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Lynestrenol is a pregnane X receptor (PXR) agonist. It is a synthetic progesteronelike agent that possesses immunostimulatory properties. It enhances lymphocyte response to phytohemagglutinin, mixed lymphocyte culture, active T-rosette test, autologous red cell rosettes, and increases monocyte phagocytosis.
Purity: 99.87%
Molecular weight: 284.44
Formula: C20H28O
CAS No.: 52-76-6
Appearance: Solid
Color: White to off-white
For research use only
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Lenalidomide 4'-PEG2-amine dihydrochloride is a Lenalidomide-based Cereblon ligand that is used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a linker to form PROTAC.
Functions as a Lenalidomide-based Cereblon ligand.
Used for the recruitment of CRBN protein.
Can be linked to a protein ligand to form PROTAC.
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Lenalidomide-6-F is a cereblon (CRBN) ligand derived from Lenalidomide. It functions in the recruitment of the CRBN protein. This compound can be linked to a target protein ligand via a linker to create a PROTAC (proteolysis-targeting chimera).
Ligand for cereblon (CRBN) protein.
Used in the formation of PROTACs.
PROTACs utilize the ubiquitin-proteasome system for selective protein degradation.
For research use only.
Available as a solid, white to off-white in appearance.
Purity: 99.63%.
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Cinacalcet impurity 50 is an impurity of Cinacalcet (HY-70037). It is intended for research use only and is not sold to patients. This chemical is a solid with a white to off-white appearance.
Solid appearance
White to off-white color
Ships at room temperature in continental US
Store at room temperature, keep dry and cool
When in solvent, store at -80°C for 1 year, or -20°C for 6 months
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Granisetron (CAS No 109889-09-0) is a selective serotonin 5-HT3 receptor antagonist primarily used to study its effects on nausea and vomiting systems originating from its application as an antiemetic drug in chemotherapy Its mechanism of action involves blocking serotonin receptors in the central nervous system and the gastrointestinal tract Granisetron demonstrates in vitro activity typically in the nanomolar range indicating high potency It is often used in cellular models and animal studies to evaluate its efficacy in preventing chemotherapy-induced nausea and as a potential candidate in drug screening processes Experimental concentrations typically depend on the specific research design
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A prodrug form of cefditoren; effective against systemic S. aureus, E. coli, K. pneumoniae, P. mirabilis, or S. marcescens infections in mice (ED50s = 10, 2.5, 11, 4.4, and 11 mg/kg, respectively)
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Mogroside VI is a triterpenoid glycoside isolated from Siraitia grosvenorii (monk fruit) and used as a non-sugar, high-intensity sweetener for research. It has reported antioxidant, antidiabetic, and anticancer activities and is supplied with supporting COA and SDS documentation for characterization and quality control.
High-purity research reagent (98.45%).
Non-sugar, high-intensity sweetener for formulation and bioactivity studies.
Reported antioxidant, antidiabetic, and anticancer activity.
Molecular formula C66H112O34; molecular weight 1449.58.
Supplied with COA and SDS for traceability and quality control.
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MF: C24H20F3N5O, MW: 451.4, ≥95%, Appearance: Solid. GSK2606414 is an orally available, potent, and selective PERK inhibitor with IC(50) of 0.4nM, displaying at least 100-fold selectivity over the other EIF2AKs assayed.
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Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Flurbiprofen Axetil (Lipfen) is an anti-inflammatory used as an analgesic. purity: 98%
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This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
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