nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A class of geranylquinol-derived polycyclic meroterpenoids from Arnebia euchroma against heart failure by reducing excessive autophagy and apoptosis in cardiomyocytes
|
Zhao, Ling-Hao |
|
|
151 |
C |
p. |
artikel |
2 |
Acovenosigenin A β-glucoside mediates JAK2-STAT3 signaling pathway by targeting GP130 in A549 and H460 cells based on integrative analysis of transcriptome and proteome and biological verification
|
Liu, Zhe |
|
|
151 |
C |
p. |
artikel |
3 |
Activity-based protein profiling in drug/pesticide discovery: Recent advances in target identification of antibacterial compounds
|
Chen, Kunlun |
|
|
151 |
C |
p. |
artikel |
4 |
Advances in HER2-Targeted Therapies: From monoclonal antibodies to dual inhibitors developments in cancer treatment
|
Bhagyalalitha, Meduri |
|
|
151 |
C |
p. |
artikel |
5 |
Alstomaphylines A–K, monoterpenoid bisindole alkaloids from Alstonia macrophylla with AChE inhibitory activity and cytotoxicity
|
Li, Zi-Wei |
|
|
151 |
C |
p. |
artikel |
6 |
7-Amino-[1,2,4]triazolo[1,5-a][1,3,5]triazines as CK1δ inhibitors: Exploring substitutions at the 2 and 5-positions
|
Grieco, Ilenia |
|
|
151 |
C |
p. |
artikel |
7 |
An innovative dual-organelle targeting NIR fluorescence probe for detecting hydroxyl radicals in biosystem and inflammation models
|
Ma, Junyan |
|
|
151 |
C |
p. |
artikel |
8 |
A novel approach to investigate the combinatorial effects of TLK1 (Tousled-Like Kinase1) inhibitors with Temozolomide for glioblastoma therapy
|
Priya, Bhanu |
|
|
151 |
C |
p. |
artikel |
9 |
Aromatase inhibitors for the treatment of breast cancer: An overview (2019–2023)
|
Bhatia, Neha |
|
|
151 |
C |
p. |
artikel |
10 |
Auto-induction, biochemical characterization and application of a novel thermo-alkaline and detergent-stable lipase (S9 peptidase domain) from Thermotoga petrophila as cleaning additive and degrading oil/fat wastes
|
Akram, Fatima |
|
|
151 |
C |
p. |
artikel |
11 |
Bio-inspired multifunctional and reusable LiP@MFO-GO and LiP@MFO-Chit hybrid enzyme complexes for efficient degradation of melanin
|
Rathour, Ranju Kumari |
|
|
151 |
C |
p. |
artikel |
12 |
Cedrol in ginger (Zingiber officinale) as a promising hair growth drug: The effects of oral and external administration on hair regeneration and its mechanism
|
Li, Tao |
|
|
151 |
C |
p. |
artikel |
13 |
Cephalostatins and ritterazines: Distinctive dimeric marine-derived steroidal pyrazine alkaloids with intriguing anticancer activities
|
Tammam, Mohamed A. |
|
|
151 |
C |
p. |
artikel |
14 |
Chitosan decorated magnetic nanobiocatalyst of Bacillus derived α-amylase as a role model for starchy wastewater treatment, detergent additive and textile desizer
|
Gupta, Nisha |
|
|
151 |
C |
p. |
artikel |
15 |
Comparative study of [18F]AlF-PAI-PDL1p and [68Ga]Ga-PAI-PDL1p as novel PD-L1 targeting PET probes for tumor imaging
|
Bai, Lu |
|
|
151 |
C |
p. |
artikel |
16 |
Corrigendum to “Design, synthesis and biological evaluation of glucose metabolism inhibitors as anticancer agents” [Bioorg. Chem. 151 (2024) 107665]
|
Cheng, Yao |
|
|
151 |
C |
p. |
artikel |
17 |
Critical review on plant-derived quorum sensing signaling inhibitors in pseudomonas aeruginosa
|
Vadakkan, Kayeen |
|
|
151 |
C |
p. |
artikel |
18 |
Design and bio-evaluation of novel millepachine derivatives targeting tubulin colchicine binding site for treatment of osteosarcoma
|
Geng, Dawei |
|
|
151 |
C |
p. |
artikel |
19 |
Design and evaluation of novel inhibitors for the treatment of clear cell renal cell carcinoma
|
