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S-Methylcysteine

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Bernaert, N.; Goetghebeur, L.; De Clercq, H.; De Loose, M.; Daeseleire, E.; Van Pamel, E.; Van Bockstaele, E.; Van Droogenbroeck, B. (2012). "Influence of Cultivar and Harvest Time on the Amounts of Isoalliin and Methiin in Leek
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Sors, Thomas G.; Ellis, Danielle R.; Na, Gun Nam; Lahner, Brett; Lee, Sangman; Leustek, Thomas; Pickering, Ingrid J.; Salt, David E. (2005).
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Imaging Agents. Structural Characterization and Solution Behavior of Complexes with Thioether-Bearing Amino Acids as Tridentate Ligands".
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He, Haiyang; Lipowska, Malgorzata; Xu, Xiaolong; Taylor, Andrew T.; Carlone, Maria; Marzilli, Luigi G. (2005). "Re(CO)
330: 619: 504: 969: 706: 642: 767:"Analysis of Sulfur and Selenium Assimilation in Astragalus plants with Varying Capacities to Accumulate Selenium" 243: 611: 607: 595: 231: 171: 954: 527: 497: 67: 50: 348: 964: 567: 93: 559: 571: 930: 879: 839: 788: 922: 871: 829: 819: 808:"The ribosome: A Hot Spot for the Identification of New Types of Protein Methyltransferases" 778: 747: 738:
Maw, George A. (1982). "Biochemistry of S-Methyl-L-Cysteine and its Principal Derivatives".
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Complexes Synthesized via an Improved Preparation of Aqueousfac-[Re(CO)
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Beyond its biological context, S-methylcysteine has been examined as a
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Except where otherwise noted, data are given for materials in their
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is an oxidized derivative of S-methylcysteine that is found in ]s.
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InChI=1S/C4H9NO2S/c1-8-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
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from alkylated DNA by zinc-cysteinate-containing repair enzymes.
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S-Methylcysteine is not genetically coded, but it arises by
603: 335: 296: 103: 8: 864:Journal of Agricultural and Food Chemistry 351: 234: 191: 26: 833: 823: 782: 680:H. It is the S-methylated derivative of 317: 730: 397: 372: 347: 212: 475:248 °C (478 °F; 521 K) 225: 379:Key: IDIDJDIHTAOVLG-VKHMYHEASA-N 170: 149: 7: 72:2-amino-3-(methylthio)propanoic acid 699:of cysteine. One pathway involves 286: 270: 25: 784:10.1111/j.1365-313X.2005.02413.x 503: 433: 427: 36: 812:Journal of Biological Chemistry 639:(at 25 °C , 100 kPa). 400:L-enantiomer: CSC(C(=O)O)N 909:]+as an Aid in Assessing 442: 436: 421: 1: 253:L-enantiomer: 214-701-6 664:with the nominal formula CH 991: 806:Clarke, Steven G. (2018). 707:S-Methylcysteine sulfoxide 752:10.1080/01961778208082422 713:Other chemical properties 633: 484: 479: 408: 388: 363: 86: 78: 66: 49: 44: 35: 825:10.1074/jbc.AW118.003235 554:Precautionary statements 975:Amino acid derivatives 68:Systematic IUPAC name 915:Inorganic Chemistry 870:(44): 10910–10919. 860:Allium ampeloprasum 818:(27): 10438–10446. 457: g·mol 346:L-enantiomer: 316:L-enantiomer: 295:L-enantiomer: 269:L-enantiomer: 211:L-enantiomer: 190:L-enantiomer: 169:L-enantiomer: 148:L-enantiomer: 127:L-enantiomer: 102:L-enantiomer: 81:3-methylthioalanine 32: 960:Sulfur amino acids 694:post-translational 688:Natural occurrence 643:Infobox references 27: 970:Alpha-Amino acids 927:10.1021/ic0501869 921:(15): 5437–5446. 876:10.1021/jf302132a 771:The Plant Journal 651:Chemical compound 649: 648: 528:Hazard statements 331:CompTox Dashboard 130:Interactive image 60: 16:(Redirected from 982: 939: 938: 894: 888: 887: 854: 848: 847: 837: 827: 803: 797: 796: 786: 762: 756: 755: 735: 629: 625: 621: 617: 613: 609: 605: 601: 597: 593: 589: 585: 581: 577: 573: 569: 565: 561: 547: 543: 539: 535: 507: 456: 444: 438: 435: 429: 423: 416:Chemical formula 356: 355: 339: 337: 321: 300: 288: 274: 246: 238: 227: 216: 195: 174: 153: 132: 107: 58: 40: 33: 31:-Methylcysteine 21: 18:S-methylcysteine 990: 989: 985: 984: 983: 981: 980: 979: 945: 944: 943: 942: 908: 904: 900: 896: 895: 891: 862:var. porrum)". 