nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Advances in the discovery of activin receptor-like kinase 5 (ALK5) inhibitors
|
Mansour, Mai A. |
|
|
147 |
C |
p. |
artikel |
2 |
Anticancer efficacy triggered by synergistically modulating the homeostasis of anions and iron: Design, synthesis and biological evaluation of dual-functional squaramide-hydroxamic acid conjugates
|
Zhi, Hai-Tao |
|
|
147 |
C |
p. |
artikel |
3 |
Antimicrobial macrozones interact with biological macromolecules via two-site binding mode of action: Fluorimetric, NMR and docking studies
|
Jednačak, Tomislav |
|
|
147 |
C |
p. |
artikel |
4 |
Antioxidant aromatic compounds from Amomum villosum and target prediction of active ingredients
|
Liang, Junming |
|
|
147 |
C |
p. |
artikel |
5 |
A path from synthesis to emergency use authorization of molnupiravir as a COVID-19 therapy
|
Sakander, Norein |
|
|
147 |
C |
p. |
artikel |
6 |
Bioisosteric replacement strategy leads to novel DNA gyrase B inhibitors with improved potencies and properties
|
Xue, Wenjie |
|
|
147 |
C |
p. |
artikel |
7 |
Biological activity and computational analysis of novel acrylonitrile derived benzazoles as potent antiproliferative agents for pancreatic adenocarcinoma with antioxidative properties
|
Beč, Anja |
|
|
147 |
C |
p. |
artikel |
8 |
Chaetoxylariones A–G: undescribed chromone-derived polyketides from co-culture of Chaetomium virescens and Xylaria grammica enabled via the molecular networking strategy
|
Zhang, Sitian |
|
|
147 |
C |
p. |
artikel |
9 |
Corrigendum to “Synthesis and preclinical evaluation of a novel molecular probe [18F]AlF-NOTA-PEG2-Asp2-PDL1P for PET imaging of PD-L1 positive tumor” [Bioorgan. Chem. 145 (2024) 107193]
|
Sun, Penghui |
|
|
147 |
C |
p. |
artikel |
10 |
Design and synthesis of novel imidazole-chalcone derivatives as microtubule protein polymerization inhibitors to treat cervical cancer and reverse cisplatin resistance
|
Liu, Zhengye |
|
|
147 |
C |
p. |
artikel |
11 |
Design and synthesis of novel JNK inhibitors targeting liver pyruvate kinase for the treatment of non-alcoholic fatty liver disease and hepatocellular carcinoma
|
Iqbal, Shazia |
|
|
147 |
C |
p. |
artikel |
12 |
Design, selective synthesis and biological activities evaluation of novel thiazol-2-ylbenzamide and thiazole-2-ylbenzimidoyl chloride derivatives
|
Xu, Zonghan |
|
|
147 |
C |
p. |
artikel |
13 |
Design, synthesis, and antitumor activity evaluation of potent fourth-generation EGFR inhibitors for treatment of Osimertinib resistant non-small cell lung cancer (NSCLC)
|
Zhang, Yuchen |
|
|
147 |
C |
p. |
artikel |
14 |
Design, synthesis, and biological evaluation of cathepsin B cleavage albumin-binding SN38 prodrug in breast cancer
|
Lu, Yingxin |
|
|
147 |
C |
p. |
artikel |
15 |
Design, synthesis, and biological evaluation of novel 2,3-Di-O-Aryl/Alkyl sulfonate derivatives of l-ascorbic acid: Efficient access to novel anticancer agents via in vitro screening, tubulin polymerization inhibition, molecular docking study and ADME predictions
|
Deshmukh, Santosh R. |
|
|
147 |
C |
p. |
artikel |
16 |
Design, synthesis, and evaluation of antitumor activity of Mobocertinib derivatives, a third-generation EGFR inhibitor
|
Fan, Dang |
|
|
147 |
C |
p. |
artikel |
17 |
Design, synthesis, docking, and antiviral evaluation of some novel pyrimidinone-based α-aminophosphonates as potent H1N1 and HCoV-229E inhibitors
|
Hekal, Hend A. |
|
|
147 |
C |
p. |
artikel |
