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                             64 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acylphloroglucinol trimers from Callistemon salignus seeds: Isolation, configurational assignment, hAChE inhibitory effects, and molecular docking studies Yu, Mu-Yuan
117 C p.
 artikel
2 A designed cyclic peptide based on Trastuzumab used to construct peptide-drug conjugates for its HER2-targeting ability Zhou, Jiaqi
117 C p.
 artikel
3 Amide-based xanthine oxidase inhibitors bearing an N-(1-alkyl-3-cyano-1H-indol-5-yl) moiety: Design, synthesis and structure-activity relationship investigation Zhang, Ting-jian
117 C p.
 artikel
4 Anticancer profile and anti-inflammatory effect of new N-(2-((4-(1,3-diphenyl-1H-pyrazol-4-yl)pyridine sulfonamide derivatives Abdel-Maksoud, Mohammed S.
117 C p.
 artikel
5 Artemicapillasins A–N, cytotoxic coumaric acid analogues against hepatic stellate cell LX2 from Artemisia capillaris (Yin-Chen) Gao, Zhen
117 C p.
 artikel
6 Assessment of elementary derivatives of 1,5-benzodiazepine as anticancer agents with synergy potential Gawandi, Sinthiya J.
117 C p.
 artikel
7 Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase Yapar, Gönül
117 C p.
 artikel
8 Caesalpinaxin, a cassane-type diterpenoid with a 21-carbon core skeleton from the seeds of Caesalpinia minax possessing pro-angiogenetic property Lou, Ruohan
117 C p.
 artikel
9 β-Carboline tethered cinnamoyl 2-aminobenzamides as class I selective HDAC inhibitors: Design, synthesis, biological activities and modelling studies Namballa, Hari Krishna
117 C p.
 artikel
10 Clavipyrrine A, a unique polycyclic nitrogenous meroterpenoid with promising anti-glioma effects isolated from the fungus Clitocybe clavipes Sun, Zhaocui
117 C p.
 artikel
11 Clickable, selective, and cell-permeable activity-based probe of human cathepsin B – Minimalistic approach for enhanced selectivity Bhuiyan, Ashif I.
117 C p.
 artikel
12 Continuous Sirtuin/HDAC (histone deacetylase) activity assay using thioamides as PET (Photoinduced Electron Transfer)–based fluorescence quencher Zessin, Matthes
117 C p.
 artikel
13 Corrigendum to “Rational design-aided discovery of novel 1,2,4-oxadiazole derivatives as potential EGFR inhibitors” [Bioorg. Chem. 114 (2021) 105124] Unadkat, Vishal
117 C p.
 artikel
14 Cytotoxic and apoptotic effects of 1,2-diborolanes with strong donor substitutes on human cancer cells Şahin, Yüksel
117 C p.
 artikel
15 Design and synthesis of naphthylchalcones as novel anti-leukaemia agents Leitão, Emília P.T.
117 C p.
 artikel
16 Design, parallel synthesis of Biginelli 1,4-dihydropyrimidines using PTSA as a catalyst, evaluation of anticancer activity and structure activity relationships via 3D QSAR studies Faizan, Syed
117 C p.
 artikel
17 Design, synthesis and binding mode of interaction of novel small molecule o-hydroxy benzamides as HDAC3-selective inhibitors with promising antitumor effects in 4T1-Luc breast cancer xenograft model Routholla, Ganesh
117 C p.
 artikel
18 Design, synthesis and biological evaluation of cinnamamide-quinazoline derivatives as potential EGFR inhibitors to reverse T790M mutation Zhang, Bin
117 C p.
 artikel
19 Design, synthesis, and evaluation of proliferation inhibitory activity of novel L-shaped ortho-quinone analogs as anticancer agents Yu, Jia
117 C p.
 artikel
20 Design, synthesis and structure-activity evaluation of novel 2-pyridone-based inhibitors of α-synuclein aggregation with potentially improved BBB permeability Mahía, Alejandro
