nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Amphiphilic azobenzenes: Antibacterial activities and biophysical investigation of their interaction with bacterial membrane lipids
|
Franche, A. |
|
|
94 |
C |
p. |
artikel |
2 |
A novel cathepsin L inhibitor prevents the progression of idiopathic pulmonary fibrosis
|
Yuan, Lei |
|
|
94 |
C |
p. |
artikel |
3 |
Anticancer, antimicrobial activities of quinoline based hydrazone analogues: Synthesis, characterization and molecular docking
|
Katariya, Kanubhai D |
|
|
94 |
C |
p. |
artikel |
4 |
Anticancer effects of sodium and potassium quercetin-5′-sulfonates through inhibition of proliferation, induction of apoptosis, and cell cycle arrest in the HT-29 human adenocarcinoma cell line
|
Czerwonka, Arkadiusz |
|
|
94 |
C |
p. |
artikel |
5 |
Apoptosis: A target for anticancer therapy with novel cyanopyridines
|
Ismail, Magda M.F. |
|
|
94 |
C |
p. |
artikel |
6 |
A review on anti-inflammatory activity of green synthesized zinc oxide nanoparticle: Mechanism-based approach
|
Agarwal, Happy |
|
|
94 |
C |
p. |
artikel |
7 |
Aromatic rosane diterpenoids from the roots of Euphorbia ebracteolata and their inhibitory effects against lipase
|
Li, Lu |
|
|
94 |
C |
p. |
artikel |
8 |
Atenolol thiourea hybrid as potent urease inhibitors: Design, biology-oriented drug synthesis, inhibitory activity screening, and molecular docking studies
|
Wahid, Sana |
|
|
94 |
C |
p. |
artikel |
9 |
Characterisation of utrophin modulator SMT C1100 as a non-competitive inhibitor of firefly luciferase
|
Wilkinson, Isabel V.L. |
|
|
94 |
C |
p. |
artikel |
10 |
Cloning and characterization of the β-xylosidase from Dictyoglomus turgidum for high efficient biotransformation of 10-deacetyl-7-xylosltaxol
|
Li, Qi |
|
|
94 |
C |
p. |
artikel |
11 |
Comparative study of the effects of ortho-, meta- and para-carboranes (C2B10H12) on the physicochemical properties, cytotoxicity and antiviral activity of uridine and 2′-deoxyuridine boron cluster conjugates
|
Saftić, Dijana |
|
|
94 |
C |
p. |
artikel |
12 |
Conjugates of tacrine and 1,2,4-thiadiazole derivatives as new potential multifunctional agents for Alzheimer’s disease treatment: Synthesis, quantum-chemical characterization, molecular docking, and biological evaluation
|
Makhaeva, Galina F. |
|
|
94 |
C |
p. |
artikel |
13 |
Conjugation of 4-aminosalicylate with thiazolinones afforded non-cytotoxic potent in vitro and in vivo anti-inflammatory hybrids
|
Abdu-Allah, Hajjaj H.M. |
|
|
94 |
C |
p. |
artikel |
14 |
Corrigendum to “Synthesis and biological evaluation of tetrazole derivatives as TNF-α, IL-6 and COX-2 inhibitors with antimicrobial activity: Computational analysis, molecular modeling study and region-specific cyclization using 2D NMR tools” [Bioorg. Chem. 92 (2019) 103301]
|
Lamie, Phoebe F. |
|
|
94 |
C |
p. |
artikel |
15 |
Coumarin Tröger’s base derivatives with cyanine substitution as selective and sensitive fluorescent lysosomal probes
|
Talianová, Veronika |
|
|
94 |
C |
p. |
artikel |
16 |
Design and synthesis of diphenylpyrimidine derivatives (DPPYs) as potential dual EGFR T790M and FAK inhibitors against a diverse range of cancer cell lines
|
Ai, Min |
|
|
94 |
C |
p. |
artikel |
17 |
Design and synthesis of novel parabanic acid derivatives as anticonvulsants
|
Aboutabl, Mona Elsayed |
|
|
94 |
C |
p. |
artikel |
18 |