18 |
Design, synthesis, in silico and biological evaluation of new indole based oxadiazole derivatives targeting estrogen receptor alpha
|
Kaur, Kamalpreet |
|
|
147 |
C |
p. |
artikel |
19 |
Design, synthesis, in vitro and in silico evaluations of new isatin-triazine- aniline hybrids as potent anti- Alzheimer multi-target directed lead compounds
|
Tamaddon-Abibigloo, Yasaman |
|
|
147 |
C |
p. |
artikel |
20 |
Development of D-π-A organic dyes for discriminating HSA from BSA and study on dye-HSA interaction
|
Cao, Hao-Wen |
|
|
147 |
C |
p. |
artikel |
21 |
Dimeric peptoids as antibacterial agents
|
Bahatheg, Ghayah |
|
|
147 |
C |
p. |
artikel |
22 |
2,2- dimethylbenzopyran derivatives containing pyridone structural fragments as selective dual-targeting inhibitors of HIF-1α and EZH2 for the treatment of lung cancer
|
Xu, Huashen |
|
|
147 |
C |
p. |
artikel |
23 |
Discovery and development of novel 10,12-disubstituted aloperine derivatives against HCoV-OC43 by targeting allosteric site of host TMPRSS2
|
Meng, Runze |
|
|
147 |
C |
p. |
artikel |
24 |
Discovery of a new class of potent pyrrolo[3,4-c]quinoline-1,3-diones based inhibitors of human dihydroorotate dehydrogenase: Synthesis, pharmacological and toxicological evaluation
|
Dimitrijević, Marina G. |
|
|
147 |
C |
p. |
artikel |
25 |
Discovery of digallic acid as XOD/URAT1 dual target inhibitor for the treatment of hyperuricemia
|
Zheng, Fengxin |
|
|
147 |
C |
p. |
artikel |
26 |
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
|
Zhu, Chenchen |
|
|
147 |
C |
p. |
artikel |
27 |
Discovery of new 2-(3-(naphthalen-2-yl)-4,5-dihydro-1H-pyrazol-1-yl)thiazole derivatives with potential analgesic and anti-inflammatory activities: In vitro, in vivo and in silico investigations
|
Mohammed, Eman R. |
|
|
147 |
C |
p. |
artikel |
28 |
Discovery of novel co-degradation CK1α and CDK7/9 PROTACs with p53 activation for treating acute myeloid leukemia
|
Wang, Kai |
|
|
147 |
C |
p. |
artikel |
29 |
Discovery of novel HER2 targeting peptide-camptothecin conjugates with effective suppression for selective cancer treatment
|
Wu, Hanyu |
|
|
147 |
C |
p. |
artikel |
30 |
Discovery of novel pyrazole based Urea/Thiourea derivatives as multiple targeting VEGFR-2, EGFRWT, EGFRT790M tyrosine kinases and COX-2 Inhibitors, with anti-cancer and anti-inflammatory activities
|
Fadaly, Wael A.A. |
|
|
147 |
C |
p. |
artikel |
31 |
Discovery of novel thiophene-3-carboxamide derivatives as potential VEGFR-2 inhibitors with anti-angiogenic properties
|
Li, Tai |
|
|
147 |
C |
p. |
artikel |
32 |
Discovery of 4-phenyl-1H-indazole derivatives as novel small-molecule inhibitors targeting the PD-1/PD-L1 interaction
|
Xu, Chenglong |
|
|
147 |
C |
p. |
artikel |
33 |
Discovery of PXR agonists from Hypericum japonicum: A class of novel nonaromatic acylphloroglucinol-terpenoid adducts
|
Su, Haiguo |
|
|
147 |
C |
p. |
artikel |
34 |
Discovery of sesquiterpenoids from the roots of Chloranthus henryi Hemsl. var. hupehensis (Pamp.) K. F. Wu and their anti-inflammatory activity by IKBα/NF-κB p65 signaling pathway suppression
|
Liu, Shuai |
|
|
147 |
C |
p. |
artikel |
35 |
Discovery of two non-UDP-mimic inhibitors of O-GlcNAc transferase by screening a DNA-encoded library
|
Balsollier, Cyril |
|
|
147 |
C |
p. |
artikel |
36 |
Dried tangerine peel polysaccharide (DTPP) alleviates hepatic steatosis by suppressing TLR4/MD-2-mediated inflammation and endoplasmic reticulum stress
|
Wang, Lingzhi |
