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                             209 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A comprehensive review of synthetic strategies and SAR studies for the discovery of PfDHODH inhibitors as antimalarial agents. Part 2: Non-DSM compounds Sharma, Manmohan

153 C p.
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2 A dual-state emission luminogen for lipid droplet imaging and photodynamic therapy Lei, Yu

153 C p.
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3 Advances in designing ternary complexes: Integrating in-silico and biochemical methods for PROTAC optimisation in target protein degradation Shaik, Shareef

153 C p.
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4 Advances in drug discovery of flavivirus NS2B-NS3pro serine protease inhibitors for the treatment of Dengue, Zika, and West Nile viruses João, Emílio Emílio

153 C p.
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5 A FRET probe based on flavonol-benzothiazole for the detection of viscosity and SO2 derivatives Xiao, Wei

153 C p.
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6 A mini review of supramolecular antagonists based on macrocyclic host compounds Li, Shanshan

153 C p.
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7 2-Aminobenzothiazole based adjuvant of polymyxin E against Gram-negative bacteria Chen, Yuce

153 C p.
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8 Amino polycarboxylic acids-modified abiraterone derivatives as potential injectable anti-prostate cancer agents Zhu, Na

153 C p.
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9 Analysis of the effects of differently charged peptides on α-amylase and their interaction mechanisms Yang, Xiaoyu

153 C p.
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10 An intramolecular charge transfer based fluorescent probe for imaging of OCl– Sun, Shu-tao

153 C p.
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11 A NIR fluorescent probe based on tricyanofuran for the detection of β-galactosidase in living ovarian tumor cells and in vivo Jiang, Wen

153 C p.
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12 Antibacterial and antibiofilm agents in the group of xanthone derivatives with piperazine moiety active against drug-resistant Helicobacter pylori strains Żelaszczyk, Dorota

153 C p.
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13 Anticancer and Antibacterial Activeness of Fused Pyrimidines: Newfangled Updates Bhatnagar, Ayushi

153 C p.
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14 Anticancer and anti-inflammatory effects of novel ethyl pyrazole derivatives having sulfonamide terminal moiety Abdel-Maksoud, Mohammed S.

153 C p.
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15 Anti-inflammatory bicyclic polyprenylated acylphloroglucinols with diverse architectures including an unprecedented 6/6/6 tricyclic core from Garcinia yunnanensis Hu, Xin-Yue

153 C p.
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16 Apigenin analogs as α-glucosidase inhibitors: Molecular docking, biochemical, enzyme kinetic, and an in vivo mouse model study Liu, Honghui

153 C p.
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17 A potent Bioorganic azapodophyllotoxin derivative Suppresses tumor Progression in Triple negative breast Cancer: An Insight into its Inhibitory effect on tubulin polymerization and Disruptive effect on microtubule assembly Gupta, Smruti

153 C p.
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18 Baliosperoid A attenuates lipopolysaccharide-induced acute lung injury by targeting SHP2 to inhibit inflammation and oxidative stress Li, Yue

153 C p.
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19 Benzylpiperidine derivatives as new dual μ-opioid and σ1 receptor ligands with potent antinociceptive effects Li, Zong-Zheng

153 C p.
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20 Biologically active franchetine-type diterpenoid alkaloids: Isolation, synthesis, anti-inflammatory, agalgesic activities, and molecular docking Xiao, Yan

153 C p.
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21 Biosynthesis of plant-derived triterpenoid asiatic acid in Saccharomyces cerevisiae cell factories Lian, Yuhan

153 C p.
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22 Butanolides and clerodane diterpenes from the twigs of Casearia grewiifolia and their effects on adiponectin secretion Nhoek, Piseth

153 C p.
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23 Cannabinoid receptor 2 (CB2) modulators: A patent review (2016–2024) Naikoo, Rayees Ahmad

153 C p.
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24 Chemo-enzymatic synthesis of NPN cofactor taking advantage of ADP-ribosyl cyclase and LarC cyclometallase promiscuous activities Vucko, Timothé

153 C p.
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25 Chlorine containing tetrahydropyrimidines: Synthesis, characterization, anticancer activity and mechanism of action Milović, Emilija

153 C p.
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26 Cholenamide-based, antiviral fluorescent probes targeting oxysterol-binding protein Nigro, Fatima

153 C p.
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27 Chromene-based compounds as drug candidates for renal and bladder cancer therapy – A systematic review Costa Cerqueira, Mónica

153 C p.
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28 Clinical and preclinical advances in PSMA-Directed Antibody-Drug conjugates (ADCs): Current status and hope for the future Mirzaei, Yousef

153 C p.
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29 Clinical applications of small-molecule GABAAR modulators for neurological disorders Chen, Guangyong

153 C p.
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30 Co-based carbon material as CYP3A4-like nanozyme with both biocatalytic activity and inhibition behaviors Wu, Dong

153 C p.
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31 Combining lavendustin C and 5-arylidenethiazolin-4-one-based pharmacophores toward multitarget anticancer hybrids Othman, Shimaa A.

