Carboxylic Acids

<p>Please enquire for more information about 4-Chloro-3,5-difluorobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Eltrombopag olamine is an orally active drug that belongs to the class of thiazolidinones. It has been used for the treatment of thrombocytopenia in patients with chronic liver disease and myelodysplastic syndrome. Eltrombopag olamine inhibits platelet aggregation by binding to glycoprotein IIb/IIIa receptors on the surface of platelets. The drug is a prodrug that is metabolized in vivo to its active form, eltrombopag. This conversion is catalysed by CYP3A4 and CYP2D6 enzymes and can be inhibited by drugs that inhibit these enzymes, such as trifluoroacetic acid and hydroxyl group-containing compounds. Eltrombopag olamine binds to erythrocytes, which may be due to its ability to form intramolecular hydrogen bonds with nitrogen atoms. The synthesis of elt</p>

<p>Please enquire for more information about tert-Butyl 4-(2-bromophenyl)piperazine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-L-aspartic acid 4-tert-butyl ester is a synthetic aminoacylase that is used in the synthesis of ergosterol. It is an efficient and economical reagent for the preparation of esters of aspartic acid, which are used in fungal antifungal agents. Boc-L-aspartic acid 4-tert-butyl ester has been shown to have various physiological functions, including the ability to inhibit ergosterol synthesis by inhibiting the enzyme polymeric ergosterol synthase in fungi. This compound can also be used to synthesize n-substituted aspartates.</p>

<p>2-Bromo-2-(4-bromophenyl)-2,2'-dimethylacetic acid (2bpd) is the sodium salt of 2-(4-bromophenyl)-2,2'-dimethylacetic acid. It is a metabolite of terfenadine and thionyl chloride. 2bpd has been shown to be an inhibitor of the histamine H1 receptor. This drug is also a brominated derivative of 2-amino-2-methyl-1-propanol, which has been shown to be an inhibitor of the histamine H1 receptor.</p>

<p>2-Thiazoleacetic acid is a heterocyclic compound that can bind to iron and is an efficient ligand for the virus. It has been used as a linker in the synthesis of biologically active methylene compounds. 2-Thiazoleacetic acid also has anti-inflammatory properties and is used to treat inflammatory diseases. The compound reacts with hydrochloric acid, forming an acetic acid derivative. This reaction is catalyzed by metal ions such as Fe2+ or Hg2+. 2-Thiazoleacetic acid can be synthesized from two molecules of formaldehyde, two molecules of hydrogen cyanide, and two molecules of hydroxamic acids.</p>

<p>Please enquire for more information about (trans)-2-Cyclopropylvinylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-amino[1,1'-biphenyl]-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(tert-Butoxycarbonyl)-4-methylpiperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Timapiprant is an amide that acts as a selective inhibitor of the prostanoid receptor CRTH2, which is involved in regulating the inflammatory response. Timapiprant inhibits skin eosinophilia, which is associated with inflammatory skin diseases such as atopic dermatitis and psoriasis. It has been shown to be safe in clinical trials and has a good safety profile. The drug's mechanism of action may be due to its ability to inhibit the production of IL-4 and IL-13 by Th2 cells and its ability to inhibit lung function. Timapiprant has shown efficacy in treating allergic rhinitis, asthma, chronic obstructive pulmonary disease, erythema multiforme, pyoderma gangrenosum, and other types of inflammatory skin diseases.</p>

<p>4-(2-Oxopyrrolidin-1-yl)benzoic acid (4-OPBA) is a hydrogen bonding inhibitor that is used to study the interactions of cavity proteins. It has shown to interact with glutathione and prostaglandin D2, which are important for hematopoietic and inflammatory responses. 4-OPBA has been observed to bind with a water molecule in the cavity, which may explain its affinity for these molecular targets. The crystal structure of 4-OPBA shows that it forms an interaction with two water molecules and one other molecule in the cavity. This may be due to its ability to form hydrogen bonds with both water molecules as well as the molecule in the cavity.</p>

<p>4-(Ethoxycarbonyl)phenylboronic acid is a potential use for picric acid detection. It has been shown to be a chemosensor with an electrochemical impedance spectroscopy response that is sensitive to chloride ions. 4-(Ethoxycarbonyl)phenylboronic acid can be used as a linker in multigram-scale synthesis of aryl halides, and its reaction mechanism has been elucidated by crystal x-ray diffraction. The synthesis of this compound is scalable and involves the formation of an apical carboxylate from ethoxycarbonyl phenyl boronic acid and an aryl halide.</p>

<p>Please enquire for more information about 1-tert-Butyl 3-methyl pyrrolidine-1,3-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Keto-7a,12a-dihydroxy-5a-cholanic acid is a steroid hormone that is synthesized from cholesterol. It is one of the major hormones involved in the regulation of the menstrual cycle and ovulation. The levels of this hormone increase during ovulation, with maximal concentration occurring at midcycle. 3-Keto-7a,12a-dihydroxy-5a-cholanic acid is converted by enzymes into estradiol and testosterone. 3-Keto-7a,12a-dihydroxy-5a-cholanic acid may also be involved in regulating peptide hormones and pheromones.</p>

<p>Please enquire for more information about tert-Butyl 4,7-diazaspiro[2.5]octane-7-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(3a,5b,12a)-3,12-Dihydroxy-7-oxocholan-24-oic acid methyl ester is an organic compound that belongs to the family of bile acids. It is synthesized in the liver by a series of reactions involving the conversion of cholesterol. The synthesis of this compound has been studied by x-ray analysis on single crystals and by various electron diffraction methods. This study revealed that the molecule is electron deficient and binds well to chloroform. (3a,5b,12a)-3,12-Dihydroxy-7-oxocholan-24-oic acid methyl ester has also been shown to have a constant molecular weight with a molecular formula of C37H64O4.</p>

<p>Please enquire for more information about Diethyl 1-[2-(1H-indol-3-yl)ethyl]-2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-Bromo-5,6-dihydro-8h-imidazo[1,2-a]pyrazine-7-carboxylic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 4-chloroacetoacetate is a neutral compound that reacts with hydrochloric acid to produce a salt, chloromethyl acetate. The reaction solution is then heated to evaporate the water and produce an organic solution. This reaction produces a molecular model of the compound, which has potent antibacterial activity against gram-positive and gram-negative bacteria.</p>

<p>Boc-L-aspartic acid a-9-fluorenylmethyl ester is a synthetic compound that mimics the structure of acetylcholine. It has been shown to be an efficient method for generating pseudopeptides and cyclic peptides. This compound may be used as a surrogate for acetylcholine in virus research, since it can bind to the same receptor. Boc-L-aspartic acid a-9-fluorenylmethyl ester has also been used to generate monoclonal antibodies that are neutralizing against foot-and-mouth disease viruses.</p>