Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(Chloromethyl)cyclohexane is a synthase gene that is responsible for synthesizing the enzyme chloromethyl cyclohexane, which is used as a solid catalyst. The synthesis of (chloromethyl)cyclohexane from phenyl groups and liquid crystal composition has been demonstrated using expression plasmids and active oxygen. The compound inhibits inflammatory diseases by preventing the production of arachidonic acid, which is an inflammatory agent. This compound also inhibits the production of prostaglandins, which are involved in the release of histamine from mast cells. Pharmaceutical preparations that contain this compound are primarily used to treat rheumatoid arthritis and other inflammatory diseases.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Bromo-2-methoxyquinoline is a versatile compound with various applications. It is commonly used as a disinfectant in ceramic compositions and research chemicals. Additionally, it has been found to have potential therapeutic benefits. Studies have shown that 6-Bromo-2-methoxyquinoline exhibits antioxidant properties and can inhibit the production of inflammatory mediators such as arachidonic acid and prostaglandins. Furthermore, it has been found to modulate potassium channels, which play a crucial role in cellular function. This compound also shows promise in the development of copolymers and other materials due to its unique chemical structure. With its wide range of applications, 6-Bromo-2-methoxyquinoline is an essential compound for various industries.</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>Cabozantinib is a small molecule that is the first to target VEGFR-2, which is a receptor tyrosine kinase involved in the development of fibrosis. Cabozantinib inhibits the activity of VEGFR-2 by binding to its ATP-binding site and blocking the phosphorylation of downstream signaling pathways. Cabozantinib has been shown to have antifibrotic properties in both preclinical and clinical models. The drug candidate has been shown to reduce kidney fibrosis in animal models. The standard dose for cabozantinib was found to be 5 mg/kg, with a maximum tolerated dose of 20 mg/kg. In vitro studies have indicated that cabozantinib binds with high affinity to the ATP-binding pocket of VEGFR-2, exhibiting competitive inhibition against other kinases such as PDGFR-beta and cKit, as well as diaryliodonium (a specific inhibitor). Caboz</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-2,5-dimethylpyridine is an organic compound that belongs to the group of amino compounds. It is a potential intermediate in the synthesis of other compounds. 4-Bromo-2,5-dimethylpyridine can react with potassium to form 4-bromopyridine and 3-bromo-4-methylpyridine. It may also be used as a reactant in aminations and as an intermediate in the preparation of n-oxides.</p>

<p>Versatile small molecule scaffold</p>

<p>2,4,5,6-Tetra(9H-carbazol-9-yl)isophthalonitrile is a redox molecule that emits light when excited by an electron or photon. It is used in organic light emitting devices (OLEDs) as the emissive material. This compound has been shown to have low chemical stability and limited transport properties. Its efficiency can be improved by increasing the concentration of the molecule. Activated 2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile emits a bright red orange emission with a maximum at 569 nm and it is activated by electron transfer from an electrode. 2,4,5,6-Tetra(9H-carbazol-9-yl)isophthalonitrile has been shown to emit blue light when excited by UV light in the presence of oxygen as an oxidant.</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>(2S)-3-Hydroxy-2-phenylpropanoic acid is an unlabelled, naturally occurring compound. It is the citric acid analog of L-phenylalanine. The structure of (2S)-3-Hydroxy-2-phenylpropanoic acid is a skeleton that consists of one hydroxyl group and one carboxylic acid group. The carboxylic acid group has a double bond in the alpha position to the carboxyl carbon, which gives this molecule an acidic character. The chloride ion is also present in this structure. This molecule can be synthesized by a kinetic reaction that involves fatty acids and brugmansia as catalysts. It can also be synthesized through a catalysed reaction using thionyl chloride as a catalyst.</p>

<p>2-Hydroxy-3-(1-methylethyl)-butanedioic acid is an organic compound that is a metabolite of the amino acid methionine. It is formed by the oxidation of the methyl group on the 2 position in methionine. The protein subunits are expressed in liver cells and it has been shown to have antioxidant properties. The analytical methods used for this compound include LC-MS/MS, which separates it into its individual isomers. This method can be used to determine the purity of 2-hydroxy-3-(1-methylethyl)-butanedioic acid. The carbonyl group in this molecule makes it susceptible to steric interactions with other molecules, which may lead to it being oxidized or reduced. It has been found that 2-hydroxy-3-(1-methylethyl)-butanedioic acid shows thermophilic and enterocolitic properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chlorobenzenethiol is a chemical compound that contains a fatty acid. It is an intramolecular hydrogen donor with the ability to form a disulfide bond. The compound also has high stability and can be used in organic synthesis reactions involving reactive sulfur groups. 4-Chlorobenzenethiol reacts with sodium carbonate to produce sodium thiocarbonate and chloroform, which are then reacted with phosphorus pentoxide for oxidation. The reaction mechanism is similar to that of the Diels-Alder reaction and the model system involves dinucleotide phosphate. 4-Chlorobenzenethiol can be reacted with hydrochloric acid or trifluoroacetic acid as an oxidizing agent.</p>

