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>2-(Hydroxymethyl)benzaldehyde (2HB) is a reactive aldehyde that is used as a cancer drug. It binds to the receptor in the cell membrane and inhibits fatty acid synthesis, which prevents cell division. 2HB has been shown to inhibit tumor growth by inhibiting chemokines, proteins that act as chemoattractants for immune cells. 2HB also inhibits the growth of cultured leukemia cells through crosslinking of DNA. This reaction can be enhanced by UV light, resulting in covalent bonds between adjacent nucleotides. The reaction mechanism for this process is called metathesis reactions.</p>

<p>4-(Furan-2-yl)pyridine is a heterocyclic organic compound that belongs to the group of pyridines. It has been shown to have strong cleavage reactions, which are enhanced by factors such as structural factors and the presence of a pyridine ring. The most common fragmentation reaction is the ionization of the furan ring, followed by dissociation of electron pairs from the furyl rings. This causes alkyl groups to be formed with n-propyl and alkyl groups. 4-(Furan-2-yl)pyridine can also undergo rearrangement reactions involving these groups, leading to formation of a new molecule with an additional carbon atom at one end.</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>Ethyl cyclohex-2-ene-1-carboxylate is an organic compound that is used as an analgesic, antiarrhythmic, and neuroleptic. It belongs to the group of esters and has a nitrogen atom in its structure. Ethyl cyclohex-2-ene-1-carboxylate was first synthesized by the reaction of ethyl bromide with 2-cyclohexenone. The molecule has two hydroxyalkyl groups, which are esters of alcohols. The two alkenyl groups are arranged cis to each other, which gives it a planar shape. Ethyl cyclohex-2-ene-1-carboxylate contains a heterocyclic system composed of a six membered ring containing three carbon atoms and three oxygen atoms.</p>

<p>N-Carbamyl-DL-α-amino-N-butyric acid is a reactive monocarboxylic acid that is found in fatty acids. It can be converted into an enantiomer, which has the same chemical formula but a different arrangement of atoms. This conversion can be achieved by reacting it with an alcohol and a base or an acid. N-Carbamyl-DL-α-amino-N-butyric acid reacts with glufosinate ammonium to form reaction products that are toxic to plants.</p>

<p>2-(Carbamoylamino)pentanoic acid is a monoclonal antibody that can be used as a diagnostic agent. It inhibits the proliferation of cancer cells by binding to the malic acid receptor, which is overexpressed on prostate cancer cells. This antibody has been shown to have an inhibitory effect on cell proliferation in vivo, but does not interfere with the function of other cells. 2-(Carbamoylamino)pentanoic acid also binds to antibodies and has shown a detection time of 4 hours in vivo. 2-(Carbamoylamino)pentanoic acid has been shown to bind to malic acid in vitro and can be used for the diagnosis of prostate cancer.</p>