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Rutinose

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278: 185: 556: 24: 409: 122: 422: 597: 327: 511:"Synthesis of Some Disaccharides Containing an L-Rhamnopyranosyl or L-Mannopyranosyl Residue, and the Substrate-specificity of α-L-Rhamnosidase from 590: 301:
InChI=1S/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12+/m0/s1
311:
InChI=1/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12+/m0/s1
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Except where otherwise noted, data are given for materials in their
23: 488: 133: 121: 111: 261: 571: 417: 509:
Kamiya, Shintaro; Sachiko Esaki; Reiko Tanaka (1985).
223: 274:DTXSID401226338 DTXSID70896972, DTXSID401226338 97: 76:6-O-(6-Deoxy-alpha-L-mannopyranosyl)-D-glucose 591: 8: 598: 584: 276: 183: 161: 74:6-O-(α-L-Rhamnopyranosyl)-D-glucopyranose, 15: 530: 243: 332: 297: 272: 174: 519:Agricultural and Biological Chemistry 304:Key: OVVGHDNPYGTYIT-BNXXONSGSA-N 141: 7: 552: 550: 314:Key: OVVGHDNPYGTYIT-BNXXONSGBT 214: 63:)-6-oxymethyl]oxane-2,3,4,5-tetrol 14: 554: 407: 362: 22: 403:(at 25 °C , 100 kPa). 368: 356: 335:O(C1O(O)(O)(O)1O)2O((O)(O)2O)C 72:6-O-(α-L-Rhamnosyl)-D-glucose, 1: 570:. You can help Knowledge by 383:326.297 g/mol 643: 549: 480:) that is present in some 397: 343: 323: 288: 81: 69: 53: 44:-Rhamnopyranosyl-(1→6)-β- 35: 30: 21: 627:Organic compound stubs 562:This article about an 487:. It is prepared from 532:10.1271/bbb1961.49.55 55:Systematic IUPAC name 18: 430:Infobox references 16: 579: 578: 513:Aspergillus niger 463: 455: 438:Chemical compound 436: 435: 257:CompTox Dashboard 123:Interactive image 47: 43: 634: 600: 593: 586: 564:organic compound 558: 551: 543: 541: 539: 534: 495:with the enzyme 461: 453: 448:also known as 6- 420: 414: 411: 410: 370: 364: 358: 351:Chemical formula 281: 280: 265: 263: 247: 227: 216: 195: 187: 176: 165: 145: 125: 101: 45: 41: 26: 19: 642: 641: 637: 636: 635: 633: 632: 631: 607: 606: 605: 604: 547: 537: 535: 508: 505: 479: 475: 471: 439: 432: 427: 426: 425:  ?) 416: 412: 408: 404: 373: 367: 361: 353: 339: 336: 331: 330: 319: 316: 315: 312: 306: 305: 302: 296: 295: 284: 266: 259: 250: 230: 217: 205: 168: 148: 128: 115: 104: 91: 77: 75: 73: 65: 64: 49: 12: 11: 5: 640: 638: 630: 629: 624: 619: 609: 608: 603: 602: 595: 588: 580: 577: 576: 559: 545: 544: 504: 501: 497:rhamnodiastase 477: 473: 469: 437: 434: 433: 428: 406: 405: 401:standard state 398: 395: 394: 391: 385: 384: 381: 375: 374: 371: 365: 359: 354: 349: 346: 345: 341: 340: 338: 337: 334: 326: 325: 324: 321: 320: 318: 317: 313: 310: 309: 307: 303: 300: 299: 291: 290: 289: 286: 285: 283: 282: 269: 267: 255: 252: 251: 249: 248: 240: 238: 232: 231: 229: 228: 220: 218: 210: 207: 206: 204: 203: 199: 197: 189: 188: 178: 170: 169: 167: 166: 158: 156: 150: 149: 147: 146: 138: 136: 130: 129: 127: 126: 118: 116: 109: 106: 105: 103: 102: 94: 92: 87: 84: 83: 79: 78: 71: 67: 66: 58: 57: 51: 50: 48:-glucopyranose 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 639: 628: 625: 623: 620: 618: 617:Disaccharides 615: 614: 612: 601: 596: 594: 589: 587: 582: 581: 575: 573: 569: 565: 560: 557: 553: 548: 533: 528: 524: 520: 516: 514: 507: 506: 502: 500: 498: 494: 490: 486: 483: 467: 459: 451: 447: 443: 431: 424: 419: 402: 396: 392: 390: 387: 386: 382: 380: 377: 376: 355: 352: 348: 347: 342: 333: 329: 322: 308: 298: 294: 287: 279: 275: 271: 270: 268: 258: 254: 253: 246: 242: 241: 239: 237: 234: 233: 226: 222: 221: 219: 213: 209: 208: 201: 200: 198: 196: 191: 190: 186: 182: 179: 177: 175:ECHA InfoCard 172: 171: 164: 160: 159: 157: 155: 152: 151: 144: 140: 139: 137: 135: 132: 131: 124: 120: 119: 117: 113: 108: 107: 100: 96: 95: 93: 90: 86: 85: 80: 68: 62: 56: 52: 38: 34: 29: 25: 20: 622:Deoxy sugars 572:expanding it 561: 546: 536:. Retrieved 525:(1): 55–62. 522: 518: 512: 449: 446:disaccharide 441: 440: 82:Identifiers 70:Other names 60: 393:1.662 g/mL 344:Properties 181:100.001.832 143:CHEBI:27522 61:2R,3S,4S,5S 611:Categories 503:References 493:hydrolysis 485:glycosides 379:Molar mass 245:0C4U3505G3 154:ChemSpider 110:3D model ( 89:CAS Number 37:IUPAC name 482:flavonoid 458:rhamnosyl 202:202-014-4 194:EC Number 17:Rutinose 442:Rutinose 466:glucose 444:is the 423:what is 421: ( 389:Density 212:PubChem 99:90-74-4 538:26 May 418:verify 415:  328:SMILES 225:441429 163:390162 31:Names 566:is a 489:rutin 293:InChI 134:ChEBI 112:JSmol 568:stub 540:2009 236:UNII 527:doi 491:by 452:-α- 262:EPA 215:CID 613:: 523:49 521:. 517:. 499:. 478:10 474:22 470:12 468:(C 372:10 366:22 360:12 40:α- 599:e 592:t 585:v 574:. 542:. 529:: 515:" 476:O 472:H 464:- 462:D 460:- 456:- 454:L 450:O 413:N 369:O 363:H 357:C 264:) 260:( 114:) 59:( 46:D 42:L

Index


IUPAC name
Systematic IUPAC name
CAS Number
90-74-4
JSmol
Interactive image
ChEBI
CHEBI:27522
ChemSpider
390162
ECHA InfoCard
100.001.832
Edit this at Wikidata
EC Number
PubChem
441429
UNII
0C4U3505G3
CompTox Dashboard
DTXSID401226338 DTXSID70896972, DTXSID401226338
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Density
standard state
verify
what is

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