Notes

Undesirable situations report associated with inactivated COVID-19 vaccine coming from 4040 health-related personnel.
The formation pathway of the two types of chars is related to both dehydration and aromatization; decarboxylation also occurs in char formation during SCWG. Humus was proved to be related to char formation during the SCWG of SS based on experimental results obtained with the model compound. This work provides insights needed to guide follow-up treatments or utilization of the char produced during the SCWG of SS.Enriched in phosphorus, sewage sludge ash has been extensively studied and applied as a secondary source for phosphorus recovery. Wet extraction, especially acid washing, is one of the most feasible methods to recover phosphorus from the ash due to its ease of operation, high efficiency and low cost. However, the management of the resultant acid residue was seldom addressed. In this study, special focus was paid to the reuse and recycling of the acid residue by an alkaline activation method. Its adsorption performance towards four different heavy metals in aqueous solutions was evaluated by batch and fixed-bed column adsorption experiments. The obtained material showed a high BET specific area (98.29 m2/g) and a total pore volume (0.114 cm3/g), and effectively removed Cd(II), Cu(II), Pb(II) and Zn(II) from aqueous solutions with the maximum adsorption capacity of around 26.8, 22.2, 53.3 and 13.5 mg/g respectively. It could be loaded in a fixed-bed column to continuously remove heavy metals especially for Pb(II). The proposed method to recycle the acid residue makes the wet extraction methods designing to recover phosphorus from incinerated sewage sludge complete without the generation of waste, which contributes to circular economy and a sustainable future.Although pyrolysis is a promising way for treating animal manure, the application is restricted with some limitations of biochar. To improve the quality of biochar derived from swine manure and enhance the immobilization of heavy metals (Cu and Zn) in it, swine manure was mixed with four types of Ca-based additives (CaO, CaCO3, Ca(OH)2, and Ca(H2PO4)2) prior to pyrolysis at 300-700 °C. The thermogravimetric characteristics of swine manure were obviously influenced The addition of CaO, CaCO3, and Ca(OH)2 during the whole decomposition process. Furthermore, with the addition of CaO and Ca(OH)2, the emission of CO2 and CO was substantially decreased at 200-500 °C, whereas the formation of CO, H2, CO2, and CH4 was drastically increased at 600-800 °C. The biochar produced with CaO addition had the highest pH, surface area and carbon content. Moreover, by addition of Ca-based additives, except for Ca(H2PO4)2, the transformation of labile Cu and Zn to the stable fraction was promoted, and the leachability and environmental risk of them were simultaneously reduced. In contrast, CaO and Ca(OH)2 were more favorable for the immobilization of Cu and Zn than CaCO3. Our study indicated that the catalytic pyrolysis using CaO was an effective and valuable method of animal manure treatment.The synthesis of a new set of triazole bisphosphonates 8a-d and 9a-d presenting an alkyl or phenyl substituent at the C-4 or C-5 position of the triazole ring is described. These compounds have been evaluated for their antiproliferative activity against MIA PaCa-2 (pancreas), MDA-MB-231 (breast) and A549 (lung) human tumor cell lines. Liproxstatin-1 mw 4-hexyl- and 4-octyltriazole bisphosphonates 8b-c both displayed remarkable antiproliferative activities with IC50 values in the micromolar range (0.75-2.4 μM) and were approximately 4 to 12-fold more potent than zoledronate. Moreover, compound 8b inhibits geranylgeranyl pyrophosphate biosynthesis in MIA PaCa-2 cells which ultimately led to tumor cells death.We report herein the synthesis of a series of novel quinoline derivatives, based on the lead compound 1a, identified from a rRSV-mGFP high-throughput screening assay. Our results revealed that target compounds 1b, 1g-h, 1af and 1ah (IC50 = 3.10-6.93 μM) had good in vitro activity against RSV, which were better than 1a and ribavirin. In addition, we found that compound 1g displayed the lower cytotoxicity (CC50 2490.33 μM) and the highest selective index (SI = 673.06), suggesting its promising potential as a candidate for further development. On the other hand, compounds 1a, 1m, 1v, 1ad-1af and 1ah-1ai (IC50s 1.87-14.28 μM) were more active against IAV than or comparable to ribavirin (IC50 15.36 ± 0.93 μM). Particularly, the most active compound 1ae (IC50 1.87 ± 0.58 μM) was found to be 8.2-fold more potent than the reference drug, which could inhibit the virus transcription and replication cycle at an early stage.The Ser/Thr kinase CK2, a member of the superfamily of eukaryotic protein kinases, has an acidophilic substrate profile with the substrate recognition sequence S/T-D/E-X-D/E, and it is inhibited by polyanionic substances like heparin. The latter, a highly sulphated glucosamino glycan composed mainly of repeating 2-O-sulpho-α-l-idopyranuronic acid/N,O6-disulpho-α-d-glucosamine disaccharide units, is the longest known substrate-competitive CK2 inhibitor. The structural basis of CK2's preference for anionic substrates and substrate-competitive inhibitors is only vaguely known which limits the value of the substrate-binding region for the structure-based development of CK2 bisubstrate inhibitors. Here, a tetragonal and a monoclinic co-crystal structure of CK2α, the catalytic subunit of CK2, with a decameric heparin fragment are described. In the tetragonal structure, the heparin molecule binds to the polybasic stretch at the beginning of CK2α's helix αC, whereas in the monoclinic structure it occupies the central substrate-recognition region around the P+1 loop. Together, the structures rationalize the inhibitory efficacy of heparin fragments as a function of chain length. The monoclinic CK2α/heparin structure, in which the heparin fragment is particularly well defined, is the first CK2 structure with an anionic inhibitor of considerable size at the central part of the substrate-recognition site. The bound heparin fragment is so close to the binding site of ATP-competitive inhibitors that it can guide the design of linkers and pave the way to efficient CK2 bisubstrate inhibitors in the future.
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