Aminoácidos (AA)

<p>3-Fluoro-4-methylaniline is a synthesized compound that is used to produce anti-cancer agents. It is an amide and has anti-cancer properties. 3-Fluoro-4-methylaniline also binds to DNA and inhibits the synthesis of proteins in cancer cells. The binding constants for ligands are found to be high. 3-Fluoro-4-methylaniline can also bind with DNA through intercalation or hybridization, which prevents transcription of RNA from DNA, thereby inhibiting protein synthesis. This results in cell death by apoptosis.</p>

<p>Please enquire for more information about (5-Methoxy-1-methyl-1H-benzimidazol-2-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>D-Leucine amide is a hydrophobic, carboxyamide amino acid that is found in the fungus Ochrobactrum anthropi. D-Leucine amide has been shown to catalyze the formation of tripeptides, such as d-alanine and d-tryptophan, from their monomers. The presence of this compound enhances the expression of genes encoding proteins involved in the synthesis of these amino acids. This compound also has been shown to enhance gene analysis by increasing the stability of DNA and RNA molecules.</p>

<p>Please enquire for more information about H-Gly-Phe-Gly-aldehyde semicarbazone acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-2-methoxy-5-methylaniline is a dye molecule that is used in the synthesis of other molecules, such as diketene. It is also used as a solvent, coupling agent, and a dye molecule. This compound can be synthetically prepared by reacting naphthylamine with pyrazolone. The reaction requires catalytic amounts of polyvalent metal salts, such as zinc chloride or iron(III) chloride. The halogenation of 4-chloro-2-methoxy-5-methylaniline to produce 2,4,5-trichlorophenol can be achieved by diazotising the molecule with sodium nitrite and potassium dichromate. 4-Chloro-2-methoxy-5 methylaniline's substituents are methyl groups on the phenyl ring (Cl) and chlorine atoms (C1). Derivatives of this</p>

<p>2-(2-Methoxyphenoxy)ethanol (2-MPE) is a metabolite of propanediol, which is a precursor in the synthesis of polyurethanes. 2-MPE can be oxidized by monooxygenases to form syringyl and other reactive metabolites. Basic hydrolysis may also produce monomers such as phenols, alcohols, and carboxylic acids. Syringyl is one of the metabolic products of 2-MPE, which has been shown to be resistant to degradation by basidiomycete fungi.</p>

<p>3-(1-Methyl-1H-indol-3-yl)propanoic acid is a potent inhibitor of serine protease. It has been shown to have no effect on fetal heart rate, but can cause bladder cancer in transgenic animals. 3-(1-Methyl-1H-indol-3-yl)propanoic acid blocks the interaction between mammalian cells and bladder cancer cells, which may be due to its ability to block the activation of serine protease in response to thymidylate. This compound also inhibits DNA synthesis and cell growth. It is highly toxic for tumor cells and normal cells, but less so for normal tissues. It also modifies the regulatory domain of cancer cells, making it possible for 3-(1-Methyl-1H-indol-3-yl)propanoic acid to modify cancer cell activity by configuring it with a different regulatory domain that regulates the expression of proteins involved in cancer development.</p>

<p>Please enquire for more information about Fmoc-N-(1-Boc-piperidin-4-yl)glycine 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 tert-Butyl 4-(aminomethyl)-4-methylpiperidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Clovamide is a bioactive compound, which is a naturally occurring phenolic amide found primarily in certain plant species. This compound is derived from sources such as the leaves of Trifolium pratense (red clover) and certain leguminous plants. With its molecular structure comprising both phenolic acid and amino acid moieties, clovamide exhibits significant antioxidant properties.</p>

<p>3-Phenylpropanal is a chemical compound that is synthesized from trifluoroacetic acid, activated chitosan polymer, and fatty acids. 3-Phenylpropanal has been shown to have a bioactive phytochemical, which has been identified as allylation. This reaction is catalyzed by the addition of an allylating agent such as propargyl bromide or propargyl chloride. The rate of this reaction is dependent on the concentration of the reactant and kinetic energy (heat). The hydroxyl group on the reactant reacts with hydrogen gas in the presence of a catalyst such as sodium carbonate or zinc oxide to form a hydroxyethyl group. This process can be monitored using kinetic data such as conversion and yield.</p>

