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Damnacanthal

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234: 159: 24: 761: 825: 398: 905: 809: 411: 505:"The antinociceptive and anti-inflammatory action of the CHCl3-soluble phase and its main active component, damnacanthal, isolated from the root of Morinda citrifolia" 544:
Faltynek CR, Schroeder J, Mauvais P, et al. (September 1995). "Damnacanthal is a highly potent, selective inhibitor of p56lck tyrosine kinase activity".
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Anekpankul T, Goto M, Sasaki M, et al. (July 2007). "Extraction of anti-cancer damnacanthal from roots of
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Okusada K, Nakamoto K, Nishida M, Fujita-Hamabe W, Kamiya K, Mizushina Y, Satake T, Tokuyama S (2011).
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In a 1995 in vitro study, damnacanthal was found to act as a potent and selective inhibitor of p56lck
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InChI=1S/C16H10O5/c1-21-16-11(7-17)12(18)6-10-13(16)15(20)9-5-3-2-4-8(9)14(10)19/h2-7,18H,1H3
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InChI=1S/C16H10O5/c1-21-16-11(7-17)12(18)6-10-13(16)15(20)9-5-3-2-4-8(9)14(10)19/h2-7,18H,1H3
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Except where otherwise noted, data are given for materials in their
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3-Hydroxy-1-methoxy-9,10-dioxo-9,10-dihydroanthracene-2-carbaldehyde
95: 85: 579: 217: 840: 783: 406: 718: 695: 662: 614: 179: 71: 906:Antineoplastic and immunomodulating drug stubs 860: 803: 591: 8: 50:3-Hydroxy-1-methoxyanthraquinone-2-aldehyde 867: 853: 810: 796: 598: 584: 576: 288:COC1=C2C(=CC(=C1C=O)O)C(=O)C3=CC=CC=C3C2=O 232: 157: 135: 15: 520: 199: 464: 285: 253: 228: 478:Separation and Purification Technology 359:532 °C (990 °F; 805 K) 148: 260:Key: IPDMWUNUULAXLU-UHFFFAOYSA-N 115: 7: 821: 819: 757: 755: 443:, using water or organic solvents. 170: 14: 823: 759: 396: 315: 22: 392:(at 25 °C , 100 kPa). 321: 309: 1: 687:1,3,8-Trihydroxyanthraquinone 682:1,2,4-Trihydroxyanthraquinone 839:. You can help Knowledge by 782:. You can help Knowledge by 490:10.1016/j.seppur.2007.01.004 927: 891:Tyrosine kinase inhibitors 818: 754: 697:Tetrahydroxyanthraquinones 649:1,8-Dihydroxyanthraquinone 644:1,4-Dihydroxyanthraquinone 639:1,3-Dihydroxyanthraquinone 437:isolated from the root of 386: 370:Related arylformaldehydes 363: 296: 276: 244: 55: 47: 35: 30: 21: 664:Trihydroxyanthraquinones 911:Aromatic compound stubs 616:Dihydroxyanthraquinones 476:by subcritical water". 831:This article about an 886:Hydroxyanthraquinones 896:Conjugated aldehydes 37:Preferred IUPAC name 558:10.1021/bi00038a038 339: g·mol 18: 522:10.1248/bpb.34.103 474:Morinda citrifolia 440:Morinda citrifolia 419:Infobox references 364:Related compounds 16: 848: 847: 791: 790: 749: 748: 606:Types of natural 427:Chemical compound 425: 424: 213:CompTox Dashboard 97:Interactive image 918: 869: 862: 855: 827: 820: 812: 805: 798: 773:immunomodulatory 763: 756: 741:Senna glycosides 600: 593: 586: 577: 570: 569: 552:(38): 12404–10. 541: 535: 534: 524: 500: 494: 493: 469: 409: 403: 400: 399: 338: 323: 317: 311: 304:Chemical formula 237: 236: 221: 219: 203: 183: 172: 161: 150: 139: 119: 99: 75: 26: 19: 926: 925: 921: 920: 919: 917: 916: 915: 876: 875: 874: 873: 817: 816: 752: 750: 745: 714: 691: 658: 610: 604: 574: 573: 543: 542: 538: 509:Biol Pharm Bull 502: 501: 497: 471: 470: 466: 461: 453:tyrosine kinase 449: 428: 421: 416: 415: 414:  ?) 