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1351:* ] is a pigment responsible for bract color in '']'' (the Siam tulip).<ref>{{Cite journal|pmid=10879491|year=2000|last1=Nakayama|first1=M|last2=Roh|first2=MS|last3=Uchida|first3=K|last4=Yamaguchi|first4=Y|last5=Takano|first5=K|last6=Koshioka|first6=M|title=Malvidin 3-rutinoside as the pigment responsible for bract color in Curcuma alismatifolia|volume=64|issue=5|pages=1093–5|journal=Bioscience, Biotechnology, and Biochemistry|doi=10.1271/bbb.64.1093|doi-access=free}}</ref> ]s are responsible for the violet color of '']''.<ref>{{Cite journal|doi=10.1016/S0031-9422(99)00095-3|title=Acylated malvidin 3-rutinosides in dusky violet flowers of Petunia integrifolia subsp. Inflata|year=1999|last1=Tatsuzawa|first1=F|journal=Phytochemistry|volume=52|issue=2|pages=351–355}}</ref> 1204:
such as blueberries ('']'') or the saskatoon berries ('']'').<ref name=mazza05>{{cite journal | last1 = Mazza | first1 = G |name-list-style=vanc | year = 2005 | title = Compositional and functional properties of saskatoon berry and blueberry | journal = International Journal of Fruit Science| volume = 5 | issue = 3| pages = 99–118 | doi = 10.1300/J492v05n03_10 | doi-access = free }}</ref><ref>{{cite journal |pmid=18066116 |year=2007 |author1=Bakowska-barczak |first2=M |first3=P |title=Survey of bioactive components in Western Canadian berries |volume=85 |issue=11 |pages=1139–52 |doi=10.1139/y07-102 |journal=Canadian Journal of Physiology and Pharmacology |last2=Marianchuk |last3=Kolodziejczyk}}</ref>
1362:* ] is a pigment responsible for the blue color in 'Johnson's Blue' and other 'blue' ]s<ref>{{Cite journal|doi=10.1016/S0031-9422(96)00831-X|title=Malvidin-3-O-glucoside-5-O-(6-acetylglucoside) and its colour manifestation in 'Johnson's Blue' and other 'Blue' geraniums|year=1997|last1=Markham|first1=Kenneth R.|last2=Mitchell|first2=Kevin A.|last3=Boase|first3=Murray R.|journal=Phytochemistry|volume=45|issue=2|pages=417–423}}</ref> 1203:
It is responsible primarily for the color of red wine, '']'' being one of its sources.<ref>{{cite web|url=http://www.phytochemicals.info/phytochemicals/malvidin.php|title=Phytochemicals: Malvidin|publisher=Top Cultures|accessdate=2009-05-20}}</ref> It is also present in other berries,
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The breakdown of malvidin releases ] as revealed in the examination of jars containing ], a drink of Ancient Egypt. Malvidin is also present in the site of the ], a 6,100-year-old winery discovered in 2007 in the Areni-1 cave complex in the village of Areni in the Vayots Dzor province of
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Malvidin is responsible for the blue color found in petals of the '']'' plants of the ''polyanthus'' group. Blue flowers of the blue pimpernel ('']'') have also a higher concentration of malvidin.
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Slightly ] and ] solutions of malvidin are characteristically of a red color, while ] solutions of malvidin yield a blue color.
