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79 gevonden resultaten

nr	titel	auteur	tijdschrift	jaar	jaarg.	afl.	pagina('s)	type
1	Albumin coated copper-cysteine nanozyme for reducing oxidative stress induced during sperm cryopreservation	Dashtestani, Fariba			80	C	p. 621-630	artikel
2	11a-N-tosyl-5-carbapterocarpans: Synthesis, antineoplastic evaluation and in silico prediction of ADMETox properties	Mendes, Joseane A.			80	C	p. 585-590	artikel
3	3-Aryl/Heteroaryl-5-amino-1-(3′,4′,5′-trimethoxybenzoyl)-1,2,4-triazoles as antimicrotubule agents. Design, synthesis, antiproliferative activity and inhibition of tubulin polymerization	Romagnoli, Romeo			80	C	p. 361-374	artikel
4	Benzimidazole scaffold based hybrid molecules for various inflammatory targets: Synthesis and evaluation	Kaur, Gaganpreet			80	C	p. 24-35	artikel
5	Bioactive secondary metabolites from the marine-associated fungus Aspergillus terreus	Liu, Mengting			80	C	p. 525-530	artikel
6	Biological properties and structural study of new aminoalkyl derivatives of benzimidazole and benzotriazole, dual inhibitors of CK2 and PIM1 kinases	Chojnacki, K.			80	C	p. 266-275	artikel
7	Characterization of inhibitory constituents of NO production from Catalpa ovata using LC-MS coupled with a cell-based assay	Park, Sangmin			80	C	p. 57-63	artikel
8	Cytoprotective and antioxidant properties of organic selenides for the myelin-forming cells, oligodendrocytes	Shaaban, Saad			80	C	p. 43-56	artikel
9	Cytotoxic macrocyclic diterpenoids from Jatropha multifida	Zhang, Jun-Sheng			80	C	p. 511-518	artikel
10	Design and Amberlyst-15 mediated synthesis of novel thienyl-pyrazole carboxamides that potently inhibit Phospholipase A2 by binding to an allosteric site on the enzyme	Kumar, Achutha Dileep			80	C	p. 444-452	artikel
11	Design and synthesis of donepezil analogues as dual AChE and BACE-1 inhibitors	Gabr, Moustafa T.			80	C	p. 245-252	artikel
12	Design and synthesis of gallocyanine inhibitors of DKK1/LRP6 interactions for treatment of Alzheimer’s disease	Thysiadis, Savvas			80	C	p. 230-244	artikel
13	Design and synthesis of novel imidazo[4,5-b]pyridine based compounds as potent anticancer agents with CDK9 inhibitory activity	Ghanem, Nada M.			80	C	p. 565-576	artikel
14	Design, synthesis and activity of light deactivatable microRNA inhibitor	Yan, Hao			80	C	p. 492-497	artikel
15	Design, synthesis and anticancer evaluation of 1H-pyrazolo[3,4-d]pyrimidine derivatives as potent EGFRWT and EGFRT790M inhibitors and apoptosis inducers	Gaber, Ahmed A.			80	C	p. 375-395	artikel
16	Design, synthesis and anti leukemia cells proliferation activities of pyrimidylaminoquinoline derivatives as DOT1L inhibitors	Zhang, Li			80	C	p. 649-654	artikel
17	Design, synthesis and antiplasmodial activity of novel imidazole derivatives based on 7-chloro-4-aminoquinoline	Kondaparla, Srinivasarao			80	C	p. 204-211	artikel
18	Design, synthesis and biological evaluation of novel pyrrole derivatives as potential ClpP1P2 inhibitor against Mycobacterium tuberculosis	Liu, Pingxian			80	C	p. 422-432	artikel
19	Design, synthesis and biological evaluation of novel 1,2,3-triazole linked coumarinopyrazole conjugates as potent anticholinesterase, anti-5-lipoxygenase, anti-tyrosinase and anti-cancer agents	Chekir, Samia			80	C	p. 189-194	artikel
20	Design, synthesis and docking study of pyridine and thieno[2,3-b] pyridine derivatives as anticancer PIM-1 kinase inhibitors	Abdelaziz, Marwa E.			80	C	p. 674-692	artikel
21	Design, synthesis and evaluation of some pyrazolo[3,4-d]pyrimidine derivatives bearing thiazolidinone moiety as anti-inflammatory agents	Tageldin, Gina N.			80	C	p. 164-173	artikel
