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Organic compounds that contain two carboxyl groups; carboxyl groups consist of a carbonyl group bonded to a hydroxy group. Includes compounds that are derived from dicarboxylic acids.
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GlyH-101 (CAS 328541-79-3) is a cell-permeable glycinyl hydrazone derivative that acts as a selective inhibitor of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel exhibiting a Ki of 1 4 M By blocking CFTR-mediated chloride transport GlyH-101 serves as a valuable tool for investigating CFTR function in epithelial physiology and pathophysiology as well as for studying mechanisms underlying cystic fibrosis and related disorders involving chloride ion dysregulation
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1,2-Dilauroyl-sn-glycero-3-phosphoethanolamine (DLPE) is a phosphatidylethanolamine derivative bearing two lauroyl (C12:0) acyl chains. It is a research-grade lipid commonly used for liposome formulation and membrane model studies; typical properties include a molecular weight of 579.75 g·mol⁻¹ and high purity (98.0%).
Phosphatidylethanolamine lipid with two lauroyl (C12:0) chains.
Suitable for liposome synthesis and membrane model studies.
High purity (98.0%) for research applications.
Molecular formula C29H58NO8P and molecular weight 579.75 g·mol⁻¹.
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Pigment Yellow 101 is a yellow bis-azomethine pigment with excitation/emission at 411 nm/512 nm. It exhibits solid-state fluorescence and is available as a commercial colorant. This product is for research use only and not sold to patients.
Yellow bis-azomethine pigment
Exhibits solid-state fluorescence
Excitation/emission: 411 nm/512 nm
Available as a commercial colorant
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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. PKUMDL-LC-101-D04 is a potent allosteric activator of glutathione peroxidase 4 (GPX4) a regulator of iron death. GPX4 activity was increased to 150% of control levels when used at a concentration of 20 uM in a cell-free assay and at a concentration of 61 uM in wild-type but not Gpx4-/- mouse embryonic fibroblast (MEF) extracts.PKUMDL-LC-101-D04 (200 uM) reduced cholesterol peroxide-induced MEF death. purity: 98%
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Lauroyl-L-carnitine chloride is an orally active absorption enhancer used in research to improve the oral bioavailability of peptide compounds. Supplied as a white to off-white solid with high purity, it is applied in formulation and permeability studies to assess and enhance intestinal uptake of peptide drugs.
Orally active absorption enhancer for peptide compounds.
Reported to improve oral bioavailability of peptides.
White to off-white solid suitable for formulation research.
High purity (~98.1%) as supplied.
Supports studies of intestinal permeability and delivery.
Store sealed at 4°C; in solvent, -80°C (6 months) or -20°C (1 month).
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UK-101 is a selective immunoproteasome β1i (LMP2) inhibitor for laboratory research. It shows reported potency with an IC50 of about 104 nM and is supplied as a high-purity solid suitable for in vitro studies; recommended solvent is DMSO.
Selective immunoproteasome β1i (LMP2) inhibitor with IC50 ≈104 nM.
High purity (≈99.6%).
Available in small research quantities, e.g., 5 mg.
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MAL3-101 is a small-molecule allosteric inhibitor of HSP70 used in biochemical and cellular research to modulate HSP70 ATPase activity and disrupt Hsp40 co-chaperone interactions. It is a membrane-permeable dihydropyrimidine analog supplied as a solid powder for laboratory use.
Allosteric inhibitor of HSP70 ATPase activity.
Disrupts Hsp40 co-chaperone interaction.
Demonstrated activity in cellular antiproliferative studies.
High purity suitable for research (>98%).
Powder form with DMSO solubility for assay preparation.
Recommended storage: powder at -20°C; in solvent at -80°C for longer storage.
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CUDC-101 is a potent multi-targeted inhibitor against HDAC EGFR and HER2 with IC50 of 4 4 nM 2 4 nM and 15 7 nM and inhibits class I/II HDACs but not class III Sir-type HDACs Phase 1
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Lauroyl-L-carnitine chloride is an orally active metabolite that significantly reverses the decrease in its target gene IL-10 and alleviates Crohn's-like colitis. This product is for research use only.
Orally active metabolite
Reverses decrease in IL-10
Alleviates Crohn's-like colitis
Exhibits anti-inflammatory effects
Improves systemic and local phenotypes of TNBS mice
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Lauroyl-L-carnitine chloride is an orally active metabolite that significantly reverses the decrease in its target gene IL-10, alleviating Crohn's-like colitis. It demonstrates anti-inflammatory effects and improves both systemic and local phenotypes in TNBS mice.
Orally active metabolite
Reverses decrease in target gene IL-10
Alleviates Crohn's-like colitis
Exhibits anti-inflammatory effects
Improves systemic and local phenotypes in TNBS mice
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Lauroyl-L-carnitine chloride is an orally active metabolite. It significantly reverses the decrease in its target gene IL-10 and alleviates Crohn's-like colitis.
Orally active metabolite
Reverses decrease in IL-10 gene
Alleviates Crohn's-like colitis
Purity: 98.14%
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Sodium lauroyl glutamate is an anionic amino acid surfactant with potential for irritant contact dermatitis and possible anti-irritating potential in surfactant mixtures on human skin.
Anionic amino acid surfactant
Potential for irritant contact dermatitis
Possible anti-irritating potential
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1,2-Dilauroyl-sn-glycerol is a saturated diacylglycerol that may participate in second messenger signal transduction. It is intended for research use only and is not sold to patients.
Potential role in second messenger signal transduction.
Crucial intracellular signaling molecules involved in regulating various physiological processes.
Specifically designated for research purposes.
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. AVN-101 is a very potent 5-HT7 receptor antagonist (Ki = 153 pM). AVN-101 also exhibits a rather high affinity toward histamine H1 (Ki = 0.58 nM) and adrenergic (alpha)2A (alpha)2B and (alpha)2C (Ki = 0.41-3.6 nM) receptors. AVN-101 shows a good oral bioavailability and facilitated brain-blood barrier permeability low toxicity and reasonable efficacy in animal models of CNS diseases. purity: 99%
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