nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Aloe emodin-conjugated sulfonyl hydrazones as novel type of antibacterial modulators against S. aureus 25923 through multifaceted synergistic effects
|
Deng, Zhao |
|
|
127 |
C |
p. |
artikel |
2 |
An insight into the interaction between Indisulam and human serum albumin: Spectroscopic method, computer simulation and in vitro cytotoxicity assay
|
Zhou, Bijia |
|
|
127 |
C |
p. |
artikel |
3 |
A novel Gboxin analog induces OXPHOS inhibition and mitochondrial dysfunction-mediated apoptosis in diffuse large B-cell lymphoma
|
Yao, Si |
|
|
127 |
C |
p. |
artikel |
4 |
A novel long excitation/emission wavelength fluorophore as platform utilized to construct NIR probes for bioimaging and biosensing
|
Qin, Jingcan |
|
|
127 |
C |
p. |
artikel |
5 |
A novel ratiometric fluorescent probe for the detection and imaging of cysteine in living cells
|
Zheng, Cheng |
|
|
127 |
C |
p. |
artikel |
6 |
Antidiabetic lanostane triterpenoids from the fruiting bodies of Ganoderma weberianum
|
Yang, Li |
|
|
127 |
C |
p. |
artikel |
7 |
Antifungal evaluation and mechanistic investigations of membrane active short synthetic peptides-based amphiphiles
|
Sharma, Komal |
|
|
127 |
C |
p. |
artikel |
8 |
An unprecedented ergostane with a 6/6/5 tricyclic 13(14 → 8)abeo-8,14-seco skeleton from Talaromyces adpressus
|
Zhang, Mi |
|
|
127 |
C |
p. |
artikel |
9 |
Applications of “linkers” in fragment-based drug design
|
Wu, Xin |
|
|
127 |
C |
p. |
artikel |
10 |
Biocatalytic hydrogen-transfer to access enantiomerically pure proxyphylline, xanthinol, and diprophylline
|
Borowiecki, Paweł |
|
|
127 |
C |
p. |
artikel |
11 |
Brujavanoids A–U, structurally diverse apotirucallane-type triterpenoids from Brucea javanica and their anti-inflammatory effects
|
Hu, Zhuo-Fan |
|
|
127 |
C |
p. |
artikel |
12 |
Cadinane-type sesquiterpenoid dimeric diastereomers hibisceusones A-C from infected stems of Hibiscus tiliaceus with cytotoxic activity against triple-negative breast cancer cells
|
Chen, De-Li |
|
|
127 |
C |
p. |
artikel |
13 |
Carbohydrate-derived bicyclic selenazolines as new dual inhibitors (cholinesterases/OGA) against Alzheimer’s disease
|
Velueta-Viveros, Martha |
|
|
127 |
C |
p. |
artikel |
14 |
Cardiac glycosides from the roots of Streblus asper Lour. with activity against Epstein-Barr virus lytic replication
|
Cai, Jing |
|
|
127 |
C |
p. |
artikel |
15 |
[11]-chaetoglobosins with cytotoxic activities from Pseudeurotium bakeri
|
Duan, Fangfang |
|
|
127 |
C |
p. |
artikel |
16 |
Corrigendum to “Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity” [Bioorg. Chem. 121 (2022) 105691]
|
Svirčev, Miloš |
|
|
127 |
C |
p. |
artikel |
17 |
Cucurbitane triterpenoid entities derived from Hemsleya penxianensis triggered glioma cell apoptosis via ER stress and MAPK signalling cross-talk
|
Li, Zongyang |
|
|
127 |
C |
p. |
artikel |
18 |
Dehydromevalonolactone ameliorates liver fibrosis and inflammation by repressing activation of NLRP3 inflammasome
|
Niu, Wei-Xiao |
|
|
127 |
C |
p. |
artikel |
19 |
Design and synthesis of novel benzimidazole-iminosugars linked a substituted phenyl group and their inhibitory activities against β-glucosidase
