Knowledge (XXG)

Aspalathin

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Bader, Michael; Mazibuko-Mbeje, Sithandiwe E.; Dludla, Phiwayinkosi V.; Johnson, Rabia; Joubert, Elizabeth; Louw, Johan; Ziqubu, Khanyisani; Tiano, Luca; Silvestri, Sonia; Orlando, Patrick; Opoku, Andy R.; Muller, Christo J. F. (2019).
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InChI=1S/C21H24O11/c22-7-14-17(28)19(30)20(31)21(32-14)16-13(27)6-12(26)15(18(16)29)10(24)4-2-8-1-3-9(23)11(25)5-8/h1,3,5-6,14,17,19-23,25-31H,2,4,7H2/t14-,17-,19+,20-,21+/m1/s1
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InChI=1/C21H24O11/c22-7-14-17(28)19(30)20(31)21(32-14)16-13(27)6-12(26)15(18(16)29)10(24)4-2-8-1-3-9(23)11(25)5-8/h1,3,5-6,14,17,19-23,25-31H,2,4,7H2/t14-,17-,19+,20-,21+/m1/s1
265: 634: 533:"Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration" 793: 812: 666: 230: 822: 627: 721: 360: 786: 194: 817: 620: 716: 156: 779: 691: 606: 46: 36: 676: 544: 434:
Bramati L; et al. (2002). "Quantitative Characterization of Flavonoid Compounds in Rooibos Tea (
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Except where otherwise noted, data are given for materials in their
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3-(3,4-Dihydroxyphenyl)-1-{2,4-dihydroxy-5-phenyl}propan-1-one
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O=C(c1c(O)c(c(O)cc1O)2O((O)(O)2O)CO)CCc3ccc(O)c(O)c3
700: 651: 475:"C-Glycosylflavonoids. The chemistry of aspalathin" 667:3′,5′-Dihydroxy-2′,4′,6′-trimethoxydihydrochalcone 181: 390:, a herbal tea prepared from the South African 73: 787: 628: 8: 794: 780: 635: 621: 613: 440:Journal of Agricultural and Food Chemistry 214: 159: 137: 15: 574: 556: 506: 473:Koeppen, B. H.; Roux, D. G. (June 1966). 426: 270: 235: 210: 150: 40:3-(3,4-Dihydroxyphenyl)-1-propan-1-one 242:Key: VCPUQYKWJRESOC-VJXVFPJBSA-N 117: 7: 748: 746: 252:Key: VCPUQYKWJRESOC-VJXVFPJBBW 172: 766:. You can help Knowledge (XXG) by 14: 407:It was first isolated in 1965 by 750: 600: 338: 300: 22: 334:(at 25 °C , 100 kPa). 306: 294: 1: 722:Neohesperidin dihydrochalcone 558:10.1371/journal.pone.0216172 643:Dihydrochalcones and their 446:(20). Elsevier: 5513–5519. 839: 813:Dihydrochalcone glycosides 745: 328: 281: 261: 226: 57: 45: 35: 30: 21: 717:Naringin dihydrochalcone 823:Aromatic compound stubs 758:This article about an 47:Systematic IUPAC name 692:Pinocembrin chalcone 609:at Wikimedia Commons 414:It has demonstrated 549:2019PLoSO..1416172M 479:Biochemical Journal 436:Aspalathus linearis 397:Aspalathus linearis 324: g·mol 18: 361:Infobox references 16: 818:Phenol glucosides 775: 774: 740: 739: 662:Dihydrokanakugiol 605:Media related to 491:10.1042/bj0990604 452:10.1021/jf025697h 438:) by LC-UV/DAD". 369:Chemical compound 367: 366: 195:CompTox Dashboard 99:Interactive image 830: 796: 789: 782: 754: 747: 701:Dihydrochalcone 677:Methyl linderone 653:Dihydrochalcones 637: 630: 623: 614: 604: 589: 588: 578: 560: 527: 521: 520: 510: 470: 464: 463: 431: 351: 345: 342: 341: 323: 308: 302: 296: 289:Chemical formula 219: 218: 203: 201: 185: 174: 163: 152: 141: 121: 101: 77: 26: 19: 838: 837: 833: 832: 831: 829: 828: 827: 803: 802: 801: 800: 743: 741: 736: 696: 647: 641: 597: 592: 543:(5): e0216172. 529: 528: 524: 472: 471: 467: 433: 432: 428: 424: 381:dihydrochalcone 370: 363: 358: 357: 356:  ?) 