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Ethyl acetoacetate-13C is a 13C labeled ester extensively used as an intermediate in the synthesis of various compounds. It is also identified as an inhibitor of bacterial biofilm, and can be utilized as a tracer and an internal standard for quantitative analysis via methods such as NMR, GC-MS, or LC-MS.
Used as a tracer
Serves as an internal standard for quantitative analysis
Incorporates carbon-13, a stable heavy isotope, for quantitation during drug development
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Ethyl palmitate (Ethyl hexadecanoate) is a Chikungunya virus (CHIKV) inhibitor with an EC50 value of 0.0068 μM. It demonstrates anti-inflammatory activity by reducing levels of TNF-α, IL-6, and NF-κB.
Inhibits expression and viral activity of CHIKV virus E2 protein.
Reduces plasma levels of TNF-α and IL-6 in endotoxemic rats.
Decreases NF-κB expression in liver and lung tissues.
Ameliorates histopathological changes caused by LPS in a rat model of endotoxemia.
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Ethyl acetoacetate-d3 is the deuterium labeled Ethyl acetoacetate Ethyl acetoacetate (Ethyl acetylacetate) is an ester widely used as an intermediate in the synthesis of many varieties of compounds[1][2][3] Ethyl acetoacetate is an inhibitor of bacterial biofilm[4]
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Sulfamethizole (Standard) is the analytical standard of Sulfamethizole (HY-B0333). It is intended for research and analytical applications. Sulfamethizole is a sulfathiazole antibiotic that inhibits the synthesis of folic acid and thymine, and selectively suppresses Photobacterium phosphoreum bioluminescence. It demonstrates antibacterial activity against Escherichia coli-mediated urinary tract infections, but not against sulII gene-positive Escherichia coli. This product is applicable for research on urinary tract infections and Photobacterium phosphoreum bioluminescence mechanisms.
Serves as a reference standard for assays
Used in qualitative, quantitative, and methodological research experiments
Applicable for HPLC, GC, and MS
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Hydroxyprogesterone caproate (CAS No 630-56-8) is a synthetic progestin used in biomedical research primarily within the fields of endocrinology and obstetrics Originating from modifications of naturally occurring progesterone this compound acts by binding to progesterone receptors influencing the regulation of menstrual cycles and maintaining pregnancy Its mechanism of action involves modulating hormonal pathways crucial for gestational support In vitro studies commonly report activity in the nanomolar to low micromolar range indicating its potent receptor affinity Typical research applications include various cell models and animal studies to investigate reproductive health with drug screening processes benefiting from its predictable biological activity Experimental concentrations typically depend on the specific research design
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