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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
44 Results for "
phenol groups
" in MedChemExpress (MCE) Product Catalog:
Products (44)
44 Results for "phenol groups" in MCE Product Catalog:
Research Areas:
Benzoic anhydride (Standard) is the analytical standard of Benzoic anhydride. This product is intended for research and analytical applications. Benzoic anhydride is a catalyst that can be used for organic synthesis reactions. Benzoic anhydride is used as a chemical titration reagent for selective quantification and deactivation of phenolic hydroxyl groups on the surface of carbon nanotubes .
Cat. No.: HY-164055
CAS No.: 202828-10-2
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HL1 is a Schiff base ligand. HL1 exhibits chelation-enhanced fluorescence effect when forming complexes and can be used as a fluorescent probe for metal ions. HL1 can be used for the research of cancer .
Cat. No.: HY-G0004R
CAS No.: 37519-14-5
Synonyms: 3-Hydroxyacetaminophen (Standard)
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Acetaminophen metabolite 3-hydroxy-acetaminophen (3-Hydroxyacetaminophen) (Standard) is the analytical standard of Acetaminophen metabolite 3-hydroxy-acetaminophen (HY-G0004). This product is intended for research and analytical applications. Acetaminophen metabolite 3-hydroxy-acetaminophen is a non-toxic metabolite and antioxidant of acetaminophen (HY-66005) with free radical scavenging activity. Acetaminophen metabolite 3-hydroxy-acetaminophen can reduce oxidative damage by exerting electron donation ability and antioxidant activity through phenolic hydroxyl groups. 3-hydroxy-acetaminophen can be used to study the toxicity mechanism and drug metabolism of acetaminophen .
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Mandelonitrile benzoate is a defensive secretion of millipedes that releases other chemicals during the cyanidation process in addition to hydrocyanic acid (HCN) and benzaldehyde. Several families of millipedes, including Polydesmidae, Paradoxosomatidae, and Euryuridae, have been shown to secrete phenols and guaiaeol, with one Paradoxosomatid also producing ethylbenzoic acid and benzoic acid. In addition, members of the Xystodesmidae family commonly produce three compounds: benzoic acid, mandelonitrile benzoate, and benzoyl cyanide. Benzoyl cyanide has not been previously discovered as a natural product. These additional natural products are discussed as defensive antipredator and antibiotic agents. Benzoyl cyanide appears to have anesthetic properties for some predators. The study provides a preliminary chemotaxonomic basis for distinguishing various taxonomic groups of millipedes.
Cat. No.: HY-N15727
CAS No.: 1251459-63-8
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Cat. No.: HY-189345
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Antileishmanial agent-45 is a C6-substituted eugenol derivative bearing a 1,2,3-triazole linker directly attached to the aromatic ring, a free phenolic hydroxyl group, and a benzyloxy substituent. Antileishmanial agent-45 retains and enhances the antileishmanial activity of its natural-product precursor eugenol. Antileishmanial agent-45 can be used for the research of leishmaniasis .
Cat. No.: HY-W140502
CAS No.: 2589-78-8
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4-Hexadecylphenol is a phenol group with a 16-carbon tail.
Cat. No.: HY-W413662
CAS No.: 119649-45-5
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4-[(4-Methoxyphenyl)methoxy]butan-1-ol is a compound with a methyl phenol group and a butanol tail. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
Cat. No.: HY-E71629
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3-(hydroxyamino)Phenol mutase (EC 5.4.4.3) belongs to the family of isomerases, specifically those intramolecular transferases transferring hydroxy groups.
Cat. No.: HY-184613
Polydopamine nanoparticles (PDA NPs) are nanoscale materials formed by the self-polymerization of dopamine monomers under specific conditions. Their structural characteristics include a polyphenolic structure and a surface rich in functional groups such as amino and phenolic hydroxyl groups, which provide abundant chemical modification sites.
