236:
468:
35:
137:
429:
Gülçin, I.; Beydemir, S.; Topal, F.; Gagua, N.; Bakuridze, A.; Bayram, R.; Gepdiremen, A. (2012). "Apoptotic, antioxidant and antiradical effects of majdine and isomajdine from Vinca herbacea Waldst. and kit".
259:
InChI=1S/C23H28N2O6/c1-12-14-10-25-8-7-23(18(25)9-13(14)15(11-31-12)21(26)30-4)16-5-6-17(28-2)20(29-3)19(16)24-22(23)27/h5-6,11-14,18H,7-10H2,1-4H3,(H,24,27)/t12-,13-,14-,18-,23+/m0/s1
269:
InChI=1/C23H28N2O6/c1-12-14-10-25-8-7-23(18(25)9-13(14)15(11-31-12)21(26)30-4)16-5-6-17(28-2)20(29-3)19(16)24-22(23)27/h5-6,11-14,18H,7-10H2,1-4H3,(H,24,27)/t12-,13-,14-,18-,23+/m0/s1
285:
528:
509:
250:
363:
502:
214:
538:
543:
533:
495:
157:
57:
47:
231:
103:
447:
177:
479:
439:
308:
113:
235:
411:
390:
357:
522:
202:
443:
384:
467:
342:
168:
451:
17:
475:
379:
189:
82:)-6,7-dimethoxy-1′-methyl-2-oxo-1,2,4′a,5′,5′a,7′,8′,10′a-octahydro-1′
148:
51:
Methyl 11,12-dimethoxy-19α-methyl-2-oxo-20α-formosanan-16-carboxylate
356:
Except where otherwise noted, data are given for materials in their
34:
136:
126:
219:
483:
293:
C12CN3CC4(3C2C(=CO1)C(=O)OC)C5=C(C(=C(C=C5)OC)OC)NC4=O
432:
Journal of Enzyme
Inhibition and Medicinal Chemistry
201:
112:
503:
8:
510:
496:
234:
176:
26:
403:
290:
255:
230:
262:Key: TTZWEOINXHJHCY-UHJVZONPSA-N
156:
7:
464:
462:
272:Key: TTZWEOINXHJHCY-UHJVZONPBK
192:
482:. You can help Knowledge (XXG) by
25:
466:
326:
320:
90:-spiroindolizine]-4′-carboxylate
33:
360:(at 25 °C , 100 kPa).
529:Alkaloids found in Apocynaceae
332:
314:
1:
444:10.3109/14756366.2011.604318
560:
461:
354:
301:
281:
246:
96:
56:
46:
41:
32:
412:"Majdine Mass Spectrum"
474:This article about an
58:Systematic IUPAC name
350: g·mol
29:
364:Infobox references
27:
539:Methoxy compounds
491:
490:
372:Chemical compound
370:
369:
215:CompTox Dashboard
138:Interactive image
16:(Redirected from
551:
512:
505:
498:
470:
463:
456:
455:
426:
420:
419:
408:
349:
334:
328:
322:
316:
309:Chemical formula
239:
238:
223:
221:
205:
194:
180:
160:
140:
116:
37:
30:
21:
559:
558:
554:
553:
552:
550:
549:
548:
519:
518:
517:
516:
460:
459:
428:
427:
423:
410:
409:
405:
400:
373:
366:
361:
347:
337:
331:
325:
319:
311:
297:
294:
289:
288:
277:
274:
273:
270:
264:
263:
260:
254:
253:
242:
232:DTXSID101045723
224:
217:
208:
195:
183:
163:
143:
130:
119:
106:
92:
91:
52:
23:
22:
15:
12:
11:
5:
557:
555:
547:
546:
544:Alkaloid stubs
541:
536:
531:
521:
520:
515:
514:
507:
500:
492:
489:
488:
471:
458:
457:
438:(4): 587–594.
421:
402:
401:
399:
396:
391:Vinca herbacea
382:isolated from
371:
368:
367:
362:
358:standard state
355:
352:
351:
345:
339:
338:
335:
329:
323:
317:
312:
307:
304:
303:
299:
298:
296:
295:
292:
284:
283:
282:
279:
278:
276:
275:
271:
268:
267:
265:
261:
258:
257:
249:
248:
247:
244:
243:
241:
240:
227:
225:
213:
210:
209:
207:
206:
198:
196:
188:
185:
184:
182:
181:
173:
171:
165:
164:
162:
161:
153:
151:
145:
144:
142:
141:
133:
131:
124:
121:
120:
118:
117:
109:
107:
102:
99:
98:
94:
93:
61:
60:
54:
53:
50:
44:
43:
39:
38:
24:
14:
13:
10:
9:
6:
4:
3:
2:
556:
545:
542:
540:
537:
535:
534:Methyl esters
532:
530:
527:
526:
524:
513:
508:
506:
501:
499:
494:
493:
487:
485:
481:
477:
472:
469:
465:
453:
449:
445:
441:
437:
433:
425:
422:
417:
413:
407:
404:
397:
395:
393:
392:
387:
386:
381:
377:
365:
359:
353:
346:
344:
341:
340:
313:
310:
306:
305:
300:
291:
287:
280:
266:
256:
252:
245:
237:
233:
229:
228:
226:
216:
212:
211:
204:
200:
199:
197:
191:
187:
186:
179:
175:
174:
172:
170:
167:
166:
159:
158:ChEMBL2333535
155:
154:
152:
150:
147:
146:
139:
135:
134:
132:
128:
123:
122:
115:
111:
110:
108:
105:
101:
100:
95:
89:
85:
81:
77:
73:
69:
65:
59:
55:
49:
45:
40:
36:
31:
19:
484:expanding it
473:
435:
431:
424:
415:
406:
389:
383:
375:
374:
97:Identifiers
87:
83:
79:
75:
71:
67:
63:
416:massbank.eu
385:Vinca minor
302:Properties
523:Categories
398:References
343:Molar mass
169:ChemSpider
125:3D model (
114:20497-42-1
104:CAS Number
62:Methyl (1′
48:IUPAC name
18:C23H28N2O6
476:alkaloid
452:21883037
380:alkaloid
203:21627963
178:10254858
28:Majdine
376:Majdine
348:428.485
190:PubChem
450:
378:is an
286:SMILES
149:ChEMBL
42:Names
478:is a
251:InChI
127:JSmol
78:,10′a
480:stub
448:PMID
388:and
86:,10′
74:,5′a
70:,4′a
440:doi
220:EPA
193:CID
525::
446:.
436:27
434:.
414:.
394:.
324:28
318:23
66:,3
511:e
504:t
497:v
486:.
454:.
442::
418:.
336:6
333:O
330:2
327:N
321:H
315:C
222:)
218:(
129:)
88:H
84:H
80:S
76:S
72:S
68:R
64:S
20:)
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
