טוען...
Triphenylbutanamines: Kinesin Spindle Protein Inhibitors with in Vivo Antitumor Activity†
[Image: see text] The human mitotic kinesin Eg5 represents a novel mitotic spindle target for cancer chemotherapy. We previously identified S-trityl-l-cysteine (STLC) and related analogues as selective potent inhibitors of Eg5. We herein report on the development of a series of 4,4,4-triphenylbutan-...
שמור ב:
| Main Authors: | , , , , , , |
|---|---|
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Chemical
Society
2012
|
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3428805/ https://ncbi.nlm.nih.gov/pubmed/22248262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm201195m |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|