Bouzian, Younos |
|
|
151 |
C |
p. |
artikel |
20 |
Design and structure-activity relationships of ether-linked alkylides: Hybrids of 3-O-descladinosyl macrolides and quinolone motifs
|
Zhang, Na |
|
|
151 |
C |
p. |
artikel |
21 |
Design and synthesis of 6,20-epoxy A-ring modified oridonin derivatives with antitumor activity through extrinsic and mitochondrial pathways
|
Li, Haonan |
|
|
151 |
C |
p. |
artikel |
22 |
Design of Multi-Target drugs of HDACs and other Anti-Alzheimer related Targets: Current strategies and future prospects in Alzheimer’s diseases therapy
|
Soltan, Osama M. |
|
|
151 |
C |
p. |
artikel |
23 |
Design, synthesis and anticancer activity of β-carboline based pseudo-natural products by inhibiting AKT/mTOR signaling pathway
|
Lv, Lijie |
|
|
151 |
C |
p. |
artikel |
24 |
Design, synthesis and antitumor activities of phthalazinone derivatives as PARP-1 inhibitors and PARP-1/HDAC-1 inhibitors
|
Wu, Jie |
|
|
151 |
C |
p. |
artikel |
25 |
Design, synthesis and bioevaluation of dual EGFR-PI3Kα inhibitors for potential treatment of NSCLC
|
Wang, Tingliang |
|
|
151 |
C |
p. |
artikel |
26 |
Design, synthesis, and biological activities of arecoline derivatives containing 1,3,4-oxadiazole structure
|
Li, Taiqing |
|
|
151 |
C |
p. |
artikel |
27 |
Design, synthesis, and biological evaluation of β-carboline-cinnamic acid derivatives as DYRK1A inhibitors in the treatment of diabetes
|
Guan, Li |
|
|
151 |
C |
p. |
artikel |
28 |
Design, synthesis and biological evaluation of glucose metabolism inhibitors as anticancer agents
|
Cheng, Yao |
|
|
151 |
C |
p. |
artikel |
29 |
Design, synthesis and biological evaluation of novel quinazoline-derived EGFR/HER-2 dual-target inhibitors bearing a heterocyclic-containing tail as potential anti-tumor agents
|
Hao, Shuang |
|
|
151 |
C |
p. |
artikel |
30 |
Design, synthesis, and biological evaluation of Pyrido[1,2-a]pyrimidin-4-one derivatives as novel allosteric SHP2 inhibitors
|
Zhang, Le |
|
|
151 |
C |
p. |
artikel |
31 |
Design, synthesis, and in vivo and in vitro biological screening of pseudolaric acid B derivatives as potential anti-tumor agents
|
Xu, Qian |
|
|
151 |
C |
p. |
artikel |
32 |
Development and biological evaluation of 68Ga-labeled peptides for potential application in HER2-positive colorectal cancer
|
Zhang, Jinglin |
|
|
151 |
C |
p. |
artikel |
33 |
Development of a fluorescent ligand that specifically binds to the c-MYC G-quadruplex by migrating the benzene group on a carbazole-benzothiazolium scaffold
|
Wang, Rui |
|
|
151 |
C |
p. |
artikel |
34 |
Development of new chiral 1,2,4-triazole-3-thiones and 1,3,4-thiadiazoles with promising in vivo anticonvulsant activity targeting GABAergic system and voltage-gated sodium channels (VGSCs)
|
Karaküçük-İyidoğan, Ayşegül |
|
|
151 |
C |
p. |
artikel |
35 |
Development of non-acidic 4-methylbenzenesulfonate-based aldose reductase inhibitors; Design, Synthesis, Biological evaluation and in-silico studies
|
Said, Gehad E. |
|
|
151 |
C |
p. |
artikel |
36 |
Directing novel ChoKα1 inhibitors using MamC-mediated biomimetic magnetic nanoparticles: a way to improve specificity and efficiency
|
Sola-Leyva, Alberto |
|
|
151 |
C |
p. |
artikel |
37 |
Discovery and development of thiazolidine-2,4-dione derivatives as Bcl-2/Mcl-1 dual inhibitors
|
Long, Jiabing |
|
|
151 |
C |
p. |
artikel |
38 |
Discovery and evolution of berberine analogues as anti-Helicobacter pylori agents with multi-target mechanisms
|
Zhang, Xin |
|
|
151 |
C |
p. |
artikel |
39 |
Discovery of new quinoline derivatives bearing 1-aryl-1,2,3-triazole motif as influenza H1N1 virus neuraminidase inhibitors
