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>5-(2-Methoxyphenyl)-1,3,4-thiadiazol-2-amine is a corrosion inhibitor that is stable in an acidic environment. It has been shown to inhibit the growth of faecalis, which are bacteria that are responsible for causing urinary tract infection. This compound has been shown to have potentiodynamic polarization properties and electrochemical impedance spectroscopy data.</p>

<p>(2E,4E)-5-Phenyl-2,4-pentadienoic Acid is an anti-inflammatory compound that can be found in the natural compounds. It has a potent inhibitory effect on cancer cells and inflammatory diseases. (2E,4E)-5-Phenyl-2,4-pentadienoic Acid has been shown to inhibit tumor necrosis factor (TNF) alpha production in LPS-stimulated human monocytes. The structure of this molecule is similar to that of cinnamic acid derivatives which are known for their anti-inflammatory properties.</p>

<p>Ethyl 1-ethyl-4-phenylpiperidine-4-carboxylate is a synthetic substance that belongs to the class of drugs. It is a metabolite of amphetamine and can be used as an impurity standard for drug product. The compound is also used for research and development in the field of pharmacopoeia and drug development.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(3-Bromophenyl)oxirane is a reactive intermediate which has been studied as a potential neuropharmacological agent. It is a strain of the drug carbamazepine and an epoxide surrogate of sulfinyl. 2-(3-Bromophenyl)oxirane has been shown to be deuterated at the α-carbon position, allowing for reproducible and high concentrations in experiments. The deuterated version can be used to determine the metabolic fate of drugs, such as dopamine.</p>

<p>1-O-Ethyl 4-O-(3-methylbutyl) butanedioate is a food additive that has been approved by the United States Food and Drug Administration (FDA). It is used as an artificial butter flavoring in imitation butter. 1-o-Ethyl 4-o-(3-methylbutyl) butanedioate is a white solid that is soluble in ethanol, ether, acetone, and chloroform. The compound also has a fruity odor. This product can be detected by its high concentration of volatile compounds such as malate, furfural, and ethyl esters. 1-o-Ethyl 4-o-(3-methylbutyl) butanedioate has been shown to have an amino acid composition profile similar to that of amino acids found in natural butterfat.</p>

<p>2-Amino-3-pyrazol-1-yl-propionic acid (APPA) is a metabolic disorder drug that is also used to control diabetes. It is an acetaldehyde derivative that decreases the production of glucose in the liver by inhibiting pyruvate dehydrogenase, which is the enzyme responsible for converting pyruvate into acetyl coenzyme A. APPA prevents the accumulation of blood sugar and improves diabetes control by reducing blood glucose levels. 2-Amino-3-pyrazol-1-yl-propionic acid has been shown to be effective in preventing or delaying type 1 diabetes in animal models and can therefore be used as a preventive medicine. This drug has been shown to have toxicological effects on histidine synthesis, as well as on cucurbitaceae plants and ether extracts from them.</p>

<p>2-Amino-4-methylpent-4-enoic acid is a medicinal chemical that inhibits the NS3 protease of the hepatitis C virus. It is a potent inhibitor of NS3 protease and has been shown to be effective against genotype 1, 2, 3, 4 and 5 hepatitis C virus in clinical trials. This drug also inhibits the replication of other viruses such as HIV and herpes simplex virus. It is currently being investigated for its potential use in patients with chronic liver disease due to its ability to reduce inflammation and cirrhosis. 2-Amino-4-methylpent-4-enoic acid may be used as an agent for the treatment of chronic liver diseases such as cirrhosis or hepatocellular carcinoma. The drug can be taken orally and has been shown to have antiviral effects in patients with chronic liver disease.<br>2-Amino-4-methylpentanoic acid is chiral, meaning it exists in</p>

<p>4-Hydroxy-8-methoxyquinoline-3-carboxylic acid is an antibacterial agent that belongs to the group of diphenyl ethers. It is used in combination with a stabilizer, such as dodecyl sulfonate, to inhibit bacterial growth. 4-Hydroxy-8-methoxyquinoline-3-carboxylic acid inhibits bacterial growth by binding to the lipid II region of the bacterial cell membrane and forming a high affinity complex with dodecyl sulfonate. This results in inhibition of bacterial DNA synthesis and protein synthesis, leading to cell death. The compound has been shown to be effective against resistant bacteria such as Enterobacteriaceae and Pseudomonas aeruginosa. 4-Hydroxy-8-methoxyquinoline-3-carboxylic acid is soluble in water and methanol but not hydrochloric acid or sodium hydroxide solutions. It also has a</p>