Cat. No.: HY-W598194
CAS No.: 1355510-12-1
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1-((4-Azidobutoxy)methyl)-4-methoxybenzene is a compound with a methyl phenol group and a butyl tail ending in a terminal azide. The azide (N3) group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage.
Cat. No.: HY-L057
1,299 compounds
Phenolic compounds are usually referred to as a diverse group of naturally occurring compounds with multiple medical properties, such as antioxidants, antimicrobial properties. Those compounds are commonly found in food and plants. They have high synthetic, medicinal and industrial values. Polyphenols are compounds with multiple phenolic functionalities. Naturally occurring polyphenols are known to have biological activities for use as drugs, for example, in diseases like AIDS, heart ailments, ulcer formation, bacterial infection, mutagenesis and neural disorders.
MCE offers a unique collection of 1,299 natural phenol compounds which is a useful tool for drug discovery as an important source of lead compounds.
Cat. No.: HY-W006081
CAS No.: 4920-77-8
3-Methyl-2-nitrophenol is a UDP-glucuronyltransferase (EC 2.4.1.17) acceptor substrate that can be confirmed to undergo glucuronidation catalyzed by the enzyme to form a glucuronide conjugate. 3-Methyl-2-nitrophenol functions as a substrate for conjugation, with glucuronidation forming a glucuronide conjugate that eliminates the parent compound’s characteristic yellow color. 3-Methyl-2-nitrophenol has higher lipid solubility that contributes to high glucuronidation conversion rate, and exhibits lower absorbance at 340 nm to act as a less interfering substrate for the NADH-NAD +-linked UDP-glucuronyltransferase assay .
Cat. No.: HY-W015811
CAS No.: 621-27-2
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3-N-Propylphenol is a small phenolic derivative containing a hydroxyl aryl group that competitively inhibits the binding of the peptide to pancreatic-specific protein disulfide isomerase (PDIp). 3-Propylphenol can be used for research on pancreatic-related diseases .
Cat. No.: HY-Y0801S
CAS No.: 1195947-64-8
Cat. No.: HY-E71131
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(S)-Stylopine synthase (EC 1.14.21.1) catalyzes an oxidation reaction that does not introduce oxygen into the product. (S)-Stylopine synthase (EC 1.14.21.1) forms a second methylenedioxy bridge in the protoberberine alkaloid stylopine by oxidatively cyclizing cheilanthifoline with adjacent phenolic hydroxyl and methoxy groups.
Cat. No.: HY-E71128
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(S)-Nandinine synthase (EC 1.14.21.12) is a cytochrome P-450 heme-thiolate enzyme catalysing an oxidative reaction that does not incorporate oxygen into the product. Forms the methylenedioxy bridge of the protoberberine alkaloid (S)-Nandinine by the oxidative ring closure of adjacent phenolic and methoxy groups of (S)-Scoulerine.
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Oxymethurea (Dimethylolurea) is a formaldehyde-releasing protein modification reagent. Under acidic conditions, Oxymethurea promotes nucleophilic substitution of tyrosine via protonation of its hydroxymethyl group, while under alkaline conditions, it promotes protein crosslinking by converting the phenolic hydroxyl group of tyrosine into a more nucleophilic phenoxide ion. Oxymethurea can be used in studies related to protein chemical modification, protein crosslinking, protein protection and genotoxicity .
Cat. No.: HY-E72110
Human UGT1A8 is a UDP-glucuronosyltransferase. Human UGT1A8 catalyzes the transfer of glucuronosyl group from UDPGA to Dihydrotestosterone, forming DHT monoglucuronide. Human UGT1A8 catalyzes the transfer of glucuronosyl group from UDPGA to DHT monoglucuronide, introducing a second glucuronosyl group at the C2 ' position of the latter to form DHT diglucuronide. Human UGT1A8 catalyzes the glucuronidation reactions of coumarins, anthraquinones, flavonoids, phenolic compounds, catechol estrogens, primary amines including 4-Aminobiphenyl, and some opioids .
Cat. No.: HY-N21584
CAS No.: 132185-42-3
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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