153 C p.
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32 Combretastatin A-4 based compounds as potential anticancer agents: A review Omar, Mai H.

153 C p.
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33 Comprehensive utilization of in silico approach and in vitro experiment to unveil the molecular mechanisms of mono (2-ethylhexyl) phthalate-induced lung adenocarcinoma Wang, Wenwen

153 C p.
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34 Computational Design, Synthesis, and Bioevaluation of 2-(Pyrimidin-4-yl) oxazole-4-carboxamide Derivatives: Dual Inhibition of EGFRWT and EGFRT790M with ADMET Profiling Raghunath Khedkar, Nilesh

153 C p.
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35 Copper(II) aromatic heterocyclic complexes of Gatifloxacin with multi-targeting capabilities for antibacterial therapy and combating antibiotic resistance Wu, Xiao-Yin

153 C p.
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36 Cordycepin alleviates diabetes mellitus-associated hepatic fibrosis by inhibiting SOX9-mediated Wnt/β-catenin signal axis Chen, Shuang

153 C p.
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37 Corrigendum to “Discovery of neuroprotective agents: Potent, brain penetrating, lipoic acid derivatives for the potential treatment of ischemic stroke by regulating oxidative stress and inflammation – A preliminary study” [Bioorg. Chem. 147 (2024) 107339] Zhu, Chenchen

153 C p.
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38 Corrigendum to “Heterocycle-functional steroidal derivatives: Design, synthesis, bioevaluation and SARs of steroidal pyrazolo[1,5-a]pyrimidines as potential ALK inhibitors” [Bioorg. Chem. 153 (2024) 107847] Liu, Fang

153 C p.
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39 Corrigendum to “Synthesis and broad-spectrum biocidal effect of novel gemini quaternary ammonium compounds” [Bioorg Chem. 151 (2024) 107646] Zivna, Natalie

153 C p.
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40 Coumarin-imidazopyridine hybrids and their first-in-class ZnII metal complexes as potent dual entry and replication inhibitors of Zika viral infection Jefferson de Arruda, Henrique

153 C p.
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41 Curcumol derivatives exhibit ameliorating effects on lipopolysaccharide-induced acute lung injury: Synthesis, biological evaluation, structure–activity relationship and action mechanism Li, Gen

153 C p.
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42 Deciphering substrate promiscuity and specificity of indolethylamine N-methyltransferase family enzymes from amphibian toads Zhang, An-An

153 C p.
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43 Design and synthesis of novel mitochondria-targeted ergosterol peroxide derivatives as potential anti-cancer agents Wang, Lu

153 C p.
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44 Design, green synthesis, and anti-glutamate damage screening of chalcone derivatives with spiro-heterocyclic structures as potential anti-ischemic brain and eye damage agents Wu, Jianzhang

153 C p.
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45 Design, synthesis, and antiproliferative activity evaluation of novel α-mangostin derivatives by ROS/MAPK signaling pathway Fredimoses, Mangaladoss

153 C p.
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46 Design, synthesis, and antitumor activity evaluation of 1,2,3-triazole derivatives as potent PD-1/PD-L1 inhibitors Xia, Yu

153 C p.
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47 Design, synthesis and bioactivity evaluation of triazole antifungal drugs with phenylthiophene structure Wu, Xudong

153 C p.
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48 Design, synthesis, and biological evaluation of adenosine derivatives targeting DOT1L and HAT as anti-leukemia agents Sethy, Bidyadhar

153 C p.
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49 Design, synthesis, and biological evaluation of novel AAK1/HDACs dual inhibitors against SARS-CoV-2 entry Mao, Nian-Dong

153 C p.
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50 Design, synthesis, and biological evaluation of novel (E)-2-cyano-3-(4,9-dioxo-4,9-dihydronaphtho[2,3-b]furan-2-yl) derivatives as potent STAT3-targeting anticolorectal cancer agents Jiang, Weiqing

153 C p.
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51 Design, synthesis, and biological evaluation of novel HPK1 inhibitors possessing 3-cyano-quinoline moiety Chen, Long