Design and synthesis of novel 1-substituted 3-(6-phenoxypyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine analogs as selective BTK inhibitors for the treatment of mantle cell lymphoma
|
Ran, Fansheng |
|
|
94 |
C |
p. |
artikel |
19 |
Design and synthesis of selective and blood-brain barrier-permeable hydroxamate-based gelatinase inhibitors
|
Bertran, Alexandra |
|
|
94 |
C |
p. |
artikel |
20 |
Design and synthesis of tetrahydropyridopyrimidine derivatives as dual GPR119 and DPP-4 modulators
|
Fang, Yuanying |
|
|
94 |
C |
p. |
artikel |
21 |
Design, molecular modeling and anticancer evaluation of thieno[2,3-d]pyrimidine derivatives as inhibitors of topoisomerase II
|
El-Metwally, Souad A. |
|
|
94 |
C |
p. |
artikel |
22 |
Design of new quinolin-2-one-pyrimidine hybrids as sphingosine kinases inhibitors
|
Vettorazzi, Marcela |
|
|
94 |
C |
p. |
artikel |
23 |
Design, preparation and biological evaluation of a 177Lu-labeled somatostatin receptor antagonist for targeted therapy of neuroendocrine tumors
|
Behnammanesh, Hossein |
|
|
94 |
C |
p. |
artikel |
24 |
Design, synthesis and anti-HBV activity of NVR3-778 derivatives
|
Lv, Kai |
|
|
94 |
C |
p. |
artikel |
25 |
Design, synthesis and biological evaluation of 2-arylaminopyrimidine derivatives bearing 1,3,8-triazaspiro[4,5]decan-4-one or piperidine-3-carboxamide moiety as novel Type-I1/2 ALK inhibitors
|
Miao, Xiuqi |
|
|
94 |
C |
p. |
artikel |
26 |
Design, synthesis and biological evaluation of bicyclic carboxylic acid derivatives as IDO1 inhibitors
|
Cai, Shi |
|
|
94 |
C |
p. |
artikel |
27 |
Design, synthesis and biological evaluation of homoerythrina alkaloid derivatives bearing a triazole moiety as PARP-1 inhibitors and as potential antitumor drugs
|
Li, Shuai |
|
|
94 |
C |
p. |
artikel |
28 |
Design, synthesis and evaluation of novel ferulic acid derivatives as multi-target-directed ligands for the treatment of Alzheimer’s disease
|
Lan, Jin-Shuai |
|
|
94 |
C |
p. |
artikel |
29 |
Design, synthesis and in vitro evaluation of fangchinoline derivatives as potential anticancer agents
|
Zhang, Yan-chun |
|
|
94 |
C |
p. |
artikel |
30 |
Design, synthesis, biological evaluation and molecular modeling of novel 1H-pyrrolo[2,3-b]pyridine derivatives as potential anti-tumor agents
|
Wang, Ruifeng |
|
|
94 |
C |
p. |
artikel |
31 |
Design, synthesis, biological evaluation and molecular modeling study of new thieno[2,3-d]pyrimidines with anti-proliferative activity on pancreatic cancer cell lines
|
Salem, Mohamed S.H. |
|
|
94 |
C |
p. |
artikel |
32 |
Design, synthesis, cytotoxicity screening and molecular docking of new 3-cyanopyridines as survivin inhibitors and apoptosis inducers
|
Sabour, Rehab |
|
|
94 |
C |
p. |
artikel |
33 |
Design, synthesis, molecular modeling, in vivo studies and anticancer evaluation of quinazolin-4(3H)-one derivatives as potential VEGFR-2 inhibitors and apoptosis inducers
|
Mahdy, Hazem A. |
|
|
94 |
C |
p. |
artikel |
34 |
Detection techniques of carboxylesterase activity: An update review
|
Lan, Lulu |
|
|
94 |
C |
p. |
artikel |
35 |
Development of carbapenem-based fluorogenic probes for the clinical screening of carbapenemase-producing bacteria
|
Kim, Juhyeon |
|
|
94 |
C |
p. |
artikel |
36 |
Development of 1,3-thiazole analogues of imidazopyridines as potent positive allosteric modulators of GABAA receptors
|
Tikhonova, Tatyana A. |
|
|
94 |
C |
p. |
artikel |
37 |
Di- and tri-substituted s-triazine derivatives: Synthesis, characterization, anticancer activity in human breast-cancer cell lines, and developmental toxicity in zebrafish embryos
