Sucres du squelette et nucléobases

Cy5 Tyramide, a red dye, amplifies signals in HRP-based immunoassays and nucleic acid hybridization.

CY3-SE: reactive dye for amino-groups in proteins, peptides, DNA. Excitation: 555 nm, Emission: 570 nm.

Please enquire for more information about 9-(2-O-Acetyl-5-O-benzoyl-3-deoxy-3-alpha-C-methyl-beta-D-ribofuranosyl)-6-chloro-9H-purine including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-n-Heptylmercaptopurine is a liquid crystal that has imbricated moieties and pyranosides. It can undergo phase transitions from the isotropic to the mesophase state. 6-n-Heptylmercaptopurine is thermotropic, which means it changes its temperature with respect to the temperature of its surroundings. 6-n-Heptylmercaptopurine is also a bilayer, long chain molecule and it has a monoclinic crystal structure. It is also intercalated in DNA, which may be due to its purine structure.

Purine analog; fluorescent probe; kinase inhibitor; mutagenic

Stability Unstable at Room Temperature Applications 7-Methyl-6-thioguanosine Chloride is a compound useful in organic synthesis.

5-Fluoro-2',3'-Dideoxy-3'-Fluorouridine (FdFO) is a nucleoside analog that inhibits the synthesis of thymine and leads to the production of uracil. FdFO is not metabolized by the liver and can be used for the treatment of hepatitis. FdFO has been shown to inhibit HIV replication in cell cultures. It binds to the noncompetitive site on DNA polymerase, preventing RNA synthesis and inhibiting DNA replication. 5-Fluoro-2',3'-Dideoxy-3'-Fluorouridine also acts as a competitive inhibitor against deoxyuridylate, which is needed in order to form thymidylate.

6-Fluorothymine is a fluorine-containing compound that is a structural analogue of thymine. It is an antiviral agent and a precursor to other drugs, such as benzoylated 6-fluoropurines. The chemical yields are high, with the use of refluxing conditions. 6-Fluorothymine has structural similarities to amines and can be synthesized by reacting primary amines with fluorine gas at elevated temperatures. 6-Fluorothymine also has vibrational frequencies in the range of infrared light, which can be used for identification purposes.