Knowledge (XXG)

Cephaeline

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InChI=1S/C28H38N2O4/c1-5-17-16-30-9-7-19-13-27(33-3)28(34-4)15-22(19)24(30)11-20(17)10-23-21-14-26(32-2)25(31)12-18(21)6-8-29-23/h12-15,17,20,23-24,29,31H,5-11,16H2,1-4H3/t17-,20-,23+,24-/m0/s1
506:
Cephaeline in the form of syrup of ipecac was once commonly recommended as an emergency treatment for accidental poisoning, but its use has been phased out due to its ineffectiveness.
452: 314: 289: 622: 524: 409: 632: 459: 232: 253: 549: 490:. Cephaeline induces vomiting by stimulating the stomach lining and is found in commercial products such as 175: 137: 480: 53: 43: 270: 83: 598: 637: 627: 588: 337: 157: 241: 491: 274: 179: 93: 430: 616: 168: 221: 575:
American Academy Of Pediatrics Committee On Injury, Violence (November 2003).
550:"Pharma Japan: Approval of 4 drugs including Seroquel recommended: CPAC panel" 523:
Lara, Alfonso; Valverde, Roberto; Gomez, Luis; Hidalgo, Nancy (July 1, 2003).
392: 371: 148: 593: 576: 486: 602: 62:)-1-{isoquinolin-2-yl]methyl}-7-methoxy-1,2,3,4-tetrahydroisoquinolin-6-ol 475: 17: 495: 208: 30: 128: 429:
Except where otherwise noted, data are given for materials in their
196: 116: 106: 187: 525:"Micropropagacion de la planta medicinal psychotria acuminata" 258: 447: 577:"Policy statement: Poison treatment in the home" 322:CC1CN2CCc3cc(c(cc32C1C4c5cc(c(cc5CCN4)O)OC)OC)OC 220: 92: 71:Cepheline; Desmethylemetine; Dihydropsychotrine 8: 273: 178: 156: 22: 592: 240: 494:. Chemically, it is closely related to 515: 319: 294: 269: 169: 301:Key: DTGZHCFJNDAHEN-OZEXIGSWSA-N 136: 7: 211: 195: 484:and other plant species including 14: 437: 355: 349: 29: 433:(at 25 °C , 100 kPa). 47:7′,10,11-Trimethoxyemetan-6′-ol 410:Occupational safety and health 361: 343: 1: 654: 554:Chemical Business Newsbase 15: 427: 407: 402: 330: 310: 285: 76: 68: 52: 42: 37: 28: 16:Not to be confused with 594:10.1542/peds.112.5.1182 529:Agronomía Costarricense 623:Isoquinoline alkaloids 481:Cephaelis ipecacuanha 387:White silky crystals 54:Systematic IUPAC name 633:Norsalsolinol ethers 487:Psychotria acuminata 556:. November 14, 2000 423:Emetic / poisonous 379: g·mol 25: 460:Infobox references 23: 478:that is found in 468:Chemical compound 466: 465: 254:CompTox Dashboard 118:Interactive image 645: 607: 606: 596: 587:(5): 1182–1185. 572: 566: 565: 563: 561: 546: 540: 539: 537: 535: 520: 502:Poison treatment 450: 444: 441: 440: 378: 363: 357: 351: 345: 338:Chemical formula 278: 277: 262: 260: 244: 224: 213: 199: 182: 171: 160: 140: 120: 96: 33: 26: 653: 652: 648: 647: 646: 644: 643: 642: 613: 612: 611: 610: 574: 573: 569: 559: 557: 548: 547: 543: 533: 531: 522: 521: 517: 512: 504: 492:syrup of ipecac 469: 462: 457: 456: 455:  ?) 