Some examples of the diverse research done by chemistry experts include discovery of new medicines and vaccines, improving understanding of environmental issues, and development of new chemical products and materials. 1631-25-0, Name is N-Cyclohexylmaleimide, molecular formula is C10H13NO2, Reference of 1631-25-0, belongs to naphthyridine compound, is a common compound. In a patnet, author is Ohkubo, Akihiro, once mentioned the new application about 1631-25-0.
A triplex-forming oligonucleotide (TFO) can recognize the homopurine-homopyrimidine sequence in DNA duplexes and inhibit the transcription of targeted mRNAs. Recently, we reported that N-acetyl-2,7-diamino-1,8-naphthyridine (N-DA(ac)), incorporated into a TFO, has high binding ability and base recognition selectivity for the pyrimidine bases in the purine-rich chain of the DNA duplex at pH 7.4. However, it was found in this study that the difference in the T-m values between the pyrimidine bases and purine bases decreased by more than 4 degrees C at pH 6.0-7.0. To improve the low base recognition selectivity of the TFO, we designed a new artificial base, (DA)Q(ac), with a quinoline skeleton. The T-m values of the triplexes containing (DA)Q(ac):T-A or (DA)Q(ac):C-G were more than 13 degrees C higher than those of the triplexes containing (DA)Q(ac):A-T or (DA)Q(ac):G-C at pH 7.4. We also observed that under more acidic conditions (pH 6.0-7.0), the base recognition selectivity of DAQac in a triplex was higher than that of N-DA(ac), although the binding ability of (DA)Q(ac) in a triplex was similar to that of N-DA(ac). Additionally, we found that (DA)Q(ac), incorporated into the TFO, could accurately recognize the C-Me-G base pair in the hairpin DNA, similar to the C-G base pair.
Reference of 1631-25-0, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 1631-25-0.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem