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Organic compounds that are derived from or have a benzene group in their molecular structure. Benzene is an aromatic organic molecule composed of 6 carbon atoms and 6 hydrogen atoms that form a ring. Includes derivatives and substituted molecules.
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3-Methylazetidin-3-ol hydrochloride is a drug intermediate for the synthesis of various active compounds. This product is for research use only and is not sold to patients.
Drug intermediate
Used for synthesis of active compounds
For research use only
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Gol-NTR is a Golgi-targetable probe characterized by its high selectivity and sensitivity. It is activated by Nitroreductase (NTR) and is capable of visualizing acute lung injury (ALI) as well as its repair function. The probe exhibits a low detection limit of 54.8 ng/mL, making it suitable for research focused on monitoring and assessing the response to sepsis-induced ALI.
High selectivity and sensitivity
Golgi-targetable
Nitroreductase (NTR)-activated
Capable of visualizing acute lung injury (ALI)
Capable of visualizing ALI repair function
Low detection limit of 54.8 ng/mL
Suitable for monitoring and assessing response to sepsis-induced ALI
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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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Olpasiran sodium is an N-acetyl galactosamine (GalNAc)-conjugated, hepatocyte-targeted siRNA. It directly inhibits LPA messenger RNA translation in hepatocytes and potently reduces Lp(a) concentration. It can be used for the research of cardiovascular disease, such as atherosclerosis.
N-acetyl galactosamine (GalNAc)-conjugated, hepatocyte-targeted small interfering RNA.
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(R)-NVS-ZP7-4 is the R-enantiomer of NVS-ZP7-4, a small-molecule inhibitor of the zinc transporter SLC39A7 (ZIP7) supplied as an optically pure research compound for biochemical and cellular studies targeting ER zinc homeostasis, Notch signaling, and ferroptosis-related pathways.
Optically pure R-enantiomer for stereochemistry-specific studies.
High purity (~98.8%) suitable for biochemical and cellular assays.
Solid, light yellow to yellow form; stable when stored at -20°C.
Solvent storage: -80°C for up to 6 months, -20°C for up to 1 month (protect from light).
Useful for probing ZIP7 function, ER zinc levels, Notch signaling, and ferroptosis mechanisms.
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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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GsMTx4 TFA is a spider venom peptide designed to selectively inhibit cationic-permeable mechanosensitive channels (MSCs) within the Piezo and TRP channel families. It acts as a pharmacological tool to investigate the role of these excitatory MSCs in both normal physiological processes and various pathological conditions.
Selectively inhibits cationic-permeable mechanosensitive channels (MSCs) belonging to Piezo and TRP families.
Blocks cation-selective stretch-activated channels in various cell types.
Attenuates lysophosphatidylcholine-induced astrocyte toxicity and microglial reactivity.
Neuroprotective in the cerebral cortex.
Reduces mechanical allodynia in models of inflammation and sciatic nerve injury.
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LXR-623 is a novel liver X-receptor(LXR) agonist with IC50 values of 179 nM and 24 nM for LXR- and LXR- respectively It is orally bioavailable and readily passes the blood-brain barrier
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