Aminoácidos (AA)

<p>Z-NH-PEG5-CH2CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG5-CH2CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>Please enquire for more information about 2-Aminomethyl-4-boc-morpholine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Alanine,n,N'-[[5-[2-amino-5-(2,2-dimethyl-1-oxopropyl)-4-thiazolyl]-2-furanyl]phosphinylidene]bis[2-methyl-,1,1'-diethylester] is a metabolic inhibitor that is used in the treatment of type 2 diabetes. It inhibits gluconeogenesis by inhibiting the enzyme phosphoenolpyruvate carboxykinase (PEPCK), which catalyzes the conversion of oxaloacetate to phosphoenolpyruvate. This compound has been shown to reduce fasting blood glucose levels in diabetic animals and humans.</p>

<p>Please enquire for more information about N-(p-Hydroxyphenethyl)-N-(3-hydroxy-4-methoxybenzyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Timapiprant is an amide that acts as a selective inhibitor of the prostanoid receptor CRTH2, which is involved in regulating the inflammatory response. Timapiprant inhibits skin eosinophilia, which is associated with inflammatory skin diseases such as atopic dermatitis and psoriasis. It has been shown to be safe in clinical trials and has a good safety profile. The drug's mechanism of action may be due to its ability to inhibit the production of IL-4 and IL-13 by Th2 cells and its ability to inhibit lung function. Timapiprant has shown efficacy in treating allergic rhinitis, asthma, chronic obstructive pulmonary disease, erythema multiforme, pyoderma gangrenosum, and other types of inflammatory skin diseases.</p>

<p>6-Chloro-3,4-dihydro-3-(a-methylbenzyl)-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide is an active metabolite of the drug benzbromarone. It is primarily administered as a diuretic to treat high blood pressure and congestive heart failure. The pharmacodynamics of this drug are related to its ability to inhibit the activity of sodium channels in vascular smooth muscle cells and thereby reduce the force of contraction and relax the vessel wall. 6CBDMTD has shown an increase in glomerular filtration rate in patients with congestive heart failure. This drug also decreases the plasma concentration of fatty acids by inhibiting the formation of lipoprotein particles. 6CBDMTD has been shown to be effective at lowering diastolic and systolic blood pressure levels in patients with hypertension.</p>

<p>Demeton-S-methyl is a chemical pesticide that belongs to the group of organophosphates. It inhibits acetylcholinesterase activity and is used for the control of insects. Demeton-S-methyl is an anticholinesterase agent that binds reversibly to the active site of acetylcholinesterase, inhibiting the enzyme's activity. This inhibition leads to accumulation of acetylcholine in nerve tissue and increased transmission at cholinergic synapses. Demeton-S-methyl has been shown to be acutely toxic in rats, mice, and dogs by inhalation or ingestion. Acute toxicities are more severe with higher dosages as well as with repeated exposures.</p>

<p>3-Bromo-7-hydroxy-4-methylchromen-2-one is an organic compound with the molecular formula CHBrNO. It is a colorless solid that is soluble in organic solvents. 3-Bromo-7-hydroxy-4-methylchromen-2-one has shown antiviral activity against the pandemic Covid 19 virus, as well as activity against influenza A and B viruses. This compound also has been shown to be active against methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. 3BRMCHM2O binds to DNA by covalent binding and inhibits the synthesis of RNA, causing cell death in bacteria. The compound can be accessed through two routes: one involving phenylhydrazine and hydrazines, and another involving ionic liquids and ionic reagents. The reaction time for this reaction is very short (10 minutes</p>

<p>12-Methyltridecanal is a lipid oxidation product that is found in animal tissues. It is produced by the oxidation of unsaturated fatty acids, such as linoleic acid, by reactive oxygen species (ROS). Lipid peroxidation can be induced by ROS generated from mitochondria, xanthine oxidase, or the activation of phospholipase A2. 12-Methyltridecanal is used to measure oxidative stress in animals and has been shown to be an important marker for leukemia cells. This compound has also been shown to be expressed in human leukemia cells.</p>