|
El-Faham, Ayman |
|
|
94 |
C |
p. |
artikel |
38 |
Discovery and optimization of novel N-benzyl-3,6-dimethylbenzo[d]isoxazol-5-amine derivatives as potent and selective TRIM24 bromodomain inhibitors with potential anti-cancer activities
|
Hu, Qingqing |
|
|
94 |
C |
p. |
artikel |
39 |
Discovery of 5-aryl-3-thiophen-2-yl-1H-pyrazoles as a new class of Hsp90 inhibitors in hepatocellular carcinoma
|
Mohamady, Samy |
|
|
94 |
C |
p. |
artikel |
40 |
Discovery of benzo[d]oxazole derivatives as the potent type-I FLT3-ITD inhibitors
|
Bao, Jiyin |
|
|
94 |
C |
p. |
artikel |
41 |
Discovery of gamma-mangostin from Garcinia mangostana as a potent and selective natural SIRT2 inhibitor
|
Yeong, Keng Yoon |
|
|
94 |
C |
p. |
artikel |
42 |
Discovery of nitrogenous sesquiterpene quinone derivatives from sponge Dysidea septosa with anti-inflammatory activity in vivo zebrafish model
|
Gui, Yu-Han |
|
|
94 |
C |
p. |
artikel |
43 |
Diterpenoids from the aerial parts of Flueggea acicularis and their activity against RANKL-induced osteoclastogenesis
|
Huang, Dane |
|
|
94 |
C |
p. |
artikel |
44 |
Diversity of complexes based on p-nitrobenzoylhydrazide, benzoylformic acid and diorganotin halides or oxides self-assemble: Cytotoxicity, the induction of apoptosis in cancer cells and DNA-binding properties
|
Jiang, Wujiu |
|
|
94 |
C |
p. |
artikel |
45 |
Editorial Board
|
|
|
|
94 |
C |
p. |
artikel |
46 |
Enzymatic synthesis of fatty acid esters of trehalose: Process optimization, characterization of the esters and evaluation of their bioactivities
|
Marathe, Sandesh J. |
|
|
94 |
C |
p. |
artikel |
47 |
E-pharmacophore guided discovery of pyrazolo[1,5-c]quinazolines as dual inhibitors of topoisomerase-I and histone deacetylase
|
Joshi, Gaurav |
|
|
94 |
C |
p. |
artikel |
48 |
Ethyl benzoate bearing pyrrolizine/indolizine moieties: Design, synthesis and biological evaluation of anti-inflammatory and cytotoxic activities
|
Attalah, Khalid M. |
|
|
94 |
C |
p. |
artikel |
49 |
Ethylenic conjugated coumarin thiazolidinediones as new efficient antimicrobial modulators against clinical methicillin-resistant Staphylococcus aureus
|
Hu, Chun-Fang |
|
|
94 |
C |
p. |
artikel |
50 |
Evaluation of biological activities, and exploration on mechanism of action of matrine–cholesterol derivatives
|
Xu, Jianwei |
|
|
94 |
C |
p. |
artikel |
51 |
Fabrication of nanoparticles from a synthesized peptide amphiphile as a versatile therapeutic cargo for high antiproliferative activity in tumor cells
|
Das, Soumi |
|
|
94 |
C |
p. |
artikel |
52 |
Fine-tuning the properties of the thrombin binding aptamer through cyclization: Effect of the 5′-3′ connecting linker on the aptamer stability and anticoagulant activity
|
Riccardi, Claudia |
|
|
94 |
C |
p. |
artikel |
53 |
Fluorinated 3,6,9-trisubstituted acridine derivatives as DNA interacting agents and topoisomerase inhibitors with A549 antiproliferative activity
|
Nunhart, Patrik |
|
|
94 |
C |
p. |
artikel |
54 |
Fluoroaryl analogs of sulforaphane – A group of compounds of anticancer and antimicrobial activity
|
Cierpiał, Tomasz |
|
|
94 |
C |
p. |
artikel |
55 |
Flurbiprofen-chalcone hybrid Mannich base derivatives as balanced multifunctional agents against Alzheimer’s disease: Design, synthesis and biological evaluation
|
Tian, Chaoquan |
|
|
94 |
C |
p. |
artikel |
56 |
