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78 results found

no	title	author	magazine	year	volume	issue	page(s)	type
1	A combined experimental and computational study on peptide nucleic acid (PNA) analogues of tumor suppressive miRNA-34a	Piacenti, Valerio			91	C	p.	article
2	Amide-tethered quinoline-resorcinol conjugates as a new class of HSP90 inhibitors suppressing the growth of prostate cancer cells	Nepali, Kunal			91	C	p.	article
3	An efficient method for the synthesis of novel derivatives 4-{5-[4-(4-amino-5-mercapto-4H-[1,2,4]triazol-3-yl)-phenyl]-3-trifluoromethyl-pyrazol-1-yl}-benzenesulfonamide and their anti-inflammatory potential	Mustafa, Ghulam			91	C	p.	article
4	Antifungal activity and tautomeric cyclization equilibria of formylphenylboronic acids	Borys, Krzysztof M.			91	C	p.	article
5	Anti-inflammatory and antiproliferative prenylated carbazole alkaloids from Clausena vestita	Liu, Yan-Ping			91	C	p.	article
6	Anti-inflammatory spiroaxane and drimane sesquiterpenoids from Talaromyces minioluteus (Penicillium minioluteum)	Chen, Chunmei			91	C	p.	article
7	Arylboronate prodrugs of doxorubicin as promising chemotherapy for pancreatic cancer	Skarbek, Charles			91	C	p.	article
8	A solid-phase method for synthesis of dimeric and trimeric ligands: Identification of potent bivalent ligands of 14-3-3σ	Lee, Yeongju			91	C	p.	article
9	Bioactivatable reductive cleavage of azobenzene for controlling functional dumbbell oligodeoxynucleotides	Lei, Huajun			91	C	p.	article
10	Bis-coumarins; non-cytotoxic selective urease inhibitors and antiglycation agents	Salar, Uzma			91	C	p.	article
11	cAMPS derivatives. A minireview over synthetic medicinal chemistry	Undheim, Kjell			91	C	p.	article
12	Chalcone derivatives and their antibacterial activities: Current development	Xu, Man			91	C	p.	article
13	Chemical constituents of the root bark of Ulmus davidiana var. japonica and their potential biological activities	So, Hae Min			91	C	p.	article
14	Chemo-sensitizing activity of natural cadinanes from Heterotheca inuloides in human uterine sarcoma cells and their in silico interaction with ABC transporters	Rodríguez-Chávez, José Luis			91	C	p.	article
15	Designing of promising medicinal scaffolds for Alzheimer’s disease through enzyme inhibition, lead optimization, molecular docking and dynamic simulation approaches	Hassan, Mubashir			91	C	p.	article
16	Design, synthesis and antibacterial activity evaluation of moxifloxacin-amide-1,2,3-triazole-isatin hybrids	Gao, Feng			91	C	p.	article
17	Design, synthesis and biological evaluation of 4-aminoquinoline-guanylthiourea derivatives as antimalarial agents	Bhagat, Shweta			91	C	p.	article
18	Design, synthesis and biological evaluation of novel perimidine o-quinone derivatives as non-intercalative topoisomerase II catalytic inhibitors	Zhou, Du-Chao			91	C	p.	article
19	Design, synthesis and biological evaluation of trinary benzocoumarin-thiazoles-azomethines derivatives as effective and selective inhibitors of alkaline phosphatase	Channar, Pervaiz Ali			91	C	p.	article
20	Design, synthesis and evaluation of phthalazinone thiohydantoin-based derivative as potent PARP-1 inhibitors	Zhong, Yi			91	C	p.	article
21	Design, synthesis, anticancer evaluation and docking studies of new pyrimidine derivatives as potent thymidylate synthase inhibitors	Amin, Lamia H.T.			91	C	p.	article
22	Design, synthesis, biological and in silico evaluation of coumarin-hydrazone derivatives as tubulin targeted antiproliferative agents	Govindaiah, Pilli			91	C	p.	article
23	Design, synthesis, molecular modeling and anti-hyperglycemic evaluation of phthalimide-sulfonylurea hybrids as PPARγ and SUR agonists	El-Zahabi, Mohamed Ayman			91	C	p.	article
24	Discovery of Michael acceptor containing 1,4-dihydropyridines as first covalent inhibitors of L-/T-type calcium channels	Aygün Cevher, Hande			91	C	p.	article
25	Discovery of novel cage-like heterocyclic hybrids as anti-inflammatory agents through the inhibition of nitrite, PGE2 and TNF-α	Kumar, Raju Suresh			91	C	p.	article
26	Discovery, synthesis and molecular substantiation of N-(benzo[d]thiazol-2-yl)-2-hydroxyquinoline-4-carboxamides as anticancer agents	Bindu, B.			91	C	p.	article
