Amino Acids (AA)

2-Aminothiophene-3-methyl carboxylate is a hydrogen bond that is derived from the amino acid methionine. It has been shown to have potent antitumor activity and can be used for the treatment of cancer. 2-Aminothiophene-3-methyl carboxylate has a molecular weight of 244.6 g/mol, an isolated yield of 0.68%, and a melting point of 245 °C.

Tributyl-(4-methoxy-phenyl)-stannane is a nucleophilic compound that can be used to synthesize 5-HT1A receptor agonists. It has been shown to have biochemical, positron and chloride properties. This chemical is synthesised by introducing a sulfur atom into the molecule. The sulfur atom reacts with the chlorine atom in chlorobenzene to form the sulfonation bond. This reaction is efficient and can be used as a method for cleaving bonds and cross-coupling carbon atoms.

Cyclo-Phe-Pro is an intermolecular hydrogen bond that has been shown to inhibit the growth of viruses. Cyclo-Phe-Pro binds to the hydrophobic region on viral capsid proteins and inhibits their uptake into cells, which may be due to its ability to form hydrogen bonds with the amino acid serine in these proteins. It also has antimicrobial activity against a number of bacterial species and can be used as a pre-preparation for high performance liquid chromatography (HPLC).

Fmoc-6-aminohexanoic acid is an amino acid that can be used as a building block for peptides and proteins. It has a hydroxide group that can be reacted with other molecules in order to form a covalent bond. The compound reacts with sodium hydroxide solution to produce a particle that is soluble in water and organic solvents. Fmoc-6-aminohexanoic acid also inhibits the protease activity of subtilisin BPN' and leucine aminopeptidase, which are enzymes that break down proteins into smaller polypeptides. This material is functionalized with carboxyl groups on both ends, making it reactive and able to react with other molecules.

2-(4-Methoxyphenoxy)acetonitrile is a chemical compound that is used to synthesize acetobromoglucose. It undergoes transformation and condensation reactions with acetobromoglucose to form 4-methoxyaceto bromoglucose.

N-a-t-Boc-N-g-trityl-L-asparagine is a recombinant human protein that has been synthesized in E. coli. It is a peptide with 17β-estradiol at its C terminus, and it binds to the oestrogen receptor α (ERα) via hydrogen bonding interactions. The linker between the asparagine and estradiol is a Boc group that can be removed by protease activity, revealing the active form of 17β-estradiol. ERα ligates to N-a-t-Boc-N-g-trityl L asparagine with high affinity, and this interaction is reversible. The linker also contains a functional group for surface attachment, which may be used to attach this peptide to a solid support or tissue culture substrate for use in cell cultures.
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2-Anilino-6-dibutylamino-3-methylfluoran is a switchable fluorescent dye that has been used to detect and measure biochemically active substances in living cells. The dye is introduced into the cell, where it binds to specific proteins or nucleic acids, causing a change in fluorescence. This change can then be detected using a microscope with an ultraviolet light source. 2-Anilino-6-dibutylamino-3-methylfluoran has also been used to detect bacteria in wastewater samples. An experiment was conducted to determine the effects of temperature on the reaction time of 2AADMF and metal ion concentration. Increasing the temperature resulted in an increase in reaction time, while increasing the concentration of metal ions had no effect on reaction time. 2AADMF also reacts differently depending on whether it is inside microcapsules or not. Microcapsules with 2AADMF reacted faster than those without it when

2-Chloro-5-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)-4-fluorophenoxyacetic acid monohydrate (2,4,5P) is a phenoxy herbicide that has been shown to be an effective broadleaf and grass weed control agent. 2,4,5P is a granule formulation that can be applied by helicopter or ground equipment. It has synergistic effects with glyphosate when applied together to soybean plants and can be used in combination with other herbicides for more effective weed control.