<p>2-(2-Methoxyphenyl)acetyl chloride is an anti-tuberculosis drug that is selective for the Mycobacterium tuberculosis complex. It has been shown to be a potent inhibitor of dna synthesis in Mycobacterium tuberculosis and other mycobacteria, with an IC50 of 0.1 μM. 2-(2-Methoxyphenyl)acetyl chloride inhibits protein synthesis by inhibiting the activity of ribosomes, which are responsible for synthesizing proteins from mRNA. This drug also has a high selectivity against the Mycobacterium tuberculosis complex (MICs ≤0.1 μM). 2-(2-Methoxyphenyl)acetyl chloride can be synthesized using anthranilic acid, amines, and anilines as starting materials. The two isomers that are formed can be differentiated by their conformational properties and phosphorus oxychloride reactivity.</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>

Versatile small molecule scaffold

<p>Methyl 5,6-dimethoxy-1H-indole-2-carboxylate is a hydroxy oxindole compound. It is used in a model system to study the functional theory of density and planarity. In this system, it is bimetallic, with an indole derivative as the ligand. The structural theory of methyl 5,6-dimethoxy-1H-indole-2-carboxylate involves hydrogen bonds between the indole ring and the metal complex. Methyl 5,6-dimethoxy-1H-indole-2-carboxylate has been shown to have spectroscopic properties that are different than those of other oxindoles.</p>

N,N-Diethyl-3-oxo-2-azatricyclo[6.3.1.0,4,12]dodeca-1(12),4,6,8,10-pentaene-9-sulfonamide is a sulfonic acid class of naphthalenes that contains a sulfonic acid moiety. The compound has shown potent activity against Mycobacterium tuberculosis and other mycobacteria, but not against Pseudomonas aeruginosa or Staphylococcus aureus. This compound has been shown to be more potent than other sulfonic acids in the same class.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2-Nitrophenyl-5(2H)-tetrazole is a synthetic compound that has been shown to be an effective inhibitor of the enzyme urokinase-type plasminogen activator. This enzyme is responsible for activating plasminogen and converting it into the active form, plasmin, which breaks down fibrin clots in blood vessels. 2-Nitrophenyl-5(2H)-tetrazole binds to the active site of urokinase-type plasminogen activator, preventing it from activating plasminogen. The conjugates of this compound have been shown to be effective in inhibiting cancer cells and inducing apoptosis by binding to DNA.</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>Boc-(2RS)-2-amino-decanoic acid is a molecule that prevents the growth of bacteria by binding to its ribosomes and interfering with protein synthesis. It is composed of the amino acid decanoic acid and ethylene. Decanoic acid is an antibiotic component that is hydrolyzed to form an ester bond with the amine group on the 2nd carbon in 2-amino-decanoic acid, forming a conjugate that can be cleaved by β-lactamase. The spacer between the two components is methylene. This molecule has antibacterial activity against Staphylococcus aureus, but not against other bacteria such as Streptococcus pneumoniae or Haemophilus influenzae. This molecule has been shown to inhibit the growth of MRSA, which has developed resistance to many antibiotics.</p>

<p>2-chloro-4-sulfamoylaniline is a sepharose, which is a type of porous polysaccharide that can be used as an affinity matrix in chromatography. It has been used to purify sulfanilamide from the reaction mixture and to separate ethoxzolamide from lactoperoxidase. The affinity of 2-chloro-4-sulfamoylaniline is determined by the proximity of the enzyme to the surface and its ability to bind with the substrate.<br>2-chloro-4-sulfamoylaniline has also been shown to deacetylate cyanogen, causing it to form cyanamide. This chemical has polluting effects on water and air due to its aliphatic nature.</p>

<p>4-Amino-3-bromobenzene-1-sulfonamide is a sulfamate that has been shown to inhibit the growth of cancer cells in vitro. It may work by inhibiting an enzyme called carbonic anhydrase, which is involved in the hydration of carbon dioxide. 4-Amino-3-bromobenzene-1-sulfonamide has also been shown to have antibacterial activity against Mycobacterium tuberculosis and Mycobacterium avium complex. This compound is structurally related to coumarin derivatives, which are known inhibitors of an enzyme called anhydrase. Coumarin derivatives have also been shown to be potent anticancer agents.</p>

