Knowledge (XXG)

Corrinoid

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565: 31: 159:. Absorption of the corrinoid on a solid phase, allows detection of cyanide even in colored samples, rendering this method appropriate for the analysis of cyanide in water, wastewater, blood, and food. Furthermore, this technology is non-toxic and considerably less prone to interference than the pyridine-barbituric acid colorimetry method. 43: 155:, reacts with free cyanide in an aqueous sample. The binding of cyanide to the corrinoid cobalt center leads to a color change from orange to violet. Quantification of the cyanide content is feasible by 477: 606: 365:
Mannel-Croise, Zelder (2009). "Side chains of cobalt corrinoids control the sensitivity and selectivity in the colorimetric detection of cyanide".
263: 243: 635: 437:"Straightforward rapid spectrophotometric quantification of total cyanogenic glycosides in fresh and processed cassava products" 599: 226:
Cracan, Valentin; Banerjee, Ruma (2013). "Chapter 10 Cobalt and Corrinoid Transport and Biochemistry". In Banci, Lucia (ed.).
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Zelder, F.H. (2008). "Specific Colorimetric Detection of Cyanide Triggered by a Conformational Switch in Vitamin B12".
131:, as in "Cob(II)alamin". When cobalt is replaced by another metal or hydrogen, the name changes accordingly, as in 592: 539: 436: 625: 136: 572: 471: 38:
numbering system, there is no 20 position. Positions 21-24 were numbered 20-23 in earlier literature.
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Dorothy Crowfoot Hodgkin (1965-11-16). "The Structure of the Corrin Nucleus from X-ray Analysis".
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Corrin ring, numbered according to the 1975 IUPAC standard. Note that for consistency with the
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Mannel-Croise, Zelder (2012). "Complex samples cyanide detection with immobilized corrinoids".
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Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences
53: 535: 619: 519: 212: 455: 564: 294: 235: 75:. These include compounds based on octadehydrocorrin, which has the trivial name 87: 293:. IUPAC-IUB Commission on Biochemical Nomenclature (CBN). 1975. Archived from 93:) are the best known members of the group. Other prominent examples include 148: 83: 72: 35: 463: 421: 386: 351: 253: 196: 30: 17: 230:. Metal Ions in Life Sciences. Vol. 12. Springer. pp. 333–374. 114: 511: 204: 76: 68: 42: 413: 378: 343: 64: 41: 29: 435:
Tivana, Da Cruz Francisco, Zelder, Bergenståhl, Dejmek (2014).
580: 291:"The Nomenclature of Corrinoids: Recommendations 1975" 546:"The Nomenclature of Corrinoids" at chem.qmul.ac.uk 63:are a group of compounds based on the skeleton of 127:rin) are cobalt derivatives, and may include an 600: 8: 476:: CS1 maint: multiple names: authors list ( 147:A solution of aquacyano-corrinoids, such as 607: 593: 538:at the U.S. National Library of Medicine 493:"Rapid visual detection of blood cyanide" 120:Compounds containing the "Cob-" prefix ( 167: 469: 402:ACS Applied Materials & Interfaces 7: 561: 559: 579:. You can help Knowledge (XXG) by 317:Inorganic Chemistry of Vitamin B12 67:, a cyclic system containing four 25: 563: 491:Mannel-Croise, Zelder (2012). 456:10.1016/j.foodchem.2014.02.066 1: 319:. Academic Press. p. 44. 236:10.1007/978-94-007-5561-1_10 636:Heterocyclic compound stubs 27:Class of chemical compounds 652: 558: 540:Medical Subject Headings 228:Metallomics and the Cell 197:10.1098/rspa.1965.0219 143:Reactions with cyanide 57: 39: 573:heterocyclic compound 571:This article about a 45: 33: 315:Pratt, J.M. (1972). 