<p>Please enquire for more information about 2-(Bromomethyl)-1-methyl-1H-benzimidazole hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-(-)-Glycidyl nosylate is an epoxide that is used in the synthesis of pharmaceuticals. It has shown mutagenic activity and can be used to produce chiral glycidyl compounds. (R)-(-)-Glycidyl nosylate has been evaluated as a potential drug for the treatment of cancer, but was found to have limited pharmacological activity. This compound binds to protein kinases and may inhibit their activity. (R)-(-)-Glycidyl nosylate also possesses aliphatic properties and is an enantiopure molecule. The stereoisomers of glycidyl nosylate are also available, with the most common being (+)glycidylether.</p>

<p>Please enquire for more information about Fructose-asparagine trifluoroacetate (Mixture of diastereomers) 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 3-(2-Methyl-1H-imidazol-1-yl)propan-1-ol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid is a synthetic amino acid that has been shown in vitro to inhibit the growth of prostate cancer cells. It is an analog of butyric acid, a naturally occurring fatty acid. Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid has been synthesized by solid phase methods and labeled with radiotracers such as indium 111 or technetium 99m. The use of Fmoc-trans-4-(aminomethyl)cyclohexane-1-carboxylic acid in vivo is limited by its short circulating half life, rapid metabolism, and high toxicity.</p>

<p>BOC-D-Ser-OH is a synthetic amino acid with an acetylated serine side chain. It is used in the synthesis of glycosidic bonds. BOC-D-Ser-OH reacts with sodium hydrogen carbonate to form the sodium salt of D-serine, which can be used to produce glycoconjugates or as a model protein. The reaction yield is low and can be improved by adding acetyl groups to the substrate, such as galactose. Glycosidic bonds are formed by transfer reactions between nucleophilic hydroxyl groups on sugar molecules and electrophilic amino groups on proteins. The glycoconjugates produced by this reaction have been shown to have anticancer activity in animal models.</p>

<p>Please enquire for more information about Pro-Gln-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-methoxyphenyl)ethyl]methylamine is a pharmacological agent that inhibits protein synthesis. It has been shown to have an optimum concentration of 1 μM, with maximal inhibition at 10 μM. 2-(4-methoxyphenyl)ethyl]methylamine binds to the basic amino acid residues of proteins and inhibits the activity of eosinophil cationic protein, which is responsible for histamine release. 2-(4-Methoxyphenyl)ethyl]methylamine has also been shown to reduce the activity of epidermal growth factor, which is responsible for cell proliferation and differentiation. The drug has been demonstrated to be an effective inhibitor of activated eosinophils, but not normal cells. 2-(4-Methoxyphenyl)ethyl]methylamine may be used as a treatment for chronic asthma patients who suffer from eosinophilic inflammation in their</p>

<p>Glycerolipid metabolism component</p>

<p>1-Naphthalenylsulfonyl-Ile-Trp-aldehyde is a recombinant protein that has protease activity. It is a serine protease that cleaves proteins at the amino acid sequence Ser-Xaa-Gly or Ser-Xaa. The recombinant protein has been shown to have proteolytic activity and can be used in assays to measure the amount of β-catenin, collagen, and growth factor in cells. 1-Naphthalenylsulfonyl-Ile-Trp-aldehyde also binds to monoclonal antibodies and can be used as a neutralizing agent for these proteins. This recombinant protein also has been shown to inhibit the growth of lung fibroblasts.</p>

<p>1-Benzyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid is a compound with an esterified hydroxyl group in the form of an acetylacetone. It can be used as a monohydrate or dihydrate and it is stabilized by hydrogen bonding. 1-Benzyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid has been studied as a potential drug for cancer treatment because it is active against tumor cells and has little toxicity to normal cells.</p>

<p>Thifensulfuron-methyl is a selective herbicide that inhibits the growth of plants by inhibiting the activity of acetyl-CoA carboxylase. Thifensulfuron-methyl is used to control weeds in wheat, barley, and rice crops. Thifensulfuron-methyl has been shown to induce glomerular filtration rate in rats with congestive heart failure, while also reducing total body weight gain and improving renal function. This drug also has synergic effects on skin cancer cells when combined with active antiretroviral therapy.</p>

