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>(5S)-5-(Propan-2-yl)pyrrolidin-2-one is a vinyl compound that is used in the production of polyvinyl acetate. It is produced by transesterification of vinyl acetate and ethylene oxide, followed by hydrolysis of the ester group. The reaction proceeds via an enzymatic process, which is initiated by lipases.br&gt;<br>(5S)-5-(Propan-2-yl)pyrrolidin-2-one can be converted to other compounds through a number of chemical reactions. For example, it can be oxidized to (5S)-5-(propane-2,3-dione)pyrrolidine with hydrogen peroxide or sodium hypochlorite. It also reacts with potassium permanganate to form (5S)-5-(propane-1,3 diol)pyrrolidine and manganese dioxide to form (5S</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-[(1H-Benzimidazol-1-yl)methyl]benzoic acid is an ionic compound. The anion has a focus with a radius of 2.6 Å and the cation has a radius of 1.9 Å. It is stable in aqueous solution and reacts with chloride to form the salt 4-[(1H-Benzimidazol-1-yl)methyl]benzoyl chloride, which is colorless, crystalline, and soluble in water. This compound can be used for analyzing ligands that bind to lanthanide ions (e.g., lanthanum). The analyzes of frameworks have been carried out by single crystal x-ray diffraction methods and fluorescence spectroscopy parameters are given in Table 1.</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-Chloro-5-ethynylthiophene (2CET) is a x-ray crystal structure that exhibits potent adenosine receptor antagonist activity. 2CET binds to the adenosine receptor in a noncompetitive manner and blocks the receptor, preventing the activation of G proteins. The binding of 2CET to the adenosine receptor leads to an increase in adenine nucleotide levels, which may contribute to its antihypertensive properties. 2CET has also been shown to be a potent agonist at A1 and A2A receptors. It was found that 2CET bound with high affinity to both receptors, but only activated A1 receptors. This indicates that 2CET is capable of stimulating cAMP production without activating other G protein coupled receptors such as angiotensin II type 1 or muscarinic acetylcholine receptors.</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-Chloro-4-methyl-5,6,7,8-tetrahydroquinoline is an organic compound that belongs to the heterocyclic category of x-ray crystallography. It was prepared in a single crystal form using perchlorate as a solvent. The anisotropic nature of 2-Chloro-4-methyl-5,6,7,8-tetrahydroquinoline has been shown through x-ray diffraction and x ray diffraction analysis.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(2-Methoxypyridin-4-yl)ethanone inhibits 5-lipoxygenase, the enzyme that converts arachidonic acid to leukotrienes. It is a non-selective inhibitor of cyclooxygenases (COXs) 1 and 2 which are responsible for the metabolism of arachidonic acid to prostaglandins. COXs are inhibited by aspirin and other nonsteroidal antiinflammatory drugs (NSAIDs). NSAIDs inhibit both COXs and can be classified as selective or nonselective based on their selectivity for COX-1 vs. COX-2. Celecoxib is a selective inhibitor of COX-2.<br>COX enzymes can be classified into two groups based on the range over which they are active: μm range or nm range. The μm range includes COX-1, COX-3, and PTGS2 and these enzymes regulate the</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>Aminopyrrolidine dihydrochloride (APDC) is a fluorescent dye that is used as an absorber in nuclear magnetic resonance spectroscopy. It has been shown to bind to the adenosine receptor and may be used to study the effect of this receptor on heart function. APDC has also been shown to inhibit the binding of quinolinium, pyridinium, and benzoate ligands to their respective receptors, which may be due to its linker group. The molecule is unsymmetrical and organic, with two absorbing groups.</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>Please enquire for more information about (1R,5R)-2-Azabicyclo[3.2.0]heptane hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</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-(Methylsulfonyl)benzyl alcohol is a synthetic molecule that modulates bone resorption by selectively binding to estrogen receptors. It is an orally active, non-steroidal compound that can be used for the treatment of osteoporosis and other conditions associated with bone loss. 2-(Methylsulfonyl)benzyl alcohol has been shown to have a high affinity for estrogen receptors and may also inhibit the production of prostaglandins in the brain, which are involved in Alzheimer's disease. The structure-based drug design approach was employed for optimization of this molecule.</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>6-Ethynylbenzo[d]thiazole is an inhibitor of the kinase ALK5, which is a receptor for growth factor-β. This inhibition prevents the phosphorylation of the receptor and subsequent activation of downstream signaling pathways. 6-Ethynylbenzo[d]thiazole also inhibits other kinases such as TGF-β and activin. 6-Ethynylbenzo[d]thiazole has been shown to inhibit cellular proliferation in vitro by inhibiting the activity of enzymes that play a role in cell division. The compound has demonstrated inhibitory activity against a number of cell lines, including human cells and tumor cells derived from human cancer patients.</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>