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. |
artikel |
2 |
A dual-state emission luminogen for lipid droplet imaging and photodynamic therapy
|
Lei, Yu |
|
|
153 |
C |
p. |
artikel |
3 |
Advances in designing ternary complexes: Integrating in-silico and biochemical methods for PROTAC optimisation in target protein degradation
|
Shaik, Shareef |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
5 |
A FRET probe based on flavonol-benzothiazole for the detection of viscosity and SO2 derivatives
|
Xiao, Wei |
|
|
153 |
C |
p. |
artikel |
6 |
A mini review of supramolecular antagonists based on macrocyclic host compounds
|
Li, Shanshan |
|
|
153 |
C |
p. |
artikel |
7 |
2-Aminobenzothiazole based adjuvant of polymyxin E against Gram-negative bacteria
|
Chen, Yuce |
|
|
153 |
C |
p. |
artikel |
8 |
Amino polycarboxylic acids-modified abiraterone derivatives as potential injectable anti-prostate cancer agents
|
Zhu, Na |
|
|
153 |
C |
p. |
artikel |
9 |
Analysis of the effects of differently charged peptides on α-amylase and their interaction mechanisms
|
Yang, Xiaoyu |
|
|
153 |
C |
p. |
artikel |
10 |
An intramolecular charge transfer based fluorescent probe for imaging of OCl–
|
Sun, Shu-tao |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
13 |
Anticancer and Antibacterial Activeness of Fused Pyrimidines: Newfangled Updates
|
Bhatnagar, Ayushi |
|
|
153 |
C |
p. |
artikel |
14 |
Anticancer and anti-inflammatory effects of novel ethyl pyrazole derivatives having sulfonamide terminal moiety
|
Abdel-Maksoud, Mohammed S. |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
16 |
Apigenin analogs as α-glucosidase inhibitors: Molecular docking, biochemical, enzyme kinetic, and an in vivo mouse model study
|
Liu, Honghui |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
18 |
Baliosperoid A attenuates lipopolysaccharide-induced acute lung injury by targeting SHP2 to inhibit inflammation and oxidative stress
|
Li, Yue |
|
|
153 |
C |
p. |
artikel |
19 |
Benzylpiperidine derivatives as new dual μ-opioid and σ1 receptor ligands with potent antinociceptive effects
|
Li, Zong-Zheng |
|
|
153 |
C |
p. |
artikel |
20 |
Biologically active franchetine-type diterpenoid alkaloids: Isolation, synthesis, anti-inflammatory, agalgesic activities, and molecular docking
|
Xiao, Yan |
|
|
153 |
C |
p. |
artikel |
21 |
Biosynthesis of plant-derived triterpenoid asiatic acid in Saccharomyces cerevisiae cell factories
|
Lian, Yuhan |
|
|
153 |
C |
p. |
artikel |
22 |
Butanolides and clerodane diterpenes from the twigs of Casearia grewiifolia and their effects on adiponectin secretion
|
Nhoek, Piseth |
|
|
153 |
C |
p. |
artikel |
23 |
Cannabinoid receptor 2 (CB2) modulators: A patent review (2016–2024)
|
Naikoo, Rayees Ahmad |
|
|
153 |
C |
p. |
artikel |
24 |
Chemo-enzymatic synthesis of NPN cofactor taking advantage of ADP-ribosyl cyclase and LarC cyclometallase promiscuous activities
|
Vucko, Timothé |
|
|
153 |
C |
p. |
artikel |
25 |
Chlorine containing tetrahydropyrimidines: Synthesis, characterization, anticancer activity and mechanism of action
|
Milović, Emilija |
|
|
153 |
C |
p. |
artikel |
26 |
Cholenamide-based, antiviral fluorescent probes targeting oxysterol-binding protein
|
Nigro, Fatima |
|
|
153 |
C |
p. |
artikel |
27 |
Chromene-based compounds as drug candidates for renal and bladder cancer therapy – A systematic review
|
Costa Cerqueira, Mónica |
|
|
153 |
C |
p. |
artikel |
28 |
