nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acid-triggered controlled release and fluorescence-switchable phthalocyanine nanoassemblies combined with O2-economizer for tumor imaging and collaborative photodynamic antitumor therapy
|
Liu, Xinxin |
|
|
143 |
C |
p. |
artikel |
2 |
A comprehensive review of small molecules targeting PI3K pathway: Exploring the structural development for the treatment of breast cancer
|
Dubey, Rahul |
|
|
143 |
C |
p. |
artikel |
3 |
Advances in synthesis and biological evaluation of CDK2 inhibitors for cancer therapy
|
Patel, Dharmesh A. |
|
|
143 |
C |
p. |
artikel |
4 |
A highly oxidized germacranolide from elephantopus tomentosus inhibits the growth of hepatocellular carcinoma cells by targeting EGFR in vitro and in vivo
|
Li, Qian |
|
|
143 |
C |
p. |
artikel |
5 |
A near-infrared aggregation-induced emission photosensitizer targeting mitochondria for depleting Cu2+ to trigger light-activated cancer cells oncosis
|
Xue, Ke |
|
|
143 |
C |
p. |
artikel |
6 |
A newly synthesized magnetic nanoparticle coated with glycidyl methacrylate monomer and 1,2,4-Triazole: Immobilization of α-Amylase from Bacillus licheniformis for more reuse, stability, and activity in the presence of H2O2
|
Kaptan Usul, Sedef |
|
|
143 |
C |
p. |
artikel |
7 |
Apigenin analogs as α-glucosidase inhibitors with antidiabetic activity
|
Liu, Honghui |
|
|
143 |
C |
p. |
artikel |
8 |
A supercritical fluid co-extract of turmeric powder and dried coconut shreds shows neuroprotection against AlCl3-induced Alzheimer’s disease in rats through nose to brain delivery
|
Sharma, Abhinav |
|
|
143 |
C |
p. |
artikel |
9 |
A turn-on fluorescent probe for detecting and bioimaging of HOCl in inflammatory and liver disease models
|
Zhang, Peng |
|
|
143 |
C |
p. |
artikel |
10 |
Bialorastins A–F, highly oxygenated and polycyclic andrastin-type meroterpenoids with proangiogenic activity from the deep-sea cold-seep-derived fungus Penicillium bialowiezense CS-283
|
Yan, Li-Hong |
|
|
143 |
C |
p. |
artikel |
11 |
Biological activity and structural modification of isosteviol over the past 15 years
|
Yang, Youfu |
|
|
143 |
C |
p. |
artikel |
12 |
Bioseparation of rare earth elements and high value-added biomaterials applications
|
Qian, Xining |
|
|
143 |
C |
p. |
artikel |
13 |
Boron-containing carbonic anhydrases inhibitors
|
Giovannuzzi, Simone |
|
|
143 |
C |
p. |
artikel |
14 |
5′-cap RNA/SAM mimetic conjugates as bisubstrate inhibitors of viral RNA cap 2′-O-methyltransferases
|
Ahmed-Belkacem, Rostom |
|
|
143 |
C |
p. |
artikel |
15 |
Carbazole-based mitochondria-targeted fluorescent probes for in vivo viscosity and cyanide detection in cells and zebrafish
|
Han, Lin-Lin |
|
|
143 |
C |
p. |
artikel |
16 |
Catalyzing a Cure: Discovery and development of LRRK2 inhibitors for the treatment of Parkinson’s disease
|
Baidya, Anurag TK |
|
|
143 |
C |
p. |
artikel |
17 |
Challenging the anticolorectal cancer capacity of quinoxaline-based scaffold via triazole ligation unveiled new efficient dual VEGFR-2/MAO-B inhibitors
|
Ayoup, Mohammed Salah |
|
|
143 |
C |
p. |
artikel |
18 |
Characteristic alkaloids from Stemona sessilifolia with lung protective effects
|
Jiang, Wanru |
|
|
143 |
C |
p. |
artikel |
19 |
Characterization of the metabolites of Eucommiae Cortex in rats provides a further insight into its estrogen-like effective substances
|
Ding, Liqin |
|
|
143 |
C |
p. |
artikel |
20 |
