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Isonotholaenic acid

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del Olmo, Esther; Armas, Marlon Garcia; López-Pérez, JL; Ruiz, G; Vargas, F; Giménez, Alberto; Deharo, Eric; San Feliciano, Arturo (2001). "Anti-Trypanosoma activity of some natural stilbenoids and synthetic related heterocyclic compounds".
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del Olmo, Esther; Armas, Marlon Garcia; Ybarra, Ma Inèss; Lopez, José Luis; Oporto, Patricia; Giménez, Alberto; Deharo, Eric; San Feliciano, Arturo (2003). "The Imidazoisoindole System. A New Skeletal Basis for Antiplasmodial Compounds".
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InChI=1S/C17H18O5/c1-21-14-7-4-11(5-8-14)3-6-12-9-13(18)10-15(22-2)16(12)17(19)20/h4-5,7-10,18H,3,6H2,1-2H3,(H,19,20)
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InChI=1/C17H18O5/c1-21-14-7-4-11(5-8-14)3-6-12-9-13(18)10-15(22-2)16(12)17(19)20/h4-5,7-10,18H,3,6H2,1-2H3,(H,19,20)
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Except where otherwise noted, data are given for materials in their
65: 55: 408: 148: 610: 509: 443: 130: 630: 420: 8: 375:Bioorganic & Medicinal Chemistry Letters 339:Bioorganic & Medicinal Chemistry Letters 637: 623: 427: 413: 405: 163: 105: 15: 328: 219: 184: 159: 191:Key: GAWSNXBLUNVZCK-UHFFFAOYSA-N 85: 7: 591: 589: 222:c2cc(OC)ccc2CCc1cc(O)cc(OC)c1C(O)=O 201:Key: GAWSNXBLUNVZCK-UHFFFAOYAW 121: 455:(3,3′-dihydroxy-5-methoxybibenzyl) 41:4-Hydroxy-2-methoxy-6-benzoic acid 14: 521:13,13'-O-Isoproylidenericcardin D 593: 249: 22: 283:(at 25 °C , 100 kPa). 255: 243: 1: 387:10.1016/s0960-894x(01)00562-5 351:10.1016/S0960-894X(03)00509-2 609:. You can help Knowledge by 677: 588: 551:Macrocyclic bis(benzyls): 315:). This compound shows an 305:found in the Andean fern 277: 230: 210: 175: 47: 35: 30: 21: 661:Aromatic compound stubs 601:This article about an 438:and their glycosides 37:Preferred IUPAC name 17:Isonotholaenic acid 574:dihydrophenanthrene 473:Isonotholaenic acid 468:Dihydro-resveratrol 299:Isonotholaenic acid 273: g·mol 18: 656:Dihydrostilbenoids 463:combretastatin B-1 445:Dihydrostilbenoids 436:Dihydrostilbenoids 308:Argyrochosma nivea 287:Infobox references 16: 618: 617: 586: 585: 381:(20): 2755–2757. 345:(16): 2769–2772. 303:dihydrostilbenoid 295:Chemical compound 293: 292: 144:CompTox Dashboard 67:Interactive image 668: 639: 632: 625: 597: 590: 572:Cyclic bibenzyl- 510:Oligomeric forms 493:Tyrolobibenzyl A 488:Notholaenic acid 429: 422: 415: 406: 399: 398: 369: 363: 362: 333: 313:Notholaena nivea 272: 257: 251: 245: 238:Chemical formula 168: 167: 152: 150: 134: 123: 109: 89: 69: 26: 19: 676: 675: 671: 670: 669: 667: 666: 665: 646: 645: 644: 643: 587: 582: 535:Neomarchantin A 505: 439: 433: 403: 402: 371: 370: 366: 335: 334: 330: 325: 296: 289: 284: 270: 260: 254: 248: 240: 226: 223: 218: 217: 206: 203: 202: 199: 193: 192: 189: 183: 182: 171: 161:DTXSID601030446 153: 146: 137: 