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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 "
divalent metal ions
" in MedChemExpress (MCE) Product Catalog:
Products (23)
23 Results for "divalent metal ions" in MCE Product Catalog:
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Framycetin (Neomycin B), an aminoglycoside antibiotic, is a potent RNase P cleavage activity inhibitor with a Ki of 35 μM. Framycetin competes for specific divalent metal ion binding sites in RNase P RNA. Framycetin inhibits hammerhead ribozyme with a Ki of 13.5 μM. Framycetin, a 5″-azido neomycin B precursor, binds the Drosha site in miR-525 and is used for hepatic encephalopathy and enteropathogenic E. coli infections .
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1 Cited Publications
Synonyms: Neomycin B sulfate; Fradiomycin B sulfate
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Framycetin sulfate (Neomycin B sulfate), an aminoglycoside antibiotic, is a potent RNase P cleavage activity inhibitor with a Ki of 35 μM. Framycetin sulfate competes for specific divalent metal ion binding sites in RNase P RNA. Framycetin sulfate inhibits hammerhead ribozyme with a Ki of 13.5 μM. Framycetin sulfate, a 5″-azido neomycin B precursor, binds the Drosha site in miR-525 and is used for hepatic encephalopathy and enteropathogenic E. coli infections .
Cat. No.: HY-Y0682S
CAS No.: 203806-08-0
Synonyms: EDTA-d12
Cat. No.: HY-W587753
CAS No.: 22601-59-8
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Synonyms: GPDH, rabbit muscle; α-Glycerophosphate dehydrogenase, rabbit muscle; Glycerol phosphate dehydrogenase, rabbit muscle
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Glycerol‑3‑phosphate dehydrogenase, rabbit muscle (GPDH; α-Glycerophosphate dehydrogenase; Glycerol phosphate dehydrogenase) is an NADH-dependent oxidoreductase derived from rabbit muscle that participates in glycolysis, gluconeogenesis, and the glycerol‑3‑phosphate shuttle metabolic pathway. Glycerol‑3‑phosphate dehydrogenase, rabbit muscle uses NADH as a reducing equivalent donor, and its substrate binding relies on the phosphate-binding site in the active center; it catalyzes the reversible reduction of dihydroxyacetone phosphate to L‑α‑glycerol‑3‑phosphate. The catalytic activity of the enzymatic reaction of Glycerol‑3‑phosphate dehydrogenase, rabbit muscle is regulated by pH and divalent metal ions. Glycerol‑3‑phosphate dehydrogenase, rabbit muscle can be used in metabolism-related studies .
Cat. No.: HY-W105699
CAS No.: 13235-36-4
Synonyms: Ethylenediaminetetraacetic acid tetrasodium tetrahydrate
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EDTA tetrasodium tetrahydrate is a metal chelator (binds to metal divalent and trivalent cations including calcium), which shows activities of anticoagulant and anti-hypercalcemic. EDTA tetrasodium tetrahydrate decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification. EDTA tetrasodium tetrahydrate can also decrease the formation of disulfide bonds .
Cat. No.: HY-Y0682S1
CAS No.: 203805-96-3
Synonyms: EDTA-d16
Cat. No.: HY-W110925
CAS No.: 1324-80-7
Synonyms: GPDH, microorganism; α-Glycerophosphate dehydrogenase, microorganism; Glycerol phosphate dehydrogenase, microorganism
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Glycerol-3-phosphate dehydrogenase, microorganism (GPDH; α-Glycerophosphate dehydrogenase; Glycerol phosphate dehydrogenase) is an NADH-dependent oxidoreductase derived from microorganism that participates in glycolysis, gluconeogenesis, and the glycerol‑3‑phosphate shuttle metabolic pathway. Glycerol-3-phosphate dehydrogenase, microorganism uses NADH as a reducing equivalent donor, and its substrate binding relies on the phosphate-binding site in the active center; it catalyzes the reversible reduction of dihydroxyacetone phosphate to L‑α‑glycerol‑3‑phosphate. The catalytic activity of the enzymatic reaction of Glycerol-3-phosphate dehydrogenase, microorganism is regulated by pH and divalent metal ions. Glycerol-3-phosphate dehydrogenase, microorganism can be used in metabolism-related studies .
