Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

4,5-Dihydroxy-2,3-dihydro-1H-isoindole-1,3-dione is a molybdenum compound with a hydroxyl group. It has been shown to inhibit the growth of bacteria that are resistant to penicillin by binding to the penicillin-binding proteins in their cell wall. 4,5-Dihydroxy-2,3-dihydro-1H-isoindole-1,3-dione has been found to be an effective inhibitor of polymer film formation when used in conjunction with 3 chloroperoxybenzoic acid. This compound also has been shown to have anti bacterial properties against Escherichia coli and Pseudomonas aeruginosa. 4,5-Dihydroxy -2,3 -dihydro -1H -isoindole -1,3 -dione may also have environmental applications due its

<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>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>

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>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>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-Iodo-1-benzofuran is an organic compound with a linear structure and a phenyl group. It has one hydrogen bond, two of which are stabilized by the phenyl ring. The other three hydrogen bonds are stabilized by the halogen bonds. The benzofuran ring is rotated in such a way that the substituents on it are dihedral. 5-Iodo-1-benzofuran has been shown to have a crystal structure that is stabilized by the halogen bond between the phenyl group and iodine.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloro-N-methyl-2-nitroaniline is an antibiotic that belongs to the group of quinolone antibiotics. It has a broad spectrum against Gram-positive and Gram-negative bacteria, including methicillin resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. 3-Chloro-N-methyl-2-nitroaniline binds to bacterial DNA gyrase and topoisomerase IV, as well as human DNA gyrase and topoisomerase II, inhibiting their activity. This leads to cell death by interfering with the production of proteins vital for cell division. The optimal parameters for this drug have been found using isothermal titration calorimetry on the enzyme gyrase in the presence of different concentrations of 3CMA. Pharmacological targets for this drug include DNA gyrase and topoisomerase IV.</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>2-Hydroxy-4,6-dimethylbenzoic acid (HMBA) is a tumor treatment drug that can be used in combination with other drugs. HMBA inhibits proton pumps and the synthesis of DNA, RNA, and protein. The proton pump inhibitors are used to treat acid reflux disease, ulcers, and gastroesophageal reflux disease. HMBA has been shown to significantly inhibit tumor growth in animal studies. This drug also has anti-inflammatory effects and may be useful for treating arthritis.</p>

<p>Benzeneacetic acid, 3,5-difluoro-hydroxy-, (S)- is a ligand that can bind to transition metals such as copper or iron. It has been shown to be a good sensing ligand for the detection of mandelate and enantioselective for the synthesis of chiral molecules. The divalent bonding between the benzeneacetic acid and the metal may be due to coordination or dipyridyl. The stability of this molecule is also dependent on the type of metal it is bonded with.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Benzothiophene-6-carboxaldehyde (BTA) is a heterocyclic compound that contains sulfur. It is a colorless liquid with a sweet odor. BTA is used in the manufacture of pesticides, pharmaceuticals, and other organic chemicals. It is also used as a building block in the synthesis of other compounds and has been shown to have anti-inflammatory properties.</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-Phenyl-1,2,4-triazolidine-3,5-dione is a molecule that can be used for biological purposes. It has the chemical formula of C6H4N2O3 and a molecular weight of 180.14 g/mol. The hydrogen bonds between the hydroxyl group and the skeleton are strong enough to keep the molecule in shape. The molecule is thermally developable; it can be developed after exposure to heat or light. 1-Phenyl-1,2,4-triazolidine-3,5-dione has been shown to react with silver ions and metal surfaces such as aluminum and titanium oxide. This compound may also be useful for coatings that are reactive to light or heat because it will form a film when exposed to either one.</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>2-Phenoxy-benzylamine is a growth factor that acts by binding to cell surface receptors. It is involved in the regulation of cellular proliferation, differentiation, and survival through interactions with its receptor. 2-Phenoxy-benzylamine binds to the extracellular domain of its receptor, which is composed of three immunoglobulin (Ig)-like domains. The protein also interacts with other proteins, such as histone H3, and can be detected using signal detection methods like Western blotting. 2-Phenoxy-benzylamine has been shown to have an effect on the expression of certain genes in tissue cultures and specifically on chondroitin sulfate in mammalian cells. It also has an endoplasmic reticulum localization sequence that allows it to be transported into the Golgi apparatus and specific primers can be designed for PCR amplification.</p>

<p>3-Iodo-4-methylfuran is a furan derivative that can be synthesized from 3,4-dimethoxybenzaldehyde. It has been shown to have antileishmanial activity via the inhibition of the sterol biosynthesis pathway. The furan ring of this compound undergoes a metathesis reaction with 2 equivalents of boronic acid to form a 4-hydroxyfuro[2,3-b]pyran ring system. This reaction is catalyzed by palladium or nickel and requires an oxidant such as cerium(IV) oxide or a peroxide. The synthesis of this compound can also be accomplished by reacting furyl bromide with aniline in the presence of sodium hydroxide in a Suzuki coupling reaction. 3-Iodo-4-methylfuran has been shown to produce yields of 84% when synthesized from 3,4-dimethoxybenzaldehyde and used as an</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>