Building Blocks

Versatile small molecule scaffold

2-Amino-5-methyl-3-nitrobenzoic acid is a heterocyclic compound that has been shown to rearrange under acidic conditions. It can be synthesized by the reaction of 2-amino-5-methylbenzoic acid and sodium nitrite in the presence of benzotriazole. This compound is used as a reagent for spectroscopy, such as NMR and IR. The IR spectrum of this compound shows absorption bands at 3351, 1707, 1671, 1533, 1492, 1377, 1283, 1166 cm−1.

Versatile small molecule scaffold

Versatile small molecule scaffold

The compound 1-Phenyl-1H-1,2,3,4-tetrazol-5-amine is a growth factor that is used in pharmaceutical preparations. The reactive functional group is amine and the drug has been shown to be biocompatible and non-toxic. It is used as a diagnostic agent for diabetes mellitus type 2 and cardiac diseases. It has also been shown to have cytotoxic effects on cancer cells lines including MDA-MB-231 cell line with EC50 of 0.8 μM.

Versatile small molecule scaffold

Iodomethylcyclohexane is a cyclohexane compound that is used as an ingredient in the production of other substances. It has been shown to have inhibitory effects on bowel disease and has a stereoisomer with a ph optimum of 7. Iodomethylcyclohexane also has an average particle diameter of 6.5 micrometers, which means it is a liquid crystal composed of molecules that are arranged in a regular and periodic manner. Iodomethylcyclohexane binds to receptors on cells, such as chloride and acid phosphatase, which are important for the regulation of cell growth. Iodomethylcyclohexane also binds to adrenergic receptors and can cause constriction of blood vessels. END>>

6-Chloro-9-phenyl-9H-purine is an antipurinic agent that inhibits the production of nucleic acids. It is a derivative of 6,6'-dichloro-2,2'-diimidazole and is used as a precursor in the synthesis of other analogues. The yield of this compound can be increased by using carbon tetrachloride as a catalyst. 6-Chloro-9-phenyl-9H-purine has been shown to be an effective catalyst for imidazolium and benzimidazolium salts. This compound also exhibits nucleophilic properties which may be due to the dipole moment created by the nitrogen atom on one side and the oxygen atom on the other side.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

7-Methylquinolin-8-amine is a chemical compound that belongs to the group of quinoline derivatives. It has been shown to inhibit collagen synthesis, which may be due to its alkalizing effect on the extracellular matrix. This agent also acts as an inhibitor of cardiac hypertrophy and modulates cardiac muscle cell proliferation. 7-Methylquinolin-8-amine also represses the transcription of protein genes and prevents the activation of cardiac tissues by chloride ions.

N-(4-Hydroxyphenyl)benzenesulfonamide (NPSA) is a potentiator of chlorine that increases the activity of monooxygenases, such as epoxide hydrolase. NPSA also has the ability to inhibit glutathione synthesis in the liver and kidneys. This inhibition leads to liver cell necrosis. It is believed that NPSA may act by inhibiting the synthesis of an intermediate in the biosynthesis of cholesterol, 3-methylcholanthrene. The chlorobenzenesulfonamide moiety reacts with glutathione to form a reactive chloride ion, which then reacts with other cellular components to cause damage.

1,3-Diphenylpropane-1,3-diol is a synthetic compound that can be used as an intermediate in organic synthesis. It is a chiral molecule with the (R) configuration at the phenyl ring. 1,3-Diphenylpropane-1,3-diol has been studied for its effects on acidemia and aciduria in humans. This chemical also inhibits phosphine toxicity by inhibiting alcohol dehydrogenase and acetaldehyde dehydrogenase. Clinical studies have shown that 1,3-diphenylpropane-1,3-diol can alleviate methylmalonic acidemia and congenital methylmalonic aciduria.

Cyclohexylmethyl)urea is a protease inhibitor that inhibits the activity of the ns3 protease, which is involved in coagulation. Cyclohexylmethyl)urea binds to the active site of the ns3 protease and prevents it from cleaving proteins. It has been shown to be beneficial for patients who have had angioplasty or other procedures that involve opening a blocked artery. Cyclohexylmethyl)urea is also used for the treatment of restenosis after angioplasty and myocardial infarction. Cyclohexylmethyl)urea is administered intravenously and can be given as an injection or infusion. The drug must be given with a co-administered agent such as hydrochloric acid, which stabilizes cyclohexylmethyl)urea by converting it into its hydrochloride salt. This pharmaceutical preparation is not indicated for use in children under 6 years of age because of its potential to cause irreversible

Diethyl 2-formylsuccinate is an organic ester that is used in pharmaceutical preparations. It is a strong electrophile that reacts with nucleophiles, such as DNA, RNA, and proteins. Diethyl 2-formylsuccinate has been shown to induce basophilic leukemia in mice. This drug also induces the expression of crth2 which is a receptor for the inflammatory response. Diethyl 2-formylsuccinate also has anti-inflammatory properties and has been shown to inhibit bowel disease. Diethyl 2-formylsuccinate has also been shown to have some activity against congestive heart failure and cyhalothrin toxicity. The anti-inflammatory effects of diethyl 2-formylsuccinate may be due to its steric interactions with the nitro group or its ability to scavenge reactive oxygen species.

2-Amino-2-methyloctanoic acid is an α-amino acid that has been shown to have a right-handed helical conformation. In the solid state, it appears as a dimer and in solution, it appears as a hexamer. The compound is chiral, which means that it can exist in two forms with different configurations of the groups around the central carbon atom. 2-Amino-2-methyloctanoic acid has been synthesized using techniques such as FTIR spectroscopy and NMR spectroscopy. It is also used to study stereoselectivity in peptides by probing their conformational preferences.

1-Chloro-3-methoxy-2-nitrobenzene is an anomalous compound that reacts with water to produce hydrochloric acid and nitrous oxide. The reaction starts with cleavage of the C–C bond, followed by a rearrangement to form the methylenedioxy group. This leads to a nucleophilic attack on the aromatic ring, which causes it to become electrophilic and react with water. The temperature of this reaction is dependent on the concentration of hydrochloric acid.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

4-Isopropylcyclohexylmethanol is a synthetic chemical that is used as a fragrance. It is found in plants such as Paeonia suffruticosa and is used in the synthesis of linalool oxide. 4-Isopropylcyclohexylmethanol has been shown to bind to histone proteins, which may have an effect on gene expression. This chemical also has a vapor pressure of 0.0013 mmHg at 25°C and can be detected by electrochemical method at a concentration of 10 ppm. 4-Isopropylcyclohexylmethanol has been shown to react with eugenol in benzene, forming methyl cinnamate and methyl ethyl alkanal.

2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane is a catalytic agent that is used in the synthesis of acetates and cyclohexanone. It can be used to produce a variety of organic compounds by using different starting materials, such as acetates and cyclohexanone. 2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane has been shown to react with epichlorohydrin to form a chloromethylated product at room temperature. The reaction proceeds via an addition-elimination mechanism and produces two products: 1,4-dioxaspiro[4.5]decane and chloroacetate.

tert-Butyl 6-aminohexanoate is a benzene derivative that is used as a spacer in organic synthesis. It reacts with potassium carbonate to form tert-butyl 6-aminocaproate and tert-butyl 2,6-dinitrophenolate. The tert-butyl group has an amino group at one end and a carboxylic acid group at the other end. This tertiary amine is made by reacting benzene with potassium hydroxide and adding 1-4c alkyl chloride. The tertiary amine functional group is reactive towards electrophilic aromatic substitution reactions, such as nitration or halogenation.

Versatile small molecule scaffold

Versatile small molecule scaffold