<p>3,4,5-Trimethoxybenzoyl Chloride is a reactive, active chemical that is used in the synthesis of cytotoxic amides. It is prepared by reacting 3,4,5-trimethoxybenzoic acid with an amine or ammonia in the presence of a base. The reaction yields an amide substituted at the 3- and 4-positions with trimethoxyphenyl groups.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 3-(cis-4-(2-(4-(2,3-Dichlorophenyl)piperazin-1-yl)ethyl)cyclohexyl)-1,1-dimethylurea including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,1'-Carbonimidoylbis-1H-imidazole is a ligand that binds to amines and isosteres. It can be activated with electrophilic reagents to form an activated linker. This ligand has been shown to inhibit the growth of xenograft tumor cells in mice by binding to functional groups on the cell surface. This drug also has been shown to bind to the receptor for advanced glycation end products (RAGE) and inhibit its function. 1,1'-Carbonimidoylbis-1H-imidazole has also been evaluated as a cancer therapeutic agent in animal models.</p>

<p>2-Chloro-3-(hydroxymethyl)pyridine is an organic compound that is used as a building block for the synthesis of other heterocycles. This compound can be synthesized from 2-chloronicotinic acid, which is obtained by oxidation of nicotine with sodium hypochlorite in the presence of potassium ion. The reaction proceeds via a cleavage of the C-Cl bond and formation of a pyridine ring. The catalytic process can be performed at room temperature and at atmospheric pressure in a variety of solvents, including water.<br>2-Chloro-3-(hydroxymethyl)pyridine has been shown to have high yields for the preparation of compounds such as 2,4-dichloropyridine and 4,5-dichloropyrimidine. It also has been used in the preparation of pharmaceuticals such as atrial natriuretic factor (ANF).</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>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 4,5-Dihydro-2-methyl-4-thiazolecarboxylic acid trifluoroacetate 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 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>Versatile small molecule scaffold</p>

<p>Methyl 2-chloro-5-iodonicotinate is a basic and yields a radioligand for use in imaging studies. It is used as a specific activity and solid-phase extraction. Methyl 2-chloro-5-iodonicotinate has been shown to be effective for radiolabeling studies of the brain following intravenous administration.</p>

<p>2,6-Dimethoxyisonicotinic acid is a cytotoxic agent that is structurally related to colchicine and combretastatin A-4. It has been shown to induce apoptosis in cancer cells by inhibiting the polymerization of tubulin. This drug also inhibits the proliferation of cancer cells by binding to DNA and disrupting the synthesis of proteins necessary for cell division. The inhibitory effect on protein synthesis may be due to its ability to inhibit the activity of RNA polymerase II and III, which are essential for transcription. 2,6-Dimethoxyisonicotinic acid also induces an anticancer effect through its ability to bind to phenolic moieties and inhibit the growth of cancer cells.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Cyano-2-methylphenylboronic acid is a high quality compound that can be used as a reagent, intermediate, or building block in the synthesis of complex compounds. This chemical is also useful as a speciality chemical and research chemical. 3-Cyano-2-methylphenylboronic acid has versatile uses in organic synthesis due to its versatility in reactions and building blocks.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 6,​7-​Dichloro-​1-​cyclopropyl-​1,​4-​dihydro-​4-​oxo-3-​quinolinecarboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Diethyl Acetylphosphonate is a synthetic chemical that is used in the production of ethyl esters, which are used as intermediates for the production of epoxides. It has shown to be a bidentate ligand and reacts with primary amines. Diethyl Acetylphosphonate can be made by reacting phosphorus pentachloride with ethyl acetate and hydrochloric acid. The reaction mechanism is similar to that of other organophosphorus compounds, in which a phosphine oxide intermediate reacts with an organic halide. Diethyl Acetylphosphonate has shown to be effective in detergent compositions and triethyl orthoformate, as well as alkanoic acid.</p>

<p>Thiodiglycolic anhydride is a synthetic reagent that is used in the synthesis of erdosteine. It also has been used in the synthesis of other products, such as magnetic particles for imaging and therapeutic uses. Thiodiglycolic anhydride can be used to synthesize erdosteine, which is a substrate for the enzyme hydroxylase and contains a hydroxy group in its structure. The hydroxyl group on erdosteine reacts with thiodiglycolic anhydride to form acrylonitrile, which then reacts with benzyl groups to form benzylthio-esters. These benzylthio-esters are then converted into acid transporters.</p>

<p>Please enquire for more information about 4,5-Dihydro-1H-imidazol-2-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 Edoxaban impurity 2 p-toluenesulfonic 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 4-Desmethyl-2-methyl celecoxib including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2S,6S)-2,6-Dimethylmorpholine is an optically pure compound that can be used to optimize the epoxidase reaction. It belongs to the class of morpholines and has two enantiomers. The (2R,6R)-enantiomer is more active than the (2S,6S)-enantiomer in catalyzing the epoxidase reaction. The temperature optima for both enantiomers are different with the (2R,6R)-enantiomer having a higher optimal temperature than the (2S,6S) enantiomer. This compound can be used as a chiral auxiliary to separate racemic mixtures by focusing on one enantiomer at a time. It can also be used as an analytical method for determining plate number and plate height.</p>

