Amino Acids (AA)

N-Acryloyl-2-methylalanine is a monomer that belongs to the group of reactive molecules. It can be used for the synthesis of polymers with different functionalities, such as cyclodehydration, copolymerization and crosslinkers. This molecule has a reactive nature and has been shown to react with chloride ions to form a particle. In cancer cells, N-acryloyl-2-methylalanine inhibits cell proliferation and induces apoptosis by binding to DNA.

Please enquire for more information about 2N-Boc-2',2''-triaminotriethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Boc-D-homophenylalanine is a potent and selective inhibitor of the bacterial efflux pump. It is an enantiomer in which the D-form has greater potency than the L-form, and it is more potent than ciprofloxacin, one of the most common fluoroquinolones. This compound has been shown to inhibit efflux pumps in gram-positive bacteria such as Staphylococcus aureus and Streptococcus pneumoniae. Boc-D-homophenylalanine also inhibits efflux pumps in gram negative bacteria such as Escherichia coli and Pseudomonas aeruginosa. The structure of this drug resembles that of peptidomimetics, which are compounds that have amino acid sequences similar to those found naturally in proteins. Boc-D-homophenylalanine is chiral, meaning it can exist as either a right or left enantiomer. As with many other

N-Boc-4-piperidineacetaldehyde is a chiral, stable, and readily available aldehyde. It has been used in the synthesis of various biologically active molecules including imidazolidinones, which are important for their use as catalysts in organic chemistry. The synthesis of this molecule by the condensation of 4-piperidineacetic acid with acetaldehyde followed by reduction with sodium borohydride is an example of this type of reaction. N-Boc-4-piperidineacetaldehyde can be used to synthesize imines and linkers that are covalently bonded to the protein backbone. This molecule also has conformational stability and is not susceptible to oxidation or radiation damage.

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N-Boc-(3S)-3-phenyl-3-aminopropionaldehyde is a synthetic chiral ligand that can be used as a building block in the synthesis of other compounds. It has been used to optimize the synthetic process, and it can be used in buffers, ammonium formate, metal chelate, and other additives to synthesize new compounds. N-Boc-(3S)-3-phenyl-3-aminopropionaldehyde is an optical isomer that can be used for supercritical fluid chromatography (SCFC) or liquid chromatography (LC). This compound has been shown to have a high affinity for ligands with a phenol group.

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Amino acid

Please enquire for more information about N-Benzyl-D-valine methyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(4-Methoxyphenyl)-2-Morpholin-4-Ylethylamine Dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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1-Methyl-1H-pyrrole-3-carboxylic acid is a chemical compound with a molecular formula of C5H5NO2. This product has predictable chemical properties and can be used in the synthesis of other compounds. It is also used as an intermediate in organic chemistry.

Please enquire for more information about 2-Chloro-9-(2-O-acetyl-5-O-(4-methylbenzoyl)-3-deoxy-3-fluoro-beta-D-ribofuranosyl)-6-phenylpurine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Fmoc-4-phosphono-Phe(Bzl)-OH is an efficient solid phase peptide synthesizer. It has been used in the synthesis of a variety of peptides, including those with short sequences and bulky side chains. Fmoc-4-phosphono-Phe(Bzl)-OH is an efficient synthesis reagent for the solid phase peptide synthesis of small or medium size peptides, which are difficult to synthesize with other methods.

2-Chloro-6-methoxyquinazoline is a quinazoline derivative that is an inhibitor of the B-Raf protein kinase. This drug has been shown to inhibit the growth of cells in vitro, where it selectively inhibits the BRAFV600E mutant form of the kinase. The pharmacokinetic properties were determined for this drug and found to be similar for both healthy subjects and patients with advanced cancer, suggesting that 2-chloro-6-methoxyquinazoline may have potential as a treatment for advanced cancer.