|
Liu, Xu |
|
|
127 |
C |
p. |
artikel |
20 |
Design and synthesis of novel benzoazoninone derivatives as potential CBSIs and apoptotic inducers: In Vitro, in Vivo, molecular docking, molecular dynamics, and SAR studies
|
Hammouda, Mohamed M. |
|
|
127 |
C |
p. |
artikel |
21 |
Design, synthesis, and anticancer evaluation of ammosamide B with pyrroloquinoline derivatives as novel BRD4 inhibitors
|
Li, Wen |
|
|
127 |
C |
p. |
artikel |
22 |
Design, synthesis and biological evaluation of a series of novel pyrrolo[2,3-d]pyrimidin/pyrazolo[3,4-d]pyrimidin-4-amine derivatives as FGFRs-dominant multi-target receptor tyrosine kinase inhibitors for the treatment of gastric cancer
|
Wu, Xiuli |
|
|
127 |
C |
p. |
artikel |
23 |
Design, synthesis and biological evaluation of N-(4-alkoxy-3-(1H-tetrazol-1-yl)phenyl) heterocyclic aromatic amide derivatives as xanthine oxidase inhibitors
|
Zhang, Ting-jian |
|
|
127 |
C |
p. |
artikel |
24 |
Design, synthesis, characterization and anticancer activity evaluation of deoxycholic acid-chalcone conjugates
|
Patel, Sejal |
|
|
127 |
C |
p. |
artikel |
25 |
Design, synthesis, in vitro, and in silico enzymatic evaluations of thieno[2,3-b]quinoline-hydrazones as novel inhibitors for α-glucosidase
|
Noori, Milad |
|
|
127 |
C |
p. |
artikel |
26 |
Development of a series of novel Mcl-1 inhibitors bearing an indole carboxylic acid moiety
|
Deng, Hongguang |
|
|
127 |
C |
p. |
artikel |
27 |
Dihydroxyphenyl-substituted thiosemicarbazone: A potent scaffold for the development of metallo-β-lactamases inhibitors and antimicrobial
|
Liu, Lu |
|
|
127 |
C |
p. |
artikel |
28 |
Directed evolution of a carbonyl reductase LsCR for the enantioselective synthesis of (1S)-2-chloro-1-(3,4-difluorophenyl) ethanol
|
Liu, Hua-Tao |
|
|
127 |
C |
p. |
artikel |
29 |
Discovery and evaluation of cytisine N-isoflavones as novel EGFR/HER2 dual inhibitors
|
Wang, Yanqing |
|
|
127 |
C |
p. |
artikel |
30 |
Discovery of a novel class of benzoxazole derivatives as histamine H3 receptor ligands for the treatment of neuropathic pain
|
Li, Ziying |
|
|
127 |
C |
p. |
artikel |
31 |
Discovery of benzamide derivatives containing urea moiety as soluble epoxide hydrolase inhibitors
|
Tian, Ye |
|
|
127 |
C |
p. |
artikel |
32 |
Discovery of carbamate-based N-salicyloyl tryptamine derivatives as novel pleiotropic agents for the treatment of Alzheimer's disease
|
Wang, Yuying |
|
|
127 |
C |
p. |
artikel |
33 |
Discovery of evodiamine derivatives as potential lead antifungal agents for the treatment of superficial fungal infections
|
Liang, Yan |
|
|
127 |
C |
p. |
artikel |
34 |
Discovery of novel 4-arylamino-quinazoline derivatives as EGFRL858R/T790M inhibitors with the potential to inhibit the non-small cell lung cancers
|
Gan, Wenhui |
|
|
127 |
C |
p. |
artikel |
35 |
Diverse polycyclic polyprenylated acylphloroglucinols with anti-neuroinflammatory activity from Hypericum beanii
|
Li, Ya-Wei |
|
|
127 |
C |
p. |
artikel |
36 |
Editorial Board
|
|
|
|
127 |
C |
p. |
artikel |
37 |
Energy metabolism as a target for cyclobenzaprine: A drug candidate against Visceral Leishmaniasis
|
Lima, Marta Lopes |
|
|
127 |
C |
p. |
artikel |
38 |