|
|
147 |
C |
p. |
artikel |
37 |
d-type peptides based fluorescent probes for “turn on” sensing of heparin
|
Xu, Huan |
|
|
147 |
C |
p. |
artikel |
38 |
Dual inhibition of oxidative phosphorylation and glycolysis to enhance cancer therapy
|
Sheng, Xi |
|
|
147 |
C |
p. |
artikel |
39 |
Dual site reactivity of indole-3-Schiff bases with S/Se/Cl substituted ketenes for stereoselective C-4 substituted indole-β-lactams, biological evaluations, magic chloro effect and molecular docking studies
|
Sharma, Kiran |
|
|
147 |
C |
p. |
artikel |
40 |
Editorial Board
|
|
|
|
147 |
C |
p. |
artikel |
41 |
Effective α-glycosidase inhibitors based on polyphenolic benzothiazole heterocycles
|
Sevimli, Esra |
|
|
147 |
C |
p. |
artikel |
42 |
Exploration and structure–activity relationship research of benzenesulfonamide derivatives as potent TRPV4 inhibitors for treating acute lung injury
|
Wang, Mengyuan |
|
|
147 |
C |
p. |
artikel |
43 |
Exploring cyclopropylamine containing cyanopyrimidines as LSD1 inhibitors: Design, synthesis, ADMET, MD analysis and anticancer activity profiling
|
Ahmad Sheikh, Khursheed |
|
|
147 |
C |
p. |
artikel |
44 |
Exploring long-range fluorine–carbon J-coupling for conformational analysis of deoxyfluorinated disaccharides: A combined computational and NMR study
|
Chaloupecká, Ema |
|
|
147 |
C |
p. |
artikel |
45 |
Exploring novel indazole derivatives as ASK1 inhibitors: Design, synthesis, biological evaluation and docking studies
|
He, Mengni |
|
|
147 |
C |
p. |
artikel |
46 |
Exploring the antileishmanial activity of dicentrine from Ocotea puberula (Lauraceae) using biomembrane models
|
Rosa, Matheus E. |
|
|
147 |
C |
p. |
artikel |
47 |
Fenamates and ibuprofen as foundational components in the synthesis of innovative, targeted COX-2 anti-inflammatory drugs, undergoing thorough biopharmacological assessments and in-silico computational studies
|
Elgohary, Mohamed K. |
|
|
147 |
C |
p. |
artikel |
48 |
Granulathiazole A protects 6-OHDA-induced Parkinson's disease from ferroptosis via activating Nrf2/HO-1 pathway
|
Kong, Luqi |
|
|
147 |
C |
p. |
artikel |
49 |
Identification of FTY720 and COH29 as novel topoisomerase I catalytic inhibitors by experimental and computational studies
|
Zeng, Huang |
|
|
147 |
C |
p. |
artikel |
50 |
Impact of GSK-3β and CK-1δ on Wnt signaling pathway in alzheimer disease: A dual target approach
|
Sharma, Vinita |
|
|
147 |
C |
p. |
artikel |
51 |
Improved synthesis and application of an alkyne-functionalized isoprenoid analogue to study the prenylomes of motor neurons, astrocytes and their stem cell progenitors
|
Suazo, Kiall F. |
|
|
147 |
C |
p. |
artikel |
52 |
Inhibition of TGF-β1/Smad3 signaling by compound 5aa: A potential treatment for idiopathic pulmonary fibrosis
|
An, Baijiao |
|
|
147 |
C |
p. |
artikel |
53 |
In vitro and in vivo antiproliferative activity on lung cancer of two acylhydrazone based zinc(II) complexes
|
Chang, Qinghua |
|
|
147 |
C |
p. |
artikel |
54 |
Issue TOC
|
|
|
|
147 |
C |
p. |
artikel |
55 |
Label-free cell phenotypic profiling of histamine H4R receptor and discovery of non-competitive H4R antagonist from natural products
|
Tang, Hongming |
|
|
147 |
C |
p. |
artikel |
56 |
Lathyrane and premyrsinane Euphorbia diterpenes against Alzheimer's disease: Bioinspired synthesis, anti-cholinesterase and neuroprotection bioactivity
|
Sun, Lian |
|
|
147 |
C |
p. |
artikel |
57 |