117 C p.
 artikel
21 Design, synthesis, in vitro, and in silico studies of 1,2,4-triazole-piperazine hybrid derivatives as potential MAO inhibitors Uslu, Harun
117 C p.
 artikel
22 Development of anti-breast cancer PI3K inhibitors based on 7-azaindole derivatives through scaffold hopping: Design, synthesis and in vitro biological evaluation Yang, Chengbin
117 C p.
 artikel
23 Discovery of bletillain, an unusual benzyl polymer with significant autophagy-inducing effects in A549 lung cancer cells through the Akt/GSK-3β/β-catenin signaling pathway Zhu, Huan
117 C p.
 artikel
24 Discovery of KRas G12C-IN-3 and Pomalidomide-based PROTACs as degraders of endogenous KRAS G12C with potent anticancer activity Li, Ling
117 C p.
 artikel
25 Discovery of new 2-phenyl-1H-benzo[d]imidazole core-based potent α-glucosidase inhibitors: Synthesis, kinetic study, molecular docking, and in vivo anti-hyperglycemic evaluation Li, Yue
117 C p.
 artikel
26 Discovery of novel ibrutinib analogues to treat malignant melanoma Ren, Sumei
117 C p.
 artikel
27 Discovery of quinazolinyl-containing benzamides derivatives as novel HDAC1 inhibitors with in vitro and in vivo antitumor activities Zhang, Zixue
117 C p.
 artikel
28 Diterpenoids from Euphorbia glomerulans with potential reversal activities against P-glycoprotein-mediated multidrug resistance Hasan, Aobulikasimu
117 C p.
 artikel
29 Editorial Board
117 C p.
 artikel
30 Growing the molecular architecture of imidazole-like ligands in HO-1 complexes Floresta, Giuseppe
117 C p.
 artikel
31 Guided rational design with scaffold hopping leading to novel histamine H3 receptor ligands Ghamari, Nakisa
117 C p.
 artikel
32 HDAC/MIF dual inhibitor inhibits NSCLC cell survival and proliferation by blocking the AKT pathway Cao, Fangyuan
117 C p.
 artikel
33 Hepatoprotective, antioxidant and anti-inflammatory potentials of Vit-E/C@SeNPs in rats: Synthesis, characterization, biochemical, radio-biodistribution, molecular and histopathological studies Aljuhr, Safa A.
117 C p.
 artikel
34 Indolin-2-one derivatives as selective Aurora B kinase inhibitors targeting breast cancer Dokla, Eman M.E.
117 C p.
 artikel
35 Issue TOC
117 C p.
 artikel
36 Meta-substituted piperlongumine derivatives attenuate inflammation in both RAW264.7 macrophages and a mouse model of colitis Wang, Ziqing
117 C p.
 artikel
37 Molecular hybridization design and synthesis of novel spirooxindole-based MDM2 inhibitors endowed with BCL2 signaling attenuation; a step towards the next generation p53 activators Lotfy, Gehad
117 C p.
 artikel
38 New α-pyrone derivatives with herbicidal activity from the endophytic fungus Alternaria brassicicola Li, Fengli
117 C p.
 artikel
39 Novel 2,4-disubstituted quinazoline analogs as antibacterial agents with improved cytotoxicity profile: Optimization of the 2,4-substituents Aboushady, Dina
117 C p.
 artikel
40 Novel natural scaffold as hURAT1 inhibitor identified by 3D-shape-based, docking-based virtual screening approach and biological evaluation Chen, Xinhua
117 C p.
 artikel
41 Novel phenanthridine amide analogs as potential anti-leishmanial agents: In vitro and in silico insights Nandikolla, Adinarayana
117 C p.
 artikel
42 Potential inhibitors and plant based technology: An alternative approach to treat corona virus Sharma, Sachin
117 C p.
 artikel
43 Probing the Ca2+ mobilizing properties on primary cortical neurons of a new stable cADPR mimic D'Errico, Stefano
117 C p.
 artikel
44 Profiling sirtuin activity using Copper-free click chemistry Curry, Alyson M.
117 C p.
 artikel
45 Property activity refinement of 2-anilino 4-amino substituted quinazolines as antimalarials with fast acting asexual parasite activity Ashton, Trent D.
