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Bryoamaride

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229: 482: 539: 150: 24: 343: 252:
InChI=1S/C36H54O12/c1-31(2,45)12-11-23(39)36(8,46)28-19(38)14-33(5)22-10-9-17-18(35(22,7)24(40)15-34(28,33)6)13-20(29(44)32(17,3)4)47-30-27(43)26(42)25(41)21(16-37)48-30/h9,13,18-19,21-22,25-28,30,37-38,41-43,45-46H,10-12,14-16H2,1-8H3/t18-,19-,21-,22+,25-,26+,27-,28+,30-,33+,34-,35+,36+/m1/s1
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Jian Chao Chen, Ming Hua Chiu, Rui Lin Nie, Geoffrey A. Cordell and Samuel X. Qiu (2005), "Cucurbitacins and cucurbitane glycosides: structures and biological activities"
356: 580: 268: 523: 573: 243: 614: 566: 609: 207: 516: 436: 363: 509: 50: 36: 599: 224: 604: 116: 44:-Glucopyranosyloxy)-16,20,25-trihydroxy-9-methyl-19-nor-9β,10α-lanosta-1,5-diene-3,11,22-trione 379: 170: 546: 481: 462: 291: 126: 228: 550: 493: 384: 334: 83:)-1--2-hydroxy-3a,6,6,9b,11a-pentamethyl-8-{oxy}-2,3,3a,3b,4,6,9a,9b,11,11a-decahydro-1 593: 195: 276:
C12C((1(CC(=O)3(2CC=C43C=C(C(=O)C4(C)C)O5((((O5)CO)O)O)O)C)C)(C)(C(=O)CCC(C)(C)O)O)O
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Except where otherwise noted, data are given for materials in their
149: 139: 212: 554: 497: 351: 461:Natural Product Reports, volume 22, pages 386-399 194: 125: 574: 517: 8: 581: 567: 524: 510: 227: 169: 15: 455: 453: 388:. It can be seen as a derivative of the 449: 273: 248: 223: 382:isolated from certain plants, notably 255:Key: QCAZYVAEXLGYLV-HPCBBFKLSA-N 7: 535: 533: 478: 476: 185: 87:-cyclopentaphenanthrene-7,10-dione 14: 537: 480: 341: 303: 22: 434:-acetylbryoamaride is found in 337:(at 25 °C , 100 kPa). 309: 297: 1: 553:. You can help Knowledge by 496:. You can help Knowledge by 425:23,24-dihydrocucurbitacin I 631: 532: 475: 437:Trichosanthes tricuspidata 419:), more specifically from 331: 284: 264: 239: 109: 93: 49: 35: 30: 21: 615:Organic compound stubs 545:This article about an 51:Systematic IUPAC name 327: g·mol 18: 610:Biochemistry stubs 430:The derivative 25- 364:Infobox references 16: 562: 561: 505: 504: 380:chemical compound 372:Chemical compound 370: 369: 208:CompTox Dashboard 151:Interactive image 103: 96:Cucurbitacin L 2- 43: 622: 583: 576: 569: 547:organic compound 541: 534: 526: 519: 512: 484: 477: 470: 467:10.1039/B418841C 457: 418: 417: 416: 408: 407: 354: 348: 345: 344: 326: 311: 305: 299: 292:Chemical formula 232: 231: 216: 214: 198: 187: 173: 153: 129: 104:-glucopyranoside 101: 41: 26: 19: 630: 629: 625: 624: 623: 621: 620: 619: 590: 589: 588: 587: 531: 530: 474: 473: 458: 451: 446: 415: 412: 411: 410: 406: 403: 402: 401: 399: 373: 366: 361: 360: 359:  ?) 