27	2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies	Taha, Muhammad			91	C	p.	article
28	Editorial Board				91	C	p.	article
29	Flavonols and 4-thioflavonols as potential acetylcholinesterase and butyrylcholinesterase inhibitors: Synthesis, structure-activity relationship and molecular docking studies	Mughal, Ehsan Ullah			91	C	p.	article
30	FtsZ inhibitors as a new genera of antibacterial agents	Tripathy, Swayansiddha			91	C	p.	article
31	Genetic dereplication of Trichoderma hypoxylon reveals two novel polycyclic lactones	Chen, Lin			91	C	p.	article
32	Identification of novel peptidomimetics targeting the polo-box domain of polo-like kinase 1	Li, Zhiyan			91	C	p.	article
33	Iizukines C−E from a saline soil fungus Aspergillus iizukae	Kang, Hui-Hui			91	C	p.	article
34	Issue TOC				91	C	p.	article
35	Labeling of VEGFR1D2 through oxime ligation	De Rosa, Lucia			91	C	p.	article
36	Lysosome imaging in cancer cells by pyrene-benzothiazolium dyes: An alternative imaging approach for LAMP-1 expression based visualization methods to avoid background interference	Abeywickrama, Chathura S.			91	C	p.	article
37	Mechanistic studies on Pyrobaculum calidifontis porphobilinogen synthase (5-aminolevulinic acid dehydratase)	Azim, Naseema			91	C	p.	article
38	Multi-target 1,4-dihydropyridines showing calcium channel blockade and antioxidant capacity for Alzheimer’s disease therapy	Malek, Rim			91	C	p.	article
39	Natural neuroprotective alkaloids from Stephania japonica (Thunb.) Miers	Xiao, Jiao			91	C	p.	article
40	New classes of carbazoles as potential multi-functional anti-Alzheimer’s agents	Choubdar, Niloufar			91	C	p.	article
41	New hexalactone derivatives and a pair of new oxaspiro-carbon epimeric glycosides from the fruits of Illicium lanceolatum	Liu, Yang-Lan			91	C	p.	article
42	New phenolic cinnamic acid derivatives as selective COX-2 inhibitors. Design, synthesis, biological activity and structure-activity relationships	Ribeiro, Daniela			91	C	p.	article
43	Novel 2-aminopyridine liganded Pd(II) N-heterocyclic carbene complexes: Synthesis, characterization, crystal structure and bioactivity properties	Erdemir, Fatoş			91	C	p.	article
44	Novel steroidal 1,3,4-thiadiazines: Synthesis and biological evaluation in androgen receptor-positive prostate cancer 22Rv1 cells	Komendantova, Anna S.			91	C	p.	article
45	N-substituted noscapine derivatives as new antiprotozoal agents: Synthesis, antiparasitic activity and molecular docking study	Babanezhad Harikandei, Kosar			91	C	p.	article
46	One-step immobilization and purification of genetic engineering CBD fusion EndoS on cellulose for antibodies Fc-glycan remodeling	Zhao, Kai			91	C	p.	article
47	Optimization of a single HPLC-PDA method for quantifying Metformin, Gliclazide, Pioglitazone, Dapagliflozin, Empagliflozin, Saxagliptin, Linagliptin and Teneligliptin using central composite design	Kant, Ravi			91	C	p.	article
48	Phytoscreening of Vochysiaceae species: Molecular identification by HPLC-ESI-MS/MS and evaluating of their antioxidant activity and inhibitory potential against human α-amylase and protein glycation	Franco, R.R.			91	C	p.	article
49	Revealing synergistic mechanism of multiple components in Stauntonia brachyanthera Hand.-Mazz. for gout by virtual screening and system pharmacological approach	Hua, Qiong-qiong			91	C	p.	article
50	Searching new structural scaffolds for BRAF inhibitors. An integrative study using theoretical and experimental techniques	Campos, Ludmila E.			91	C	p.	article
51	Small molecule HDAC inhibitors: Promising agents for breast cancer treatment	Huang, Meiling			91	C	p.	article
52	Strategy and validation of a structure-based method for the discovery of selective inhibitors of PAK isoforms and the evaluation of their anti-cancer activity	Song, Pei-Lu			91	C	p.	article
53	Structural modifications and in vitro pharmacological evaluation of 4-pyridyl-piperazine derivatives as an active and selective histamine H3 receptor ligands	Szczepańska, Katarzyna			91	C	p.	article
54	1,8-Substituted anthraquinones, anthrones and bianthrones as potential non-azole leads against fungal infections	Jalab, Murhaf			91	C	p.	article
