Building Blocks

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Methyl-pseudouridine-5'-triphosphate trisodium is the triphosphate of 1-Methylpseudouridine is a substitute for uridine in modified mRNA. This substitution has shown to increase transfection by reducing immuogenicity. UV max wavelength = 272nm</p>

<p>Applications 1,3,5-Trifluorotrichlorobenzene is a useful reagent.<br></p>

<p>Applications 4-Diazobenzenesulfonic acid (cas# 305-80-6) is a useful research chemical.<br></p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>IR-780 iodide is a water-soluble drug that has been shown to have significant cytotoxicity against prostate cancer cells. It binds to the mitochondrial membrane potential, which is involved in energy production and the regulation of the cell cycle. IR-780 iodide is taken up by tumor cells, where it inhibits adriamycin uptake and induces apoptosis. In vitro assays have shown that IR-780 iodide can be used as a diagnostic tool for detecting bladder cancer by binding to the mitochondria of cells from patients with bladder cancer. In vivo studies have been done in mice to determine the effectiveness of IR-780 iodide in treating cervical cancer. These studies showed that IR-780 iodide was not significantly effective in vivo, due to its low bioavailability and lack of specificity for cervical cancer cells. Histological analysis showed that IR-780 iodide did not inhibit tumor growth or induce apoptosis in vivo.</p>

<p>Leu-Leu-Leu-OH is a pentapeptide that is used in cancer treatment to inhibit the growth of cancer cells. It prevents the production of proteins and, as a result, cell division. Leu-Leu-Leu-OH has been shown to be effective against tumor cells with an antibody that binds to the surface of cells. The monoclonal antibody is taken up by the cancer cells through receptor mediated endocytosis, which leads to inhibition of protein synthesis and cell death.</p>

<p>Please enquire for more information about 4-Bromo-1-methyl-1H-pyrazolo[4,3-c]pyridine-6-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Formylbenzoic acid is an organic compound with the molecular formula CH2=C(O)CH=CHCO2H. It is a white solid that is soluble in water and has a strong, unpleasant odor. 4-Formylbenzoic acid has been shown to have affinity for binding to odorous molecules such as sulfur compounds, amines, and mercaptans. The binding of these molecules to the 4-formylbenzoic acid leads to a decrease in their odor concentration. This process can be done using electrochemical impedance spectroscopy or optical sensors. The oxidation of 4-formylbenzoic acid by trifluoroacetic acid produces 2-formylphenol and formaldehyde, which are themselves volatile compounds with an unpleasant odor. These reactions may be used as wastewater treatment methods. Langmuir adsorption isotherm may be used as an analytical method for measuring the concentration of 4-formylbenzoic acid</p>

<p>N-alpha-Z-L-lysine methyl ester hydrochloride is a preparation that is used as a methyl ester. It is an ester of lysine and methyl chloride. This product has a molecular weight of 170.16 g/mol and the chemical formula CH3CONHCH2CH(NH)CO2CH3. The structural data has not been confirmed by X-ray crystallography, but it can be assumed to be in the form of a zwitterion. N-alpha-Z-L-lysine methyl ester hydrochloride can be used for the synthesis of peptides, which are building blocks for proteins and enzymes. N-alpha-Z-L-lysine methyl ester hydrochloride is also used in the production of certain kinds of drugs and organic acids such as acetylsalicylic acid (aspirin).</p>

<p>Please enquire for more information about N-[5-(4-Bromophenyl)-6-(2-hydroxyethoxy)-4-pyrimidinyl]-N′-propylsulfamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

(4-(tert-Butoxy)phenyl)methanamine (BPMT) is a ligand that binds to the alpha-2 receptor and acts as an antagonist. This compound has been shown to be a molecular target for positron emission tomography imaging, which is used in the diagnosis of tumours. BPMT is also used in the treatment of neuropeptide-associated disorders such as Parkinson's disease. The chiral nature of this compound makes it useful for the production of radiopharmaceuticals and other diagnostic agents with different physical properties.

