Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>2,5-Diethoxyterephthalohydrazide is an organic compound that has been used for the synthesis of linkers with various functional groups. It is a reactive intermediate in the synthesis of amines and compounds containing amine functional groups. 2,5-Diethoxyterephthalohydrazide has been shown to be stable under environmental conditions and can be used as a linker in organic solvents such as amines, alcohols or esters. This compound has also been shown to exhibit photocatalytic activity when irradiated by UV light. Techniques such as analytical chemistry and techniques can be used to characterize this compound's reactivity and stability.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

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

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>3,5-Bis(trifluoromethyl)-1H-pyrazole-4-carboxylic acid is a chiral compound that has been shown to be an active building block for coordination frameworks. It is prepared from the reaction of 3,5-bis(trifluoromethyl)-1H-pyrazole with a carboxylic acid and can be used in the synthesis of metalloporphyrins. 3,5-Bis(trifluoromethyl)-1H-pyrazole-4-carboxylic acid has been shown to form stable coordination complexes with ligands such as bidentate or tridentate phosphoramidites and dimethylammonium chloride. This compound undergoes thermal treatment during the preparation process and reacts with various solvents and reagents.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Ethyl cyclopropaneacetate is an organic compound that belongs to the class of aminophenyl ethyl esters. It has been shown to inhibit neutrophil migration and angiotensin II-induced vasoconstriction in cerebral arteries, suggesting that it may have a role in the treatment of chronic bronchitis. Ethyl cyclopropaneacetate has also been shown to have antimycotic activity against Candida albicans and Aspergillus niger, as well as cancer-fighting effects. This compound is synthesized by reacting triethyl orthoformate with adenosine under mild conditions. The reaction system is high yielding and can be used for the synthesis of other drugs.</p>

<p>5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole is an activator that is used in palladium catalyzed reactions to form a phosphine ligand. 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole is also used as a vasotropic agent and reagent for organic synthesis. It is used to synthesize ethylesters and salts of 5-(5'-bromo)-2,2'-dihydroquinoline carboxylic acid. This compound can be hydrolyzed with alkaline solution to produce the corresponding amine.</p>

Methyl 3,3-bis(methylthio)-2-cyanoacrylate is a diphenyl ether that is used as a bactericide. It has been shown to be effective against both Gram-positive and Gram-negative bacteria. Methyl 3,3-bis(methylthio)-2-cyanoacrylate is synthesized by the reaction of malonate with dimethylamine chloride in the presence of hydrochloric acid salt in order to produce chloride ions. The reaction is then heated, which causes the methyl 3,3-bis(methylthio)-2-cyanoacrylate to form. This compound is soluble in organic solvents such as formic acid and can be purified by recrystallization or by distillation.

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</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>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>CASIN is a lysine-derived antimicrobial agent that inhibits the growth of bacteria by binding to the peptide chains of collagen, which are found in skin and mucous membranes. CASIN has been shown to inhibit the growth of many bacterial species, including those that are resistant to other antibiotics. CASIN can be used for the treatment of infectious diseases caused by bacteria, such as bacterial vaginosis or chlamydia. CASIN has also been shown to reduce body mass index in animal models. The mechanism of action is not known but may involve interference with an enzyme that controls the biosynthesis of fatty acids. The use of CASIN in humans is limited due to its toxicity on human cells and potential safety concerns.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Tadalafil is a synthetic drug that is used as a treatment for erectile dysfunction. It works by inhibiting the PDE5 enzyme, which is responsible for breaking down cGMP. Tadalafil has been shown to be effective in the treatment of male erectile dysfunction and pulmonary hypertension, with few side effects. This drug is taken orally, with a meal or without one, and can be administered with or without food. To improve absorption, tadalafil should be taken at least 30 minutes before sexual activity. The dosage of tadalafil ranges from 2.5 to 20 mg, and it should not exceed 40 mg per day.</p>

1,3,5,7-Tetrabromoadamantane is a molecule that has been synthesized and introduced as a mediator to introduce oxidants. The introduction of the oxidant is mediated by 1,3,5,7-tetrabromoadamantane. This molecule has been shown to be synthesized in two steps from hexamethylenetetramine (HMT) and iodomethane. The synthesis of this molecule can also be achieved by reacting synthons such as tetraphenylmethane with hydrochloric acid. 1,3,5,7-Tetrabromoadamantane is an equivalence mediator because it can mediate a redox reaction in which the oxidizing agent is reduced and the reducing agent is oxidized.

