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Stictic acid

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Wassman, Christopher D.; Baronio, Roberta; Demir, Ă–zlem; Wallentine, Brad D.; Chen, Chiung-Kuang; Hall, Linda V.; Salehi, Faezeh; Lin, Da-Wei; Chung, Benjamin P.; Wesley Hatfield, G.; Richard Chamberlin, A.; Luecke, Hartmut; Lathrop, Richard H.; Kaiser, Peter; Amaro, Rommie E. (2013).
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Lohézic-Le Dévéhat, Françoise; Tomasi, Sophie; Elix, John A.; Bernard, Aurélie; Rouaud, Isabelle; Uriac, Philippe; Boustie, Joël (2007). "Stictic Acid Derivatives from the Lichen
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InChI=1S/C19H14O9/c1-6-4-9(25-3)8(5-20)15-10(6)17(22)27-14-7(2)13(21)11-12(16(14)26-15)19(24)28-18(11)23/h4-5,19,21,24H,1-3H3
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Stictic acid is the subject of preliminary biomedical research. Stictic acid has
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Correché, ER; Enriz, RD; Piovano, M; Garbarino, J; Gómez-Lechón, MJ (2004).
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Except where otherwise noted, data are given for materials in their
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O=C1OC(O)C2=C3C(OC(C(C(C)=CC(OC)=C4C=O)=C4O3)=O)=C(C)C(O)=C21
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1,4-Dihydroxy-10-methoxy-5,8-dimethyl-3,7-dioxo-1,3-dihydro-7
182: 358: 54:-2,6,12-trioxabenzocycloheptaindene-11-carbaldehyde 643: 164: 76: 626: 569: 633: 619: 576: 562: 197: 142: 120: 500: 434: 193: 644: 133: 225:Key: SKCUFZLDTAYNBZ-UHFFFAOYSA-N 585: 524: 382:and Their Antioxidant Activities". 155: 13: 423:Alternatives to Laboratory Animals 14: 693: 589: 528: 273: 31: 22: 307:(at 25 Â°C , 100 kPa). 459: 410: 371: 279: 267: 1: 364: 605:. You can help Knowledge by 548:. You can help Knowledge by 7: 384:Journal of Natural Products 10: 698: 584: 523: 436:10.1177/026119290403200611 301: 254: 234: 209: 60: 44: 39: 30: 21: 682:Aromatic compound stubs 597:This article about an 473:Nature Communications 46:Systematic IUPAC name 334:secondary metabolism 662:Oxygen heterocycles 536:This article about 485:2013NatCo...4.1407W 336:in some species of 297: g·mol 18: 493:10.1038/ncomms2361 311:Infobox references 16: 614: 613: 557: 556: 396:10.1021/np070145k 319:Chemical compound 317: 316: 178:CompTox Dashboard 102:Interactive image 689: 635: 628: 621: 593: 586: 578: 571: 564: 532: 525: 515: 514: 504: 463: 457: 456: 438: 414: 408: 407: 380:Usnea articulata 375: 330:organic compound 296: 281: 275: 269: 262:Chemical formula 202: 201: 186: 184: 168: 157: 146: 135: 124: 104: 80: 35: 26: 19: 15: 697: 696: 692: 691: 690: 688: 687: 686: 672:Lichen products 642: 641: 640: 639: 583: 582: 521: 519: 518: 464: 460: 415: 411: 376: 372: 367: 332:, a product of 320: 313: 308: 294: 284: 278: 272: 264: 250: 247: 242: 241: 230: 227: 226: 223: 217: 216: 205: 187: 180: 171: 158: 127: 107: 94: 83: 70: 56: 55: 12: 11: 5: 695: 685: 684: 679: 677:Mycology stubs 674: 669: 664: 659: 654: 652:Phenolic acids 638: 637: 630: 623: 615: 612: 611: 601:compound is a 594: 581: 580: 573: 566: 558: 555: 554: 533: 517: 516: 458: 409: 390:(7): 1218–20. 