<p>Please enquire for more information about L-b-Homotyrosine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

9-Fluoro-11b,21-dihydroxy-16a-methylpregna-1,4-diene-3,20-dione is a potent antiandrogen that is used to treat alopecia areata and other skin disorders. 9-Fluoro-11b,21-dihydroxy-16a-methylpregna-1,4-diene-3,20-dione has been shown to have an inhibitory effect on the growth of skin tumors in mice. This drug also has a protective effect against chemical stability. It binds to fatty acids and epidermal growth factor (EGF), which may be related to its ability to regulate transcriptional processes and inflammatory skin diseases.

<p>Please enquire for more information about 1-(4-Amino-3,5-dichloro-phenyl)-2-bromo-ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>O-tert-Butyl-D-tyrosine is an organogelator. It is a low molecular weight organic liquid that can form a gel when mixed with a solvent. O-tert-Butyl-D-tyrosine is soluble in hydrophobic solvents such as butanol, and insoluble in water. The gelation properties of this substance are due to its ability to interact with the surface of the solvent droplet and form a network that holds other solute molecules in place. This interaction is called physisorption, which means that it does not need any chemical bonds to form the gel. Gels formed by O-tert-Butyl-D-tyrosine are stable at room temperature, but will melt when heated or exposed to pH extremes.</p>

<p>Oxytocin is an endogenous hormone.</p>

<p>Please enquire for more information about Z-L-leucine-N-hydroxysuccinimide ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Tyrosine is a non-essential amino acid with versatile building block properties. It can be used as a reagent in organic synthesis, as a building block for complex compounds, and as a speciality chemical. L-Tyrosine is also useful as a reaction component in the synthesis of peptides and proteins. L-Tyrosine is an important intermediate in the production of pharmaceuticals, agrochemicals, dyes, flavors and fragrances. The CAS number for L-Tyrosine is 60-18-4.</p>

<p>Phthaloyl-L-alanine is a molecule with a hydrochloric acid group and a carbonyl group. It has been shown to have the ability to bind to peptidyl molecules and immobilize them, leading to an inhibition of the reaction mechanism. This process can be induced by enzymatic inactivation or by hydrogen bonding with chloride. The cisplatin-induced apoptosis of cancer cells has been demonstrated using patch-clamp technique on human erythrocytes. Caspases are proteins that are activated during apoptosis and have been found to interact with Phthaloyl-L-alanine in vitro. Molecular modeling studies suggest that Phthaloyl-L-alanine may inhibit caspases by binding to the enzyme's active site.</p>

<p>2-Methyl-4-chlorophenoxyacetic acid is a sodium salt of 2-methyl-4-chlorophenoxyacetic acid. It is a herbicide that inhibits photosynthesis by disrupting the electron transport chain in chloroplasts. The hydroxyl group on the phenoxy ring is responsible for its herbicidal activity. 2-Methyl-4-chlorophenoxyacetic acid has been shown to cause significant cell death in tissue culture, which may be due to its ability to inhibit enzymes such as acetylcholinesterase, phosphodiesterase, and carboxypeptidase A2. This chemical also has carcinogenic potential, but no toxicological studies have been conducted in humans or animals.</p>

<p>L-threo-droxidopa is a prodrug that is hydrolyzed in the liver to L-3,4-dihydroxyphenylalanine (L-DOPA) and then metabolized by dopamine β-hydroxylase to form dopamine. This drug has been shown to be effective for the treatment of Parkinson's disease. The long-term efficacy of this drug is unknown, but it has been shown to be safe and well tolerated for up to six months. L-threo-droxidopa has also been shown to be effective in lowering systolic blood pressure in patients with mild hypertension. The side effects of this drug include symptoms such as nausea, vomiting, dizziness, headache, and insomnia. However, these side effects are often transient and do not require discontinuation of treatment with this medication. There are no known interactions between L-threo-droxidopa and other drugs or foods. Pharmacological</p>

