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Lunularic acid

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Pryce, Robert J.; Linton, Linda (1974). "Lunularic acid decarboxylase from the liverwort Conocephalum conicum".
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InChI=1S/C15H14O4/c16-12-8-5-10(6-9-12)4-7-11-2-1-3-13(17)14(11)15(18)19/h1-3,5-6,8-9,16-17H,4,7H2,(H,18,19)
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InChI=1S/C15H14O4/c16-12-8-5-10(6-9-12)4-7-11-2-1-3-13(17)14(11)15(18)19/h1-3,5-6,8-9,16-17H,4,7H2,(H,18,19)
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InChI=1/C15H14O4/c16-12-8-5-10(6-9-12)4-7-11-2-1-3-13(17)14(11)15(18)19/h1-3,5-6,8-9,16-17H,4,7H2,(H,18,19)
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Gorham, John (1977). "Lunularic acid and related compounds in liverworts, algae and Hydrangea".
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Pryce, R. J. (1971). "Lunularic acid, a common endogenous growth inhibitor of liverworts".
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Except where otherwise noted, data are given for materials in their
128: 87: 77: 119: 488: 190: 690: 589: 523: 152: 63: 710: 500: 8: 717: 703: 507: 493: 485: 205: 107: 15: 172: 274:C1=CC(=C(C(=C1)O)C(=O)O)CCC2=CC=C(C=C2)O 383: 271: 226: 201: 368:has been detected from the liverwort 243:Key: GFSQDOUEUWXRSL-UHFFFAOYSA-N 233:Key: GFSQDOUEUWXRSL-UHFFFAOYSA-N 7: 671: 669: 253:Key: GFSQDOUEUWXRSL-UHFFFAOYAI 143: 127: 535:(3,3′-dihydroxy-5-methoxybibenzyl) 14: 601:13,13'-O-Isoproylidenericcardin D 673: 22: 327:(at 25 °C , 100 kPa). 1: 475:10.1016/S0031-9422(00)86926-5 448:10.1016/S0031-9422(00)86795-3 689:. You can help Knowledge by 366:lunularic acid decarboxylase 757: 668: 631:Macrocyclic bis(benzyls): 317:258.27 g/mol 321: 282: 262: 217: 47: 35: 30: 21: 41:2-Hydroxy-6-benzoic acid 741:Aromatic compound stubs 349:found in the liverwort 681:This article about an 358:Hydrangea macrophylla 518:and their glycosides 371:Conocephalum conicum 355:and in the roots of 37:Preferred IUPAC name 654:dihydrophenanthrene 553:Isonotholaenic acid 548:Dihydro-resveratrol 18: 736:Dihydrostilbenoids 543:combretastatin B-1 525:Dihydrostilbenoids 516:Dihydrostilbenoids 405:10.1007/BF00390214 352:Lunularia cruciata 331:Infobox references 16: 698: 697: 666: 665: 469:(11): 2497–2501. 347:dihydrostilbenoid 339:Chemical compound 337: 336: 186:CompTox Dashboard 89:Interactive image 748: 719: 712: 705: 677: 670: 652:Cyclic bibenzyl- 590:Oligomeric forms 573:Tyrolobibenzyl A 568:Notholaenic acid 509: 502: 495: 486: 479: 478: 458: 452: 451: 431: 425: 424: 388: 290:Chemical formula 210: 209: 194: 192: 176: 156: 145: 131: 111: 91: 67: 26: 19: 756: 755: 751: 750: 749: 747: 746: 745: 726: 725: 724: 723: 667: 662: 615:Neomarchantin A 585: 519: 513: 483: 482: 460: 459: 455: 433: 432: 428: 390: 389: 385: 380: 340: 333: 328: 306: 302: 298: 292: 278: 275: 270: 269: 258: 255: 254: 251: 245: 244: 241: 235: 234: 231: 225: 224: 213: 195: 188: 179: 159: 146: 134: 114: 94: 81: 70: 57: 43: 42: 17:Lunularic acid 12: 11: 5: 754: 752: 744: 743: 738: 728: 727: 722: 721: 714: 707: 699: 696: 695: 685:compound is a 678: 664: 663: 661: 660: 649: 648: 639: 628: 627: 622: 617: 612: 603: 597:Bis(bibenzyls) 593: 591: 587: 586: 584: 583: 570: 565: 560: 558:Lunularic acid 555: 550: 545: 539:Combretastatin 536: 529: 527: 521: 520: 514: 512: 511: 504: 497: 489: 481: 480: 463:Phytochemistry 453: 442:(2): 249–253. 