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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
100 Results for "
dioxide
" in MedChemExpress (MCE) Product Catalog:
Products (100)
100 Results for "dioxide" in MCE Product Catalog:
Cat. No.: HY-W098585R
CAS No.: 59804-25-0
Target:
Methyl 4-hydroxy-2-methyl-2H-thieno[2,3-e][1,2]thiazine-3-carboxylate 1,1-dioxide (Standard) is the analytical standard of Methyl 4-hydroxy-2-methyl-2H-thieno[2,3-e][1,2]thiazine-3-carboxylate 1,1-dioxide. This product is intended for research and analytical applications.
Cat. No.: HY-W075496
CAS No.: 23613-32-3
Synonyms: Dibenzothiophene-5,5'-dioxide-3,7-dicarboxylic acid
5,5-Dioxo-5H-dibenzo[b,d]thiophene-3,7-dicarboxylic acid (Dibenzothiophene-5,5'-dioxide-3,7-dicarboxylic acid) is a metal-organic framework (MOF).
Cat. No.: HY-128974R
CAS No.: 69227-93-6
Synonyms: Lauryl Maltoside (Standard)
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N-Dodecyl-β-D-maltoside (Standard) is the analytical standard of N-Dodecyl-β-D-maltoside (HY-128974). This product is intended for research and analytical applications. N-Dodecyl-β-D-maltoside (Lauryl Maltoside) is a non-ionic detergent. N-Dodecyl-β-D-maltoside has strong adsorption on alumina, titanium dioxide and hematite. N-Dodecyl-β-D-maltoside can promote the reactivation of various proteins. N-Dodecyl-β-D-maltoside can effectively stabilize photoactive reaction center complexes (RCs) and inhibit the degradation of Rhodopseudomonas spheroides R-26 reaction center in solution. N-Dodecyl-β-D-maltoside can be used for purification and stabilization of RNA polymerase and for detection of protein-lipid interactions .
Cat. No.: HY-P1775B
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Carbonic Anhydrase, Human (EC 4.2.1.1) is a zinc metalloenzyme that catalyzes the hydration of carbon dioxide to form carbonic acid. Carbonic Anhydrase participates in a variety of important physiological processes, such as the maintenance of pH and carbon dioxide homeostasis, the transport of bicarbonate and carbon dioxide, biosynthetic reactions, bone resorption, calcification, and tumorigenesis.
Cat. No.: HY-E70986
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Carbonic Anhydrase I, Human (EC 4.2.1.1) is a zinc metalloenzyme that catalyzes the hydration of carbon dioxide to form carbonic acid. Carbonic Anhydrase I participates in a variety of important physiological processes, such as the maintenance of pH and carbon dioxide homeostasis, the transport of bicarbonate and carbon dioxide, biosynthetic reactions, bone resorption, calcification, and tumorigenesis.
Carbonic acid is a diprotic acid, acidulant and anesthetic. Carbonic acid penetrates living cells more easily than most other acids, exhibits stronger toxicity than inorganic acids at equivalent concentrations, and exacerbates ocean acidification. Carbonic acid binds reversibly to cellular proteins, acidifies cell sap and protoplasmic inclusions, inhibits Paramecium growth and various cellular functions, induces reversible cellular changes, produces lethal effects at high doses, decomposes into carbon dioxide and H2O, and participates in the maintenance of physiological pH balance .
Cat. No.: HY-79019
CAS No.: 14101-58-7
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N-Benzylsulfamide is a benzyl-substituted sulfamide reagent. N-Benzylsulfamide can be used as a synthetic precursor to generate dioxides of bicyclic thiadiazines .
Cat. No.: HY-P11577
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Cat. No.: HY-E71035
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Carbonic anhydrase II, Bovine (EC 4.2.1.1) catalyzes the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa) , a reversible reaction that occurs relatively slowly in the absence of a catalyst.
Cat. No.: HY-E71035A
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Research Areas:
Carbonic anhydrase II, Human (EC 4.2.1.1) catalyzes the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa) , a reversible reaction that occurs relatively slowly in the absence of a catalyst.
Cat. No.: HY-P1775C
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Carbonic anhydrase, E. coli (EC 4.2.1.1) catalyzes the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa) , a reversible reaction that occurs relatively slowly in the absence of a catalyst.
Cat. No.: HY-W013767R
CAS No.: 59669-26-0
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Thiodicarb (Standard) is the analytical standard of Thiodicarb. This product is intended for research and analytical applications. Thiodicarb is a carbamate insecticide used to control flies in animal and poultry houses and dairies. Thiodicarb is metabolized into methomyl in animals and plants, and subsequently degraded into carbon dioxide and acetonitrile .
Cat. No.: HY-E70938
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L-Tyrosine Decarboxylase Apoenzyme, Streptococcus faecalis (EC 4.1.1.25), is a carboxyl lyase capable of cleaving carbon-carbon bonds. L-Tyrosine Decarboxylase Apoenzyme participates in tyrosine metabolism and alkaloid biosynthesis. L-Tyrosine Decarboxylase Apoenzyme uses a cofactor—pyridoxal phosphate. L-Tyrosine Decarboxylase Apoenzyme has one substrate, L-tyrosine, and two products: tyramine and carbon dioxide.
Cat. No.: HY-P2825A
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L-Tyrosine Decarboxylase, Streptococcus faecalis (EC 4.1.1.25), is a carboxyl lyase capable of cleaving carbon-carbon bonds. L-Tyrosine Decarboxylase Apoenzyme participates in tyrosine metabolism and alkaloid biosynthesis. L-Tyrosine Decarboxylase Apoenzyme uses a cofactor—pyridoxal phosphate. L-Tyrosine Decarboxylase Apoenzyme has one substrate, L-tyrosine, and two products: tyramine and carbon dioxide.
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Cat. No.: HY-W127787R
CAS No.: 6131-98-2
Synonyms: L-(+)-Tartaric acid sodium hydrate (Standard)
Cat. No.: HY-B1191S1
Synonyms: 2,6-Lupetidine-d5
Cat. No.: HY-W009690
CAS No.: 10543-57-4
Synonyms: Tetraacetylethylenediamine; TAED
Research Areas:
N,N,N',N'-Tetraacetylethylenediamine (Tetraacetylethylenediamine; TAED) is a disinfectant and bleach activator. N,N,N',N'-Tetraacetylethylenediamine is a common bleach activator in phosphorus-free laundry detergent formulations, which acts to activate sodium perborate and improve bleaching efficiency at low temperatures. N,N,N',N'-Tetraacetylethylenediamine reacts with sodium percarbonate in water to produce peracetic acid with strong oxidative bactericidal activity. This reaction is environmentally friendly, and the final degradation products are sodium carbonate, acetic acid, ammonia, carbon dioxide, oxygen and water .
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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
