20:
409:
272:
Cole, Derek C.; Stock, Joseph R.; Lennox, William J.; Bernotas, Ronald C.; Ellingboe, John W.; Boikess, Steve; Coupet, Joseph; Smith, Deborah L.; Leung, Louis; Zhang, Guo-Ming; Feng, Xidong (2007-11-01). "Discovery of N1-(6-Chloroimidazothiazole-5-sulfonyl)tryptamine as a Potent, Selective, and
191:
Andreani, Aldo; Granaiola, Massimiliano; Leoni, Alberto; Locatelli, Alessandra; Morigi, Rita; Rambaldi, Mirella; Varoli, Lucilla; Lannigan, Deborah; Smith, Jeff; Scudiero, Dominic; Kondapaka, Sudhir (2011-09-01). "Imidazothiazole guanylhydrazones as RSK2 inhibitors ".
376:
Amarouch, Hamid; Loiseau, Philippe R; Bacha, Catarina; Caujolle, Raymond; Payard, Marc; Loiseau, Philippe M; Bories, Christian; Gayral, Philippe (1987-09-01). "Imidazothiazoles: analogues du lévamisole".
308:
Güzeldemirci, Nuray Ulusoy; Küçükbasmacı, Ömer (2010-01-01). "Synthesis and antimicrobial activity evaluation of new 1,2,4-triazoles and 1,3,4-thiadiazoles bearing imidazothiazole moiety".
237:
Park, Jin-Hun; El-Gamal, Mohammed I.; Lee, Yong Sup; Oh, Chang-Hyun (2011-12-01). "New imidazothiazole derivatives: Synthesis, in vitro anticancer evaluation, and in silico studies".
111:
Fascio, Mirta L.; Errea, María Inés; D'Accorso, Norma
Beatriz (2015-01-27). "Imidazothiazole and related heterocyclic systems. Synthesis, chemical and biological properties".
450:
156:
Gürsoy, Elif; Güzeldemirci, Nuray Ulusoy (2007-03-01). "Synthesis and primary cytotoxicity evaluation of new imidazothiazole derivatives".
345:"Synthesis, characterization and evaluation for antifungal activity of substituted diaryl imidazo [2, 1, b]-benzothiazole"
469:
474:
484:
479:
443:
19:
436:
325:
290:
254:
219:
173:
138:
420:
386:
356:
317:
282:
246:
209:
201:
165:
128:
120:
463:
390:
92:
76:
72:
416:
84:
321:
250:
205:
169:
124:
34:
361:
344:
80:
68:
50:
88:
38:
329:
294:
258:
223:
177:
142:
408:
63:
54:
42:
31:
214:
133:
286:
58:
46:
343:
Malik, Jitender K.; Soni, Himesh; Singhai, A.K. (2013-01-01).
16:
Class of chemical compounds comprising a bicyclic heterocycle
61:
atom. Imidazothiazole derivatives show a broad spectrum of
424:
30:are a class of chemical compounds containing a
444:
8:
451:
437:
23:The general structure of imidazothiazoles.
360:
213:
132:
37:(a double ring system) consisting of an
18:
379:European Journal of Medicinal Chemistry
310:European Journal of Medicinal Chemistry
273:Orally Active 5-HT6 Receptor Agonist".
239:European Journal of Medicinal Chemistry
194:European Journal of Medicinal Chemistry
158:European Journal of Medicinal Chemistry
113:European Journal of Medicinal Chemistry
103:
45:ring. The structure contains three non-
7:
405:
403:
423:. You can help Knowledge (XXG) by
95:, fungi and worms, respectively).
14:
407:
71:", activity such as anticancer,
275:Journal of Medicinal Chemistry
1:
391:10.1016/0223-5234(87)90037-7
349:Journal of Pharmacy Research
322:10.1016/j.ejmech.2009.09.024
251:10.1016/j.ejmech.2011.08.024
206:10.1016/j.ejmech.2011.07.001
170:10.1016/j.ejmech.2006.10.012
125:10.1016/j.ejmech.2014.12.012
501:
402:
362:10.1016/j.jopr.2013.01.002
419:-related article is a
24:
470:Nitrogen heterocycles
22:
475:Sulfur heterocycles
485:Pharmacology stubs
25:
432:
431:
287:10.1021/jm070521y
281:(23): 5535–5538.
