Amines

<p>Please enquire for more information about tert-Butyl 2-amino-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Intermediate in the synthesis of edoxaban</p>

<p>Please enquire for more information about Amyloid beta-Protein (17-40) ammonium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Dimethylaminoethanol (+)-bitartrate salt is a potent, reversible inhibitor of protein synthesis that binds reversibly to the 50S ribosomal subunit. It is used in regulatory toxicology and clinical pathology as a positive control for the study of chronic toxicity and long-term effects. 2-Dimethylaminoethanol (+)-bitartrate salt has shown no treatment effect on ovary weight or estrous cycle length in female Sprague-Dawley rats after chronic exposure and long-term exposure at doses up to 1,000 mg/kg/day. This drug has also shown no effect on rat fertility or reproductive performance, indicating it does not cause reproductive toxicity.</p>

<p>Please enquire for more information about Gastrin I (1-14) (human) ammonium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2-Furylmethyl)methylamine is a protein inhibitor that has been shown to inhibit γ-secretase, an enzyme responsible for the cleavage of amyloid precursor protein (APP) and the production of beta-amyloid. It has also been shown to be effective in treating cancer and Alzheimer's disease when administered as an intravenous injection or oral medication. The effects on animals were observed in a study involving mice with bladder cancer. (2-Furylmethyl)methylamine was found to inhibit the growth of bladder cancer cells and induce apoptosis. This compound also inhibits glycogen synthase kinase 3 (GSK3), which is involved in cell proliferation. Trichophyton mentagrophytes, a fungus that causes athlete's foot, has also been found to be sensitive to this drug. Heterocycles are not affected by this compound because they lack nitrogen atoms at their positions corresponding to those in the amide group</p>

<p>3,7-Diamino-2,8-dimethyldibenzothiophene sulfone (contains 2,6-Dimethyl isomer) is a hydrophilic aromatic hydrocarbon that is used in the production of polymers. It is a copolymerization agent and monomer for epoxy resins and vulcanizates. The product contains impurities such as benzene and sulfur.</p>

<p>(R,S)-AMPA is a synthetic analog of the excitatory neurotransmitter glutamate, specifically designed to activate AMPA receptors, a subtype of ionotropic glutamate receptors. These receptors are pivotal in mediating fast synaptic transmission in the central nervous system. (R,S)-AMPA serves as a prototypical agonist for AMPA receptors, facilitating the study of receptor function and synaptic plasticity.​</p>

<p>Please enquire for more information about Ethyl 4-amino-2-mercaptopyrimidine-5-carboxylate 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-N-(4-boc-aminobutyl)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 5-tert-Butyl-1,3,4-oxadiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Mozavaptan is a pharmacological agent that acts as a vasopressin V2 receptor antagonist. It is derived through synthetic chemical processes designed to target specific neurohormonal pathways in the body. Mozavaptan exerts its effects by inhibiting the action of vasopressin, a hormone that promotes water reabsorption in the kidneys. By blocking the vasopressin receptors, it enhances water excretion and corrects imbalances in electrolyte levels, particularly addressing conditions like hyponatremia.</p>

<p>Please enquire for more information about (Cys2)-Neuropeptide Y (1-4)-8-aminooctanoyl-(D-Cys27)-Neuropeptide Y (25-32) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Fluoroamphetamine hydrochloride (3FAH) is a histological and microscopic technique used to study the effects of analgesics on human skin. 3FAH is an analgesic that has been shown to reduce pain in a number of studies. It has also been observed to enhance the effects of laser treatments on human skin, as it reduces inflammation and increases transdermal permeation. This drug is applied topically or injected for the treatment of pain, muscle spasms, or Parkinson’s disease. 3FAH can be administered by iontophoresis or permeation techniques, which are both effective ways to deliver drugs through skin.</p>

<p>Please enquire for more information about 12-(Boc-aminooxy)-dodecanoic 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 5-(H-Gly-Pro-Gly-Pro-amido)-9-[di-(3-sulfonylpropyl)amino]-benzo[a]phenoxazonium perchlorate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-3,5,6-trichloropyridine-2-carboxylic acid (4ATC) is a herbicide that inhibits the activity of pyridoxal phosphate (PLP)-dependent enzymes. 4ATC has been shown to be more toxic to plants than temozolomide and is used in vitro to study the effects of herbicides on cells. It inhibits cell growth and induces apoptosis in human cancer cells. In addition, 4ATC has been shown to inhibit the enzyme activities of group P2 proteins and nucleic acid synthesis. 4ATC also inhibits protein synthesis by inhibiting RNA synthesis in eukaryotic cells. 4ATC is not active against bacteria or fungi.</p>