16: 1152:'''Malvidin''' is an ], the 3',5'-methoxy derivative of ]. As a primary ], its ]s are highly abundant in nature. 166: 173: 477:| SystematicName=3,5,7-Trihydroxy-2-(4-hydroxy-3,5-dimethoxy)-1λ<sup>4</sup>-benzopyran-1-ylium 228: 79: 206: 155: 50: 784: 719: 210: 177: 389: 370: 349: 319: 217: 36: 93: 8: 857:| Formula=C<sub>17</sub>H<sub>15</sub>O<sub>7</sub>+ 162: 850:
Formula=C<sub>17</sub>H<sub>15</sub>O<sub>7</sub>+
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Saving copy of the {{chembox}} taken from revid 464319253 of page
104: 103: 531:| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} 524:
ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
636:| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} 629:| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} 126: 752:| SMILES = O(c1cc(cc(OC)c1O)c3c2cc(O)cc(O)c2cc3O)C 803:| SMILES = Oc1cc2c(O)cc(O)cc2c1c3cc(OC)c(O)c(OC)c3 248: 652:| StdInChIKey = KZMACGJDUUWFCH-UHFFFAOYSA-O 645:| StdInChIKey = KZMACGJDUUWFCH-UHFFFAOYSA-O 207:Latest revision as of 20:36, 13 August 2023 580:| ChEMBL2_Ref = {{ebicite|correct|EBI}} 10: 790: 765:| KEGG_Ref = {{keggcite|correct|kegg}} 725: 612:| ChEMBL_Ref = {{ebicite|correct|EBI}} 605:| ChEMBL_Ref = {{ebicite|correct|EBI}} 1255:The breakdown of malvidin releases ]. 558:| ChEBI_Ref = {{ebicite|changed|EBI}} 395: 376: 355: 325: 145:Revision as of 10:59, 6 December 2011 69: 26: 1275:== Use as a marker in archaeology == 713:| UNII_Ref = {{fdacite|correct|FDA}} 255:: doi added to citation with #oabot. 135: 118: 247: 216: 204: 189: 154: 142: 14: 107: 1486: 87: 73: 44: 30: 1329:* ] is the malvidin-3-glucoside. 672:| CASNo_Ref = {{cascite|correct| 661:| CASNo_Ref = {{cascite|correct| 512:|Section1={{Chembox Identifiers 197:Chem/Drugbox validation project 838:|Section2={{Chembox Properties 9: 1: 1471: 1462: 1451: 1442: 1431: 1420: 1411: 1400: 1389: 1378: 1369: 1358: 1347: 1340:* ] is the 3-O-] of malvidin. 1336: 1325: 1314: 1303: 1294: 1282: 1271: 1262: 1251: 1242: 1231: 1220: 1211: 1199: 1190: 1179: 1168: 1159: 1148: 1139: 1094: 1085: 1074: 1064: 1055: 1045: 1036: 1026: 999: 986: 975: 962: 951: 938: 927: 914: 903: 892: 883: 872: 862: 853: 843: 834: 824: 799: 772: 761: 748: 739: 709: 698: 681: 668: 657: 576: 565: 554: 527: 517: 508: 498: 473: 443: 421: 339: 309: 280: 271: 199:(updated: 'CASNo'). 876:| MolarMass = 331.2968 g/mol 690:<!-- blanked - oldvalue: 7: 1040:|Section3={{Chembox Hazards 1491: 869:MolarMass = 331.2968 g/mol 439:dimethoxyphenyl)chromenium 313:| Verifiedfields = changed 11:(Difference between pages) 1469: 1460: 1449: 1440: 1429: 1418: 1409: 1398: 1387: 1376: 1367: 1356: 1345: 1334: 1323: 1312: 1301: 1292: 1280: 1269: 1260: 1249: 1240: 1229: 1218: 1209: 1197: 1188: 1177: 1172:== Natural occurrences == 1166: 1157: 1146: 1137: 1101: 1083: 1006: 899: 896:| ExactMass = 331.081778 881: 797: 781: 770: 759: 755: 737: 733: 707: 620: 617: 574: 563: 552: 471: 386: 367: 363: 343:| Watchedfields = changed 337: 333: 307: 287: 275:{{distinguish|Malvidine}} 269: 264: 261: 203: 141: 547:| ChemSpiderID = 140095 540:| ChemSpiderID = 140095 140: 1318:* ] is a malvidin di]. 