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Durantin A

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InChI=1S/C22H20O9/c1-11(23)28-10-17-19(12-4-6-14(24)15(8-12)26-2)31-21-16(27-3)9-13-5-7-18(25)30-20(13)22(21)29-17/h4-9,17,19,24H,10H2,1-3H3/t17-,19-/m1/s1
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InChI=1/C22H20O9/c1-11(23)28-10-17-19(12-4-6-14(24)15(8-12)26-2)31-21-16(27-3)9-13-5-7-18(25)30-20(13)22(21)29-17/h4-9,17,19,24H,10H2,1-3H3/t17-,19-/m1/s1
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Ahmad, Nisar; Zeb, Fozia; Ahmad, Ijaz; Wang, Fanghai (July 2009). "Repenins A–D, four new antioxidative coumarinolignoids from Duranta repens Linn".
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Except where otherwise noted, data are given for materials in their
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CC(=O)OC1(OC2=C(C=C3C=CC(=O)OC3=C2O1)OC)C4=CC(=C(C=C4)O)OC
384: 130: 404: 8: 330:Bioorganic & Medicinal Chemistry Letters 411: 397: 163: 105: 15: 320: 219: 184: 159: 191:Key: ICLAWMWLMZMRGC-IEBWSBKVSA-N 85: 7: 365: 363: 201:Key: ICLAWMWLMZMRGC-IEBWSBKVBP 121: 305:isolated from the flowering plant 14: 367: 249: 22: 283:(at 25 °C , 100 kPa). 41:benzodioxin-2-yl]methyl acetate 255: 243: 1: 435:O-methylated natural phenols 383:. You can help Knowledge by 456: 362: 342:10.1016/j.bmcl.2009.05.006 277: 230: 210: 175: 47: 35: 30: 21: 440:Aromatic compound stubs 375:This article about an 37:Preferred IUPAC name 273: g·mol 18: 287:Infobox references 16: 430:Coumarinolignoids 392: 391: 336:(13): 3521–3524. 295:Chemical compound 293: 292: 144:CompTox Dashboard 67:Interactive image 447: 413: 406: 399: 371: 364: 354: 353: 325: 303:coumarinolignoid 301:is a bio-active 272: 257: 251: 245: 238:Chemical formula 168: 167: 152: 150: 134: 123: 109: 89: 69: 26: 19: 455: 454: 450: 449: 448: 446: 445: 444: 420: 419: 418: 417: 360: 358: 357: 327: 326: 322: 317: 296: 289: 284: 270: 260: 254: 248: 240: 226: 223: 218: 217: 206: 203: 202: 199: 193: 192: 189: 183: 182: 171: 161:DTXSID401045489 153: 146: 137: 124: 112: 92: 72: 59: 43: 42: 12: 11: 5: 453: 451: 443: 442: 437: 432: 422: 421: 416: 415: 408: 401: 393: 390: 389: 379:compound is a 372: 356: 355: 319: 318: 316: 313: 308:Duranta repens 294: 291: 290: 285: 281:standard state 278: 275: 274: 268: 262: 261: 258: 252: 246: 241: 236: 233: 232: 228: 227: 225: 224: 221: 213: 212: 211: 208: 207: 205: 204: 200: 197: 196: 194: 190: 187: 186: 178: 177: 176: 173: 172: 170: 169: 156: 154: 142: 139: 138: 136: 135: 127: 125: 117: 114: 113: 111: 110: 102: 100: 94: 93: 91: 90: 82: 80: 74: 73: 71: 70: 62: 60: 53: 50: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 452: 441: 438: 436: 433: 431: 428: 427: 425: 414: 409: 407: 402: 400: 395: 394: 388: 386: 382: 378: 373: 370: 366: 361: 351: 347: 343: 339: 335: 331: 324: 321: 314: 312: 310: 309: 304: 300: 288: 282: 276: 269: 267: 264: 263: 242: 239: 235: 234: 229: 220: 216: 209: 195: 185: 181: 174: 166: 162: 158: 157: 155: 145: 141: 140: 133: 129: 128: 126: 120: 116: 115: 108: 104: 103: 101: 99: 96: 95: 88: 84: 83: 81: 79: 76: 75: 68: 64: 63: 61: 57: 52: 51: 46: 38: 34: 29: 25: 20: 385:expanding it 374: 359: 333: 329: 323: 306: 298: 297: 87:ChEMBL495830 48:Identifiers 231:Properties 17:Durantin A 424:Categories 315:References 299:Durantin A 266:Molar mass 98:ChemSpider 54:3D model ( 377:aromatic 350:19464173 132:11224109 271:428.393 119:PubChem 107:9399162 348:  215:SMILES 78:ChEMBL 31:Names 180:InChI 56:JSmol 381:stub 346:PMID 338:doi 149:EPA 122:CID 426:: 344:. 334:19 332:. 311:. 253:20 247:22 412:e 405:t 398:v 387:. 352:. 340:: 259:9 256:O 250:H 244:C 151:) 147:( 58:)

Index


Preferred IUPAC name
JSmol
Interactive image
ChEMBL
ChEMBL495830
ChemSpider
9399162
PubChem
11224109
CompTox Dashboard
DTXSID401045489
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
coumarinolignoid
Duranta repens
doi
10.1016/j.bmcl.2009.05.006
PMID
19464173
Stub icon
aromatic
stub
expanding it
v

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