Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Isobutyl-1H-benzimidazole is a potent and selective inhibitor of cell proliferation. It inhibits the growth of cancer cells by targeting the catalytic activity of topoisomerase II. The in vitro cytotoxic activity of 1-isobutyl-1H-benzimidazole has been investigated on human cancer cells and endometrial cancer cells. The IC50 values for cisplatin, a chemotherapeutic agent, and 1-isobutyl-1H-benzimidazole were found to be identical at 10 μM. Endometrial cancer cells were more sensitive to 1-isobutyl-1H-benzimidazole than human cancer cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>MLN-4760 is a new chemical entity with potent inhibitory effects against the angiotensin II type 1 receptor. It also has an inhibitory effect on the renin-angiotensin system, which is involved in regulating blood pressure and heart function. MLN-4760 binds to the angiotensin II type 1 receptor and blocks its interaction with angiotensin II, leading to reduced cardiac hypertrophy, heart failure, and death in animal models of cardiac hypertrophy. In addition, MLN-4760 has been shown to have antitumor properties in vitro and in vivo. This compound is a natural product that was isolated from Chinese herbs used for centuries for their therapeutic benefits.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 4-(Methoxycarbonyl)bicyclo[2.1.1]hexane-1-carboxylic acid 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>L-Abrine is a plant toxin that belongs to the group of abrinoids. It is a chiral molecule and can exist as an L-form or D-form. The L-form is used in some analytical methods, such as gas chromatography, while the D-form is used in medical purposes. L-Abrine has been shown to have anti-HIV effects by inhibiting reverse transcriptase and deoxyribonuclease activity. It has also been shown to inhibit colony stimulating factor production and decrease bacterial growth in vitro. L-Abrine inhibits the replication of bacteria by binding to adenylate cyclase and blocking the enzyme's ability to synthesize cAMP from ATP. This inhibition prevents protein synthesis, leading to cell death.</p>

<p>Magnesium acetate tetrahydrate is a white crystalline solid that is soluble in water and is used as a nutritional supplement. It is produced by the reaction of magnesium carbonate with an aqueous solution of acetic acid. The particle size varies depending on the synthesis method used. Magnesium acetate tetrahydrate has been shown to be effective for treating diabetes mellitus, as it helps regulate blood sugar levels by promoting insulin release from pancreatic cells and increasing glucose uptake into these cells. This compound also has been found to be effective in reducing hiv infection rates, which may be due to its ability to increase the activity of CD4+ T-cells.</p>

<p>Volatile compound with banana scent</p>

<p>Methanesulfonic anhydride is a white crystalline solid that is soluble in water and ethanol. It has been shown to be a potent inhibitor of acetaminophen metabolism and the formation of reactive metabolites. Methanesulfonic anhydride inhibits the metabolic activity of cytochrome P450 enzymes, which are responsible for the oxidation of acetaminophen. This inhibition leads to lower levels of toxic metabolites and less tissue damage. Methanesulfonic anhydride also modulates other assays, such as those for nitric oxide synthase and prostaglandin E2 receptors. Methanesulfonic anhydride is used as a catalyst in chemical reactions, including those that produce hydrogen sulfide gas for use in gold mining. It has also been used to study the localization of various proteins by using probes labeled with methanesulfonic anhydride. Methanesulfonic anhydride may cause hypertension due to its ability to inhibit the degradation of norepinephrine, leading to increased</p>

<p>2-Methyl-2-propanethiol is an electron acceptor and a reagent that can be used for the synthesis of organic compounds. It is soluble in polar solvents, but insoluble in nonpolar solvents. 2-Methyl-2-propanethiol has been shown to react with thiols at concentrations below its optimum concentration. The reaction mechanism is believed to involve adsorption and intramolecular hydrogen transfer. The adsorption process occurs on the surface of the substrate and the intramolecular hydrogen transfer occurs through an intermolecular hydrogen bond with the substrate's hydroxyl group or disulfide bond. When 2-methyl-2-propanethiol reacts with a thiol, it forms a mercaptan group called p2 that contains two substituents, one on each carbon atom. This reaction produces a disulfide bond as well as an electrochemical detector signal known as "activated."</p>

