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Fluorogestone acetate is a synthetic progesterone analog used to inhibit ovulation and synchronize the estrous cycle in cattle by suppressing luteinizing hormone (LH) release. It is supplied as a high-purity reagent in weighed milligram quantities for research and veterinary reproductive management applications.
Inhibits ovulation and synchronizes the estrous cycle in cattle.
Acts by suppressing luteinizing hormone (LH) release.
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Oxyphenisatin acetate is the acetylated prodrug of oxyphenisatin, historically used as a laxative. This listing describes a research-grade chemical supplied for analytical and laboratory studies; it is intended for research use only and not for human or veterinary use.
Acetylated prodrug of oxyphenisatin.
Used in biochemical and autophagy-related research.
CAS number: 115-33-3.
Molecular formula C24H19NO5 and molecular weight ~401.41.
Typically supplied as a solid with high purity (commonly ≥98%).
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Levonorgestrel is an orally active inhibitor of progesterone. It has anticancer activity and can induce apoptosis. It can be used as a contraceptive and in combination with other medications. Levonorgestrel can also be used in the study of osteoporosis and uterine leiomyoma.
Orally active inhibitor of progesterone.
Exhibits anticancer activity.
Induces apoptosis.
Used as a contraceptive.
Can be used in combination with other medications.
Applicable in the study of osteoporosis and uterine leiomyoma.
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5-Cholesten-24(RS)-methyl-3β-ol-d3 is a deuterium labeled compound intended for research use. It can serve as a tracer or an internal standard for quantitative analysis. Deuteration is noted for its potential impact on the pharmacokinetic and metabolic profiles of drugs.
Used as a tracer.
Internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Stable heavy isotopes incorporated into drug molecules for quantitation during drug development.
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UCL-TRO-1938 is a potent allosteric activator of PI3Kα with an EC50 value of approximately 60 μM. UCL-TRO-1938 can induce cell proliferation and has cardioprotective and neural regeneration effects.
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An oxysterol; inhibits the proliferation of HGC-27 cells at 1 µM, an effect that can be enhanced by knockdown of LXRβ; tumor levels are increased in patients with gastric cancer
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α-Cholestane-d4 is a deuterium-labeled analogue of α-cholestane used as a stable isotope internal standard and tracer in analytical workflows. It supports accurate quantitation, method development, and tracer studies in mass spectrometry and isotope-dilution assays, with high isotopic and chemical purity for reliable results.
Deuterium-labeled internal standard for mass spectrometry
High isotopic and chemical purity for accurate quantitation
Suitable for isotope-dilution assays and tracer studies
Available in small pack sizes for analytical use
Molecular formula C27H44D4 and CAS 205529-74-4 for identification
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TRO 19622 (CAS 22033-87-0) also known as Olesoxime is a cholesterol-like small molecule that modulates mitochondrial function contributing to cellular resilience under stress conditions Preclinical studies demonstrate that TRO 19622 attenuates neurodegeneration supports nerve function and facilitates neuroregeneration following traumatic nerve injury in both in vitro and in vivo models This compound is utilized in research exploring neuroprotection and mechanisms underlying neuronal survival with potential applications in models of neurodegenerative diseases and peripheral nerve trauma
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