436:Phytochemistry 426: 399:(4): 354–357. 382: 381: 379: 376: 343:Lunularic acid 338: 335: 334: 329: 325:standard state 322: 319: 318: 315: 309: 308: 304: 300: 296: 293: 288: 285: 284: 280: 279: 277: 276: 273: 265: 264: 263: 260: 259: 257: 256: 252: 249: 248: 246: 242: 239: 238: 236: 232: 229: 228: 220: 219: 218: 215: 214: 212: 211: 203:DTXSID40177826 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: 96: 95: 93: 92: 84: 82: 75: 72: 71: 69: 68: 60: 58: 53: 50: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 753: 742: 739: 737: 734: 733: 731: 720: 715: 713: 708: 706: 701: 700: 694: 692: 688: 684: 679: 676: 672: 659: 655: 651: 650: 647: 643: 640: 638: 634: 630: 629: 626: 623: 621: 618: 616: 613: 611: 607: 604: 602: 598: 595: 594: 592: 588: 582: 578: 574: 571: 569: 566: 564: 561: 559: 556: 554: 551: 549: 546: 544: 540: 537: 534: 533:Batatasin-III 531: 530: 528: 526: 522: 517: 510: 505: 503: 498: 496: 491: 490: 487: 476: 472: 468: 464: 457: 454: 449: 445: 441: 437: 430: 427: 422: 418: 414: 410: 406: 402: 398: 394: 387: 384: 377: 375: 373: 372: 367: 362: 360: 359: 354: 353: 348: 344: 332: 326: 320: 316: 314: 311: 310: 294: 291: 287: 286: 281: 272: 268: 261: 247: 237: 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: 101: 98: 97: 90: 86: 85: 83: 79: 74: 73: 66: 62: 61: 59: 56: 52: 51: 46: 38: 34: 29: 25: 20: 691:expanding it 680: 656:derivative: 633:Marchantin A 620:Plagiochin E 606:Marchantin B 557: 466: 462: 456: 439: 435: 429: 396: 392: 386: 369: 363: 356: 350: 342: 341: 48:Identifiers 658:Cavicularin 642:Riccardin B 625:Riccardin H 283:Properties 730:Categories 378:References 313:Molar mass 174:9ZQ3FYV21C 100:ChemSpider 76:3D model ( 65:23255-59-6 55:CAS Number 563:Lunularin 683:aromatic 413:24493279 421:6984399 307: 141:PubChem 419:  411:  393:Planta 267:SMILES 154:161413 129:C10268 109:141785 31:Names 417:S2CID 345:is a 222:InChI 78:JSmol 687:stub 644:and 635:and 608:and 579:and 541:and 409:PMID 165:UNII 120:KEGG 471:doi 444:doi 401:doi 191:EPA 144:CID 732:: 599:: 575:, 467:13 465:. 440:16 438:. 415:. 407:. 397:97 395:. 374:. 364:A 361:. 301:14 297:15 718:e 711:t 704:v 693:. 646:C 637:C 610:E 581:C 577:B 508:e 501:t 494:v 477:. 473:: 450:. 446:: 423:. 403:: 305:4 303:O 299:H 295:C 193:) 189:( 80:)

Index


Preferred IUPAC name
CAS Number
23255-59-6
JSmol
Interactive image
ChemSpider
141785
KEGG
C10268
PubChem
161413
UNII
9ZQ3FYV21C
CompTox Dashboard
DTXSID40177826
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InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
dihydrostilbenoid
Lunularia cruciata
Hydrangea macrophylla
lunularic acid decarboxylase
Conocephalum conicum
doi
10.1007/BF00390214

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