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>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-Triazol-4-ylbenzoic acid is a bifunctional molecule that can be used to activate carboxylate groups. 4-Triazol-4-ylbenzoic acid contains chloride and nitrogen atoms, which are necessary for the chemical stability of the compound. This molecule has been shown to have luminescence properties in the presence of various metals and metal ions, such as copper and silver ions. 4-Triazol-4-ylbenzoic acid is also stable in basic solutions due to its basic structure. The crystal x-ray diffraction of this molecule shows that it has a linker that can bind with water molecules and form an H2O tetramer.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Iodobut-3-enoic acid is a nitro compound that is used for the synthesis of various organic compounds. It has been shown to be a versatile reagent in organic synthesis and can be used in both cross-coupling reactions and nucleophilic substitution reactions. 3-Iodobut-3-enoic acid may be used as a precursor to synthesize other nitro compounds, such as 1,1'-dinitrobenzene or 1,2,4-trinitrobenzene. This reagent is also useful for the preparation of halogenated aromatic compounds. 3-Iodobut-3-enoic acid has been shown to be an effective functional group modifier for palladium catalysis, due to its ability to bind strongly to palladium metal and form stable complexes with other ligands.</p>

<p>Versatile small molecule scaffold</p>

<p>Tert-butyl 4-chloro-3-nitrobenzoate is a molecule inhibitor that binds to the active site of peroxidase. Tert-butyl 4-chloro-3-nitrobenzoate has been shown to have an anti-cancer effect on cancer cells by inhibiting the production of reactive oxygen species and reducing their proliferation. The drug also inhibits the activity of kinases, which are enzymes that regulate cell division. Tert-butyl 4-chloro-3-nitrobenzoate has been shown to be clinically effective for the treatment of myocardial infarction in rats.</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>(2R,3S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid is a peptide that can be synthesized on the solid phase. It has been shown to have an adsorption mechanism that is similar to that of natural peptides. This compound has conformational and structural homology with other peptides, such as l-amino acids and threonine. The glycopeptide is a glycosylated molecule with an α-(1→6)-linked glucose at the nonterminal amino group.</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-[4-(Difluoromethoxy)phenyl]-4,4,4-trifluorobutane-1,3-dione is a trichloroacetic acid derivative that has been used as a catalyst in acylation reactions. It is also a hydrogen bond donor and can be used to form amides from chloroformates. The structural analysis of 1-[4-(Difluoromethoxy)phenyl]-4,4,4-trifluorobutane-1,3-dione shows that it contains an intramolecular hydrogen bond between the carbonyl group and the amide nitrogen atom. This compound also has a kinetic isotope effect due to the presence of deuterium atoms. The NMR spectra of this compound show signals at δ 2.8 ppm and δ 3.5 ppm corresponding to the two protonated nitrogen atoms.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 4-(3-(difluoromethoxy)phenyl)-2,4-dioxobutanoate (MDE) is a hydrogen-bonding acid methyl ester that can be synthesized from 3,4-dihydroxybenzaldehyde and 2,4-dimethoxyphenylacetic acid. MDE has significant cytotoxicity in cultured cells and causes death of neurons. It also has antiinflammatory activity and can be used as a therapeutic agent for bowel disease. MDE is a picolinic acid analog. Picolinic acid is an antagonist of the N-methyl d-aspartate receptor (NMDA), which may contribute to its neuroprotective effects. The analytical method for MDE was developed by Etoac Extract Company in Japan with the help of other companies like Tokyo Chemical Industry Company Ltd., Sumitomo Chemical Co., Ltd., and Showa Denko KK.</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>

<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>tert-Butyl 2-chloronicotinate is an activated synthetic molecule that activates the nucleophile of an amide or a proton. It has been shown to be a biomimetic and can be used in catalysis. Activation of tert-Butyl 2-chloronicotinate is accomplished by a nucleophilic attack on the carbonyl carbon atom, followed by proton transfer from the leaving group to the electrophilic carbon atom. The tertiary butyl group of this compound is activated as a nucleophile and is capable of transferring its proton to either an amide or a proton. The chloro substituent on tert-Butyl 2-chloronicotinate can also act as a ligand for metal ions, which facilitates catalytic reactions.</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-(3,4-Dimethylbenzenesulfonamido)butanoic acid is a synthetic amino acid that has been shown to inhibit receptor-mediated activation of ion channels. It has also been shown to inhibit the binding of ligands and activators to receptors. This chemical was used in research as a tool for studying protein interactions, ion channels, and cell biology. 4-(3,4-Dimethylbenzenesulfonamido)butanoic acid has CAS number 857041-67-9 and can be used as a reagent for life science research.</p>

<p>Versatile small molecule scaffold</p>