856: 855: 851: 805: 804: 800: 764: 763: 759: 737: 736: 732: 727: 719:chelating agent 715: 701:methyl transfer 690: 679: 675: 671: 667: 658:-Methylcysteine 652: 645: 640: 556: 530: 516: 500: 454: 441: 432: 426: 418: 404: 401: 396: 395: 384: 381: 380: 377: 371: 370: 359: 340: 333: 324: 303: 289: 277: 256: 219: 198: 177: 156: 135: 121: 110: 96: 82: 74: 73: 62: 23: 22: 15: 12: 11: 5: 988: 986: 978: 977: 972: 967: 962: 957: 947: 946: 941: 940: 906: 902: 898: 889: 849: 798: 777:(6): 785–797. 757: 740:Sulfur Reports 729: 728: 726: 723: 714: 711: 689: 686: 677: 673: 669: 665: 650: 647: 646: 641: 637:standard state 634: 631: 630: 592:P305+P351+P338 557: 552: 549: 548: 531: 526: 523: 522: 517: 512: 509: 508: 501: 496: 493: 492: 482: 481: 477: 476: 473: 467: 466: 463: 459: 458: 452: 446: 445: 439: 430: 424: 419: 414: 411: 410: 406: 405: 403: 402: 399: 391: 390: 389: 386: 385: 383: 382: 378: 375: 374: 366: 365: 364: 361: 360: 358: 357: 349:DTXSID50862579 343: 341: 329: 326: 325: 323: 322: 313: 311: 305: 304: 302: 301: 292: 290: 282: 279: 278: 276: 275: 266: 264: 258: 257: 255: 254: 250: 248: 240: 239: 229: 221: 220: 218: 217: 208: 206: 200: 199: 197: 196: 187: 185: 179: 178: 176: 175: 166: 164: 158: 157: 155: 154: 145: 143: 137: 136: 134: 133: 124: 122: 115: 112: 111: 109: 108: 99: 97: 92: 89: 88: 84: 83: 80: 76: 75: 71: 70: 64: 63: 53: 47: 46: 42: 41: 24: 14: 13: 10: 9: 6: 4: 3: 2: 987: 976: 973: 971: 968: 966: 963: 961: 958: 956: 953: 952: 950: 936: 932: 928: 924: 920: 916: 912: 893: 890: 885: 881: 877: 873: 869: 865: 861: 853: 850: 845: 841: 836: 831: 826: 821: 817: 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739: 733: 716: 705: 691: 655: 654: 653: 519: 486: 465:white solid 172:ChEMBL394875 87:Identifiers 79:Other names 54: 28: 697:methylation 514:Signal word 462:Appearance 409:Properties 232:100.013.365 151:CHEBI:45658 965:Thioethers 949:Categories 725:References 662:amino acid 498:Pictograms 450:Molar mass 319:A34I1H07YM 183:ChemSpider 116:3D model ( 94:CAS Number 51:IUPAC name 620:P403+P233 612:P337+P313 608:P332+P313 588:P304+P340 584:P302+P352 580:P301+P312 489:labelling 245:EC Number 105:1187-84-4 61:-cysteine 935:16022542 884:23020262 844:29743234 793:15941393 746:: 1–26. 682:cysteine 480:Hazards 204:DrugBank 57:-Methyl- 835:6036201 660:is the 520:Warning 284:PubChem 933:  882:  842:  832:  791:  455:135.18 393:SMILES 272:C22040 162:ChEMBL 45:Names 905:(H2O) 672:CH(NH 368:InChI 298:24417 214:02216 193:22826 141:ChEBI 118:JSmol 931:PMID 880:PMID 840:PMID 789:PMID 628:P501 624:P405 616:P362 604:P330 600:P321 596:P312 576:P280 572:P271 568:P270 564:P264 560:P261 546:H335 542:H319 538:H315 534:H302 309:UNII 262:KEGG 923:doi 872:doi 830:PMC 820:doi 816:293 779:doi 748:doi 676:)CO 668:SCH 487:GHS 336:EPA 287:CID 951:: 929:. 919:44 917:. 911:Tc 878:. 868:60 866:. 838:. 828:. 814:. 810:. 787:. 775:42 773:. 769:. 742:. 721:. 626:, 622:, 618:, 614:, 610:, 606:, 602:, 598:, 594:, 590:, 586:, 582:, 578:, 574:, 570:, 566:, 562:, 544:, 540:, 536:, 491:: 937:. 925:: 907:3 903:3 899:3 886:. 874:: 858:( 846:. 822:: 795:. 781:: 754:. 750:: 744:2 678:2 674:2 670:2 666:3 656:S 443:S 440:2 437:O 434:N 431:9 428:H 425:4 422:C 338:) 334:( 120:) 59:L 55:S 29:S 20:)

Index

S-methylcysteine

IUPAC name
Systematic IUPAC name
CAS Number
1187-84-4
JSmol
Interactive image
ChEBI
CHEBI:45658
ChEMBL
ChEMBL394875
ChemSpider
22826
DrugBank
02216
ECHA InfoCard
100.013.365
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EC Number
KEGG
C22040
PubChem
24417
UNII
A34I1H07YM
CompTox Dashboard
DTXSID50862579
Edit this at Wikidata
InChI

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