Chemical synthesis of a 28 kDa full-length PET degrading enzyme ICCG by the removable backbone modification strategy
|
Gao, Yun-Pu |
|
|
143 |
C |
p. |
artikel |
21 |
Click chemistry in the synthesis of antibody-drug conjugates
|
Dudchak, Rostyslav |
|
|
143 |
C |
p. |
artikel |
22 |
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 |
|
|
143 |
C |
p. |
artikel |
23 |
Corrigendum to “Molecular hybridization design and synthesis of novel spirooxindole-based MDM2 inhibitors endowed with BCL2 signaling attenuation; a step towards the next generation p53 activators” [Bioorg. Chem. 117 (2021) 105427]
|
Lotfy, Gehad |
|
|
143 |
C |
p. |
artikel |
24 |
Corrigendum to “Novel spirooxindole based benzimidazole scaffold: In vitro, nanoformulation and in vivo studies on anticancer and antimetastatic activity of breast adenocarcinoma” [Bioorg. Chem. 129 (2022) 106124]
|
Barakat, Assem |
|
|
143 |
C |
p. |
artikel |
25 |
Corrigendum to “The active phthalate metabolite, DHEP, induces proliferation and metastasis of prostate cancer cells via upregulation of β-catenin and downregulation of KLF7” [Bioorganic Chem., 141 (2023) 106864]
|
Li, Hecheng |
|
|
143 |
C |
p. |
artikel |
26 |
C3-Spirooxindoles: Divergent chemical synthesis and bioactivities (2018–2023)
|
Helal, Mohamed H. |
|
|
143 |
C |
p. |
artikel |
27 |
Decaging-to-labeling: Development and investigation of quinone methide warhead for protein labeling
|
Guo, Fuhu |
|
|
143 |
C |
p. |
artikel |
28 |
Deciphering single-cell protein secretion and gene expressions by constructing cell-antibody conjugates
|
Li, Yachao |
|
|
143 |
C |
p. |
artikel |
29 |
Design and synthesis of luotonin A-derived topoisomerase targeting scaffold with potent antitumor effect and low genotoxicity
|
Li, Xin-Wei |
|
|
143 |
C |
p. |
artikel |
30 |
Design of balanced dual-target inhibitors of EGFR and microtubule
|
Liu, Yifan |
|
|
143 |
C |
p. |
artikel |
31 |
Design, synthesis, and biological evaluation of novel capsaicin-tacrine hybrids as multi-target agents for the treatment of Alzheimer's disease
|
Long, Juanyue |
|
|
143 |
C |
p. |
artikel |
32 |
Design, synthesis, and biological evaluation of novel donepezil-tacrine hybrids as multi-functional agents with low neurotoxicity against Alzheimer’s disease
|
Wang, Ningwei |
|
|
143 |
C |
p. |
artikel |
33 |
Design, synthesis, and biological evaluation of novel tryptanthrin derivatives as selective acetylcholinesterase inhibitors for the treatment of Alzheimer's disease
|
Xia, Jucheng |
|
|
143 |
C |
p. |
artikel |
34 |
Design, synthesis, and biological evaluation of N-(pyridin-3-yl)pyrimidin-4-amine analogues as novel cyclin-dependent kinase 2 inhibitors for cancer therapy
|
Zeng, Wen-Bin |
|
|
143 |
C |
p. |
artikel |
35 |
Design, synthesis and biological evaluation of potent epidermal growth factor receptor tyrosine kinase (EGFR-TK) inhibitors against resistance mutation for lung cancer treatment
|
Wang, Cheng |
|
|
143 |
C |
p. |
artikel |
36 |
Design, synthesis, and evaluation of pirfenidone-NSAIDs conjugates for the treatment of idiopathic pulmonary fibrosis
|
Lu, Xiang |
|
|
143 |
C |
p. |
artikel |
37 |
Design, synthesis and evaluation of quinazoline derivatives as Gαq/11 proteins inhibitors against uveal melanoma
|
Fan, Guangjin |
|
|
143 |
C |
p. |
artikel |
38 |
Design, synthesis, and evaluation of VHL-based EZH2 degraders for breast cancer
|
Xiao, Boren |
|
|
143 |
C |
p. |
artikel |
39 |
