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Organic compounds that consist of five-membered heterocyclic molecules containing a nitrogen atom and at least one other non-carbon atom as part of the ring.
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Phthalazinone pyrazole is a potent, selective, orally active small-molecule inhibitor of Aurora-A kinase used for research in cell biology and oncology. It has a biochemical IC50 of 0.031 μM against Aurora-A and shows cellular activity in multiple cancer cell lines.
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Filastatin is a small-molecule antifungal research reagent that inhibits Candida albicans filamentation and adhesion. It blocks the yeast-to-hyphal morphological transition and inhibits adhesion across multiple pathogenic Candida species (IC50 ≈ 3 μM in a GFP-based adhesion assay), making it suitable for in vitro studies of fungal morphogenesis and host-pathogen interactions.
Inhibits Candida albicans filamentation and adhesion.
Reduces fungal adhesion to surfaces and human cells.
Blocks the yeast-to-hyphal morphological transition.
Useful for in vitro antifungal and pathogenesis research.
High purity appropriate for biochemical assays.
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YL-5092 is a selective YT521-B homology (YTH) domain-containing protein 1 (YTHDC1) inhibitor with an IC50 of 7.4 nM and a KD of 29.6 nM. It can suppress cancer cell proliferation and induce cell G0/G1 phase arrest and apoptosis. YL-5092 is used for cancer research, including acute myeloid leukemia (AML).
Selectively inhibits YT521-B homology (YTH) domain-containing protein 1.
Suppresses cancer cell proliferation.
Induces cell G0/G1 phase arrest.
Promotes apoptosis in cancer cells.
Impairs leukemogenesis and improves survival rates in mouse tumor models.
Reduces leukemia infiltration in peripheral blood, spleen, and bone marrow.
Decreases the expression of YTHDC1 target genes like MYC, FOXM1, GINS1, MCM2, MCM4, and MCM5.
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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Varespladib methyl (A-002; LY333013) is a selective inhibitor of group II secretory phospholipase A2 (PLA2). It is an orally-administered methyl ester pro-drug that is metabolized to LY315920. It demonstrates high-level secretory PLA2 (sPLA2) inhibition at nanomolar and picomolar concentrations against 28 medically important snake venoms from six continents.
Selective inhibitor of group II secretory phospholipase A2 (PLA2).
Orally-administered methyl ester pro-drug.
Metabolized to LY315920.
Exhibits high-level sPLA2 inhibition against 28 snake venoms.
Purity: 99.90%.
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More