<p>2-Amino-5-cyano-3-methylbenzoic acid is a diester of methylamine. It is an acid ester that has been used in the synthesis of other compounds. 2-Amino-5-cyano-3-methylbenzoic acid is an intermediate in the synthesis of some pharmaceuticals, such as carbamazepine and methylphenidate. This compound has not been shown to have any biological activity.</p>

2-(7-Amino-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid is a monoclonal antibody that recognizes basic proteins. It is used to study the receptor binding of these proteins and their role in inflammatory diseases. 2-(7-Amino-4-methyl-2-oxo-2H-chromen-3,6-)acetic acid is an amino function that enhances the localization of cholinergic receptors at the apical membrane of epithelial cells. It also inhibits the efflux pump activity of bacteria, which may be useful for treating bacterial infections.

<p>3,3-Diethoxypropan-1-amine is a synthetic drug that reversibly inhibits the growth of bacteria. It has been shown to be effective against methicillin resistant strains of Staphylococcus aureus and Clostridium perfringens, with no detectable activity against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. 3,3-Diethoxypropan-1-amine is a heterobifunctional compound that binds to epidermal growth factor with high affinity. 3,3-Diethoxypropan-1-amine can also bind to collagen and liposomal formulations, which may be useful for the treatment of wounds. This drug has been shown to inhibit δ opioid receptors in mice and rats, which is thought to contribute to its analgesic effects.</p>

<p>L-Tyrosine ethyl ester hydrochloride is a non-protein amino acid that inhibits the activity of metalloproteases, which are enzymes that break down proteins. It has been shown to be effective against bowel disease and cancer by inhibiting the release of inflammatory cytokines. L-Tyrosine ethyl ester hydrochloride also has anti-inflammatory properties and can be used in the treatment of depression and liver cirrhosis. This drug is an inhibitor of hydroxylase, which is an enzyme involved in the synthesis of melanin. It is a structural analogue to L-DOPA, which is used for Parkinson's disease. L-Tyrosine ethyl ester hydrochloride has been shown to have antihypertensive effects and can be used as a diuretic agent.</p>

Z-Tyr-OBzl is a reactive solvent that is used in the synthesis of polypeptides and peptides. It has been shown to react with amino acids and acetonitrile, forming a trifluoroacetyl group. This group can be easily removed by hydrolysis or reductive amination. The solvents used in this reaction are non-polar and do not dissolve water, which makes this process an excellent choice for synthesizing materials that are insoluble in water. Z-Tyr-OBzl is also able to form oxone, which is a powerful oxidant that can be used for the oxidation of aromatic rings.

<p>Metal-chelating agent</p>

<p>Versatile small molecule scaffold</p>

Please enquire for more information about N-​Nitroso hydrochlorothiazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

(S)-1-N-Boc-2-methylpiperazine is a quinolone synthon that has been shown to have antibacterial activity against bacteria. The synthesis of this compound is done through the condensation of piperazine with an N-Boc protected 2,6-dichloroquinoline. This reaction proceeds in good yield and enantioselectivity. The antibacterial properties of (S)-1-N-Boc-2-methylpiperazine are not yet known.

Methyl 3-bromobenzoate is a cross-coupled compound with three functional groups: a methyl group, an acid bromo group, and a carboxylic acid benzoic ester. It is used in the synthesis of antigens that are chemically reactive to trifluoroacetic acid gas. The clinical studies have shown that the efficiency of this study is low because it has been found to be difficult to synthesize methyl 3-bromobenzoate in large quantities. This molecule can be prepared by the reaction of vinylene with an electrophile in non-polar solvents or by catalytic mechanisms.