369: 368: 366: 363: 361:reactivation. 318: 315: 314: 309: 305:standard state 302: 299: 298: 292: 286: 285: 282: 276: 270: 265: 260: 257: 256: 252: 251: 249: 248: 245: 237: 236: 235: 232: 231: 229: 228: 224: 221: 220: 212: 211: 210: 207: 206: 204: 203: 195:DTXSID20972053 190: 188: 176: 173: 172: 170: 169: 161: 159: 151: 148: 147: 137: 129: 128: 126: 125: 117: 115: 109: 108: 106: 105: 97: 95: 88: 85: 84: 82: 81: 73: 71: 66: 63: 62: 58: 57: 49: 48: 42: 41: 37: 36: 28: 27: 9: 6: 4: 3: 2: 694: 683: 680: 678: 675: 673: 670: 668: 665: 663: 660: 658: 657:Phenol ethers 655: 653: 650: 649: 647: 636: 631: 629: 624: 622: 617: 616: 610: 608: 604: 600: 595: 592: 588: 587: 579: 574: 572: 567: 565: 560: 559: 553: 551: 547: 543: 539: 534: 531: 527: 526: 522: 512: 508: 503: 498: 494: 490: 486: 482: 478: 474: 470: 462: 454: 450: 446: 442: 437: 432: 429:(6): 605–15. 428: 424: 420: 413: 405: 401: 397: 393: 389: 385: 381: 374: 370: 362: 360: 356: 355: 350: 346: 341: 339: 335: 331: 328: 324: 312: 306: 300: 293: 291: 288: 287: 266: 263: 259: 258: 253: 244: 243: 240: 233: 219: 218: 215: 208: 200: 196: 192: 191: 189: 179: 175: 174: 167: 163: 162: 160: 154: 150: 149: 145: 141: 138: 136: 134:ECHA InfoCard 131: 130: 123: 119: 118: 116: 114: 111: 110: 103: 99: 98: 96: 92: 87: 86: 79: 75: 74: 72: 69: 65: 64: 59: 53: 47: 43: 38: 34: 29: 25: 20: 17:Stictic acid 607:expanding it 596: 550:expanding it 535: 520: 476: 472: 461: 426: 422: 412: 387: 383: 379: 373: 352: 342: 323:Stictic acid 322: 321: 61:Identifiers 51: 542:lichenology 255:Properties 140:100.161.455 646:Categories 365:References 290:Molar mass 113:ChemSpider 89:3D model ( 68:CAS Number 349:apoptotic 345:cytotoxic 667:Lactones 599:aromatic 511:23360998 479:: 1407. 453:31487885 445:15757498 404:17629329 354:in vitro 351:effects 327:aromatic 78:549-06-4 538:lichens 502:3562459 481:Bibcode 338:lichens 295:386.312 153:PubChem 509:  499:  451:  443:  402:  325:is an 239:SMILES 40:Names 544:is a 449:S2CID 214:InChI 166:73677 122:66327 91:JSmol 603:stub 546:stub 507:PMID 441:PMID 400:PMID 347:and 540:or 497:PMC 489:doi 431:doi 392:doi 359:p53 183:EPA 156:CID 648:: 505:. 495:. 487:. 475:. 471:. 447:. 439:. 427:32 425:. 421:. 398:. 388:70 386:. 340:. 277:14 271:19 634:e 627:t 620:v 609:. 577:e 570:t 563:v 552:. 513:. 491:: 483:: 477:4 455:. 433:: 406:. 394:: 283:9 280:O 274:H 268:C 185:) 181:( 93:) 52:H

Index



Systematic IUPAC name
CAS Number
549-06-4
JSmol
Interactive image
ChemSpider
66327
ECHA InfoCard
100.161.455
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PubChem
73677
CompTox Dashboard
DTXSID20972053
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
aromatic
organic compound
secondary metabolism
lichens
cytotoxic
apoptotic
in vitro

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