Knowledge

Arcapillin

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Nurul Islam, M; Jung, HA; Sohn, HS; Kim, HM; Choi, JS (2013). "Potent α-glucosidase and protein tyrosine phosphatase 1B inhibitors from Artemisia capillaris".
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InChI=1S/C18H16O8/c1-23-13-4-8(9(19)5-10(13)20)12-6-11(21)16-14(26-12)7-15(24-2)18(25-3)17(16)22/h4-7,19-20,22H,1-3H3
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InChI=1/C18H16O8/c1-23-13-4-8(9(19)5-10(13)20)12-6-11(21)16-14(26-12)7-15(24-2)18(25-3)17(16)22/h4-7,19-20,22H,1-3H3
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Except where otherwise noted, data are given for materials in their
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2-(2,4-Dihydroxy-5-methoxyphenyl)-5-hydroxy-6,7-dimethoxy-4
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COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O
166: 77: 475: 8: 40:2′,4′,5-Trihydroxy-5′,6,7-trimethoxyflavone 482: 468: 219: 141: 15: 186: 383: 275: 240: 215: 247:Key: IZWKTABKAJGBFW-UHFFFAOYSA-N 121: 7: 436: 434: 257:Key: IZWKTABKAJGBFW-UHFFFAOYAR 157: 14: 438: 305: 22: 339:(at 25 °C , 100 kPa). 393:Archives of Pharmacal Research 311: 299: 1: 454:. You can help Knowledge by 363:protein tyrosine phosphatase 527: 433: 405:10.1007/s12272-013-0069-7 333: 286: 266: 231: 61: 45: 35: 30: 21: 511:Organic compound stubs 501:Phosphatase inhibitors 446:This article about an 47:Systematic IUPAC name 371:Artemisia capillaris 329: g·mol 55:-1-benzopyran-4-one 18: 343:Infobox references 16: 463: 462: 351:Chemical compound 349: 348: 200:CompTox Dashboard 103:Interactive image 518: 484: 477: 470: 448:organic compound 442: 435: 425: 424: 388: 328: 313: 307: 301: 294:Chemical formula 224: 223: 208: 206: 190: 170: 159: 145: 125: 105: 81: 26: 19: 526: 525: 521: 520: 519: 517: 516: 515: 491: 490: 489: 488: 431: 429: 428: 390: 389: 385: 380: 352: 345: 340: 326: 316: 310: 304: 296: 282: 279: 274: 273: 262: 259: 258: 255: 249: 248: 245: 239: 238: 227: 217:DTXSID001003170 209: 202: 193: 173: 160: 148: 128: 108: 95: 84: 71: 57: 56: 41: 12: 11: 5: 524: 522: 514: 513: 508: 503: 493: 492: 487: 486: 479: 472: 464: 461: 460: 443: 427: 426: 382: 381: 379: 376: 368:isolated from 350: 347: 346: 341: 337:standard state 334: 331: 330: 324: 318: 317: 314: 308: 302: 297: 292: 289: 288: 284: 283: 281: 280: 277: 269: 268: 267: 264: 263: 261: 260: 256: 253: 252: 250: 246: 243: 242: 234: 233: 232: 229: 228: 226: 225: 212: 210: 198: 195: 194: 192: 191: 183: 181: 175: 174: 172: 171: 163: 161: 153: 150: 149: 147: 146: 138: 136: 130: 129: 127: 126: 118: 116: 110: 109: 107: 106: 98: 96: 89: 86: 85: 83: 82: 74: 72: 67: 64: 63: 59: 58: 50: 49: 43: 42: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 523: 512: 509: 507: 504: 502: 499: 498: 496: 485: 480: 478: 473: 471: 466: 465: 459: 457: 453: 449: 444: 441: 437: 432: 422: 418: 414: 410: 406: 402: 399:(5): 542–52. 398: 394: 387: 384: 377: 375: 373: 372: 367: 364: 360: 359:α-glucosidase 356: 344: 338: 332: 325: 323: 320: 319: 298: 295: 291: 290: 285: 276: 272: 265: 251: 241: 237: 230: 222: 218: 214: 213: 211: 201: 197: 196: 189: 185: 184: 182: 180: 177: 176: 169: 165: 164: 162: 156: 152: 151: 144: 140: 139: 137: 135: 132: 131: 124: 120: 119: 117: 115: 112: 111: 104: 100: 99: 97: 93: 88: 87: 80: 76: 75: 73: 70: 66: 65: 60: 54: 48: 44: 38: 34: 29: 25: 20: 456:expanding it 445: 430: 396: 392: 386: 369: 354: 353: 62:Identifiers 52: 287:Properties 123:CHEBI:81339 17:Arcapillin 495:Categories 378:References 355:Arcapillin 322:Molar mass 188:S53LT52TKY 134:ChemSpider 90:3D model ( 79:83162-82-7 69:CAS Number 37:IUPAC name 421:207410409 366:inhibitor 506:Flavones 413:23435948 327:360.318 155:PubChem 419:  411:  357:is an 271:SMILES 168:158311 143:139285 31:Names 450:is a 417:S2CID 236:InChI 114:ChEBI 92:JSmol 452:stub 409:PMID 361:and 179:UNII 401:doi 205:EPA 158:CID 497:: 415:. 407:. 397:36 395:. 374:. 309:16 303:18 483:e 476:t 469:v 458:. 423:. 403:: 315:8 312:O 306:H 300:C 207:) 203:( 94:) 53:H

Index


IUPAC name
Systematic IUPAC name
CAS Number
83162-82-7
JSmol
Interactive image
ChEBI
CHEBI:81339
ChemSpider
139285
PubChem
158311
UNII
S53LT52TKY
CompTox Dashboard
DTXSID001003170
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
α-glucosidase
protein tyrosine phosphatase
inhibitor
Artemisia capillaris
doi
10.1007/s12272-013-0069-7

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