Please enquire for more information about 3-Methyl-2-(methylthio)benzo[d]thiazol-3-ium iodide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about Methyl 2-Bromo-5-iodobenzoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>5-Hydroxypyrazine-2-carboxylic acid is a drug that inhibits the activation of proteins involved in cell signaling pathways. It has been shown to have an inhibitory effect on the activation of protein kinase C, which plays a key role in the proliferation and differentiation of cells. 5-Hydroxypyrazine-2-carboxylic acid also inhibits sorafenib, a drug used for the treatment of cancer. Sorafenib is metabolized in rats by cytochrome P450 (CYP) enzymes, which are found in human liver tissue as well. The metabolism rate of sorafenib can be reduced by coadministration with caffeine or other substances that induce CYP activity. 5-Hydroxypyrazine-2-carboxylic acid is not active against pyrazinoic acid and pyrazine-2 carboxylate, which are metabolites produced by CYP enzymes.</p>

Fmoc-Dap(Ac)-OH is a fine chemical that is used as a building block in the synthesis of complex compounds. It reacts with various nucleophiles to form an amide bond, and has been shown to be useful for both research and industrial applications. Fmoc-Dap(Ac)-OH can also be used as a reagent to synthesize peptides, which are biologically active compounds that form the basis of many drugs. This versatile intermediate is also used as a scaffold in the construction of more complex molecules. Fmoc-Dap(Ac)-OH has CAS No. 181952-29-4 and is classified as a speciality chemical by the International Union of Pure and Applied Chemistry (IUPAC).

<p>Fmoc-L-aspartic acid beta-allyl ester is a specific interaction between an amide and an enzyme target. It has been shown to have anti-inflammatory properties by inhibiting the activity of COX-2, which inhibits the production of prostaglandins. Fmoc-L-aspartic acid beta-allyl ester is a cyclic peptide with a lactam ring system that has been synthesized in a stepwise manner on a solid phase. This molecule interacts with cell line A549 and blocks the proliferation of cancer cells. Fmoc-L-aspartic acid beta-allyl ester also contains a disulfide bond that stabilizes its structure.</p>

Fmoc-N-methylglycine is a modified form of the amino acid glycine, which has been modified to include a reactive group that can be used to link other molecules. This molecule has gram-negative bacterial activity and exhibits potent antibacterial activity against many gram-positive bacteria. Fmoc-N-methylglycine is also an antimicrobial peptide with binding constants in the nanomolar range. It is also an agent that binds to serotonin, which may explain its effects on mood and sleep. Fmoc-N-methylglycine can be synthesized using stepwise solid phase synthesis methods or by conjugation with other molecules.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>3,4-Difluoro-1H-Pyrrole is a neutral compound with a molecular weight of 136.17 g/mol. It has the chemical formula C6H3F2N and it can be found in reactions involving the congener and coordination chemistry. 3,4-Difluoro-1H-Pyrrole is an intermediate in organic synthesis that is used as starting material for other organic compounds such as pharmaceuticals and agrochemicals. The redox potential of 3,4-Difluoro-1H-Pyrrole is -0.42 V for the reaction with chloride solution and its basicity is 0.89 mM at 25°C. This molecule has been studied by X-ray crystallography and by titration calorimetry for hydrogen bonding interactions.</p>

<p>2,4-Dichloropyrido [2,3-D] pyrimidine is a regioselective chlorination agent that can be used for the synthesis of various organic compounds. It is often used in cross-coupling reactions to form carbon-carbon bonds. 2,4-Dichloropyrido [2,3-D] pyrimidine has been shown to give high yields and is selective for disubstituted or monosubstituted substrates. This compound is also useful for the functionalization of C-H bonds via palladium-catalyzed coupling reactions.</p>

<p>1,4-Dicyanobenzene is an organic compound that is used as a reactant in the production of other chemicals. It has been shown to be reactive with nucleophiles such as amines and alcohols. 1,4-Dicyanobenzene has shown good transport properties and can be used in industrial preparation of polymers such as polyurethane. The reaction mechanism for 1,4-dicyanobenzene is nucleophilic attack by a nucleophile on the carbonyl carbon of the double bond. This reaction yields two products: an amide or an aliphatic hydrocarbon. 1,4-Dicyanobenzene can also undergo reactions involving hydrogen bonds with other molecules in order to form new compounds.</p>

