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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-[(1,1-Dioxo-1,2-benzothiazol-3-yl)amino]butanoic acid is a ligand of the nicotinic acetylcholine receptor (nAChR). It has been shown to inhibit or activate nAChRs depending on the receptor subtype. 4-[(1,1-Dioxo-1,2-benzothiazol-3-yl)amino]butanoic acid has also been shown to be an effective inhibitor of the sodium channel. 4-[(1,1-Dioxo-1,2-benzothiazol-3-yl)amino]butanoic acid is a peptide with a molecular weight of 269.30 Da and purity greater than 99%. This compound is a research tool that can be used as an antibody for cell biology and immunology experiments.</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>8-Chloroquinoline-3-carboxylic acid is an industrial chemical that is used as a pharmaceutical. It is also an antibacterial agent that has been shown to be effective against sulfite-reducing bacteria, such as Clostridium difficile and Helicobacter pylori. This drug inhibits bacterial growth by damaging the cell membrane and preventing the production of essential proteins for DNA replication. 8-Chloroquinoline-3-carboxylic acid is produced by treating quinoline with chlorination, followed by reaction with sulfuryl chloride or quinoline carboxylic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-oxo-1,4-Dihydroquinoline-3-carbonitrile (4ODQ) is a synthetic compound that is acidic in nature. It hydrolyzes in acidic conditions to form a carboxylic acid and ammonia. 4ODQ can also react with amines to form azides, chloride to form chloramines, methyl anthranilate to form piperidines, trifluoride to form triflates, and morpholine to form morpholines. The chemical structure of 4ODQ consists of an anthranilate moiety which has been decarboxylated and an amine group which has been enaminated.<br>4ODQ inhibits the growth of cancer cells by binding to the ATP binding site on the enzyme kinase B (BRAF), thereby preventing phosphorylation of downstream proteins that are involved in cell proliferation. This inhibition leads to apoptosis or programmed cell death.</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-Methoxy-5-methylbenzene-1,3-dicarbaldehyde (MMDA) is a reactive molecule that has been used for cross linking and insolubilizing polymers. It is an important intermediate in the synthesis of methyl methacrylate, which is used in the production of acrylic adhesives and coatings. 2-Methoxy-5-methylbenzene-1,3-dicarbaldehyde can be used as a monomer or comonomer to produce polymers with various functionalities. This molecule undergoes bifunctional reactions with acceptor molecules such as phenols, amines and alcohols. 2-Methoxy-5-methylbenzene-1,3-dicarbaldehyde reacts with triplet oxygen to form singlet oxygen. This reaction results in the formation of reactive radicals that can cause oxidation reactions on the acceptor molecule. Monitoring this process is possible through monitoring the accept</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>5-Amino-1,3-dihydroxymethylbenzene is a ligand that binds to acetyl coenzyme A. It has been used in the cross-coupling of aryl halides with alkyl or aryl Grignard reagents. 5-Amino-1,3-dihydroxymethylbenzene is recycled and used as a ligand in reaction conditions that are not compatible with other ligands. The efficiency of this method is dependent on the use of magnetic nanoparticles for separation and filtering. 5-Amino-1,3-dihydroxymethylbenzene can be linked to diphosphine ligands by heating and stirring in order to create an efficient catalyst system.</p>