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Aromatic organic heterocyclic compounds that contain a benzene ring fused with a six-membered ring that contains one nitrogen atom and five carbon atoms. Includes compounds that are derived from quinolines.
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GSK1070916 (CAS 942918-07-2) is a selective ATP-competitive inhibitor targeting Aurora kinase B and C displaying Ki values of 0 38 nM and 1 5 nM respectively The compound demonstrates marked selectivity over Aurora kinase A with IC50 values of approximately 5 nM (Aurora B) versus 1259 nM (Aurora A) In vitro studies show that GSK1070916 inhibits proliferation of human lung cancer cells (A549) with an EC50 of roughly 7 nM Additionally the compound effectively reduces phosphorylation of histone H3 an Aurora B substrate and exhibits tumor growth inhibition in HL-60 xenograft mouse models GSK1070916 is utilized in tumor biology research investigating Aurora kinase signaling pathways
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SARS-CoV-2-IN-86 is a small-molecule research compound that inhibits SARS-CoV-2 methyltransferases (nsp14 and nsp16) and is reported as an andrographolide derivative. It is supplied as a solid or as a 10 mM solution in DMSO for in vitro antiviral and enzymatic studies. Batch-specific certificates of analysis and safety documentation are available from the supplier.
Inhibits SARS-CoV-2 methyltransferases (nsp14 and nsp16).
Andrographolide derivative for antiviral research.
Available as solid and 10 mM solution in DMSO.
High purity (≈99.4%) per supplier documentation.
Suitable for in vitro enzymatic and antiviral assays.
Powder stable at -20°C; solvent storage guidelines available.
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SARS-CoV-2-IN-86 is a research-grade small molecule inhibitor of SARS-CoV-2 methyltransferases (nsp14 and nsp16), provided for in vitro biochemical and antiviral studies. It is available as solid material and as a 10 mM solution in DMSO, with documented purity and storage recommendations to support reproducible experimental use.
High purity (99.35%) for reproducible results.
Available as 10 mM solution in DMSO or as solid for flexible assay workflows.
Well-characterized chemical identity (CAS 368866-07-3) and formula for traceability.
Suitable for biochemical methyltransferase and antiviral research applications.
Defined storage conditions to preserve stability in powder and solution formats.
Datasheet available with specification and handling information.
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Hexestrol (CAS 84-16-2) is a small-molecule agonist targeting estrogen receptors ER and ER It is designed to selectively activate these receptors thereby regulating hormone-responsive gene expression and associated biological pathways Hexestrol exerts its biological activity primarily through direct agonist-mediated activation of ER and ER In in vitro studies Hexestrol demonstrates potent activation with reported EC50 values of approximately 0 07 nM for ER and 0 175 nM for ER Based on these pharmacological properties Hexestrol holds research potential in studies involving estrogen receptor signaling hormone-dependent cellular responses and pathologies related to estrogen deficiency
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