<p>2-[(Chlorocarbonyl)oxy]ethanesulfonyl}methane (CESM) is an organic solvent that has been shown to initiate polymerization of vinyl monomers. It reacts with electrophiles such as hydroxyl groups and fluorine, and undergoes ligation reactions with reactive functional groups. CESM is also used as a reagent in chemical ligation reactions, which have been used for the synthesis of proteins with novel sequences. The use of CESM in these reactions has been shown to be more efficient than traditional methods, with the rate of reaction being increased by up to five times. This agent has also been shown to be effective against infectious diseases such as HIV-1 and other retroviruses. CESM deprotects nitro groups from peptides and proteins, enabling their cleavage by proteases or reduction by hydrogenation agents. The trifluoromethyl group on CESM can react with hydrocarbon groups</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>

Versatile small molecule scaffold

<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>6-Amino-3-methyl-1,4-diphenyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile is a synthetic compound that has antioxidant properties and has been shown to induce apoptosis in cancer cells. It also shows antibacterial activity against Gram negative bacteria and has been shown to have antifungal properties. 6-Amino-3-methyl-1,4-diphenylpyrano [2,3 c] pyrazole 5 carbonitrile induces apoptotic cell death by inhibiting the phosphorylation of the protein kinase B (PKB) downstream of the insulin receptor substrate 1 (IRS1). This inhibition leads to an increased release of cytochrome C from mitochondria and activation of caspases. 6 aminopyrano[2,3 c]pyrazole 5 carbonitrile also inhibits the synthesis</p>

<p>Versatile small molecule scaffold</p>

<p>5-(4-Iodophenyl)-2H-tetrazole is a ligand that can be used for optical imaging. It has been modified with methyl groups and was found to have increased uptake by cells. The modification of 5-(4-iodophenyl)-2H-tetrazole with methyl groups on the phenyl ring increased the uptake by cells, while the modification of the tetrazole moiety had no effect on cellular uptake. 5-(4-iodophenyl)-2H-tetrazole has also been shown to bind to DNA, RNA, and proteins in a perinuclear pattern. This ligand is also luminescent and can be used for optical imaging.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

3-Bromo-2,3-dihydrothiophene 1,1-dioxide is a synthetic chemical that has been shown to react with magnesium in an ionic liquid to form 3-bromo-2,3-dihydrothiophene. This compound can be analyzed using elemental analysis and organic reactions. It has been studied extensively for its use as a catalyst in organic reactions such as alkylation and nucleophilic substitution. This compound also has a number of congener groups including the alizarin group, the naphthalene group, and the monocyclic group. 3-Bromo-2,3-dihydrothiophene 1,1-dioxide is also used for the synthesis of sodium salicylate.

<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>2-Amino-1-(3-chlorophenyl)ethan-1-ol is an iodide compound that has been shown to have insulin-like growth factor activity. It has been developed for clinical use in the treatment of cancer and other diseases. 2-Amino-1-(3-chlorophenyl)ethan-1-ol has been shown to reduce borohydride and peracid, which are compounds that are used in organic synthesis. The stereoisomers of this compound have also been characterized by X-ray crystallography. This iodide has been found to stimulate the growth of cells in vitro, as well as increase fatty acid production, thus making it a potential candidate for the treatment of obesity.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>N,N,2,2-Tetramethyl-1,3-propanediamine is a disulfide compound. It crystallizes in the orthorhombic system and exhibits an axial ligand. It has been shown to be a good ligand for many metal ions such as copper and zinc. The crystal structure of N,N,2,2-Tetramethyl-1,3-propanediamine is most likely a perchlorate salt with polymeric chains. The topology of the N,N,2,2-Tetramethyl-1,3-propanediamine molecule is anions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N'-Hydroxy-2-thiophenecarboximidamide is a factor-1 inhibitor that has been shown to inhibit the hypoxia inducible transcription factors (HIF) 1α and HIF2α. These proteins are involved in cellular response to hypoxia, which can lead to metastasis. This drug also inhibits the development of xenograft tumors by inhibiting cellular responses. N'-Hydroxy-2-thiophenecarboximidamide has been shown to be more effective than other inhibitors at preventing tumor growth and angiogenesis. It is also an important advance for cancer therapy as it provides a new target for cancer therapeutics.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 2-(benzylamino)acetate is a carboxyalkyl compound that is involved in the biosynthesis of β-unsaturated ketones. It can be used as a substrate for the oxidation of molecules such as quinazolines, piperidines and piperazines. Methyl 2-(benzylamino)acetate can also act as an acceptor for hydrogen atoms or electrons from other molecules. The methyl group in this molecule has been shown to be able to donate or accept electrons from other molecules, allowing it to participate in many different reactions. Methyl 2-(benzylamino)acetate is synthesized by bacteria such as Bacillus subtilis.</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>

