2-Aminoadenosine, obtained by silylation-amination from guanosine, is readily converted by KNO2/ HF/Pyridine in up to 80% yield into 2-fluoradenosine, which is a convenient starting material for the preparation of 9(beta-D-arabinafulanosyl)-2-fluoroadenine 5'-phosphate (Fludara). N-6,N-6-Pentamethylene-2-aminoadenosine, and guanosine afford likewise the corresponding 2-fluoropurine nucleosides in high yields.
[EN] METHODS OF QUANTIFYING METHYLGLYOXAL-INDUCED NUCLEIC ACID ADDUCTS<br/>[FR] PROCÉDÉS DE QUANTIFICATION D'ADDUITS À L'ACIDE NUCLÉIQUE INDUITS PAR LE MÉTHYLGLYOXAL
申请人:HOPE CITY
公开号:WO2019152728A1
公开(公告)日:2019-08-08
Methods of quantifying a N 2 -(1-carboxyethyl)-2'-deoxyguanosine (CEdG) and N 2 -(1-carboxyethyl)-guanosine (CEG) levels in biological samples and comparing those levels to known normal levels can diagnose a number of metabolic disorders or complications associated therewith, including diabetes, its associated complications, and cancer. Methods can also determine whether therapies for disorders are effective by measuring CEdG and CEG levels before and after treatment. Measurement of CEdG and CEG levels is achieved by using liquid chromatography electrospray ionization tandem mass spectrometry.
The present invention provides oligomers which are specifically hybridizable with a selected sequence of RNA or DNA wherein at least one of the nucleoside moieties of the oligomer is modified to include a guanidinium group. These oligomers are useful for diagnostic, therapeutic and investigative purposes.
Aminooxy functionalized oligomers, oligomer arrays and methods of using them
申请人:——
公开号:US20030113769A1
公开(公告)日:2003-06-19
The present invention provides oligomers which are specifically hybridizable with a selected sequence of RNA or DNA wherein at least one of the nucleoside moieties of the oligomer is modified to include an aminooxy linkage. These oligomers are useful for diagnostic, therapeutic and investigative purposes.
[EN] NEW METHOD OF PREPARING 2-FLUOROPURINE DERIVATIVES
申请人:SCHERING AKTIENGESELLSCHAFT
公开号:WO1993011144A1
公开(公告)日:1993-06-10
(DE) Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung von 2-Fluorpurin-Derivaten aus 2-Aminopurin-Derivaten, die in HF/Pyridin oder HF/Pyridin/H2O in Gegenwart eines Nitrits umgesetzt werden.(EN) The invention concerns a method for the preparation of 2-fluoropurine derivatives from 2-aminopurine derivatives which are transformed into HF/pyridine or HF/pyridine/H2O in the presence of a nitrite.(FR) L'invention concerne un procédé de fabrication de dérivés de la 2-fluoropurine à partir de dérivés de la 2-aminopurine, par transformation en HF/pyridine ou HF/pyridine/H2O, en présence d'un nitrite.
(DE) 本发明涉及一种制备2-Fluoropurin-Derivates的方法,从2-Aminopurin-Derivates制备,后者在HF/Pyridin或HF/Pyridin/H2O条件下,当受硝酸盐转化时。
(EN) The invention concerns a method for the preparation of 2-fluoropurine derivatives from 2-aminopurine derivatives which are transformed into HF/pyridine or HF/pyridine/H2O in the presence of a nitrite.
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NEUES VERFAHREN ZUR HERSTELLUNG VON 2-FLUORPURIN-DERIVATEN