Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Phenylthiomorpholine is a drug that is used as an antiarrhythmic agent. This drug has been shown to be effective in the treatment of arrhythmias and can be used to decrease the frequency of ventricular tachycardia, ventricular fibrillation, and atrial fibrillation. 2-Phenylthiomorpholine inhibits the activity of cysteamine, which is an amino acid that plays a major role in the regulation of blood pressure. It also has anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis, as well as analgesic effects due to its activity on ligand-gated ion channels.

Ethyl 1-benzylpiperidine-2-carboxylate is an organic compound that belongs to the class of benzhydryl compounds. It is a colorless liquid at room temperature and has a boiling point of 60°C. Ethyl 1-benzylpiperidine-2-carboxylate can be synthesized by reacting methanol with piperidine in the presence of aluminum chloride and sodium borohydride in a catalytic amount. The nitrogen atom in this compound is a chiral center, which means it cannot exist as two enantiomers. This product also reacts with chloride to form ethylmagnesium chloride, which is used for the production of aminoalcohols.

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Butoxypyridine is a hydrophobic, potent inducers of the cytochrome P450 system. It can be used as a substrate for molecular modeling studies and has been shown to react with chlorine atom in mass spectrometric studies. The reaction products are pyridine compounds that are chlorinating agents. The chlorination reaction rate can be controlled by various techniques such as temperature, solvent, and concentration.

Versatile small molecule scaffold

3-Amino-5-chloropyridine-2-carboxamide is a phosphoinositide (PI) analog that has been shown to inhibit the growth of cancer cells. It also inhibits the production of proteins, such as cyclin D1 and Bcl-xL, which are required for cancer cell proliferation. 3-Amino-5-chloropyridine-2-carboxamide has been shown to be effective in vivo in animal models and in vitro in human cancer cells. The compound has been shown to have no effect on normal cells, leading to a low level of toxicity. This drug can be used as an anticancer agent or as part of a combined therapy regimen with other chemotherapeutic agents.

Benzene-1,2-disulfonamide is a sulfonamide that inhibits bacterial enzymes. It is an inhibitor of carbonic anhydrase, a human enzyme that catalyzes the conversion of carbon dioxide and water to bicarbonate. Benzene-1,2-disulfonamide has been shown to inhibit the growth of bacteria in vitro. The compound also has been found to be effective against some types of cancer cells, including those which are resistant to platinum-based chemotherapy. Benzene-1,2-disulfonamide binds to the active site of the bacterial enzyme and blocks its activity. The drug's high potency against anaerobic bacteria may be due to its ability to bind with nitro groups on proteins such as tetrahydrofolate reductase and cytochrome c oxidase.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

N-Benzyl-1H-1,3-benzodiazol-2-amine is an antihistaminic that has been shown to be a potent inhibitor of histamine release from mast cells. It has been used in the treatment of anaphylaxis, cutaneous and mucocutaneous leishmaniasis, as well as in vitro activity against Leishmania species. This drug does not inhibit the release of histamine from basophils or eosinophils.
N-Benzyl-1H-1,3-benzodiazol-2-amine is a competitive inhibitor of leukotriene C4 synthase and is an antagonist at the H2 receptor. It also inhibits the activity of amastigotes and other intracellular targets.