<p>Please enquire for more information about Edoxaban impurity G benzenesulfonate 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 Domperidone N-oxide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Iodo-1-methyl-1H-pyrazole-5-carbonitrile is a tetrazole molecule that has been shown to have potent and selective inhibitory activity against human PCSK9. This compound binds to the catalytic site of PCSK9 and prevents the formation of an active enzyme, therefore inhibiting the production of LDL cholesterol. 4-Iodo-1-methyl-1H-pyrazole-5-carbonitrile is a prodrug that is metabolized by acetaldehyde dehydrogenase to form an active inhibitor. The reaction proceeds in a chiral and enantioselective manner, which allows for the synthesis of racemic mixtures of this drug.</p>

<p>Please enquire for more information about Ethyl 2-(3-phthalimidopropyl)acetoacetate 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 Depropyl rotigotine 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 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-3-oxo-5-isobenzofurancarbonitrile 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>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>

<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>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-4-hydroxypyridine (2AH) is a synthetic, isomeric compound that has been synthesized in two different forms: 3-bromo-5-hydroxypyridine and hydroxy group. 2AH has been shown to be chemically stable at room temperature and pH levels of less than 7. It also withstands the loss of membrane fluidity induced by amides, such as 3-amino-2-bromopyridine. 2AH can be used to synthesize oxindole derivatives, which are found in natural gas, and piperidines. This chemical can also be used for aminations with pyrrole or 2 amino 4 hydroxypyridine.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-[[(3aS,4R,6S,6aa)-4-[7-[[(1R,2S)-2-(3,4-Difluorophenyl)cyclopropyl]amino]-5-(propylthio)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]- 2,2-dimethyl-tetrahydro-3aH-cyclopenta[d][1,3]dioxol-6-yl]oxy]ethanol-d7 is a compound with brominated sparfloxacin. It has various applications in the field of biochemistry and research chemicals. This compound has been found to have interactions with adipocytes and adipose tissues. Additionally, it has shown potential effects on glycan metabolism and potassium ion channels. Furthermore, this compound has been studied for its potential as an herbicide and its interaction with other substances such as</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Doxazosin is a research chemical that has shown potential in various fields. It is a water-soluble compound that has been studied for its effects on microcystins, cytidine, and vitamins. Doxazosin has also been found to have aldehyde and particulate properties, making it a versatile compound for different applications. In the field of medicine, Doxazosin has been researched for its potential in treating certain conditions. Studies have shown that Doxazosin can interact with 1-hydroxy-2-naphthoic acid and glutamate, which are important molecules involved in various biological processes. Additionally, Doxazosin has shown promising results in inhibiting the growth of e. cloacae bacteria, making it a potential candidate for antibacterial treatments. Furthermore, Doxazosin has been studied in the field of chemistry due to its unique properties. It can undergo derivatization reactions with fatty acids and z</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-Amino-3-methylisothiazole HCl is a pyridine-5-carboxylic acid that inhibits bacterial growth by binding to the 50S ribosomal subunit. It has been shown to inhibit the growth of both aeruginosa and nalidixic acid resistant strains of S. aureus, P. aeruginosa, and P. mirabilis in vitro. 5-Amino-3-methylisothiazole HCl has also been shown to be active against E. coli, quinolone resistant strains of Proteus mirabilis, and methicillin resistant strains of Staphylococcus aureus in vitro.</p>

<p>(1H-Indazol-4-yl)acetic acid is a cation that has been shown to have pharmacological activity. It is hydrolyzable and is used as an anti-inflammatory agent. This compound also decarboxylates and hydrolyzes, which are processes that produce carboxyl and fluoro groups. (1H-Indazol-4-yl)acetic acid has been shown to be an anti-inflammatory agent, with effects against inflammation in the central nervous system. This drug also inhibits the production of inflammatory cytokines, including tumor necrosis factor alpha (TNFα), interleukin 1β (IL1β), and IL6.</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>Chromane-2-carboxylic acid is an amide with a hydroxy group that has inhibitory effects on alkoxyphenols. It has been shown to have the ability to inhibit the growth of cancer cells in mammalian tissue and has been used in synthesizing nitro compounds. Chromane-2-carboxylic acid also inhibits matrix metalloproteinases, which are enzymes that break down proteins in the extracellular matrix and are associated with tumor invasion and metastasis. This compound also has radical scavenging activities, which may be due to its ability to form hydrogen bonds or intramolecular hydrogen bonds with aromatic hydrocarbons or fatty acids.</p>

<p>3-Aminopyrrolidin-2-one hcl is an antibiotic that is used to treat tuberculosis. It inhibits the enzyme transacylase, which catalyses the conversion of L-lysine into L-pipecolic acid in bacteria. This antibiotic has been shown to be effective against Mycobacterium tuberculosis and Mycobacterium avium complex. 3-Aminopyrrolidin-2-one hcl has a broad spectrum of activity against gram positive and gram negative bacteria, but it is not active against acid-fast bacteria.</p>

<p>Versatile small molecule scaffold</p>