<p>4-Methoxybenzylamine is an organic amine that has a redox potential of -0.14 V (vs. SHE) and a pK a of 10.5. It is used in the synthesis of trifluoroacetic acid esters, which are used as pharmaceutical intermediates. 4-Methoxybenzylamine has been shown to be effective in alleviating pain in animal models, and its mechanism of action may be due to inhibition of the enzyme cyclooxygenase. The kinetic data for this reaction were obtained by studying the deuterium isotope effect, which is characterized by a low energy barrier and rapid reaction rate. The hydrolysis step is also important for the reaction mechanism, with protocatechuic acid being an intermediate product. Hydrochloric acid is needed for dehydration of the reactants, while an aryl halide can be used instead in some cases. In these reactions, there are many possible reaction</p>

<p>1-Methyl-4-piperidinol is a hydroxylated piperidine that has been shown to inhibit the growth of cancer cells in culture. It was also found to be cytotoxic against human leukemia cells and murine myeloma cells. 1-Methyl-4-piperidinol has been shown to bind to the receptors on cell membranes, which may be responsible for its anti-cancer effects. The structure of 1-methyl-4-piperidinol is similar to that of pyrrolidine and piperazine, which are known to have antihistamine properties. In addition, 1-methyl-4-piperidinol binds with magnesium salt and forms a complex that inhibits the activity of hydrogen bond formation by amines and fatty acids. This inhibition leads to an increase in pH levels inside the cell, which may lead to cancer cell death.</p>

<p>Maleic acid is dicarboxylic acid.  It is the cis isomer.  The trans isomer is fumaric acid</p>

<p>5-Methyl-L-norleucine is an amide that is a natriuretic and has been shown to have physiological activities. It has been shown to have restenosis and tumor treatment properties, as well as antimicrobial resistance. 5-Methyl-L-norleucine also acts as a cyclic peptide, which may be due to its disulfide bond. This compound is not only effective in treating microbial infections, but it also has anti-inflammatory properties. 5-Methyl-L-norleucine is found in the genus of plants called "Acorus," so it can be used for plant physiology research.</p>

<p>Putrescine is a metabolite that is produced by the breakdown of amino acids and proteins. It can be synthesized from ornithine, citrulline, and arginine. Putrescine is a precursor to polyamines such as spermidine and spermine, which are important for cell growth. Mouse studies have shown that putrescine is a conjugate base that may act as a neurotransmitter or neuromodulator in the central nervous system.</p>

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

<p>2-Methyl-1H-imidazole-5-carboxylic acid is a molecule that belongs to the class of antibiotics. It has been shown to be an effective inhibitor of lipases and other enzymes, which is due to its carboxylate group. The immobilization of this molecule has been studied by X-ray crystallography. The oxygen atoms in the molecule are covalently immobilized on a silica surface via a linker chain, which prevents the loss of these atoms. Dichroism spectroscopy was used to study the effects of different solvents on this molecule's ability to rotate light. 2-Methyl-1H-imidazole-5-carboxylic acid was also successfully immobilized using an enzyme called lipase, with residue carboxylate groups positioned at the bottom of the binding cavity.</p>

<p>Please enquire for more information about 3-(3-Methylcyclopentyl)propan-1-ol 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 Melarsomine dihydrochloride 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-MPPF dihydrochloride 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 MidazolamEPimpurityGmaleate 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 Mafosfamide sodium 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-2-undecyl-1,3-dioxolan-4-yl)methoxy]-1-propanesulfonate sodium including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 2-bromo-6-iodobenzoate (MIBI) is a synthetic compound that has been shown to have anti-proliferative effects in vitro and in vivo. MIBI inhibits the proliferation of cancer cells by arresting the cell cycle at G1 phase and inducing apoptosis. It also binds to DNA, which prevents transcription and replication. In addition, it inhibits the production of factor-1, which is a protein that promotes angiogenesis. MIBI has been found to be active against many different types of human cancer cells, including colon carcinoma cells, prostate carcinoma cells, pancreatic adenocarcinoma cells, leukemia cells, lung cancer cells, breast cancer cells, and ovarian cancer cells. These anticancer activities are due to its ability to inhibit cell growth and induce apoptosis.</p>

