no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Activity and specificity studies of the new thermostable esterase EstDZ2
|
Myrtollari, Kamela |
|
|
104 |
C |
p. |
article |
2 |
Agallolides A-M, including two rearranged ent-atisanes featuring a bicyclo[3.2.1]octane motif, from the Chinese Excoecaria agallocha
|
Jiang, Zhong-Ping |
|
|
104 |
C |
p. |
article |
3 |
Aminotriazines with indole motif as novel, 5-HT7 receptor ligands with atypical binding mode
|
Kułaga, Damian |
|
|
104 |
C |
p. |
article |
4 |
(+)- and (–)-Corydecumbenines A and B, two pairs of novel quaternary protoberberine alkaloid cycloadduct enantiomers with anti-neuroinflammatory and neuroprotective activities from the rhizomes of Corydalis decumbens
|
Yin, Xu |
|
|
104 |
C |
p. |
article |
5 |
Anticandidal formyl phloroglucinol meroterpenoids: Biomimetic synthesis and in vitro evaluation
|
Zhong, Lin–Fang |
|
|
104 |
C |
p. |
article |
6 |
Antidiabetic and cytotoxic polyhydroxylated oleanane and ursane type triterpenoids from Salvia grossheimii
|
Zare, Somayeh |
|
|
104 |
C |
p. |
article |
7 |
Anti-inflammatory and antioxidant properties of chemical constituents of Broussonetia papyrifera
|
Malaník, Milan |
|
|
104 |
C |
p. |
article |
8 |
Antimicrobial chloro-hydroxylactones derived from the biotransformation of bicyclic halolactones by cultures of Pleurotus ostreatus
|
Grabarczyk, Małgorzata |
|
|
104 |
C |
p. |
article |
9 |
Antimycobacterial activity of azepanobetulin and its derivative: In vitro, in vivo, ADMET and docking studies
|
Kazakova, Oxana |
|
|
104 |
C |
p. |
article |
10 |
Antiproliferative abietane quinone diterpenoids from the roots of Salvia deserta
|
Zheng, Xiaofeng |
|
|
104 |
C |
p. |
article |
11 |
Antitumor activity, multitarget mechanisms, and molecular docking studies of quinazoline derivatives based on a benzenesulfonamide scaffold: Cell cycle analysis
|
El-Azab, Adel S. |
|
|
104 |
C |
p. |
article |
12 |
A perspective on potential target proteins of COVID-19: Comparison with SARS-CoV for designing new small molecules
|
Kumar, Devendra |
|
|
104 |
C |
p. |
article |
13 |
A review on kinases phosphorylating the carboxyl-terminal domain of RNA polymerase II—Biological functions and inhibitors
|
Zhang, Jianru |
|
|
104 |
C |
p. |
article |
14 |
A trifunctional Pt(II) complex alleviates the NHEJ/HR-related DSBs repairs to evade cisplatin-resistance in NSCLC
|
Wang, Xing |
|
|
104 |
C |
p. |
article |
15 |
Bioactive sesquiterpene coumarins from the resin of Ferula sinkiangensis targeted on over-activation of microglia
|
Guo, Tingting |
|
|
104 |
C |
p. |
article |
16 |
Bioassay-guided isolation of cyclooxygenase-2 inhibitory and antioxidant phenylpropanoid derivatives from the roots of Dendropanax dentiger
|
Yang, Li |
|
|
104 |
C |
p. |
article |
17 |
Cadinane- and drimane-type sesquiterpenoids produced by Paecilomyces sp. TE-540, an endophyte from Nicotiana tabacum L., are acetylcholinesterase inhibitors
|
Xu, Kuo |
|
|
104 |
C |
p. |
article |
18 |
Characterization of a novel thermostable glucose-tolerant GH1 β-glucosidase from the hyperthermophile Ignisphaera aggregans and its application in the efficient production of baohuoside I from icariin and total epimedium flavonoids
|
Xie, Jingcong |
|
|
104 |
C |
p. |
article |
19 |
Chlorotrimethylsilane promoted one-flask heterocyclic synthesis of 1,2,4-triazoles from nitrilimines: Modeling studies and bioactivity evaluation of LH-21 and Rimonabant analogues
|
Tsai, Shuo-En |
|
|
104 |
C |
p. |
article |
20 |
Combination of DN604 with gemcitabine led to cell apoptosis and cell motility inhibition via p38 MAPK signaling pathway in NSCLC
