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                             64 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Additional alkaloids from Zoanthus vietnamensis with neuroprotective and anti-angiogenic effects Chen, Shu-Rong
109 C p.
 artikel
2 A new twist of rubredoxin function in M. tuberculosis Sushko, Tatsiana
109 C p.
 artikel
3 An insight into the structure of 5-spiro aromatic derivatives of imidazolidine-2,4-dione, a new group of very potent inhibitors of tumor multidrug resistance in T-lymphoma cells Żesławska, Ewa
109 C p.
 artikel
4 Antibacterial activity of a new monocarbonyl analog of curcumin MAC 4 is associated with divisome disruption Polaquini, Carlos R.
109 C p.
 artikel
5 Antioxidant and anti-sickling activity of glucal-based triazoles compounds – An in vitro and in silico study Vieira Veloso, Rodinei
109 C p.
 artikel
6 Antiproliferative activity, enzymatic inhibition and apoptosis-promoting effects of benzoxazole-based hybrids on human breast cancer cells Omar, A.-Mohsen M.E.
109 C p.
 artikel
7 Asymmetric synthesis and in vivo/in vitro characterization of new hybrid anticonvulsants derived from (2,5-dioxopyrrolidin-1-yl)phenylacetamides Abram, Michał
109 C p.
 artikel
8 Cathepsin K inhibitors based on 2-amino-1,3,4-oxadiazole derivatives Gontijo, Talita B.
109 C p.
 artikel
9 Chaetocochin J, an epipolythiodioxopiperazine alkaloid, induces apoptosis and autophagy in colorectal cancer via AMPK and PI3K/AKT/mTOR pathways Hu, Song
109 C p.
 artikel
10 Combining cross-coupling reaction and Knoevenagel condensation in the synthesis of glyco-BODIPY probes for DC-SIGN super-resolution bioimaging Biagiotti, Giacomo
109 C p.
 artikel
11 Deciphering structural bases of intestinal and hepatic selectivity in targeting pregnane X receptor with indole-based microbial mimics Li, Hao
109 C p.
 artikel
12 Design and synthesis of 4-anilinoquinazolines as Raf kinase inhibitors. Part 1. Selective B-Raf/B-RafV600E and potent EGFR/VEGFR2 inhibitory 4-(3-hydroxyanilino)-6-(1H-1,2,3-triazol-4-yl)quinazolines Lee, Cheng-I
109 C p.
 artikel
13 Design and synthesis of new carbamates as inhibitors for fatty acid amide hydrolase and cholinesterases: Molecular dynamic, in vitro and in vivo studies Maleki, Mahdi Faal
109 C p.
 artikel
14 Design and synthesis of novel 3,4-dihydrocoumarins as potent and selective monoamine oxidase-B inhibitors with the neuroprotection against Parkinson’s disease Liu, Li
109 C p.
 artikel
15 Design, synthesis and anti-rheumatoid arthritis evaluation of double-ring conjugated enones Zhou, Shiyang
109 C p.
 artikel
16 Design, synthesis and biological assessment of novel CDK4 inhibitor with potent anticancer activity Li, Yongtao
109 C p.
 artikel
17 Design, synthesis and biological evaluations of diverse Michael acceptor-based phenazine hybrid molecules as TrxR1 inhibitors Zhong, Yucheng
109 C p.
 artikel
18 Design, synthesis, and cytotoxic activity of novel 2H-imidazo[1,2-c]pyrazolo[3,4-e]pyrimidine derivatives Zheng, You-Guang
109 C p.
 artikel
19 Design, synthesis and in vitro anticancer research of novel tetrandrine and fangchinoline derivatives Gao, Xiu-zheng
109 C p.
 artikel
20 Design, synthesis and molecular modeling of new quinazolin-4(3H)-one based VEGFR-2 kinase inhibitors for potential anticancer evaluation Abdallah, Abdallah E.