<p>Trans-2-[3-(4-tert-butylphenyl)-2-methyl-2-propenylidene]malononitrile is a reactive chemical that has been used to study the mechanism of tubular transport. This compound has been shown to be a potential cancer gene therapy agent, as it can stimulate the growth of cells in culture and induce tumor regression in mice. Trans-2-[3-(4-tert-butylphenyl)-2-methyl-2-propenylidene]malononitrile binds to fatty acids and causes them to coordinate with metal ions, which may be responsible for its antitumor properties. Trans-2-[3-(4-tert-butylphenyl)-2-methyl-2-propenylidene]malononitrile also binds to DNA polymerase and transcription factors, inhibiting their function and rendering them incapable of binding RNA polymerase. The sensitivity of this compound</p>

<p>N10-Methyl pteroic acid is a novel immunosuppressant that inhibits T-cell proliferation and promotes regression of inflammatory bowel disease. It has been shown to be effective in treating cancer patients, with the terminal half-life being approximately 20 hours. N10-Methyl pteroic acid is a potent inhibitor of human acute lymphoblastic leukemia cells. It can also be used as an immunosuppressant for organ transplantation, with desorption from gels using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) and bioanalytical methods such as high performance liquid chromatography (HPLC).</p>

<p>3-(2-Pyridyl)-D-alanine is an amino acid that is a precursor to the peptide antibiotic, pyrithione. It can be prepared from 2-pyridylacetic acid and D-alanine. 3-(2-Pyridyl)-D-alanine is a chiral molecule with two stereogenic centres, which means it has four different optical isomers: L-, D-, S-, and R-. The L form of 3-(2-pyridyl)-D-alanine was found in Streptomyces sp. strain NRRL 8057. This amino acid is synthesized by a peptide synthetase enzyme. The sequence of this biosynthetic gene has not been determined yet.</p>

<p>Boc-L-Propargylglycine is an antibacterial agent that can be used for the treatment of cancer. It has been shown to have specificities against cancer cells, as well as a high potency and low toxicity. Boc-L-Propargylglycine may be useful in biochemistry experiments because it can form conjugates with amines, hydroxyl groups, and amino acids. This drug also binds to DNA by forming triplexes and high-potency complexes with guanine residues. Boc-L-propargylglycine has been shown to inhibit the growth of cancer cells in vitro. It is orally bioactive, which means that it is absorbed and distributed throughout the body when taken by mouth.</p>

<p>The N-alpha-Boc-L-tryptophan N-alpha-carboxy anhydride is a postulated intermediate in the ring opening of the ester of tryptophan. The kinetics of this reaction, which is influenced by the basicity and acidity of the environment, have been studied using techniques such as crystal violet, formamide and radiolabeling.</p>

<p>Please enquire for more information about (R,S)-Z-3-Amino-7-chloro-2-oxo-5-phenyl-1,4-benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(4-Fluorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-L-Ala-NHS ester is a methyl ester that is used as a fluorescent probe for the detection of amines and other amino acids. It can be used to measure the pH of solutions, as well as in the detection of enzyme substrates and aldehydes. Z-L-Ala-NHS ester has been shown to have high fluorescence properties, which are sensitive to changes in pH.</p>

<p>Please enquire for more information about Benzyl-O-benzyl-serine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Demeton-S-methyl sulfoxide is a broad spectrum insecticide that is used to control insects in agriculture and public health. It has been shown to exhibit genotoxic effects, which may be due to its ability to inhibit the activity of the glutamate pyruvate transaminase enzyme. This inhibition blocks the conversion of pyruvate into acetyl coenzyme A, which is required for fatty acid synthesis. Demeton-S-methyl sulfoxide also inhibits the function of ryanodine receptors, which are calcium channels found in muscle cells. The chronic exposure of animals to this chemical causes lung damage and an increased frequency of spontaneous tremors.</p>

<p>Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid is a synthetic amide that is used as an intermediate in the synthesis of peptides. It has a conformational structure and can be labeled with dyes to study the structures of proteins or peptides. Fmoc-1-amino-4,7,10-trioxa-13-tridecanamine succinimic acid has been used as an immunogen in the preparation of monoclonal antibodies. It also can be conjugated to drugs or other compounds for use as bioconjugates. This compound has been shown to have enzymatic activity and can be used as a substrate for enzyme linked immunosorbent assays (ELISA). Trifluoroacetic acid is commonly used in the synthesis of this compound.</p>