|
Wang, Xinyi |
|
|
104 |
C |
p. |
article |
21 |
Copper (II)-based halogen-substituted chromone antitumor drug entities: Studying biomolecular interactions with ct-DNA mediated by sigma hole formation and cytotoxicity activity
|
Arjmand, Farukh |
|
|
104 |
C |
p. |
article |
22 |
Core modified 8–17 DNAzymes with 2′-deoxy-2′-C-methylpyrimidine nucleosides
|
Dellafiore, María |
|
|
104 |
C |
p. |
article |
23 |
Correlation study on methoxylation pattern of flavonoids and their heme-targeted antiplasmodial activity
|
Ortiz, Sergio |
|
|
104 |
C |
p. |
article |
24 |
Corrigendum to “Hyperpatulols A-I, spirocyclic acylphloroglucinol derivatives with anti-migration activities from the flowers of hypericum patulum” [Bioorg. Chem. 87 (2019) 409–416]
|
Liu, Yang-Yang |
|
|
104 |
C |
p. |
article |
25 |
Coumarin-chalcone hybrids targeting insulin receptor: Design, synthesis, anti-diabetic activity, and molecular docking
|
Konidala, Sathish Kumar |
|
|
104 |
C |
p. |
article |
26 |
Cytochalasins from an endophytic fungus Phoma multirostrata XJ-2-1 with cell cycle arrest and TRAIL-resistance-overcoming activities
|
Peng, Xiaogang |
|
|
104 |
C |
p. |
article |
27 |
Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAFV600E dual inhibitors
|
Al-Wahaibi, Lamya H. |
|
|
104 |
C |
p. |
article |
28 |
Design and synthesis of novel 4-thiazolidinone derivatives with promising anti-breast cancer activity: Synthesis, characterization, in vitro and in vivo results
|
Tahmasvand, Raheleh |
|
|
104 |
C |
p. |
article |
29 |
Design and synthesis of quinoxaline-1,3,4-oxadiazole hybrid derivatives as potent inhibitors of the anti-apoptotic Bcl-2 protein
|
Ono, Yukari |
|
|
104 |
C |
p. |
article |
30 |
Design and synthesis of some barbituric and 1,3-dimethylbarbituric acid derivatives: A non-classical scaffold for potential PARP1 inhibitors
|
Eldin A. Osman, Essam |
|
|
104 |
C |
p. |
article |
31 |
Design, efficient synthesis, docking studies, and anticancer evaluation of new quinoxalines as potential intercalative Topo II inhibitors and apoptosis inducers
|
Abbass, Eslam M. |
|
|
104 |
C |
p. |
article |
32 |
Design, green synthesis, molecular docking and anticancer evaluations of diazepam bearing sulfonamide moieties as VEGFR-2 inhibitors
|
Saleh, Nashwa M. |
|
|
104 |
C |
p. |
article |
33 |
Design, synthesis, and anticancer evaluation of benzophenone derivatives bearing naphthalene moiety as novel tubulin polymerization inhibitors
|
Wang, Guangcheng |
|
|
104 |
C |
p. |
article |
34 |
Design, synthesis and antitumor evaluation of novel 5-methylpyrazolo[1,5-a]pyrimidine derivatives as potential c-Met inhibitors
|
Luo, Guolin |
|
|
104 |
C |
p. |
article |
35 |
Design, synthesis, and biological evaluation of new challenging thalidomide analogs as potential anticancer immunomodulatory agents
|
El-Zahabi, Mohamed Ayman |
|
|
104 |
C |
p. |
article |
36 |
Design, synthesis and biological evaluation of novel carbohydrate-based sulfonamide derivatives as antitumor agents
|
Hao, Shuang |
|
|
104 |
C |
p. |
article |
37 |
Design, synthesis and biological evaluation of novel plumbagin derivatives as potent antitumor agents with STAT3 inhibition
|
Li, Na |
|
|
104 |
C |
p. |
article |
38 |
Design, synthesis and biological evaluation of thieno[3,2-d]pyrimidine derivatives containing aroyl hydrazone or aryl hydrazide moieties for PI3K and mTOR dual inhibition
|
Han, Yufei |
|
|
104 |
C |
p. |
article |
39 |
Design, synthesis and evaluation of antiproliferative and antitubulin activities of 5-methyl-4-aryl-3-(4-arylpiperazine-1-carbonyl)-4H-1,2,4-triazoles