Please enquire for more information about 5-Methyl-2-nitropyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Bromo-3-methylthiophene (2BMT) is an organic chemical compound that has been used for the Suzuki coupling reaction. It can be prepared by reacting 2-bromo-3-methylthiophene with potassium hydroxide in a hydroxide solution. 2BMT has shown to inhibit the activity of tiagabine hydrochloride, which is a drug that regulates GABA neurotransmission. 2BMT is also used as an intermediate in the synthesis of carbonyl group compounds and halides. The structure and physical properties of 2BMT have been studied in detail by x-ray crystallography and nmr spectroscopy.

1-Phenyl-3-(4-chlorostyrene)pyrazole is a high quality reagent that can be used as an intermediate in the production of complex compounds. It is also used as a building block in the synthesis of speciality chemicals, research chemicals, and versatile building blocks. 1-Phenyl-3-(4-chlorostyrene)pyrazole has been shown to be useful as a reaction component in the synthesis of fine chemicals and useful scaffolds.

Boc-Lys-OMe HCl is an ester hydrochloride of N-Boc-Lysine. It is a macrocyclic compound that has been used in the laboratory as an acidifying agent to convert sodium borohydride to methyl ester hydrochloride. Boc-Lys-OMe HCl is also used in the synthesis of macrocyclic compounds, such as n-boc-l-lysine and other polyamino compounds.

3-Phenyl-2-propen-1-ol is a cinnamyl compound that is found in plants, such as cinnamon and cassia. It has been shown to have an inhibitory effect on the enzyme activities of sorbitol dehydrogenase, which is involved in the synthesis of polysaccharides. 3-Phenyl-2-propen-1-ol also has a transcriptional regulatory effect on genes that encode enzymes involved in the synthesis of polymers. The reaction mechanism for this reaction has been proposed to be through an initial nucleophilic attack by the hydroxyl group on the electrophilic carbonyl carbon atom followed by protonation and elimination of water.
3-Phenyl-2-propen-1-ol has also been shown to be a signal peptide, which is used to identify proteins for transport within cells. This polymerase chain reaction (PCR) model system can be used to determine

Boc-L-histidine is a histidine derivative with a boronic acid group that can be used to synthesize imines. It is an organic solvent and can be used in magnetic resonance spectroscopy. Boc-L-histidine has been shown to inhibit the tyrosine activity of tyrosinase, which is involved in melanin synthesis. This compound also inhibits cancer cells by inhibiting the cellular process of protein synthesis and, as such, may be useful for the treatment of cancers.

2-Methoxy-2-phenylethanol is a molecule that has been found to be a good catalyst for the ring-opening of epoxides. It is also used as a solid catalyst in kinetic studies and as an additive in organic syntheses. 2-Methoxy-2-phenylethanol is soluble in water and reacts with fatty acids to form acetylated products. This molecule has been shown to have an inhibitory effect on human liver alcohol dehydrogenase, which may be due to it's ability to bind to the enzyme's active site.

Boc-S-trityl-L-homocysteine is a synthetic molecule that is used as a prodrug to introduce the amino acid homocysteine into cells. It has been shown to have anti-cancer and estrogen receptor modulating properties. Boc-S-trityl-L-homocysteine is synthesized by reacting L-homocysteine with diisopropylamino chlorides in the presence of sodium hydroxide, followed by ligation with dicyclohexylcarbodiimide. The compound adopts a centrosymmetric conformation due to the presence of two chiral centers at C3 and C4 positions on the pyridyl ring. The active site consists of an aromatic ring with three substituents, one of which is an amide group. This chemical transformation occurs through a nucleophilic attack by the amide group on an electrophilic carbonyl carbon atom.

2-Acetyl-7-methoxybenzofuran is an antibacterial agent that has potent inhibitory activity against methicillin-resistant Staphylococcus aureus and other bacterial species. It also inhibits the growth of endophytic fungus in plants. 2-Acetyl-7-methoxybenzofuran is synthesized by the fungus Cereus, which is used in traditional medicine to treat various ailments. This compound binds to the 16S ribosomal RNA, which inhibits protein synthesis and cell division. 2-Acetyl-7-methoxybenzofuran also shows potent inhibitory activity against methicillin-resistant Staphylococcus aureus, as well as other bacterial species. This antibiotic binds to the 16S ribosomal RNA, inhibiting protein synthesis and cell division.