Design, synthesis, molecular docking and biological evaluation of 1,3,5-trisubstituted-1H-pyrazole derivatives as anticancer agents with cell cycle arrest, ERK and RIPK3- kinase activities
|
Boshta, Nader M. |
|
|
143 |
C |
p. |
artikel |
40 |
Development of multi-targetable chalcone derivatives bearing N-aryl piperazine moiety for the treatment of Alzheimer's disease
|
Bajad, Nilesh Gajanan |
|
|
143 |
C |
p. |
artikel |
41 |
Development of new thieno[2,3-d]pyrimidines as dual EGFR and STAT3 inhibitors endowed with anticancer and pro-apoptotic activities
|
Elsebaie, Heba A. |
|
|
143 |
C |
p. |
artikel |
42 |
Development of safe and antioxidant COX-2 inhibitors; Synthesis, molecular docking analysis and biological evaluation of novel pyrrolizine 5-carboxamides
|
K. A. Abdelall, Eman |
|
|
143 |
C |
p. |
artikel |
43 |
Discovery and characterization of natural product luteolin as an effective inhibitor of human pyridoxal kinase
|
Zhu, Yunmei |
|
|
143 |
C |
p. |
artikel |
44 |
Discovery of a near-infrared fluorescent probe for G-quadruplexes by exploiting the concept of unfolding-intramolecular-aggregation-induced emission
|
Wang, Xiao-Dong |
|
|
143 |
C |
p. |
artikel |
45 |
Discovery of a potent and selective covalent threonine tyrosine kinase (TTK) inhibitor
|
Sun, Yaoliang |
|
|
143 |
C |
p. |
artikel |
46 |
Discovery of highly efficient CRBN-recruiting HPK1-PROTAC as a potential chemical tool for investigation of scaffolding roles in TCR signaling
|
Zeng, Shenxin |
|
|
143 |
C |
p. |
artikel |
47 |
Discovery of α-Ketoamide inhibitors of SARS-CoV-2 main protease derived from quaternized P1 groups
|
Huang, Qiao |
|
|
143 |
C |
p. |
artikel |
48 |
Discovery of LH10, a novel fexaramine-based FXR agonist for the treatment of liver disease
|
Huang, Wanqiu |
|
|
143 |
C |
p. |
artikel |
49 |
Discovery of novel 1H-benzo[d]imidazole-4,7-dione based transglutaminase 2 inhibitors as p53 stabilizing anticancer agents in renal cell carcinoma
|
Kim, Ga-Ram |
|
|
143 |
C |
p. |
artikel |
50 |
Divergent synthesis of fractionated Cannabis sativa extract led to multiple cannabinoids C-&O-glycosides with anti-proliferative/anti-metastatic properties
|
Nalli, Yedukondalu |
|
|
143 |
C |
p. |
artikel |
51 |
Dual chemodynamic/photothermal therapeutic nanoplatform based on DNA-functionalized prussian blue
|
Zeng, Qin |
|
|
143 |
C |
p. |
artikel |
52 |
Editorial Board
|
|
|
|
143 |
C |
p. |
artikel |
53 |
Enhancement efficiency delivery of antiviral Molnupiravir-drug via the loading with self-assembly nanoparticles of pycnogenol and cellulose which are decorated by zinc oxide nanoparticles for COVID-19 therapy
|
El-Shafai, Nagi M. |
|
|
143 |
C |
p. |
artikel |
54 |
Enhancing nicotinamide N-methyltransferase bisubstrate inhibitor activity through 7-deazaadenosine and linker modifications
|
Li, Pengyu |
|
|
143 |
C |
p. |
artikel |
55 |
Evaluation of a biomarker (NO) dynamics in inflammatory zebrafish and periodontitis saliva samples via a fast-response and sensitive fluorescent probe
|
Zhang, Yibin |
|
|
143 |
C |
p. |
artikel |
56 |
Evaluation of antihypertensive activity and molecular docking analysis of Padina boergesenii extract
|
Patel, Nidhi |
|
|
143 |
C |
p. |
artikel |
57 |
Exploration of costunolide derivatives as potential anti-inflammatory agents for topical treatment of atopic dermatitis by inhibiting MAPK/NF-κB pathways
|
Lu, Cheng |
|
|
143 |
C |
p. |
artikel |
58 |
Exploring the plasticity of the InhA substrate-binding site using new diaryl ether inhibitors
|
Tamhaev, Rasoul |
|
|
143 |
C |
p. |
artikel |
