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Medroxyprogesterone (Standard) is the analytical standard of Medroxyprogesterone, intended for research and analytical applications. This product is for research use only and not sold to patients.
Used as an analytical standard
Suitable for qualitative, quantitative, and methodological research experiments
Applicable in techniques such as HPLC, GC, and MS
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Medroxyprogesterone acetate (MPA) is a synthetic steroidal derivative structurally related to the endogenous hormone progesterone classified as a progestin Acting primarily through binding to progesterone receptors it modulates gene transcription influencing endometrial proliferation and reproductive pathways Additionally MPA exhibits affinity toward glucocorticoid receptors which may contribute to its physiological effects In biomedical research MPA serves as a standard experimental tool to investigate progesterone receptor signaling mechanisms and steroid hormone interactions Furthermore it is widely used in studies focused on reproductive biology contraceptive mechanisms hormone replacement therapy models oncology research involving hormone-responsive tumors and conditions such as endometriosis
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Norethindrone acetate (Standard) is the analytical standard of Norethindrone acetate, intended for research and analytical applications. It is a female hormone used for the research of endometriosis. It also functions as a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. This product is for research use only and not sold to patients.
Analytical standard, reference standard supplied assay.
Commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
Molecular weight: 340.46
Formula: C₂₂H₂₈O₃
Appearance: Solid
Color: White to off-white
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Norethisterone enanthate is a long-acting parenteral progestogen, orally active, and functions as a click chemistry reagent. It contains an alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing azide groups. This compound is intended for research use only.
Deoxycorticosterone acetate (56-47-3) is a small-molecule agonist targeting mineralocorticoid receptors (MR) It is designed to activate MR thereby regulating renal sodium reabsorption and potassium excretion Deoxycorticosterone acetate exerts its biological activity primarily through interaction with cytoplasmic mineralocorticoid receptors leading to nuclear translocation and modulation of electrolyte balance Typical IC50 values associated with its mineralocorticoid receptor binding affinity have been reported in the nanomolar range Based on these pharmacological properties Deoxycorticosterone acetate holds research potential in studies of electrolyte balance adrenal insufficiency modeling and the pathophysiology of hypertension as well as models investigating mineralocorticoid receptor-dependent signaling and renal or cardiovascular physiology
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Deoxycorticosterone acetate (56-47-3) is a small-molecule agonist targeting mineralocorticoid receptors (MR) It is designed to activate MR thereby regulating renal sodium reabsorption and potassium excretion Deoxycorticosterone acetate exerts its biological activity primarily through interaction with cytoplasmic mineralocorticoid receptors leading to nuclear translocation and modulation of electrolyte balance Typical IC50 values associated with its mineralocorticoid receptor binding affinity have been reported in the nanomolar range Based on these pharmacological properties Deoxycorticosterone acetate holds research potential in studies of electrolyte balance adrenal insufficiency modeling and the pathophysiology of hypertension as well as models investigating mineralocorticoid receptor-dependent signaling and renal or cardiovascular physiology
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Medroxyprogesterone (CAS 520-85-4) is a small-molecule agonist targeting the progesterone receptor It is designed to activate progesterone receptor-mediated intracellular signaling pathways thereby regulating cellular proliferation Medroxyprogesterone exerts its biological activity primarily through agonism of the progesterone receptor modulating pathways such as PI3K/Akt signaling In preclinical mouse models medroxyprogesterone demonstrates inhibitory activity on atherosclerotic lesion formation Based on these pharmacological properties medroxyprogesterone holds research potential in the study of progesterone receptor-mediated biological processes cellular proliferation and vascular pathology
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Cagrilintide acetate is a non-selective AMYR/CTR agonist and a long-acting acylated amylase analogue. It reduces food intake and causes significant weight loss in a dose-dependent manner, making it suitable for obesity studies.
Non-selective AMYR/CTR agonist
Long-acting acylated amylase analogue
Reduces food intake
Causes significant weight loss in a dose-dependent manner
Suitable for obesity studies
For research use only
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Bazedoxifene (acetate)-D is the D-crystal form compound of Bazedoxifene acetate, an orally active, nonsteroidal selective estrogen receptor modulator (SERM) with IC50s of 23 nM for ERα and 99 nM for ERβ.
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Fluorogestone acetate is a synthetic progestin used in veterinary and research settings to inhibit ovulation and synchronize estrous cycles. Supplied as a solid, high-purity reagent, it is characterized by formula C23H31FO5 and a molecular weight of 406.49 g·mol⁻¹; handle and store sealed away from moisture and light as recommended in the SDS.
High purity: 99.6%.
Molecular formula: C23H31FO5.
Molecular weight: 406.49 g·mol⁻¹.
Available in multiple pack sizes including 50 mg.
Recommended storage: 4°C sealed; in solvent, -80°C (6 months) or -20°C (1 month).
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