350: 346: 342: 338: 324: 314: 308: 302: 294: 280: 277: 272: 271: 260: 257: 256: 253: 247: 246: 235: 217: 210: 201: 188: 176: 156: 143: 132: 119: 105: 89: 88: 45: 12: 11: 5: 628: 626: 618: 617: 612: 607: 602: 592: 591: 586: 585: 578: 571: 563: 560: 559: 542: 529: 528: 521: 514: 506: 503: 502: 485: 472: 471: 448: 447: 445: 442: 421:cucurbitacin L 413: 404: 385:Bryonia dioica 371: 368: 367: 362: 340: 339: 335:standard state 332: 329: 328: 322: 316: 315: 312: 306: 300: 295: 290: 287: 286: 282: 281: 279: 278: 275: 267: 266: 265: 262: 261: 259: 258: 254: 251: 250: 242: 241: 240: 237: 236: 234: 233: 225:DTXSID30658770 220: 218: 206: 203: 202: 200: 199: 191: 189: 181: 178: 177: 175: 174: 166: 164: 158: 157: 155: 154: 146: 144: 137: 134: 133: 131: 130: 122: 120: 115: 112: 111: 107: 106: 95: 91: 90: 54: 53: 47: 46: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 627: 616: 613: 611: 608: 606: 603: 601: 598: 597: 595: 584: 579: 577: 572: 570: 565: 564: 558: 556: 552: 548: 543: 540: 536: 527: 522: 520: 515: 513: 508: 507: 501: 499: 495: 492:article is a 491: 486: 483: 479: 469: 468: 464: 456: 454: 450: 443: 441: 439: 438: 433: 428: 426: 422: 397: 394: 391: 387: 386: 381: 377: 365: 358: 353: 336: 330: 323: 321: 318: 317: 296: 293: 289: 288: 283: 274: 270: 263: 249: 245: 238: 230: 226: 222: 221: 219: 209: 205: 204: 197: 193: 192: 190: 184: 180: 179: 172: 168: 167: 165: 163: 160: 159: 152: 148: 147: 145: 141: 136: 135: 128: 124: 123: 121: 118: 114: 113: 108: 99: 92: 86: 82: 78: 74: 70: 66: 62: 58: 52: 48: 38: 34: 29: 25: 20: 555:expanding it 544: 498:expanding it 490:biochemistry 487: 460: 435: 431: 429: 383: 375: 374: 110:Identifiers 97: 94:Other names 84: 80: 76: 72: 68: 64: 60: 56: 17:Bryoamaride 600:Triterpenes 396:cucurbitane 393:hydrocarbon 376:Bryoamaride 285:Properties 605:Glucosides 594:Categories 444:References 390:triterpene 320:Molar mass 162:ChemSpider 138:3D model ( 127:61105-51-9 117:CAS Number 37:IUPAC name 196:44584115 171:23264945 357:what is 355: ( 325:678.816 183:PubChem 352:verify 349:  269:SMILES 31:Names 549:is a 488:This 378:is a 244:InChI 140:JSmol 40:2-(β- 551:stub 494:stub 79:,11a 463:doi 423:or 213:EPA 186:CID 100:-β- 75:,9b 71:,9a 67:,3b 63:,3a 596:: 452:^ 440:. 427:. 414:54 405:30 313:12 307:54 301:36 59:,2 55:(1 582:e 575:t 568:v 557:. 525:e 518:t 511:v 500:. 465:: 432:O 409:H 400:C 398:( 347:Y 310:O 304:H 298:C 215:) 211:( 142:) 102:D 98:O 85:H 81:R 77:R 73:R 69:S 65:S 61:R 57:R 42:D

Index


IUPAC name
Systematic IUPAC name
CAS Number
61105-51-9
JSmol
Interactive image
ChemSpider
23264945
PubChem
44584115
CompTox Dashboard
DTXSID30658770
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
verify
what is
Infobox references
chemical compound
Bryonia dioica
triterpene
hydrocarbon
cucurbitane
cucurbitacin L
23,24-dihydrocucurbitacin I
Trichosanthes tricuspidata

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