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Filtered Search Results
Cayman Chemical EstradIol CypIonate 1g
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A synthetic estrogen; reduces estrogen-depletion induced spikes in basal tail temperature in ovariectomized wild-type, ERα-/-, and ERβ-/- mice at 0.1 mg/kg per day; increases the rate of pregnancy in cows induced to ovulate small dominant follicles; reduces edema and articular joint neutrophil infiltration in an ovariectomized mouse model of zymosan-induced arthritis
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000664636 ACOLTREMON-D3 10MG
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Medchemexpress LLC Vitamin D2 (ergocalciferol) | 50-14-6 | 99.1% | C28H44O | 10 G
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Vitamin D2 (Ergocalciferol) is derived from plant sources or dietary supplements and can be used as a supplement of Vitamin D. This product is intended for research use only.
- Derived from plant sources
- Can be used as a supplement of vitamin D
- For research use only
- Molecular weight: 396.65
- Appearance: solid
- Color: white to light yellow
- Structure classification: steroids
- Initial source: plants other families
- Endogenous metabolite: human gut microbiota metabolites
- Shipping at room temperature in continental US
- Store at -20°C, protected from light, under nitrogen
- Unstable in solutions; freshly prepared is recommended
- Solubility (in vitro): DMSO: 31.25 mg/mL (78.78 mM)
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Medchemexpress LLC Alosetron-d3 hydrochloride | 1189919-71-8 | 99.0% | C17H16D3ClN4O | 5 MG
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Alosetron-d3 hydrochloride is a deuterium labeled Alosetron, functioning as a serotonin 5HT3-receptor antagonist. It is suitable for use as a tracer and an internal standard in NMR, GC-MS, or LC-MS analysis for quantitative applications.
- Deuterium labeled compound
- Serotonin 5HT3-receptor antagonist
- Internal standard for quantitative analysis
- Used in neurological disease research
- Supports drug concentration detection
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eMolecules 112965-21-6 | Medchem Express | Calcipotriol | 5mg | 446254737 | HY-10001 | MFCD00866630 | 412.614 | C27H40O3
Ambeed | 4-(Dimethylamino)benzonitrile | 5g | 573000594 | A814924 | 1197-19-9 | MFCD00001815 | 146.193 | C9H10N2
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eMolecules Building Block Tool
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Medchemexpress LLC R -Nicardipine-d3 10mg | 10MG
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R -Nicardipine-d3 10mg | 10MG
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eMolecules Sodium taurocholate dihydrate | 345909-26-4 | MFCD00150132 | 1g
Combi-Blocks | Sodium taurocholate dihydrate | 1g | 401040224 | QB-6959 | 96.000 | 345909-26-4 | MFCD00150132 | 573.720 | C26H48NNaO9S
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Medchemexpress LLC GelHP Protein Gel B 10pcs | 10PCS
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GelHP Protein Gel B 10pcs | 10PCS
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Medchemexpress LLC Velmupressin acetate | 1647120-04-4 | 1006.64 g/mol | 1 MG
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Velmupressin acetate is a potent, selective, and short-acting peptidic V2 receptor (V2R) agonist. It exhibits EC50 values of 0.07 nM for human V2R (hV2R) and 0.02 nM for rat V2R (rV2R). This product is stable under recommended storage conditions and is not classified as a hazardous substance or mixture according to safety data.
- Potent, selective, and short-acting peptidic V2 receptor (V2R) agonist
- EC50 values of 0.07 nM for human V2R (hV2R)
- EC50 values of 0.02 nM for rat V2R (rV2R)
- Stable under recommended storage conditions
- Not a hazardous substance or mixture
- For research use only
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Cayman Chemical OctnoIc AcId-d3 10mg
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An internal standard for the quantification of octanoic acid by GC- or LC-MS
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Apexbio Technology LLC Cortisone acetate 50-04-4 100mg
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Cortisone acetate (50-04-4) is a glucocorticoid receptor agonist targeting the glucocorticoid receptor It is designed to modulate glucocorticoid signaling thereby regulating gene transcription and downstream immune and inflammatory responses Cortisone acetate exerts its biological activity primarily through enzymatic conversion to cortisol which subsequently activates glucocorticoid receptors to influence cellular stress and inflammatory pathways Based on these pharmacological properties cortisone acetate holds research potential in the investigation of glucocorticoid signaling pathways receptor-mediated transcriptional regulation cellular stress responses and inflammatory condition models
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Medchemexpress LLC Fluorogestone acetate | 2529-45-5 | 99.6% | 406.49 g·mol⁻¹ | C23H31FO5 | 50MG
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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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Medchemexpress LLC Fluorogestone acetate | 2529-45-5 | MFCD00243094 | 99.6% | 406.49 | C23H31FO5 | 100MG
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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.
- High purity: 99.6%.
- Molecular formula: C23H31FO5; molecular weight: 406.49.
- Available in multiple package sizes, including 100 mg.
- Provided in weighed quantities suitable for formulation and analytical use.
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Apexbio Technology LLC TRO 19622 22033-87-0 5mg
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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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Cayman Chemical EstradIol 3 DGlucuronIde 25mg
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A non-cholestatic regioisomer of E217G that acts as a substrate for MRP2, competing with E217G for MRP2-mediated transport (IC50 = 14.2 µM)
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