Building Blocks

<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>

<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>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-[(5-Methylthiophen-2-yl)formamido]acetic acid is a research tool that is used as an activator of G protein coupled receptors. It binds to the receptor, which induces activation and signaling via second messengers. 2-[(5-Methylthiophen-2-yl)formamido]acetic acid has been shown to activate ion channels in cells and is also a ligand for the receptor. This compound has been shown to be a potent inhibitor of GABA (gamma amino butyric acid) binding in rat brain synaptosomes.</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>

<p>2,2-Dimethyl-4-pentenoic acid is a decarboxylating agent that converts the carboxylic acid group to an aldehyde. It is commonly used as a reducing agent in organic synthesis, especially for the conversion of esters and nitriles to alcohols and amines respectively. The synthesis of 2,2-dimethyl-4-pentenoic acid is achieved by reacting piperidine with propylene oxide. This reaction proceeds via a six-membered ring intermediate that decomposes to form the final product. The reaction can be catalyzed with peroxide or hydrogen peroxide, which leads to a high yield. 2,2-Dimethyl-4-pentenoic acid has been shown to be effective against hyperproteinemia and lipogenous disorders such as steatosis and cholestasis.</p>

<p>Versatile small molecule scaffold</p>

<p>6-Propyl-5,6-dihydro-2H-pyran-2-one belongs to the class of isoquinoline alkaloids. It is found in leguminosae plants and has a strong spectrum of activity against bacteria, viruses and fungi. This compound is also used for the treatment of malaria and as an antihelminthic agent. The index of this substance is unknown, but it has been shown to have a mass spectrum that corresponds with that of prosopis. 6-Propyl-5,6-dihydro-2H-pyran-2-one is semiarid and indehiscent, with volatile fruit.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(Bromomethyl)-2,1,3-benzothiadiazole is a heterocyclic compound that is used as an intermediate in the synthesis of pharmaceuticals. It has been shown to have biological activity when hydrolyzed by malonic esterases and phosphodiesterases. 4-(Bromomethyl)-2,1,3-benzothiadiazole has also been shown to be a potent inhibitor of acid hydrolysis in rat erythrocytes and to cause inotropic effects. 4-(Bromomethyl)-2,1,3-benzothiadiazole can be nitrated by potassium nitrate to form a diazonium salt that is used as a reagent for the determination of amines.</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 6-isothiocyanatohexanoate is a reactive organic compound that reacts with thiophosgene to form methyl 2,6-dithiocyanatohexanoate. This reaction product is unstable and breaks down to release carbon dioxide and sulfur dioxide. Methyl 6-isothiocyanatohexanoate reacts with theophylline to produce methyl 3,7-dithiocyanatooctanoate. This reaction product can be hydrolyzed by esterases or glucuronidases to release caffeine. Methyl 6-isothiocyanatohexanoate also reacts with theophylline to form methyl 7-dithiocyanatooctanoate in an oxidative process, which releases carbon monoxide and hydrogen cyanide.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Phenylpentanoic acid is a chemical compound that is found in nature. It is used as an additive to enhance the properties of styrene, which is a colorless liquid with a sweet odor and it can be combustible. 4-Phenylpentanoic acid has been shown to inhibit the degradation of styrene by carbon tetrachloride, but its mechanism of action is not yet known. This substance has also been shown to be selective for alkali metals such as potassium and sodium, while exhibiting no selectivity for other metal ions such as magnesium or iron. This chemical also effectively removes hydroxides from metal surfaces and reacts with aliphatic hydrocarbons to form a variety of products. The nature of 4-phenylpentanoic acid's constant is not yet known.</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>

<p>1-Chloronaphthalen-2-amine is an organic compound that belongs to the group of amines. It is a colorless liquid with a molecular weight of 122.14 and a boiling point of 164°C. This compound is an isomer of naphthalene, which means it has the same chemical formula but different arrangement of atoms within the molecule. 1-Chloronaphthalen-2-amine can be used in pharmaceuticals as well as in nature, where it reacts with singlet oxygen to form nitrosonium ion, which can then react with benzoate to produce nitrobenzene. The enzyme catalysis process involves the use of 1-chloronaphthalen-2-amine as a substrate and acetonitrile as a catalyst to produce 2,6 -dichloroisonicotinic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Diaminopyrazole is a heterocyclic compound that has been used as a colorant in the textile industry. It is also known to be an effective acceptor for hydrogen bonding in human keratin. 3,4-Diaminopyrazole reacts with primary alcohols to form chalcones and the long-term exposure of this compound has been shown to cause fatty alcohols. This heterocyclic compound undergoes a bathochromic shift under UV light and can be used as a spectral marker in vitro.</p>

<p>Versatile small molecule scaffold</p>

<p>The protonation of 4-methyl-1H,2H,3H-pyrrolo[2,3-b]pyridine can be described by the following equilibrium equation:</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Lidamine is a potential drug candidate for use in cancer therapy. It has been shown to be cytotoxic, meaning it kills cancer cells. Lidamine was also found to inhibit the growth of cancer cells in vitro and in vivo. More research is needed to investigate lidamine as a potential treatment for cancer.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>