347: 343: 339: 335: 321: 311: 305: 299: 291: 277: 274: 269: 268: 257: 254: 253: 250: 244: 243: 240: 234: 233: 222: 204: 197: 188: 175: 144: 124: 104: 91: 80: 67: 53: 52: 41: 12: 11: 5: 836: 834: 826: 825: 820: 815: 805: 804: 799: 798: 791: 784: 776: 773: 772: 762:compound is a 755: 738: 737: 735: 734: 729: 724: 719: 714: 708: 706: 698: 697: 695: 694: 689: 684: 679: 674: 669: 664: 658: 656: 649: 648: 642: 640: 639: 632: 625: 617: 611: 610: 596: 595:External links 593: 591: 590: 522: 485:(3): 604–609. 465: 425: 423: 420: 409:chromatography 368: 365: 364: 359: 337: 336: 332:standard state 329: 326: 325: 319: 313: 312: 309: 303: 297: 292: 287: 284: 283: 279: 278: 276: 275: 272: 264: 263: 262: 259: 258: 256: 255: 251: 248: 247: 245: 241: 238: 237: 229: 228: 227: 224: 223: 221: 220: 212:DTXSID90726949 207: 205: 193: 190: 189: 187: 186: 178: 176: 168: 165: 164: 154: 146: 145: 143: 142: 134: 132: 126: 125: 123: 122: 114: 112: 106: 105: 103: 102: 94: 92: 85: 82: 81: 79: 78: 70: 68: 63: 60: 59: 55: 54: 50: 49: 43: 42: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 835: 824: 821: 819: 816: 814: 811: 810: 808: 797: 792: 790: 785: 783: 778: 777: 771: 769: 765: 761: 756: 753: 749: 744: 733: 730: 728: 725: 723: 720: 718: 715: 713: 710: 709: 707: 704: 699: 693: 690: 688: 685: 683: 680: 678: 675: 673: 670: 668: 665: 663: 660: 659: 657: 654: 650: 646: 638: 633: 631: 626: 624: 619: 618: 615: 608: 603: 599: 598: 594: 586: 582: 577: 572: 568: 564: 559: 554: 550: 546: 542: 538: 534: 526: 523: 518: 514: 509: 504: 500: 496: 492: 488: 484: 480: 476: 469: 466: 461: 457: 453: 449: 445: 441: 437: 430: 427: 421: 419: 417: 412: 410: 405: 403: 399: 398: 393: 392:rooibos plant 389: 385: 382: 378: 374: 362: 355: 350: 333: 327: 320: 318: 315: 314: 293: 290: 286: 285: 280: 271: 267: 260: 246: 236: 232: 225: 217: 213: 209: 208: 206: 196: 192: 191: 184: 180: 179: 177: 171: 167: 166: 162: 158: 155: 153: 151:ECHA InfoCard 148: 147: 140: 136: 135: 133: 131: 128: 127: 120: 116: 115: 113: 111: 108: 107: 100: 96: 95: 93: 89: 84: 83: 76: 72: 71: 69: 66: 62: 61: 56: 48: 44: 38: 34: 29: 25: 20: 768:expanding it 757: 742: 711: 540: 536: 525: 482: 478: 468: 443: 439: 435: 429: 416:antidiabetic 413: 406: 395: 372: 371: 58:Identifiers 388:rooibos tea 282:Properties 157:100.233.299 119:CHEBI:79078 17:Aspalathin 807:Categories 727:Nothofagin 712:Aspalathin 703:glycosides 682:Pedicellin 672:Kanakugiol 645:glycosides 607:Aspalathin 422:References 418:activity. 373:Aspalathin 317:Molar mass 130:ChemSpider 86:3D model ( 65:CAS Number 37:IUPAC name 732:Phlorizin 687:Phloretin 567:1932-6203 499:0264-6021 386:found in 384:glucoside 75:6027-43-6 760:aromatic 585:31048842 537:PLOS ONE 460:12236672 402:Fabaceae 379:-linked 183:11282394 576:6497260 545:Bibcode 517:4290475 508:1265048 354:what is 352: ( 322:452.412 170:PubChem 139:9457391 583:  573:  565:  515:  505:  497:  458:  349:verify 346:  266:SMILES 31:Names 375:is a 231:InChI 110:ChEBI 88:JSmol 764:stub 581:PMID 563:ISSN 513:PMID 495:ISSN 456:PMID 571:PMC 553:doi 503:PMC 487:doi 448:doi 404:). 200:EPA 173:CID 809:: 579:. 569:. 561:. 551:. 541:14 539:. 535:. 511:. 501:. 493:. 483:99 481:. 477:. 454:. 444:50 442:. 411:. 394:, 310:11 304:24 298:21 795:e 788:t 781:v 770:. 705:: 655:: 636:e 629:t 622:v 587:. 555:: 547:: 519:. 489:: 462:. 450:: 400:( 377:C 344:N 307:O 301:H 295:C 202:) 198:( 90:)

Index


IUPAC name
Systematic IUPAC name
CAS Number
6027-43-6
JSmol
Interactive image
ChEBI
CHEBI:79078
ChemSpider
9457391
ECHA InfoCard
100.233.299
Edit this at Wikidata
PubChem
11282394
CompTox Dashboard
DTXSID90726949
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
verify
what is
Infobox references
C
dihydrochalcone
glucoside

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