|
Wang, Chao |
|
|
104 |
C |
p. |
article |
40 |
Design, synthesis and evaluation of diaryl γ-dihydropyrone derivatives as cyclocurcumin mimetics and inhibitors of the aggregation of amyloid β
|
Hotsumi, Mayumi |
|
|
104 |
C |
p. |
article |
41 |
Design, synthesis, and pharmacological evaluation of novel 1,2,4-triazol-3-amine derivatives as potential agonists of GABAA subtype receptors with anticonvulsant and hypnotic effects
|
Jahani, Reza |
|
|
104 |
C |
p. |
article |
42 |
Design, synthesis and structure-activity relationship studies of novel partial FXR agonists for the treatment of fatty liver
|
Qiu, Qianqian |
|
|
104 |
C |
p. |
article |
43 |
Design, synthesis and the structure-activity relationship of agonists targeting on the ALDH2 catalytic tunnel
|
Cheng, Ming-Che |
|
|
104 |
C |
p. |
article |
44 |
Design, synthesis, antimicrobial activity and molecular docking studies of some novel di-substituted sulfonylquinoxaline derivatives
|
Ammar, Yousry A. |
|
|
104 |
C |
p. |
article |
45 |
Development of activity-based probes for the protein deacylase Sirt1
|
Goetz, Christopher J. |
|
|
104 |
C |
p. |
article |
46 |
Development of diarylpentadienone analogues as alpha-glucosidase inhibitor: Synthesis, in vitro biological and in vivo toxicity evaluations, and molecular docking analysis
|
Abdullah, Maryam Aisyah |
|
|
104 |
C |
p. |
article |
47 |
β,γ-Diaryl α-methylene-γ-butyrolactones as potent antibacterials against methicillin-resistant Staphylococcus aureus
|
Hamann, Henry J. |
|
|
104 |
C |
p. |
article |
48 |
Dimethylated acylphloroglucinol meroterpenoids with anti-oral-bacterial and anti-inflammatory activities from Hypericum elodeoides
|
Li, Qi-Ji |
|
|
104 |
C |
p. |
article |
49 |
Discovery and rational design of 2-aminopyrimidine-based derivatives targeting Janus kinase 2 (JAK2) and FMS-like tyrosine kinase 3 (FLT3)
|
Li, Yingxiu |
|
|
104 |
C |
p. |
article |
50 |
Discovery, biological evaluation and docking studies of novel N-acyl-2-aminothiazoles fused (+)-nootkatone from Citrus paradisi Macf. as potential α-glucosidase inhibitors
|
Guo, Yong |
|
|
104 |
C |
p. |
article |
51 |
Discovery of a cobalt (III) salen complex that induces apoptosis in Burkitt like lymphoma and leukemia cells, overcoming multidrug resistance in vitro
|
Hopff, Sina M. |
|
|
104 |
C |
p. |
article |
52 |
Discovery of derivatives of 6(7)-amino-3-phenylquinoxaline-2-carbonitrile 1,4-dioxides: novel, hypoxia-selective HIF-1α inhibitors with strong antiestrogenic potency
|
Buravchenko, Galina I. |
|
|
104 |
C |
p. |
article |
53 |
Discovery of dihydro-β-agarofurans from Tripterygium wilfordii with their H2O2-induced SH-SY5Y cell protective effects
|
Zhou, Le |
|
|
104 |
C |
p. |
article |
54 |
Discovery of novel artemisinin-sulfonamidehybrids as potential carbonicanhydraseIX inhibitors with improved antiproliferative activities
|
An, Ran |
|
|
104 |
C |
p. |
article |
55 |
Discovery of novel indazole-acylsulfonamide hybrids as selective Mcl-1 inhibitors
|
Wan, Yichao |
|
|
104 |
C |
p. |
article |
56 |
Discovery of trisubstituted pyrazolines as a novel scaffold for the development of selective phosphodiesterase 5 inhibitors
|
Abdel-Halim, Mohammad |
|
|
104 |
C |
p. |
article |
57 |
DNA binding studies of novel diazatruxenones analogs as potential anticancer agents: Synthesis, antitumor investigation, DNA binding, SAR and molecular modeling calculation
|
El Sayed, Mardia T. |
|
|
104 |
C |
p. |
article |
58 |
Druggable targets of SARS-CoV-2 and treatment opportunities for COVID-19
|
Faheem, |
|
|
104 |
C |
p. |
article |