153 C p.
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52 Design, synthesis, and biological evaluation of novel 5,7,4′-trimethoxyflavone sulfonamide-based derivatives as highly potent inhibitors of LRPPRC/STAT3/CDK1 Wu, Rui

153 C p.
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53 Design, synthesis and biological evaluation of prostate-specific membrane antigen (PSMA)-targeted SIRT2 inhibitors Yu, Junhui

153 C p.
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54 Design, synthesis, and biological evaluation of tetrahydropyrimidine analogue as GSK-3β/Aβ aggregation inhibitor and anti-Alzheimer’s agent Sukanya, Sukanya

153 C p.
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55 Design, synthesis, and evaluation of dual son of sevenless 1 (SOS1) and epidermal growth factor receptor (EGFR) inhibitors for the treatment of cancers Zeng, Yi

153 C p.
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56 Design, synthesis and FXR partial agonistic activity of anthranilic acid derivatives bearing aryloxy moiety as therapeutic agents for metabolic dysfunction-associated steatohepatitis Chen, Cong

153 C p.
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57 Design, synthesis, and in silico insights of novel N’-(2-oxoindolin-3-ylidene)piperidine-4-carbohydrazide derivatives as VEGFR-2 inhibitors Eldehna, Wagdy M.

153 C p.
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58 Design, synthesis and optimization of pyrazolo[3,4-b] pyridine derivatives as Hsp110-STAT3 interaction disruptors for the treatment of pulmonary arterial hypertension Li, Mengqi

153 C p.
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59 Design, synthesis, and structure–activity relationships of xanthine derivatives as broad-spectrum inhibitors of coronavirus replication Chen, Xiaofang

153 C p.
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60 Design, synthesis, biological evaluation study of spirocyclic POM analogues as novel MmpL3 anti-tubercular agent Mi Kim, Young

153 C p.
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61 Design, synthesis, molecular docking, and evaluation of sulfonyl quinazoline analogues as promising liver cancer drugs Venkatesan, Gopalakrishnan

153 C p.
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62 Design, synthesis, molecular modeling and evaluation of 2,4-diaminopyrimidine analogues as promising colorectal cancer drugs Venkatesan, Gopalakrishnan

153 C p.
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63 Developing new anticancer agents: Design, synthesis, biological evaluation and in silico study of several functionalized pyrimidine-5-carbonitriles as small molecules modulators targeting breast cancer Badawi, Waleed A.

153 C p.
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64 Development and preclinical evaluation of a cyclic PET tracer targeting integrin-α6 on colorectal cancer models Chen, Liping

153 C p.
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65 Development of an at-line coupling of LC-QTOF-ESI-MS/MS to steroid 5-alpha reductase inhibition assay, a fast bioactive targeting and guided purification of natural complex sample, Impatiens balsamina Linn. Srivilai, Jukkarin

153 C p.
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66 Development of natural product-based targeted protein degraders as anticancer agents Chen, Cheng

153 C p.
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67 Development of new LSM-83177 analogues as anti-tumor agents against colorectal cancer targeting p53-MDM2 interaction Elgohary, Mohamed K.

153 C p.
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68 Development of novel aza-stilbenes as a new class of selective MAO-B inhibitors for the treatment of Parkinson’s disease Knez, Damijan

153 C p.
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69 Development of novel imipridone derivatives with potent anti-cancer activities as human caseinolytic peptidase P (hClpP) activators Zhang, Yanzhi

153 C p.
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70 Disclosing novel melanogenesis pathways: Formation of unexpected biphenyl-type dimers through radical–radical coupling by solid-state oxidation of the melanin biosynthetic precursor 5,6-dihydroxyindole Viggiano, Sara

153 C p.
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71 Discovery and optimization of novel 4-morpholinothieno[3,2-d]pyrimidine derivatives as potent BET inhibitors for cancer therapy Ran, Kai

153 C p.
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72 Discovery and structure − activity relationships of 2,4,5-trimethoxyphenyl pyrimidine derivatives as selective D5 receptor partial agonists Kumar, Sakesh

153 C p.
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73 Discovery and synthesis of novel glyrrhizin-analogs containing furanoylpiperazine and the activity against myocardial injury in sepsis Li, Wei

153 C p.
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74 Discovery of a Potent, selective and orally bioavailable CDK9 degrader for targeting transcription regulation in Triple-Negative breast cancer Nie, Hui-Jun

153 C p.
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75 Discovery of Daclatasvir as a potential PD-L1 inhibitor from drug repurposing Sun, Mengmeng

