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Cysteine proteases Cp are widely distributed
2020-08-04
Cysteine proteases (Cp) are widely distributed among living organisms, found in both prokaryotes and eukaryotes (e.g. bacteria, parasites, plants, invertebrates and vertebrates) [13], [14]. The catalytic mechanism of these pretomanid receptor involves a cysteine group in the active site. Cp compris
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The excitatory amino acid L
2020-08-04
The excitatory amino Amphotericin B L-glutamate or glutamate mediates most of the excitatory neurotransmission within the mammalian central nervous system (CNS) and has been implicated in numerous peripheral nervous system (PNS) pathways. The excitatory amino acids, including glutamate, are of great
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The CYP A structure manifest larger active site and
2020-08-04
The CYP3A4 structure manifest larger active site and a closely existing large solvent channel to facilitate oxidation of larger or multiple substrate. This solvent channel is formed by interaction among tyrosine (Y-53), aspartic CJ-42794 (D-61), aspartic acid (D-76), arginine (R-106), arginine (R-37
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Collectively our structures offer novel structural insights
2020-08-04
Collectively, our structures offer novel structural insights into the action of diverse CRTH2 antagonists, which will facilitate CRTH2 drug development for a number of inflammatory diseases, including asthma. They also reveal interesting features of the ligand binding pocket and suggest a novel mech
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mst1 kinase A priori CK might influence the level
2020-08-04
A priori, CK2 might influence the level of HSP27 either by affecting its stability or by modulating the transcription of its gene. However, taking into account that in C2C12 HSP27 is selectively regulated by CK2 while other HSPs, namely HSP70, HSP90 and HSP105, are not (see Fig. 1a), and that these
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According to the study by Frasco et
2020-08-04
According to the study by Frasco et al. (2005) metals tend to chemically react with the products resulting from the main reaction of the Ellman’s method. This a major interference of such methodology, and these interferences by metals are difficult to identify and/or quantify. From all tested metals
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br Conflict of interest br Acknowledgements This work was su
2020-08-04
Conflict of interest Acknowledgements This work was supported by Breast Cancer Research Foundation for the MNU/rat study and spheroid experiment and Lynn Sage Cancer Research Foundation for the DMBA/mouse study. The authors would like to thank Repros Therapeutics, Inc., and HRA-Pharma (Paris,
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The relationship of DDR expression to tumor aggressiveness o
2020-08-04
The relationship of DDR1 wst-1 sale to tumor aggressiveness or patient outcome has been investigated for other types of cancer, but these other investigations have typically only considered expression of tDDR1 protein. For example, Quan et al. reported that the DDR1 protein was highly expressed in
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It was hypothesized that if modafinil acts primarily
2020-08-04
It was hypothesized that if modafinil acts primarily via a noradrenergic mechanism, Dbh −/− mice should be non-responsive since they completely lack NE. In contrast, if modafinil acts mainly through DA systems, these mice should be hypersensitive. Modafinil was tested in Dbh −/− mice using both loco
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br The central role of DNA PK
2020-08-04
The central role of DNA-PK in non-homologous end-joining repair DNA DSBs are considered the most cytotoxic type of DNA lesion. DNA DSBs result from endogenous events such as V(D)J recombination and the production of reactive oxygen species (ROS) during cellular metabolism, as well as from exogeno
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The recent crystal structure of human DNA ligase I complexed
2020-08-04
The recent crystal structure of human DNA ligase I complexed with a nicked substrate depicts the modular organization of this enzyme, in which three conserved domains, DNA binding (DBD) adenylation (AD) and oligonucleotide/oligosaccharide binding fold (OB), encircle a nicked DNA [9]. The adenylation
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GBM cells are also highly resistant to
2020-08-04
GBM cells are also highly resistant to the anticancer deoxyribonucleoside analog gemcitabine [2,2′-difluorodeoxycytidine (dFdC)]. Interestingly, the cytotoxicity of dFdC was markedly enhanced in human GBM cell lines and ALDH+ CSCs when administered in combination with the specific ALDH inhibitor tet
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Anti inflammatory effects of two coumarins
2020-08-03
Anti-inflammatory effects of two coumarins, columbianetin 27 and libanoridin 28 isolated from Corydalis heterocarpa in lipopolysaccharide (LPS)-stimulated HT-29 human colon carcinoma akt pathway were studied by Kang et al., further 28 inhibited the protein expression levels of inflammatory mediator
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Further tested compounds linarin pectolinarin
2020-08-03
Further tested compounds linarin (11), pectolinarin (11a), erigeroside (13), 6″-caffeoylerigeroside (13a) and chlorogenic YM201636 (14) had very weak effect (IC50 values over 40 μM) on CK2 activity independently from the used substrate and examined subunit. To assess the mechanism by which the fla
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Recently pharmacological studies have revealed that natural
2020-08-03
Recently, pharmacological studies have revealed that natural compounds achieve increasing attention due to its high therapeutic effectiveness and low adverse effect, compared with the chemically synthesized compounds. Emodin is a kind of natural anthraquinone derivative enriched in traditional Chin
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