<p>Please enquire for more information about 3-Amino-2-bromo-6-chloropyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminobutyrophenone is a butyrophenone, a nitro compound that is the amine derivative of 4-aminobutyric acid. This product is used as a control agent in pest control and as an intermediate for pharmaceuticals and dyes. It has been used to produce methemoglobin, which is used to treat nitrate poisoning. 4-Aminobutyrophenone undergoes acylation reactions with chloride or sulfoxide groups to form chlorohydrins and thiohydrins respectively. These products are bioisosteres of the carbonyl group, which can be hydrolyzed with acid or alkali to produce carboxylic acids or alcohols respectively. Friedel-Crafts acylation with phenol gives benzoylphenylhydroxylamine, which can be oxidized by hydrogen peroxide to give the corresponding nitro compound.</p>

<p>Please enquire for more information about Boc-epi-statine (3R,4S)-4-(Boc-amino)-3-hydroxy-6-methyl-heptanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Allylamine HCl is a chemical that belongs to the group of allylamines. It can be used as an analytical method for wastewater treatment because it reacts with sodium salts and forms water-soluble products. Allylamine HCl has been used in the production of microcapsules, which are polymeric particles that contain drugs or other substances. The biological properties of allylamine HCl have been studied, and it has been found to be nontoxic to mice when consumed orally. Allylamine HCl is also toxic to tumor cells and could be effective in cancer therapy. Allylamine HCl has also been shown to inhibit transfer reactions involving water vapor, such as intramolecular hydrogen transfer.</p>

<p>2,7-Bis[2-(diethylamino)ethoxy]-9-fluorenone dihydrochloride (2,7-BDFE) is a potent inducer of interferon. It is a natural compound that has been shown to have significant cytotoxicity against murine sarcoma virus and opportunistic fungal infections. 2,7-BDFE has also been shown to induce toll-like receptor 4 (TLR4), which triggers the production of other cytokines and chemokines. 2,7-BDFE has also been found to inhibit the growth of cancer cells in vitro and in vivo. This drug is used as an inhibitor for benzalkonium chloride for the prevention of bacterial contamination on surfaces.</p>

<p>Please enquire for more information about 4-Methyl-benzhydrylamine resin (100-200 mesh)·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>9-Aminoacridine is a potential anticancer agent that intercalates into the DNA and prevents the replication process. It has been shown to inhibit the growth of bacteria resistant to tetracycline by interfering with bacterial DNA replication. 9-Aminoacridine also has anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

<p>4-Methyloxy-phenyl)-piperazin-1-yl]-phenylamine is an organic compound that has a reactive silicon group. It contains two phenyl groups, one of which is attached to the silicon. This compound exhibits phase equilibrium in water and can be used as a monomer for fabricating inorganic materials with orderly patterns, such as glass and metal oxides. This product also has impurities and can be grown at different rates depending on the conditions, such as temperature. The optical properties of 4-methyloxy-phenyl)-piperazin-1-yl]-phenylamine are dependent on its environment and it has been shown to have exothermic properties when reacting with iron powder.</p>

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

<p>1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol) 2000] (ammonium salt) 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. 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol) 2000] (ammonium salt) 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>2-(Dimethylamino)acetaldehyde sulfite is a white crystalline solid with a melting point of around 100°C. It is soluble in water and slightly soluble in organic solvents. 2-(Dimethylamino)acetaldehyde sulfite can be used as a reagent to prepare alkali solutions and acid hydrochlorides. It can also be used as an intermediate for the synthesis of methacrylic acid, methyl acetate, and other organic compounds. 2-(Dimethylamino)acetaldehyde sulfite can be synthesized using a high-yield synthetic method involving lithium, acidification, and an organic solvent.</p>