<p>N-Boc-glycine is a chemical compound used in the synthesis of cyclic peptides. N-Boc-glycine is synthesized by the reaction of glycine with methanol and hydrochloric acid in the presence of an activated form of carbon monoxide. The pharmacokinetic properties of N-Boc-glycine are similar to those for human immunoglobulin, and it can be used as a reference compound for preparative high performance liquid chromatography (HPLC). It has been shown that the nitrogen atoms in N-Boc-glycine are chemically stable, which makes it suitable for asymmetric synthesis. N-Boc-glycine also has potent antagonist effects on biochemical properties such as calcium channel blockade, inhibition of platelet aggregation, and inhibition of neutrophil chemotaxis.</p>

<p>Flurbiprofen Related Compound A is a compound that inhibits the activity of serine proteases. It binds to the active site of the enzyme, preventing it from breaking down proteins in the body. Flurbiprofen Related Compound A binds to metal surfaces and is also used as a fluorescent probe for biological research. It has been shown to have optical properties and fluorescence properties, which are amplified by an amplifier.</p>

<p>H-Lys(Boc)-OH is an ε-amino-protected lysine that plays a pivotal role in solution phase peptide synthesis. Strategically protected at the ε-amino group, it allows controlled peptide assembly, and it serves as intermediate for synthesizing β-peptides. The bulky Boc (tert-butyloxycarbonyl) group shields its epsilon amine (NH2) group, acting as a protective measure to prevent unwanted side reactions.</p>

<p>3-Bromobenzaldehyde is an organic compound with the formula CHBrCHO. It is a colorless liquid that is soluble in many organic solvents. 3-Bromobenzaldehyde can be synthesized by the reaction of ethyl acetoacetate and anhydrous sodium in methanol, and can be purified by distillation or recrystallization from ethanol. This compound has been used as a solvent for analytical methods, such as GC-MS analysis, due to its high boiling point and low volatility. 3-Bromobenzaldehyde also reacts with hydrogen chloride to form benzoyl chloride, which can then be reacted with alcohols to produce esters. 3-Bromobenzaldehyde has been shown to react with chalcones to form optical active compounds, such as curcumin analogues. These reactions are typically carried out in solution using acetic acid or sulfuric acid as a catalyst.br&gt;br&gt;</p>

Versatile small molecule scaffold

<p>Laudanosine is a gamma-aminobutyric acid (GABA) analog that is metabolized by the liver to form laudanosine. Laudanosine has been shown to be a competitive antagonist of benzodiazepine binding sites, including those of atracurium, mivacurium chloride, and diazepam. Laudanosine has also been shown to inhibit cyclic nucleotide phosphodiesterases in vitro, with clinical relevance for its use as an anti-epileptic drug.</p>

8-Boc-3,8-diaza-bicyclo[3.2.1]octane is a functional group that can be used in the preparation of pharmaceutical preparations. It is insoluble in water and soluble in organic solvents. This compound has been shown to be effective in the treatment of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. 8-Boc-3,8-diaza-bicyclo[3.2.1]octane has also been shown to have protective effects against sae-cd induced cytotoxicity by upregulating the expression of antiapoptotic proteins Bcl2 and Bclxl, which are important for neuronal cell survival.

<p>(S)-1-Boc-3-methylpiperazine is a hydrophobic compound that is structurally modified from the tetracyclic family of drugs. It has been shown to inhibit tumor cell growth by binding to the oncogene, KRASG12C, and downregulating its expression. (S)-1-Boc-3-methylpiperazine also inhibits cancer cell growth through the inhibition of the PI3K/AKT signaling pathway. The pharmacological effects of (S)-1-Boc-3-methylpiperazine are dependent on its ability to bind with high affinity to KRASG12C and inhibit its activity.</p>

<p>1,3-Bis(diphenylphosphino)propane is a chelate ligand that forms complexes with a wide range of transition metal ions. It has been shown to be an effective catalyst for the conversion of aryl halides to acid derivatives. The compound has been found to have an excellent stability in aqueous solutions and does not hydrolyze readily in human serum or water. 1,3-Bis(diphenylphosphino)propane is also used as an additive in many industrial processes, such as the production of nylon and polyester fibers.</p>

5'-Bromo-2'-hydroxyacetophenone is a chemical that is used as a substrate in the preparation of other chemicals. The reaction solution contains 5'-bromo-2'-hydroxyacetophenone, nitrogen atoms, and a biological sample. This substrate reacts with trifluoroacetic acid to form an intramolecular hydrogen bond. The magnetic resonance spectrum of this product reveals the presence of two carbon atoms, three hydrogen atoms, and one oxygen atom. The resulting chemical structure is that of 2-Aminobenzamide.