Functionalization of 8-17 DNAzymes modulates catalytic efficiency and divalent metal ion preference
|
Du, Shanshan |
|
|
94 |
C |
p. |
artikel |
57 |
Functionalization of 9-thioxanthone at the 1-position: From arylamino derivatives to [1]benzo(thio)pyrano[4,3,2-de]benzothieno[2,3-b]quinolines of biological interest
|
Mokhtari Brikci-Nigassa, Nahida |
|
|
94 |
C |
p. |
artikel |
58 |
Green and facile synthesis of Ag nanoparticles using Crataegus pentagyna fruit extract (CP-AgNPs) for organic pollution dyes degradation and antibacterial application
|
Ebrahimzadeh, Mohammad Ali |
|
|
94 |
C |
p. |
artikel |
59 |
Halogenated aromatic thiosemicarbazones as potent inhibitors of tyrosinase and melanogenesis
|
Hałdys, Katarzyna |
|
|
94 |
C |
p. |
artikel |
60 |
Highly oxygenated polyketides produced by Trichoderma koningiopsis QA-3, an endophytic fungus obtained from the fresh roots of the medicinal plant Artemisia argyi
|
Shi, Xiao-Shan |
|
|
94 |
C |
p. |
artikel |
61 |
ICP-MS and HPLC analyses, enzyme inhibition and antioxidant potential of Achillea schischkinii Sosn.
|
Türkan, Fikret |
|
|
94 |
C |
p. |
artikel |
62 |
Identification and characterization of human interferon alpha inhibitors through a WISH cell line-based reporter gene assay
|
Bürgi, Milagros |
|
|
94 |
C |
p. |
artikel |
63 |
Identification of inhibitors of the immunosuppressive enzyme IL4I1
|
Presset, Marc |
|
|
94 |
C |
p. |
artikel |
64 |
Inhibition of nitric oxide and prostaglandin E2 production by pyrrolylated-chalcones: Synthesis, biological activity, crystal structure analysis, and molecular docking studies
|
Mohd Faudzi, Siti Munirah |
|
|
94 |
C |
p. |
artikel |
65 |
Insight into the binding affinity of thiourea in the calcium binding pocket of proteinase K, through high resolution X-ray crystallography
|
Ahmad, Malik Shoaib |
|
|
94 |
C |
p. |
artikel |
66 |
Introducing of acyclonucleoside analogues tethered 1,2,4-triazole as anticancer agents with dual epidermal growth factor receptor kinase and microtubule inhibitors
|
Aouad, Mohamed Reda |
|
|
94 |
C |
p. |
artikel |
67 |
In-vitro Anti-cancer assay and apoptotic cell pathway of newly synthesized benzoxazole-N-heterocyclic hybrids as potent tyrosine kinase inhibitors
|
Desai, Sulaksha |
|
|
94 |
C |
p. |
artikel |
68 |
In vivo evaluation and atom-based 3D-QSAR studies on saponins from shells of Xanthoceras sorbifolium Bunge as anti-AD agents
|
Chen, Gang |
|
|
94 |
C |
p. |
artikel |
69 |
Isobenzofuranone monomer and dimer derivatives from the mangrove endophytic fungus Epicoccum nigrum SCNU-F0002 possess α-glucosidase inhibitory and antioxidant activity
|
Yan, Zhangyuan |
|
|
94 |
C |
p. |
artikel |
70 |
Issue TOC
|
|
|
|
94 |
C |
p. |
artikel |
71 |
Modification on the 1,2-dihydro-2-oxo-pyridine-3-carboxamide core to obtain multi-target modulators of endocannabinoid system
|
Gado, Francesca |
|
|
94 |
C |
p. |
artikel |
72 |
Molecular docking, antiproliferative and anticonvulsant activities of swertiamarin isolated from Enicostemma axillare
|
Vaijanathappa, Jaishree |
|
|
94 |
C |
p. |
artikel |
73 |
Neurological and psychiatric management using COMT inhibitors: A review
|
Akhtar, Md Jawaid |
|
|
94 |
C |
p. |
artikel |
74 |
New quinoline-2-one/pyrazole derivatives; design, synthesis, molecular docking, anti-apoptotic evaluation, and caspase-3 inhibition assay
|
Aly, Ashraf A. |
|
|
94 |
C |
p. |
artikel |
75 |
New 2,6,9-trisubstituted purine derivatives as Bcr-Abl and Btk inhibitors and as promising agents against leukemia