Evaluation of the cell permeability of bicyclic peptoids and bicyclic peptide-peptoid hybrids
|
Wang, Hee Myeong |
|
|
127 |
C |
p. |
artikel |
39 |
Flavone-1,2,3-triazole derivatives as potential α-glucosidase inhibitors: Synthesis, enzyme inhibition, kinetic analysis and molecular docking study
|
Dhameja, Manoj |
|
|
127 |
C |
p. |
artikel |
40 |
From EGFR kinase inhibitors to anti-inflammatory drugs: Optimization and biological evaluation of (4-(phenylamino)quinazolinyl)-phenylthiourea derivatives as novel NF-κB inhibitors
|
Wagdy, Reem A. |
|
|
127 |
C |
p. |
artikel |
41 |
Further studies on C2′-substituted 1-phenylbenzazepines as dopamine D1 receptor ligands
|
Giri, Rajan |
|
|
127 |
C |
p. |
artikel |
42 |
Genus Thermotoga: A valuable home of multifunctional glycoside hydrolases (GHs) for industrial sustainability
|
Akram, Fatima |
|
|
127 |
C |
p. |
artikel |
43 |
Heterocyclic ring expansion yields anthraquinone derivatives potent against multidrug resistant tumor cells
|
Tikhomirov, Alexander S. |
|
|
127 |
C |
p. |
artikel |
44 |
Hexa-substituted cyclotriphosphazene derivatives containing hetero-ring chalcones: Synthesis, in vitro cytotoxic activity and their DNA damage determination
|
Beytur, Asiye |
|
|
127 |
C |
p. |
artikel |
45 |
Imidazo[4,5-b]pyridine derived tubulin polymerization inhibitors: Design, synthesis, biological activity in vitro and computational analysis
|
Boček, Ida |
|
|
127 |
C |
p. |
artikel |
46 |
Implications of N7-hydrogen and C8-keto on the base pairing, mutagenic potential and repair of 8-oxo-2′-deoxy-adenosine: Investigation by nucleotide analogues
|
Wu, Junjie |
|
|
127 |
C |
p. |
artikel |
47 |
Investigation of binding mechanism for human plasminogen Kringle 5 with its potential receptor vWA1 domain in Cochlin by bio-specific technologies and molecular dynamic simulation
|
Zhang, Jiaxin |
|
|
127 |
C |
p. |
artikel |
48 |
Investigation of carbonic anhydrase inhibitory effects and cytotoxicities of pyrazole-based hybrids carrying hydrazone and zinc-binding benzenesulfonamide pharmacophores
|
Yamali, Cem |
|
|
127 |
C |
p. |
artikel |
49 |
Investigation on the potential targets of Astragaloside IV against intracerebral hemorrhage based on network pharmacology and experimental validation
|
Zheng, Yingyi |
|
|
127 |
C |
p. |
artikel |
50 |
(+)-Isocryptotanshinone derivatives and its simplified analogs as STAT3 signaling pathway inhibitors
|
Shi, Xiang |
|
|
127 |
C |
p. |
artikel |
51 |
Isolation, derivatization, in-vitro, and in-silico studies of potent butyrylcholinesterase inhibitors from Berberis parkeriana Schneid
|
Ali, Rabia |
|
|
127 |
C |
p. |
artikel |
52 |
Issue TOC
|
|
|
|
127 |
C |
p. |
artikel |
53 |
Menisperdaurines A-W, structurally diverse isoquinoline alkaloids from Menispermum dauricum and their dopamine D1 receptor activities
|
Wei, Hong-Li |
|
|
127 |
C |
p. |
artikel |
54 |
Modified peroxamide-based reactive oxygen species (ROS)-responsive doxorubicin prodrugs
|
Jafari, Mina |
|
|
127 |
C |
p. |
artikel |
55 |
Nanogel-mediated drug delivery system for anticancer agent: pH stimuli responsive poly(ethylene glycol/acrylic acid) nanogel prepared by gamma irradiation
|
El-Sattar, Nour E.A. Abd |
|
|
127 |
C |
p. |
artikel |
56 |
