Building Blocks
Subcategorías de "Building Blocks"
- Ácidos borónicos y derivados del ácido borónico(5.784 productos)
- Building Blocks quirales(1.242 productos)
- Building Blocks de hidrocarburos(6.105 productos)
- Building Blocks orgánicos(61.065 productos)
Se han encontrado 205418 productos de "Building Blocks"
(1R,2S,3R,4R,5S)-Tricyclo[3.2.1.0,2,4]octane-3-carboxylic acid
CAS:Versatile small molecule scaffold
Fórmula:C9H12O2Pureza:Min. 95%Peso molecular:152.19 g/mol2,3-Dihydro-1H-indene-2-carbaldehyde
CAS:2,3-Dihydro-1H-indene-2-carbaldehyde is a bioisostere of the aromatic compound 2,3-dihydrobenzo[b]thiophene. It has been shown to be potent and selective antagonists of the rhodium complex that binds to the topoisomerase I enzyme found in bacteria. The carbonyl group on this molecule is in an active conformation, which makes it a good inhibitor for topoisomerase 1.Fórmula:C10H10OPureza:Min. 95%Peso molecular:146.19 g/mol4-(1,3-Dioxolan-2-yl)-4-methylpentan-1-amine
CAS:Versatile small molecule scaffoldFórmula:C9H19NO2Pureza:Min. 95%Peso molecular:173.25 g/mol1,2-Dimethyl-1H-1,3-benzodiazol-5-ol
CAS:Versatile small molecule scaffoldFórmula:C9H10N2OPureza:Min. 95%Peso molecular:162.19 g/mol1-(Adamantan-1-yl)imidazolidine-2,4,5-trione
CAS:Versatile small molecule scaffoldFórmula:C13H16N2O3Pureza:Min. 95%Peso molecular:248.28 g/mol6-Chloro-3,4-dihydro-1,2,3-benzotriazin-4-one
CAS:6-Chloro-3,4-dihydro-1,2,3-benzotriazin-4-one is a potent anti-inflammatory agent that belongs to the group of organic compounds. It has been shown to be more effective in inhibiting inflammation than other classes of drugs such as nonsteroidal anti-inflammatory agents. 6-Chloro-3,4-dihydro-1,2,3-benzotriazin-4-one also blocks the production of prostaglandins by inhibiting cyclooxygenase and lipoxygenases. This drug is not a nitrite but is converted into one by sodium nitrite in a reaction that releases nitric oxide. Nitric oxide causes vasodilation and inhibits platelet aggregation, which reduces blood clot formation.Fórmula:C7H4ClN3OPureza:Min. 95%Peso molecular:181.58 g/mol3-(Furan-2-yl)-1-methyl-4,5-dihydro-1H-pyrazol-5-one
CAS:Versatile small molecule scaffold
Fórmula:C8H8N2O2Pureza:Min. 95%Peso molecular:164.16 g/mol1,3-Dimethyl 2-phenylpropanedioate
CAS:1,3-Dimethyl 2-phenylpropanedioate is a molecule that is used in the production of malonic acid. The reaction mechanism involves an enzymatic homogenization of the reactants, which leads to the formation of carbonyl oxygens and reaction intermediates. The carbonyl oxygens are then protonated by ethyl diazoacetate to form allyl carbonates. This process occurs in the presence of immobilized enzymes and chemical reactions.Fórmula:C11H12O4Pureza:Min. 95%Peso molecular:208.21 g/molMethyl 2-[(1R,3S)-rel-3-hydroxycyclopentyl]acetate
CAS:Versatile small molecule scaffold
Fórmula:C8H14O3Pureza:Min. 95%Peso molecular:158.19 g/mol3H-Imidazo[4,5-b]pyridine-5,7-diamine dihydrochloride
CAS:Versatile small molecule scaffoldFórmula:C6H8ClN5Pureza:Min. 95%Peso molecular:185.61 g/molN-[3-(Prop-2-en-1-yloxy)phenyl]acetamide
CAS:Versatile small molecule scaffoldFórmula:C11H13NO2Pureza:Min. 95%Peso molecular:191.23 g/mol2-Isocyanato-1-methoxy-2-methylpropane
CAS:Versatile small molecule scaffoldFórmula:C6H11NO2Pureza:Min. 95%Peso molecular:129.2 g/mol1-Ethoxy-2-isocyanato-2-methylpropane
CAS:Versatile small molecule scaffoldFórmula:C7H13NO2Pureza:Min. 95%Peso molecular:143.2 g/mol2-Isocyanato-1-methoxybutane
CAS:Versatile small molecule scaffoldFórmula:C6H11NO2Pureza:Min. 95%Peso molecular:129.2 g/mol4-(Tetrahydro-1,1-dioxido-2H-1,2-thiazin-2-yl)-benzenamine
CAS:Versatile small molecule scaffoldFórmula:C10H14N2O2SPureza:Min. 95%Peso molecular:226.3 g/mol4a-Methyl-decahydroquinoline
CAS:Versatile small molecule scaffoldFórmula:C10H19NPureza:Min. 95%Peso molecular:153.26 g/mol1-Phenylbut-3-en-2-one
CAS:1-Phenylbut-3-en-2-one is an n-oxide that is the product of the reaction between 2,4,6-trinitrobenzenesulfonic acid and phenylacetic acid. It has been used as a horticultural agent for controlling mildew on plants. It has also been shown to have a potent inhibitory effect against cell growth in vitro at doses of 50 μmol/L. 1-Phenylbut-3-en-2-one will react with chlorine atoms in the environment to form chlorinated derivatives that may be more toxic than the parent compound. 1Phenylbut-3-en-2-one has neuroprotective properties and has been shown to reduce the incidence of cancer in rats by inhibiting carcinogenesis studies. This drug also exhibits antiangiogenic properties, which may be due to its inhibition of DNA synthesis and protein synthesis.
Fórmula:C10H10OPureza:Min. 95%Peso molecular:146.19 g/mol2,2-Dimethoxycyclobutane-1-carbonitrile
CAS:Versatile small molecule scaffoldFórmula:C7H11NO2Pureza:Min. 95%Peso molecular:141.2 g/mol5-(Morpholin-4-yl)-1,2,3,4-tetrahydropyrimidine-2,4-dione
CAS:Versatile small molecule scaffoldFórmula:C8H11N3O3Pureza:Min. 95%Peso molecular:197.19 g/mol5-(Trifluoromethyl)-1,3,4-thiadiazole-2-thiol
CAS:Versatile small molecule scaffold
Fórmula:C3HF3N2S2Pureza:Min. 95%Peso molecular:186.18 g/mol