22	Design, synthesis and molecular modeling study of certain 4-Methylbenzenesulfonamides with CDK2 inhibitory activity as anticancer and radio-sensitizing agents	Ghorab, Mostafa M.			80	C	p. 276-287	artikel
23	Design, synthesis, biological activities and DFT calculation of novel 1,2,4-triazole Schiff base derivatives	Jin, Ru-Yi			80	C	p. 253-260	artikel
24	Design, synthesis, docking study, α-glucosidase inhibition, and cytotoxic activities of acridine linked to thioacetamides as novel agents in treatment of type 2 diabetes	Mohammadi-Khanaposhtani, Maryam			80	C	p. 288-295	artikel
25	Design, synthesis, in-vitro thymidine phosphorylase inhibition, in-vivo antiangiogenic and in-silico studies of C-6 substituted dihydropyrimidines	Iftikhar, Fatima			80	C	p. 99-111	artikel
26	Design, synthesis of novel azolyl flavonoids and their protein tyrosine Phosphatase-1B inhibitory activities	Zhang, Ling			80	C	p. 195-203	artikel
27	Design, synthesis of novel isoindoline hybrids as COX-2 inhibitors: Anti-inflammatory, analgesic activities and docking study	Labib, Madlen B.			80	C	p. 70-80	artikel
28	Development of dilipid polymyxins: Investigation on the effect of hydrophobicity through its fatty acyl component	Domalaon, Ronald			80	C	p. 639-648	artikel
29	Dicoumarol derivatives: Green synthesis and molecular modelling studies of their anti-LOX activity	Simijonović, Dušica			80	C	p. 741-752	artikel
30	Discovery of dihydrobenzofuran neolignans from Rubus ideaus L. with enantioselective anti-Aβ 1–42 aggregation activity	Zhou, Le			80	C	p. 64-69	artikel
31	Discovery of polar spirocyclic orally bioavailable urea inhibitors of soluble epoxide hydrolase	Lukin, Alexey			80	C	p. 655-667	artikel
32	Dual EGFR/HER2 inhibitors and apoptosis inducers: New benzo[g]quinazoline derivatives bearing benzenesulfonamide as anticancer and radiosensitizers	Ghorab, Mostafa M.			80	C	p. 611-620	artikel
33	Editorial Board				80	C	p. i	artikel
34	Efficient chemoenzymatic synthesis of (S)-α-amino-4-fluorobenzeneacetic acid using immobilized penicillin amidase	Lin, Chao-Ping			80	C	p. 174-179	artikel
35	Efficient synthesis of the ketone body ester (R)-3-hydroxybutyryl-(R)-3-hydroxybutyrate and its (S,S) enantiomer	Budin, Noah			80	C	p. 560-564	artikel
36	Enhancement in anti-tubercular activity of indole based thiosemicarbazones on complexation with copper(I) and silver(I) halides: Structure elucidation, evaluation and molecular modelling	Khan, Ashiq			80	C	p. 303-318	artikel
37	Imidazopyridine linked triazoles as tubulin inhibitors, effectively triggering apoptosis in lung cancer cell line	Sayeed, Ibrahim Bin			80	C	p. 714-720	artikel
38	Imidazo[2′,1′:2,3]thiazolo[4,5-d]pyridazinone as a new scaffold of DHFR inhibitors: Synthesis, biological evaluation and molecular modeling study	Ewida, Menna A.			80	C	p. 11-23	artikel
39	Improvement of carbonyl reductase activity for the bioproduction of tert-butyl (3R,5S)-6-chloro-3,5-dihydroxyhexanoate	Liu, Zhi-Qiang			80	C	p. 733-740	artikel
40	Investigation of salicylanilide and 4-chlorophenol-based N-monosubstituted carbamates as potential inhibitors of acetyl- and butyrylcholinesterase	Krátký, Martin			80	C	p. 668-673	artikel
41	Issue TOC				80	C	p. ii-xxiv	artikel
42	Lambertellin from Pycnoporus sanguineus MUCL 51321 and its anti-inflammatory effect via modulation of MAPK and NF-κB signaling pathways	Jouda, Jean-Bosco			80	C	p. 216-222	artikel
43	Lipid reducing activity of novel cholic acid (CA) analogs: Design, synthesis and preliminary mechanism study	Luo, Guoshun			80	C	p. 396-407	artikel
44	Multi-targetable chalcone analogs to treat deadly Alzheimer’s disease: Current view and upcoming advice	Zhang, Xu			80	C	p. 86-93	artikel
45	Natural constituents from Cortex Mori Radicis as new pancreatic lipase inhibitors	Hou, Xu-Dong			80	C	p. 577-584	artikel