Versatile small molecule scaffold

<p>6-Chloro-7-hydroxy-4-phenyl-2H-chromen-2-one (6CHC) is a chromene derivative that binds to nuclear DNA and can be used for the diagnosis of cancer. 6CHC has been shown to inhibit the growth of cancer cells by binding to their nuclear DNA. The compound has also been shown to bind to the PPAR receptors and thereby inhibiting the proliferation of cancer cells. 6CHC has been shown to be a more sustainable alternative for phaseolus, which is currently being used as an inhibitor in wastewater treatment. This compound is resistant to acid molecules, making it a good candidate for use in wastewater treatment with high concentrations of acid. 6CHC is also an antioxidant that can be used as an corrosion inhibitor in wastewater treatment systems.</p>

<p>N-Benzyl-N-methylthiourea is an isomeric, bicyclic compound. It has antiaromatic properties and belongs to the thiazole class of compounds. It was isolated from a reaction mixture in which benzyl chloride and methylisothiourea were heated together with sodium amide. It has been reinvestigated as a possible intermediate for heterocyclic synthesis. The substance is stable at room temperature, but decomposes on heating.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Aminomethylidene)-2,3-dihydro-1H-inden-1-one is a lipophilic drug that is used in pharmaceutical preparations. It is a non-irritating and non-sensitizing agent that does not cause any significant sensitization reactions. It is used as a diagnostic aid for the detection of fatty acid esters in tissue samples, an enhancement agent during cavity preparation, and as pharmaceutical dosage for treatment of depression. This compound has been shown to act as a transporter gene modulator and can be found in tissues such as the brain, heart, kidney, liver, spleen, adrenal gland and pancreas. 2-(Aminomethylidene)-2,3-dihydro-1H-inden-1-one may be conjugated with glutathione or sulfate and excreted into bile. Fatty acids are transported into cells by carriers</p>

<p>Versatile small molecule scaffold</p>

<p>5,6,7,8-Tetrahydro-8-quinolinecarbothioamide is a pyridine compound with the molecular formula C4H5N. It is an anti-ulcer agent that has been used in the synthesis of other organic compounds. This compound contains a pyridine ring with a nitrogen atom at position 8 that is substituted with a cyano group. It also contains two hydrocarbon rings and one nitro group at position 5. 5,6,7,8-Tetrahydro-8-quinolinecarbothioamide can be synthesized by reacting 2 equivalents of carbonyl fluoride with 1 equivalent of sodium nitrite in the presence of copper metal.</p>

<p>6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a dermatological active substance that is used in the treatment of skin diseases. It has been shown to be an immunosuppressant in animals and humans and can also be used in the treatment of respiratory disease. It has vasotropic properties and is an antiinflammatory agent. 6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a topoisomerase II inhibitor that binds to DNA and prevents the unwinding of DNA strands by inhibiting the formation of topoisomerases II–DNA complexes. The compound binds to the C1 position on the cyclohexane ring, which contains both unsubstituted alkyl and unsubstituted aryl groups as well as elements such as silver halide.</p>

<p>Bromomethanesulfonamide is a synthetic drug that is used to treat acute lymphoblastic leukemia and hepatitis. It inhibits the activity of the enzyme ns5b polymerase, which is involved in viral replication. Bromomethanesulfonamide is also an NS5B polymerase inhibitor, which may be effective against some types of chronic hepatitis caused by a virus. This drug has been shown to inhibit serotonin synthesis in animals, but this effect has not been observed in humans. Bromomethanesulfonamide has also been used as a control agent for pharmaceutical preparations and carbonic anhydrase inhibitors for glaucoma treatment.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-Methylthiophene-2-sulfonamide is an inhibitor of arylsulfonamides. It can be used to investigate the conformational and torsional effects of arylsulfonamides and their relationship to the inhibition of sulfonamide. N-Methylthiophene-2-sulfonamide has been shown to have good inhibitory activity against sulfonamide with conformation and torsional effects, which may be due to its ability to bind to the sulfanilamide in the active site. The computational results also show that this compound has potential for use as a drug candidate.</p>

<p>7-Chloro-6-nitroquinazolin-4(1H)-one is a manipulator that has been shown to be effective in the treatment of epidermal growth. The compound was found to be an efficient inhibitor of protein kinases and histone deacetylases, which are important for the regulation of cellular proliferation. 7-Chloro-6-nitroquinazolin-4(1H)-one is also a nucleophile that reacts with electrophiles such as organic peroxides and nitrosating agents. This reaction leads to the production of reactive oxygen species, which may contribute to its antitumor activity.</p>