Leucine zipper as a bridge for transaminase self-assembly: A fusion enzyme for efficient chiral conversion of d-phenylglycine
|
Liu, Jiali |
|
|
147 |
C |
p. |
artikel |
58 |
Membrane interactions in Alzheimer’s disease treatment strategies with multitarget molecules
|
Zambrano, Pablo |
|
|
147 |
C |
p. |
artikel |
59 |
Molecular docking approach for the design and synthesis of new pyrazolopyrimidine analogs of roscovitine as potential CDK2 inhibitors endowed with pronounced anticancer activity
|
Hamed, Ola Alaa |
|
|
147 |
C |
p. |
artikel |
60 |
Natural anti-neuroinflammatory inhibitors in vitro and in vivo from Aglaia odorata
|
Yin, Qianqian |
|
|
147 |
C |
p. |
artikel |
61 |
Natural products from Odontonema strictum promote neurite outgrowth in neuronal PC12 cells
|
Luhata, Lokadi Pierre |
|
|
147 |
C |
p. |
artikel |
62 |
N-Containing triterpenoid saponins from Mussaenda densiflora and identification of heinsiagenin A as a potent immunosuppressant
|
Du, Xiuying |
|
|
147 |
C |
p. |
artikel |
63 |
New meroterpenoids and polyketides from the endophytic fungus Paraphaeosphaeria sp. C-XB-J-1 and their anti-inflammatory and SARS-CoV-2 Mpro inhibitory activities
|
Li, Qi |
|
|
147 |
C |
p. |
artikel |
64 |
Non-peptidic inhibitors targeting SARS-CoV-2 main protease: A review
|
Xiao, Ya-Qi |
|
|
147 |
C |
p. |
artikel |
65 |
Novel CCR3-targeted cyclic peptides as potential therapeutic agents for age-related macular degeneration via inhibiting angiogenesis and reducing retinal photoreceptor damage
|
Li, Yuanyuan |
|
|
147 |
C |
p. |
artikel |
66 |
Novel guanidine derivatives targeting leukemia as selective Src/Abl dual inhibitors: Design, synthesis and anti-proliferative activity
|
Moustafa, Amr H. |
|
|
147 |
C |
p. |
artikel |
67 |
Novel 1,3,4-oxadiazole derivatives as highly potent microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitors
|
Gür Maz, Tuğçe |
|
|
147 |
C |
p. |
artikel |
68 |
Novel partially reversible NDM-1 inhibitors based on the naturally occurring houttuynin
|
Wang, Lifang |
|
|
147 |
C |
p. |
artikel |
69 |
Novel Pt(IV) complexes containing salvigenin ligand reverse cisplatin-induced resistance by inhibiting Rap1b-mediated cancer cell stemness in esophageal squamous cell carcinoma treatments
|
Zhao, Jia |
|
|
147 |
C |
p. |
artikel |
70 |
13-Oxyingenol-dodecanoate inhibits the growth of non-small cell lung cancer cells by targeting ULK1
|
Wang, Xin-Ye |
|
|
147 |
C |
p. |
artikel |
71 |
Peroxynitrite-activated fluorescent probe with two reaction triggers for pathological diagnosis and therapeutic evaluation of inflammation
|
Liu, Feiyan |
|
|
147 |
C |
p. |
artikel |
72 |
Photocatalytic regeneration of nicotinamide cofactor biomimetics drives biocatalytic reduction by Old Yellow enzymes
|
Luo, Feifan |
|
|
147 |
C |
p. |
artikel |
73 |
PI3Kδ and mTOR dual inhibitors: Design, synthesis and anticancer evaluation of 3-substituted aminomethylquinoline analogues
|
Yevale, Digambar |
|
|
147 |
C |
p. |
artikel |
74 |
Protein coupled thionine acetate probed silica nanoparticles: An integrated laser-assisted therapeutic approach for treating cancer
|
Kumar, Pankaj |
|
|
147 |
C |
p. |
artikel |
75 |
Pyrano[2,3-c]pyrazole fused spirooxindole-linked 1,2,3-triazoles as antioxidant agents: Exploring their utility in the development of antidiabetic drugs via inhibition of α-amylase and DPP4 activity
|
Chahal, Sandhya |
|
|
147 |
C |
p. |
artikel |
76 |
Rapid identifying of COX-2 inhibitors from turmeric (Curcuma longa) by bioaffinity ultrafiltration coupled with UPLC-Q Exactive-Orbitrap-MS and zebrafish-based in vivo validation