<p>Fluoxetine is a potent inhibitor of the enzyme cytochrome P450 (CYP) 2C19. The inhibition of CYP2C19 by fluoxetine may lead to an increase in the plasma concentration of other drugs that are metabolized by this enzyme, such as glipizide and hydroxycyclohexyl. Fluoxetine inhibits human uric acid secretion and increases plasma concentrations of uric acid. This drug also inhibits human erythrocyte dihydropyrimidine dehydrogenase, leading to increased blood levels of pyrimidines, especially cytotoxic ones like 6-fluoro-3-indoxyl-beta-D-galactopyranoside. Fluoxetine has been shown to have a protective effect against acetaminophen toxicity in rats because it enhances the conversion of acetaminophen to its less toxic metabolite N-acetylcysteine.</p>

<p>Z-NH-PEG12-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-PEG12-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 (3-Methyl-isoxazol-5-yl)methylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide is an anticancer drug that belongs to the class of phenethyl derivatives. It is a radiosensitizer that inhibits DNA and RNA synthesis, leading to cancer cell death. The drug has been shown to have a chiral center and two enantiomers, with the (S)-enantiomer being more active than the (R)-enantiomer. N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide has been shown to be effective in animal models for brain tumors and breast cancer cells. It has also been shown to be effective against leukemia cells, which are resistant to other treatments. N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4</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 Fmoc-S-4-methyltrityl-L-cysteine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Methylglutaric acid is an organic compound that belongs to the group of alkanocarboxylic acids. It has been shown to reduce the formation of malonic acid, which can be toxic to the heart and cause congestive heart failure. 3-Methylglutaric acid also inhibits oxidation catalysts and increases the production of energy in cells by providing electrons. The kinetic data for 3-methylglutaric acid have been determined using a gas chromatography technique on a high-temperature conversion reactor at a pH of 7.0 with a concentration of 0.1 M potassium phosphate buffer (pH 7) and a temperature of 70°C. 3-Methylglutaric acid has been shown to inhibit monoclonal antibody cationic polymerization, which may be due to its reactive nature and its ability to donate hydrogen ions or electrons.</p>

<p>Gly-Ala-OH is a leukocyte antigen that belongs to the group of transcription-polymerase chain reaction (PCR) inhibitors. It has been shown to inhibit the transcription of DNA into RNA by binding to the polymerase, preventing it from adding nucleotides onto the 3’ end of DNA. This inhibition can be seen in experimental solubility data and nmr spectra. Gly-Ala-OH also binds to type strain bacteria, such as Escherichia coli, Bacillus subtilis, Streptococcus pneumoniae, and Staphylococcus aureus. Gly-Ala-OH has been shown to bind with high affinity to ubiquitin ligases. This property may be due to its ability to form hydrogen bonds with these enzymes. Gly-Ala-OH binds more tightly than ATP and is therefore able to stabilize these enzymes for an extended period of time.</p>

<p>Z-NH-PEG2-CH2COOH 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-PEG2-CH2COOH 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>N-Succinimdyl-N-methylcarbamate is a reactive, antimicrobial agent that inhibits the activity of an enzyme in the cycle of cellular respiration. It binds to the active site of the enzyme, preventing it from functioning. N-Succinimdyl-N-methylcarbamate has been shown to inhibit hepatitis by inducing apoptosis. The drug has a phase transition temperature of approximately -6°C and is stable at higher temperatures. N-Succinimdyl-N-methylcarbamate has been shown to have an inhibitory effect on cyclic peptides, including those found in bacteria such as Helicobacter pylori and Chlamydia trachomatis.</p>

<p>2-Ethyl-2-phenylmalonamide (2-EPMA) is a metabolite of primidone that acts as an inhibitor of glutamate dehydrogenase and may be used in the treatment of epilepsy. It has been shown to be effective in treating seizures caused by carbamazepine, phenobarbital, or phenytoin. 2-EPMA is also used to measure enzyme activities in serum, which can be used as a diagnostic tool for liver diseases. 2-EPMA is typically prepared for use as an enzyme inhibitor by diluting it with high salt or human serum. This compound may have carcinogenic potential and should not be administered with single doses greater than 100 mg/kg body weight. 2-EPMA interacts with many other drugs such as phenobarbital, phenytoin, and carbamazepine.</p>