|
Sabt, Ahmed |
|
|
151 |
C |
p. |
artikel |
40 |
Discovery of novel amide derivatives against VEGFR-2/tubulin with potent antitumor and antiangiogenic activity
|
Liu, Zhenling |
|
|
151 |
C |
p. |
artikel |
41 |
Discovery of novel pyrazolo[1,5-a]pyrimidine derivatives as selective ROCK2 inhibitors with anti-breast cancer migration and invasion activities
|
Cao, Zhi |
|
|
151 |
C |
p. |
artikel |
42 |
Discovery of pyrimidine-2,4-diamine analogues as efficiency anticancer drug by targeting GTSE1
|
Xing, Sunhui |
|
|
151 |
C |
p. |
artikel |
43 |
Editorial Board
|
|
|
|
151 |
C |
p. |
artikel |
44 |
Fragment-based design and synthesis of coumarin-based thiazoles as dual c-MET/STAT-3 inhibitors for potential antitumor agents
|
Naguib, Bassem H. |
|
|
151 |
C |
p. |
artikel |
45 |
Haperforatones A-M, thirteen undescribed limonoids from Harrisonia perforata with anti-inflammatory activity
|
Wang, Qing |
|
|
151 |
C |
p. |
artikel |
46 |
Heteryunine A, an amidated tryptophan-catechin-spiroketal hybrid with antifibrotic activity from Heterosmilax yunnanensis
|
Du, Rong-Rong |
|
|
151 |
C |
p. |
artikel |
47 |
Identification of antimycobacterial 8-hydroxyquinoline derivatives as in vitro enzymatic inhibitors of Mycobacterium tuberculosis enoyl-acyl carrier protein reductase
|
Joaquim, Angélica Rocha |
|
|
151 |
C |
p. |
artikel |
48 |
Identification of diterpenoids from Salvia castanea Diels f. tomentosa Stib and their antitumor activities
|
Wang, Dong-Dong |
|
|
151 |
C |
p. |
artikel |
49 |
Intersite communication in dimeric enzymes highlighted by structural and thermodynamic analysis of didansyltyrosine binding to thymidylate synthases
|
Venturelli, Alberto |
|
|
151 |
C |
p. |
artikel |
50 |
Intriguing steroid glycosides for cancer therapy by suppressing the DNA damage response and mTOR/S6K signaling pathways
|
An, Pei-Pei |
|
|
151 |
C |
p. |
artikel |
51 |
Investigating the effect of ligand structure on the anticancer properties of several new Co(II) complexes of vitaminB3-based phosphoramides
|
Oroujzadeh, Nasrin |
|
|
151 |
C |
p. |
artikel |
52 |
Investigation of relationships between metabolic chemical reporter structures and S-glyco-modification effects
|
Dou, Biao |
|
|
151 |
C |
p. |
artikel |
53 |
Issue TOC
|
|
|
|
151 |
C |
p. |
artikel |
54 |
Macrocyclic peptides derived from AcPHF6* and AcPHF6 to selectively modulate the Tau aggregation
|
Dangi, Abha |
|
|
151 |
C |
p. |
artikel |
55 |
Metal-free internal nucleophile-triggered domino route for synthesis of fused quinoxaline [1,4]-diazepine hybrids and the evaluation of their DNA binding properties
|
Majhi, Bhim |
|
|
151 |
C |
p. |
artikel |
56 |
Mitochondrial targeted modification and anticancer mechanism of natural product ergosterol peroxide
|
Liu, Peng |
|
|
151 |
C |
p. |
artikel |
57 |
Multi-component forms of the 2nd generation H1 receptor antagonist drug, Bilastine and its enhanced physicochemical characteristics
|
Kar, Ananya |
|
|
151 |
C |
p. |
artikel |
58 |
N-Acyl phenothiazines as mycobacterial ATP synthase inhibitors: Rational design, synthesis and in vitro evaluation against drug sensitive, RR and MDR-TB
|
Reddyrajula, Rajkumar |
|
|
151 |
C |
p. |
artikel |
59 |
New cyclometalated iridium(III) complexes bearing substituted 2-(1H-benzimidazol-2-yl)quinoline: Synthesis, characterization, electrochemical and anticancer studies
|
Sahin, Cigdem |
|
|
151 |
C |
p. |
artikel |
60 |
New polycyclic polyprenylated acylphloroglucinols with antidepressant activities from Hypericum perforatum L.