446: 442: 438: 434: 420: 376: 366: 360: 354: 348: 340: 326: 323: 318: 317: 306: 303: 302: 299: 293: 292: 281: 271:DTXSID501016520 263: 256: 247: 227: 214: 202: 163: 143: 123: 110: 99: 86: 72: 64: 63: 48: 21: 12: 11: 5: 651: 649: 641: 640: 635: 630: 625: 615: 614: 609: 608: 567: 541: 514: 513: 511: 508: 503: 500: 467: 464: 463: 458: 436: 435: 431:standard state 428: 425: 424: 421: 418: 415: 414: 405: 404: 400: 399: 396: 389: 388: 385: 381: 380: 374: 368: 367: 364: 358: 352: 346: 341: 336: 333: 332: 328: 327: 325: 324: 321: 313: 312: 311: 308: 307: 305: 304: 300: 297: 296: 288: 287: 286: 283: 282: 280: 279: 266: 264: 252: 249: 248: 246: 245: 237: 235: 229: 228: 226: 225: 217: 215: 207: 204: 203: 201: 200: 192: 190: 184: 183: 173: 165: 164: 162: 161: 153: 151: 145: 144: 142: 141: 133: 131: 125: 124: 122: 121: 113: 111: 104: 101: 100: 98: 97: 89: 87: 82: 79: 78: 74: 73: 70: 66: 65: 57: 56: 50: 49: 46: 40: 39: 35: 34: 13: 10: 9: 6: 4: 3: 2: 650: 639: 636: 634: 631: 629: 626: 624: 621: 620: 618: 604: 600: 595: 590: 586: 582: 578: 571: 568: 555: 551: 545: 542: 530: 526: 519: 516: 509: 507: 501: 499: 497: 493: 489: 488: 483: 482: 477: 473: 461: 454: 449: 432: 426: 422: 417: 416: 412: 411: 406: 401: 397: 394: 391: 390: 386: 383: 382: 375: 373: 370: 369: 342: 339: 335: 334: 329: 320: 316: 309: 295: 291: 284: 276: 272: 268: 267: 265: 255: 251: 250: 243: 239: 238: 236: 234: 231: 230: 223: 219: 218: 216: 210: 206: 205: 198: 194: 193: 191: 189: 186: 185: 181: 177: 174: 172: 170:ECHA InfoCard 167: 166: 159: 155: 154: 152: 150: 147: 146: 139: 135: 134: 132: 130: 127: 126: 119: 115: 114: 112: 108: 103: 102: 95: 91: 90: 88: 85: 81: 80: 75: 67: 61: 55: 51: 45: 41: 36: 32: 27: 19: 584: 580: 570: 558:. Retrieved 553: 544: 532:. Retrieved 528: 518: 505: 485: 479: 471: 470: 419:Main hazards 408: 138:ChEMBL255708 77:Identifiers 69:Other names 59: 560:26 December 534:26 December 413:(OHS/OSH): 395:in ethanol 384:Appearance 331:Properties 176:100.006.902 24:Cephaeline 617:Categories 581:Pediatrics 510:References 472:Cephaeline 393:Solubility 372:Molar mass 242:QA971541A1 149:ChemSpider 105:3D model ( 84:CAS Number 44:IUPAC name 603:14595067 476:alkaloid 403:Hazards 398:Soluble 94:483-17-0 18:cephalin 638:Emetics 628:Phenols 496:emetine 453:what is 451: ( 377:466.622 209:PubChem 601:  474:is an 448:verify 445:  315:SMILES 222:442195 197:C09390 158:390702 129:ChEMBL 38:Names 290:InChI 107:JSmol 599:PMID 562:2009 536:2009 233:UNII 188:KEGG 589:doi 585:112 259:EPA 212:CID 619:: 597:. 583:. 579:. 552:. 527:. 498:. 353:38 347:28 58:(1 605:. 591:: 564:. 538:. 443:Y 365:4 362:O 359:2 356:N 350:H 344:C 261:) 257:( 109:) 60:R 20:.

Index

cephalin

IUPAC name
Systematic IUPAC name
CAS Number
483-17-0
JSmol
Interactive image
ChEMBL
ChEMBL255708
ChemSpider
390702
ECHA InfoCard
100.006.902
Edit this at Wikidata
KEGG
C09390
PubChem
442195
UNII
QA971541A1
CompTox Dashboard
DTXSID501016520
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Solubility
Occupational safety and health

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