59 |
Expression of a thermostable glucose-stimulated β-glucosidase from a hot-spring metagenome and its promising application to produce gardenia blue
|
Mo, Haiying |
|
|
143 |
C |
p. |
artikel |
60 |
Fluorinated azoles as effective weapons in fight against methicillin-resistance staphylococcus aureus (MRSA) and its SAR studies
|
Zhao, Xuanming |
|
|
143 |
C |
p. |
artikel |
61 |
Fourteen new 2-benzylbenzofuran glycosides with cardioprotective activity from Heterosmilax yunnanensis
|
Du, Rong-Rong |
|
|
143 |
C |
p. |
artikel |
62 |
Fructooligosaccharides from Cynoglossum tubiflorus: Effect of the molecular size on their antidiabetic activity in high-fat diet and alloxan induced diabetic rats
|
Dallali, Dhouha |
|
|
143 |
C |
p. |
artikel |
63 |
Green approach to the synthesis of α-aminophosphonate-tetrahydroisoquinoline hybrids and their anti-cholinesterase activity
|
Marchán-García, Joaquín |
|
|
143 |
C |
p. |
artikel |
64 |
Groebke Blackburn Bienaymé-mediated multi-component synthesis of selective HDAC6 inhibitors with anti-inflammatory properties
|
Kraft, Fabian B. |
|
|
143 |
C |
p. |
artikel |
65 |
Human serum albumin as a potential drug delivery system for N-methylated hot spot insulin analogs inhibiting hormone aggregation
|
Wasko, Joanna |
|
|
143 |
C |
p. |
artikel |
66 |
Identification and evolution of non-traditional nitrilase from Spirosoma linguale DSM 74 with high hydration activity
|
Sun, Yangyang |
|
|
143 |
C |
p. |
artikel |
67 |
Identification of diverse sesquiterpenoids with anti-fibrotic potential from Inula japonica Thunb.
|
Peng, Yulin |
|
|
143 |
C |
p. |
artikel |
68 |
Identification of (E)-1-((1H-indol-3-yl)methylene)-4-substitute-thiosemicarbazones as potential anti-hepatic fibrosis agents
|
Lin, Gang |
|
|
143 |
C |
p. |
artikel |
69 |
Identification of novel ureido benzothiophenes as dual VEGFR-2/EGFR anticancer agents
|
Eldehna, Wagdy M. |
|
|
143 |
C |
p. |
artikel |
70 |
In situ interaction between the hormone 17α-ethynylestradiol and the liquid-ordered phase composed of the lipid rafts sphingomyelin and cholesterol
|
Ruiz, Gilia Cristine Marques |
|
|
143 |
C |
p. |
artikel |
71 |
In vitro α-amylase and α-glucosidase inhibition study of dihydropyrimidinones synthesized via one-pot Biginelli reaction in the presence of a green catalyst
|
Kamat, Vinuta |
|
|
143 |
C |
p. |
artikel |
72 |
Iodoquinazoline-derived VEGFR-2 and EGFRT790M dual inhibitors: Design, synthesis, molecular docking and anticancer evaluations
|
Mohamed, Abeer A. |
|
|
143 |
C |
p. |
artikel |
73 |
Issue TOC
|
|
|
|
143 |
C |
p. |
artikel |
74 |
Molecular glues targeting GSPT1 in cancers: A potent therapy
|
Zhang, Dandan |
|
|
143 |
C |
p. |
artikel |
75 |
Molecular hybrids of substituted phenylcarbamoylpiperidine and 1,2,4-triazole methylacetamide as potent 15-LOX inhibitors: Design, synthesis, DFT calculations and molecular docking studies
|
Nawaz, Zahid |
|
|
143 |
C |
p. |
artikel |
76 |
Near-infrared light controlled protein degradation by photo-caged lenalidomide and pomalidomide
|
Zhu, Yaoji |
|
|
143 |
C |
p. |
artikel |
77 |
New chromone derivatives bearing thiazolidine-2,4-dione moiety as potent PTP1B inhibitors: Synthesis and biological activity evaluation
|
Zheng, Yingying |
|
|
143 |
C |
p. |
artikel |
78 |
New fusidane-type nortriterpenoids from the Arctic marine-derived fungus Simplicillium lamellicola culture medium with their inhibitory effect on benign prostatic hyperplasia
|
Kwon, Haeun |
|
|
