About 11 results found for searched term "57-62-5" (0.057 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M6305 | Olverembatinib | Src-bcr-Abl |
| GZD824; HQP1351 | ||
| Olverembatinib is a novel orally bioavailable Bcr-Abl inhibitor for Bcr-Abl(WT) and Bcr-Abl(T315I) with IC50 of 0.34 nM and 0.68 nM, respectively. | ||
| M7512 | Chlorotetracycline | Antibiotic |
| Aureomycin; U-6780 | ||
| Chlortetracycline is a tetracycline antibiotic and commonly used to treat conjunctivitis in cats. | ||
| M10958 | JNJ-63576253 | Androgen Receptor |
| TRC-253 | ||
| JNJ-63576253 (TRC-253) is a potent and orally active complete antagonist of the androgen receptor against F877L mutant AR and wild-type AR in LNCaP cells IC50 The values are 37 and 54 nM, respectively. JNJ-63576253 can be used in the study of castration-resistant prostate cancer (CRPC). | ||
| M10976 | Moslosooflavone | ROS |
| Moslosooflavoneone is a flavonoid isolated from snow lotus. Moslofoflavone has anti-hypoxic and anti-inflammatory activities. | ||
| M21840 | Alvimopan monohydrate | Others |
| Alvimopan monohydrate | ||
| M28071 | S116836 | Src-bcr-Abl |
| S116836, a potent, orally active BCR-ABL tyrosine kinase inhibitor, blocks both wild-type as well as T315I Bcr-Abl. S116836 arrests the cells in the G0/G1 phase of cell cycle, induces apoptosis, increases ROS production, and decreases GSH production in BaF3/WT and BaF3/T315I cells. S116836 also inhibits SRC, LYN, HCK, LCK and BLK, and receptor tyrosine kinases such as FLT3, TIE2, KIT, PDGFR-β. Antitumor activies. | ||
| M28616 | Rezvilutamide | Androgen Receptor |
| SHR3680 | ||
| Rezvilutamide (SHR3680) is an androgen receptor antagonist. Rezvilutamide (SHR3680) is used for the study of prostate cancer. | ||
| M29067 | Farglitazar | PPAR |
| GI262570; GI262570X | ||
| Farglitazar is a PPARγ agonist that has significant therapeutic benefits such as glycemic control in type 2 diabetic patients. | ||
| M29251 | JNJ-63576253 free base | Androgen Receptor |
| TRC-253 free base | ||
| JNJ-63576253 (TRC-253) free base is a potent and orally active full antagonist of androgen receptor (AR), with IC50s of 37 and 54 nM for F877L mutant AR and wild-type AR in LNCaP cells. JNJ-63576253 free base can be used for the research of castration-resistant prostate cancer (CRPC). | ||
| M30315 | PRL-3 Inhibitor 2 | Phosphatase |
| PRL-3 Inhibitor 2 (compound 2) is a potent PRL-3 inhibitor with an IC50 value of 28.1 µM. | ||
| M40437 | Piperenone | Others |
| Piperenone can be isolated from M. lilijporu. | ||
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