109 C p.
 artikel
21 Discovery of higenamine as a potent, selective and cellular active natural LSD1 inhibitor for MLL-rearranged leukemia therapy Fang, Yuan
109 C p.
 artikel
22 Discovery of novel 2H-chromene-3-carbonyl derivatives as selective estrogen receptor degraders (SERDs): Design, synthesis and biological evaluation Lu, Xiang
109 C p.
 artikel
23 Editorial Board
109 C p.
 artikel
24 Enhancing the chemosensitivity of HepG2 cells towards cisplatin by organoselenium pseudopeptides Shaaban, Saad
109 C p.
 artikel
25 ESIPT-based fluorescent probe for bioimaging and identification of group IIIA ions in live cells and zebrafish Zheng, Qinxiang
109 C p.
 artikel
26 Flavonoids from Pterogyne nitens as Zika virus NS2B-NS3 protease inhibitors Lima, Caroline Sprengel
109 C p.
 artikel
27 Gancochlearols E − I, meroterpenoids from Ganoderma cochlear against COX-2 and triple negative breast cancer cells and the absolute configuration assignment of ganomycin K Li, Yan-Peng
109 C p.
 artikel
28 Green catalyst Cu(II)-enzyme-mediated eco-friendly synthesis of 2-pyrimidinamines as potential larvicides against Culex quinquefasciatus mosquito and toxicity investigation against non-target aquatic species Chidambaram, SathishKumar
109 C p.
 artikel
29 Identification of a new natural biflavonoids against breast cancer cells induced ferroptosis via the mitochondrial pathway Xie, Yang
109 C p.
 artikel
30 In vitro anti-melanogenic effects of chimeric compounds, 2-(substituted benzylidene)-1,3-indanedione derivatives with a β-phenyl-α, β -unsaturated dicarbonyl scaffold Ryu, Il Young
109 C p.
 artikel
31 In vivo and in vitro anti-inflammatory, antipyretic and ulcerogenic activities of pyridone and chromenopyridone derivatives, physicochemical and pharmacokinetic studies Fayed, Eman A.
109 C p.
 artikel
32 Issue TOC
109 C p.
 artikel
33 Lipopeptides production by a newly Halomonas venusta strain: Characterization and biotechnological properties Cheffi, Meriam
109 C p.
 artikel
34 Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa Nocedo-Mena, Deyani
109 C p.
 artikel
35 New substituted pyrazolones and dipyrazolotriazines as promising tyrosyl-tRNA synthetase and peroxiredoxin-5 inhibitors: Design, synthesis, molecular docking and structure-activity relationship (SAR) analysis Othman, Ismail M.M.
109 C p.
 artikel
36 Non-classical cardenolides from Calotropis gigantea exhibit anticancer effect as HIF-1 inhibitors Zheng, Zhiyuan
109 C p.
 artikel
37 Novel α-Aminophosphonates of imatinib Intermediate: Synthesis, anticancer Activity, human Abl tyrosine kinase Inhibition, ADME and toxicity prediction Aita, Saikiran
109 C p.
 artikel
38 Novel, natural allosteric inhibitors and enhancers of Candida rugosa lipase activity Menden, Ariane
109 C p.
 artikel
39 Novel thienopyrimidine analogues as potential metabotropic glutamate receptors inhibitors and anticancer activity: Synthesis, In-vitro, In-silico, and SAR approaches Khedr, Mohammed A.
109 C p.
 artikel
40 Overcome the tumor immunotherapy resistance by combination of the HDAC6 inhibitors with antitumor immunomodulatory agents Yussuf Khamis, Mussa
109 C p.
 artikel
41 Peptide-targeted dendrimeric prodrugs of 5-aminolevulinic acid: A novel approach towards enhanced accumulation of protoporphyrin IX for photodynamic therapy Tewari, K.M.