59 |
Drug-like biimidazole derivatives dually target c-MYC/BCL-2 G-quadruplexes and inhibit acute myeloid leukemia
|
Hu, Ming-Hao |
|
|
104 |
C |
p. |
article |
60 |
Editorial Board
|
|
|
|
104 |
C |
p. |
article |
61 |
Enantiomeric chromene derivatives with anticancer effects from Mallotus apelta
|
Kiem, Phan Van |
|
|
104 |
C |
p. |
article |
62 |
Enantiomeric 8-O-4′-type neolignans from Crataegus pinnatifida exhibit cytotoxic effect via apoptosis and autophagy in Hep3B cells
|
Shang, Xin-Yue |
|
|
104 |
C |
p. |
article |
63 |
Evaluation and comparison of the commonly used bioassays of human indoleamine 2,3-dioxygenase 1 (IDO1) and tryptophan 2,3-dioxygenase (TDO)
|
Zhang, Shengnan |
|
|
104 |
C |
p. |
article |
64 |
Evaluation of sulfonate and sulfamate derivatives possessing benzofuran or benzothiophene nucleus as inhibitors of nucleotide pyrophosphatases/phosphodiesterases and anticancer agents
|
Anbar, Hanan S. |
|
|
104 |
C |
p. |
article |
65 |
Exploiting azido-dichloro-triazine as a linker for regioselective incorporation of peptides through their N, O, S functional groups
|
Sharma, Anamika |
|
|
104 |
C |
p. |
article |
66 |
Fluorescently-labelled amyloid paired helical filaments (PHF) in monitoring its fibrillation kinetics
|
Šmidlehner, Tamara |
|
|
104 |
C |
p. |
article |
67 |
Fungal mediated biotransformation of melengestrol acetate, and T-cell proliferation inhibitory activity of biotransformed compounds
|
Javed, Saira |
|
|
104 |
C |
p. |
article |
68 |
68Ga-Labeled bismacrocyclic methylene phosphonate as potential bone seeking PET radiopharmaceutical
|
Chauhan, Kanchan |
|
|
104 |
C |
p. |
article |
69 |
Geissoschizoline, a promising alkaloid for Alzheimer’s disease: Inhibition of human cholinesterases, anti-inflammatory effects and molecular docking
|
Lima, Josélia A. |
|
|
104 |
C |
p. |
article |
70 |
Highly oxygenated lanostane triterpenoids from Ganoderma applanatum as a class of agents for inhibiting lipid accumulation in adipocytes
|
Su, Hai-Guo |
|
|
104 |
C |
p. |
article |
71 |
History of the development of antifungal azoles: A review on structures, SAR, and mechanism of action
|
Shafiei, Mohammad |
|
|
104 |
C |
p. |
article |
72 |
Identification of a potent heme oxygenase-2 (HO-2) inhibitor by targeting the secondary hydrophobic pocket of the HO-2 western region
|
Floresta, Giuseppe |
|
|
104 |
C |
p. |
article |
73 |
Inhibition of zika virus infection by fused tricyclic derivatives of 1,2,4,5-tetrahydroimidazo[1,5-a]quinolin-3(3aH)-one
|
Xu, Bin |
|
|
104 |
C |
p. |
article |
74 |
In vitro study and structure-activity relationship analysis of stilbenoid derivatives as powerful vasorelaxants: Discovery of new lead compound
|
Chan, Sock Ying |
|
|
104 |
C |
p. |
article |
75 |
Is oseltamivir suitable for fighting against COVID-19: In silico assessment, in vitro and retrospective study
|
Tan, Qi |
|
|
104 |
C |
p. |
article |
76 |
Issue TOC
|
|
|
|
104 |
C |
p. |
article |
77 |
Metabolites with phytopathogenic fungi inhibitory activities from the mangrove endophytic fungus Botryosphaeria ramose
|
Hu, Zhibo |
|
|
104 |
C |
p. |
article |
78 |
Natural iridoids from Patrinia heterophylla showing anti-inflammatory activities in vitro and in vivo
|
Wu, Peng |
|
|
104 |
C |
p. |
article |
79 |
New cembrane-type diterpenoids from the South China Sea soft coral Sinularia crassa and their α-glucosidase inhibitory activity
|
Wu, Meng-Jun |
|
|
104 |
C |
p. |
article |
80 |
New indole-7-aldehyde derivatives as melatonin analogues; synthesis and screening their antioxidant and anticancer potential
|
Shirinzadeh, Hanif |