153 C p.
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76 Discovery of ent-kaurane diterpenoid glucosides as potent analgesics from the leaves of Pieris formosa Feng, Yuanyuan

153 C p.
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77 Discovery of epigenetic modulators targeting HDACs and EZH2 simultaneously for the treatment of hematological malignancies Zhang, Jinwei

153 C p.
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78 Discovery of flavonoid-containing compound Lupalbigenin as anti-NSCLC cancer agents via suppression of EGFR and ERK1/2 pathway Cuan, Xiangdan

153 C p.
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79 Discovery of N-Benzylpiperidinol derivatives as USP7 inhibitors against Hematology Pan, Youlu

153 C p.
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80 Discovery of new 4-aminoquinoline derivatives containing an amine or hydroxamic acid terminal as multifunctional agents for the treatment of Alzheimer’s disease Zhai, Bochao

153 C p.
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81 Discovery of new molecular hybrid derivatives with coumarin scaffold bearing pyrazole/oxadiazole moieties: Molecular docking, POM analyses, in silico pharmacokinetics and in vitro antimicrobial evaluation with identification of potent antitumor pharmacophore sites Tataringa, Gabriela

153 C p.
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82 Discovery of novel and potent sulfonamide derivatives as orally available drug for psoriasis Qi, Liang

153 C p.
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83 Discovery of novel diaryl urea-oxindole hybrids as BRAF kinase inhibitors targeting BRAF and KRAS mutant cancers Ghannam, Iman A.Y.

153 C p.
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84 Discovery of novel Macrocyclic small molecules Based on 2-Amino-4-thiazolylpyridineas selective EGFR inhibitors with high Blood-Brain barrier penetration for the treatment of glioblastoma Wu, Guowu

153 C p.
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85 Discovery of novel 5-phenyl-1H-pyrrole-2-carboxylic acids as Keap1-Nrf2 inhibitors for acute lung injury treatment Tang, Jiaqin

153 C p.
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86 Discovery of novel 20S proteasome subunit β5 PROTAC degraders as potential therapeutics for pharyngeal carcinoma and Bortezomib-resistant multiple myeloma Wang, Shumei

153 C p.
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87 Discovery of potent hypoxia-inducible factor-1α (HIF-1α) degraders by proteolysis targeting chimera (PROTAC) Li, Yuying

153 C p.
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88 Discovery of the FXR/CES2 dual modulator LE-77 for the treatment of irinotecan-induced delayed diarrhea Cao, Zhijun

153 C p.
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89 DNA and hemoglobin binding activities: Investigation of coumarin-thiosemicarbazone hybrids Çelik, Esra

153 C p.
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90 Eco-conscious synthesis of novel 1,2,4-triazolo[1,5-a]pyrimidine derivatives as potent Anti-microbial agent and comparative study of cell viability and cytotoxicity in HEK-293 cell line utilizingIndian gooseberry (Phyllanthus emblica) fruit extract Bhatt, Bhaktiben R.

153 C p.
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91 Editorial Board
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92 Effect of lathyrane-type diterpenoids in neural stem cell physiology: Microbial transformations, molecular docking and dynamics studies Escobar-Montaño, Felipe

153 C p.
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93 Enabling oral novel Taxanes-based Chemotherapy with Lipophilic prodrug Self-nanoemulsifying drug delivery system Miao, Yifan

153 C p.
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94 Enhancing rhamnolipid production via immobilized Pseudomonas stutzeri lipase: A comparative study Cruz, Guillermo

153 C p.
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95 Evaluation of expanded 2-aminobenzothiazole library as inhibitors of a model histidine kinase and virulence suppressors in Pseudomonas aeruginosa Fihn, Conrad A.

153 C p.
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96 Evaluation of the antifungal activity of novel bis-pyrazole carboxamide derivatives and preliminary investigation of the mechanism Song, Yaping

153 C p.
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97 Exploring fluorinated heptose phosphate analogues as inhibitors of HldA and HldE, key enzymes in the biosynthesis of lipopolysaccharide Cao, Jun

153 C p.
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98 Exploring the antifungal potential of novel carbazate derivatives as promising drug candidates against emerging superbug, Candida auris Fatima, Tazeen

153 C p.
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99 Exploring the selective incorporation of 15β-senecioyloxi-ent-kaurenoic acid methyl ester in Langmuir monolayers mimicking cell membranes da Silva, Gustavo H.O.