367:Inorganic Chemistry 332:Inorganic Chemistry 189:1965RSPSA.288..294H 157:UV-vis spectroscopy 137:hydrogenobamic acid 512:10.1039/c2ay25595b 500:Analytical Methods 105:and its hexaamide 97:and its hexaamide 58: 40: 588: 587: 414:10.1021/am201357u 379:10.1021/ic900053h 344:10.1021/ic702368b 264:978-94-007-5561-1 245:978-94-007-5560-4 183:(1414): 294–305. 71:rings similar to 50: 16:(Redirected from 643: 609: 602: 595: 567: 560: 524: 523: 506:(9): 2632–2634. 497: 488: 482: 481: 475: 467: 441: 432: 426: 425: 397: 391: 390: 373:(4): 1272–1274. 362: 356: 355: 338:(4): 1264–1266. 327: 321: 320: 312: 306: 305: 303: 302: 287: 281: 258:electronic-book 257: 223: 217: 216: 172: 48: 21: 651: 650: 646: 645: 644: 642: 641: 640: 616: 615: 614: 613: 556: 532: 527: 495: 490: 489: 485: 468: 439: 434: 433: 429: 399: 398: 394: 364: 363: 359: 329: 328: 324: 314: 313: 309: 300: 298: 289: 288: 284: 246: 225: 224: 220: 174: 173: 169: 165: 145: 133:ferrobamic acid 129:oxidation state 91: 51: 28: 23: 22: 15: 12: 11: 5: 649: 647: 639: 638: 633: 628: 618: 617: 612: 611: 604: 597: 589: 586: 585: 568: 554: 553: 548: 543: 531: 530:External links 528: 526: 525: 483: 444:Food Chemistry 427: 408:(2): 725–729. 392: 357: 322: 307: 282: 244: 218: 166: 164: 161: 144: 141: 95:cobyrinic acid 89: 54:cyanocobalamin 47: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 648: 637: 634: 632: 629: 627: 626:Tetrapyrroles 624: 623: 621: 610: 605: 603: 598: 596: 591: 590: 584: 582: 578: 574: 569: 566: 562: 557: 552: 549: 547: 544: 541: 537: 534: 533: 529: 521: 517: 513: 509: 505: 501: 494: 487: 484: 479: 473: 465: 461: 457: 453: 449: 445: 438: 431: 428: 423: 419: 415: 411: 407: 403: 396: 393: 388: 384: 380: 376: 372: 368: 361: 358: 353: 349: 345: 341: 337: 333: 326: 323: 318: 311: 308: 297:on 2012-10-28 296: 292: 286: 283: 280: 276: 272: 268: 265: 261: 255: 251: 247: 241: 237: 233: 229: 222: 219: 214: 210: 206: 202: 198: 194: 190: 186: 182: 178: 171: 168: 162: 160: 158: 154: 150: 142: 140: 138: 134: 130: 126: 123: 118: 116: 112: 108: 104: 100: 96: 92: 85: 80: 78: 74: 70: 66: 62: 55: 44: 37: 32: 19: 581:expanding it 570: 555: 503: 499: 486: 472:cite journal 447: 443: 430: 405: 401: 395: 370: 366: 360: 335: 331: 325: 316: 310: 299:. Retrieved 295:the original 285: 227: 221: 180: 176: 170: 146: 124: 121: 119: 111:cobamic acid 103:cobinic acid 99:cobyric acid 81: 60: 59: 273:electronic- 631:Corrinoids 620:Categories 536:Corrinoids 301:2006-06-19 163:References 153:cobinamide 107:cobinamide 84:cobalamins 73:porphyrins 61:Corrinoids 18:Corrinoids 450:: 20–27. 279:1868-0402 271:1559-0836 149:cobalamin 88:vitamin B 46:Vitamin B 36:porphyrin 551:Goldbook 520:96719554 464:24731309 422:22211318 387:19161297 352:18205304 254:23595677 213:95235740 115:cobamide 205:2415001 185:Bibcode 77:corrole 69:pyrrole 542:(MeSH) 518:  462:  420:  385:  350:  277:  269:  262:  252:  242:  211:  203:  65:corrin 575:is a 516:S2CID 496:(PDF) 440:(PDF) 209:S2CID 201:JSTOR 577:stub 478:link 460:PMID 418:PMID 383:PMID 348:PMID 275:ISSN 267:ISSN 260:ISBN 250:PMID 240:ISBN 113:and 82:The 508:doi 452:doi 448:158 410:doi 375:doi 340:doi 232:doi 193:doi 181:288 151:or 135:or 125:cor 122:not 622:: 514:. 502:. 498:. 474:}} 470:{{ 458:. 446:. 442:. 416:. 404:. 381:. 371:48 369:. 346:. 336:47 334:. 248:. 238:. 207:. 199:. 191:. 179:. 139:. 117:. 109:; 101:; 90:12 79:. 49:12 608:e 601:t 594:v 583:. 522:. 510:: 504:4 480:) 466:. 454:: 424:. 412:: 406:4 389:. 377:: 354:. 342:: 304:. 256:. 234:: 215:. 195:: 187:: 86:( 56:) 52:( 20:)

Index

Corrinoids

porphyrin

cyanocobalamin
corrin
pyrrole
porphyrins
corrole
cobalamins
vitamin B12
cobyrinic acid
cobyric acid
cobinic acid
cobinamide
cobamic acid
cobamide
oxidation state
ferrobamic acid
hydrogenobamic acid
cobalamin
cobinamide
UV-vis spectroscopy
Bibcode
1965RSPSA.288..294H
doi
10.1098/rspa.1965.0219
JSTOR
2415001
S2CID

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