4,4'-Dimethyl-2,2'-bipyridine is a molecule that belongs to the group of p2 metal complexes. It has been shown to have synergistic effects with ruthenium complexes in analytical chemistry and electrochemical studies. Theoretical calculations have been performed for 4,4'-dimethyl-2,2'-bipyridine and its derivatives. These calculations show that the molecule is planar and that it can be considered as a diazonium salt. The photochemical properties of 4,4'-dimethyl-2,2'-bipyridine have also been studied in detail. This substance emits light when excited by ultraviolet light or visible light, which makes it an excellent candidate for use as a luminescent material in optical displays.

<p>2,4-Dibromopyridine is a brominated derivative of pyridine. It is synthesized through the substitution of two bromine atoms for two hydrogens on the pyridine ring. This synthesis can be achieved by disubstitution or cross-coupling reactions. The reaction products are nucleophilic and react with electrophiles to produce substitution products. The reaction mechanism is thought to involve a six-membered transition state, which has been observed using X-ray absorption spectroscopy.</p>

2,4-Dimethyl-3-hydroxypyridine is a hydroxypyridine compound with epoxide. It inhibits cytochrome P450 enzymes and is used as an organic solvent. 2,4-Dimethyl-3-hydroxypyridine is also used in research to study the structure of the pyridine ring and the hydroxyl group.

Versatile small molecule scaffold

tert-Butyl 2-(hydroxymethyl)azetidine-1-carboxylate is a versatile compound that has various applications across different industries. It is commonly used as a building block in the synthesis of shikimic acid, which is a key intermediate in the production of inhibitors and herbicides. Additionally, this compound can be utilized in electrode fabrication and is often sought after by researchers for their chemical studies. Another notable application of tert-Butyl 2-(hydroxymethyl)azetidine-1-carboxylate is its use in the pharmaceutical industry. It serves as an important starting material for the synthesis of cetirizine, an antihistamine medication used to alleviate allergy symptoms. Furthermore, it has been studied for its potential therapeutic effects on conditions such as psoriasis and photocatalytic reactions. In addition to its pharmaceutical applications, tert-Butyl 2-(hydroxymethyl)azetidine-1-carboxylate

<p>Versatile small molecule scaffold</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>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>Potassium 3-(phenylsulfonyl)benzenesulfonate is a chemical compound that is used as an anti-aging agent. It has been shown to reduce the viscosity of acrylonitrile, and is most effective when it is at a concentration of 1%. Potassium 3-(phenylsulfonyl)benzenesulfonate also reduces the strain on polymer fibers, which can be caused by temperatures or deionized water. The optimum temperature for this compound is about 50°C. Potassium 3-(phenylsulfonyl)benzenesulfonate does not have any adverse effects with other chemicals in the production process, and does not react with hexamethylenetetramine or aminopropyl naphthenate. This chemical also has a low cost and high tolerance for additives such as styrene or additives such as resistant</p>

<p>4-Phenyl-piperidine is a nitro compound that has been shown to be toxic for the kidneys and nervous system. 4-Phenyl-piperidine has been shown to inhibit dopamine uptake in the striatum and locomotor activity in rats. It also inhibits the hydrolysis of hydrochloric acid, which produces hydrogen ion (H+) ions, resulting in an acidic environment. The chemical structures of 4-phenyl-piperidine are similar to those of tricyclic antidepressants drugs, such as amitriptyline and imipramine, with a phenyl ring attached to an amine group. This drug is used as a pharmaceutical preparation for treating depression by inhibiting the reuptake of serotonin and norepinephrine, which are neurotransmitters that affect mood.</p>

4-Methylenepiperidine hydrochloride is a synthetic, ethylene oxide derivative that is used as an antifungal drug. It is also used in the synthesis of other compounds and as a reagent in organic chemistry. 4-Methylenepiperidine hydrochloride can be synthesized by reacting ethylene with an alkoxide, followed by adding a metal halide such as organolithium reagents to form the desired product. The yield rate of this reaction is high and it is easy to perform on a large scale.

