Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Methyl 2-(dimethylamino)-6-methylpyrimidine-4-carboxylate (MDMP) is a natural compound that has been shown to have biological properties. It has a locomotor activity in mice and inhibits the growth of methicillin-resistant Staphylococcus aureus and Mycobacterium tuberculosis. MDMP is an inhibitor molecule that blocks the enzyme DNA polymerase, thereby inhibiting DNA synthesis. This drug also inhibits the production of phosphatidylcholine, which is important for maintaining cell membrane integrity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Iodo-4-methoxybenzaldehyde is a chiral compound that can be synthesized through an intramolecular, stereoselective cyclic annulation reaction. The key step in this process is the arylation of 2-iodo-4-methoxybenzaldehyde with ethyl bromide. This compound can also be synthesized by reacting 2-iodobenzoic acid with formaldehyde in the presence of a base. In addition, 2-Iodo-4-methoxybenzaldehyde can be produced by the sequence of nitrogen substitution and tricyclic annulation.</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>4-Isothiocyanatophenol (4ITCP) is an anticancer agent that has been shown to inhibit the growth of cancer cells in vivo. It is a metabolite of etoposide, which is used to treat certain types of cancer. 4ITCP inhibits the growth of cancer cells by enhancing mitochondrial membrane potential and inhibiting cell proliferation. This compound also inhibits cell growth by binding to phenyl groups on proteins, including enzymes and structural proteins. 4ITCP has been shown to act as a prodrug in vivo, where it is converted into 4-nitrophenol before being activated. 4ITCP also has optical properties that can be detected using spectroscopy and fluorescence.</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>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>Octanenitrile is a colorless liquid with a boiling point of 29.8 °C. It is soluble in water, ether, and chloroform, but insoluble in hexane. Octanenitrile has been shown to have an effect on the phase transition temperature by using deuterium isotopes. This compound can also be used to study the deuterium isotope effect on autoimmune diseases and cancer. The amine group in octanenitrile can be used to synthesize methylamines, one of which is malonic acid. The ph optimum for octanenitrile is 7-8. Octanenitrile reacts with hydrochloric acid to produce hydrogen chloride gas and dipropyl ether (CH3-CH2-O-CH3). Octanenitrile also has intramolecular hydrogen bonding that stabilizes the molecule, reducing activation energies for subsequent reactions such as fatty acid synthesis or polyunsaturated fatty acid synthesis</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxybenzaldehyde oxime is a white solid with a molecular weight of 178.33 and a melting point of 241°C. It has the chemical formula C7H6O3NO2, which consists of a hydrogen atom, two halides, and an oxime group. The molecule is made up of three functional groups: the peroxy group (a hydrogen bond), the alkylating group (an acrylonitrile), and the intramolecular hydrogen bond. 4-Hydroxybenzaldehyde oxime reacts with amines to form β-unsaturated ketones in a mesomorphic state. 4-Hydroxybenzaldehyde oxime is also known to react with peracid to generate peroxy radicals that are used as oxidizing agents in organic synthesis.</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-Chloro-6-hydroxy-7-methylpurine (2CHM) is a betaine that is found in the leaves of the plant Cinchona ledgeriana. It can be obtained by methylation of 2,6-dichloropurine and has been shown to inhibit bacterial growth. The 2CHM isomer shows antibacterial activity against Escherichia coli, Staphylococcus aureus, Streptococcus pyogenes, and Bacillus subtilis. This compound inhibits protein synthesis by binding to DNA or RNA. It also inhibits cell growth by interfering with transcription and translation. The alkali form of CHM is also effective against bacteria as it binds to DNA and affects protein synthesis.</p>

<p>Methyl 2-isothiocyanatobenzoate is a heterocyclic compound that is used as a precursor in the synthesis of many other compounds. It reacts with electrophiles such as hydrogen, chlorine, and bromine to form alkylating agents. Methyl 2-isothiocyanatobenzoate has shown anticancer activity and can be used for the treatment of cancer. This compound is membrane permeable and can cross the blood brain barrier. In addition, methyl 2-isothiocyanatobenzoate is a good substrate for nitroreductases and can be activated by radiation or chloride ions to form an alkylating agent that inhibits DNA synthesis. The magnetic resonance spectroscopy of this compound shows it has a relatively high level of chloride ions.</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>O-Anisidine Hydrochloride is a sulfa drug that belongs to the group of sulfonamides. It inhibits bacterial growth by interfering with the synthesis of folic acid, which is necessary for cell growth. O-Anisidine Hydrochloride has been shown to have genotoxic effects in vitro and in vivo, as well as carcinogenic potential. Studies have also shown that it has synergistic effects when combined with other drugs. Chronic oral administration of o-anisidine hydrochloride can cause long-term toxicity and genotoxicity, including atp levels.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Bromo-2,2-dimethoxypropane is a drug that is used in the synthesis of other compounds. It has been shown to have an inhibitory effect on the reuptake of serotonin, dopamine and norepinephrine by 5-HT1A receptors. This drug may also act as an agonist at β-adrenergic receptors. 1-Bromo-2,2-dimethoxypropane selectively binds to 5-HT1A receptors, leading to increased serotonin levels in the brain.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methylcyclohexanone is an organic compound that is a colorless liquid at room temperature. It is classified as an enolate and has the chemical formula of CH3COCHO. The asymmetric synthesis of 2-methylcyclohexanone can be achieved by adding sodium ethoxide to ethyl formate in the presence of anhydrous sodium. This method produces a 1,3-diketone that can be hydrolyzed to give 2-methylcyclohexanone. Hydrogen bonding interactions between the methyl group and the carbonyl group are important for the stability of this molecule. The solubility data for 2-methylcyclohexanone ranges from 0.015 g/mL at 20 °C to 0.05 g/mL at 100 °C. Activation energies for this molecule range from -2.4 kcal/mol to -1.9 kcal/mol, with a viscosity of 8 cP at</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>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>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>