|
Bertrand, Jeanluc |
|
|
94 |
C |
p. |
artikel |
76 |
Novel halogenated sulfonamide biguanides with anti-coagulation properties
|
Markowicz-Piasecka, Magdalena |
|
|
94 |
C |
p. |
artikel |
77 |
Novel 2-methylimidazolium salts: Synthesis, characterization, molecular docking, and carbonic anhydrase and acetylcholinesterase inhibitory properties
|
Bal, Selma |
|
|
94 |
C |
p. |
artikel |
78 |
O-GlcNAcylation of truncated NAC segment alters peptide-dependent effects on α-synuclein aggregation
|
Ryan, Philip |
|
|
94 |
C |
p. |
artikel |
79 |
Optimization of the benzamide fragment targeting the S2′ site leads to potent dipeptidyl peptidase-IV inhibitors
|
Deng, Xiaoyan |
|
|
94 |
C |
p. |
artikel |
80 |
Organic small molecular receptors as fluorimetric/bioimaging probe for extracellular/intracellular zinc sensation
|
Hanif, Muhammad |
|
|
94 |
C |
p. |
artikel |
81 |
Polycyclic furanobutenolide-derived norditerpenoids from the South China Sea soft corals Sinularia scabra and Sinularia polydactyla with immunosuppressive activity
|
Cui, Wan-Xiang |
|
|
94 |
C |
p. |
artikel |
82 |
Polyprenylated xanthones from the twigs and leaves of Garcinia nujiangensis and their cytotoxic evaluation
|
Liu, Xiao-Jia |
|
|
94 |
C |
p. |
artikel |
83 |
Preclinical evaluation of 1,2,4-triazole-based compounds targeting voltage-gated sodium channels (VGSCs) as promising anticonvulsant drug candidates
|
Kaproń, Barbara |
|
|
94 |
C |
p. |
artikel |
84 |
Preparation and anti-Raji lymphoma efficacy of a novel pH sensitive and magnetic targeting nanoparticles drug delivery system
|
Cai, Xiaohui |
|
|
94 |
C |
p. |
artikel |
85 |
Prospective computational design and in vitro bio-analytical tests of new chemical entities as potential selective CYP17A1 lyase inhibitors
|
Gumede, N.J. |
|
|
94 |
C |
p. |
artikel |
86 |
Protective effects of polydatin on multiple organ ischemia-reperfusion injury
|
Sun, Zhicheng |
|
|
94 |
C |
p. |
artikel |
87 |
Purification and characterization of β-galactosidase from newly isolated Aspergillus terreus (KUBCF1306) and evaluating its efficacy on breast cancer cell line (MCF-7)
|
Vidya, B. |
|
|
94 |
C |
p. |
artikel |
88 |
ω-Quinazolinonylalkyl aryl ureas as reversible inhibitors of monoacylglycerol lipase
|
Dato, Florian M. |
|
|
94 |
C |
p. |
artikel |
89 |
Rational approaches of drug design for the development of selective estrogen receptor modulators (SERMs), implicated in breast cancer
|
Makar, Subhajit |
|
|
94 |
C |
p. |
artikel |
90 |
Semisynthesis and biological evaluation of some novel Mannich base derivatives derived from a natural lignan obovatol as potential antifungal agents
|
Yang, Chun |
|
|
94 |
C |
p. |
artikel |
91 |
Steering the antitumor drug discovery campaign towards structurally diverse indolines
|
Thakur, Amandeep |
|
|
94 |
C |
p. |
artikel |
92 |
Structural and clinical impact of anti-allergy agents: An overview
|
Kapoor, Yagyesh |
|
|
94 |
C |
p. |
artikel |
93 |
Structure-based discovery of novel small molecule inhibitors of platelet-derived growth factor-B
|
Zarei, Omid |
|
|
94 |
C |
p. |
artikel |
94 |
Structure elucidation {spectroscopic, single crystal X-ray diffraction and computational DFT studies} of new tailored benzenesulfonamide derived Schiff base copper(II) intercalating complexes: Comprehensive biological profile {DNA binding, pBR322 DNA cleavage, Topo I inhibition and cytotoxic activity}