<p>Zofenopril calcium is a potassium-containing salt of zofenopril, a prodrug that is hydrolyzed in vivo to the active form, 4-phenylthio-L-proline. Zofenopril calcium is used as an antihypertensive agent and has a low incidence of adverse effects. It inhibits the enzyme angiotensin converting enzyme (ACE) in the renin-angiotensin system, which results in decreased levels of angiotensin II and subsequent vasodilation.</p>

<p>Diphenylprolinol is a synthetic cannabinoid that is used as an agonist of the CB1 and CB2 receptors in the brain. It has been shown to have high affinity for both the CB1 and CB2 receptors, with Ki values of 0.07 and 0.05 nM respectively. Diphenylprolinol is a full agonist of the CB1 receptor, but only a partial agonist of the CB2 receptor. Diphenylprolinol binds to these receptors in a manner that resembles endocannabinoids, which are endogenous cannabinoids produced by animals. This drug has shown antipsychotic effects through its binding to serotonin reuptake inhibitors and its ability to block dopamine release in the prefrontal cortex. Diphenylprolinol also acts as a potent growth factor by stimulating cell proliferation via activation of protein kinase C (PKC). PKC activation leads to increased levels of intracellular calcium ions (Ca2+) and stimulates growth factor production such as</p>

<p>Please enquire for more information about 1-Methyl-1H-imidazole-2-carbohydrazide 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 tert-Butyl (1-methyl-1H-imidazol-5-yl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R,S)-1-Methyl-3-nicotinoylpyrrolidine is a nicotinic acid derivative with a pyrrolidine ring at the 1-position. It is used as an intermediate in the synthesis of other compounds and has been used as a stabilizer for cellulose. The stability study showed that the compound was stable to evaporation and oxidation products in ethanol solutions. The adsorption index (AI) was found to be 0.9.</p>

<p>Please enquire for more information about Methyl 3-(1-methyl-1H-benzimidazol-2-yl)propanoate 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 Fmoc-4-hydrazinobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 4-methylthiazole-5-carboxylate (MTMC) is a compound with high chemical and biological activity. MTMC has been shown to inhibit the growth of S. aureus, and also exhibits cytotoxic effects on human cancer A549 cells in vitro. MTMC has been shown to be active against HIV in cell culture and also inhibits the replication of influenza virus. MTMC has significant activity against cancer, and is also effective against immunodeficiencies that are due to viral infection. It can be synthesized by a high-yielding process involving the reaction of methyl 4-nitrobenzoate with thiourea in an organic solvent under reflux conditions. The crystal structure of MTMC was determined by X-ray diffraction methods, revealing that it is centrosymmetric with four molecules present in the asymmetric unit.</p>

<p>7-Phenylacetamide-3-chloromethyl-3-cephem-4-carboxylic acid diphenylmethyl ester is an organic solution that is used in the detoxification of chemical substances. It has a hydroxyl group and is soluble in nonpolar solvents. 7PAMC has been shown to be effective against bone lesions caused by acylation reactions. This drug also binds to the enzyme called cytochrome P450, which is involved in the metabolism of many drugs. It also inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, enzymes that maintain bacterial DNA integrity. The particle size of this drug is small, with a diameter of less than 10 microns. 7PAMC has a viscosity of 1 cps at 25°C and a melting point of 129°C.</p>

<p>2-Methylaminoethanol is a colorless, water-soluble liquid. It is an alkanolamine that has a dipole moment of 1.8 debye. 2-Methylaminoethanol can be synthesized by reacting potassium dichromate with ethanolamine in the presence of borohydride and ammonia. The reaction yield for this process is about 50%. 2-Methylaminoethanol reacts with maleic acid to form maleate salt. Maleate salt molecules have two amine groups attached to a carbonyl group, which are used as raw materials for the production of various other chemicals like nylon 11, nylon 12, and polyethylene terephthalate (PET). Maleates also serve as intermediates in the manufacture of esters and nitrites from alcohols and phenols. 2-Methylaminoethanol has been shown to cause blood pressure reduction in mammals due to its ability to inhibit vasoconstriction caused by</p>

