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A straightforward synthetic pathway was adopted
2024-01-04

A straightforward synthetic pathway was adopted to synthesize the target compounds as outlined in . The starting chloromethylquinazolinones (–) were synthesized from anthranilic Agarose GPG/LMP low melt in two steps following reported procedures., , , The first step involves chloroacetylation of a
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Although several studies indicate that ALDH
2024-01-04

Although several studies indicate that ALDH2 protects the heart from injury and maladaptive remodeling (reviewed in [11], [12], [13]), accumulating evidence indicates that deficiency of the enzyme could be protective as well. For example, mice expressing the defective Aldh2*2 mutation show lower ald
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Y-27632 There has been growing interest over computational m
2024-01-04

There has been growing interest over computational methods to predict the biological activity by chemical structure, so as to decide whether it Y-27632 has objective qualities or not. In this contribution, the well-known method, which is called quantitative structure–activity relationship (QSAR) [13
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MafB a member of the Maf protein family is
2024-01-04

MafB, a member of the Maf protein family, is essential for terminal differentiation of macrophages (Kelly et al., 2000). The phagocytic activity of polystyrene beads was found to be enhanced in SKF38393 HCl with exogenous expression of MafB (Tillmanns et al., 2007). However, in alveolar macrophages
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Our current knowledge on autophagy broadly differentiates
2024-01-04

Our current knowledge on autophagy broadly differentiates it into three types: macroautophagy, microautophagy, and chaperone-mediated autophagy. Macroautophagy mainly involves the sequestration of cytoplasmic contents in a double-walled membrane followed by the fusion with the lysosomes. The lysosom
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In summary this report demonstrates another successful appli
2024-01-03

In summary, this report demonstrates another successful application of gene editing in iPSCs. Despite the lack of efficient metabolic functional repair after transplantation, the application of gene correction into HLCs might still be a realistic goal for ex vivo gene therapy of liver diseases with
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abk br Materials and methods br Results and discussion br Co
2024-01-03

Materials and methods Results and discussion Conclusion The preparation of acrylic nanoparticles as aminosugar carriers could not be achieved by direct functionalization of poly(t-butyl acrylate) particles with saccharide groups. A four-step procedure starting from a protected derivative of
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Finally intracrine androgen synthesis metabolism
2024-01-03

Finally, intracrine androgen synthesis/metabolism can be activated thus allowing 5(S),6(R)-7-trihydroxymethyl Heptanoate receptor to bypass the low levels of androgens in the circulation by producing androgens themselves (Cai and Balk, 2011, Rahman et al., 2004). Moreover, changes in AR co-regulato
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br Role of AMPK in
2024-01-03

Role of AMPK in inflammation signaling Pro-inflammatory cytokines, such as interleukin (IL)-6 and tumor necrosis factor-α (TNF-α), activate Ikβ kinase (IKKβ), which phosphorylates IκBα, triggering the degradation of proteasomal IκB. This liberates active nuclear factor kB (NF-kB) to translocate i
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br Materials and methods br Results br Discussion We have
2024-01-03

Materials and methods Results Discussion We have in this study used semi-nested degenerative PCR to identify the lipoxygenases expressed in the lung tissue from M. fascicularis and report on the identification of 5- and 12/15-LO transcripts from this tissue. Although we did not find transcr
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br Aldehyde sensors to monitor
2024-01-03

Aldehyde sensors to monitor substrate levels Previous efforts to ameliorate metabolic diseases frequently relied on biochemical methods which could measure the levels of toxic substrates in dpp-4 inhibitors or bodily fluids (blood and serum or plasma, urine, cerebrospinal fluid). Therapeutic eff
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During the course of our ACK inhibitor program a high
2024-01-03

During the course of our ACK1 inhibitor program, a high-throughput screening (HTS) campaign of our internal sample collection was conducted. A series of -aryl pyrimidine-5-carboxamides of the general structure () was identified. Earlier studies of the structure–activity relationship (SAR) of ident
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Anti LT therapy by LO inhibition
2024-01-02

Anti-LT therapy by 5-LO inhibition has been hampered by occurring liver toxicities by Zileuton or the clinical phase II compound Atreleuton [36], [37] However both compounds possess a thiophene as well as an N-hydroxyurea moiety. These features could be linked with reactive thiophene intermediates [
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dpp-4 inhibitors br Introduction The principal pathways of a
2024-01-02

Introduction The principal pathways of adrenal and gonadal steroidogenesis have been known for over 50 years (reviewed by Miller and Auchus, 2011). Cholesterol is first converted to pregnenolone via three reactions, 20-hydroxylation, 22-hydroxylation and scission of the 20,22 carbon–carbon bond,
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Western blot results showed that the
2024-01-02

Western blot results showed that the expressions of SOCS1 and SOCS3 significantly increased after administration of rGas6 24h after MCAO (Fig. 7A–C p Discussion After ischemic stroke, inflammation has been shown to be an important secondary injury mediator in patients, as well as in animals (Herz
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