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Organic compounds that contain one or more carbonyl (a carbon atom with a double bond to an oxygen atom) functional groups. Includes compounds with functional groups that contain a carbonyl in their structure such as ketones, aldehydes, and others.
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. (beta)-NF-JQ1 is a PROTAC that recruits aryl hydrocarbon receptor E3 (AhR E3) ligase to target proteins. (beta)-NF-JQ1 uses (beta)-NF as an AhR ligand to target bromodomain (BRD)-containing proteins and induce AhR and BRD protein interactions. (beta)-NF-JQ1 shows potent anticancer activity associated with protein knockdown activity. . purity: 99%
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Tris(2,4-di-tert-butylphenyl)phosphate is an active compound derived from the leaves of Vitex negundo L. This compound demonstrates anti-inflammatory activity, primarily by inhibiting secretory Phospholipase A2 (sPLA2) through molecular docking mechanisms. It has shown significant anti-inflammatory effects in in vivo studies.
Inhibits secretory Phospholipase A2 (sPLA2)
Derived from Vitex negundo L.
Demonstrates anti-inflammatory activity
Significant anti-inflammatory effects in carrageenan-induced paw edema model
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VinylMyristate(stabilizedwithMEHQ) is a biochemical reagent that can be used as a biological material or organic compound for life science related research
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YK-3-237 is a research-grade small molecule SIRT1 activator that targets mutant p53 and has demonstrated antiproliferative activity against triple-negative breast cancer cell lines. Supplied in solid form or as a DMSO solution for in vitro research use.
Acts as a SIRT1 activator targeting mutant p53.
Inhibits proliferation of triple-negative breast cancer cells.
Provided as solid and as a DMSO solution for in vitro research.
High purity (99.54%) suitable for research applications.
Molecular weight 372.18 and chemical formula C19H21BO7 for reference.
Recommended storage: powder at -20°C (long-term) or 4°C (short-term); in solvent at -80°C (long-term) or -20°C (short-term).
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2'-Deoxy-2'-fluoroinosine is a purine nucleoside analog that demonstrates broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include inhibition of DNA synthesis and induction of apoptosis.
Purine nucleoside analog
Demonstrates broad antitumor activity
Targets indolent lymphoid malignancies
Inhibits DNA synthesis
Induces apoptosis
Appears as a white to off-white solid
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