About 6 results found for searched term "53-43-0" (0.056 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2699 | Fexofenadine hydrochloride | Histamine Receptor |
| MDL 16455A | ||
| Fexofenadine inhibits histamine H1 receptor with IC50 of 246 nM. | ||
| M5882 | Pirarubicin HCl | Topoisomerase |
| THP Hydrochloride | ||
| Pirarubicin Hcl is an analogue of the anthracycline anti-neoplastic doxorubicin, which is an inhibitor of Topo II. | ||
| M8375 | S 26948 | Others |
| S 26948 is a selective PPARγ modulator (SPPARγM). | ||
| M9061 | Dehydroepiandrosterone | Animal Modeling |
| DHEA; Prasterone; Dehydroisoandrosterone | ||
| Dehydroepiandrosterone is a potent anti-apoptotic factor with some degree of androgenic activity and is a low affinity (Ki = 1 micron) partial agonist for the androgen receptor (AR). In addition, Dehydroepiandrosterone can also be used to construct a rat polycystic ovary syndrome model. | ||
| M18234 | Syringetin-3-O-rutinoside | Others |
| Syringetin-3-O-rutinoside | ||
| M41613 | Topoisomerase II inhibitor 14 | Topoisomerase |
| Topoisomerase II inhibitor 14 is a potent inhibtor of Topoisomerase II, with anticancer activity. | ||
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