Building Blocks

<p>Versatile small molecule scaffold</p>

<p>4-(Prop-2-yn-1-yloxy)benzoic acid is a colorless to white crystalline solid. It is soluble in water, ethanol, ether and benzene. The substance is an intermediate in the synthesis of pharmaceuticals such as propofol and etoposide. 4-(Prop-2-yn-1-yloxy)benzoic acid can be used for the synthesis of polymers that are polymerizable and have a high degree of crosslinking. This substance can also be used as a reagent for the conversion of halides, azobenzene, anthracene, phenols, and naphthalenes into their corresponding ethers.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

(3-Methylphenyl)(phenyl)methanol is a radical cation that has been shown to undergo intramolecular hydrogen abstraction. This chemical can be found as two isomers, 3-methylphenol and 3-methylbenzaldehyde. The molecule has six-membered ring transition states and molecular ion peaks with m/z of 136 and 138, respectively. The gaseous form of this compound is metastable, which means it will spontaneously decompose into the more stable radical anion (m/z = 164). The radical cations are formed when the methyl group on the phenyl ring is abstracted by a hydrogen atom from another molecule. Fragmentation of this molecule yields substituent radicals and radical cations (m/z = 110).

<p>o-Benzyl-(D)-serine benzyl ester is a molecule that can be synthesized in high yields by reacting o-benzyl-D-serine with benzaldehyde. This synthetic route produces the target molecule, which can then be used for experimental purposes. The experimental result of this reaction was found to be 98% yield and the reaction conditions were found to be an activating methodology and a reagent condition of deprotecting.</p>

3-Bromobutyl)benzene is a nucleophile that reacts with an alkyl halide. The nucleophile attacks the electrophilic carbon atom of the alkyl halide, forming a covalent bond with it. This reaction is called alkylation. The product of this reaction is called an alkyl bromide. 3-Bromobutyl)benzene can also react with primary amines to form (3-bromobutyl)anilines. These reactions are catalyzed by palladium, which is used as a catalyst for these reactions because of its ability to bind to both the nucleophile and the amine in these reactions.

<p>Versatile small molecule scaffold</p>

<p>(Ethenesulfonyl)cyclohexane is a monomer that is used in the production of pharmaceutical formulations and devices. It has been shown to inhibit the hydrolysis of 5-hydroxytryptamine (5-HT), which leads to increased levels of serotonin (5-HT). This compound also inhibits the binding of 5-HT to its receptor, which may be due to its ability to bind with high affinity at the 5-HT1A receptor.</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>

Versatile small molecule scaffold

<p>5-Methoxy-3-methyl-1H-indole is an oxygenated aromatic amine that is produced as a phytoalexin. It has been shown to inhibit the growth of gram negative bacteria, such as Salmonella and E. coli, by inhibiting the synthesis of proteins required for cellular respiration. 5-Methoxy-3-methyl-1H-indole also inhibits the activity of an enzyme called phospholipase A2, which is responsible for the hydrolysis of lipid molecules in cell membranes. This inhibition prevents the release of arachidonic acid from phospholipids, leading to a decrease in prostaglandins and leukotrienes. 5-Methoxy-3-methyl-1H indole has also been shown to have antioxidant properties due to its ability to scavenge free radicals.</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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>5-Benzyl-thiazol-2-ylamine is a nitrogenous compound that has been shown to interact with ferrite, a magnetic material. It has proapoptotic effects on human glioblastoma cells, t98g cells, and mouse fibroblasts. The interactions of 5-benzyl-thiazol-2-ylamine with ferrite are reportedly stabilized by the presence of iron ions. This interaction can be studied using resonance energy techniques such as fluorescence microscopy, nuclear magnetic resonance spectroscopy, and electron paramagnetic resonance spectroscopy.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

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>

<p>Versatile small molecule scaffold</p>

<p>3-(3,4-dimethoxybenzenesulfonamido)propanoic acid is an inhibitor of phosphodiesterase 4 (PDE4). It is a white powder that is soluble in water. The purity of this product is greater than or equal to 98%.</p>

<p>3-(2-Chlorobenzenesulfonamido)propanoic acid (CAS No. 746655-82-3) is a potent, selective inhibitor of the human serotonin receptor 5-HT2A. It has been shown to inhibit the binding of ligands with high affinity and selectivity to 5-HT2A receptors. 3-(2-Chlorobenzenesulfonamido)propanoic acid has also been shown to exhibit an affinity for other ion channels and peptides, such as the NMDA glutamate receptor and the CGRP calcitonin gene related peptide receptor.</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>