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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
19 Results for "
α-trehalose
" in MedChemExpress (MCE) Product Catalog:
Products (19)
19 Results for "α-trehalose" in MCE Product Catalog:
10
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10
10 Cited Publications
Synonyms: D-trehalose dihydrate; α,α-trehalose dihydrate
Category:
other families Polysaccharides Microorganisms Animals Other Diseases Plants Disease Research Fields Saccharides
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Synonyms: Tre6P potassium
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Cat. No.: HY-N1132AR
CAS No.: 6138-23-4
Synonyms: D-trehalose dihydrate (Standard); α,α-trehalose dihydrate (Standard)
Cat. No.: HY-N1132S
CAS No.: 2028292-31-9
Synonyms: D-trehalose-d14; α,α-trehalose-d14
Category:
Cat. No.: HY-131368A
CAS No.: 4484-88-2
Synonyms: Tre6P
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Cat. No.: HY-W768345
CAS No.: 1313730-07-2
Synonyms: D-trehalose-13C12; α,α-trehalose-13C12
Cat. No.: HY-W400427
CAS No.: 59-56-3
Research Areas:
α-D-Glucose-1-phosphate is a derivative of D-glucose (HY-B0389). α-D-Glucose-1-phosphate serves as a starting material for glucuronic acid synthesis. Glucuronic acid acts as a Ca 2+ chelator and also functions as a biosynthetic substrate for the production of linear maltooligosaccharides or α,α-trehalose. α-D-Glucose-1-phosphate can be used as a cytostatic compound, Antibiotic, and immunosuppressant essential for heart disease management. α-D-Glucose-1-phosphate is applicable to the research of heart disease .
Cat. No.: HY-131368R
CAS No.: 136632-28-5
Synonyms: Tre6P potassium (Standard)
Cat. No.: HY-E71207
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Research Areas:
α,α-Trehalose synthase (EC 2.4.1.245) requires Mg2+ for maximal activity. The enzyme-catalysed reaction is reversible. In the reverse direction to that shown above, α,α-Trehalose synthase (EC 2.4.1.245) is specific for α,α-Trehalose as substrate, as it cannot use α-or β-paranitrophenyl glucosides, maltose, sucrose, lactose or cellobiose.
Cat. No.: HY-N1132S1
CAS No.: 1334376-67-8
Synonyms: D-trehalose-d2; α,α-trehalose-d2
Cat. No.: HY-E71206
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α,α-Trehalose phosphorylase (EC 2.4.1.64) belongs to the family of glycosyltransferases, specifically the hexosyltransferases.
Cat. No.: HY-E71205
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α,α-Trehalose (EC 3.2.1.28) is an anomer-inverting glucosidase that catalyses the hydrolysis of the α-glucosidic O-linkage of α,α-Trehalose, releasing initially equimolar amounts of α-and β-D-glucose.
Cat. No.: HY-145536
CAS No.: 150399-99-8
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α-D-Glucose-1-phosphate disodium tetrahydrate is a derivative of D-glucose (HY-B0389). α-D-Glucose-1-phosphate disodium tetrahydrate serves as a starting material for glucuronic acid synthesis. Glucuronic acid acts as a Ca 2+ chelator and also functions as a biosynthetic substrate for the production of linear maltooligosaccharides or α,α-trehalose. α-D-Glucose-1-phosphate disodium tetrahydrate can be used as a cytostatic compound, Antibiotic, and immunosuppressant essential for heart disease management. α-D-Glucose-1-phosphate disodium tetrahydrate is applicable to the research of heart disease .
Cat. No.: HY-E70898
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Research Areas:
Trehalose-6-phosphate hydrolase, Escherichia coli (EC 3.2.1.93), belongs to the hydrolase family and is a glycosidase that hydrolyzes O- and S-glycoside compounds. Trehalose-6-phosphate hydrolase participates in the metabolism of starch and sucrose. Its substrates are α,α'-trehalose-6-phosphate and water, and its products are D-glucose and D-glucose-6-phosphate.
Cat. No.: HY-E70898A
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Research Areas:
Trehalose-6-phosphate hydrolase, Bacillus subtilis (EC 3.2.1.93), belongs to the hydrolase family and is a glycosidase that hydrolyzes O- and S-glycoside compounds. Trehalose-6-phosphate hydrolase participates in the metabolism of starch and sucrose. Its substrates are α,α'-trehalose-6-phosphate and water, and its products are D-glucose and D-glucose-6-phosphate.
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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