505:{{Chembox Identifiers 397:| ImageFile=malvidin. 357:| ImageFile=malvidin. 831:{{Chembox Properties 174:Edit filter managers 101: 58: 743:| UNII = GL5KGZ4D8U 61: 18: 1089:| AutoignitionPt = 596:| ChEMBL2 = 592005 589:| ChEMBL2 = 592005 465:dimethoxyflavylium 425:| IUPACName=3,5,7- 378:| verifiedrevid = 327:| verifiedrevid = 214: 152: 66: 23: 1479: 1033:{{Chembox Hazards 416:| ImageSize=250px 409:| ImageSize=250px 205: 143: 89: 75: 62: 46: 32: 19: 1482: 1455:{{Anthocyanins}} 1424:== References == 1307:== Glycosides == 1098:| Autoignition= 792:| PubChem=159287 702:| CASNo=643-84-5 256: 250: 242: 232: 213: 200: 184: 170: 151: 132: 131: 129: 124: 122: 114: 111: 105: 90: 76: 65: 47: 33: 22: 1490: 1489: 1485: 1484: 1483: 1481: 1480: 1476: 1465: 1456: 1445: 1436: 1425: 1414: 1405: 1394: 1383: 1372: 1363: 1352: 1341: 1330: 1319: 1308: 1297: 1288: 1276: 1265: 1256: 1245: 1236: 1225: 1224:== Chemistry == 1214: 1205: 1193: 1184: 1173: 1162: 1153: 1142: 1133: 1126: 1117: 1110: 1099: 1090: 1079: 1072: 1070: 1060: 1053: 1051: 1041: 1034: 1032: 1022: 1015: 1004: 995: 993: 984: 982: 971: 969: 960: 958: 947: 945: 936: 934: 923: 921: 912: 910: 897: 888: 877: 870: 868: 858: 851: 849: 839: 832: 830: 820: 813: 804: 793: 777: 776:| KEGG = C08716 766: 753: 744: 731: 729: 714: 703: 696: 695: 691: 687: 677: 675: 666: 664: 653: 646: 637: 630: 613: 606: 597: 590: 581: 570: 559: 548: 541: 532: 525: 523: 513: 506: 504: 494: 487: 478: 467: 466: 462: 458: 454: 450: 441: 440: 436: 432: 431:2-(4-hydroxy- 3 428: 417: 410: 401: 400: 382: 381: 361: 360: 344: 331: 330: 314: 303: 296: 285: 276: 257: 253:Open access bot 251: 246: 245: 244: 240: 238: 222: 220: 215: 209: 201: 190: 188: 187: 186: 182: 180: 160: 158: 153: 147: 139: 138: 137: 136: 134: 133: 127: 125: 120: 117: 115: 112: 110:Content deleted 109: 106: 102: 100: 99: 98: 97: 96: 95: 94: 86: 83: 82: 81: 80: 72: 63: 59: 57: 56: 55: 54: 53: 52: 51: 43: 40: 39: 38: 37: 29: 20: 13: 12: 5: 1488: 1478: 1477: 1474: 1472: 1470: 1467: 1466: 1463: 1461: 1458: 1457: 1454: 1452: 1450: 1447: 1446: 1443: 1441: 1438: 1437: 1434: 1432: 1430: 1427: 1426: 1423: 1421: 1419: 1416: 1415: 1412: 1410: 1407: 1406: 1403: 1401: 1399: 1396: 1395: 1392: 1390: 1388: 1385: 1384: 1382:== See also == 1381: 1379: 1377: 1374: 1373: 1370: 1368: 1365: 1364: 1361: 1359: 1357: 1354: 1353: 1350: 1348: 1346: 1343: 1342: 1339: 1337: 1335: 1332: 1331: 1328: 1326: 1324: 1321: 1320: 1317: 1315: 1313: 1310: 1309: 1306: 1304: 1302: 1299: 1298: 1295: 1293: 1290: 1289: 1285: 1283: 1281: 1278: 1277: 1274: 1272: 1270: 1267: 1266: 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865: 863: 860: 859: 856: 854: 852: 848: 846: 844: 841: 840: 837: 835: 833: 829: 827: 825: 822: 821: 818: 816: 814: 811: 809: 806: 805: 802: 800: 798: 