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Prostratin

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In 2010, AIDS Research Alliance in Los Angeles, California announced that it signed a new licensing agreement with Stanford University, transferring exclusive rights of the technology developed by the Stanford research team. Phase I human
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and a team at the U.S. National Cancer Institute. Samoan healers use the mamala tree to treat hepatitis. Research indicated that prostratin has potential to be useful in the treatment of
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InChI=1S/C22H30O6/c1-11-6-16-20(26,18(11)25)9-14(10-23)7-15-17-19(4,5)21(17,28-13(3)24)8-12(2)22(15,16)27/h6-7,12,15-17,23,26-27H,8-10H2,1-5H3/t12-,15+,16-,17-,20-,21+,22-/m1/s1
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InChI=1/C22H30O6/c1-11-6-16-20(26,18(11)25)9-14(10-23)7-15-17-19(4,5)21(17,28-13(3)24)8-12(2)22(15,16)27/h6-7,12,15-17,23,26-27H,8-10H2,1-5H3/t12-,15+,16-,17-,20-,21+,22-/m1/s1
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Prostratin is of interest because of its unique ability to activate latent viral reservoirs, while preventing healthy cells from infection, as well as its discovery through
697: 541: 486:. Pioneering agreements to protect indigenous intellectual property rights of the Samoan people were established between the Samoan government and the 376: 597: 517:. This practical synthesis produces gram quantities of prostratin, and is a major step forward in pharmaceutical development of prostratin. 296: 707: 554:
Wang, Man-Tzu; Holderfield, Matthew; Galeas, Jacqueline; Delrosario, Reyno; To, Minh D.; Balmain, Allan; McCormick, Frank (2015).
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Press Release-AIDS Research Alliance Gains Exclusive Rights To New Technology from Stanford University
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of prostratin will be carried out by the AIDS ReSearch Alliance in Los Angeles, California.
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and UC Berkeley agreed to share equally in any commercial proceeds from the gene product.
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is trying to isolate the gene sequence responsible for prostratin biosynthesis.
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Except where otherwise noted, data are given for materials in their
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U.S. University Shares Drug Royalties with Samoa for Tree Gene
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Berkeley searches for AIDS cure in a Samoan indigenous tree
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In 2008, a team at Stanford University led by chemist
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O=C1\C(=C/23(O)(/C=C(/CO)C12O)4(OC(=O)C)(C3C)C4(C)C)C
617:; Jung-Min Kee; Jeffrey M. Warrington (May 2008). 402:activator found in the bark of the mamala tree of 714: 192: 103: 678:Paul Wender and Stanford Prostratin synthesis 245: 167: 650: 571: 542:Prostratin and the AIDS Research Alliance 212: 241: 715: 448:as it could flush viral reservoirs in 273:Key: BOJKFRKNLSCGHY-HXGSDTCMSA-N 147: 604:, AIDS Research Alliance, 2001-12-13 73:-cyclopropabenzoazulen-9a-yl acetate 509:has published an elegant four-step 283:Key: BOJKFRKNLSCGHY-HXGSDTCMBJ 183: 13: 492:University of California, Berkeley 14: 754: 683:Jay Keasling and Prostratin Genes 671: 693:Prostratin Agreements with Samoa 361: 22: 357:(at 25 °C , 100 kPa). 607: 588: 547: 544:, AIDS Research Alliance, 2006 535: 1: 528: 7: 477: 10: 759: 573:10.1016/j.cell.2015.10.041 420:from species of the genus 347:390.47 g/mol 82:12-Deoxyphorbol-13-acetate 440:village by ethnobotanist 351: 312: 292: 257: 87: 79: 35: 30: 21: 595:Prostratin Press Release 643:10.1126/science.1154690 688:Ethnobotanist Paul Cox 488:AIDS Research Alliance 436:of Samoan healers in 434:traditional knowledge 494:where a team led by 37:Preferred IUPAC name 635:2008Sci...320..649W 513:of prostratin from 468:Alzheimer's disease 18: 511:chemical synthesis 458:As a modulator of 409:Homalanthus nutans 384:Infobox references 16: 629:(5876): 649–652. 