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Various organic compounds consisting of carbon, hydrogen, and oxygen atoms that are found in foods and living tissues; typically broken down to release energy; includes sugars, sugar alcohols, sugar acids and derivatives, glycosyl compounds, and more.
We are committed to bringing youAGreenerAAlternative Products which adhere to one or more of The 12 Principles ofAGreenerAChemistry. This product has been enhanced for energy efficiency and waste prevention when used in fuel cell research. for more information see the article in biofiles.
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1-Linoleoyl glycerol is a LpPLA2 inhibitor. It acts as a precursor for synthesizing various functional lipids, such as phospholipids. It mitigates inflammation induced by Apolipoprotein CIII (reduction of IL-6).
Acts as a LpPLA2 inhibitor
Precursor for synthesizing various functional lipids, such as phospholipids
Mitigates inflammation induced by Apolipoprotein CIII (reduction of IL-6)
(R)-1-Linoleoyl glycerol and (S)-1-Linoleoyl glycerol exhibit Lp-PLA2 inhibitory activities
Metabolized by human eosinophils to 13-HODE-G and 13-HODE
Metabolized by human neutrophils to produce 15-LO metabolite
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D-Glucosyl-β-1,1′-N-palmitoylsphingosine is an endogenous Mincle ligand with immunostimulatory activity. It binds to and activates macrophage-inducible C-type lectin (Mincle).
Applicable to the research of immune system diseases
Endogenous Mincle ligand
Immunostimulatory activity
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Gum ghatti is a natural, high-molecular-weight polysaccharide exudate used as a biochemical reagent and functional excipient for research applications. It serves as a thickener, stabilizer, and matrix component in formulation and assay workflows; supplied as a solid powder for laboratory use (CAS 9000-28-6).
Natural polysaccharide exudate suitable for research use only.
Functions as a thickener, stabilizer, and emulsifying agent.
High molecular weight provides viscosity and film-forming properties.
Available in solid form for ease of weighing and formulation.
Applicable in biochemical assays, formulation development, and excipient research.
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Glucose 6-phosphate dehydrogenase (G-6-P-DH) is a key regulatory enzyme in the first step of the pentose phosphate pathway. G-6-P-DH is a glycoprotein with a molecular mass of 128 kDa (gel filtration).
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Azidoethyl-SS-PEG2-Boc is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent due to its Azide group, allowing it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules containing Alkyne groups. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
Utilized in the synthesis of PROTACs
Functions as a click chemistry reagent
Contains an azide group
Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules
Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups
PROTACs leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins
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Azidoethyl-SS-PEG2-Boc is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring an Azide group. This allows it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing Alkyne groups, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
Peg-based PROTAC linker
Click chemistry reagent
Contains an Azide group for CuAAc and SPAAC reactions
For research use only
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3-O-Methyl-D-glucopyranose is a methylated glucose derivative supplied as a biochemical reagent for laboratory research. It is commonly used as a non-metabolizable glucose analog and substrate in transport, uptake, and metabolic studies, provided as a white to off-white powder for experimental assays.
High purity: 99.93%.
Molecular formula: C7H14O6.
Molecular weight: 194.18 g/mol.
Non-metabolizable glucose analog for transport and metabolic assays.
Available in multiple laboratory sizes, including 1 G.
Includes structural identifiers suitable for computational use (SMILES, InChI).
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