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Phosphorylase b is one of the two forms of phosphorylase present in skeletal muscle. The other is Phosphorylase a, which can be transformed into one another. The conversion process requires the addition of divalent metal ions and ATP .
Cat. No.: HY-121858
CAS No.: 34441-14-0
Cat. No.: HY-17624AR
CAS No.: 4146-30-9
Synonyms: Neomycin B sulfate (Standard); Fradiomycin B sulfate (Standard)
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Framycetin (sulfate) (Standard) is the analytical standard of Framycetin (sulfate). This product is intended for research and analytical applications. Framycetin sulfate (Neomycin B sulfate), an aminoglycoside antibiotic, is a potent RNase P cleavage activity inhibitor with a Ki of 35 μM. Framycetin sulfate competes for specific divalent metal ion binding sites in RNase P RNA. Framycetin sulfate inhibits hammerhead ribozyme with a Ki of 13.5 μM. Framycetin sulfate, a 5″-azido neomycin B precursor, binds the Drosha site in miR-525 and is used for hepatic encephalopathy and enteropathogenic E. coli infections .
Cat. No.: HY-P11825
Cat. No.: HY-E71580
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2-Keto-myo-inositol isomerase (EC 5.3.99.11) requires a divalent metal ion for activity.
Cat. No.: HY-E71101
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(R)-Limonene synthase (EC 4.2.3.20) requires divalent metal ions (preferably Mn2+) for catalysis. (R)-Limonene synthase (EC 4.2.3.20) is found in plants of the genera Citrus, Carum, and Anethum.
Cat. No.: HY-E71073
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(4S)-Limonene synthaseis a recombinant enzyme (also known as a monoterpene synthase or cyclase) from the grand fir (Abies grandis) requires Mn2+ and K+ for activity. Mg2+ is essentially ineffective as the divalent metal ion cofactor.
Cat. No.: HY-E71529
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2-epi-Valiolone synthase (EC 4.2.3.155) can produce 2-epi-valine ketone, which requires a divalent metal ion (Zn2+ or Co2+) and a NAD+ cofactor. The NAD+ cofactor is briefly reduced during the reaction.
Cat. No.: HY-17624S
Synonyms: Neomycin B-d2; Fradiomycin B-d2
Cat. No.: HY-E71528
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2-epi-5-epi-Valiolone synthase (EC 4.2.3.152) exhibits high specificity for α-D-sedaripogonanone-7-phosphate. 2-epi-5-epi-Valiolone synthase (EC 4.2.3.152) requires a divalent metal ion (Zn2+ or Co2+) and a NAD+ cofactor, the latter of which is transiently reduced during the reaction. 2-epi-5-epi-Valiolone synthase (EC 4.2.3.152) participates in the biosynthesis of C7N-aminocyclic alcohols.
Cat. No.: HY-P2765B
Synonyms: GPDH, Rabbit; α-Glycerophosphate dehydrogenase, Rabbit; Glycerol phosphate dehydrogenase, Rabbit
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Glycerol-3-phosphate dehydrogenase, Rabbit (GPDH; α-Glycerophosphate dehydrogenase; Glycerol phosphate dehydrogenase) is an NADH-dependent oxidoreductase derived from Rabbit that participates in glycolysis, gluconeogenesis, and the glycerol‑3‑phosphate shuttle metabolic pathway. Glycerol-3-phosphate dehydrogenase, Rabbit uses NADH as a reducing equivalent donor, and its substrate binding relies on the phosphate-binding site in the active center; it catalyzes the reversible reduction of dihydroxyacetone phosphate to L‑α‑glycerol‑3‑phosphate. The catalytic activity of the enzymatic reaction of Glycerol-3-phosphate dehydrogenase, Rabbit is regulated by pH and divalent metal ions. Glycerol-3-phosphate dehydrogenase, Rabbit can be used in metabolism-related studies .
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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