<p>Please enquire for more information about tert-butyl (2S)-2-Methyl-4-oxopiperidine-1-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 6-(Methoxycarbonyl)spiro[3.3]heptane-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Morpholinopropylamine is a nitrogen-containing heterocyclic organic amine. It has been shown to bind to receptor cells and inhibit the uptake of chloride ions by liver cells, which may be due to its ability to form hydrogen bonds with chloride ions. The binding constants for this drug have also been determined using X-ray crystallography and nuclear magnetic resonance spectroscopy. 3-Morpholinopropylamine has been shown to have anticancer properties and is able to bind with DNA in a manner that inhibits DNA synthesis. This drug also inhibits the production of hydrochloric acid in the stomach, which may be due to its ability to interact electrochemically with amines.</p>

<p>Please enquire for more information about 1-(4-Methoxybenzyl)piperidine-2,4-dione 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 Methyl 6-bromoquinoline-2-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 Methyl 2-chloropyrimidine-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 [(5-Methyl-4-phenyl-4H-1,2,4-triazol-3-yl)thio]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate is a pyrethroid insecticide. It is formulated as an emulsifiable concentrate and applied to the soil surface or injected into the root zone of plants. This insecticide is also used in combination with other pesticides to provide broad spectrum control of insect pests. Methyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate is chemically synthesized from 2,3-dihydro-1,3-benzodioxole and chloroacetic acid. The mechanism of action for this pesticide is not well understood but may be due to its ability to inhibit hydrolase enzymes. This product also has a low toxicity on mammals and birds that are exposed orally or through inhalation at high concentrations.</p>

<p>Methyl 4-chloro-4-oxobutanoate is a chemical compound that is used as a medicine. It has been shown to have an affinity for the human immunodeficiency virus (HIV) and can be used to treat HIV infection. Methyl 4-chloro-4-oxobutanoate is also used in other types of medicines, such as those for treating high blood pressure and heart disease. This chemical binds to the receptors on cells that are responsible for regulating blood pressure and heart rate, which leads to inhibition of cyclic guanosine monophosphate (cGMP) production. Methyl 4-chloro-4-oxobutanoate inhibits the activity of lipolytic enzymes, which break down fats into smaller units, by binding at the active site of these enzymes. It also binds to chloride ions and prevents them from being released from cells, which causes a rise in intracellular chloride levels. This increase in chloride</p>

<p>1-Methylimidazole is a compound with the molecular formula CH3N2H. It is soluble in water, but insoluble in organic solvents. 1-Methylimidazole has been found to bind to human serum and p-nitrophenyl phosphate. The fluorescence of 1-methylimidazole is quenched by hydrogen bonding interactions, which are the same as those that occur in natural compounds such as hemoglobin and chlorophyll. The nitrogen atoms on the surface of 1-methylimidazole can be detected using infrared spectroscopy. This method can also be used to analyze group P2 molecules, such as benzene, phenol, and cyclohexane.</p>

<p>Mesityl oxide is a nitro compound that is used as an intermediate for the synthesis of other compounds. It is prepared by the reaction of acetone and malonic acid in the presence of phosphorus pentoxide. The optimum concentration for this reaction is 1.5 M in acetone and 0.1 M in malonic acid. The product is purified by solid phase extraction using a microextraction device and then recrystallized from acetone-methanol to obtain pure mesityl oxide. Mesityl oxide has been shown to inhibit prostate cancer cells, which may be due to its ability to react with hydroxyl groups on proteins to form methoxy radicals, which break down DNA molecules.</p>

<p>Fmoc-O-trityl-L-serine is a synthetic molecule that is not naturally occurring. It has been shown to have inhibitory effects on the growth of cancer cells in vitro and in vivo, but does not affect healthy cells. Fmoc-O-trityl-L-serine binds to the membrane of cancer cells and inhibits protein synthesis by binding to ribosomes. This drug also inhibits cell growth by interfering with the membrane interactions necessary for cellular metabolism. Fmoc-O-trityl-L-serine is toxic to red blood cells, which may be due to its ability to induce hemolysis.</p>