143 |
C |
p. |
artikel |
79 |
New resveratrol analogs as improved biologically active structures: Design, synthesis and computational modeling
|
Mlakić, Milena |
|
|
143 |
C |
p. |
artikel |
80 |
New thiophene-1,3,4-oxadiazole-thiazolidine-2,4-dione hybrids: Synthesis, MCF-7 inhibition and binding studies
|
Doddagaddavalli, Manasa A. |
|
|
143 |
C |
p. |
artikel |
81 |
N-(3-Methoxyphenyl)-6-(7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridin-3-yl)pyridin-2-amine is an inhibitor of the FLT3-ITD and BCR-ABL pathways, and potently inhibits FLT3-ITD/D835Y and FLT3-ITD/F691L secondary mutants
|
Wang, Xiuqi |
|
|
143 |
C |
p. |
artikel |
82 |
Novel GSH-responsive prodrugs derived from indole-chalcone and camptothecin trigger apoptosis and autophagy in colon cancer
|
Wang, Hui |
|
|
143 |
C |
p. |
artikel |
83 |
Novel heptafluoroisopropyl N-phenylpyrazole aryl amides containing cyanoalkyl groups: Design, synthesis, insecticidal activity, docking studies and theoretical calculations
|
Liu, Dongdong |
|
|
143 |
C |
p. |
artikel |
84 |
Novel indolinone-tethered benzothiophenes as anti-tubercular agents against MDR/XDR M. tuberculosis: Design, synthesis, biological evaluation and in vivo pharmacokinetic study
|
Eldehna, Wagdy M. |
|
|
143 |
C |
p. |
artikel |
85 |
Novel 1,3,4-oxadiazole hybrids of 3-n-butylphthalide derivatives as potential anti-ischemic stroke agents
|
Yu, Qinyang |
|
|
143 |
C |
p. |
artikel |
86 |
Novel quinazolinone Derivatives: Design, synthesis and in vivo evaluation as potential agents targeting Alzheimer disease
|
Moftah, Hadeer K. |
|
|
143 |
C |
p. |
artikel |
87 |
Novel sulfonyl-substituted tetrandrine derivatives for colon cancer treatment by inducing mitochondrial apoptosis and inhibiting PI3K/AKT/mTOR pathway
|
Ling, Jie |
|
|
143 |
C |
p. |
artikel |
88 |
NQO-1 activatable NIR photosensitizer for visualization and selective killing of breast cancer cells
|
Li, Zhipeng |
|
|
143 |
C |
p. |
artikel |
89 |
Old trees bloom new flowers, lysosome targeted near-infrared fluorescent probe for ratiometric sensing of hypobromous acid in vitro and in vivo based on Nile red skeleton
|
Zhao, Wanqing |
|
|
143 |
C |
p. |
artikel |
90 |
Panaxadiol carbamate derivatives: Synthesis and biological evaluation as potential multifunctional anti-Alzheimer agents
|
Quan, Yin-Sheng |
|
|
143 |
C |
p. |
artikel |
91 |
Pathology, target discovery, and the evolution of XO inhibitors from the first discovery to recent advances (2020–2023)
|
Kumar, Nitish |
|
|
143 |
C |
p. |
artikel |
92 |
Penicimides A and B, two novel diels–alder [4 + 2] cycloaddition ergosteroids from Penicillium herquei
|
Deng, Mengyi |
|
|
143 |
C |
p. |
artikel |
93 |
Platanosides from Platanus × acerifolia: New molecules, SAR, and target validation of a strong lead for drug-resistant bacterial infections and the associated sepsis
|
Wu, Xi-Ying |
|
|
143 |
C |
p. |
artikel |
94 |
Potential therapeutic medicines for renal fibrosis: Small-molecule compounds and natural products
|
Xiang, Yu |
|
|
143 |
C |
p. |
artikel |
95 |
Programming and monitoring surface-confined DNA computing
|
Sun, Chenyun |
|
|
143 |
C |
p. |
artikel |
96 |
Recent advances in the synthesis and antimalarial activity of 1,2,4-trioxanes
|
Rathi, Komal |
|
|
143 |
C |
p. |
artikel |
97 |
Recent advances of vacuolar protein-sorting 34 inhibitors targeting autophagy
|
Chen, Long |
|
|
143 |
C |
p. |
artikel |
98 |
Recent developments of P-glycoprotein inhibitors and its structure–activity relationship (SAR) studies