<p>Please enquire for more information about Methyl (3S)-3-aminopent-4-ynoate hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Iodo-2-methoxypyridine-3-carboxaldehyde is a disubstituted compound that has insulin-like properties. It inhibits the activity of the insulin receptor, which may contribute to its insulin-like growth factor effects. This inhibitor also targets the protein kinase, which is responsible for the response of cells to insulin. 4-Iodo-2-methoxypyridine 3 carboxaldehyde has been shown to inhibit IGF1R and malonate ion, and it may have potential as an oral treatment for diabetes.</p>

<p>N-Cbz-L-serine is a synthetic amino acid that has been shown to have antimicrobial effects. It has been found to inhibit the growth of bacteria, fungi, and protozoa by inhibiting their cell membranes. This amino acid also inhibits the synthesis of phospholipids in bacterial cell walls and may be used as an antimicrobial agent for industrial applications. N-Cbz-L-serine contains both a hydroxy group and a hydroxyl group, which are essential for its antibacterial activity. The fatty acids present in this compound can be either saturated or unsaturated. Multigram quantities of N-Cbz-L-serine have been produced with high purity using asymmetric synthesis methods.</p>

<p>Please enquire for more information about R-(-)-Methamphetamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(2-Methyl-1H-imidazol-1-yl)ethanol is a synthetic intermediate that has been used to synthesize antibiotics and antiviral agents. It has a terminal half-life of about 2 days and its pharmacokinetics are linear with an oral dose range from 10 to 100 mg/kg. The fruit extract of Camptotheca acuminata contains alkaloids, which can be converted into 2-(2-methyl-1H-imidazol-1-yl)ethanol by alkalization. 2-(2-Methyl-1H-imidazol-1-yl)ethanol is effective against hordeolum, acne, and infectious diseases caused by viruses such as herpes simplex. This drug has antibacterial properties and can be used in the treatment of bacterial infections such as staphylococcal skin infections, streptococcal throat infections, or gonorrhea. Dehydration is an</p>

<p>Please enquire for more information about H-Gln-pNA trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-2-Methylpyrrolidine is a synthetic quaternary ammonium compound that is a reaction yield enhancer. It has been shown to have histamine-lowering effects in vitro and in vivo. The pharmacokinetic properties of (R)-2-Methylpyrrolidine are characterized by moderate distribution and elimination half-life times. It is also active at the h3 receptors, which may be related to its wake-promoting effects. (R)-2-Methylpyrrolidine has been shown to increase the levels of amines in the brain, which may be associated with its antidepressant activity. This drug also has environmental effects such as increasing the absorption of heavy metal ions such as lead and cadmium.</p>

<p>4,7-Dihydroxy-1,10-phenanthroline is an organometallic compound that has been shown to inhibit the growth of tumour cells. It is a protonated molecule and can be classified as a reactive intermediate. The reaction mechanism for this intermediate is nucleophilic attack by the hydroxy group on the carbon atom adjacent to the aromatic ring. This results in the formation of a cationic intermediate, which undergoes protonation to form the final product. 4,7-Dihydroxy-1,10-phenanthroline has been found to have anti-tumor effects against l1210 murine leukemia cell lines.</p>

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

<p>N-Chloroacetyl-L-tyrosine is a synthetic, proteolytic enzyme that hydrolyzes proteins containing the amino acid L-tyrosine. It has been shown to inhibit the growth of bacteria by inhibiting the activity of enzymes involved with protein synthesis and peptide bond formation. N-Chloroacetyl-L-tyrosine inhibits the activity of diazonium salt and conjugates, which are involved in polypeptide synthesis and DNA replication. It also has an inhibitory effect on functional groups, such as hydroxyl, amine, sulfhydryl, carboxylate, phosphate, and phosphoric acid.</p>