|
Pan, Xue-Ge |
|
|
151 |
C |
p. |
artikel |
61 |
New sesquiterpenes and viridin derivatives from Penicillium sp. Ameliorates NAFLD by regulating the PINK1/Parkin mitophagy pathway
|
Zhang, Hang |
|
|
151 |
C |
p. |
artikel |
62 |
New Smoothened ligands based on the purine scaffold as potential agents for treating pancreatic cancer
|
Espinosa-Bustos, Christian |
|
|
151 |
C |
p. |
artikel |
63 |
Novel antibody-drug conjugates based on DXd-ADC technology
|
Chen, Rong |
|
|
151 |
C |
p. |
artikel |
64 |
Novel imidazo[2,1-b]thiazoles and imidazo[1,2-a]pyridines tethered with indolinone motif as VEGFR-2 inhibitors and apoptotic inducers: Design, synthesis and biological evaluations
|
Elkotamy, Mahmoud S. |
|
|
151 |
C |
p. |
artikel |
65 |
Novel mandelic acid derivatives containing piperazinyls as potential candidate fungicides against Monilinia fructicola: Design, synthesis and mechanism study
|
Zheng, Ya |
|
|
151 |
C |
p. |
artikel |
66 |
Novel PROTAC probes targeting FOSL1 degradation to eliminate head and neck squamous cell carcinoma cancer stem cells
|
Zaman, Shadid U. |
|
|
151 |
C |
p. |
artikel |
67 |
Oleanane-type triterpenoids from Sabia limoniacea and their anti-inflammatory activities
|
Huang, Yan |
|
|
151 |
C |
p. |
artikel |
68 |
Pyrimidine-based sulfonamides and acetamides as potent antimicrobial Agents: Synthesis, Computational Studies, and biological assessment
|
Indalkar, Supriya |
|
|
151 |
C |
p. |
artikel |
69 |
Rational design on loop regions for precisely regulating flexibility of catalytic center to mitigate overoxidation of prazole sulfides by Baeyer-Villiger monooxygenase
|
Su, Bingmei |
|
|
151 |
C |
p. |
artikel |
70 |
Rosmarinic acid turned α-syn oligomers into non-toxic species preserving microtubules in Raw 264.7 cells
|
Flores, Nicolás |
|
|
151 |
C |
p. |
artikel |
71 |
Saponins from Dolichos lablab seeds with anti-inflammatory activity
|
Zhang, Wei |
|
|
151 |
C |
p. |
artikel |
72 |
Scutellarein derivatives with histamine H3 receptor antagonism and cholinesterase inhibitory potency as multi target-directed ligands for possible Alzheimer’s disease therapy
|
Chen, Jiao |
|
|
151 |
C |
p. |
artikel |
73 |
13,14-seco withaphysalins from Physalis minima and their inhibitory effects on NLRP3 inflammasome activation
|
Hu, Bintao |
|
|
151 |
C |
p. |
artikel |
74 |
Sesquiterpenoids from Carpesium abrotanoides and their anti-inflammatory activity both in vitro and in vivo
|
Zhang, Xiao-Fang |
|
|
151 |
C |
p. |
artikel |
75 |
Synthesis and antimicrobial activity testing of quaternary ammonium silane compounds
|
Kuruca, Tuğçe |
|
|
151 |
C |
p. |
artikel |
76 |
Synthesis and biological evaluation of novel isoxazoloquinone derivatives as potent STAT3-targeting antipsoriasis agents
|
Chen, Ling |
|
|
151 |
C |