153 C p.
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100 Expression of PPAR-γ TF by newly synthesized thiazolidine-2,4-diones to manage glycemic control: Insights from in silico, in vitro and experimental pharmacology in wistar rats Gharge, Shankar

153 C p.
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101 Facile constructed meroterpenoids with novel hexadecahydroacephenanthrylene carbon skeleton using the biotransformation and chemical synthesis method Yan, Die

153 C p.
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102 Filicinic acid based meroterpenoids from Hypericum elodeoides and their anti-Alzheimer’s disease effects Li, Jing-Dian

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103 First dual inhibitors of human topoisomerase IIα and Hsp90 C-terminal domain inhibit the growth of Ewing sarcoma in vitro and in vivo Dernovšek, Jaka

153 C p.
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104 FL118: A potential bladder cancer therapeutic compound targeting H2A.X identified through library screening Fan, Guangrui

153 C p.
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105 Flexible 2,4-diaminopyrimidine bearing a butyrolactone as Plasmodium falciparum dihydrofolate reductase inhibitors Decharuangsilp, Sasithorn

153 C p.
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106 Fluoroquinolones tackling antimicrobial resistance: Rational design, mechanistic insights and comparative analysis of norfloxacin vs ciprofloxacin derivatives Khanna, Aanchal

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107 Functional interplay between short antimicrobial peptides and model lipid membranes Gratino, Lorena

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108 68Ga labeled Olmutinib: Design, synthesis, and evaluation of a novel PET EGFR probe Cheng, Hua

153 C p.
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109 Glycoconjugate coumarins exploiting metabolism-enhanced fluorescence and preferential uptake: New optical tools for tumor cell staining Iacopini, Dalila

153 C p.
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110 Halogenated monopyridinium oximes are less effective in reactivation of phosphylated cholinesterases than bisquaternary oximes Kohoutova, Zuzana

153 C p.
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111 Harnessing potential COX-2 engagement for boosting anticancer activity of substituted 2-mercapto-4(3H)-quinazolinones with promising EGFR/VEGFR-2 inhibitory activities Hamdi, Abdelrahman

153 C p.
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112 5H-benzo[c]fluorene derivative exhibits antiproliferative activity via microtubule destabilization Fatima, Eram

153 C p.
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113 HDAC6 mediates tumorigenesis during mitosis and the development of targeted deactivating agents Peng, Jie

153 C p.
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114 Heterocycle-functional steroidal derivatives: Design, synthesis, bioevaluation and SARs of steroidal pyrazolo[1,5-a]pyrimidines as potential ALK inhibitors Liu, Fang

153 C p.
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115 Hyaluronan and Glucose Dual-targeting Probe: Synthesis and Application Zhang, Henan

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116 Identification of adenosine analogues as nsp14 N7‑methyltransferase inhibitors for treating coronaviruses infection Chen, Qishu

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117 Identification of indole-grafted pyrazolopyrimidine and pyrazolopyridine derivatives as new anti-cancer agents: Synthesis, biological assessments, and molecular modeling insights Eldehna, Wagdy M.

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118 Identification of novel RANKL inhibitors through in silico analysis Jiang, Yingying

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119 Identification of sanguinarine as c-MYC transcription inhibitor through enhancing the G-quadruplex-NM23-H2 interactions Zhong, Li-Ting

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120 Impact of lipidation site on the activity of α-helical antimicrobial peptides Makowska, Marta

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121 Indole-based COX-2 inhibitors: A decade of advances in inflammation, cancer, and Alzheimer’s therapy Shah, Moksh

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122 Interpret the potential role of zinc against oxidative stress in inflammation with a practical fluorescent assay Lin, Zengyan

153 C p.
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123 In vitro and in vivo studies of a decanuclear Ni(II) complex as a potential anti-breast cancer agent Zhu, Haitao

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124 In vitro anti-inflammatory activity and molecular docking of Peperomia pellucida (L.) Kunth extract via the NF-κB and PPAR-γ signalling in human retinal pigment epithelial cells Ho, Keat Lam

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125 In vitro evaluation of promiscuity and toxicity of a small molecule targeting wild and T164I β2-adrenergic receptors Bandaru, Srinivas

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126 Issue TOC
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127 Lipophilic derivatives of EGCG as potent α-amylase and α-glucosidase inhibitors ameliorating oxidative stress and inflammation Kothari, Manan

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128 Medicinal chemistry insights into PRMT5 inhibitors Jiao, Zhihao

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129 Molecular hybridization, synthesis, in vitro α-glucosidase inhibition, in vivo antidiabetic activity and computational studies of isatin based compounds Patil, Sunidhi

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130 Molecular tweaking by generative cheminformatics and ligand–protein structures for rational drug discovery Nangia, Ashwini K.