Clinical and preclinical advances in PSMA-Directed Antibody-Drug conjugates (ADCs): Current status and hope for the future
|
Mirzaei, Yousef |
|
|
153 |
C |
p. |
artikel |
29 |
Clinical applications of small-molecule GABAAR modulators for neurological disorders
|
Chen, Guangyong |
|
|
153 |
C |
p. |
artikel |
30 |
Co-based carbon material as CYP3A4-like nanozyme with both biocatalytic activity and inhibition behaviors
|
Wu, Dong |
|
|
153 |
C |
p. |
artikel |
31 |
Combining lavendustin C and 5-arylidenethiazolin-4-one-based pharmacophores toward multitarget anticancer hybrids
|
Othman, Shimaa A. |
|
|
153 |
C |
p. |
artikel |
32 |
Combretastatin A-4 based compounds as potential anticancer agents: A review
|
Omar, Mai H. |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
36 |
Cordycepin alleviates diabetes mellitus-associated hepatic fibrosis by inhibiting SOX9-mediated Wnt/β-catenin signal axis
|
Chen, Shuang |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
42 |
Deciphering substrate promiscuity and specificity of indolethylamine N-methyltransferase family enzymes from amphibian toads
|
Zhang, An-An |
|
|
153 |
C |
p. |
artikel |
43 |
Design and synthesis of novel mitochondria-targeted ergosterol peroxide derivatives as potential anti-cancer agents
|
Wang, Lu |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
45 |
Design, synthesis, and antiproliferative activity evaluation of novel α-mangostin derivatives by ROS/MAPK signaling pathway
|
Fredimoses, Mangaladoss |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
47 |
Design, synthesis and bioactivity evaluation of triazole antifungal drugs with phenylthiophene structure
|
Wu, Xudong |
|
|
153 |
C |
p. |
artikel |
48 |
Design, synthesis, and biological evaluation of adenosine derivatives targeting DOT1L and HAT as anti-leukemia agents
|
Sethy, Bidyadhar |
|
|
153 |
C |
p. |
artikel |
49 |
Design, synthesis, and biological evaluation of novel AAK1/HDACs dual inhibitors against SARS-CoV-2 entry
|
Mao, Nian-Dong |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
51 |
Design, synthesis, and biological evaluation of novel HPK1 inhibitors possessing 3-cyano-quinoline moiety
|
Chen, Long |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
53 |
Design, synthesis and biological evaluation of prostate-specific membrane antigen (PSMA)-targeted SIRT2 inhibitors
|
Yu, Junhui |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
59 |
Design, synthesis, and structure–activity relationships of xanthine derivatives as broad-spectrum inhibitors of coronavirus replication
|
Chen, Xiaofang |
|
|
153 |
C |
p. |
artikel |
60 |
Design, synthesis, biological evaluation study of spirocyclic POM analogues as novel MmpL3 anti-tubercular agent
|
Mi Kim, Young |
|
|
153 |
C |
p. |
artikel |
61 |
Design, synthesis, molecular docking, and evaluation of sulfonyl quinazoline analogues as promising liver cancer drugs
|
Venkatesan, Gopalakrishnan |
|
|
153 |
C |
p. |
artikel |
62 |
Design, synthesis, molecular modeling and evaluation of 2,4-diaminopyrimidine analogues as promising colorectal cancer drugs
|
Venkatesan, Gopalakrishnan |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
64 |
Development and preclinical evaluation of a cyclic PET tracer targeting integrin-α6 on colorectal cancer models
|
Chen, Liping |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
66 |
Development of natural product-based targeted protein degraders as anticancer agents
|
Chen, Cheng |
|
|
153 |
C |
p. |
artikel |
67 |