<p>4-Fluoroaniline is an antimicrobial agent that inhibits microbial metabolism by binding to enzymes and blocking their activity. The enzyme activities are affected by the hydrogen bonding interactions between the 4-fluoroaniline molecule and other molecules in the enzyme active site. 4-Fluoroaniline can be used for wastewater treatment, as it has been shown to inhibit bacterial growth and help remove nitrogen from wastewater. Hydrogen fluoride (HF) is generated when 4-fluoroaniline is exposed to water, which may be toxic to aquatic life. The reaction mechanism of 4-fluoroaniline with a tetrazolium dye is dependent on the presence of nitrogens. Nitrogen atoms in the 4-fluoroaniline react with diazonium salt to form a diazonium intermediate, which reacts with a tetrazolium dye to produce a red compound that can be detected at low concentrations. A model system of 4-fluoro</p>

<p>6-Fluoro-3-(4-piperidinyl)-1,2-benzisoxazole is a drug candidate that belongs to a new class of atypical antipsychotics. It has been synthesized using an efficient method and was found to bind to the m1 receptor with high affinity. 6-Fluoro-3-(4-piperidinyl)-1,2-benzisoxazole has shown efficacy in vitro studies against 5HT1a receptors and in vivo studies against fibroblast cells. This drug is also effective against serotonin levels, which may be due to its ability to inhibit the reuptake of serotonin by blocking the serotonin transporter.</p>

<p>Please enquire for more information about Fluocinolone acetonide-21-carboxylic 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 Fmoc-Arg(Pbf)-OH (U-13C6, U-15N4) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%.</p>

<p>Versatile small molecule scaffold</p>

<p>This chemical is an inhibitor of protein interactions. It has been used as a research tool and as a pharmacological agent. This product is a ligand that binds to receptors or ion channels, which are proteins found in the cell membrane or cell wall. When these proteins interact with ligands, they can initiate a response inside the cell, such as opening or closing ion channels or initiating other cellular processes. The efficacy of this product depends on its concentration and binding affinity for the receptor or ion channel. This product has been shown to inhibit the activity of both potassium and calcium channels at high concentrations.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(4-Bromophenyl)methyl 2-hydroxybenzoate is a natural product of plant origin. It is an analytical standard for HPLC, and is used as a reference material in the analysis of secondary metabolites and natural products. (4-Bromophenyl)methyl 2-hydroxybenzoate has been isolated from "Paeonia suffruticosa".</p>

<p>2-Bromo-5-ethynylthiophene is a terminal alkyne that can be used as a ligand, an additive, or as an intermediate in organic synthesis. 2-Bromo-5-ethynylthiophene can be obtained by heating ethynylacetylene with bromine and sulfuric acid. It is insoluble in water and other solvents, and has two different conformations. The two isomers are distinguished by their reaction time to form the diacetate monomer. The diacetate monomer reacts more quickly than the monoacetate monomer because it has a higher energy barrier. 2-Bromo-5-ethynylthiophene can also be used in devices such as OLEDs and solar cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloropyrazin-2(1H)-one is an organic compound with the molecular formula C6H5ClO. It is a colorless liquid that spontaneously polymerizes. 3-Chloropyrazin-2(1H)-one has been shown to have a number of functions, including reactions with cyclohexanone and acetone to produce ethyl formate, as well as reactions with acetonitrile and ethyl formate to produce 2-ethoxyethyl acetate. Phase equilibrium data for 3-chloropyrazin-2(1H)-one are given in terms of the liquid and vapor phases at various pressures and temperatures. The solvents used in crystallographic studies of 3-chloropyrazin-2(1H)-one include tetrahydrofuran (THF) and dimethyl sulfoxide (DMSO). Experimental data for 3-chloropyrazin-2(1H)-one is</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid is a compound that has been shown to inhibit the polymerization of polymers. This chemical can be used as a sealant due to its ability to form a protective film on surfaces. It is also an effective polymerization inhibitor for polymers such as polyvinyl chloride and polystyrene, which are both used in the production of solar cells. 5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid can also be used to enhance the performance of solar cells by preventing water vapor from degrading the polymers that they are made of. The optimal wavelength range for this chemical is between 200 and 400 nm.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>