Z-O-tert-Butyl-L-tyrosine is a fine chemical that is soluble in water and has a wide range of uses. It is a versatile scaffold for the synthesis of complex compounds, and can be used as a building block or reaction component in research chemicals. Z-O-tert-Butyl-L-tyrosine is an important reagent for organic synthesis, especially when combined with other chemicals. This chemical can also be used as a speciality chemical to produce high quality products.

2-(3-Methyl-1,2,4-oxadiazol-5-yl)ethyl]amine hydrochloride is a high quality chemical reagent that can be used as a complex intermediate in organic synthesis. It is also a useful scaffold for the synthesis of other complex compounds. 2-(3-Methyl-1,2,4-oxadiazol-5-yl)ethyl]amine hydrochloride is an excellent building block for the synthesis of various fine chemicals and research chemicals. This compound has many uses as a versatile building block in chemical reactions due to its reactivity.

4-(Aminomethyl)-3-phenylbutyric acid hydrochloride is a reagent that can be used as a building block in synthesizing new chemical compounds. It is also an intermediate for the synthesis of 4-(aminomethyl)benzoic acid, which is useful for producing pharmaceuticals, pesticides, and other agrochemicals. 4-(Aminomethyl)-3-phenylbutyric acid hydrochloride has a CAS number of 860252-34-2 and can be used in reactions with a variety of reagents to produce fine chemicals, research chemicals, and speciality chemicals.

DL-Alanine is a small molecule drug that has been used as a fluorescence probe for the detection of human hepatitis B virus (HBV) DNA. DL-Alanine has also been shown to be an inhibitor of the polymerase chain reaction, which is a technique used for amplifying DNA. The fluorescence of DL-alanine is quenched by HBV, and the intensity of this interaction can be measured using an ultraviolet spectrophotometer. DL-Alanine was found to inhibit HBV replication in a model system when it was added at concentrations between 1 and 10 mM. The inhibition was attributed to its ability to scavenge anion radicals generated during the course of HBV replication. DL-Alanine inhibits both wild type and mutant strains of HBV, with no significant difference in potency between them.

4-Methylpyrimidine is a molecule used in the treatment of cancer. It is an inhibitor of the enzyme topoisomerase II, which is involved in DNA replication and repair. 4-Methylpyrimidine binds to the active site of topoisomerase II and blocks its activity. 4-Methylpyrimidine has been shown to be effective against Covid-19 pandemic, which was responsible for a severe outbreak of pneumonia in 2009. The reaction mechanism of 4-methylpyrimidine involves methylpyrazine, a chloride ligand, and molybdenum as the metal center. FT-IR spectroscopy has been used to identify the structural analysis of this molecule.

O-Phospho-L-tyrosine is a phosphorylated form of L-tyrosine. It is used as an immunogen in the production of monoclonal antibodies. O-Phospho-L-tyrosine has also been shown to inhibit the enzyme indole alkaloids, which are responsible for the development of oral pathogens. The dephosphorylation of O-Phospho-L-tyrosine by tyrosine phosphatases leads to its conversion back to L-tyrosine. This compound can be detected by chromatographic analysis and is commonly used in analytical methods to identify natural compounds.

6-Methoxy-1H-indol-5-ol, also known as 5-hydroxytryptophan (5HTP) is a natural amino acid that is found in the human body. It is converted into serotonin by the enzyme tryptophan hydroxylase and becomes an intermediate in the metabolic pathway of serotonin (5HT). Serotonin affects mood and behavior and is used to treat depression. 6-Methoxy-1H-indol-5-ol has been shown to be effective in treating depression and obesity. This drug has a number of side effects, including nausea, vomiting, diarrhea, dizziness, anxiety, agitation, headache, insomnia, tachycardia (fast heartbeat), high blood pressure, mania or psychosis.