|
Lan, Zhenwei |
|
|
147 |
C |
p. |
artikel |
77 |
Research progress of PROTACs for neurodegenerative diseases therapy
|
Cai, Zhifang |
|
|
147 |
C |
p. |
artikel |
78 |
Secondary metabolites with fungicide potentials from the deep-sea seamount-derived fungus Talaromyces scorteus AS-242
|
Wang, Ying |
|
|
147 |
C |
p. |
artikel |
79 |
Selective activation of prodrugs in breast cancer using metabolic glycoengineering and the tetrazine ligation bioorthogonal reaction
|
Mitry, Madonna M.A. |
|
|
147 |
C |
p. |
artikel |
80 |
Structure-guided design of novel biphenyl-quinazoline derivatives as potent non-nucleoside reverse transcriptase inhibitors featuring improved anti-resistance, selectivity, and solubility
|
Wang, Jin-Si |
|
|
147 |
C |
p. |
artikel |
81 |
Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer
|
Elsayad, Khaled A. |
|
|
147 |
C |
p. |
artikel |
82 |
Synergistic promotion of angiogenesis after intracerebral hemorrhage by ginsenoside Rh2 and chrysophanol in rats
|
Li, Mengying |
|
|
147 |
C |
p. |
artikel |
83 |
Synthesis and biological evaluation of Halogen-Substituted novel α-Ketoamides as potential protein aggregation modulators in Alzheimer’s disease
|
Das, Bhanuranjan |
|
|
147 |
C |
p. |
artikel |
84 |
Synthesis and evaluation of pentacyclic triterpenoids conjugates as novel HBV entry inhibitors targeting NTCP receptor
|
Chen, Yixin |
|
|
147 |
C |
p. |
artikel |
85 |
Synthesis and preclinical evaluation of a novel probe [18F]AlF-NOTA-IPB-GPC3P for PET imaging of GPC3 positive tumor
|
Mo, Chunwei |
|
|
147 |
C |
p. |
artikel |
86 |
Synthesis and unexpected binding of monofluorinated N,Nʹ-diacetylchitobiose and LacdiNAc to wheat germ agglutinin
|
Kurfiřt, Martin |
|
|
147 |
C |
p. |
artikel |
87 |
Synthesis of obovatol and related neolignan analogues as α-glucosidase and α-amylase inhibitors
|
Sciacca, Claudia |
|
|
147 |
C |
p. |
artikel |
88 |
Synthesis, physicochemical characterization, and investigation of anti-inflammatory activity of water-soluble PEGylated 1,2,4-Triazoles
|
Li, Sin-Min |
|
|
147 |
C |
p. |
artikel |
89 |
Synthesis, structural, multitargeted molecular docking analysis of anti-cancer, anti-tubercular, DNA interactions of benzotriazole based macrocyclic ligand
|
Pon Matheswari, P. |
|
|
147 |
C |
p. |
artikel |
90 |
Targeted genetic and small molecule disruption of N-Ras CaaX cleavage alters its localization and oncogenic potential
|
Hildebrandt, Emily R. |
|
|
147 |
C |
p. |
artikel |
91 |
The effects of histidine substitution of aromatic residues on the amyloidogenic properties of the fragment 264–277 of nucleophosmin 1
|
Florio, Daniele |
|
|
147 |
C |
p. |
artikel |
92 |
The emerging role of deubiquitylating enzyme USP21 as a potential therapeutic target in cancer
|
Shi, Zhen-Yuan |
|
|
147 |
C |
p. |
artikel |
93 |
The novel small molecule E0924G dually regulates bone formation and bone resorption through activating the PPARδ signaling pathway to prevent bone loss in ovariectomized rats and senile mice
|
Li, Yining |
|
|
147 |
C |
p. |
artikel |
94 |
TMV-CP based rational design and discovery of α-Amide phosphate derivatives as anti plant viral agents
|
Chen, Shunhong |
|
|
147 |
C |
p. |
artikel |
95 |
Unveiling the tyrosinase inhibitory potential of phenolics from Centaurium spicatum: Bridging in silico and in vitro perspectives
|
Alruhaimi, Reem S. |
|
|
147 |
C |
p. |
artikel |