<p>Please enquire for more information about Gly-Amyloid b-Protein (15-25)-Gly-epsilon-aminocaproyl(-Lys)6 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 (3R)-3-[(tert-Butoxycarbonyl)amino]-4-(2,4-difluorophenyl)butanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tridodecylmethylammonium chloride (TDMAC) is a biocompatible and non-toxic polymer that is used in the manufacture of sensors. TDMAC can be used as a coating on electrodes to increase their sensitivity to changes in pH and ionic strength. TDMAC is also used as a blood substitute, and has been shown to have anticoagulant properties. TDMAC has been shown to be effective at preventing heparin-induced thrombocytopenia when combined with dextran sulfate. This polymer has also been studied for use in biosensors and bioelectrochemical impedance spectroscopy devices.</p>

<p>Please enquire for more information about PAL resin (200-400 mesh) 4-Alkoxy-2,6-dimethoxybenzylamine 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 2-Amino-3-fluorobenzoic acid ethyl ester 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-Amino-5-chloropyrazine-2-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromoquinolin-8-amine is a topoisomerase inhibitor that can be used as an antitumor agent. It has been shown to inhibit the growth of tumor cell lines and suppress the growth of colon carcinoma cells in rats and human colon carcinomas in mice. 5-Bromoquinolin-8-amine interacts with DNA, specifically inhibiting the formation of supercoiled DNA. This interaction may lead to the inhibition of tumor cell growth. 5-Bromoquinolin-8-amine also inhibits protein synthesis by interacting with proteins at the ribosomal level, leading to inhibited cell growth.</p>

<p>Myristyl dimethylamine oxide is a surfactant that is used in wastewater treatment. It is also an antimicrobial agent that exhibits broad-spectrum activity against bacteria, yeast and moulds. Myristyl dimethylamine oxide has been shown to have a low toxicity to humans and other mammals. The antimicrobial activity of this compound may be due to its ability to inhibit microbial growth by disrupting the cell membrane or by inhibiting protein synthesis. Myristyl dimethylamine oxide can be found in many household products, including soaps, shampoos, toothpaste, mouthwash, and cosmetics. !-- --&gt;Myristyl dimethylamine oxide is also used in the prevention of HIV infection by blocking the binding of HIV to the CD4 receptor on cells. This compound has been shown to block HIV-1 entry into human cells and inhibit HIV replication in vitro with high values for protonation.</p>

<p>(2R,3S)-3-Amino-2-hydroxy-3-phenylpropanoic acid hydrochloride is an organic compound that is used in the manufacture of taxol, an anticancer drug. It is synthesized by reacting chloroacetic acid with a metal hydroxide, such as sodium hydroxide or potassium hydroxide. The reaction proceeds spontaneously to form the enantiomerically pure (2R,3S) form and unreacted (2S,3R) form. The (2R,3S) enantiomer has been found to be more reactive than the (2S,3R) form. Quaternary ammonium salts are formed when the (2R,3S) enantiomer reacts with quaternary ammonium compounds such as benzyltrimethylammonium chloride. This compound can also be used in catalytic reactions to produce drugs such as carbapenems and pen</p>

<p>4-Amino-3-methoxypyridine (4AMMP) is a naturally occurring amino acid that can be found in the nuclei of innervated tissues. It is an inhibitor of the enzyme tyrosine hydroxylase and inhibits the synthesis of catecholamines. The concentration of 4AMMP in blood was measured by radioactivity. This agent has been used for studies on the thalamic nucleus and cortex, as well as for measuring catecholamine levels in tissue homogenates.</p>

<p>Please enquire for more information about 3-Aminoazepan-2-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N1-Glutathionyl-spermidine disulfide (N1-GS) is a molecule that has been shown to have clinical use in the treatment of chronic hepatitis C infection. The N1-GS molecule is composed of a glutathione (GSH) scaffold with two sulfhydryl groups and an amino acid side chain. N1-GS has a hydrophobic nature, which allows it to penetrate the cellular membrane and enter cells. It is also able to form hydrogen bonds and act as a catalyst for reactions. Fluorescence analysis revealed that this molecule is selective for disulfides over thiols, amines, or alcohols. Disulfides are very important in biological systems since they can be found in enzymes, proteins, and cellular membranes. The insolubility of the N1-GS molecule makes it difficult to analyze its structure using traditional methods such as gas chromatography or nuclear magnetic resonance spectroscopy. However, fluorescence</p>