Pro-Gly-OH is a cyclic peptide that has been shown to have antimicrobial activity. Pro-Gly-OH has been shown to be an intramolecular hydrogen acceptor, which leads to the formation of a carbonyl group. This compound also has site specific interactions with the cell membrane and is taken up by cells. It is active at acidic pHs and can be activated by growth factors.
The conformational properties of Pro-Gly-OH are due to hydrogen bonding interactions and amide bond formation.

Stable under physiological and chemical conditions, 1-Boc-azetidine-3-yl-methanol is a linker that forms permanent bonds in conjugates, particularly in antibody-drug conjugates (ADCs) and as a linker in PROTAC (PROteolysis TArgeting Chimera) molecules for targeted protein degradation. It is also a versatile chemical intermediate used to synthesize complex organic molecules, particularly in pharmaceuticals, agrochemicals, and research chemicals.

N-Acetyl-D-tryptophan is a form of tryptophan that has been shown to have neuroprotective effects. It binds to the neurokinin 1 receptor, inhibiting the release of neurotoxic substances and preventing neuronal cell death. N-Acetyl-D-tryptophan is also able to inhibit the formation of reactive oxygen species, which are responsible for cellular damage. N-Acetyl-D-tryptophan has been shown to have neuroprotective effects in bacterial strain, gamma-aminobutyric acid (GABA) binding constants, reaction solution, inhibitor binding, mitochondrial cytochrome c amide and atherosclerotic cardiovascular disease urine samples.

4-Fluoro-3-methoxybenzonitrile (4FM) is an orally active dihydrobenzofuran derivative that has been optimized for oral bioavailability. The drug is a potent inhibitor of efflux and can be used to lower the oral bioavailability of drugs that are substrates for efflux. 4FM also inhibits heterocycle metabolism, which can be used as a strategy to evolve drugs with improved physicochemical properties. 4FM has shown preclinical efficacy in lowering heterocycle levels, including lowering of methadone levels in humans. The drug is a competitive inhibitor of the enzyme P450 2D6, which is responsible for the metabolism of many drugs. This inhibition may have adverse effects on these drugs and should be monitored closely during treatment with 4FM.

O-Methyldomesticine is a type of alkaloid, which is a naturally occurring organic compound primarily found in certain plant species. These compounds often have complex structures and are typically derived from plant secondary metabolites. O-Methyldomesticine’s mode of action is thought to involve interactions with central nervous system receptors, although the precise mechanisms remain under investigation. Its chemical structure allows it to potentially modulate biochemical pathways, making it of interest to pharmacological research.

Glycyl-glycine is a biological buffer with a pH range of 7.5-8.9 and a pKa of 8.2. It is a zwitterionic compound and is low in toxicity, meaning it is suitable for many applications

1-Phenyl-3-oxabicyclo[3.1.0]hexan-2-one (1POX) is a monomer that belongs to the class of cyclopropane compounds and can be used in the synthesis of polymers. It has been shown to react with benzene, irradiation, monoxide, oxiranyl, acetonitrile and trimeric dyes to form reactive intermediates such as ketones and carboxylic acids. These intermediates can undergo photolysis to produce products such as ketones and carboxylic acids. The wavelength of the light used for photolysis can influence the product formation. 1POX is also a substrate for cyclopropane ring formation reactions, which are known for their high reactivity due to the stability of this ring system. The carbonyl group on 1POX is electron withdrawing and stabilizes the planar geometry of 1POX.

