Building Blocks

Versatile small molecule scaffold

Phthaloyl-L-alanine is a molecule with a hydrochloric acid group and a carbonyl group. It has been shown to have the ability to bind to peptidyl molecules and immobilize them, leading to an inhibition of the reaction mechanism. This process can be induced by enzymatic inactivation or by hydrogen bonding with chloride. The cisplatin-induced apoptosis of cancer cells has been demonstrated using patch-clamp technique on human erythrocytes. Caspases are proteins that are activated during apoptosis and have been found to interact with Phthaloyl-L-alanine in vitro. Molecular modeling studies suggest that Phthaloyl-L-alanine may inhibit caspases by binding to the enzyme's active site.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

3-Amino-N-phenylpropanamide is a synthetic chemical that has been used as an optical sensor to detect the presence of β-glucosidase. It reacts with β-glucosidase, which hydrolyses 3-amino-N-phenylpropanamide to produce colorless products. The reaction is detected by a change in the optical properties of the substrate, which can be observed using a colorimetric assay or an enzymatic hydrolysis assay. This product was synthesised from 3 amino N phenyl propanamide and trifluoroacetic acid (TFA) salt, which is hydrolysed by β-glucosidase to form the sodium salt of 3 amino N phenyl propanoic acid and acetic acid.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Perfluoroheptanoyl chloride is a fluorinated hydrocarbon that is used as a surfactant in detergent compositions. It has been shown to be biostable, which means it does not react with other molecules in the environment. This compound also has low environmental toxicity because of its resistance to peroxidation and its ability to form stable complexes with metals. Perfluoroheptanoyl chloride has been shown to cause allergic reactions in some people and may cause adverse effects on animal health. Research on the effects of perfluoroheptanoyl chloride on Xenopus oocytes has demonstrated that this compound can affect gene expression and result in cell death.

2-Fluoro-4,5-dimethoxybenzoic acid is a fluorinated electrophilic side-chain oxazoline. It is synthesized by lithiation of 2,4,5-trimethoxybenzaldehyde followed by oxidation with hydrogen peroxide and reductive cleavage with sodium borohydride. The fluorination of the 2-position of the benzoic acid moiety provides a convenient method for preparing fluorinated analogues that are resistant to degradation.

Versatile small molecule scaffold

3-Methylbutanimidamide hydrochloride (3MBAM) is a quaternary ammonium salt that is used primarily in the treatment of tuberculosis. It inhibits the biosynthesis of mycolic acids, which are important for the growth and survival of Mycobacterium tuberculosis. 3MBAM binds to the enzyme ATPase, which is essential for energy production and cell division. 3MBAM also has strong inhibitory activity against various strains of Mycobacterium tuberculosis resistant to other drugs. 3MBAM is metabolized by hydrolysis, forming formamide and methylsulfonyl chloride in the liver.

(1R,2S)-Boc-Achc is a versatile research chemical that belongs to the class of carboxylic acids. It is a bifunctional scaffold that can be used as a building block in various chemical reactions and synthesis processes. The compound, also known as (1R,2S)-2-tert-Butoxycarbonylamino-cyclohexanecarboxylic acid, is an aliphatic carboxylic acid with a N-Boc amino acid group attached. (1R,2S)-Boc-Achc serves as a valuable tool for scientists and researchers in the field of organic chemistry. Its unique structure and properties make it suitable for the development of new compounds and drug candidates. It can be used as a starting material or intermediate in the synthesis of pharmaceuticals, agrochemicals, and other bioactive molecules. With its Boc protecting group, (1R,2S)-Boc

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2-N-Ethylpyridine-2,3-diamine is a small molecule inhibitor that binds to the ATP binding site of HIV reverse transcriptase and inhibits its activity. It has been shown to inhibit the proliferation of human tumor cells in culture. This compound also prevents the formation of new virus particles and leads to a decrease in viral load. 2-N-Ethylpyridine-2,3-diamine does not bind to the same site as nevirapine, but instead binds to a different amino acid residue on the reverse transcriptase enzyme called Y181C. Residues at this location are found in all HIV strains resistant to nevirapine.

Versatile small molecule scaffold

Versatile small molecule scaffold

4-Chloro-1-methylquinolin-2(1H)-one is a molecule with analgesic activity. It has been shown to produce analgesia in the rat tail flick and hot plate tests, as well as anti-nociceptive effects in the mouse formalin test. The analgesic effect of 4-chloro-1-methylquinolin-2(1H)-one is thought to be due to its ability to inhibit the release of excitatory neurotransmitters from peripheral sensory neurons. This molecule has also been shown to have anti-inflammatory properties and is an intermediate for the synthesis of other drugs, such as diclofenac sodium.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Methyl 3-methanesulfonamidobenzoate is an organic compound that is used as a reagent in organic synthesis. It has the chemical formula CH3O2C(CH2)2SO2CH=NOH. Methyl 3-methanesulfonamidobenzoate is a methyl ester of benzoic acid, which is also known as methyl benzoate. This compound has been shown to react with DNA, forming adducts with guanine and cytosine bases.

Versatile small molecule scaffold