109 C p.
 artikel
42 Preclinical assessment of stem of Nicotiana tabacum on excision wound model Sharma, Yash
109 C p.
 artikel
43 Procerolides A-B from Microcionidae marine sponge Clathria procera: Anti-inflammatory macrocylic lactones with selective cyclooxygenase-2 attenuation properties Chakraborty, Kajal
109 C p.
 artikel
44 Quinazolinone-dihydropyrano[3,2-b]pyran hybrids as new α-glucosidase inhibitors: Design, synthesis, enzymatic inhibition, docking study and prediction of pharmacokinetic Sherafati, Maedeh
109 C p.
 artikel
45 Quinolines, a perpetual, multipurpose scaffold in medicinal chemistry Yadav, Pratibha
109 C p.
 artikel
46 Seven new prenylated flavanones from the roots of Sophora flavescens and their anti-proliferative activities Yang, Ya-nan
109 C p.
 artikel
47 STAT3-induced HLA-F-AS1 promotes cell proliferation and stemness characteristics in triple negative breast cancer cells by upregulating TRABD Wu, Di
109 C p.
 artikel
48 Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity Xiang, Zhi-Nan
109 C p.
 artikel
49 Synthesis and antiplasmodial evaluation of 1H-1,2,3-triazole grafted 4-aminoquinoline-benzoxaborole hybrids and benzoxaborole analogues Saini, Anu
109 C p.
 artikel
50 Synthesis and biological evaluation of novel 8- substituted sampangine derivatives as potent inhibitor of Zn2+-Aβ complex mediated toxicity, oxidative stress and inflammation Xie, Ren-ren
109 C p.
 artikel
51 Synthesis and biological evaluation of pentacyclic triterpenoid derivatives as potential novel antibacterial agents Wu, Panpan
109 C p.
 artikel
52 Synthesis and structure-activity relationship of lipo-diterpenoid alkaloids with potential target of topoisomerase IIα for breast cancer treatment Luan, Shangxian
109 C p.
 artikel
53 Synthesis, anticancer evaluation and mechanism studies of novel indolequinone derivatives of ursolic acid Wang, Wen-Yan
109 C p.
 artikel
54 Synthesis, in vitro and computational studies of novel glycosyl-1, 2, 3-1H-triazolyl methyl benzamide derivatives as potential α-glucosidase inhibitory activity Shukla, Akhilesh Kumar
109 C p.
 artikel
55 Synthesis, in-vitro evaluation, molecular docking, and kinetic studies of pyridazine-triazole hybrid system as novel α-glucosidase inhibitors Moghimi, Setareh
109 C p.
 artikel
56 Synthesis of 4,6-diphenylpyrimidin-2-ol derivatives as new benzodiazepine receptor ligands Khoramjouy, Mona
109 C p.
 artikel
57 Synthesis of nigranoic acid and manwuweizic acid derivatives as HDAC inhibitors and anti-inflammatory agents Ni, Dong-Xuan
109 C p.
 artikel
58 Synthesis, X-ray, Hirshfeld surface analysis, exploration of DNA binding, urease enzyme inhibition and anticancer activities of novel adamantane-naphthyl thiourea conjugate Arshad, Nasima
109 C p.
 artikel
59 Tailoring an aldo-keto reductase KmAKR for robust thermostability and catalytic efficiency by stepwise evolution and structure-guided consensus engineering Li, Shu-Fang
109 C p.
 artikel
60 Targeting GRP receptor: Design, synthesis and preliminary biological characterization of new non-peptide antagonists of bombesin Palmioli, Alessandro
109 C p.
 artikel
61 Tautomeric preference in lumazines, deazalumazines, isoalloxazines and pyrimidines and its effect on the reactivity of alkyl groups Kondrashova, Svetlana A.
109 C p.
 artikel
62 Telomerase activators from 20(27)-octanor-cycloastragenol via biotransformation by the fungal endophytes Duman, Seda
109 C p.
 artikel
63 Therapeutic potential of N4 -substituted thiosemicarbazones as new urease inhibitors: Biochemical and in silico approach Islam, Muhammad
109 C p.
 artikel
64 Verifying the role of 3-hydroxy of 17-cyclopropylmethyl-4,5α-epoxy-3,14β-dihydroxy-6β-[(4′-pyridyl) carboxamido]morphinan derivatives via their binding affinity and selectivity profiles on opioid receptors Huang, Boshi
109 C p.
 artikel
                             64 gevonden resultaten
 
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