Nanotechnology applications for treatment of hepatic infections via modulating Hepatic histopathological and DNA alterations
|
Gad, Sameh S. |
|
|
127 |
C |
p. |
artikel |
57 |
Natural product protulactone A: Total synthesis from D-galactose, X-ray analysis and biological evaluation
|
Djokić, Sanja |
|
|
127 |
C |
p. |
artikel |
58 |
New benzimidazole based hybrids: Synthesis, molecular modeling study and anticancer evaluation as TopoII inhibitors
|
Nawareg, Nareman A. |
|
|
127 |
C |
p. |
artikel |
59 |
New dihydrobenzoxanthone derivatives with bacterial neuraminidase inhibitory activity isolated from Artocarpus elasticus
|
Baiseitova, Aizhamal |
|
|
127 |
C |
p. |
artikel |
60 |
New fluorinated diarylureas linked to pyrrolo[2,3-d]pyrimidine scaffold as VEGFR-2 inhibitors: Molecular docking and biological evaluation
|
Adel, Mai |
|
|
127 |
C |
p. |
artikel |
61 |
New phthalimide-based derivatives as EGFR-TK inhibitors: Synthesis, biological evaluation, and molecular modeling study
|
Mansour, Nayera I. |
|
|
127 |
C |
p. |
artikel |
62 |
New thiophene, thienopyridine and thiazoline-based derivatives: Design, synthesis and biological evaluation as antiproliferative agents and multitargeting kinase inhibitors
|
Alamshany, Zahra M. |
|
|
127 |
C |
p. |
artikel |
63 |
Nile crab Potamonautes niloticus shell extract: Chromatographic and molecular elucidation of potent antioxidant and anti-inflammatory capabilities
|
Galal-Khallaf, Asmaa |
|
|
127 |
C |
p. |
artikel |
64 |
Novel chlorpromazine derivatives as anti-endometrial carcinoma agents with reduced extrapyramidal side effects
|
Li, Lijuan |
|
|
127 |
C |
p. |
artikel |
65 |
Novel donepezil-chalcone-rivastigmine hybrids as potential multifunctional anti-Alzheimer's agents: Design, synthesis, in vitro biological evaluation, in vivo and in silico studies
|
Sang, Zhipei |
|
|
127 |
C |
p. |
artikel |
66 |
One pot domino synthesis of new 3,5-disubstituted-tetrahydro-2H-1,3,5-thiadiazine-2-thiones (THTTs) as anti-inflammatory and antinociceptive candidates: A proof from in-vivo to in-vitro and in-silico mechanistic studies
|
Raheem, Sumaya |
|
|
127 |
C |
p. |
artikel |
67 |
Rational drug design strategies for the development of promising multi-target directed indole hybrids as Anti-Alzheimer agents
|
George, Namy |
|
|
127 |
C |
p. |
artikel |
68 |
Recent developments in promiscuous enzymatic reactions for carbon–nitrogen bond formation
|
Xia, Hui |
|
|
127 |
C |
p. |
artikel |
69 |
SAR study culminates in a series of HDAC6 selective inhibitors featuring Schisandrin C-analogous Cap as potential immunomodulatory agents for cancer therapy
|
Tao, Qiangqiang |
|
|
127 |
C |
p. |
artikel |
70 |
Scopariusicides D–M, ent-clerodane-based isomeric meroditerpenoids with a cyclobutane-fused γ/δ-lactone core from Isodon scoparius
|
Li, Xing-Ren |
|
|
127 |
C |
p. |
artikel |
71 |
Six pairs of enantiomeric phthalide dimers from the rhizomes of Ligusticum chuanxiong and their absolute configurations and anti-inflammatory activities
|
Huang, Lu |
|
|
127 |
C |
p. |
artikel |
72 |
Small molecules enhancers of amyloid aggregation of C-terminal domain of Nucleophosmin 1 in acute myeloid leukemia
|
Florio, Daniele |
|
|
127 |
C |
p. |
artikel |
73 |