|
|
104 |
C |
p. |
article |
81 |
New insight of red seaweed derived Callophycin A as an alternative strategy to treat drug resistance vaginal candidiasis
|
Ganeshkumar, Arumugam |
|
|
104 |
C |
p. |
article |
82 |
New methyl 5-(halomethyl)-1-aryl-1H-1,2,4-triazole-3-carboxylates as selective COX-2 inhibitors and anti-inflammatory agents: Design, synthesis, biological evaluation, and docking study
|
Li, Sin-Min |
|
|
104 |
C |
p. |
article |
83 |
New synthetic analogues of natural 5Z,9Z-dienoic acids: Stereoselective synthesis and study of the anticancer activity
|
Makarov, Alexey A. |
|
|
104 |
C |
p. |
article |
84 |
Nonpeptidal compounds from the insect Polyphaga plancyi and their biological evaluation
|
Zhu, Hong-Jie |
|
|
104 |
C |
p. |
article |
85 |
Novel adamantyl retinoid-related molecules with POLA1 inhibitory activity
|
Cincinelli, Raffaella |
|
|
104 |
C |
p. |
article |
86 |
Novel anti-tubercular and antibacterial based benzosuberone-thiazole moieties: Synthesis, molecular docking analysis, DNA gyrase supercoiling and ATPase activity
|
Omar, Mohamed A. |
|
|
104 |
C |
p. |
article |
87 |
Novel coumarin-pyridazine hybrids as selective MAO-B inhibitors for the Parkinson’s disease therapy
|
Rodríguez-Enríquez, Fernanda |
|
|
104 |
C |
p. |
article |
88 |
Novel cyclic thiourea derivatives of aminoalcohols at the presence of AlCl3 catalyst as potent α-glycosidase and α-amylase inhibitors: Synthesis, characterization, bioactivity investigation and molecular docking studies
|
Sujayev, Afsun |
|
|
104 |
C |
p. |
article |
89 |
Novel enantiopure isoxazolidine and C-alkyl imine oxide derivatives as potential hypoglycemic agents: Design, synthesis, dual inhibitors of α-amylase and α-glucosidase, ADMET and molecular docking study
|
Ghannay, Siwar |
|
|
104 |
C |
p. |
article |
90 |
Novel N-(aryl/heteroaryl)-2-chlorobenzenesulfonamide derivatives: Synthesis and anticancer activity evaluation
|
Bułakowska, Anita |
|
|
104 |
C |
p. |
article |
91 |
Novel oligomeric neolignans with PTP1B inhibitory activity from the bark of Magnolia officinalis var. biloba
|
Li, Chuan |
|
|
104 |
C |
p. |
article |
92 |
Novel tetrazole-based selective COX-2 inhibitors: Design, synthesis, anti-inflammatory activity, evaluation of PGE2, TNF-α, IL-6 and histopathological study
|
Labib, Madlen B. |
|
|
104 |
C |
p. |
article |
93 |
Pehuén (Araucaria araucana) seed residues are a valuable source of natural antioxidants with nutraceutical, chemoprotective and metal corrosion-inhibiting properties
|
Gallia, María C. |
|
|
104 |
C |
p. |
article |
94 |
Potent α-amylase inhibitors and radical (DPPH and ABTS) scavengers based on benzofuran-2-yl(phenyl)methanone derivatives: Syntheses, in vitro, kinetics, and in silico studies
|
Ali, Irfan |
|
|
104 |
C |
p. |
article |
95 |
Prenylated xanthones and benzophenones from the fruits of Garcinia bracteata and their potential antiproliferative and anti-inflammatory activities
|
Xue, Qing |
|
|
104 |
C |
p. |
article |
96 |
Preparation and assessment of a new radiotracer technetium-99m-6-hydrazinonicotinic acid-tyrosine as a targeting agent in tumor detecting through single photon emission tomography
|
Mogadam, Hemat Yaghoubi |
|
|
104 |
C |
p. |
article |
97 |
P2X7 receptor inhibition by 2-amino-3-aryl-1,4-naphthoquinones
|
de Luna Martins, Daniela |
|
|
104 |
C |
p. |
article |
98 |
(2R)- and (2S)- 2-hydroxy- hexanoyl and octanoyl-l-homoserine lactones: New highly potent Quorum Sensing modulators with opposite activities
|
Zhang, Qiang |
|
|
104 |
C |
p. |
article |
99 |
