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Oxaline

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InChI=1S/C24H25N5O4/c1-6-22(2,3)23-12-19(32-4)21(31)28-18(11-15-13-25-14-26-15)20(30)27-24(23,28)29(33-5)17-10-8-7-9-16(17)23/h6-14H,1H2,2-5H3,(H,25,26)(H,27,30)/b18-11+/t23-,24-/m1/s1
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InChI=1/C24H25N5O4/c1-6-22(2,3)23-12-19(32-4)21(31)28-18(11-15-13-25-14-26-15)20(30)27-24(23,28)29(33-5)17-10-8-7-9-16(17)23/h6-14H,1H2,2-5H3,(H,25,26)(H,27,30)/b18-11+/t23-,24-/m1/s1
472: 226: 438: 191: 431: 155: 482: 304: 467: 457: 487: 424: 352:"Oxaline, a fungal alkaloid, arrests the cell cycle in M phase by inhibition of tubulin polymerization" 172: 462: 44: 373: 118: 477: 363: 249: 54: 176: 98: 408: 298: 451: 143: 368: 351: 396: 283: 109: 330: 17: 377: 404: 321: 130: 297:
Except where otherwise noted, data are given for materials in their
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CC(C)(C=C)12C=C(C(=O)N\31(NC(=O)/C3=C\c4ccn4)N(c5c2cccc5)OC)OC
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Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
160: 412: 350:Koizumi, Y; Arai, M; Tomoda, H; Omura, S (2004). 142: 53: 432: 319:is a fungal isolate with anticancer activity 8: 439: 425: 175: 117: 22: 367: 342: 231: 196: 171: 203:Key: SOHAVULMGIITDH-SSDCDQDPSA-N 97: 7: 393: 391: 473:Heterocyclic compounds with 4 rings 213:Key: SOHAVULMGIITDH-SSDCDQDPBU 133: 16:For the short for glyoxaline, see 14: 395: 267: 261: 29: 301:(at 25 °C , 100 kPa). 273: 255: 1: 411:. You can help Knowledge by 369:10.1016/j.bbamcr.2004.04.013 504: 390: 329:-methylated derivative of 15: 295: 242: 222: 187: 37: 28: 403:This article about an 291: g·mol 25: 305:Infobox references 23: 483:Methoxy compounds 420: 419: 313:Chemical compound 311: 310: 156:CompTox Dashboard 79:Interactive image 495: 468:Indole alkaloids 441: 434: 427: 399: 392: 382: 381: 371: 347: 290: 275: 269: 263: 257: 250:Chemical formula 180: 179: 164: 162: 146: 135: 121: 101: 81: 57: 33: 26: 503: 502: 498: 497: 496: 494: 493: 492: 458:Allyl compounds 448: 447: 446: 445: 388: 386: 385: 349: 348: 344: 339: 314: 307: 302: 288: 278: 272: 266: 260: 252: 238: 235: 230: 229: 218: 215: 214: 211: 205: 204: 201: 195: 194: 183: 165: 158: 149: 136: 124: 104: 84: 71: 60: 47: 21: 12: 11: 5: 501: 499: 491: 490: 488:Alkaloid stubs 485: 480: 475: 470: 465: 460: 450: 449: 444: 443: 436: 429: 421: 418: 417: 400: 384: 383: 341: 340: 338: 335: 312: 309: 308: 303: 299:standard state 296: 293: 292: 286: 280: 279: 276: 270: 264: 258: 253: 248: 245: 244: 240: 239: 237: 236: 233: 225: 224: 223: 220: 219: 217: 216: 212: 209: 208: 206: 202: 199: 198: 190: 189: 188: 185: 184: 182: 181: 173:DTXSID60893990 168: 166: 154: 151: 150: 148: 147: 139: 137: 129: 126: 125: 123: 122: 114: 112: 106: 105: 103: 102: 94: 92: 86: 85: 83: 82: 74: 72: 65: 62: 61: 59: 58: 50: 48: 43: 40: 39: 35: 34: 13: 10: 9: 6: 4: 3: 2: 500: 489: 486: 484: 481: 479: 476: 474: 471: 469: 466: 464: 461: 459: 456: 455: 453: 442: 437: 435: 430: 428: 423: 422: 416: 414: 410: 406: 401: 398: 394: 389: 379: 375: 370: 365: 361: 357: 353: 346: 343: 336: 334: 332: 328: 324: 323: 318: 306: 300: 294: 287: 285: 282: 281: 254: 251: 247: 246: 241: 232: 228: 221: 207: 197: 193: 186: 178: 174: 170: 169: 167: 157: 153: 152: 145: 141: 140: 138: 132: 128: 127: 120: 116: 115: 113: 111: 108: 107: 100: 96: 95: 93: 91: 88: 87: 80: 76: 75: 73: 69: 64: 63: 56: 52: 51: 49: 46: 42: 41: 36: 32: 27: 19: 413:expanding it 402: 387: 362:(1): 47–55. 359: 355: 345: 326: 320: 316: 315: 38:Identifiers 325:. It is an 243:Properties 99:CHEBI:70400 463:Imidazoles 452:Categories 337:References 284:Molar mass 110:ChemSpider 66:3D model ( 55:55623-37-5 45:CAS Number 331:meleagrin 18:Imidazole 405:alkaloid 378:15276324 322:in vitro 119:10225680 24:Oxaline 478:Lactams 317:Oxaline 289:447.495 144:6438440 131:PubChem 376:  227:SMILES 407:is a 192:InChI 90:ChEBI 68:JSmol 409:stub 374:PMID 360:1693 364:doi 161:EPA 134:CID 454:: 372:. 358:. 354:. 333:. 265:25 259:24 440:e 433:t 426:v 415:. 380:. 366:: 327:O 277:4 274:O 271:5 268:N 262:H 256:C 163:) 159:( 70:) 20:.

Index

Imidazole

CAS Number
55623-37-5
JSmol
Interactive image
ChEBI
CHEBI:70400
ChemSpider
10225680
PubChem
6438440
CompTox Dashboard
DTXSID60893990
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
in vitro
meleagrin
"Oxaline, a fungal alkaloid, arrests the cell cycle in M phase by inhibition of tubulin polymerization"
doi
10.1016/j.bbamcr.2004.04.013
PMID
15276324
Stub icon
alkaloid

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