Building Blocks

<p>Etoricoxib is a nonsteroidal anti-inflammatory drug that is marketed for the relief of osteoarthritis and rheumatoid arthritis. Etoricoxib is an inhibitor of cyclooxygenase-2, which is involved in the inflammatory response. It also inhibits the activity of lipoxygenases, which are enzymes that oxidize fatty acids to form leukotrienes. Etoricoxib has been found to be a potent inhibitor of cytochrome P450 (CYP) 2C9, CYP2C19, CYP2D6 and CYP3A4. Etoricoxib was also found to bind to DNA in calf thymus tissue with high affinity. This binding may inhibit transcription or replication.</p>

<p>Isoxazolo[5,4-c]pyridin-3-amine is an inhibitor of fatty acid amide hydrolase (FAAH), a metabolic enzyme that catalyzes the hydrolysis of the endogenous fatty acid amides. This inhibition results in increased levels of endocannabinoids, which are known to reduce pain and inflammation. Isoxazolo[5,4-c]pyridin-3-amine has been shown to be effective against a number of FAAH inhibitors, including other inhibitors such as URB597 and JZL184. These compounds have also been shown to produce analgesic effects in mice by inhibiting the production of proinflammatory cytokines such as tumor necrosis factor α (TNFα) and IL-1β.</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>7-Chloroindoline is a cyclohexanone derivative that has shown in vitro activity against b. subtilis and S. aureus. It has antimicrobial properties and is classified as an antimicrobial agent. 7-Chloroindoline has been shown to inhibit the growth of bacteria by binding to their DNA, preventing RNA synthesis and protein production. The mechanism of action is similar to the other cyclohexanones, but the antimicrobial properties are not as potent. 7-Chloroindoline also shows antifungal activity against Candida albicans, Coccidioides immitis, and Cryptococcus neoformans.</p>

<p>Versatile small molecule scaffold</p>

<p>Paliperidone is an antipsychotic drug that belongs to the group of thiophenylpiperazines. It is used in the treatment of schizophrenia and bipolar disorder, as well as in the prevention of psychosis in people with a history of such disorders. Paliperidone has been shown to be effective for treating psychotic symptoms in children. This drug is also effective for preventing cancer by inhibiting cell growth and inducing apoptosis. Paliperidone has been shown to have long-term safety and low toxicity levels, with no increase in the risk of death or cancer.</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>2-Amino-4-bromopyridin-3-ol is an organometallic compound that is synthesized from benzyl alcohol and 2-chloro-5 nitrobenzaldehyde. It has a molecular weight of 263.2 g/mol and a melting point of 171 degrees Celsius. The compound has been observed as a white crystalline powder with a melting point range of 119 to 173 degrees Celsius. The compound exhibits electron microscopy morphology, which is spherical in shape with a size range of 1 to 10 nm. 2-Amino-4 bromopyridin-3-ol has been shown to be selective for the benzyl alcohol substrate, yielding high yields of up to 98%.</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>2-Bromo-alpha-methylbenzyl alcohol is a chiral molecule that has two enantiomers, which are mirror images of each other. The (S)-(+)-enantiomer is the active form and the (R)-(-)-enantiomer has no biological activity. 2-Bromo-alpha-methylbenzyl alcohol can be hydrogenated to form (+) -2-bromo-alpha-methylbenzaldehyde, which is an allylic compound with a conjugate diastereomeric relationship to it. This means that the two enantiomers have different chemical properties because they are structurally related in a way that does not allow for rotation about a single bond. The (S)-(+)-enantiomer of 2-bromo-alpha-methylbenzyl alcohol exhibits high affinity for phosphorus ligands, while the (R)-(-)-enantiomer has no affinity.</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>Temozolomide is an organic compound with a nitro group at the 8-position. It is used as a cytotoxic agent to treat cancer. Temozolomide has been shown to yield high yields of up to 98% when synthesized in acidic conditions, such as hydrochloric acid and methyl isocyanate. This compound can also be synthesized in basic ph conditions using carbamate chemistry. The sensitivity of this compound to nitrophenyl, nitrite, and chloride can be used to determine its purity. Organic synthesis of temozolomide requires an understanding of organic chemistry principles and the use of basic laboratory equipment such as a vacuum pump, a glassware set, and a drying oven.</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>Cyclohexyl 2-aminoacetate hydrochloride is a phosphodiesterase inhibitor that belongs to the group of cyclic amp inhibitors. It is an optical isomer and its structure includes a pyrrolidinyl, sulfur, alkoxy group, and cycloalkyl ring. Cyclohexyl 2-aminoacetate hydrochloride has been shown to have inotropic effects in animals by increasing the force of contraction of the heart. It has also been found to be antithrombotic in animals with experimentally induced thrombosis. Cyclohexyl 2-aminoacetate hydrochloride can be used as an optical isomer for the production of other compounds with similar structures.</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>