4-(2-Methoxyphenoxy)benzoic acid is a white crystalline solid with a melting point of 50°C. It is soluble in water, ethanol, ether, and chloroform. 4-(2-Methoxyphenoxy)benzoic acid has been used as a starting material for the synthesis of pharmaceuticals such as carbamazepine (Tegretol). The compound has two methoxy groups on the phenyl ring that are susceptible to nucleophilic attack by strong bases. This reaction occurs at room temperature and can be reversed by heating the solution to 150°C. The compound also undergoes polycondensation reactions when heated in the presence of an oxidizing agent.

N-alpha-Z-L-histidine is a nitrogenous compound that is an amide formed by the reaction of histidine and trifluoroacetic acid. It has been shown to be anticancer and to have an effect on tumor vasculature, with efficacy against solid tumors. N-alpha-Z-L-histidine inhibits the cell cycle at the G1 phase and blocks DNA synthesis, which arrests cells in the M phase. This drug also inhibits tumor angiogenesis by blocking vascular endothelial growth factor (VEGF) signaling. N-alpha-Z-L-histidine is a molecule that has been synthesized using solid phase chemistry and purified by high performance liquid chromatography.

1,2-Phenylenediamine is an aromatic amine that can be used as a precursor for the synthesis of various heterocyclic compounds. It has been shown to have an acidic character, which is due to its coordination geometry with three of its nitrogen atoms in the form of pyramidal nitrogen atoms. 1,2-Phenylenediamine is also a ligand for toll-like receptor (TLR) 4 and TLR9. It has been shown to activate these receptors by binding and activating downstream signaling pathways such as NF-κB and MAPK. This compound also has the ability to induce apoptosis in HL60 cells through inhibition of protein synthesis and activation of caspases.

Methyl 3,5-dibromo-2-methoxybenzoate is a fine chemical that is useful as a scaffold for the preparation of a variety of compounds. It is also used as an intermediate in the synthesis of pharmaceuticals and research chemicals. Methyl 3,5-dibromo-2-methoxybenzoate can be used as a reaction component to generate complex compounds with high purity and quality. This compound has been classified as a speciality chemical and may be reclassified due to its usefulness in research.

Boc-S-benzyl-D-cysteine is a fine chemical that is used as a research chemical and reagent. It is a versatile building block for the synthesis of complex compounds. Boc-S-benzyl-D-cysteine has been used in the synthesis of natural products, pharmaceuticals, and other organic molecules. It can also be synthesized from benzylcysteamine and glutathione. The compound can be purified by recrystallization or chromatography.

3,5-Dimethoxy-4-methylbenzoic acid methyl ester (DMMBME) is a synthetic compound that is used as an immunogen to generate antibodies against fungal proteins. DMMBME is specifically used to identify the presence of bryoria and australian fungi in plants. The chemical structure of DMMBME can be oxidized by depsidones, which leads to the production of reactive oxygen species that are believed to be responsible for the oxidative coupling of target proteins. This reaction can be catalyzed by a number of enzymes such as nidulin, which is found in plant roots.

2,3-Diphenyl-3-phenylaminoacrylonitrile (DPAN) is a fine chemical that is used as a building block in the synthesis of more complex compounds. DPAN can be used as a reagent and speciality chemical in research and development. It has been shown to react with other chemicals to form new compounds, some of which have been shown to have potential therapeutic properties. This compound has also been shown to have potential use as a scaffold for drug discovery.

Beta-cyano-l-alanine is a naturally occurring amino acid that is found in plants. It is synthesized by the enzyme beta-cyanoalanine synthase and is involved in plant metabolism. Beta-cyano-l-alanine is a precursor of the neurotransmitter gamma aminobutyric acid, or GABA, which has been shown to regulate the opening and closing of calcium channels in brain cells. In addition, it has been shown to inhibit enzymes such as phosphofructokinase and pyruvate kinase that are involved in the breakdown of glucose and other nutrients. Beta-cyano-l-alanine has also been shown to inhibit ryanodine receptors and other enzymes involved in muscle contraction. This amino acid can be used as an indicator for tissue culture experiments because it can be detected by sephadex G-100 chromatography.