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64 results found

no	title	author	magazine	year	volume	issue	page(s)	type
1	Additional alkaloids from Zoanthus vietnamensis with neuroprotective and anti-angiogenic effects	Chen, Shu-Rong			109	C	p.	article
2	A new twist of rubredoxin function in M. tuberculosis	Sushko, Tatsiana			109	C	p.	article
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.	article
4	Antibacterial activity of a new monocarbonyl analog of curcumin MAC 4 is associated with divisome disruption	Polaquini, Carlos R.			109	C	p.	article
5	Antioxidant and anti-sickling activity of glucal-based triazoles compounds – An in vitro and in silico study	Vieira Veloso, Rodinei			109	C	p.	article
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.	article
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.	article
8	Cathepsin K inhibitors based on 2-amino-1,3,4-oxadiazole derivatives	Gontijo, Talita B.			109	C	p.	article
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.	article
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.	article
11	Deciphering structural bases of intestinal and hepatic selectivity in targeting pregnane X receptor with indole-based microbial mimics	Li, Hao			109	C	p.	article
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.	article
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.	article
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.	article
15	Design, synthesis and anti-rheumatoid arthritis evaluation of double-ring conjugated enones	Zhou, Shiyang			109	C	p.	article
16	Design, synthesis and biological assessment of novel CDK4 inhibitor with potent anticancer activity	Li, Yongtao			109	C	p.	article
17	Design, synthesis and biological evaluations of diverse Michael acceptor-based phenazine hybrid molecules as TrxR1 inhibitors	Zhong, Yucheng			109	C	p.	article
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.	article
19	Design, synthesis and in vitro anticancer research of novel tetrandrine and fangchinoline derivatives	Gao, Xiu-zheng			109	C	p.	article
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.	article
21	Discovery of higenamine as a potent, selective and cellular active natural LSD1 inhibitor for MLL-rearranged leukemia therapy	Fang, Yuan			109	C	p.	article
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.	article
23	Editorial Board				109	C	p.	article
24	Enhancing the chemosensitivity of HepG2 cells towards cisplatin by organoselenium pseudopeptides	Shaaban, Saad			109	C	p.	article
25	ESIPT-based fluorescent probe for bioimaging and identification of group IIIA ions in live cells and zebrafish	Zheng, Qinxiang			109	C	p.	article
26	Flavonoids from Pterogyne nitens as Zika virus NS2B-NS3 protease inhibitors	Lima, Caroline Sprengel			109	C	p.	article
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.	article
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.	article
29	Identification of a new natural biflavonoids against breast cancer cells induced ferroptosis via the mitochondrial pathway	Xie, Yang			109	C	p.	article
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.	article
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.	article
32	Issue TOC				109	C	p.	article
33	Lipopeptides production by a newly Halomonas venusta strain: Characterization and biotechnological properties	Cheffi, Meriam			109	C	p.	article
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.	article
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.	article
36	Non-classical cardenolides from Calotropis gigantea exhibit anticancer effect as HIF-1 inhibitors	Zheng, Zhiyuan			109	C	p.	article
37	Novel α-Aminophosphonates of imatinib Intermediate: Synthesis, anticancer Activity, human Abl tyrosine kinase Inhibition, ADME and toxicity prediction	Aita, Saikiran			109	C	p.	article
38	Novel, natural allosteric inhibitors and enhancers of Candida rugosa lipase activity	Menden, Ariane			109	C	p.	article
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.	article
40	Overcome the tumor immunotherapy resistance by combination of the HDAC6 inhibitors with antitumor immunomodulatory agents	Yussuf Khamis, Mussa			109	C	p.	article
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.	article
42	Preclinical assessment of stem of Nicotiana tabacum on excision wound model	Sharma, Yash			109	C	p.	article
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.	article
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.	article
45	Quinolines, a perpetual, multipurpose scaffold in medicinal chemistry	Yadav, Pratibha			109	C	p.	article
46	Seven new prenylated flavanones from the roots of Sophora flavescens and their anti-proliferative activities	Yang, Ya-nan			109	C	p.	article
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.	article
48	Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity	Xiang, Zhi-Nan			109	C	p.	article
49	Synthesis and antiplasmodial evaluation of 1H-1,2,3-triazole grafted 4-aminoquinoline-benzoxaborole hybrids and benzoxaborole analogues	Saini, Anu			109	C	p.	article
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.	article
51	Synthesis and biological evaluation of pentacyclic triterpenoid derivatives as potential novel antibacterial agents	Wu, Panpan			109	C	p.	article
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.	article
53	Synthesis, anticancer evaluation and mechanism studies of novel indolequinone derivatives of ursolic acid	Wang, Wen-Yan			109	C	p.	article
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.	article
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.	article
56	Synthesis of 4,6-diphenylpyrimidin-2-ol derivatives as new benzodiazepine receptor ligands	Khoramjouy, Mona			109	C	p.	article
57	Synthesis of nigranoic acid and manwuweizic acid derivatives as HDAC inhibitors and anti-inflammatory agents	Ni, Dong-Xuan			109	C	p.	article
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.	article
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.	article
60	Targeting GRP receptor: Design, synthesis and preliminary biological characterization of new non-peptide antagonists of bombesin	Palmioli, Alessandro			109	C	p.	article
61	Tautomeric preference in lumazines, deazalumazines, isoalloxazines and pyrimidines and its effect on the reactivity of alkyl groups	Kondrashova, Svetlana A.			109	C	p.	article
62	Telomerase activators from 20(27)-octanor-cycloastragenol via biotransformation by the fungal endophytes	Duman, Seda			109	C	p.	article
63	Therapeutic potential of N4 -substituted thiosemicarbazones as new urease inhibitors: Biochemical and in silico approach	Islam, Muhammad			109	C	p.	article
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.	article

64 results found

Koninklijke Bibliotheek - National Library of the Netherlands