Structural and biosynthetic studies of botrycinereic acid, a new cryptic metabolite from the fungus Botrytis cinerea
|
Pinto, Ana A. |
|
|
127 |
C |
p. |
artikel |
74 |
Structurally diverse metabolites from a soil-derived fungus Aspergillus calidoustus
|
Li, Fengli |
|
|
127 |
C |
p. |
artikel |
75 |
Structure-activity relationship analysis of novel GSPT1 degraders based on benzotriazinone scaffold and its antitumor effect on xenograft mouse model
|
Takwale, Akshay D. |
|
|
127 |
C |
p. |
artikel |
76 |
Structure-activity relationships reveal a 2-furoyloxychalcone as a potent cytotoxic and apoptosis inducer for human U-937 and HL-60 leukaemia cells
|
del Rosario, Henoc |
|
|
127 |
C |
p. |
artikel |
77 |
Styryl dyes with N-Methylpiperazine and N-Phenylpiperazine Functionality: AT-DNA and G-quadruplex binding ligands and theranostic agents
|
Zonjić, Iva |
|
|
127 |
C |
p. |
artikel |
78 |
Synthesis and anti-inflammatory activity of paeonol derivatives with etherized aryl urea by regulating TLR4/MyD88 signaling pathway in RAW264.7 cell
|
Gong, Xiaobao |
|
|
127 |
C |
p. |
artikel |
79 |
Synthesis and biological evaluation of antibacterial activity of novel clarithromycin derivatives incorporating 1,2,3-triazole moieties at the 4″- and 11-OH positions
|
Qin, Yinhui |
|
|
127 |
C |
p. |
artikel |
80 |
Synthesis and evaluation of avermectin–imidazo[1,2-a]pyridine hybrids as potent GABAA receptor modulators
|
Volkova, Yulia A. |
|
|
127 |
C |
p. |
artikel |
81 |
Synthesis and structure–activity relationship study of saponin-based membrane fusion inhibitors against SARS-CoV-2
|
Jang, Youngho |
|
|
127 |
C |
p. |
artikel |
82 |
Synthesis, biological evaluation and molecular docking studies of novel diosgenin derivatives as anti-inflammatory agents
|
Zhang, Sheng-Nan |
|
|
127 |
C |
p. |
artikel |
83 |
Synthesis, biological evaluation and structure-activity relationship of 2-(2-hydroxyaryl)alkenylphosphonium salts with potency as anti-MRSA agents
|
Terekhova, Natalia V. |
|
|
127 |
C |
p. |
artikel |
84 |
Synthesis of mitochondria-targeted ferulic acid amide derivatives with antioxidant, anti-inflammatory activities and inducing mitophagy
|
Xie, Yu |
|
|
127 |
C |
p. |
artikel |
85 |
Synthesis of novel 4,7-disubstituted quinoline derivatives as autophagy inducing agents via targeting stabilization of ATG5
|
Li, Xiangpan |
|
|
127 |
C |
p. |
artikel |
86 |
Synthesis of the new nucleoside 5′-alpha-iminophosphates using Staudinger reaction
|
Vasilyeva, Svetlana V. |
|
|
127 |
C |
p. |
artikel |
87 |
The effect of novel synthetic semicarbazone- and thiosemicarbazone-linked 1,2,3-triazoles on the apoptotic markers, VEGFR-2, and cell cycle of myeloid leukemia
|
Othman, Esraa M. |
|
|
127 |
C |
p. |
artikel |
88 |
Twelve novel sesquiterpenes with anti-inflammatory and cholesterol-lowering activities from burdock leaves
|
Liang, Hanjing |
|
|
127 |
C |
p. |
artikel |
89 |
Unusual sesquilignans with anti-inflammatory activities from the resin of Ferula sinkiangensis
|
Li, Qian |
|
|
127 |
C |
p. |
artikel |
90 |
Violacein switches off low molecular weight tyrosine phosphatase and rewires mitochondria in colorectal cancer cells
|
Faria, Alessandra V.S. |
|
|
127 |
C |
p. |
artikel |