Knowledge

Mustakone

Source 📝

193: 563: 24: 604: 232: 597: 207: 471:
Kapadia VH, Nagasampagi BA, Naik VG, Dev S (January 1965). "Studies in sesquiterpenes—XXII: Structure of mustakone and copaene".
94: 638: 419:"Essential Oils from Leaves of Medicinal Plants of Brazilian Flora: Chemical Composition and Activity against Candida Species" 590: 623: 171: 341: 633: 36: 188: 508:/M Phase and Cell Death in HepG2 Cells and Inhibits the Development of Tumors in a Xenograft Model" 390: 60: 396: 539: 450: 134: 628: 570: 529: 519: 480: 440: 430: 383: 373: 255: 216:
InChI=1S/C15H22O/c1-8(2)10-5-6-15(4)13-9(3)7-11(16)14(15)12(10)13/h7-8,10,12-14H,5-6H2,1-4H3
417:
Costa MD, Silva AG, Silva AP, Lima VL, Bezerra-Silva PC, Rocha SK, et al. (May 2017).
192: 498:
Nogueira ML, Lima EJ, Adrião AA, Fontes SS, Silva VR, Santos LS, et al. (June 2020).
70: 114: 574: 534: 499: 445: 418: 335: 484: 617: 360: 293: 159: 309: 562: 524: 303: 280: 125: 435: 357: 543: 454: 504:
L. (Cyperaceae) Rhizome Essential Oil Causes Cell Cycle Arrest in the G
326: 146: 23: 382:. Mustakone can be found in a variety of plants and their oils like 334:
Except where otherwise noted, data are given for materials in their
379: 105: 93: 83: 176: 371:
O. It is named after the plant it was first extracted from
578: 158: 40:1,5-dimethyl-8-propan-2-yltricyclodec-4-en-3-one 69: 598: 8: 605: 591: 191: 133: 15: 533: 523: 466: 464: 444: 434: 409: 378:which had the common name "mustuka" in 237: 212: 187: 219:Key: CTFSUCDHRVDRKG-UHFFFAOYSA-N 113: 7: 559: 557: 149: 14: 561: 267: 22: 338:(at 25 °C , 100 kPa). 273: 261: 240:CC1=CC(=O)C2C3C1C2(CCC3C(C)C)C 1: 485:10.1016/S0040-4020(01)82231-6 577:. You can help Knowledge by 363:with the chemical formula C 655: 556: 525:10.3390/molecules25112687 332: 315: 248: 228: 203: 53: 45: 35: 30: 21: 436:10.3390/medicines4020027 639:Organic compound stubs 569:This article about an 624:Tricyclic compounds 502:Cyperus articulatus 391:Cyperus articulatus 288: g·mol 18: 397:Hymenaea courbaril 342:Infobox references 316:Related compounds 16: 586: 585: 350:Chemical compound 348: 347: 322:Related compounds 172:CompTox Dashboard 95:Interactive image 646: 607: 600: 593: 571:organic compound 565: 558: 548: 547: 537: 527: 495: 489: 488: 468: 459: 458: 448: 438: 414: 385:Myrcia sylvatica 374:Cyperus rotundus 298:128-129 °C 287: 275: 269: 263: 256:Chemical formula 196: 195: 180: 178: 162: 151: 137: 117: 97: 73: 26: 19: 654: 653: 649: 648: 647: 645: 644: 643: 614: 613: 612: 611: 554: 552: 551: 507: 497: 496: 492: 470: 469: 462: 416: 415: 411: 406: 370: 366: 361:sesquiterpenoid 351: 344: 339: 323: 285: 272: 266: 258: 244: 241: 236: 235: 224: 221: 220: 217: 211: 210: 199: 189:DTXSID501318673 181: 174: 165: 152: 140: 120: 100: 87: 76: 63: 49: 41: 12: 11: 5: 652: 650: 642: 641: 636: 634:Sesquiterpenes 631: 626: 616: 615: 610: 609: 602: 595: 587: 584: 583: 566: 550: 549: 505: 490: 479:(2): 607–618. 