About 12 results found for searched term "91-33-8" (0.444 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1745 | AMG-458 | c-Met |
| AMG458 | ||
| AMG-458 is a potent, selective and orally bioavailable c-Met inhibitor, with Ki values of 1.2 nM and 2.0 nM for human and mouse c-Met, respectively. | ||
| M2206 | TH-302 (Evofosfamide) | Others |
| Evofosfamide | ||
| TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. | ||
| M2444 | Benzthiazide | Carbonic Anhydrase |
| Benzothiazide | ||
| Benzthiazide is a thiazide diuretic, promoting water loss from the body. | ||
| M3793 | Deferitrin | Others |
| GT-56-252 | ||
| Deferitrin is a desferrioxanthin (DFT) analog as well as an orally active iron chelator.D may be used in studies related to severe β-thalassemia. | ||
| M4812 | Genz-123346 | Others |
| Genz-123346 is an inhibitor of GL1 synthase that blocks the conversion of ceramide to GL1. | ||
| M6035 | Trimebutine | Opioid Receptor |
| Mebutin | ||
| Trimebutine is an agonist of peripheral mu, kappa and delta opiate receptors, used as spasmolytic agent for treatment of both acute and chronic abdominal pain. | ||
| M14034 | Almorexant hydrochloride | OX Receptor |
| ACT-078573 hydrochloride | ||
| Almorexant hydrochloride (ACT 078573 hydrochloride) is a potent and competitive dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist with Ki values of 1.3 and 0.17 nM, respectively. | ||
| M20743 | AMG-1 | c-Met |
| c-Met/RON Dual Kinase Inhibitor, RON-IN-1 | ||
| AMG-1 (c-Met/RON Dual Kinase Inhibitor, RON-IN-1) is a potent inhibitor of human c-Met and RON with IC50 of 4 nM and 9 nM, respectively. | ||
| M24875 | Zagotenemab | Microtubule |
| LY33003560 | ||
| Zagotenemab (LY3303560) is a humanised anti-tau antibody that selectively binds and neutralises tau deposits in the brain. Zagotenemab can be used in Alzheimer's disease research. | ||
| M43441 | PROTAC GPX4 degrader-1 | PROTAC |
| PROTAC GPX4 degrader-1 (DC-2) is a PROTAC-based GPX4 degrader, with a DC50 of 0.03 μM in HT1080 cells. | ||
| M45314 | Ac-ESMD-CHO | Caspase |
| Ac-ESMD-CHO is an inhibitor of caspase-3 and caspase-7 that inhibits the proteolytic cleavage of caspase-3 precursor peptide (CPP32) at the Glu-Ser-Met-Asp (ESMD) site. | ||
| M53423 | Ac-IETD-CHO | Apoptosis |
| Ac-IETD-CHO is a potent, reversible inhibitor of granzyme B and caspase-8. | ||
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