Building Blocks

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>1-Ethenyl-1H-imidazole-2-carboxaldehyde is a molecule that contains a vinyl group and a hydrogen bond. It has an intramolecular interaction with the carbonyl group and interactions with the formyl group and the pyridine ring. The vinyl group is also able to interact with other vinyl groups in other molecules, creating cycles of these molecules.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>5-Aminopyrimidin-4(3H)-one is an imidazole that is a precursor to the purines, which are nucleic acid bases. It is synthesized from the reaction of ammonium persulfate and 5-aminouracil with diacetate. This compound can be used as a fungicide and can also be used in the synthesis of 5-amino-1-(2,4,6-trichlorophenoxy)pyrimidine (5-ATP), a chemotherapeutic agent.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-Methyl-1H-indole-2-carboxamide is a molecule that has been optimized for antibacterial activity. It belongs to an indole family of molecules and has been shown to be active against the fungus, Neosartorya fischeri. In theory, this molecule could have potential as a drug agent for the prevention of bacterial infection. The optimization process was based on parameters such as carboxamide functional theory, nmr spectra, and potentials. The experimental data collected from NMR spectra and antibacterial activity confirmed that this molecule had a high degree of antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus and Gram-negative bacteria such as Escherichia coli.</p>

<p>2-Acetamidothiazole-5-sulfonyl chloride (2A5C) is a sulfonamide anticancer drug that exhibits cytotoxic activity. 2A5C is an indole derivative that has been synthesized for the purpose of developing a new class of anticancer agents. This drug has shown to have significant anti-tumor activity in molecular docking studies and can be used as a lead compound for future research.</p>

<p>Versatile small molecule scaffold</p>

<p>3-(aminocarbonyl)benzenesulfonyl chloride (3-ACBSCl) is a compound that inhibits the life cycle of the HIV virus. It is a hexamer and binds to viral proteins, inhibiting the process of viral assembly. 3-ACBSCl helps to optimize lead compounds for antiviral drugs. This inhibitor has been shown to be active against HIV-1, and also inhibits other viruses that have an analogous life cycle. 3-ACBSCl has been shown to inhibit HIV-1 infection by binding to the capsid protein and preventing it from assembling into a functional virus particle.</p>

<p>2-Methylene-1,3-dioxepane is a biodegradable polymer that is used in the production of polyesters for use in film and packaging. It is synthesized by cationic polymerization, which involves the formation of ester linkages. 2-Methylene-1,3-dioxepane has been shown to be biocompatible in cell culture and can be used as a growth factor for tissue engineering. The melting point of this polymer is dependent on the molecular weight and it undergoes phase transition at temperatures around 130°C. This polymer degrades through hydrolysis when exposed to alkali or hydrogen chloride.2-Methylene-1,3-dioxepane has been observed to have an FTIR spectrum containing carbonyl absorption bands at 1710 cm−1 and 1650 cm−1. This material also displays a 13C NMR spectrum with peaks at -18 ppm and -7 ppm</p>

Versatile small molecule scaffold

<p>2-(Naphthalen-2-ylformamido)acetic acid (Nafamid) is a toxic agent that can be used to induce experimental diabetes in animals. Nafamid is metabolized to benzoate and then to chloride, which can be detected in urine. Chromatographic experiments showed that Nafamid was not metabolized by rats or mice, but was eliminated as the mercapturic acid (MNA) and mercapturic acid glucuronide (MAG). MNA has been isolated from urine samples of rats injected with Nafamid. The metabolic pathways for Nafamid are the same for animals and humans.</p>