55	Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors	Chiaramonte, Niccolò			91	C	p.	article
56	Synthesis and application of a “turn on” fluorescent probe for glutathione based on a copper complex of coumarin hydrazide Schiff base derivative	He, Guangjie			91	C	p.	article
57	Synthesis and biological evaluation of bergenin-1,2,3-triazole hybrids as novel class of anti-mitotic agents	Pavan Kumar, P.			91	C	p.	article
58	Synthesis, biological evaluation and molecular docking studies of bis-chalcone derivatives as xanthine oxidase inhibitors and anticancer agents	Burmaoglu, Serdar			91	C	p.	article
59	Synthesis, in silico and in vitro studies of new 1,4-dihydropiridine derivatives for antitumor and P-glycoprotein inhibitory activity	Mollazadeh, Shirin			91	C	p.	article
60	Synthesis, in-vitro α-glucosidase inhibition, antioxidant, in-vivo antidiabetic and molecular docking studies of pyrrolidine-2,5-dione and thiazolidine-2,4-dione derivatives	Hussain, Fida			91	C	p.	article
61	Synthesis, molecular docking analysis and carbonic anhydrase I-II inhibitory evaluation of new sulfonamide derivatives	Sağlık, Begüm Nurpelin			91	C	p.	article
62	Synthesis, molecular docking, and biological evaluation of 3-oxo-2-tolylhydrazinylidene-4,4,4-trifluorobutanoates bearing higher and natural alcohol moieties as new selective carboxylesterase inhibitors	Makhaeva, Galina F.			91	C	p.	article
63	Synthesis of 3-indolylmethyl substituted (pyrazolo/benzo)triazinone derivatives under Pd/Cu-catalysis: Identification of potent inhibitors of chorismate mutase (CM)	Reddy, Gangireddy Sujeevan			91	C	p.	article
64	Synthesis of new arylhydrazide bearing Schiff bases/thiazolidinone: α-Amylase, urease activities and their molecular docking studies	Rahim, Fazal			91	C	p.	article
65	Synthesis of novel methyl jasmonate derivatives and evaluation of their biological activity in various cancer cell lines	Sucu, Bilgesu Onur			91	C	p.	article
66	Synthesis of novel (R)-4-fluorophenyl-1H-1,2,3-triazoles: A new class of α-glucosidase inhibitors	Avula, Satya Kumar			91	C	p.	article
67	Synthesis, physicochemical and biological evaluation of tacrine derivative labeled with technetium-99m and gallium-68 as a prospective diagnostic tool for early diagnosis of Alzheimer’s disease	Gniazdowska, Ewa			91	C	p.	article
68	The 5-hydrazino-3-methylisothiazole-4-carboxylic acid, its new 5-substituted derivatives and their antiproliferative activity	Jęśkowiak, Izabela			91	C	p.	article
69	The influence of cationic dendrimers on antibacterial activity of phage endolysin against P. aeruginosa cells	Ciepluch, Karol			91	C	p.	article
70	The novel economical synthesis and antimicrobial activity of a trithiocarbonate derivative	Mabkhot, Yahia N.			91	C	p.	article
71	Thiohydantoin derivatives incorporating a pyrazole core: Design, synthesis and biological evaluation as dual inhibitors of topoisomerase-I and cycloxygenase-2 with anti-cancer and anti-inflammatory activities	Abdellatif, Khaled R.A.			91	C	p.	article
72	Three new cyclopiane-type diterpenes from a deep-sea derived fungus Penicillium sp. YPGA11 and their effects against human esophageal carcinoma cells	Cheng, Zhongbin			91	C	p.	article
73	Tyrosine-based asymmetric urea ligand for prostate carcinoma: Tuning biological efficacy through in silico studies	Sengupta, Sagnik			91	C	p.	article
74	Tyrosol from marine Fungi, a novel Quorum sensing inhibitor against Chromobacterium violaceum and Pseudomonas aeruginosa	Chang, Aiping			91	C	p.	article
75	Ugi efficient synthesis, biological evaluation and molecular docking of coumarin-quinoline hybrids as apoptotic agents through mitochondria-related pathways	Taheri, Salman			91	C	p.	article
76	Ureidobenzenesulfonamides as efficient inhibitors of carbonic anhydrase II	Serbian, Immo			91	C	p.	article
77	Utilization of tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidinone as a cap moiety in design of novel histone deacetylase inhibitors	Mohamed, Mamdouh F.A.			91	C	p.	article
78	Water soluble thioglycosylated BODIPYs for mitochondria targeted cytotoxicity	Kesavan, Praseetha E.			91	C	p.	article

78 results found

Koninklijke Bibliotheek - National Library of the Netherlands