450:latently infected 392:Chemical compound 390: 389: 226:CompTox Dashboard 129:Interactive image 750: 665: 664: 654: 611: 605: 592: 586: 585: 575: 566:(5): 1237–1251. 551: 545: 539: 472:pancreatic tumor 460:protein kinase C 400:protein kinase C 374: 368: 365: 364: 320:Chemical formula 250: 249: 234: 232: 216: 196: 185: 171: 151: 131: 107: 26: 19: 15: 758: 757: 753: 752: 751: 749: 748: 747: 713: 712: 674: 669: 668: 612: 608: 593: 589: 552: 548: 540: 536: 531: 523:clinical trials 480: 393: 386: 381: 380: 379:  ?) 370: 366: 362: 358: 336: 332: 328: 322: 308: 305: 300: 299: 288: 285: 284: 281: 275: 274: 271: 265: 264: 253: 235: 228: 219: 199: 186: 174: 154: 134: 121: 110: 97: 83: 75: 74: 12: 11: 5: 756: 746: 745: 743:Phorbol esters 740: 735: 730: 725: 723:Acetate esters 711: 710: 705: 700: 695: 690: 685: 680: 673: 672:External links 670: 667: 666: 615:Paul A. Wender 606: 600:2007-01-06 at 587: 546: 533: 532: 530: 527: 479: 476: 391: 388: 387: 382: 360: 359: 355:standard state 352: 349: 348: 345: 339: 338: 334: 330: 326: 323: 318: 315: 314: 310: 309: 307: 306: 303: 295: 294: 293: 290: 289: 287: 286: 282: 279: 278: 276: 272: 269: 268: 260: 259: 258: 255: 254: 252: 251: 243:DTXSID10893788 238: 236: 224: 221: 220: 218: 217: 209: 207: 201: 200: 198: 197: 189: 187: 179: 176: 175: 173: 172: 164: 162: 156: 155: 153: 152: 144: 142: 136: 135: 133: 132: 124: 122: 115: 112: 111: 109: 108: 100: 98: 93: 90: 89: 85: 84: 81: 77: 76: 40: 39: 33: 32: 28: 27: 9: 6: 4: 3: 2: 755: 744: 741: 739: 738:Cyclopentenes 736: 734: 733:Cyclopropanes 731: 729: 726: 724: 721: 720: 718: 709: 706: 704: 701: 699: 696: 694: 691: 689: 686: 684: 681: 679: 676: 675: 662: 658: 653: 648: 644: 640: 636: 632: 628: 624: 620: 616: 610: 603: 602:archive.today 599: 596: 591: 583: 579: 574: 569: 565: 561: 557: 550: 543: 538: 534: 526: 524: 518: 516: 512: 508: 503: 501: 497: 493: 489: 485: 475: 473: 469: 465: 461: 456: 454: 451: 447: 443: 442:Paul Alan Cox 439: 435: 431: 427: 423: 419: 418:phorbol ester 415: 414:Euphorbiaceae 411: 410: 405: 401: 397: 385: 378: 373: 356: 350: 346: 344: 341: 340: 324: 321: 317: 316: 311: 302: 301: 298: 291: 277: 267: 266: 263: 256: 248: 244: 240: 239: 237: 227: 223: 222: 215: 211: 210: 208: 206: 203: 202: 195: 191: 190: 188: 182: 178: 177: 170: 166: 165: 163: 161: 158: 157: 150: 146: 145: 143: 141: 138: 137: 130: 126: 125: 123: 119: 114: 113: 106: 102: 101: 99: 96: 92: 91: 86: 78: 72: 68: 64: 60: 56: 52: 48: 44: 38: 34: 29: 25: 20: 626: 622: 609: 590: 563: 559: 549: 537: 519: 504: 496:Jay Keasling 481: 457: 453:CD4+ T-cells 421: 407: 395: 394: 149:ChEMBL170518 88:Identifiers 80:Other names 70: 66: 62: 58: 54: 50: 46: 42: 507:Paul Wender 484:ethnobotany 426:Thymelaceae 313:Properties 17:Prostratin 728:Diterpenes 717:Categories 529:References 396:Prostratin 343:Molar mass 214:KO94U6DIQ6 160:ChemSpider 116:3D model ( 105:60857-08-1 95:CAS Number 438:Falealupo 430:Australia 661:18451298 598:Archived 582:26590425 478:Overview 652:2704988 631:Bibcode 623:Science 515:phorbol 422:Pimelea 377:what is 375: ( 337: 181:PubChem 659:  649:  580:  464:cancer 372:verify 369:  297:SMILES 194:454217 169:399975 140:ChEMBL 31:Names 500:Samoa 428:) in 404:Samoa 398:is a 262:InChI 118:JSmol 657:PMID 578:PMID 560:Cell 466:and 205:UNII 647:PMC 639:doi 627:320 568:doi 564:163 446:HIV 231:EPA 184:CID 65:,9a 57:,7b 53:,7a 49:,4a 45:,1b 41:(1a 719:: 655:. 645:. 637:. 625:. 621:. 576:. 562:. 558:. 474:. 455:. 406:, 331:30 327:22 61:,8 663:. 641:: 633:: 584:. 570:: 424:( 412:( 367:N 335:6 333:O 329:H 325:C 233:) 229:( 120:) 71:H 67:S 63:R 59:R 55:S 51:R 47:S 43:R

Index


Preferred IUPAC name
CAS Number
60857-08-1
JSmol
Interactive image
ChEMBL
ChEMBL170518
ChemSpider
399975
PubChem
454217
UNII
KO94U6DIQ6
CompTox Dashboard
DTXSID10893788
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
verify
what is
Infobox references
protein kinase C
Samoa
Homalanthus nutans
Euphorbiaceae
phorbol ester

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