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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
7 Results for "
benzoyl-CoA
" in MedChemExpress (MCE) Product Catalog:
Products (7)
7 Results for "benzoyl-CoA" in MCE Product Catalog:
Target:
Research Areas:
Benzoyl coenzyme A (Benzoyl CoA) is A derivative of Coenzyme A (CoA) in which the mercaptan group of CoA binds to the benzoyl group. Benzoyl coenzyme A is involved in the catalytic reaction as a substrate for the acyl transfer reaction. Benzoyl coenzyme A is a versatile metabolic intermediate that can be used to reveal substrate specificity of enzymes, metabolic regulation, and drug metabolism .
Synonyms: benzoyl CoA trilithium
Cat. No.: HY-134129B
Synonyms: benzoyl CoA sodium
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Benzoyl coenzyme A (sodium) is the sodium salt form of Benzoyl coenzyme A (HY-134129). Benzoyl coenzyme A (sodium) is A derivative of Coenzyme A (CoA) in which the mercaptan group of CoA binds to the benzoyl group. Benzoyl coenzyme A (sodium) is involved in the catalytic reaction as a substrate for the acyl transfer reaction. Benzoyl coenzyme A (sodium) is a versatile metabolic intermediate that can be used to reveal substrate specificity of enzymes, metabolic regulation, and drug metabolism .
Cat. No.: HY-E71423
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2,3-Epoxybenzoyl-CoA dihydrolase (EC 4.1.2.44) participates in the aerobic benzoyl-CoA catabolic pathway of the bacterium Azoarcus evansii. It converts 2,3-epoxy-2,3-dihydrobenzoyl-CoA into its oxepin form prior to ring opening and the formation of a dialdehyde intermediate.
Cat. No.: HY-E71157
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1,4-Dihydroxy-2-naphthoyl-CoA hydrolase (EC 3.1.2.28) participates in the synthesis of menaquinones, phylloquinone, as well as several plant pigments. 1,4-Dihydroxy-2-naphthoyl-CoA hydrolase (EC 3.1.2.28) does not accept benzoyl-CoA or phenylacetyl-CoA as substrates.
Cat. No.: HY-E71837
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4-Hydroxybenzoyl-CoA reductase (EC 1.3.7.9) is an oxidoreductase that can convert oxidized 2[4Fe-4S]-[ferredoxin], benzoyl-CoA and H2O into 4-hydroxybenzoyl-CoA, reduced 2[4Fe-4S]-[ferredoxin] and 2 H +.
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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