Recent advancements in the medicinal chemistry of bacterial type II topoisomerase inhibitors
|
Jaswal, Shalini |
|
|
104 |
C |
p. |
article |
100 |
Reductive domino reaction to access chromeno[2,3-c]isoquinoline-5-amines with antiproliferative activities against human tumor cells
|
Yue, Xiaoyi |
|
|
104 |
C |
p. |
article |
101 |
Role of heterocyclic compounds in SARS and SARS CoV-2 pandemic
|
Negi, Meenakshi |
|
|
104 |
C |
p. |
article |
102 |
Sesquiterpenoids, phenolic and lignan glycosides from the roots and rhizomes of Clematis hexapetala Pall. and their bioactivities
|
Cai, Lu |
|
|
104 |
C |
p. |
article |
103 |
Some thiocarbamoyl based novel anticathepsin agents
|
Kaur, Ravinder |
|
|
104 |
C |
p. |
article |
104 |
Structure-activity relationship studies of prostate-specific membrane antigen (PSMA) inhibitors derived from α-amino acid with (S)- or (R)-configuration at P1′ region
|
Kwon, Hongmok |
|
|
104 |
C |
p. |
article |
105 |
Structure based drug discovery and in vitro activity testing for DNA gyrase inhibitors of Salmonella enterica serovar Typhi
|
Sharma, Priyanka |
|
|
104 |
C |
p. |
article |
106 |
Study on enhanced serum protein protecting and anti-cathepsin activities of various curcumin formulations containing traditional excipients and bio-enhancers
|
Raghav, Neera |
|
|
104 |
C |
p. |
article |
107 |
Syntheses and evaluation of daphnetin derivatives as novel G protein-coupled receptor inhibitors and activators
|
Wang, Yinan |
|
|
104 |
C |
p. |
article |
108 |
Synthesis, ADMET prediction and reverse screening study of 3,4,5-trimethoxy phenyl ring pendant sulfur‐containing cyanopyrimidine derivatives as promising apoptosis inducing anticancer agents
|
Nainwal, Lalit Mohan |
|
|
104 |
C |
p. |
article |
109 |
Synthesis and biological evaluation of 3-amino-1,2,4-triazole derivatives as potential anticancer compounds
|
Grytsai, Oleksandr |
|
|
104 |
C |
p. |
article |
110 |
Synthesis and biological evaluation of β-ionone oriented proapoptosis agents by enhancing the ROS generation
|
Yang, Jie |
|
|
104 |
C |
p. |
article |
111 |
Synthesis and biological evaluation of some coumarin hybrids as selective carbonic anhydrase IX and XII inhibitors
|
Thacker, Pavitra S. |
|
|
104 |
C |
p. |
article |
112 |
Synthesis and biological evaluation of substituted phenyl azetidine-2-one sulphonyl derivatives as potential antimicrobial and antiviral agents
|
Mandal, Milan Kumar |
|
|
104 |
C |
p. |
article |
113 |
Synthesis and biological study of class I selective HDAC inhibitors with NO releasing activity
|
Ding, Qin'ge |
|
|
104 |
C |
p. |
article |
114 |
Synthesis, biological evaluation and computational studies of acrylohydrazide derivatives as potential Staphylococcus aureus NorA efflux pump inhibitors
|
Kumar, Gautam |
|
|
104 |
C |
p. |
article |
115 |
Synthesis, biological evaluation and molecular docking studies of novel thiopyrimidine analogue as apoptotic agent with potential anticancer activity
|
Haffez, Hesham |
|
|
104 |
C |
p. |
article |
116 |
Synthesis, DNA/RNA-interaction and biological activity of benzo[k,l]xanthene lignans
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Synthesis, physicochemical properties and biological activities of novel alkylphosphocholines with foscarnet moiety
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Synthetic strategies in construction of organic low molecular-weight carrier-drug conjugates
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TCF3-activated FAM201A enhances cell proliferation and invasion via miR-186-5p/TNKS1BP1 axis in triple-negative breast cancer
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