<p>2-Methylbenzhydrol is an organic compound that belongs to the group of five-membered heterocyclic compounds. The crystal structure of 2-methylbenzhydrol has been determined by X-ray crystallography, and it reacts with a rhesus monkey in a stereoselective manner. It is also found as one of two diastereomers in the reaction between benzaldehyde and hydroxylamine. The molecular ion peak for 2-methylbenzhydrol can be detected using mass spectrometry, and the major product ions are ions corresponding to the loss of methanol (CHOH) from the molecule. Other functional groups present in this compound include an aldehyde and a hydroxy group. The reversed-phase high performance liquid chromatography (HPLC) plates used to separate 2-methylbenzhydrol from other similar compounds should be stable at room temperature, but will become unstable if heated to more than 40°C.</p>

<p>Please enquire for more information about 3-Methoxy methamphetamine hydrochloride 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 Boc-(2R,5S)-5-phenylpyrrolidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Docosahexanoyl-sn-glycero-3-phosphocholine (DHA) is a dietary phospholipid that has been shown to have biological activity in several animal models. DHA is a polyunsaturated fatty acid that can be found in the brain and muscle tissue. DHA is important for maintaining the integrity of cellular membranes, which are biomimetic lipid bilayers. These structures make up the outer layer of cells and allow for communication between cells and other molecules outside of the cell membrane. DHA has been shown to delay neurodegenerative diseases such as Alzheimer's disease by preventing oxidative damage to neurons.</p>

<p>Please enquire for more information about O-Benzyl-L-tyrosine methyl ester hydrochloride 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 L-Cysteinesulfinic acid, monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-NH-PEG8-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-PEG8-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 4-Amino-1-Boc-piperidine-4-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-Thr-OPAC is a solid-phase peptide synthesis reagent. It is used to synthesize α-amino acid peptides. Fmoc-Thr-OPAC has been used in the preparation of various peptides, including polypeptide hormones such as insulin and vasopressin. The compound has also been used in the crystalline form for the synthesis of α-amino acid derivatives.</p>

<p>N-alpha-Benzoyl-L-lysine is a lysine analogue that has been shown to have anaphylactic effects in pigs. This compound is synthesized by reacting the benzoyl chloride with L-lysine. The reaction scheme for this synthesis can be found in Figure 1 below. In order to produce this product, it is necessary to first dissolve the reactants in a solvent such as dichloromethane or chloroform. The solvents are then removed by evaporation and the residue obtained is purified by recrystallization or chromatography. N-alpha-Benzoyl-L-lysine has also been shown to be able to elicit formyl amides from plant cells, which may lead to new insights into how plants respond to environmental cues.</p>

<p>Please enquire for more information about 4-[1-(2-Methoxyethyl)-1H-indol-3-yl]butanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-L-aspartic acid 4-tert-butyl ester is a synthetic aminoacylase that is used in the synthesis of ergosterol. It is an efficient and economical reagent for the preparation of esters of aspartic acid, which are used in fungal antifungal agents. Boc-L-aspartic acid 4-tert-butyl ester has been shown to have various physiological functions, including the ability to inhibit ergosterol synthesis by inhibiting the enzyme polymeric ergosterol synthase in fungi. This compound can also be used to synthesize n-substituted aspartates.</p>

<p>3-(Chloromethyl)-4-methoxybenzaldehyde is a natural product that can be extracted from the rhizomes of the plant. It has been shown to have antibacterial activity in laboratory experiments and has been used in traditional medicine for the treatment of fungus infections. 3-(Chloromethyl)-4-methoxybenzaldehyde is an imidazolylmethyl derivative with a hexane structure. It reacts with hydrochloric acid to form a molecule called chloromethylation, which is also known as an esterification reaction. Piperazine acts as a catalyst in this reaction, increasing its scalability and making it suitable for large-scale production. The compound exhibits radical scavenging activity, which may be due to its ability to donate electrons or hydrogen atoms to free radicals.</p>

<p>Please enquire for more information about N,N'-bis-Fmoc-diaminoacetic acid 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 3-Methoxy-7a-methyl-estra-2,5(10)-dien-17-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-proline analogue</p>

<p>Beta-alanine amide HCl is a research chemical that belongs to the class of beta-amino acid derivatives. Beta-alanine amide HCl is an activator of nucleophiles and can be used in analytical chemistry as an indicator for chloride ions. It has been shown to react with asparagine, yielding beta-alanine and ammonia. The reaction system can be analysed by measuring the elimination of a hydrogen chloride ion from the beta-alanine amide HCl molecule and the subsequent increase in pH. The analytical method has also been used to measure concentrations of deamination reactions and redox potentials at high concentrations.</p>