|
Afsan, Zeenat |
|
|
94 |
C |
p. |
artikel |
95 |
Studies on the selectivity of proline hydroxylases reveal new substrates including bicycles
|
Smart, Tristan J. |
|
|
94 |
C |
p. |
artikel |
96 |
Synthesis and antibacterial activity of 11,12-cyclic carbonate 4″-O-aralkylacetylhydrazineacyl azithromycin derivatives
|
Yan, Mi |
|
|
94 |
C |
p. |
artikel |
97 |
Synthesis and antibacterial evaluation against resistant Gram-negative bacteria of monobactams bearing various substituents on oxime residue
|
Li, Zhi–Wen |
|
|
94 |
C |
p. |
artikel |
98 |
Synthesis and antibacterial evaluation of a novel library of 2-(thiazol-5-yl)-1,3,4-oxadiazole derivatives against methicillin-resistant Staphylococcus aureus (MRSA)
|
Hannoun, Mohamed H. |
|
|
94 |
C |
p. |
artikel |
99 |
Synthesis and biological effects of small molecule enhancers for improved recombinant protein production in plant cell cultures
|
Rebelo, Bárbara A. |
|
|
94 |
C |
p. |
artikel |
100 |
Synthesis and biological evaluation of 1-(benzofuran-3-yl)-4-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazole derivatives as tubulin polymerization inhibitors
|
Qi, Zhi-Yuan |
|
|
94 |
C |
p. |
artikel |
101 |
Synthesis and biological evaluation of new chloro/acetoxy substituted isoindole analogues as new tyrosine kinase inhibitors
|
Köse, Aytekin |
|
|
94 |
C |
p. |
artikel |
102 |
Synthesis and biological evaluation of novel millepachine derivative containing aminophosphonate ester species as novel anti-tubulin agents
|
Huang, Xiaochao |
|
|
94 |
C |
p. |
artikel |
103 |
Synthesis and biological evaluations of novel isoxazoles and furoxan derivative as anti-inflammatory agents
|
Abdelall, Eman K.A. |
|
|
94 |
C |
p. |
artikel |
104 |
Synthesis and cytotoxic activity of chalcone analogues containing a thieno[2,3-d]pyrimidin-2-yl group as the A-ring or B-ring
|
Wang, Fu-Cheng |
|
|
94 |
C |
p. |
artikel |
105 |
Synthesis and discovery of pyrazolo-pyridine analogs as inflammation medications through pro- and anti-inflammatory cytokine and COX-2 inhibition assessments
|
Dennis Bilavendran, J. |
|
|
94 |
C |
p. |
artikel |
106 |
Synthesis and evaluation of antioxidant and antiproliferative activity of 2-arylbenzimidazoles
|
Baldisserotto, Anna |
|
|
94 |
C |
p. |
artikel |
107 |
Synthesis and evaluation of methoxy substituted 2-benzoyl-1-benzofuran derivatives as lead compounds for the development adenosine A1 and/or A2A receptor antagonists
|
Janse van Rensburg, Helena D. |
|
|
94 |
C |
p. |
artikel |
108 |
Synthesis and evaluation of the antitumor activity of Calix[4]arene l-proline derivatives
|
Oguz, Mehmet |
|
|
94 |
C |
p. |
artikel |
109 |
Synthesis and in-vitro anti-proliferative evaluation of some pyrazolo[1,5-a]pyrimidines as novel larotrectinib analogs
|
Attia, Mohamed H. |
|
|
94 |
C |
p. |
artikel |
110 |
Synthesis and molecular docking studies of imines as α-glucosidase and α-amylase inhibitors
|
Aispuro-Pérez, Analy |
|
|
94 |
C |
p. |
artikel |
111 |
Synthesis and molecular docking studies of some novel antimicrobial benzamides
|
Acar, Cemre |
|
|
94 |
C |
p. |
artikel |
112 |
Synthesis, characterization and molecular docking of some novel hydrazonothiazolines as urease inhibitors
|
Shehzad, Muhammad Tariq |
|
|
94 |
C |
p. |
artikel |
113 |
Synthesis, in vitro alpha-glucosidase inhibitory potential of benzimidazole bearing bis-Schiff bases and their molecular docking study
|
Rahim, Fazal |
|
|
94 |
C |
p. |
artikel |