795: 794: 789: 787: 782: 779: 778: 775: 773: 771: 768: 767: 764: 762: 760: 757: 756: 754: 751: 749: 746: 745: 742: 740: 738: 735: 734: 732: 730:PubChem=159287 728: 724: 722: 716: 715: 712: 710: 708: 705: 704: 701: 699: 697: 693: 689: 686: 684: 682: 679: 678: 673: 671: 669: 667: 662: 660: 658: 655: 654: 651: 649: 647: 644: 642: 639: 638: 635: 633: 631: 628: 626: 623: 622: 619: 615: 614: 611: 609: 607: 604: 602: 599: 598: 595: 593: 591: 588: 586: 583: 582: 579: 577: 575: 572: 571: 569:| ChEBI = 6674 568: 566: 564: 561: 560: 557: 555: 553: 550: 549: 546: 544: 542: 539: 537: 534: 533: 530: 528: 526: 522: 520: 518: 515: 514: 511: 509: 507: 503: 501: 499: 496: 495: 492: 490: 488: 485: 483: 480: 479: 476: 474: 472: 469: 468: 464: 460: 456: 452: 448: 446: 444: 442: 438: 434: 430: 426: 424: 422: 419: 418: 415: 413: 411: 408: 406: 403: 402: 398: 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977: 974: 964: 953: 950: 940: 929: 926: 916: 905: 902: 894: 891: 887:| Appearance= 885: 880: 874: 864: 861: 855: 845: 842: 836: 826: 823: 817: 815: 810: 808: 807: 801: 796: 791: 788: 786: 783: 780: 774: 769: 763: 758: 750: 747: 741: 736: 726: 723: 721: 718: 717: 711: 706: 700: 683: 680: 670: 659: 656: 650: 648: 643: 641: 640: 634: 632: 627: 625: 624: 616: 610: 608: 603: 601: 600: 594: 592: 587: 585: 584: 578: 573: 567: 562: 556: 551: 545: 543: 538: 536: 535: 529: 519: 516: 510: 500: 497: 493:| OtherNames= 491: 489: 486:| OtherNames= 484: 482: 481: 475: 470: 447:| IUPACName=3 445: 423: 420: 414: 412: 407: 405: 404: 396: 393: 391: 388: 385: 377: 374: 372: 369: 366: 356: 353: 351: 348: 347: 341: 336: 326: 323: 321: 318: 317: 311: 306: 300: 298: 293: 291: 290: 282: 279: 273: 268: 260: 254: 237: 230: 226: 221: 212: 208: 198: 194: 179: 175: 168: 164: 159: 150: 146: 130: 123: 113:Content added 1052:MainHazards= 453:Tetrahydroxy 1435:{{Reflist}} 1078:| FlashPt= 1030:|Section3= 992:Solubility 909:Appearance 828:|Section2= 502:|Section1= 427:trihydroxy 88:Revision 2 45:Revision 1 981:BoilingPt 968:BoilingPt 957:MeltingPt 944:MeltingPt 380:464371038 329:440126448 302:{{chembox 295:{{chembox 1071:FlashPt= 785:⚫ 720:⚫ 692:643-84-5 621:Line 24: 618:Line 18: 390:⚫ 371:⚫ 350:⚫ 320:⚫ 229:contribs 195:for the 193:Malvidin 167:contribs 157:Beetstra 128:Wikitext 933:Density 920:Density 685:| CASNo 265:Line 1: 262:Line 1: 241:431,569 183:171,922 694:--> 121:Visual 74:Page 2 64:Page 2 31:Page 1 21:Page 1 451:,5,7- 243:edits 219:OAbot 185:edits 236:Bots 225:talk 211:edit 163:talk 149:edit 1404:* ] 1393:* ] 674:CAS 449:,4′ 399:svg 359:png 1287:]. 1132:}} 1125:}} 1116:}} 1109:}} 1021:}} 1014:}} 990:| 979:| 966:| 955:| 942:| 931:| 918:| 907:| 819:}} 812:}} 676:}} 665:}} 663:?? 461:5′ 457:3′ 227:| 176:, 165:| 1475:] 1068:| 1049:| 994:= 983:= 970:= 959:= 946:= 935:= 922:= 911:= 866:| 847:| 727:| 688:= 521:| 463:- 459:, 455:- 437:- 435:5 433:, 429:- 249:m 231:) 223:( 169:) 161:(

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