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131 Multifrequency-STD NMR unveils the first Michaelis complex of an intramolecular trans-sialidase from Ruminococcus gnavus Monaco, Serena

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132 Multiomics-guided mining and characterization of epoxide hydrolase involved in camptothecin biosynthesis from Camptotheca acuminata Pu, Xiang

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133 Muti-target rationale design of novel substituted N-phenyl-2-((6-phenylpyridazin-3-yl)thio)acetamide candidates as telomerase/JAK1/STAT3/TLR4 inhibitors: In vitro and in vivo investigations Shaldam, Moataz A.

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134 1,3-Naphthoxazine derivatives: Synthesis, in silico pharmacokinetic studies, antioxidant and photoprotective properties Pelit, Emel

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135 Naphthyl-functionalized acetamide derivatives: Promising agents for cholinesterase inhibition and antioxidant therapy in Alzheimer’s disease Camargo-Ayala, Lorena

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136 New benzophenone analogs from Nigrospora sphaerica and their inhibitory activity against PD-1/PD-L1 interactions Kuang, Qi-Xuan

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137 New stilbenes from Cajanus cajan inhibit adipogenesis in 3T3-L1 adipocytes through down-regulation of PPARγ Yao, Liyuan

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138 Nigenolides A–H, 13 new microperfuranones with ferroptosis inhibitory activity from the deep-sea-derived Aspergillus niger Zou, Zheng-Biao

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139 Novel benzenesulfonamide derivatives as potential selective carbonic anhydrase IX, XII inhibitors with anti-proliferative activity: Design, synthesis and in silico studies Fadaly, Wael A.A.

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140 “Novel chemo-enzymatic synthesis, structural elucidation and first antiprotozoal activity profiling of the atropoisomeric dimers of trans-8-Hydroxycalamenene” Bassanini, Ivan

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141 Novel co-delivery nanomedicine for photodynamic enlarged immunotherapy by cascade immune activation and efficient Immunosuppression reversion Zhang, Yimei

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142 Novel flavonoid derivatives containing 1,2,4-triazole Schiff bases as potential antifungal agents: design, synthesis, and biological evaluation Meng, Kaini

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143 Novel 5-Fluorouracil analogues versus perfluorophenyl ureas as potent anti-breast cancer agents: Design, robust synthesis, in vitro, molecular docking, pharmacokinetics ADMET analysis and dynamic simulations Sroor, Farid M.

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144 Novel purine derivatives as selective CDK2 inhibitors with potential anticancer activities: Design, synthesis and biological evaluation Shah, Alpesh

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145 Opportunities and challenges for targeting HPK1 in cancer immunotherapy Xu, Jiamei

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146 Optical control of butyrylcholinesterase (BChE) activity via photoswitchable azobenzene for potential treatment of Alzheimer’s disease Wang, Lei

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147 Penisimplinoids A-K, highly oxygenated andrastin-type meroterpenoids with diverse activities from the marine-derived fungus Penicillium simplicissimum Yang, Yanan

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148 Phenylboronic acid-functionalized copper nanoclusters with sensitivity and selectivity for the ratiometric detection of luteolin Hou, Xingyu

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149 Photochemical Metal-Free synthesis and biological Assessment of isocryptolepine analogues targeting estrogen receptor Alpha in breast cancer cells Bogdanov, F.B.

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150 Pin1: Advances in pancreatic cancer therapeutic potential and inhibitors research Wang, Nan

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151 Pleiotropically activation of azaphilone biosynthesis by overexpressing a pathway-specific transcription factor in marine-derived Aspergillus terreus RA2905 Zheng, Yao-Yao

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152 Pomalidomide sensitizes lung cancer cells to TRAIL/CDDP-induced apoptosis via directly targeting electron transfer flavoprotein alpha subunit Li, Liangping

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153 Preclinical evaluation of a new technetium-99m labeled neurotensin analogue for NTSR1 targeted radionuclide imaging Erfani, Mostafa

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154 Probing class I histone deacetylases (HDAC) with proteolysis targeting chimera (PROTAC) for the development of highly potent and selective degraders Ibrahim, Hany S.

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155 Pyrrolo[2,3-d]pyrimidines as potential kinase inhibitors in cancer drug discovery: A critical review Sai Madhurya, Malyala

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156 Quinazoline derivatives inhibit cell growth of prostate cancer as a WRN helicase dependent manner by regulating DNA damage repair and microsatellite instability Yu, Jia

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157 Rational design of new quinoline-benzimidazole scaffold bearing piperazine acetamide derivatives as antidiabetic agents Ghasemi, Mehran

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158 Rationale design and synthesis of new roflumilast analogues as preferential selective and potent PDE-4B inhibitors Moussa, Ahmed M.