405: 401: 397: 393: 377: 371: 336: 326: 320: 314: 306: 292: 289: 284: 283: 272: 269: 268: 262: 261: 258: 252: 251: 240: 222: 215: 206: 186: 173: 142: 122: 102: 89: 78: 65: 51: 43: 42: 12: 11: 5: 924: 922: 914: 913: 908: 903: 898: 893: 888: 878: 877: 872: 871: 864: 857: 849: 846: 845: 835:compound is a 828: 815: 814: 807: 800: 792: 789: 788: 769:antineoplastic 764: 747: 746: 744: 743: 738: 737: 736: 725: 723: 716: 715: 713: 712: 707: 701: 699: 693: 692: 690: 689: 684: 679: 674: 668: 666: 660: 659: 657: 656: 651: 646: 641: 636: 631: 626: 620: 618: 612: 611: 608:anthraquinones 605: 603: 602: 595: 588: 580: 572: 571: 536: 495: 484:(3): 343–349. 463: 462: 460: 457: 448: 445: 426: 423: 422: 417: 395: 394: 390:standard state 387: 384: 383: 372: 369: 366: 365: 361: 360: 357: 351: 350: 347: 341: 340: 334: 328: 327: 324: 318: 312: 307: 302: 299: 298: 294: 293: 291: 290: 287: 279: 278: 277: 274: 273: 271: 270: 266: 265: 263: 259: 256: 255: 247: 246: 245: 242: 241: 239: 238: 230:DTXSID10197253 225: 223: 211: 208: 207: 205: 204: 196: 194: 188: 187: 185: 184: 176: 174: 166: 163: 162: 152: 144: 143: 141: 140: 132: 130: 124: 123: 121: 120: 112: 110: 104: 103: 101: 100: 92: 90: 83: 80: 79: 77: 76: 68: 66: 61: 58: 57: 53: 52: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 923: 912: 909: 907: 904: 902: 901:Phenol ethers 899: 897: 894: 892: 889: 887: 884: 883: 881: 870: 865: 863: 858: 856: 851: 850: 844: 842: 838: 834: 829: 826: 822: 813: 808: 806: 801: 799: 794: 793: 787: 785: 781: 778:article is a 777: 774: 770: 765: 762: 758: 753: 742: 739: 735: 734:Carminic acid 732: 731: 730: 729:Kermesic acid 727: 726: 724: 721: 717: 711: 708: 706: 703: 702: 700: 698: 694: 688: 685: 683: 680: 678: 675: 673: 670: 669: 667: 665: 661: 655: 652: 650: 647: 645: 642: 640: 637: 635: 632: 630: 627: 625: 622: 621: 619: 617: 613: 609: 601: 596: 594: 589: 587: 582: 581: 578: 567: 563: 559: 555: 551: 547: 540: 537: 532: 528: 523: 518: 514: 510: 506: 499: 496: 491: 487: 483: 479: 475: 468: 465: 458: 456: 454: 446: 444: 442: 441: 436: 435:anthraquinone 432: 420: 413: 408: 391: 385: 382: 381: 376: 373: 368: 367: 362: 358: 356: 355:Boiling point 353: 352: 348: 346: 343: 342: 335: 333: 330: 329: 308: 305: 301: 300: 295: 286: 282: 275: 264: 254: 250: 243: 235: 231: 227: 226: 224: 214: 210: 209: 202: 198: 197: 195: 193: 190: 189: 182: 178: 177: 175: 169: 165: 164: 160: 156: 153: 151: 149:ECHA InfoCard 146: 145: 138: 134: 133: 131: 129: 126: 125: 118: 114: 113: 111: 109: 106: 105: 98: 94: 93: 91: 87: 82: 81: 74: 70: 69: 67: 64: 60: 59: 54: 46: 38: 34: 29: 25: 20: 17:Damnacanthal 841:expanding it 830: 784:expanding it 766: 751: 719: 705:quinalizarin 634:Damnacanthal 633: 549: 546:Biochemistry 545: 539: 515:(1): 103–7. 512: 508: 498: 481: 477: 473: 467: 450: 447:Pharmacology 438: 431:Damnacanthal 430: 429: 378: 117:ChEMBL212948 56:Identifiers 48:Other names 629:Aloe emodin 349:1.461 g/mL 297:Properties 155:100.208.625 880:Categories 710:rheoemodin 459:References 332:Molar mass 201:WUC3CB63CD 128:ChemSpider 84:3D model ( 63:CAS Number 380:Pyridoxal 833:aromatic 672:Parietin 624:Alizarin 531:21212526 375:Gossypol 73:477-84-9 566:7547985 412:what is 410: ( 345:Density 337:282.251 168:PubChem 677:Emodin 564:  529:  433:is an 407:verify 404:  281:SMILES 108:ChEMBL 31:Names 767:This 654:Rhein 249:InChI 86:JSmol 837:stub 780:stub 776:drug 720:Misc 562:PMID 527:PMID 192:UNII 181:2948 137:2843 771:or 554:doi 517:doi 486:doi 218:EPA 171:CID 882:: 560:. 550:34 548:. 525:. 513:34 511:. 507:. 482:55 480:. 455:. 319:10 313:16 868:e 861:t 854:v 843:. 811:e 804:t 797:v 786:. 722:: 599:e 592:t 585:v 568:. 556:: 533:. 519:: 492:. 488:: 402:N 325:5 322:O 316:H 310:C 220:) 216:( 88:)

Index

Chemical structure of damnacanthal
Preferred IUPAC name
CAS Number
477-84-9
JSmol
Interactive image
ChEMBL
ChEMBL212948
ChemSpider
2843
ECHA InfoCard
100.208.625
Edit this at Wikidata
PubChem
2948
UNII
WUC3CB63CD
CompTox Dashboard
DTXSID10197253
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Density
Boiling point
Gossypol
Pyridoxal
standard state
verify

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