<p>Please enquire for more information about 2-Methyl-2H-indazol-5-ylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Maleimidocaproic acid N-hydroxysuccinimide ester (6MCA-NHS) is a fluorescent probe that reacts with the hydroxyl group of fatty acids in human serum and other biological samples. 6MCA-NHS binds to the carboxylic acid group at the end of a fatty acid molecule, forming a covalent bond. This process generates light emission that can be detected by a fluorescence probe to measure changes in pH or other chemical properties within the solution. 6MCA-NHS has been used as a tumor treatment, where laser ablation is used to break up tumor cells and release 6MCA-NHS into the cytoplasm. The drug can then bind to DNA molecules and inhibit protein synthesis, which results in cell death.</p>

Methyl 4-amino-2-methoxybenzoate is a solute with anticancer activity. It has been shown to inhibit the growth of erythrocytes and cancer cells in vitro. The mechanism of action is associated with its ability to bind to aminobenzothiazole, which inhibits the production of DNA and RNA. Methyl 4-amino-2-methoxybenzoate has also been shown to inhibit the proliferation of human muscle cells and induce their differentiation. This drug does not have any effect on lipid or protein synthesis in cells, which may be due to its solvent perturbation properties.

1-Methyl-1,2,4-triazole is a molecule containing nitrogen atoms. It can be used as a monomer in the preparation of polymers or materials. 1-Methyl-1,2,4-triazole has been shown to be effective for the equilibration of mixtures of organic compounds in analytical methods and matrix effect studies. The reaction vessel must be unsymmetrical to prevent the polymer from sticking to it and causing potential problems with the separation process.

2-Mercaptopyridine is a quinone that has been used as an inhibitor of the HIV reverse transcriptase enzyme. It binds to the active site of the enzyme and inhibits its activity by forming a stable covalent bond with two cysteine residues in the enzyme. The molecule is stabilized by two adjacent sulfide bonds, which form a six-membered ring with three nitrogen atoms and one oxygen atom. This ring coordinates to the zinc ion in the active site of the enzyme. 2-Mercaptopyridine has also been found to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. 2-Mercaptopyridine binds to DNA at positions where it is complementary to guanine or adenine nucleotides, thus preventing RNA synthesis and replication.

<p>Isocytosine is a prodrug that has been synthesized with the intramolecular hydrogen on the nitrogen atoms, which makes it more chemically stable. Isocytosine is a reactive molecule, and can react with tautomers to form isocytosine derivatives. Isocytosine contains three hydrogen atoms that are transferable through reactions to other molecules. The chemical stability of isocytosine allows for its use in wastewater treatment. It also has metabolic effects, such as the inhibition of colorectal adenocarcinoma and metabolic disorders. Isocytosine can be used as a model system for studying transfer reactions and reaction mechanisms.</p>

<p>2-Iodobenzoic acid is a synthetic compound that is used in the treatment of wastewater. It is produced by the reaction of benzoate and nitrite in the presence of sodium hydroxide. The intramolecular hydrogen atom transfer from the 2-iodobenzoic acid to benzoate is a reversible reaction. This process can be catalyzed by palladium, which has been shown to be effective in coupling 2-iodobenzoic acid with other compounds to produce cyclic peptides. The use of 2-iodobenzoic acid as a contraceptive has been investigated for its ability to inhibit acetylcholinesterase activity, which may lead to increased levels of acetylcholine and inhibition of muscle contractions.</p>

<p>2-Iodobenzoic acid methyl ester is a palladium complex that can be used as a catalyst for the hydrolysis of ketoesters, imines, and halides. The reaction mechanism involves the coordination of the metal center to the carboxylate or amine group on the substrate, followed by a nucleophilic attack at the benzoate or chloride group. The resulting product is an alkyl halide. 2-Iodobenzoic acid methyl ester has been shown to catalyze the cross-coupling of diphenyl ethers with various amines in water and in organic solvents.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>