<p>Please enquire for more information about 2-Amino-5-(trifluoromethoxy)benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>DL-3-Amino-3-phenylpropionic acid is an amino acid that is synthesized by the reaction of malonic acid and ethyl ester. This compound is a competitive inhibitor of the enzyme pyruvate carboxylase and inhibits this enzyme in the conversion of pyruvic acid to acetyl CoA, which plays a key role in metabolism. DL-3-Amino-3-phenylpropionic acid has been shown to inhibit the growth of bacteria such as Escherichia coli, Salmonella typhimurium and Staphylococcus aureus. The inhibition of pyruvate carboxylase by DL-3-Amino-3-phenylpropionic acid prevents the production of acetaldehyde from pyruvate, which is toxic to cells.</p>

<p>Please enquire for more information about TCO-amine 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 (p-Amino-Phe6)-Angiotensin II including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-1-Boc-3-Aminopyrrolidine is a small molecule that inhibits 3-kinase. It has been shown to bind to the ATP binding site of PI3Kδ and inhibit its activity. This results in the inhibition of phosphoinositide production, which leads to decreased cell proliferation and survival. (R)-1-Boc-3-Aminopyrrolidine has also been shown to have selectivity for isoform α over β, γ, and δ. The drug binds specifically to the ATP binding site on PI3Kδ, but does not disrupt other interactions such as hydrogen bonding or pi stacking interactions with residues in the vicinity of the ATP binding site. The IC50 values for (R)-1-Boc-3-Aminopyrrolidine were determined using siRNA knockdown experiments against human isoform α PI3Kδ.</p>

<p>1,3,4-Oxadiazol-2-amine is a synthetic compound that belongs to the group of peptidomimetics. It is an alkylating agent that has been shown to inhibit glycogen synthase kinase 3 (GSK3) and prevent the formation of amyloid plaques in Alzheimer's disease. 1,3,4-Oxadiazol-2-amine also has antibacterial activity against Gram-positive and Gram-negative bacteria. This compound can be synthesized by reacting chloroacetaldehyde with 2-(2'-aminophenoxy)ethanol in the presence of acid. The molecular weight for this compound is 167.260 g/mol. Crystals are obtained from melting the substance at 180 °C under vacuum and then allowing it to cool down to room temperature over a period of 4 hours. The crystal system for this molecule is monoclinic and its space group is P21/c. X-ray diffraction</p>

<p>Fmoc-4-(Boc-amino)-L-phenylalanine is a useful building block, which is used in the synthesis of complex compounds and research chemicals. It is also a reaction component in the synthesis of compounds. Fmoc-4-(Boc-amino)-L-phenylalanine has CAS No. 174132-31-1 and can be used as a versatile building block to produce high quality reagents.</p>

<p>N-(3-Dimethylaminopropyl)acrylamide is a polymerization initiator that is used in the synthesis of polymers. It is also a model protein, which can be used to study bacterial growth rates and tissue metabolism. N-(3-Dimethylaminopropyl)acrylamide has been shown to have biological properties similar to human serum, as well as to serve as a model for primary cells. The FT-IR spectroscopy of N-(3-Dimethylaminopropyl)acrylamide reveals the presence of chloride ions in its molecular structure. The reaction mechanism for this compound has been determined by deionized water and ionic reactions with chloride ions.</p>

<p>3-[(Dimethylamino)methyl]-1,2,4-oxadiazol-5-amine hydrochloride is a versatile building block that is used as an intermediate in the synthesis of fine chemicals. It is also a useful scaffold for the synthesis of biologically active compounds and research chemicals. 3-[(Dimethylamino)methyl]-1,2,4-oxadiazol-5-amine hydrochloride can be prepared by reacting methylamine with 2-aminothiophenol in the presence of a base. This reagent is also useful for the preparation of other compounds such as carbamates and cyclic ureas.</p>

<p>3-(Aminomethyl)phenol is a potent inhibitor of growth factor receptor kinase (GRK) and protein kinase C. It has been shown to have inhibitory effects on cellular proliferation in mammalian cells and is being investigated as an adjuvant therapy for cancer treatment. 3-(Aminomethyl)phenol has also been shown to inhibit the enzyme cyclooxygenase-2, which is involved in the synthesis of prostaglandins.<br>DISCUSSION: The carbonyl group of 3-(aminomethyl)phenol makes it a potent inhibitor of GRKs and protein kinases C. Kinases are enzymes that catalyze the addition of phosphate groups onto proteins, which affects their activity. As such, 3-(aminomethyl)phenol inhibits the activity of GRKs and protein kinases C by binding to the ATP-binding site, preventing ATP from binding and phosphorylating the enzyme's target proteins</p>