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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
26 Results for "
esterification reaction
" in MedChemExpress (MCE) Product Catalog:
Products (26)
26 Results for "esterification reaction" in MCE Product Catalog:
16
16 Cited Publications
Cat. No.: HY-D0178
CAS No.: 25952-53-8
1
1 Cited Publications
Cat. No.: HY-15929
CAS No.: 14348-40-4
Synonyms: 2,4,6-Tribromo-3-hydroxybenzoic acid
Cat. No.: HY-W020983
CAS No.: 2923-28-6
Synonyms: Triflic acid silver; Perfluoromethanesulfonic acid silver; Fluorad FC 24 silver
Target:
Research Areas:
Chloramphenicol palmitate is an orally active prodrug of Chloramphenicol (HY-B0239), obtained from the esterification reaction between the agent and Palmitic acid (HY-N0830). Chloramphenicol palmitate is rapidly and completely hydrolyzed by intestinal esterase, releasing Chloramphenicol. Chloramphenicol is an orally effective broad-spectrum antibiotic .
Cat. No.: HY-W061674
CAS No.: 13991-37-2
Synonyms: (E)-Pent-2-enoic acid
Cat. No.: HY-34643
CAS No.: 30964-00-2
Synonyms: Hept-6-ynoic acid
Target:
Research Areas:
Hexanoylic acid (Hex-6-ynoic acid) is a drug intermediate. Hexanoylic acid can be functionalized by esterification reaction to paclitaxel (HY-B0015), enabling it to undergo an efficient ring addition reaction with β-cyclodextrin, thereby enhancing its water solubility, stability and targeting properties .
Cat. No.: HY-E70600
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Research Areas:
Human CES1 Enzyme is a recombinantly expressed CES1 enzyme. Human CES1 Enzyme, an enzyme responsible for the hydrolysis of ester- and amide-containing molecules, is mainly expressed in the liver where it is crucial for the processing of active metabolites and is also involved in trans-esterification reactions .
Cat. No.: HY-W088501
CAS No.: 1617-32-9
Cat. No.: HY-W015695
CAS No.: 137-00-8
Target:
Cat. No.: HY-186012
CAS No.: 3032193-08-8
Target:
Research Areas:
TPP@CUR is the product formed by the esterification reaction between Curcumin (HY-N0005) and (5-hydroxy-5-oxopentyl)triphenylphosphonium bromide (TPP). TPP@CUR can be used to synthesize Ser@TPP@CUR (HY-151342), which can then be used in studies of acute kidney injury .
Cat. No.: HY-E70611
Target:
Research Areas:
C. rugosa Lipase is a biocatalyst that has recently attracted much attention because of its regio-selectivity in various types of reactions, such as trans-esterification, hydrolysis, and esterification .
Cat. No.: HY-W036734
CAS No.: 23868-34-0
Target:
Research Areas:
Chloramphenicol palmitate (Standard) is the analytical standard of Chloramphenicol palmitate (HY-B1599). This product is intended for research and analytical applications. Chloramphenicol palmitate is an orally active prodrug of Chloramphenicol (HY-B0239), obtained from the esterification reaction between the agent and Palmitic acid (HY-N0830). Chloramphenicol palmitate is rapidly and completely hydrolyzed by intestinal esterase, releasing Chloramphenicol. Chloramphenicol is an orally effective broad-spectrum antibiotic .
Cat. No.: HY-183003
Cat. No.: HY-183003A
Cat. No.: HY-183003B
Cat. No.: HY-183003C
Cat. No.: HY-183003D
Cat. No.: HY-183163
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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