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Fmoc-NH-PEG4-CH2COOH is a pegylation reagent that is widely used in the pharmaceutical and biotechnology industries. Pegylation refers to the process of attaching polyethylene glycol (PEG) molecules to a target molecule, such as a protein or peptide, to improve its stability, solubility, and pharmacokinetic properties. This product is a protected PEG derivative with an Fmoc (fluorenylmethoxycarbonyl) group at one end and a carboxylic acid group at the other end. The Fmoc group can be easily removed using mild base conditions, allowing for further modifications or conjugations. The PEG4 spacer in this reagent provides flexibility and helps to minimize steric hindrance between the attached molecule and its surroundings. The carboxylic acid group allows for easy conjugation with amino groups through peptide coupling reactions. Fmoc-NH-PEG4-CH2COOH is commonly

Please enquire for more information about 2-Chloro-N-{2-methyl-1-[(4-oxo-1,2,3-benzotriazin-3(4H)-yl)methyl]propyl}acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about [2-Methyl-3-(1-naphthyl)propyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications (4-Methyl-1H-imidazol-5-yl)methanol hydrochloride (cas# 38585-62-5) is a useful research chemical.

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N-Me-Thr-OMe·HCl is an analogue of the drug deglycobleomycin. It has a high selectivity for DNA cleavage, which abolishes inherent resistance to bleomycin. N-Me-Thr-OMe·HCl also has structural and efficiency advantages over other analogues. This drug has been shown to be effective in treating leukemia and lymphoma, where it prevents the synthesis of DNA and RNA by inhibiting dna cleavage. The hydrogen bond between l-threonine and threonine is essential for the formation of this drug. The epimerization of l-threonine to dl-threonine is essential for the synthesis of this drug.

M03127 - H-Glu(OCHex)-OH

H-Glu-Ser-OH is a tryptic fragment of the protein hormone erythropoietin that is produced by the kidneys. It is one of the major hormones involved in regulating red blood cell production. Erythropoietin stimulates the proliferation of hematopoietic cells, which are responsible for making new blood cells, and also plays an important role in wound healing. The amino acid sequence of this peptide consists of two alpha helices and four beta sheets. Structural analysis has shown that H-Glu-Ser-OH can be cleaved by proteases to produce the amino acid sequence H-Glu-Arg-OH. This fragment has been shown to have a bitter taste receptor binding activity and may play a role in casein coagulation.

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This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

2,6-Dimethoxy-4-methylbenzyl alcohol is a high quality, versatile building block that is used as a reagent. The chemical has been shown to be a useful intermediate in the production of fine chemicals and speciality chemicals. 2,6-Dimethoxy-4-methylbenzyl alcohol can be used as a reaction component in the production of research chemicals and versatile building blocks. This compound can be found on CAS registry number 875664-51-0.

Applications 1-Methyl-3-phenylpropylamine is used in the synthesis of N-substituted derivatives of (1-methyl-3- phenylpropyl)amine.

4-Chloro-2-methoxybenzoic acid is a chloroacetic acid that is used as an antibacterial agent. It has been shown to have a broad spectrum of activity against bacteria, including gram-positive and gram-negative bacteria. 4-Chloro-2-methoxybenzoic acid is active against both stationary and mobile phases of growth. It has also been shown to be effective in inhibiting the growth of fungi, such as Aspergillus niger, Aspergillus fumigatus, Penicillium notatum, and Fusarium oxysporum. This compound can be synthesized from carboxylic acids by reacting them with sodium nitrite in the presence of dry nitrogen gas to form chloroacetic acid. The chemical formula for this compound is CHClOOC(CH)COOH.

2-Phenyl-1,3-indandione is a coumarin derivative that is used as an anti-inflammatory drug. It inhibits the release of arachidonic acid from phospholipids in the cell membrane and consequently inhibits the formation of prostaglandins. The drug has been shown to inhibit light-induced tumor promotion in mice with cervical cancer, which may be due to its ability to inhibit the activity of oxidative enzymes such as cytochrome P450. 2-Phenyl-1,3-indandione also inhibits sodium-dependent glucose transport and energy metabolism by binding to potassium channels. This drug also has immunosuppressive effects on lymphocyte transformation and autoimmune diseases through hydrogen bonding interactions with protein molecules.

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