C1)OC)Br)C(=O)NCCC2=CC(=C(C(=C2)Br)OCCCN(C)C)Br
239:
Except where otherwise noted, data are given for materials in their
439: 291: 272: 224:
A: CN(C)CCCOC1=C(C=C(C=C1Br)CCNC(=O)(CC2=CC(=C(C=C2)OC)Br)N)Br
74: 66: 267: 145: 36: 23: 86: 55: 337:. Walter de Gruyter GmbH & Co KG. pp. 112–113. 361: 261:
are chemical compounds that have been isolated from
492: 166: 158: 475: 417:. Gulf Professional Publishing. p. 86. 482: 468: 132: 124: 411:Cordell, Geoffrey A. (23 August 2005). 410: 493: 203:Key: MNNHZXNEKPRDII-NRFANRHFSA-N 193:Key: CPOMDHYOIBOZBW-FQEVSTJZSA-N 103: 95: 434: 414:The Alkaloids: Chemistry and Biology 330: 393:"Total Synthesis of Suberedamine a" 148: 13: 14: 537: 390: 331:Zhou, Jiaju (23 September 2019). 438: 355: 35: 22: 271:. The compounds are brominated 243:(at 25 °C , 100 kPa). 324: 285: 1: 278: 454:. You can help Knowledge by 7: 364:Journal of Natural Products 298:Journal of Natural Products 10: 542: 433: 237: 212: 177: 47: 34: 21: 526:Organic compound stubs 446:This article about an 275:dimer derivatives. 18: 247:Infobox references 16: 511:Methoxy compounds 463: 462: 424:978-0-12-469561-0 376:10.1021/np010077g 344:978-3-11-065519-3 334:Alkaloids, Part 1 310:10.1021/np300102z 255:Chemical compound 253: 252: 76:Interactive image 68:Interactive image 533: 484: 477: 470: 448:organic compound 442: 435: 428: 407: 405: 403: 387: 349: 348: 328: 322: 321: 289: 170: 162: 150: 136: 128: 107: 99: 78: 70: 39: 26: 19: 15: 541: 540: 536: 535: 534: 532: 531: 530: 516:Tertiary amines 491: 490: 489: 488: 425: 401: 399: 358: 353: 352: 345: 329: 325: 304:(6): 1090–101. 290: 286: 281: 256: 249: 244: 233: 230: 225: 220: 219: 208: 205: 204: 201: 195: 194: 191: 185: 184: 173: 151: 139: 110: 81: 59: 43: 40: 30: 27: 12: 11: 5: 539: 529: 528: 523: 518: 513: 508: 503: 501:Sponge biology 487: 486: 479: 472: 464: 461: 460: 443: 432: 431: 429: 423: 408: 397:acs.confex.com 388: 370:(7): 980–982. 357: 354: 351: 350: 343: 323: 283: 282: 280: 277: 263:marine sponges 254: 251: 250: 245: 241:standard state 238: 235: 234: 232: 231: 228: 226: 223: 215: 214: 213: 210: 209: 207: 206: 202: 199: 198: 196: 192: 189: 188: 180: 179: 178: 175: 174: 172: 171: 163: 154: 152: 144: 141: 140: 138: 137: 129: 120: 118: 112: 111: 109: 108: 100: 91: 89: 83: 82: 80: 79: 71: 62: 60: 53: 50: 49: 45: 44: 42:Suberedamine B 41: 32: 31: 29:Suberedamine A 28: 9: 6: 4: 3: 2: 538: 527: 524: 522: 519: 517: 514: 512: 509: 507: 504: 502: 499: 498: 496: 485: 480: 478: 473: 471: 466: 465: 459: 457: 453: 449: 444: 441: 437: 436: 430: 426: 420: 416: 415: 409: 398: 394: 391:Xiong, Fong. 389: 385: 381: 377: 373: 369: 365: 360: 359: 356:Extra reading 346: 340: 336: 335: 327: 319: 315: 311: 307: 303: 299: 295: 288: 284: 276: 274: 270: 269: 265:in the genus 264: 260: 259:Suberedamines 248: 242: 236: 227: 222: 221: 218: 211: 197: 187: 186: 183: 176: 169: 164: 161: 156: 155: 153: 147: 143: 142: 135: 130: 127: 122: 121: 119: 117: 114: 113: 106: 101: 98: 93: 92: 90: 88: 85: 84: 77: 72: 69: 64: 63: 61: 57: 52: 51: 46: 38: 33: 25: 20: 17:Suberedamine 456:expanding it 445: 413: 400:. Retrieved 396: 367: 363: 333: 326: 301: 297: 287: 266: 258: 257: 105:ChEMBL465833 97:ChEMBL464660 48:Identifiers 506:Bromoarenes 402:15 November 495:Categories 279:References 116:ChemSpider 54:3D model ( 384:11473442 318:22620987 273:tyrosine 168:10258717 165:B: 160:10484217 157:A: 131:B: 123:A: 102:B: 94:A: 73:B: 65:A: 268:Suberea 146:PubChem 134:8434200 126:8659624 521:Amides 421:  382:  341:  316:  217:SMILES 87:ChEMBL 450:is a 182:InChI 56:JSmol 452:stub 419:ISBN 404:2020 380:PMID 339:ISBN 314:PMID 372:doi 306:doi 149:CID 497:: 395:. 378:. 368:64 366:. 312:. 302:75 300:. 296:. 483:e 476:t 469:v 458:. 427:. 406:. 386:. 374:: 347:. 320:. 308:: 58:)

Index



JSmol
Interactive image
Interactive image
ChEMBL
ChEMBL464660
ChEMBL465833
ChemSpider
8659624
8434200
PubChem
10484217
10258717
InChI
SMILES
standard state
Infobox references
marine sponges
Suberea
tyrosine
"Synthesis and biological evaluation of purpurealidin E-derived marine sponge metabolites: aplysamine-2, aplyzanzine A, and suberedamines A and B"
doi
10.1021/np300102z
PMID
22620987
Alkaloids, Part 1
ISBN
978-3-11-065519-3
doi

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.