Building Blocks

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

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>3-Amino-2,4-dichlorobenzoic acid is a metabolite of malonate that inhibits the synthesis of fatty acids by inhibiting the activity of fatty acid synthetase. It has been shown to inhibit lipid accumulation in plants and may be used as an inhibitor in plant physiology experiments. 3-Amino-2,4-dichlorobenzoic acid can be applied to explants before or after treatment with test compounds to determine its inhibitory effect on fatty acid synthetase activity. 3-Amino-2,4-dichlorobenzoic acid is also a potent inhibitor of endogenous lipogenic enzymes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>2-(3-Aminophenoxy)ethan-1-ol is a nitro compound that has been synthesized from 3-aminophenol and ethyl chloroformate. The synthesis of this compound involves the use of a copper catalyst to form the nitro group. This chemical is an intermediate in the production of other nitro compounds, such as 2,4-dinitrophenol, which are used in explosives and dyes. 2-(3-Aminophenoxy)ethan-1-ol can be used as a stabilizing agent for nanoparticles because it contains amines that can bind to metal ions. It also has optical properties that can be exploited for various purposes, such as catalyzed reactions or optical studies. 2-(3-Aminophenoxy)ethan-1-ol is also useful when analyzing nitroarenes by using techniques such as chemoselective oxidation and hydrolysis.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

3,5-Dichloro-2,6-dimethylpyridin-4-amine is a phytotoxic compound that belongs to the group of heterocyclic compounds. It has been used in hydroponic cultures as a carboxyl herbicide and for the control of clopidol-resistant weeds. The symptoms induced by 3,5-dichloro-2,6-dimethylpyridin-4-amine are similar to those observed in plants treated with picolinic acid. Ingestion of this substance can lead to symptoms such as vomiting and diarrhea. The chemical is toxic and ingestion can result in death.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

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

This compound is an indole carboxylic acid with a tert-butoxycarbonyl group. It has a functional group of an ester at the C3 position, which is positioned at the 2-position on the indole ring. The molecule is a heterocycle and can be found in nature. This compound is bioactive and has been shown to have an affinity for human inflammatory receptors. It can also act as a surrogate for other molecules that might be too difficult to synthesize or too expensive to produce.

<p>Versatile small molecule scaffold</p>

Methyl 3-amino-4-butanamido-5-methylbenzoate is a chemical compound that has been used as a pharmacological agent. It has an affinity for acidic sites on muscle and blocks angiotensin II, which causes vasodilatation of blood vessels, increases blood flow to the heart, and lowers blood pressure. Methyl 3-amino-4-butanamido-5-methylbenzoate is also a strong blocker of angiotensin receptors in the brain. This drug is usually administered in the form of its hydrochloride salt. The physicochemical properties of this compound are determined by elemental analysis and chromatographic methods. Methyl 3-amino-4-butanamido-5-methylbenzoate can be synthesized from 4-(dimethylamino) butyric acid and methyl 3-(aminomethyl) benzoate through the following reaction:

Versatile small molecule scaffold

<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

<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

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>5-Amino-1H-pyrazole-3-carbonitrile (APC) is a pyrazolopyrimidine compound. It is used as a starting material in organic synthesis, for example to prepare dithioesters and dithioacetals. The transformation of the APC molecule is accomplished by reacting it with either an alcohol or acid chloride.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>1,4,7-Tribenzyl-1,4,7-triazonane is a crystalline compound that belongs to the group of ligands. This compound has a benzyl group in its structure and can be used as a transition metal complexing agent. The bond cleavage reaction of 1,4,7-tribenzyl-1,4,7-triazonane is catalyzed by a coordination chemical reaction with transition metals. It has been shown to form complexes with nickel and palladium. The kinetic isotope effect for this process has been reported to be large due to the presence of two hydrogen atoms in one molecule. This means that the molecule is more reactive at the site where it contains the hydrogen atom that is heavier isotopically.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Ethyl 1-benzyl-4-hydroxypyrrolidin-2-one can be synthesized in high yield by reacting benzyl amine with methanol and sodium carbonate in ethanol. This compound is a natural product found in marine organisms, such as sponges, sea cucumbers, and tunicates. It has been shown to have antibiotic properties against bacteria and fungi. The pharmaceutical industry has expressed interest in this compound because of its potential use as an anti-inflammatory agent.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>1-Carbamoylpyrrolidine-2-carboxylic acid is an antimicrobial agent that belongs to the class of cyclic amino acid derivatives. It crystallizes well and has a high yield of approximately 91%. The antimicrobial activity of 1-carbamoylpyrrolidine-2-carboxylic acid is due to its ability to inhibit microbial cell parameters, such as axial rotation and hydrolysis. This compound also has the ability to bind to benzyl groups with a high affinity and inhibit microbial growth by interfering with protein synthesis. Furthermore, 1-carbamoylpyrrolidine-2-carboxylic acid is inexpensively synthesized from benzoic acid.</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>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>