114 |
Synthesis, in vitro α-amylase inhibitory, and radicals (DPPH & ABTS) scavenging potentials of new N-sulfonohydrazide substituted indazoles
|
Rafique, Rafaila |
|
|
94 |
C |
p. |
artikel |
115 |
Synthesis, in vitro and in vivo biological evaluation of dihydroartemisinin derivatives with potential anti-Toxoplasma gondii agents
|
Deng, Hao |
|
|
94 |
C |
p. |
artikel |
116 |
Synthesis, molecular docking, dynamic simulations, kinetic mechanism, cytotoxicity evaluation of N-(substituted-phenyl)-4-{(4-[(E)-3-phenyl-2-propenyl]-1-piperazinyl} butanamides as tyrosinase and melanin inhibitors: In vitro, in vivo and in silico approaches
|
Raza, Hussain |
|
|
94 |
C |
p. |
artikel |
117 |
Synthesis of chlorophyll-a homologs by C132-substitutions and their physico- and biochemical properties
|
Ogasawara, Shin |
|
|
94 |
C |
p. |
artikel |
118 |
Synthesis of d-ring modified acid hydrazide derivatives of podophyllotoxin and their anticancer studies as Tubulin inhibiting agents
|
Nerella, Srinivas |
|
|
94 |
C |
p. |
artikel |
119 |
Synthesis of naphthalimide-carborane and metallacarborane conjugates: Anticancer activity, DNA binding ability
|
Nekvinda, Jan |
|
|
94 |
C |
p. |
artikel |
120 |
Synthesis of new indazole based dual inhibitors of α-glucosidase and α-amylase enzymes, their in vitro, in silico and kinetics studies
|
Rafique, Rafaila |
|
|
94 |
C |
p. |
artikel |
121 |
Synthesis of novel 2-aminobenzothiazole derivatives as potential antimicrobial agents with dual DNA gyrase/topoisomerase IV inhibition
|
Ismail, Magda M.F. |
|
|
94 |
C |
p. |
artikel |
122 |
Synthesis of 1,2,4-triazolo[1,5-a]pyrimidine derivatives: Antimicrobial activity, DNA Gyrase inhibition and molecular docking
|
Abd El-Aleam, Rehab H. |
|
|
94 |
C |
p. |
artikel |
123 |
Taxumarienes A–G, seven new α-glucosidase inhibitory taxane-diterpenoids from the leaves of Taxus mairei
|
Chen, Kang |
|
|
94 |
C |
p. |
artikel |
124 |
The anti-cancer compound Schweinfurthin A targets Osh2 and disrupts lipid metabolism in the yeast model
|
Moosavi, Behrooz |
|
|
94 |
C |
p. |
artikel |
125 |
The first enzyme-promoted addition of nitromethane to imines (aza-Henry reaction)
|
Janicki, Ignacy |
|
|
94 |
C |
p. |
artikel |
126 |
The larvicidal activity of natural inspired piperine-based dienehydrazides against Culex pipiens
|
Tantawy, Ahmed H. |
|
|
94 |
C |
p. |
artikel |
127 |
The noncovalent conjugations of bovine serum albumin with three structurally different phytosterols exerted antiglycation effects: A study with AGEs-inhibition, multispectral, and docking investigations
|
Sobhy, Remah |
|
|
94 |
C |
p. |
artikel |
128 |
Thermostability detection and optimization of glycoengineered antibodies and antibody-drug conjugates based on differential scanning flouremitry analysis
|
Qin, Ken |
|
|
94 |
C |
p. |
artikel |
129 |
The synthetic flavanone 6-methoxy-2-(naphthalen-1-yl)chroman-4-one induces apoptosis and activation of the MAPK pathway in human U-937 leukaemia cells
|
Saavedra, Ester |
|
|
94 |
C |
p. |
artikel |
130 |
Three new bioactive natural products from the fungus Talaromyces assiutensis JTY2
|
Cai, Jin |
|
|
94 |
C |
p. |
artikel |
131 |
Total synthesis and anti-inflammatory evaluation of violacin A and its analogues
|
Liu, Qingyin |
|
|
94 |
C |
p. |
artikel |
132 |
Water-soluble betaines and amines based on thiacalix[4]arene scaffold as new cholinesterase inhibitors
|
Padnya, Pavel L. |
|
|
94 |
C |
p. |
artikel |