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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
35 Results for "
Gluconate
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "Gluconate" in MCE Product Catalog:
Cat. No.: HY-E71955
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Research Areas:
6-Deoxy-6-sulfo-D-gluconate dehydratase (EC 4.2.1.162) is a lyase that can convert 6-deoxy-6-sulfo-D-gluconate into 2-dehydro-3,6-dideoxy-6-sulfo-D-gluconate and H2O.
Cat. No.: HY-E70977
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6-phospho-D-gluconate dehydrogenase, E. coli (EC 1.1.1.44) is an oxidoreductase that acts on the CH-OH group of a donor molecule and uses NAD+ or NADP+ as an acceptor. The two substrates of 6-phospho-D-gluconate dehydrogenase, E. coli (EC 1.1.1.44) are 6-phospho-D-gluconate and NADP+, while its three products are D-ribulose-5-phosphate, CO2, and NADPH.
Cat. No.: HY-E71516
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2-Deoxy-D-gluconate 3-dehydrogenase (EC 1.1.1.125) belongs to the oxidoreductase family, which refers to oxidoreductases that use NAD+ or NADP+ as acceptors and act on the CH-OH group of donor molecules. 2-Deoxy-D-gluconate 3-dehydrogenase (EC 1.1.1.125) participates in the interconversion between pentoses and glucuronic acid.
Cat. No.: HY-E71498
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2-Dehydro-3-deoxy-D-gluconate 5-dehydrogenase (EC 1.1.1.127) is an oxidoreductase that catalyzes the oxidation of 2-dehydro-3-deoxy-D-gluconate (KDG), using NAD+ (or NADP+ in some strains) as the electron acceptor.
Cat. No.: HY-E71500
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2-Dehydro-3-deoxy-D-gluconate aldolase (EC 4.1.2.51) from the archaeon Picrophilus torridus is involved in D-glucose and D-galactose catabolism via the nonphosphorylative variant of the Entner-Doudoroff pathway; in the direction of aldol synthesis the enzyme catalyses the formation of 2-dehydro-3-deoxy-D-gluconate and 2-dehydro-3-deoxy-D-galactonate at a similar ratio.
Cat. No.: HY-E71437
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2,5-Didehydrogluconate reductase (2-dehydro-D-gluconate-forming) (EC 1.1.1.274) is involved in the catabolism of 2,5-didehydrogluconate. cf.
Cat. No.: HY-E71499
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2-Dehydro-3-deoxy-D-gluconate 6-dehydrogenase (EC 1.1.1.126) belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor.
Cat. No.: HY-E71911
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5-Dehydro-2-deoxygluconokinase (EC 2.7.1.92) is a transferase that can convert 5-dehydro-2-deoxy-D-gluconate and ATP into 6-phospho-5-dehydro-2-deoxy-D-gluconate, ADP and H +.
Cat. No.: HY-185401A
CAS No.: 191486-46-1
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(E,E)-ATSM is a chelating agent. (E,E)-ATSM can react with the metallized ligand Copper gluconate. (E,E)-ATSM can be used in research on central nervous system diseases .
Cat. No.: HY-E71916
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5-Deoxy-glucuronate isomerase (EC 5.3.1.30) is an isomerase that can convert 5-deoxy-D-glucuronate into 5-dehydro-2-deoxy-D-gluconate.
Cat. No.: HY-E71912
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5-Dehydro-2-deoxyphosphogluconate aldolase (EC 4.1.2.29) is a lyase that can convert 6-phospho-5-dehydro-2-deoxy-D-gluconate into 3-oxopropanoate and dihydroxyacetone phosphate.
Cat. No.: HY-E71505
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2-Dehydro-3-deoxygluconokinase (EC 2.7.1.45) is a phosphotransferase that acts on alcoholic hydroxyl groups as acceptors. This enzyme catalyzes the phosphorylation of 2-dehydro-3-deoxy-D-gluconate (KDG) and is a key enzyme in the bacterial Entner–Doudoroff (ED) pathway.
Cat. No.: HY-E71956
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6-Deoxy-6-sulfogluconolactonase (EC 3.1.1.99) is a hydrolase that can convert 6-deoxy-6-sulfo-D-glucono-1,5-lactone and H2O into 6-deoxy-6-sulfo-D-gluconate and H +.
Cat. No.: HY-E71510
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2-Dehydro-3-deoxy-phosphogluconate aldolase (EC 4.1.2.14) is an aldolase and a key enzyme in the bacterial Entner–Doudoroff (ED) pathway; it catalyzes the cleavage of KDPG (6-phospho-2-keto-3-deoxy-D-gluconate) into pyruvate and glyceraldehyde-3-phosphate (G3P).
Cat. No.: HY-E71504
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2-Dehydro-3-deoxyglucono/galactono-kinase (EC 2.7.1.178) from the archaeon Sulfolobus solfataricus is involved in glucose and galactose catabolism via the branched variant of the Entner-Doudoroff pathway, and phosphorylates 2-dehydro-3-deoxy-D-gluconate and 2-dehydro-3-deoxy-D-galactonate with similar catalytic efficiency. cf.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