p. |
artikel |
77 |
Synthesis and broad-spectrum biocidal effect of novel gemini quaternary ammonium compounds
|
Zivna, Natalie |
|
|
151 |
C |
p. |
artikel |
78 |
Synthesis and evaluation of 5,15-diaryltetrabenzoporphyrins as photosensitizers for photo-diagnosis and photodynamic activity of tumors
|
Mi, Le |
|
|
151 |
C |
p. |
artikel |
79 |
Synthesis, biological evaluation, and molecular docking studies of novel N-substituted piperazine-tethered thiophene-3-carboxamide selenides as potent antiproliferative agents with EGFR kinase inhibitory activity
|
Makhal, Priyanka N. |
|
|
151 |
C |
p. |
artikel |
80 |
Synthetic routes and clinical application of Small-Molecule HER2 inhibitors for cancer therapy
|
Liu, He-Nan |
|
|
151 |
C |
p. |
artikel |
81 |
Targeting DNA methyltransferases for cancer therapy
|
Wang, Kaiyue |
|
|
151 |
C |
p. |
artikel |
82 |
Targeting histone methylation and demethylation for non-alcoholic fatty liver disease
|
Du, Yuanbing |
|
|
151 |
C |
p. |
artikel |
83 |
Targeting next-generation PDE4 inhibitors in search of potential management of rheumatoid arthritis and psoriasis
|
Bhuktar, Harshavardhan |
|
|
151 |
C |
p. |
artikel |
84 |
Tetrahydropyridine appended 8-aminoquinoline derivatives: Design, synthesis, in silico, and in vitro antimalarial studies
|
Sharma, Ganesh |
|
|
151 |
C |
p. |
artikel |
85 |
The potential of marine natural Products: Recent Advances in the discovery of Anti-Tuberculosis agents
|
Peng, Xinyu |
|
|
151 |
C |
p. |
artikel |
86 |
The utility of Streptococcus mutans undecaprenol kinase for the chemoenzymatic synthesis of diverse non-natural isoprenoids
|
Kumar, Vikas |
|
|
151 |
C |
p. |
artikel |
87 |
Transcriptomic analysis of MCF7 breast cancer cells treated with MGBs reveals a profound inhibition of estrogen receptor genes
|
Alniss, Hasan Y. |
|
|
151 |
C |
p. |
artikel |
88 |
TRIP13 − a potential drug target in cancer pharmacotherapy
|
Jacob Bunu, Samuel |
|
|
151 |
C |
p. |
artikel |
89 |
Unlocking the potential of higher-molecular-weight 5-HT7R ligands: Synthesis, affinity, and ADMET examination
|
Pyka, Patryk |
|
|
151 |
C |
p. |
artikel |
90 |
Unveiling anti-diabetic potential of new thiazole-sulfonamide derivatives: Design, synthesis, in vitro bio-evaluation targeting DPP-4, α-glucosidase, and α-amylase with in-silico ADMET and docking simulation
|
Khamees Thabet, Hamdy |
|
|
151 |
C |
p. |
artikel |
91 |
Unveiling the potential of isatin-grafted phenyl-1,2,3-triazole derivatives as dual VEGFR-2/STAT-3 inhibitors: Design, synthesis and biological assessments
|
Elsebaie, Heba A. |
|
|
151 |
C |
p. |
artikel |
92 |
Visualization of nonsmall-cell lung cancer by near-infrared fluorescence imaging with tumor-targeting peptide ABT-510
|
Tu, Yuanbiao |
|
|
151 |
C |
p. |
artikel |