Development of new LSM-83177 analogues as anti-tumor agents against colorectal cancer targeting p53-MDM2 interaction
|
Elgohary, Mohamed K. |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
69 |
Development of novel imipridone derivatives with potent anti-cancer activities as human caseinolytic peptidase P (hClpP) activators
|
Zhang, Yanzhi |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
72 |
Discovery and structure − activity relationships of 2,4,5-trimethoxyphenyl pyrimidine derivatives as selective D5 receptor partial agonists
|
Kumar, Sakesh |
|
|
153 |
C |
p. |
artikel |
73 |
Discovery and synthesis of novel glyrrhizin-analogs containing furanoylpiperazine and the activity against myocardial injury in sepsis
|
Li, Wei |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
75 |
Discovery of Daclatasvir as a potential PD-L1 inhibitor from drug repurposing
|
Sun, Mengmeng |
|
|
153 |
C |
p. |
artikel |
76 |
Discovery of ent-kaurane diterpenoid glucosides as potent analgesics from the leaves of Pieris formosa
|
Feng, Yuanyuan |
|
|
153 |
C |
p. |
artikel |
77 |
Discovery of epigenetic modulators targeting HDACs and EZH2 simultaneously for the treatment of hematological malignancies
|
Zhang, Jinwei |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
79 |
Discovery of N-Benzylpiperidinol derivatives as USP7 inhibitors against Hematology
|
Pan, Youlu |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
82 |
Discovery of novel and potent sulfonamide derivatives as orally available drug for psoriasis
|
Qi, Liang |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
87 |
Discovery of potent hypoxia-inducible factor-1α (HIF-1α) degraders by proteolysis targeting chimera (PROTAC)
|
Li, Yuying |
|
|
153 |
C |
p. |
artikel |
88 |
Discovery of the FXR/CES2 dual modulator LE-77 for the treatment of irinotecan-induced delayed diarrhea
|
Cao, Zhijun |
|
|
153 |
C |
p. |
artikel |
89 |
DNA and hemoglobin binding activities: Investigation of coumarin-thiosemicarbazone hybrids
|
Çelik, Esra |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
91 |
Editorial Board
|
|
|
|
153 |
C |
p. |
artikel |
92 |
Effect of lathyrane-type diterpenoids in neural stem cell physiology: Microbial transformations, molecular docking and dynamics studies
|
Escobar-Montaño, Felipe |
|
|
153 |
C |
p. |
artikel |
93 |
Enabling oral novel Taxanes-based Chemotherapy with Lipophilic prodrug Self-nanoemulsifying drug delivery system
|
Miao, Yifan |
|
|
153 |
C |
p. |
artikel |
94 |
Enhancing rhamnolipid production via immobilized Pseudomonas stutzeri lipase: A comparative study
|
Cruz, Guillermo |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
96 |
Evaluation of the antifungal activity of novel bis-pyrazole carboxamide derivatives and preliminary investigation of the mechanism
|
Song, Yaping |
|
|
153 |
C |
p. |
artikel |
97 |
Exploring fluorinated heptose phosphate analogues as inhibitors of HldA and HldE, key enzymes in the biosynthesis of lipopolysaccharide
|
Cao, Jun |
|
|
153 |
C |
p. |
artikel |
98 |
Exploring the antifungal potential of novel carbazate derivatives as promising drug candidates against emerging superbug, Candida auris
|
Fatima, Tazeen |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
101 |
Facile constructed meroterpenoids with novel hexadecahydroacephenanthrylene carbon skeleton using the biotransformation and chemical synthesis method
|
Yan, Die |
|
|
153 |
C |
p. |
artikel |
102 |
Filicinic acid based meroterpenoids from Hypericum elodeoides and their anti-Alzheimer’s disease effects