46	New C-2 diastereomers of flavanone glycosides conjugated with 3-hydroxy-3-methylglutaric acid from the pericarp of Citrus grandis (L.) Osbeck	Ma, Shuang-Gang			80	C	p. 519-524	artikel
47	New monoterpenoid by biotransformation of thymoquinone using Aspergillus niger	Mohammad, Mohammad Yasin			80	C	p. 212-215	artikel
48	Nitric oxide inhibitory constituents from Siegesbeckia pubescens	Jang, Hari			80	C	p. 81-85	artikel
49	Novel benzotriazole N-acylarylhydrazone hybrids: Design, synthesis, anticancer activity, effects on cell cycle profile, caspase-3 mediated apoptosis and FAK inhibition	Kassab, Asmaa E.			80	C	p. 531-544	artikel
50	Novel pyrrol-2(3H)-ones and pyridazin-3(2H)-ones carrying quinoline scaffold as anti-proliferative tubulin polymerization inhibitors	Abdelbaset, Mahmoud S.			80	C	p. 151-163	artikel
51	Promiscuous enzyme-catalyzed cascade reaction: Synthesis of xanthone derivatives	Fu, Yajie			80	C	p. 555-559	artikel
52	QM/MM study of the reaction mechanism of Cl-cis,cis-muconate with muconate lactonizing enzyme	Zhu, Ledong			80	C	p. 453-460	artikel
53	Sam domain-based stapled peptides: Structural analysis and interaction studies with the Sam domains from the EphA2 receptor and the lipid phosphatase Ship2	Mercurio, Flavia Anna			80	C	p. 602-610	artikel
54	2-S-cysteinylhydroquinone is an intermediate for the firefly luciferin biosynthesis that occurs in the pupal stage of the Japanese firefly, Luciola lateralis	Kanie, Shusei			80	C	p. 223-229	artikel
55	Structural comparison of Mtb-DHFR and h-DHFR for design, synthesis and evaluation of selective non-pteridine analogues as antitubercular agents	Sharma, Kalicharan			80	C	p. 319-333	artikel
56	Structure-based design of free fatty acid receptor 1 agonists bearing non-biphenyl scaffold	Li, Zheng			80	C	p. 296-302	artikel
57	Structure-based design of some isonicotinic acid hydrazide analogues as potential antitubercular agents	Atta, Amal			80	C	p. 721-732	artikel
58	Studies on the lipid-regulating mechanism of alisol-based compounds on lipoprotein lipase	Xu, Fei			80	C	p. 347-360	artikel
59	Syntheses, antiviral activities and induced resistance mechanisms of novel quinazoline derivatives containing a dithioacetal moiety	Xie, Dandan			80	C	p. 433-443	artikel
60	Synthesis, α-amylase inhibitory potential and molecular docking study of indole derivatives	Taha, Muhammad			80	C	p. 36-42	artikel
61	Synthesis and biological evaluation of benzo[b]furo[3,4-e][1,4]diazepin-1-one derivatives as anti-cancer agents	Malayeri, Sina Omid			80	C	p. 631-638	artikel
62	Synthesis and biological evaluation of some N-(3-(1H-tetrazol-5-yl) phenyl)acetamide derivatives as novel non-carboxylic PTP1B inhibitors designed through bioisosteric modulation	Maheshwari, Neelesh			80	C	p. 145-150	artikel
63	Synthesis and cholinesterase inhibitory activity of new 2-benzofuran carboxamide-benzylpyridinum salts	Abedinifar, Fahimeh			80	C	p. 180-188	artikel
64	Synthesis and DNase I inhibitory properties of some 5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidines	Ts. Mavrova, Anelia			80	C	p. 693-705	artikel
65	Synthesis and dopaminergic activity of a series of new 1-aryl tetrahydroisoquinolines and 2-substituted 1-aryl-3-tetrahydrobenzazepines	Lucena-Serrano, Cristina			80	C	p. 480-491	artikel
66	Synthesis and molecular docking study of some novel 2,3-disubstituted quinazolin-4(3H)-one derivatives as potent inhibitors of urease	Akyüz, Gülay			80	C	p. 121-128	artikel
67	Synthesis, biological activities, and molecular docking studies of 2-mercaptobenzimidazole based derivatives	Ali, Mumtaz			80	C	p. 472-479	artikel
68	Synthesis, biological evaluation and docking study of 1,3,4-thiadiazole-thiazolidinone hybrids as anti-inflammatory agents with dual inhibition of COX-2 and 15-LOX	Omar, