Knowledge (XXG)

Vanilloid

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213: 83: 69: 90: 97: 104: 76: 460: 397: 559: 283: 530: 350:"20-hydroxyeicosatetraenoic acid (20-HETE) is a pivotal endogenous ligand for TRPV1-mediated neurogenic inflammation in the skin" 163: 413:"Actions of two naturally occurring saturated N-acyldopamines on transient receptor potential vanilloid 1 (TRPV1) channels" 181: 476:"Endovanilloid control of pain modulation by the rostroventromedial medulla in an animal model of diabetic neuropathy" 82: 68: 212: 89: 96: 154:. Endogenously generated chemicals that trigger the TRPV1 channel of the vanilloids class are referred to as 167: 607: 474:
Silva, M.; Martins, D.; Charrua, A.; Piscitelli, F.; Tavares, I.; Morgado, C.; Di Marzo, V. (2016-08-01).
454: 391: 44: 475: 103: 552:"Vanilloid and Isovanilloid Analogues as Inhibitors of Methionyl-tRNA and Isoleucyl-tRNA Synthetases" 200: 75: 597: 309:"Endovanilloids. Putative endogenous ligands of transient receptor potential vanilloid 1 channels" 379: 189: 550:
Lee, Jeewoo; Uk Kang, Sang; Yeon Kim, Su; Eun Kim, Sung; Joon Jo, Yeong; Kim, Sunghoon (2001).
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Hamers A, Primus CP, Whitear C, Kumar NA, Masucci M, Montalvo Moreira SA; et al. (2022).
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De Petrocellis L, Chu CJ, Moriello AS, Kellner JC, Walker JM, Di Marzo V (2004).
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which naturally responds to noxious stimuli such as high temperatures and acidic
275: 150:. This action is responsible for the burning sensation experienced after eating 143: 231: 220: 196: 159: 499: 128: 52: 580: 507: 446: 428: 375: 334: 293: 270:. Handbook of Experimental Pharmacology. Vol. 179. pp. 155–171. 151: 32: 175: 366: 349: 185: 139: 138:
A number of vanilloids, most notably capsaicin, bind to the
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Capsaicin receptor: TRPV1 a promiscuous TRP channel
521:Carlson, Neil R.; Birkett, Melissa A. (2017). 16:Chemical compounds containing a vanillyl group 230:Outside the food industry vanilloids such as 140:transient receptor potential vanilloid type 1 8: 560:Bioorganic & Medicinal Chemistry Letters 459:: CS1 maint: multiple names: authors list ( 396:: CS1 maint: multiple names: authors list ( 241:Other vanilloids which act at TRPV1 include 436: 365: 324: 266:Pingle, SC; Matta, JA; Ahern, GP (2007). 207: 63: 258: 452: 389: 525:(12 ed.). Pearson. p. 212. 7: 307:Van Der Stelt M, Di Marzo V (2004). 14: 492:10.1016/j.neuropharm.2016.03.007 326:10.1111/j.1432-1033.2004.04081.x 211: 102: 95: 88: 81: 74: 67: 164:20-hydroxyeicosatetraenoic acid 170:(NADA) and N-oleoyl-dopamine ( 23:are compounds which possess a 1: 573:10.1016/S0960-894X(01)00096-8 276:10.1007/978-3-540-34891-7_9 188:for endovanilloid, and the 624: 182:Fatty acid amide hydrolase 234:are used commercially in 168:N-arachidonoyl dopamine 55:, etc. Isomers are the 523:Physiology of Behavior 429:10.1038/sj.bjp.0705924 201:cannabinoid receptors 184:(FAAH), is a crucial 142:(TRPV1) receptor, an 45:vanillylmandelic acid 199:at TRPV1, and other 193:-acylethanolamines 480:Neuropharmacology 367:10.1111/bph.15726 285:978-3-540-34889-4 226: 225: 134: 133: 49:homovanillic acid 615: 584: 556: 537: 536: 518: 512: 511: 471: 465: 464: 458: 450: 440: 408: 402: 401: 395: 387: 369: 360:(7): 1450–1469. 345: 339: 338: 328: 304: 298: 297: 263: 215: 208: 111:vanillyl alcohol 106: 99: 92: 85: 78: 71: 64: 29:vanillyl alcohol 623: 622: 618: 617: 616: 614: 613: 612: 588: 587: 554: 549: 546: 541: 540: 533: 520: 519: 515: 473: 472: 468: 451: 410: 409: 405: 388: 347: 346: 342: 319:(10): 1827–34. 306: 305: 301: 286: 265: 264: 260: 255: 243:resiniferatoxin 27:. They include 17: 12: 11: 5: 621: 619: 611: 610: 605: 600: 590: 589: 586: 585: 567:(8): 965–968. 545: 542: 539: 538: 531: 513: 466: 417:Br J Pharmacol 403: 354:Br J Pharmacol 340: 299: 284: 257: 256: 254: 251: 238:formulations. 228: 227: 224: 223: 217: 216: 156:endovanilloids 136: 135: 132: 131: 126: 121: 118: 115: 112: 108: 107: 100: 93: 86: 79: 72: 25:vanillyl group 15: 13: 10: 9: 6: 4: 3: 2: 620: 609: 608:Phenol ethers 606: 604: 601: 599: 596: 595: 593: 582: 578: 574: 570: 566: 562: 561: 553: 548: 547: 543: 534: 532:9780134320823 528: 524: 517: 514: 509: 505: 501: 497: 493: 489: 485: 481: 477: 470: 467: 462: 456: 448: 444: 439: 434: 430: 426: 422: 418: 414: 407: 404: 399: 393: 385: 381: 377: 373: 368: 363: 359: 355: 351: 344: 341: 336: 332: 327: 322: 318: 314: 313:Eur J Biochem 310: 303: 300: 295: 291: 287: 281: 277: 273: 269: 262: 259: 252: 250: 248: 244: 239: 237: 233: 222: 219: 218: 214: 210: 209: 206: 205: 204: 202: 198: 194: 192: 187: 183: 179: 177: 173: 169: 165: 161: 157: 153: 152:spicy peppers 149: 145: 141: 130: 127: 125: 124:Vanillylamine 122: 120:acetovanillon 119: 117:vanillic acid 116: 113: 110: 109: 105: 101: 98: 94: 91: 87: 84: 80: 77: 73: 70: 66: 65: 62: 61: 60: 58: 57:isovanilloids 54: 50: 46: 42: 41:acetovanillon 38: 37:vanillic acid 34: 30: 26: 22: 564: 558: 522: 516: 483: 479: 469: 455:cite journal 423:(2): 251–6. 420: 416: 406: 392:cite journal 357: 353: 343: 316: 312: 302: 267: 261: 240: 236:pepper spray 229: 190: 180: 155: 137: 20: 18: 172:CID 5282106 166:(20-HETE), 144:ion channel 598:Vanilloids 592:Categories 544:Literature 253:References 232:nonivamide 221:Anandamide 197:catabolism 160:anandamide 158:including 21:vanilloids 500:0028-3908 486:: 49–57. 384:243939400 129:Capsaicin 53:capsaicin 581:11327601 508:26965218 447:15289293 376:34755897 335:15128293 294:17217056 195:(NAEs), 114:vanillin 33:vanillin 603:Phenols 438:1575334 247:olvanil 176:PubChem 579:  529:  506:  498:  445:  435:  382:  374:  333:  292:  282:  186:enzyme 555:(PDF) 380:S2CID 174:from 577:PMID 527:ISBN 504:PMID 496:ISSN 461:link 443:PMID 398:link 372:PMID 331:PMID 290:PMID 280:ISBN 245:and 19:The 569:doi 488:doi 484:107 433:PMC 425:doi 421:143 362:doi 358:179 321:doi 317:271 272:doi 178:). 594:: 575:. 565:11 563:. 557:. 502:. 494:. 482:. 478:. 457:}} 453:{{ 441:. 431:. 419:. 415:. 394:}} 390:{{ 378:. 370:. 356:. 352:. 329:. 315:. 311:. 288:. 278:. 249:. 203:. 162:, 148:pH 59:. 51:, 47:, 43:, 39:, 35:, 31:, 583:. 571:: 535:. 510:. 490:: 463:) 449:. 427:: 400:) 386:. 364:: 337:. 323:: 296:. 274:: 191:N

Index

vanillyl group
vanillyl alcohol
vanillin
vanillic acid
acetovanillon
vanillylmandelic acid
homovanillic acid
capsaicin
isovanilloids
Structure of vanillyl alcohol
Structure of Vanillin
Structure of vanillic acid
Structure of acetovanillon
Structure of vanillylamine
Structure of Capsaicin
Vanillylamine
Capsaicin
transient receptor potential vanilloid type 1
ion channel
pH
spicy peppers
anandamide
20-hydroxyeicosatetraenoic acid
N-arachidonoyl dopamine
CID 5282106
PubChem
Fatty acid amide hydrolase
enzyme
N-acylethanolamines
catabolism

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