|
Li, Jing-Dian |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
104 |
FL118: A potential bladder cancer therapeutic compound targeting H2A.X identified through library screening
|
Fan, Guangrui |
|
|
153 |
C |
p. |
artikel |
105 |
Flexible 2,4-diaminopyrimidine bearing a butyrolactone as Plasmodium falciparum dihydrofolate reductase inhibitors
|
Decharuangsilp, Sasithorn |
|
|
153 |
C |
p. |
artikel |
106 |
Fluoroquinolones tackling antimicrobial resistance: Rational design, mechanistic insights and comparative analysis of norfloxacin vs ciprofloxacin derivatives
|
Khanna, Aanchal |
|
|
153 |
C |
p. |
artikel |
107 |
Functional interplay between short antimicrobial peptides and model lipid membranes
|
Gratino, Lorena |
|
|
153 |
C |
p. |
artikel |
108 |
68Ga labeled Olmutinib: Design, synthesis, and evaluation of a novel PET EGFR probe
|
Cheng, Hua |
|
|
153 |
C |
p. |
artikel |
109 |
Glycoconjugate coumarins exploiting metabolism-enhanced fluorescence and preferential uptake: New optical tools for tumor cell staining
|
Iacopini, Dalila |
|
|
153 |
C |
p. |
artikel |
110 |
Halogenated monopyridinium oximes are less effective in reactivation of phosphylated cholinesterases than bisquaternary oximes
|
Kohoutova, Zuzana |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
112 |
5H-benzo[c]fluorene derivative exhibits antiproliferative activity via microtubule destabilization
|
Fatima, Eram |
|
|
153 |
C |
p. |
artikel |
113 |
HDAC6 mediates tumorigenesis during mitosis and the development of targeted deactivating agents
|
Peng, Jie |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
115 |
Hyaluronan and Glucose Dual-targeting Probe: Synthesis and Application
|
Zhang, Henan |
|
|
153 |
C |
p. |
artikel |
116 |
Identification of adenosine analogues as nsp14 N7‑methyltransferase inhibitors for treating coronaviruses infection
|
Chen, Qishu |
|
|
153 |
C |
p. |
artikel |
117 |
Identification of indole-grafted pyrazolopyrimidine and pyrazolopyridine derivatives as new anti-cancer agents: Synthesis, biological assessments, and molecular modeling insights
|
Eldehna, Wagdy M. |
|
|
153 |
C |
p. |
artikel |
118 |
Identification of novel RANKL inhibitors through in silico analysis
|
Jiang, Yingying |
|
|
153 |
C |
p. |
artikel |
119 |
Identification of sanguinarine as c-MYC transcription inhibitor through enhancing the G-quadruplex-NM23-H2 interactions
|
Zhong, Li-Ting |
|
|
153 |
C |
p. |
artikel |
120 |
Impact of lipidation site on the activity of α-helical antimicrobial peptides
|
Makowska, Marta |
|
|
153 |
C |
p. |
artikel |
121 |
Indole-based COX-2 inhibitors: A decade of advances in inflammation, cancer, and Alzheimer’s therapy
|
Shah, Moksh |
|
|
153 |
C |
p. |
artikel |
122 |
Interpret the potential role of zinc against oxidative stress in inflammation with a practical fluorescent assay
|
Lin, Zengyan |
|
|
153 |
C |
p. |
artikel |
123 |
In vitro and in vivo studies of a decanuclear Ni(II) complex as a potential anti-breast cancer agent
|
Zhu, Haitao |
|
|
153 |
C |
p. |
artikel |
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 |
|
|
153 |
C |
p. |
artikel |
125 |
In vitro evaluation of promiscuity and toxicity of a small molecule targeting wild and T164I β2-adrenergic receptors
|
Bandaru, Srinivas |
|
|
153 |
C |
p. |
artikel |
126 |
Issue TOC
|
|
|
|
153 |
C |
p. |
artikel |
127 |
Lipophilic derivatives of EGCG as potent α-amylase and α-glucosidase inhibitors ameliorating oxidative stress and inflammation
