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Aromatic organic compounds that consist of a phenyl functional group (−C6H5) bonded to a hydroxyl functional group (−OH). Includes compounds with more substitutions and derivatives.
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Methoxamine hydrochloride is a selective alpha1-adrenergic receptor agonist. It causes vasoconstriction and increased peripheral vascular resistance, and significantly increased the overflow of ATP, ADP, and AMP by a prazosin-sensitive mechanism. This product is for research use only.
Selective alpha1-adrenergic receptor agonist.
Causes vasoconstriction.
Increases peripheral vascular resistance.
Increases overflow of ATP, ADP, and AMP.
Target: Noradrenergic α1.
In vivo studies show greater effect on peripheral resistance vessels than Winkessel vessels in rat systemic circulation.
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Recombinant mouse L-selectin (CD62L) is the extracellular domain of the protein expressed in HEK293 cells with a C-terminal His tag. It is supplied as a 0.22 μm filtered PBS solution (pH 7.4) at 0.34 mg/mL, with an approximate molecular weight of 70-80 kDa and high purity suitable for research applications in immunology and cell adhesion studies.
Recombinant mouse extracellular domain suitable for in vitro assays.
Expressed in HEK293 for mammalian-like post-translational modifications.
C-terminal His tag facilitates purification and detection.
Supplied as a filtered PBS solution ready for dilution or use.
High purity (≥98.0%) supports biochemical and binding studies.
Concentration provided for convenient aliquoting and dosing.
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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Verbenalin is an orally active terpenoid glycoside extracted from the medicinal plant *Verbena officinalis*. It exhibits anti-inflammatory, antiviral, and neuroprotective effects. It binds strongly to the nsp-12 protein of the SARS-CoV-2 virus and is used in research for inflammatory and nervous system diseases such as hepatitis and Alzheimer's disease.
Orally active terpenoid glycoside
Exhibits anti-inflammatory effects
Exhibits antiviral effects
Exhibits neuroprotective effects
Binds strongly to nsp-12 protein of SARS-CoV-2 virus
Used in research for inflammatory diseases
Used in research for nervous system diseases
Purity: 99.90%
Appearance: Solid
Color: White to off-white
For research use only
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. LCS3 is a reversible and non-competitive synergistic inhibitor of glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) with IC50s of 3.3 uM and 3.8 uM respectively. LCS3 has antitumour activity induces apoptosis and can be used in the study of lung adenocarcinoma (LUAD). purity: 99%
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More