Building Blocks
Sottocategorie di "Building Blocks"
- Acidi boronici e derivati dell'acido boronico(5.780 prodotti)
- Building Blocks Chirali(1.241 prodotti)
- Building Blocks Idrocarburici(6.100 prodotti)
- Building Blocks organici(61.017 prodotti)
Trovati 205265 prodotti di "Building Blocks"
2-[(4-Fluorophenyl)methyl]oxirane
CAS:Versatile small molecule scaffold
Formula:C9H9FOPurezza:Min. 95%Peso molecolare:152.16 g/molPropan-2-yl (2S)-2-amino-3-methylbutanoate
CAS:Propan-2-yl (2S)-2-amino-3-methylbutanoate is an amino acid derivative that is used as a chiral auxiliary. The compound has been used in the synthesis of amides, esters, and other amine products. It has also been used in the preparation of enantiomerically pure protonated amines. Propan-2-yl (2S)-2-amino-3-methylbutanoate can be used as a chiral auxiliary in chromatographic techniques to separate racemic mixtures into their enantiomers. This compound is mesomorphic at low temperatures and becomes isotropic at higher temperatures. Propan-2-yl (2S)-2-amino-3-methylbutanoate is also soluble in solvents with different polarities, such as water and chloroform, and has a molecular weight of 158.25 g/mol.Formula:C8H17NO2Purezza:Min. 95%Peso molecolare:159.23 g/mol4-Isocyanato-2-methoxy-1-methylbenzene
CAS:Versatile small molecule scaffold
Formula:C9H9NO2Purezza:Min. 95%Peso molecolare:163.17 g/mol2-(1-Methyl-1H-pyrrol-2-yl)ethan-1-ol
CAS:Versatile small molecule scaffold
Formula:C7H11NOPurezza:Min. 95%Peso molecolare:125.17 g/mol2-[3,5-Dimethoxy-4-(propan-2-yloxy)phenyl]ethan-1-amine hydrochloride
CAS:Prodotto controllatoVersatile small molecule scaffoldFormula:C13H22ClNO3Purezza:Min. 95%Peso molecolare:275.77 g/mol2-(3,5-Dimethoxy-4-propoxyphenyl)ethan-1-amine hydrochloride
CAS:Prodotto controllatoVersatile small molecule scaffold
Formula:C13H22ClNO3Purezza:Min. 95%Peso molecolare:275.77 g/molcis-4-methoxy-cyclohexylamine hcl
CAS:Versatile small molecule scaffold
Formula:C7H16ClNOPurezza:Min. 95%Peso molecolare:165.66 g/molEthyl 4-methyl-5-oxopyrrolidine-3-carboxylate
CAS:Versatile small molecule scaffold
Formula:C8H13NO3Purezza:Min. 95%Peso molecolare:171.19 g/mol4-(Difluoromethyl)-1-fluoro-2-nitrobenzene
CAS:Versatile small molecule scaffold
Formula:C7H4F3NO2Purezza:Min. 95%Peso molecolare:191.11 g/mol4-(4-Chlorophenyl)-2-hydrazino-1,3-thiazole
CAS:Versatile small molecule scaffold
Formula:C9H8ClN3SPurezza:Min. 95%Peso molecolare:225.7 g/mol3-Hydroxy-4-propoxybenzaldehyde
CAS:3-Hydroxy-4-propoxybenzaldehyde is a metabolically stable inhibitor of the enzyme, phenylalanine 4-hydroxylase. 3HPA inhibits the production of phenolic compounds and reduces the risk of cancer. It has been shown to be potently active against human leukemia cells in vitro, but less active against other cell lines. 3HPA is also selective for tumor cells, which may be due to its ability to inhibit DNA synthesis by preventing the formation of n-substituted benzylamino compounds. 3HPA stabilizes DNA and RNA synthesis, which may help prevent tumor growth.
Formula:C10H12O3Purezza:Min. 95%Peso molecolare:180.2 g/mol2-(Pyridin-2-yl)pyrimidin-4-amine
CAS:2-(Pyridin-2-yl)pyrimidin-4-amine (PPPA) is an antimicrobial agent that is used in the treatment of bacterial infections. It binds to the chloride ion in the cell wall and prevents the formation of a functional pore, causing leakage of cellular contents. PPPA reacts with cyanamide to form 2-(pyridin-2-yl)pyrimidin-4(1H)-one (PPPOH), which is more reactive than PPPA. The reactivity of PPPOH causes damage to the cell's cytoplasmic membrane, leading to cell death. PPPA also reacts with nitro, alkynyl, and alkylaminoalkyl groups, as well as carboxy, cyano, and alkenyl groups on proteins and amino acids. PPPA hydrolyzes phenoxy and cyclohexane rings found in some antibiotics such as tetracycline.
Formula:C9H8N4Purezza:Min. 95%Peso molecolare:172.19 g/mol4-Ethyl-1,2-dihydroquinolin-2-one
CAS:Versatile small molecule scaffold
Formula:C11H11NOPurezza:Min. 95%Peso molecolare:173.21 g/mol3-bromo-5-methylthiophene-2-carboxylic acid
CAS:3-Bromo-5-methylthiophene-2-carboxylic acid (3BMT) is a drug that inhibits the enzyme succinate dehydrogenase. Succinate dehydrogenase is an enzyme that catalyzes the conversion of succinate to fumarate in the citric acid cycle, which is a series of biochemical reactions in cellular respiration. 3BMT prevents the formation of acetyl coenzyme A, which is needed for the production of energy in cells. This drug also has a pyrrole moiety that can be oxidized by difluoromethylating it and then reacting with pyrrole to form 2,4-dichloropyrimidine. 3BMT has been shown to inhibit carboxamides such as L-aspartate oxidase and glutamate decarboxylase.
Formula:C6H5BrO2SPurezza:Min. 95%Peso molecolare:221.1 g/mol2-Hydroxy-3-methoxy-4-nitrobenzoic acid
CAS:Versatile small molecule scaffoldFormula:C8H7NO6Purezza:Min. 95%Peso molecolare:213.14 g/mol4H,5H,6H,7H,8H-Furo[3,2-c]azepin-4-one
CAS:Versatile small molecule scaffold
Formula:C8H9NO2Purezza:Min. 95%Peso molecolare:151.16 g/mol1-(Naphthalen-2-ylmethyl)piperazine
CAS:Versatile small molecule scaffold
Formula:C15H18N2Purezza:Min. 95%Peso molecolare:226.32 g/mol3-Methoxy-6-methyl-1,2,4-triazine
CAS:Versatile small molecule scaffold
Formula:C5H7N3OPurezza:Min. 95%Peso molecolare:125.13 g/mol2-(3-chlorophenyl)morpholine
CAS:Versatile small molecule scaffold
Formula:C10H12ClNOPurezza:Min. 95%Peso molecolare:197.66 g/molMethyl 2-[(2-hydroxyethyl)sulfanyl]acetate
CAS:Versatile small molecule scaffold
Formula:C5H10O3SPurezza:Min. 95%Peso molecolare:150.2 g/mol
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