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159 Recent advances in the natural product analogues for the treatment of neurodegenerative diseases Zhang, Jinling

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160 Research progress and development strategy of PI3K inhibitors for breast cancer treatment: A review (2016-present) Peng, Rujue

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161 Rhodesain inhibitors on the edge of reversibility-irreversibility Agost-Beltrán, Laura

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162 Rivastigmine structure-based hybrids as potential multi-target anti-Alzheimer’s drug candidates Leuci, Rosalba

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163 Searching for the Holy Grail − Highly Potent Bridged Endoperoxides for Targeted Cancer Therapy Tiwari, Mohit K.

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164 Simplified scalable synthesis of a water-soluble toll-like receptor 2 agonistic lipopeptide adjuvant for use with protein-based viral vaccines Brar, Deshkanwar S.

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165 Simultaneous visualization of lipid droplets and tracking of the endogenous hypochlorous acid in psoriatic mice models with a novel fluorescent probe in a wash-free fashion Zhao, Xuan

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166 Sodium cromoglycate exerts anti-pulmonary fibrosis effects by targeting the Keap1 protein to activate Nrf2 signaling Liu, Xiaofeng

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167 Spatial metabolomics to discover hypertrophic scar relevant metabolic alterations and potential therapeutic strategies: A preliminary study Li, Jingyun

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168 Stereochemical influence of 4ʹ-methyl substitutions on truncated 4ʹ-thioadenosine derivatives: Impact on A3 adenosine receptor binding and antagonism Kim, Minjae

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169 Steroid and bioactive molecule conjugates: Improving therapeutic approaches in disease management Kawka, Anna

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170 Structural characterization and Bacteroides proliferation promotion activity of a novel homogeneous arabinoglucuronoxylan from Commelina communis L. Wang, Xiaojiang

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171 Structurally diverse design and synthesis of novel 2-phenylindole amide derivatives with anti-canine breast cancer activity Wu, Pan

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172 Structurally diverse phenylpropanoyl phloroglucinol derivatives from Mallotus philippensis and their anti-bacterial activities Chen, Yeqi

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173 Structurally diverse triterpenoids with antibacterial activities from Euphorbia humifusa Xia, Ru-Feng

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174 Structure-Based identification of a potent KDM7A inhibitor exerts anticancer activity through transcriptionally reducing MKRN1 in taxol- resistant and -sensitive triple-negative breast cancer cells Shi, Jin-Jin

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175 Sulfonyl-acetohydrazide derivatives as juvenile hormone mimics to be insect growth regulators Kumari, Neetika

153 C p.
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176 Sustainable synthesis of ZnO and FexOy nanoparticles and their nanocomposite ZnFe2O4: Comprehensive characterization and applications in antioxidant activity and antibiotics degradation efficiency Abdullah, Johar Amin Ahmed

153 C p.
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177 Synergy trap for guardian angels of DNA: Unraveling the anticancer potential of phthalazinone-thiosemicarbazone hybrids through dual PARP-1 and TOPO-I inhibition Elkafoury, Eman M.

153 C p.
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178 Synthesis and bioactivity evaluation of glycosylated resveratrol derivatives as antioxidative neuroprotection agents against cerebral Ischemia-Reperfusion injury Xu, Yanning

153 C p.
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179 Synthesis and biological evaluation of a new class of azole urea compounds as Akt inhibitors with promising anticancer activity in pancreatic cancer models Pecoraro, Camilla

153 C p.
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180 Synthesis and evaluation of anticancer activity of new 4,5,6,7-tetrabromo-1H-benzimidazole derivatives Łukowska-Chojnacka, Edyta

153 C p.
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181 Synthesis and immunotherapy efficacy of a PD-L1 small-molecule inhibitor combined with its 131I-iodide labelled isostructural compound Lv, Gaochao

153 C p.
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182 Synthesis and in vitro exploration of the 8-carbo substituted 5-methoxyflavones as anti-breast and anti-lung cancer agents targeting protein kinases (VEGFR-2 & EGFR) Nkoana, Jackson K.

