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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
29 Results for "
reducing power
" in MedChemExpress (MCE) Product Catalog:
Products (29)
29 Results for "reducing power" in MCE Product Catalog:
6
6 Cited Publications
Synonyms: Sodium lauryl sulfate; Laurylsulfuric acid sodium salt
Research Areas:
Sodium dodecyl sulfate is an anionic surfactant commonly used as a detergent, emulsifier, and protein denaturant in various industrial processes, especially in the production of personal care products, cleaners, and laboratory reagents. Sodium dodecyl sulfate has unique chemical properties that make it an effective ingredient in many applications, helping to reduce surface tension and enhance cleaning power.
1
1 Cited Publications
Cat. No.: HY-W127785
CAS No.: 1643-20-5
Synonyms: N,N-Dimethyldodecan-1-amine oxide; Dodecyldimethylamine oxide
Target:
Research Areas:
N,N-Dimethyldodecylamine N-oxide is an amine oxide surfactant commonly used as a detergent, emulsifier and wetting agent in various industrial processes, especially in personal care products and household cleaning in the production of agents. N,N-Dimethyldodecylamine N-oxide has unique chemical properties that make it an effective ingredient in many product formulations to help reduce surface tension and enhance cleaning power.
Cat. No.: HY-W130648
CAS No.: 126-92-1
Cat. No.: HY-N2307A
CAS No.: 54383-28-7
Synonyms: (+)-Lirinidine
Category:
Alkaloids Plant Monophenols Nelumbo nucifera Gaertn. Extract Phenols Nymphaeaceae Extract Disease Research Fields Isoquinoline Alkaloids Cancer
Target:
Cat. No.: HY-125863C
CAS No.: 9001-40-5
Synonyms: G6PD, Bacillus sp.
Target:
Research Areas:
Glucose-6-phosphate dehydrogenase, Bacillus sp. (G6PD, Bacillus sp.) (EC 1.1.1.49) is an NADP-dependent antioxidant metabolic enzyme. Glucose-6-phosphate dehydrogenase, Bacillus sp. is induced by sublethal doses of Menadione (HY-B0332) and increasing concentrations of NaCl in Bacillus sp. F26. Glucose-6-phosphate dehydrogenase, Bacillus sp. catalyzes the oxidation of glucose-6-phosphate (G6P) to 6-phosphoglucono-δ-lactone, while reducing NADP + to NADPH, providing reducing power for the antioxidant defense system and cellular redox balance of Bacillus sp. F26. Glucose-6-phosphate dehydrogenase, Bacillus sp. is used in research related to diabetic complications .
Cat. No.: HY-N9588
CAS No.: 22860-72-6
Target:
Cat. No.: HY-125863A
CAS No.: 9001-40-5
Synonyms: G6PD (Leuconostoc sp., recombinant)
Target:
Research Areas:
Glucose-6-phosphate dehydrogenase (Leuconostoc sp., recombinant) (G6PD (Leuconostoc sp., recombinant)) (EC 1.1.1.49) is an NADP-dependent antioxidant metabolic enzyme. Glucose-6-phosphate dehydrogenase (Leuconostoc sp., recombinant) can be induced by sublethal doses of Menadione (HY-B0332) and increasing concentrations of NaCl. Glucose-6-phosphate dehydrogenase (Leuconostoc sp., recombinant) catalyzes the oxidation of glucose-6-phosphate (G6P) to 6-phosphoglucono-δ-lactone, while reducing NADP + to NADPH, providing reducing power for the antioxidant defense system and cellular redox balance of bacteria. Glucose-6-phosphate dehydrogenase (Leuconostoc sp., recombinant) is used in research related to diabetic complications .
Cat. No.: HY-19682
CAS No.: 68576-86-3
Target:
Research Areas:
Enciprazine is an orally active non-benzodiazepine anxiolytic. Enciprazine acts as an agonist of 5-HT1A receptor (5-HT1AR) and an antagonist of α1-adrenergic receptor (α1-adrenergic receptor) . Enciprazine induces drug-related electroencephalogram changes by reducing the average power of δ waves and θ waves, and increasing the average power of α waves and fast β waves. Enciprazine exhibits anti-aggressive activity, with only weak sedative and ataxic effects. Enciprazine regulates plasma corticosterone levels and activates the hypothalamic-pituitary-adrenal axis. Enciprazine can be used in research related to anxiety disorders, generalized anxiety syndrome and psychosis .
Cat. No.: HY-N10770
CAS No.: 1221762-70-4
Target:
Cat. No.: HY-W127785R
CAS No.: 1643-20-5
Synonyms: N,N-Dimethyldodecan-1-amine oxide (Standard); Dodecyldimethylamine oxide (Standard)
Research Areas:
N,N-Dimethyldodecylamine N-oxide (Standard) is the analytical standard of N-ethyl-N-oxido-dodecan-1-amine. This product is intended for research and analytical applications. N,N-Dimethyldodecylamine N-oxide is an amine oxide surfactant commonly used as a detergent, emulsifier and wetting agent in various industrial processes, especially in personal care products and household cleaning in the production of agents. N,N-Dimethyldodecylamine N-oxide has unique chemical properties that make it an effective ingredient in many product formulations to help reduce surface tension and enhance cleaning power.
Cat. No.: HY-W710279
Cat. No.: HY-N21603
CAS No.: 1909225-92-8
Target:
Cat. No.: HY-N21589
CAS No.: 1619977-01-3
Category:
Plant Flavonoids Cyperaceae Extract Flavanols Phenols Polyphenols Eleocharis dulcis (Burm. f.) Trin. ex Hensch. Extract
Target:
Cat. No.: HY-N21598
CAS No.: 1619977-00-2
Category:
Flavonols Plant Flavonoids Cyperaceae Extract Eleocharis dulcis (Burm. f.) Trin. ex Hensch. Extract
Target:
Category:
Plant Artemisia tridentata Nutt. Extract Terpenoids Sesquiterpenes Compositae/Asteraceae Extract
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Cat. No.: HY-N7648A
CAS No.: 54749-97-2
Synonyms: Atherospermine hydrochloride
Target:
Cat. No.: HY-E71546
Target:
Research Areas:
2-Hydroxy-4-carboxymuconate semialdehyde hemiacetal dehydrogenase (EC 1.1.1.312) is an NADP+-dependent dehydrogenase belonging to the class of oxidoreductases. It catalyzes the oxidation of the substrate to acetate, producing CO2 and NADPH, and plays a role in microbial carbon metabolism and the generation of reducing power.
Cat. No.: HY-N21588
CAS No.: 1619976-96-3
Category:
Flavonols Plant Flavonoids Cyperaceae Extract Eleocharis dulcis (Burm. f.) Trin. ex Hensch. Extract
Target:
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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