|
Zhao, Xuanming |
|
|
143 |
C |
p. |
artikel |
99 |
Revealing protein trafficking by proximity labeling-based proteomics
|
Wang, Yankun |
|
|
143 |
C |
p. |
artikel |
100 |
RNA-binding MSI proteins and their related cancers: A medicinal chemistry perspective
|
Liu, Chenxin |
|
|
143 |
C |
p. |
artikel |
101 |
Selective inhibition of SIRT2: A disputable therapeutic approach in cancer therapy
|
Kaya, Selen Gozde |
|
|
143 |
C |
p. |
artikel |
102 |
Structural diversity of microbial secondary metabolites based on chemical epigenetic manipulation
|
Lv, Huawei |
|
|
143 |
C |
p. |
artikel |
103 |
Structurally diverse amides from Chloranthus henryi var. hupehensis and their anti-inflammatory activities by blocking Akt phosphorylation
|
Zhang, Dan-Yang |
|
|
143 |
C |
p. |
artikel |
104 |
Structurally diverse stilbenes from Gnetum parvifolium and their anti-neuroinflammatory activities
|
Yan, Qi-Wei |
|
|
143 |
C |
p. |
artikel |
105 |
Sucrosephenylpropanoid esters and isoflavonoids isolated from Belamcanda chinensis roots and their potential anti-osteoclastogenic activity
|
Ha, Manh Tuan |
|
|
143 |
C |
p. |
artikel |
106 |
Sulfonamidyl derivatives of sigmacidin: Protein-protein interaction inhibitors targeting bacterial RNA polymerase and sigma factor interaction exhibiting antimicrobial activity against antibiotic-resistant bacteria
|
Ye, Jiqing |
|
|
143 |
C |
p. |
artikel |
107 |
Synthesis and application of clinically approved small-molecule drugs targeting androgen receptor
|
Gao, Hua |
|
|
143 |
C |
p. |
artikel |
108 |
Synthesis and biological evaluation of 2′-hydroxychalcone derivatives as AMPK activators
|
Vu Nguyen, Duy |
|
|
143 |
C |
p. |
artikel |
109 |
Synthesis and biological evaluations of 8-biaryl-2,2-dimethylbenzopyranamide derivatives against Alzheimer's disease and ischemic stroke
|
Cao, Ruolin |
|
|
143 |
C |
p. |
artikel |
110 |
Synthesis and characterization of bis-amide SSE1917 as a microtubule-stabilizing anticancer agent
|
Iqbal, Sana |
|
|
143 |
C |
p. |
artikel |
111 |
Synthesis and photodynamic activity of novel thieno[3,2–b]thiophene fused BODIPYs with good bio-solubility and anti-aggregation effect
|
Cao, Ning |
|
|
143 |
C |
p. |
artikel |
112 |
Synthesis, in vitro, and in silico studies of new derivatives of diphenylpiperazine scaffold: A key substructure for MAO inhibition
|
El-Halaby, Lamiaa O. |
|
|
143 |
C |
p. |
artikel |
113 |
Synthesis, molecular docking and biological evaluation of 1,2,4-oxadiazole based novel non-steroidal derivatives against prostate cancer
|
Kumar, Shubham |
|
|
143 |
C |
p. |
artikel |
114 |
Synthesis, molecular docking, electrochemical and fluorimetric analysis of new caffeic and cinnamic acid-conjugated hemorphin derivatives designed as potential anticonvulsant and antinociceptive agents
|
Todorov, Petar |
|
|
143 |
C |
p. |
artikel |
115 |
Synthetic and pharmacological developments in the hybrid s-triazine moiety: A review
|
Bareth, Diksha |
|
|
143 |
C |
p. |
artikel |
116 |
Tailored horseshoe-shaped nicotinonitrile scaffold as dual promising c-Met and Pim-1 inhibitors: Design, synthesis, SAR and in silico study
|
Mohamady, Samy |
|
|
143 |
C |
p. |
artikel |
117 |
Targeting JAK2/STAT3 for the treatment of cancer: A review on recent advancements in molecular development using structural analysis and SAR investigations
|
Kohal, Rupali |
|
|
143 |
C |
p. |
artikel |
118 |
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