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-1-fluoro-2-nitrobenzene is a boron trifluoride compound that reacts with sulfuric acid to form the target product, 4-bromo-2-fluorobenzenesulfonic acid. It is used in the production of dyes and pharmaceuticals. The reaction is conducted at a temperature of 60°C in a reaction time of 8 hours. The repeatability of this process was found to be high, with a relative standard deviation (RSD) of 2.5% and an RSD for peak area of 3%. Experiments have been conducted to optimize the reaction conditions and determine the optimum reaction time and target product yield. A sulfuric acid concentration of 1M has been found to produce the highest yield, while maintaining the lowest RSD values.</p>

Boc-Tyr(tBu)-OH is a chemical compound that is part of the class of lactams. It has been shown to have antitumor activity in vitro and in vivo, but it has not yet been tested for its cytotoxicity. This compound is synthesized by solid-phase synthesis and contains a disulfide bond, which may contribute to its cytotoxicity. Boc-Tyr(tBu)-OH has also been shown to have high affinity for the alpha 2A adrenergic receptor subtype and other receptors with an isosteric carbonyl group.

Benzophenone hydrazone is a benzophenone derivative that belongs to the group of pharmaceutical preparations. It is a hydrazone compound that contains one nitrogen atom and one phosphorus pentoxide group. The reaction mechanism of this molecule involves oxidation catalyzed by a radiation or light source. The diphenylmethanone, which acts as an electron donor, reacts with the benzophenone compound to produce the benzophenone hydrazone product. This reaction has been shown in solution and in solid form by reacting with potassium dichromate and hydrogen peroxide in the presence of hydrochloric acid.

<p>1-Bromo-4-iodobenzene is an aryl halide that can be synthesized by the cross coupling of ethyl formate and hydrochloric acid. This compound is useful in analytical applications, such as chromatographic methods, due to its high solubility in organic solvents. It is also used in synthetic procedures for the preparation of other aryl halides. 1-Bromo-4-iodobenzene has been used to synthesize calcium carbonate via the Suzuki coupling reaction with sodium salts, which are nucleophiles. The carbonyl group on this molecule reacts with the nucleophile, forming an alkyl group and a metal salt. Transfer reactions involving these salts can produce other products with different functional groups.</p>

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

<p>Versatile small molecule scaffold</p>

<p>Boc-His(Trt)-OH is a chemical compound that has been used in the laboratory to study uptake and binding of compounds. It is stable in complex with albumin, which has led to its use as a model system for studying hepatic steatosis. This chemical can be synthesized by solid-phase synthesis with trifluoroacetic acid and polypeptide synthesis. FT-IR spectroscopy has been used to characterize Boc-His(Trt)-OH, revealing its chemical diversity.</p>

Versatile small molecule scaffold

2-Ethynyl-3-methoxypyridine is a chiral, alkynyl compound that can be synthesized from the reaction of acetone and ethyne. This compound is axially chiral and has two rotational isomers, which are optically active. The synthesis of this compound was first reported in 1952 by cyclizing 2-ethynylpyridine with methoxyacetophenone in the presence of acetic acid. The photochemical reactions of this compound have been studied extensively and it has shown to be a useful substrate for pyridines.

<p>Versatile small molecule scaffold</p>

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

<p>Gly-Gly-OMe·HCl is a diagnostic agent that can be used to diagnose atherosclerotic lesions. It is conjugated to an organic molecule and then radiolabeled. The conjugate can be detected by cyclopentadienyl, which emits gamma rays when it decays. This conjugate has been shown to selectively accumulate in atherosclerotic lesions of the coronary arteries, where it accumulates with a higher concentration than in the surrounding tissue. This product also has gastroprotective effects on the stomach and liver and can reduce lipid levels in hyperlipidaemic patients.</p>

<p>Fmoc-b-Ala-Ala-Pro-OH is a reaction component that can be used in the synthesis of peptides and other compounds. It is a building block for the preparation of complex compounds, such as small molecules, polymers and natural products. Fmoc-b-Ala-Ala-Pro-OH has been shown to be useful in the synthesis of various types of reagents, including antibiotics and pharmaceuticals. This chemical has been reported as a useful scaffold for the preparation of high quality research chemicals. Fmoc-b-Ala-Ala-Pro is also an intermediate in the synthesis of speciality chemicals and fine chemicals.</p>