<p>Please enquire for more information about 17-Methylestra-3,5-diene-3,17b-diol diacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>This is a broad-spectrum antibacterial agent that inhibits bacterial DNA gyrase. It is active against atypical bacterial species, such as Chlamydia and Mycoplasma, and has been shown to be effective against certain strains of the methicillin-resistant Staphylococcus aureus (MRSA) bacteria. This drug also inhibits the growth of other bacteria by binding to their DNA. The drug is used in combination with other antibiotics to treat infections caused by Clostridium difficile, Helicobacter pylori, Borrelia burgdorferi, and Salmonella enterica. However, this drug does not work against Pseudomonas aeruginosa or Enterobacteriaceae infections.</p>

<p>Bz-Gly-Gly-OH is a peptide that is used in biochemical analyses. It has been shown to bind to amides, fatty acids, and collagen. Bz-Gly-Gly-OH also has the ability to activate human serum and fibroblast proliferation. This peptide can be synthesized by chemical ligation of hippuric acid, malic acid, and carbapenem.</p>

<p>1,2-Dilinoleoyl-3-palmitoyl-rac-glycerol (DLPG) is a lipid molecule that is structurally similar to the sphingolipid ceramide. It has been shown to be an inhibitor of cellular uptake and growth rate and also has long-term toxicity effects. DLPG has been shown to inhibit the signal transduction pathway by binding to microprocessors in the cell membrane and changing their frequency. DLPG also has a profile that can be used as an analog for dextran sulfate, which is a chemical compound that inhibits the uptake of glucose in mammalian cells. The uptake of DLPG can be decoupled from its signaling activity by using constant magnetic fields, which can be generated with superparamagnetic iron oxides or iron particles.</p>

<p>Please enquire for more information about N-(8-Methoxy-4-methylquinazolin-2-yl)guanidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Phenylacetic acid 2-phenylethyl ester is an ester of caproic acid and phenylethyl. It is used as a control agent in the manufacture of chemical substances, detergent compositions, and lemongrass oil. Phenylacetic acid 2-phenylethyl ester can be synthesized by reacting methyl anthranilate with benzoic acid in the presence of phosphotungstic acid. The required starting materials are available from commercial sources. The product has a structural formula that can be confirmed by nmr spectroscopy.</p>

<p>Please enquire for more information about Boc-L-Tyr(Bzl)-Merrifield Resin 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 N'-(1-Methylazepan-4-yl)benzohydrazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Phenylquinazoline-2,4(1H,3H)-dione is an efficient synthesis of hydrazine. It can be used in the synthesis of other molecules.</p>

<p>1-Methyl-1H-benzimidazole-2-carboxylic acid is a synthetic compound that can be used as an antiprotozoal. It has been shown to have good activity against intestinalis, vaginalis, and intestinalis species. 1-Methyl-1H-benzimidazole-2-carboxylic acid binds to the acetyl groups of the parasite's cell membrane and inhibits the formation of the cytoplasmic membrane. This prevents the parasite from synthesizing ATP, which causes them to die. 1-Methyl-1H-benzimidazole-2-carboxylic acid also has strong activity against Giardia lamblia, which is caused by its ability to inhibit protein synthesis in this organism.</p>

<p>Please enquire for more information about [1-(2-Methoxyethyl)-1H-indol-3-yl]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-alpha-Acetyl-L-ornithine is an intermediate in the urea cycle that has been shown to be a potential biomarker for metabolic disorders. It has also been shown to inhibit glutamate synthesis and nitrogen oxidation by inhibiting arginase and nitric oxide synthase. N-alpha-Acetyl-L-ornithine is synthesized from L-arginine and acetyl coenzyme A, catalyzed by synthetases. The reaction requires ATP, magnesium ion, and a molecule of NADPH. This synthetic pathway can be monitored using high performance liquid chromatography (HPLC). N-alpha-Acetyl-L ornithine can be used as a precursor in the production of caproic acid, which is an important organic acid used in chemical biology.</p>

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