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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
23 Results for "
D-Gluconate
" in MedChemExpress (MCE) Product Catalog:
Products (23)
23 Results for "D-Gluconate" in MCE Product Catalog:
1
1 Cited Publications
Synonyms: Calcium D-Gluconate; Gluconic acid hemicalcium salt
Synonyms: D-Gluconic acid sodium salt; Sodium D-Gluconate; D-Gluconate sodium salt
Cat. No.: HY-W105875
CAS No.: 22830-45-1
Synonyms: D-Gluconic acid iron(II) salt dihydrate, 98%
Cat. No.: HY-Y0569H
CAS No.: 59625-89-7
Cat. No.: HY-W768336
CAS No.: 2687960-00-3
Synonyms: D-Gluconic acid-13C6 sodium; D-Gluconate-13C6 sodium
Cat. No.: HY-B1092AS
CAS No.: 2687959-99-3
Synonyms: D-Gluconic acid sodium salt-1-13C; Sodium D-Gluconate-1-13C; D-Gluconate sodium salt-1-13C
Synonyms: Calcium D-Gluconate (Standard); Gluconic acid hemicalcium salt (Standard)
Category:
Cat. No.: HY-B1092AR
CAS No.: 527-07-1
Synonyms: D-Gluconic acid sodium salt (Standard); Sodium D-Gluconate (Standard); D-Gluconate sodium salt (Standard)
Cat. No.: HY-E71955
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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-B1092AS2
Synonyms: D-Gluconic acid sodium salt-d6; Sodium D-Gluconate-d6; D-Gluconate sodium salt-d6
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-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.
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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