|
Kothari, Manan |
|
|
153 |
C |
p. |
artikel |
128 |
Medicinal chemistry insights into PRMT5 inhibitors
|
Jiao, Zhihao |
|
|
153 |
C |
p. |
artikel |
129 |
Molecular hybridization, synthesis, in vitro α-glucosidase inhibition, in vivo antidiabetic activity and computational studies of isatin based compounds
|
Patil, Sunidhi |
|
|
153 |
C |
p. |
artikel |
130 |
Molecular tweaking by generative cheminformatics and ligand–protein structures for rational drug discovery
|
Nangia, Ashwini K. |
|
|
153 |
C |
p. |
artikel |
131 |
Multifrequency-STD NMR unveils the first Michaelis complex of an intramolecular trans-sialidase from Ruminococcus gnavus
|
Monaco, Serena |
|
|
153 |
C |
p. |
artikel |
132 |
Multiomics-guided mining and characterization of epoxide hydrolase involved in camptothecin biosynthesis from Camptotheca acuminata
|
Pu, Xiang |
|
|
153 |
C |
p. |
artikel |
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. |
|
|
153 |
C |
p. |
artikel |
134 |
1,3-Naphthoxazine derivatives: Synthesis, in silico pharmacokinetic studies, antioxidant and photoprotective properties
|
Pelit, Emel |
|
|
153 |
C |
p. |
artikel |
135 |
Naphthyl-functionalized acetamide derivatives: Promising agents for cholinesterase inhibition and antioxidant therapy in Alzheimer’s disease
|
Camargo-Ayala, Lorena |
|
|
153 |
C |
p. |
artikel |
136 |
New benzophenone analogs from Nigrospora sphaerica and their inhibitory activity against PD-1/PD-L1 interactions
|
Kuang, Qi-Xuan |
|
|
153 |
C |
p. |
artikel |
137 |
New stilbenes from Cajanus cajan inhibit adipogenesis in 3T3-L1 adipocytes through down-regulation of PPARγ
|
Yao, Liyuan |
|
|
153 |
C |
p. |
artikel |
138 |
Nigenolides A–H, 13 new microperfuranones with ferroptosis inhibitory activity from the deep-sea-derived Aspergillus niger
|
Zou, Zheng-Biao |
|
|
153 |
C |
p. |
artikel |
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. |
|
|
153 |
C |
p. |
artikel |
140 |
“Novel chemo-enzymatic synthesis, structural elucidation and first antiprotozoal activity profiling of the atropoisomeric dimers of trans-8-Hydroxycalamenene”
|
Bassanini, Ivan |
|
|
153 |
C |
p. |
artikel |
141 |
Novel co-delivery nanomedicine for photodynamic enlarged immunotherapy by cascade immune activation and efficient Immunosuppression reversion
|
Zhang, Yimei |
|
|
153 |
C |
p. |
artikel |
142 |
Novel flavonoid derivatives containing 1,2,4-triazole Schiff bases as potential antifungal agents: design, synthesis, and biological evaluation
|
Meng, Kaini |
|
|
153 |
C |
p. |
artikel |
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. |
|
|
153 |
C |
p. |
artikel |
144 |
Novel purine derivatives as selective CDK2 inhibitors with potential anticancer activities: Design, synthesis and biological evaluation
|
Shah, Alpesh |
|
|
153 |
C |
p. |
artikel |
145 |
Opportunities and challenges for targeting HPK1 in cancer immunotherapy
|
Xu, Jiamei |
|
|
153 |
C |
p. |
artikel |
146 |
Optical control of butyrylcholinesterase (BChE) activity via photoswitchable azobenzene for potential treatment of Alzheimer’s disease
|
Wang, Lei |
|
|
153 |
C |
p. |
artikel |
147 |
Penisimplinoids A-K, highly oxygenated andrastin-type meroterpenoids with diverse activities from the marine-derived fungus Penicillium simplicissimum
|
Yang, Yanan |
|
|
153 |
C |
p. |
artikel |
148 |
Phenylboronic acid-functionalized copper nanoclusters with sensitivity and selectivity for the ratiometric detection of luteolin
|
Hou, Xingyu |
|
|
153 |
C |
p. |