117 C p.
 artikel
46 Receptor mapping using methoxy phenyl piperazine derivative: Preclinical PET imaging Mann, Garima
117 C p.
 artikel
47 Secoiridoid dimers and their biogenetic precursors from the fruits of Cornus officinalis with potential therapeutic effects on type 2 diabetes Peng, Zhong-Can
117 C p.
 artikel
48 Site selective synthesis and anti-inflammatory evaluation of Spiro-isoxazoline stitched adducts of arteannuin B Ur Rasool, Javeed
117 C p.
 artikel
49 Structurally diverse biflavonoids from the fruits of Citrus medica L. var. sarcodactylis Swingle and their hypolipidemic and immunosuppressive activities Ma, Qin-Ge
117 C p.
 artikel
50 Structural simplification and bioisostere principle lead to Bis-benzodioxole-fibrate derivatives as potential hypolipidemic and hepatoprotective agents Xie, Yundong
117 C p.
 artikel
51 Structure–activity relationship and biological evaluation of 12 N-substituted aloperine derivatives as PD-L1 down-regulatory agents through proteasome pathway Zeng, Qing–Xuan
117 C p.
 artikel
52 Synthesis and biological evaluation of cationic TopFluor cholesterol analogues Jurášek, Michal
117 C p.
 artikel
53 Synthesis and hyperglycemic, biochemical and histopathological evaluation of novel sulfonylbiguanide and sulfonylurea derivatives as potent anti-diabetic agents Basyouni, Wahid M.
117 C p.
 artikel
54 Synthesis and in vitro evaluation of anti-inflammatory, antioxidant, and anti-fibrotic effects of new 8-aminopurine-2,6-dione-based phosphodiesterase inhibitors as promising anti-asthmatic agents Wójcik-Pszczoła, Katarzyna
117 C p.
 artikel
55 Synthesis and in vitro evaluation of chlorogenic acid amides as potential hypoglycemic agents and their synergistic effect with acarbose Cardullo, Nunzio
117 C p.
 artikel
56 Synthesis, biological evaluation and molecular docking of new sulfonamide-based indolinone derivatives as multitargeted kinase inhibitors against leukemia El-Hussieny, Marwa
117 C p.
 artikel
57 Synthesis, biological evaluation, and molecular docking studies of deoxygenated C-glycosides as LpxC inhibitors Dreger, Alexander
117 C p.
 artikel
58 Synthesis of a new series of pyrazolo[1,5-a]pyrimidines as CDK2 inhibitors and anti-leukemia Almehmadi, Samar J.
117 C p.
 artikel
59 Synthesis of aspirin-curcumin mimic conjugates of potential antitumor and anti-SARS-CoV-2 properties Srour, Aladdin M.
117 C p.
 artikel
60 The development of modulators for lysophosphatidic acid receptors: A comprehensive review Liu, Wenjie
117 C p.
 artikel
61 The Mpro structure-based modifications of ebselen derivatives for improved antiviral activity against SARS-CoV-2 virus Qiao, Zhen
117 C p.
 artikel
62 Triterpenoids and meroterpenoids with α-glucosidase inhibitory activities from the fruiting bodies of Ganoderma australe Guo, Jiao-Cen
117 C p.
 artikel
63 Triterpenoid saponins from the leaves and stems of Pericampylus glaucus and their insulin mimetic activities Lee, Hee-Ju
117 C p.
 artikel
64 Water-soluble pillar[5]arene sulfo-derivatives self-assemble into biocompatible nanosystems to stabilize therapeutic proteins Shurpik, Dmitriy N.
117 C p.
 artikel
                             64 gevonden resultaten
 
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