<p>2-Fluoropyridine-5-carboxaldehyde is a reactive chemical that can be used as an acceptor in organic synthesis. It has been shown to have antibacterial properties, and is also a synthon for the production of prosthetic groups. 2-Fluoropyridine-5-carboxaldehyde reacts with dopamine to form diphenyl ethers, which are used as labels for immunoassays. This chemical can be catalysed and has been shown to be resistant to catalysis. 2-Fluoropyridine-5-carboxaldehyde can also be used in the synthesis of cycloalkanes.</p>

<p>2-Fluoro-3-pyridineboronic acid is an amide that can be used as a catalyst for transfer reactions. It forms a complex with copper chloride and isohexane, which is then heated to produce the desired product. 2-Fluoro-3-pyridineboronic acid has been used in analytical methods such as constant pressure and methyl ethyl method. This compound also has high resistance to water vapor, hexane, and organic solvents. 2-Fluoro-3-pyridineboronic acid has been shown to inhibit the MCL-1 protein, which plays a role in regulating apoptosis. It can be used as a potential therapeutic agent against infectious diseases such as tuberculosis and HIV/AIDS due to its ability to inhibit MCL-1 protein expression.</p>

<p>Please enquire for more information about H-D-ASN-L-ASP-OH 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-Tyr(Et)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>1,9-Nonanediol is a chemical substance that has been synthesized with the use of a constant pressure process. It is an asymmetric synthesis with light exposure. The molecule has been characterized by chromatographic methods and has the molecular formula CH3(CH2)9O. 1,9-Nonanediol is a dodecanedioic acid and an aliphatic hydrocarbon. It exists in two forms: one hydroxyl group and one hydrogen bond, which are both involved in the dehydration process. This substance does not have any chloride or magnetic resonance spectroscopy properties because it does not contain any chlorine atoms or hydrogen atoms.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>(S)-(-)-1-Phenylpropylamine is a compound that can be synthesized by the asymmetric synthesis of 1-phenylethylamine. It is an amine that is used in the production of other compounds and has been shown to be reactive with a number of different compounds. The chemical profile of (S)-(-)-1-Phenylpropylamine consists mainly of aldehydes, amides, amines, and alkylating agents. This chiral molecule can be used for the production of drugs or as a precursor for other chemicals.</p>

Versatile small molecule scaffold

<p>Please enquire for more information about 5-Bromo-2-fluoro-1,3-dimethylbenzene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Fmoc-D-Ala-OH is a synthetic cyclic peptide that has been shown to have anticancer properties. This compound was synthesized by solid-phase chemistry and exhibits an inhibitory effect on cancer cells. Fmoc-D-Ala-OH blocks the synthesis of proteins in cancer cells, leading to cell death. It also inhibits the activity of serine proteases such as degarelix acetate, which are important for cancer cell growth and metastasis.</p>

<p>Versatile small molecule scaffold</p>

<p>7-Bromo-1-methylnaphthalene is a fluorescent dye that can be used to measure the concentration of DNA, RNA, and proteins. This compound is an intercalator, which means that it can bind to double stranded DNA or RNA near the center of the molecule where there is a space for binding. It has been used in the study of the thymic gland because it binds to DNA and RNA in cells from this organ. 7-Bromo-1-methylnaphthalene has also been used as a skeleton for organic compounds, such as dimethylammonium. The bromine atom in this compound can be replaced with other atoms like iodine or chlorine to make different colored dyes.</p>

<p>Versatile small molecule scaffold</p>

<p>Monomethyl glutarate is a monomer for the synthesis of polymers. It has been used in the past as a precursor for the production of polyacrylic acid and its copolymers. Monomethyl glutarate is synthesized by the reaction of hydrochloric acid, high salt, and an expression plasmid containing glutarate dehydrogenase. This compound is also used as a reagent in kinetic studies of fatty acids and glutaric acid. Monomethyl glutarate is an acidic compound with a pKa value of 3.5 at 25°C. It is rapidly hydrolyzed in water to form monomethyl glutarate acid, which has a pKa value of 2.4 at 25°C. Monomethyl glutarate can be ingested orally or applied topically due to its low energy requirements for hydrolysis in water.</p>

Versatile small molecule scaffold

N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide is an environmental and industrial chemical that is used as a formate, benzoate, and methyl benzoate intermediate. It reacts with nitric acid to form N-(4-aminophenyl)-N-methyl-2-(4-nitrophenoxy)acetamide (NPA). NPA has been shown to have antiangiogenic properties. NPA inhibits the proliferation of endothelial cells by interfering with the cell cycle and inducing apoptosis.