artikel |
149 |
Photochemical Metal-Free synthesis and biological Assessment of isocryptolepine analogues targeting estrogen receptor Alpha in breast cancer cells
|
Bogdanov, F.B. |
|
|
153 |
C |
p. |
artikel |
150 |
Pin1: Advances in pancreatic cancer therapeutic potential and inhibitors research
|
Wang, Nan |
|
|
153 |
C |
p. |
artikel |
151 |
Pleiotropically activation of azaphilone biosynthesis by overexpressing a pathway-specific transcription factor in marine-derived Aspergillus terreus RA2905
|
Zheng, Yao-Yao |
|
|
153 |
C |
p. |
artikel |
152 |
Pomalidomide sensitizes lung cancer cells to TRAIL/CDDP-induced apoptosis via directly targeting electron transfer flavoprotein alpha subunit
|
Li, Liangping |
|
|
153 |
C |
p. |
artikel |
153 |
Preclinical evaluation of a new technetium-99m labeled neurotensin analogue for NTSR1 targeted radionuclide imaging
|
Erfani, Mostafa |
|
|
153 |
C |
p. |
artikel |
154 |
Probing class I histone deacetylases (HDAC) with proteolysis targeting chimera (PROTAC) for the development of highly potent and selective degraders
|
Ibrahim, Hany S. |
|
|
153 |
C |
p. |
artikel |
155 |
Pyrrolo[2,3-d]pyrimidines as potential kinase inhibitors in cancer drug discovery: A critical review
|
Sai Madhurya, Malyala |
|
|
153 |
C |
p. |
artikel |
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 |
|
|
153 |
C |
p. |
artikel |
157 |
Rational design of new quinoline-benzimidazole scaffold bearing piperazine acetamide derivatives as antidiabetic agents
|
Ghasemi, Mehran |
|
|
153 |
C |
p. |
artikel |
158 |
Rationale design and synthesis of new roflumilast analogues as preferential selective and potent PDE-4B inhibitors
|
Moussa, Ahmed M. |
|
|
153 |
C |
p. |
artikel |
159 |
Recent advances in the natural product analogues for the treatment of neurodegenerative diseases
|
Zhang, Jinling |
|
|
153 |
C |
p. |
artikel |
160 |
Research progress and development strategy of PI3K inhibitors for breast cancer treatment: A review (2016-present)
|
Peng, Rujue |
|
|
153 |
C |
p. |
artikel |
161 |
Rhodesain inhibitors on the edge of reversibility-irreversibility
|
Agost-Beltrán, Laura |
|
|
153 |
C |
p. |
artikel |
162 |
Rivastigmine structure-based hybrids as potential multi-target anti-Alzheimer’s drug candidates
|
Leuci, Rosalba |
|
|
153 |
C |
p. |
artikel |
163 |
Searching for the Holy Grail − Highly Potent Bridged Endoperoxides for Targeted Cancer Therapy
|
Tiwari, Mohit K. |
|
|
153 |
C |
p. |
artikel |
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. |
|
|
153 |
C |
p. |
artikel |
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 |
|
|
153 |
C |
p. |
artikel |
166 |
Sodium cromoglycate exerts anti-pulmonary fibrosis effects by targeting the Keap1 protein to activate Nrf2 signaling
|
Liu, Xiaofeng |
|
|
153 |
C |
p. |
artikel |
167 |
Spatial metabolomics to discover hypertrophic scar relevant metabolic alterations and potential therapeutic strategies: A preliminary study
|
Li, Jingyun |
|
|
153 |
C |
p. |
artikel |
168 |
Stereochemical influence of 4ʹ-methyl substitutions on truncated 4ʹ-thioadenosine derivatives: Impact on A3 adenosine receptor binding and antagonism
|
Kim, Minjae |
|
|
153 |
C |
p. |
artikel |
169 |
Steroid and bioactive molecule conjugates: Improving therapeutic approaches in disease management
|
Kawka, Anna |
|
|
153 |
C |
p. |
artikel |
170 |
Structural characterization and Bacteroides proliferation promotion activity of a novel homogeneous arabinoglucuronoxylan from Commelina communis L.