245:(12): 5769–5777.
87:(against cancer,
492:
480:Imidazothiazoles
453:
446:
439:
411:
404:
395:
394:
373:
367:
366:
364:
340:
334:
333:
305:
299:
298:
269:
263:
262:
234:
228:
227:
217:
200:(9): 4311–4323.
188:
182:
181:
153:
147:
146:
136:
108:
41:ring fused to a
28:Imidazothiazoles
500:
499:
495:
494:
493:
491:
490:
489:
460:
459:
458:
457:
400:
398:
375:
374:
370:
342:
341:
337:
307:
306:
302:
271:
270:
266:
236:
235:
231:
190:
189:
185:
155:
154:
150:
110:
109:
105:
101:
67:, i.e. "in the
17:
12:
11:
5:
498:
496:
488:
487:
482:
477:
472:
462:
461:
456:
455:
448:
441:
433:
430:
429:
412:
397:
396:
385:(5): 463–466.
368:
335:
300:
264:
229:
183:
164:(3): 320–326.
148:
102:
100:
97:
93:microorganisms
57:atoms and one
15:
13:
10:
9:
6:
4:
3:
2:
497:
486:
483:
481:
478:
476:
473:
471:
468:
467:
465:
454:
449:
447:
442:
440:
435:
434:
428:
426:
422:
418:
413:
410:
406:
401:
392:
388:
384:
381:(in French).
380:
372:
369:
363:
358:
354:
350:
346:
339:
336:
331:
327:
323:
319:
315:
311:
304:
301:
296:
292:
288:
284:
280:
276:
268:
265:
260:
256:
252:
248:
244:
240:
233:
230:
225:
221:
216:
211:
207:
203:
199:
195:
187:
184:
179:
175:
171:
167:
163:
159:
152:
149:
144:
140:
135:
130:
126:
122:
118:
114:
107:
104:
98:
96:
94:
90:
86:
82:
78:
77:antimicrobial
74:
73:antipsychotic
70:
66:
65:
60:
56:
52:
48:
44:
40:
36:
33:
29:
21:
425:expanding it
417:pharmacology
414:
399:
382:
378:
371:
355:(1): 39–46.
352:
348:
338:
316:(1): 63–68.
313:
309:
303:
278:
274:
267:
242:
238:
232:
215:11585/105011
197:
193:
186:
161:
157:
151:
116:
112:
106:
85:anthelmintic
62:
27:
26:
134:11336/17776
119:: 666–683.
51:heteroatoms
35:heterocycle
464:Categories
99:References
81:antifungal
69:petri dish
89:psychosis
39:imidazole
330:19939519
295:17948978
259:22033063
224:21794960
178:17145120
143:25499987
64:in vitro
55:nitrogen
43:thiazole
32:bicyclic
328:
293:
257:
222:
176:
141:
83:, and
59:sulfur
53:: two
47:carbon
415:This
421:stub
326:PMID
291:PMID
255:PMID
220:PMID
174:PMID
139:PMID
387:doi
357:doi
318:doi
283:doi
247:doi
210:hdl
202:doi
166:doi
129:hdl
121:doi
49:or
466::
383:22
351:.
347:.
324:.
314:45
312:.
289:.
279:50
277:.
253:.
243:46
241:.
218:.
208:.
198:46
196:.
172:.
162:42
160:.
137:.
127:.
117:90
115:.
91:,
79:,
75:,
452:e
445:t
438:v
427:.
393:.
389::
365:.
359::
353:7
332:.
320::
297:.
285::
261:.
249::
226:.
212::
204::
180:.
168::
145:.
131::
123::
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.