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Vitamin D4 (22-Dihydroergocalciferol) is a vitamin D derived from fungi. The precursor of vitamin D4 is 22,23-dihydroergosterol. It is for research use only and not sold to patients.
Appearance: Solid
Color: Off-white to light yellow
Molecular weight: 398.66
Solubility: 25 mg/mL in DMSO
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Vitamin D Receptor Antibody is a rabbit-derived and non-conjugated IgG polyclonal antibody, targeting the Vitamin D Receptor. It is for research use only.
Immunohistochemistry-Paraffin (IHC-P): 1:100-500 dilution ratio
Immunohistochemistry-Frozen (IHC-F): 1:100-500 dilution ratio
Immunocytochemistry/Immunofluorescence (ICC/IF): 1:100-500 dilution ratio
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R5 peptide (acetate) is a synthetic peptide known for its silica-precipitating activity. It is provided as a solid and is intended for research purposes only, not for patient use.
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Actinine-d9 chloride is the deuterium labeled Actinine chloride. Actinine chloride is an angiopathic substance produced as an intermediary metabolite by gut microbiota that feed on carnitine in dietary red meat. Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
Can be used as a tracer.
Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Contains a stable heavy isotope.
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rel-PROTAC PARP1 degrader is the relative configuration of ROTAC PARP1 degrader (HY-114324). ROTAC PARP1 degrader is a PARP1 degrader based on MDM2 E3 ligand. It induces significant PARP1 cleavage and programmed cell death. PROTAC PARP1 degrader at 10 μM at 24 h inhibits MDA-MB-231 cell line with an IC50 of 6.12 μM.
Relative configuration of ROTAC PARP1 degrader
Based on MDM2 E3 ligand
Induces significant PARP1 cleavage
Induces programmed cell death
Inhibits MDA-MB-231 cell line with an IC50 of 6.12 μM at 10 μM (24 h)
Purity: 98.99%
Molecular weight: 1145.09
Appearance: Solid
Color: White to off-white
Soluble in DMSO (110 mg/mL)
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Endoxifen E-isomer (E-Endoxifen) is an E-isomer of Endoxifen, identified as an impurity in Endoxifen Z-isomer agent substance. This compound demonstrates antiestrogenic effects and is for research use only.
Inhibits PGR gene expression in E2-induced MCF-7 cells.
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Pyridoxine (vitamin B6) is a water-soluble vitamin and enzymatic cofactor involved in amino acid, lipid, and neurotransmitter metabolism. Supplied as a high-purity research reagent, this material is intended for laboratory and analytical use and is not for human or clinical applications.
High-purity reagent suitable for biochemical assays and analytical methods.
Water-soluble vitamin and cofactor in metabolic reactions.
Suitable for cell studies and enzymology experiments.
Supplied in a 10 mg package for small-scale laboratory use.
Not for human consumption; intended for research use only.
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rel-Bedaquiline is a drug impurity related to the anti-tuberculosis agent bedaquiline and is supplied as an analytical reference for research use only. It is intended for chromatographic and analytical method development, impurity profiling, and stability studies. Consult the Certificate of Analysis for batch-specific purity and storage conditions.
Intended for research use only; not for human or clinical use.
Impurity standard for analytical and chromatographic method development.
High purity reference: 97.56% by HPLC (batch dependent).
Suitable for impurity profiling and stability studies.
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Ulipristal acetate (126784-99-4) is a selective progesterone receptor modulator (SPRM) targeting progesterone receptors It is designed to modulate receptor-mediated signaling thereby regulating endometrial tissue proliferation and fibroid cell growth Ulipristal acetate exerts its biological activity primarily through reversible inhibition of progesterone-dependent signaling pathways Based on these pharmacological properties ulipristal acetate holds research potential in studies of progesterone signaling pathways uterine physiology hormonal regulation mechanisms and benign gynecological conditions such as uterine myoma
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MW 430.7 Da, Purity >98%. Fat-soluble antioxidant. Peroxyl radical scavenger that protects polyunsaturated fatty acids in membranes and lipoproteins. Anticarcinogen.
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Goserelin acetate is a synthetic GnRH (gonadotropin-releasing hormone) agonist peptide supplied for research use in studies of hormone-dependent cancers and reproductive biology. The acetate salt is formulated for laboratory assays and preclinical work where a defined GnRH receptor agonist is required.
High reported purity (99.87%) suitable for research applications.
Well-characterized molecular formula and weight for identity confirmation.
Supplied in small milligram quantities for laboratory experiments.
Appropriate for in vitro and preclinical cancer biology studies.
Datasheet and handling instructions available for proper storage and use.
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MW 726.9 Da, Purity >98%. Antioxidant. Protects against lipid peroxidation by inhibiting the activity of the inducible nitric oxide synthase. Blood brain barrier permeable. Active both in vivo and in vitro.