About 7 results found for searched term "86-73-7" (0.052 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1907 | Org 27569 | Cannabinoid |
| Org 27569 is a potent and selective allosteric modulator of the cannabinoid CB1 receptor. | ||
| M10511 | TAS-115 mesylate | VEGFR/PDGFR |
| Pamufetinib mesylate | ||
| TAS-115 (Pamufetinib) mesylate inhibited the kinase activity of both VEGFR2 and MET and their signal-dependent cell growth as strongly as other known VEGFR or MET inhibitors. | ||
| M14698 | ERAP1-IN-1 | Others |
| ERAP1-IN-1 is an endoplasmic reticulum aminopeptidase 1 (ERAP1) inhibitor. ERAP1-IN-1 competitively inhibits ERAP1 activity towards a nonamer peptide representative of physiological substrates. | ||
| M14702 | Fluorene | Others |
| Fluorene, a polycyclic aromatic hydrocarbon (PAH), is a precursor to other fluorene compounds. Fluorene and its derivative can be used as a precursor to fluorene-based dyes. | ||
| M21513 | Vemurafenib-d7 | Raf |
| PLX4032-d7; RG7204-d7; RO5185426-d7 | ||
| Vemurafenib (PLX4032; RG7204; RO5185426) is a first-in-class selective B-RAF inhibitor that inhibits the activity of RAFV600E and c-RAF-1 with IC50 at 31 nM and 48 nM, respectively. Vemurafenib can induce autophagy. | ||
| M30753 | LBW242 | IAP |
| LBW242, a 3-mer and Smac mimetic, is a potent and orally active proapoptotic IAP inhibitor. LBW242 shows effects on mutant FLT3-expressing cells. LBW242 has activity against multiple myeloma, and potentiates TRAIL- and anticancer agent-mediated cell death of ovarian cancer cells. | ||
| M51130 | BNP (1-21), Pro (Human) | Others |
| BNP (1-21), Pro (Human) is a peptide containg 21 amino acids. | ||
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