|
Wang, Xiaojiang |
|
|
153 |
C |
p. |
artikel |
171 |
Structurally diverse design and synthesis of novel 2-phenylindole amide derivatives with anti-canine breast cancer activity
|
Wu, Pan |
|
|
153 |
C |
p. |
artikel |
172 |
Structurally diverse phenylpropanoyl phloroglucinol derivatives from Mallotus philippensis and their anti-bacterial activities
|
Chen, Yeqi |
|
|
153 |
C |
p. |
artikel |
173 |
Structurally diverse triterpenoids with antibacterial activities from Euphorbia humifusa
|
Xia, Ru-Feng |
|
|
153 |
C |
p. |
artikel |
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 |
|
|
153 |
C |
p. |
artikel |
175 |
Sulfonyl-acetohydrazide derivatives as juvenile hormone mimics to be insect growth regulators
|
Kumari, Neetika |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
178 |
Synthesis and bioactivity evaluation of glycosylated resveratrol derivatives as antioxidative neuroprotection agents against cerebral Ischemia-Reperfusion injury
|
Xu, Yanning |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
180 |
Synthesis and evaluation of anticancer activity of new 4,5,6,7-tetrabromo-1H-benzimidazole derivatives
|
Łukowska-Chojnacka, Edyta |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
183 |
Synthesis and modification of noscapine derivatives as promising future anticancer agents
|
Nemati, Faezeh |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
185 |
Synthesis of 5-hydroxyisatin thiosemicarbazones, spectroscopic investigation, protein-ligand docking, and in vitro anticancer activity
|
Chaudhary, Upendra |
|
|
153 |
C |
p. |
artikel |
186 |
Synthesis of 3-hydroxy-4-pyridinone hexadentate chelators, and biophysical evaluation of their affinity towards lipid bilayers
|
Vinhas, Sílvia |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
189 |
Synthesis, structural modification, and biological activity of a novel bisindole alkaloid iheyamine A
|
Guo, Xin |
|
|
153 |
C |
p. |
artikel |
190 |
Synthetic biology of metabolic cycles for Enhanced CO2 capture and Sequestration
|
Dowaidar, Moataz |
|
|
153 |
C |
p. |
artikel |
191 |
Targeting JNK kinase inhibitors via molecular docking: A promising strategy to address tumorigenesis and drug resistance
|
Alkafaas, Samar Sami |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
193 |
The pivotal role of histidine 976 in human histone deacetylase 4 for enzyme function and ligand recognition
|
Schweipert, Markus |
|
|
153 |
C |
p. |
artikel |
194 |
Therapeutic role of NLRP3 inflammasome inhibitors against Alzheimer’s disease
|
Tantra, Tanmoy |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
196 |
The sugar moiety in protopanaxadiol ginsenoside affects its ability to target glucocorticoid receptor to regulate lipid metabolism
|
Li, Weili |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
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. |
artikel |
199 |
Tryptophanol-derived oxazoloisoindolinone fluorescent probes for cellular localization studies of p53 activators
|
Barros, Hélio L. |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
201 |
Unlocking lysosomal acidity to activate membranolytic module for accurately cancer theranostics
|
Li, Zhuo |
|
|
153 |
C |
p. |
artikel |
202 |
Unprecedented nor-seco-diterpene lactones inhibited osteogenic differentiation of valve interstitial cells
|
Wei, Jiangchun |
|
|
153 |
C |
p. |
artikel |
203 |
Unravelling the role of natural and synthetic products as DNA topoisomerase inhibitors in hepatocellular carcinoma
|
Ren, Qing |
|
|
153 |
C |
p. |
artikel |
204 |
Unveiling cofactor inhibition mechanisms in horse liver alcohol dehydrogenase: An allosteric driven regulation
|
Vetrano, Alice |
|
|
153 |
C |
p. |
artikel |
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. |
artikel |
206 |
Unveiling the anticancer potential of novel spirooxindole-tethered pyrazolopyridine derivatives
|
Eldehna, Wagdy M. |
|
|
153 |
C |
p. |
artikel |
207 |
Virtual screening-led design of inhibitor scaffolds for the NLRP3 inflammasome
|
El-Sayed, Sherihan |
|
|
153 |
C |
p. |
artikel |
208 |
Virtual screening, molecular dynamics simulations, and in vitro validation of EGFR inhibitors as breast cancer therapeutics
|
Shetty, Swathi R. |
|
|
153 |
C |
p. |
artikel |
209 |
Y9, a Gboxin analog, displays anti-tumor effect in non-small cell lung cancer by inducing lysosomal dysfunction and apoptosis
|
Yin, Jie |
|
|
153 |
C |
p. |
artikel |