<p>2,4,6-Trichloropyrimidine is an antimicrobial agent that belongs to the chemical class of pyrimidine compounds. It inhibits bacterial growth by cross-linking with amino acids and nucleic acids in the cell wall, thereby inhibiting protein synthesis. 2,4,6-Trichloropyrimidine is also a cross-linking agent for polymers such as polyurethane and vinyl chloride. This compound has been shown to be effective against P. aeruginosa and other bacteria that are resistant to antibiotics. 2,4,6-Trichloropyrimidine reacts with water vapor or oxygen nucleophiles to form hydrogen chloride and amine groups. These reactions can be used for identification of this compound in the laboratory.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 1,1',1''-(1,3,5-Triazinane-1,3,5-triyl)tris(2-bromoethan-1-one) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,2-Dimethylbut-3-enoic acid is a bioactive compound that is used to synthesize other compounds. It has been shown to have a number of functions, such as being an electrolyte and having an electron deficient group in its structure. 2,2-Dimethylbut-3-enoic acid reacts with electrophilic functional groups at high temperatures to form allylation products. This reaction is called cheletropic and has been shown to be reversible.</p>

<p>3-Ethynylbenzenesulfonamide is a synthetic, hydrophobic, antimicrobial compound that disrupts the cell membrane. It has been shown to be effective against both mammalian and microbial cells. The antimicrobial use of this compound is still under study, but it may provide an alternative to the current antibiotics. 3-Ethynylbenzenesulfonamide is amphipathic in nature and has an extremely large expansion ratio. This molecule is also hydrophobic, which may help with its ability to penetrate the cell membrane. Antimicrobial compounds are designed to inhibit or kill microorganisms such as bacteria or fungi by disrupting their cellular membranes. They work by interacting with specific targets on the surface of the target organism and producing a lethal effect on its function. 3-Ethynylbenzenesulfonamide interacts with proteins found on bacterial membranes called porins, resulting in a loss of osmotic stability and then permeability through the bilayer. This leads</p>

Please enquire for more information about DL-Tropic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about Tert-butyl N-(8-bromooctyl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2,3,4-Tetrahydropyridin-4-one is an organic compound that can be synthesized by a cross-coupling reaction between a pyridine and chloroformate. The reaction mechanism involves nucleophilic addition of the amine to the electrophile followed by reductive elimination. This process leads to the formation of a tetrahydroquinoline skeleton with stereoselectivity. Tetrahydropyridin-4-one can also be synthesized from an iminium ion or an activated pyridinium salt. The resulting product will have a different skeleton because it was synthesized through different mechanisms.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(2R,3S)-Benzyl 6-oxo-2,3-diphenylmorpholine-4-carboxylate is a molecule with an enantioselective synthesis and a preparative method. It has been catalysed by chiral reagents such as chiral catalysts, chiral auxiliaries, and chiral ligands. This molecule can be synthesized in racemic form or in the form of its two enantiomers. The two enantiomers have different physical properties and biological activities. (2S,3S)-Benzyl 6-oxo-2,3-diphenylmorpholine-4-carboxylate is known to be an inhibitor of protein kinase C (PKC) that causes the release of intracellular calcium ions from cytoplasmic stores. The other enantiomer (2R,3S)-benzyl 6-oxo-2,3-d</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>1-Trityl-1H-imidazole-4-carbaldehyde is a phosphorane that has been synthesized in the laboratory. It is an organometallic compound with a chloroformate ligand and a mononuclear, dimethylformamide complex. 1-Trityl-1H-imidazole-4-carbaldehyde has shown to be an electrophile and binds to receptor sites with high affinity. This may be due to its ability to form hydrogen bonds with the receptor site, which often occurs for pharmacokinetic profiles.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

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

Versatile small molecule scaffold

<p>2-Bromo-4-iodoanisole is an electrophilic intermediate that can be synthetically prepared by regioselective halogenations of 4-iodoanisole. It is also a substrate for sequential halogenations with bromine or iodine. The 2-bromo-4-iodoanisole reacts with aluminum to form an aluminate, which can be used as a catalyst in organic synthesis. 2-Bromo-4-iodoanisole has been shown to react with aromatic rings by electrophilically attacking the ring and adding a second bromine atom to the ring, leading to quenching of the molecule and formation of structurally diverse products.</p>

<p>Metal-chelating agent</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>