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Salicyluric acid

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165: 142: 29: 394: 374: 255: 435: 358: 275: 231: 464: 81: 474: 121: 346: 469: 459: 428: 160: 454: 110: 421: 137: 41: 368: 354: 177: 90: 305: 70: 164: 141: 50: 405: 309: 448: 325: 242: 153: 283:
InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
401: 321: 20: 207: 61: 28: 393: 313: 302: 317: 101: 230: 221: 126: 409: 241: 219: 206: 176: 171: 152: 120: 100: 80: 60: 40: 35: 312:and is the primary form in which salicylates are 320:. The pathway is very similar to the pathway of 49: 429: 8: 19: 436: 422: 373:: CS1 maint: location missing publisher ( 163: 140: 69: 27: 353:(Second ed.). Weinheim. p. 70. 89: 337: 280: 260: 136: 366: 347:"Biotransformations of Salicylic Acid" 154: 18: 109: 7: 390: 388: 14: 247:164–165 °C (327–329 °F) 392: 194: 188: 288:Key:ONJSZLXSECQROL-UHFFFAOYSA-N 197: 182: 1: 408:. You can help Knowledge by 491: 387: 263:c1ccc(c(c1)C(=O)NCC(=O)O)O 172:Chemical and physical data 271: 251: 26: 316:from the body, via the 465:Amino acid derivatives 404:-related article is a 351:Acetylsalicylic acid 23: 475:Pharmacology stubs 470:Human metabolites 460:Alpha-Amino acids 417: 416: 360:978-3-527-68502-8 345:Schrör K (2016). 296: 295: 232:Interactive image 122:CompTox Dashboard 16:Chemical compound 482: 438: 431: 424: 396: 389: 379: 378: 372: 364: 342: 299:Salicyluric acid 234: 214: 199: 196: 190: 184: 167: 156: 145: 144: 130: 128: 113: 93: 73: 53: 31: 24: 22: 21:Salicyluric acid 490: 489: 485: 484: 483: 481: 480: 479: 445: 444: 443: 442: 385: 383: 382: 365: 361: 344: 343: 339: 334: 292: 289: 284: 279: 278: 267: 264: 259: 258: 237: 212: 202: 193: 187: 148: 124: 116: 96: 76: 56: 17: 12: 11: 5: 488: 486: 478: 477: 472: 467: 462: 457: 447: 446: 441: 440: 433: 426: 418: 415: 414: 397: 381: 380: 359: 336: 335: 333: 330: 310:salicylic acid 294: 293: 291: 290: 287: 285: 282: 274: 273: 272: 269: 268: 266: 265: 262: 254: 253: 252: 249: 248: 245: 239: 238: 236: 235: 227: 225: 217: 216: 210: 204: 203: 200: 191: 185: 180: 174: 173: 169: 168: 158: 150: 149: 147: 146: 138:DTXSID70197592 133: 131: 118: 117: 115: 114: 106: 104: 98: 97: 95: 94: 86: 84: 78: 77: 75: 74: 66: 64: 58: 57: 55: 54: 46: 44: 38: 37: 33: 32: 15: 13: 10: 9: 6: 4: 3: 2: 487: 476: 473: 471: 468: 466: 463: 461: 458: 456: 455:Salicylamides 453: 452: 450: 439: 434: 432: 427: 425: 420: 419: 413: 411: 407: 403: 398: 395: 391: 386: 376: 370: 362: 356: 352: 348: 341: 338: 331: 329: 327: 326:hippuric acid 324:excretion as 323: 319: 315: 311: 307: 304: 300: 286: 281: 277: 270: 261: 257: 250: 246: 244: 243:Melting point 240: 233: 229: 228: 226: 223: 218: 211: 209: 205: 181: 179: 175: 170: 166: 162: 159: 157: 155:ECHA InfoCard 151: 143: 139: 135: 134: 132: 123: 119: 112: 108: 107: 105: 103: 99: 92: 88: 87: 85: 83: 79: 72: 68: 67: 65: 63: 59: 52: 48: 47: 45: 43: 39: 34: 30: 25: 410:expanding it 402:pharmacology 399: 384: 350: 340: 322:benzoic acid 298: 297: 215: g·mol 161:100.006.965 36:Identifiers 449:Categories 332:References 220:3D model ( 208:Molar mass 91:5BR3P7J05U 62:ChemSpider 42:CAS Number 369:cite book 306:conjugate 111:ChEMBL586 314:excreted 51:487-54-7 318:kidneys 303:glycine 301:is the 213:195.174 178:Formula 357:  256:SMILES 102:ChEMBL 400:This 276:InChI 222:JSmol 406:stub 375:link 355:ISBN 82:UNII 71:9835 308:of 127:EPA 451:: 371:}} 367:{{ 349:. 328:. 437:e 430:t 423:v 412:. 377:) 363:. 224:) 201:4 198:O 195:N 192:9 189:H 186:9 183:C 129:) 125:(

Index


CAS Number
487-54-7
ChemSpider
9835
UNII
5BR3P7J05U
ChEMBL
ChEMBL586
CompTox Dashboard
DTXSID70197592
Edit this at Wikidata
ECHA InfoCard
100.006.965
Edit this at Wikidata
Formula
Molar mass
JSmol
Interactive image
Melting point
SMILES
InChI
glycine
conjugate
salicylic acid
excreted
kidneys
benzoic acid
hippuric acid
"Biotransformations of Salicylic Acid"

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