153 C p.
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183 Synthesis and modification of noscapine derivatives as promising future anticancer agents Nemati, Faezeh

153 C p.
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184 Synthesis and structural proof of novel oxazolo[5,4-d]pyrimidine derivatives as potential VEGFR2 inhibitors. In vitro study of their anticancer activity Sochacka-Ćwikła, Aleksandra

153 C p.
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185 Synthesis of 5-hydroxyisatin thiosemicarbazones, spectroscopic investigation, protein-ligand docking, and in vitro anticancer activity Chaudhary, Upendra

153 C p.
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186 Synthesis of 3-hydroxy-4-pyridinone hexadentate chelators, and biophysical evaluation of their affinity towards lipid bilayers Vinhas, Sílvia

153 C p.
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187 Synthesis of novel 1,2,3-triazole-tethered N-acyl hydrazones as a new class of carbonic anhydrase II inhibitors: In vitro and in silico potentials Fatima, Noor

153 C p.
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188 Synthesis of S-alkylated oxadiazole bearing imidazo[2,1-b]thiazole derivatives targeting breast cancer: In vitro cytotoxic evaluation and in vivo radioactive tracing studies Mohammed, Eman R.

153 C p.
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189 Synthesis, structural modification, and biological activity of a novel bisindole alkaloid iheyamine A Guo, Xin

153 C p.
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190 Synthetic biology of metabolic cycles for Enhanced CO2 capture and Sequestration Dowaidar, Moataz

153 C p.
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191 Targeting JNK kinase inhibitors via molecular docking: A promising strategy to address tumorigenesis and drug resistance Alkafaas, Samar Sami

153 C p.
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192 Tetrahydrocarbazoles incorporating 5-arylidene-4-thiazolinones as potential antileukemia and antilymphoma targeting tyrosine kinase and tubulin polymerase enzymes: Design, synthesis, structural, biological and molecular docking studies Ali, Basma S.

153 C p.
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193 The pivotal role of histidine 976 in human histone deacetylase 4 for enzyme function and ligand recognition Schweipert, Markus

153 C p.
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194 Therapeutic role of NLRP3 inflammasome inhibitors against Alzheimer’s disease Tantra, Tanmoy

153 C p.
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195 The RIP3 activator C8 regulates the autophagy flux mediated by p62 and promotes the immunogenic form of cell death in human gastric cancer cells Liu, Xiaojie

153 C p.
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196 The sugar moiety in protopanaxadiol ginsenoside affects its ability to target glucocorticoid receptor to regulate lipid metabolism Li, Weili

153 C p.
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197 Towards antimicrobial agents: Design and antibacterial activity of a hybrid fluorophore where porphyrin and Rose Bengal moieties are linked through the hydroxyl group of a xanthene dye Mamardashvili, G.

153 C p.
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198 3-(2-Trifluoromethyl-3-aryl-4H-chromen-4-yl)-1H-indoles: Mastering anti-inflammation and analgesia while mitigating gastrointestinal side effects Cai, Nan

153 C p.
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199 Tryptophanol-derived oxazoloisoindolinone fluorescent probes for cellular localization studies of p53 activators Barros, Hélio L.

153 C p.
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200 Tyrosine modifications of insulin-degrading enzyme enable favorable control of substrate specificity for both Alzheimer’s disease and type-2 diabetes mellitus Hatakawa, Yusuke

153 C p.
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201 Unlocking lysosomal acidity to activate membranolytic module for accurately cancer theranostics Li, Zhuo

153 C p.
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202 Unprecedented nor-seco-diterpene lactones inhibited osteogenic differentiation of valve interstitial cells Wei, Jiangchun

153 C p.
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203 Unravelling the role of natural and synthetic products as DNA topoisomerase inhibitors in hepatocellular carcinoma Ren, Qing

153 C p.
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204 Unveiling cofactor inhibition mechanisms in horse liver alcohol dehydrogenase: An allosteric driven regulation Vetrano, Alice

153 C p.
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205 Unveiling the anti-cancer potentiality of phthalimide-based Analogues targeting tubulin polymerization in MCF-7 cancerous Cells: Rational design, chemical Synthesis, and Biological-coupled Computational investigation Aljuhani, Ateyatallah

153 C p.
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206 Unveiling the anticancer potential of novel spirooxindole-tethered pyrazolopyridine derivatives Eldehna, Wagdy M.

153 C p.
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207 Virtual screening-led design of inhibitor scaffolds for the NLRP3 inflammasome El-Sayed, Sherihan

153 C p.
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208 Virtual screening, molecular dynamics simulations, and in vitro validation of EGFR inhibitors as breast cancer therapeutics Shetty, Swathi R.

153 C p.
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209 Y9, a Gboxin analog, displays anti-tumor effect in non-small cell lung cancer by inducing lysosomal dysfunction and apoptosis Yin, Jie

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                             209 gevonden resultaten
 
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