124: 112: 92: 72: 59: 43: 42: 12: 11: 5: 674: 672: 664: 663: 658: 648: 647: 642: 641: 634: 627: 619: 616: 615: 605:compound is a 598: 584: 583: 581: 580: 569: 568: 559: 548: 547: 542: 537: 532: 523: 517:Bis(bibenzyls) 513: 511: 507: 506: 504: 503: 490: 485: 480: 478:Lunularic acid 475: 470: 465: 459:Combretastatin 456: 449: 447: 441: 440: 434: 432: 431: 424: 417: 409: 401: 400: 364: 327: 326: 324: 321: 294: 291: 290: 285: 281:standard state 278: 275: 274: 268: 262: 261: 258: 252: 246: 241: 236: 233: 232: 228: 227: 225: 224: 221: 213: 212: 211: 208: 207: 205: 204: 200: 197: 196: 194: 190: 187: 186: 178: 177: 176: 173: 172: 170: 169: 156: 154: 142: 139: 138: 136: 135: 127: 125: 117: 114: 113: 111: 110: 102: 100: 94: 93: 91: 90: 82: 80: 74: 73: 71: 70: 62: 60: 53: 50: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 673: 662: 659: 657: 654: 653: 651: 640: 635: 633: 628: 626: 621: 620: 614: 612: 608: 604: 599: 596: 592: 579: 575: 571: 570: 567: 563: 560: 558: 554: 550: 549: 546: 543: 541: 538: 536: 533: 531: 527: 524: 522: 518: 515: 514: 512: 508: 502: 498: 494: 491: 489: 486: 484: 481: 479: 476: 474: 471: 469: 466: 464: 460: 457: 454: 453:Batatasin-III 451: 450: 448: 446: 442: 437: 430: 425: 423: 418: 416: 411: 410: 407: 396: 392: 388: 384: 380: 376: 368: 365: 360: 356: 352: 348: 344: 340: 332: 329: 322: 320: 318: 317:anti-chagasic 314: 310: 309: 304: 300: 288: 282: 276: 269: 267: 264: 263: 242: 239: 235: 234: 229: 220: 216: 209: 195: 185: 181: 174: 166: 162: 158: 157: 155: 145: 141: 140: 133: 129: 128: 126: 120: 116: 115: 108: 104: 103: 101: 99: 96: 95: 88: 84: 83: 81: 79: 76: 75: 68: 64: 63: 61: 57: 52: 51: 46: 38: 34: 29: 25: 20: 611:expanding it 600: 576:derivative: 553:Marchantin A 540:Plagiochin E 526:Marchantin B 472: 378: 374: 367: 342: 338: 331: 312: 306: 298: 297: 48:Identifiers 578:Cavicularin 562:Riccardin B 545:Riccardin H 231:Properties 87:ChEMBL68178 650:Categories 323:References 319:activity. 311:(formerly 266:Molar mass 98:ChemSpider 54:3D model ( 483:Lunularin 603:aromatic 395:11591517 359:12873511 132:10017784 271:302.326 119:PubChem 107:8193357 393:  357:  215:SMILES 78:ChEMBL 31:Names 301:is a 180:InChI 56:JSmol 607:stub 564:and 555:and 528:and 499:and 461:and 391:PMID 355:PMID 383:doi 347:doi 149:EPA 122:CID 652:: 519:: 495:, 389:. 379:11 377:. 353:. 343:13 341:. 253:18 247:17 638:e 631:t 624:v 613:. 566:C 557:C 530:E 501:C 497:B 428:e 421:t 414:v 397:. 385:: 361:. 349:: 259:5 256:O 250:H 244:C 151:) 147:( 58:)

Index

Chemical structure of isonotholaenic acid
Preferred IUPAC name
JSmol
Interactive image
ChEMBL
ChEMBL68178
ChemSpider
8193357
PubChem
10017784
CompTox Dashboard
DTXSID601030446
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InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
dihydrostilbenoid
Argyrochosma nivea
anti-chagasic
doi
10.1016/S0960-894X(03)00509-2
PMID
12873511
doi
10.1016/s0960-894x(01)00562-5
PMID
11591517

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