460: 408: 407: 405: 402: 368: 364: 349: 346: 345: 340: 336:standard state 333: 330: 329: 324: 321: 318: 317: 313: 312: 306: 300: 299: 296: 290: 289: 283: 277: 276: 270: 264: 259: 254: 251: 250: 246: 245: 243: 242: 239: 231: 230: 229: 226: 225: 223: 222: 218: 215: 214: 206: 205: 204: 201: 200: 198: 197: 184: 182: 170: 167: 166: 164: 163: 155: 153: 145: 142: 141: 139: 138: 130: 128: 122: 121: 119: 118: 110: 108: 102: 101: 99: 98: 90: 88: 81: 78: 77: 75: 74: 66: 64: 59: 56: 55: 51: 50: 48:3-Copaen-2-one 47: 43: 42: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 651: 640: 637: 635: 632: 630: 627: 625: 622: 621: 619: 608: 603: 601: 596: 594: 589: 588: 582: 580: 576: 572: 567: 564: 560: 555: 545: 541: 536: 531: 526: 521: 517: 513: 509: 503: 494: 491: 486: 482: 478: 474: 467: 465: 461: 456: 452: 447: 442: 437: 432: 428: 424: 420: 413: 410: 403: 401: 399: 398: 393: 392: 387: 386: 381: 377: 375: 362: 359: 355: 343: 337: 331: 328: 325: 320: 319: 314: 311: 307: 305: 302: 301: 297: 295: 294:Boiling point 292: 291: 284: 282: 279: 278: 260: 257: 253: 252: 247: 238: 234: 227: 213: 209: 202: 194: 190: 186: 185: 183: 173: 169: 168: 161: 157: 156: 154: 148: 144: 143: 136: 132: 131: 129: 127: 124: 123: 116: 112: 111: 109: 107: 104: 103: 96: 92: 91: 89: 85: 80: 79: 72: 68: 67: 65: 62: 58: 57: 52: 44: 38: 34: 29: 25: 20: 579:expanding it 568: 553: 518:(11): 2687. 515: 511: 501: 493: 476: 472: 426: 422: 412: 395: 389: 384: 372: 353: 352: 54:Identifiers 46:Other names 473:Tetrahedron 310:cyclohexane 308:Soluble in 249:Properties 115:CHEBI:66416 618:Categories 404:References 304:Solubility 281:Molar mass 126:ChemSpider 82:3D model ( 61:CAS Number 37:IUPAC name 17:Mustakone 512:Molecules 429:(2): 27. 423:Medicines 354:Mustakone 71:1209-91-2 544:32527068 455:28930242 358:tricylic 160:12313013 135:28639001 629:Ketones 535:7321242 446:5590063 327:Copaene 286:218.340 147:PubChem 542:  532:  453:  443:  394:, and 233:SMILES 31:Names 573:is a 380:Hindi 356:is a 208:InChI 106:ChEBI 84:JSmol 575:stub 540:PMID 451:PMID 530:PMC 520:doi 481:doi 441:PMC 431:doi 177:EPA 150:CID 620:: 538:. 528:. 516:25 514:. 510:. 477:21 475:. 463:^ 449:. 439:. 425:. 421:. 400:. 388:, 369:22 365:15 271:22 265:15 606:e 599:t 592:v 581:. 546:. 522:: 506:2 500:" 487:. 483:: 457:. 433:: 427:4 376:, 367:H 274:O 268:H 262:C 179:) 175:( 86:)

Index


IUPAC name
CAS Number
1209-91-2
JSmol
Interactive image
ChEBI
CHEBI:66416
ChemSpider
28639001
PubChem
12313013
CompTox Dashboard
DTXSID501318673
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Boiling point
Solubility
cyclohexane
Copaene
standard state
Infobox references
tricylic
sesquiterpenoid
Cyperus rotundus
Hindi
Myrcia sylvatica

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.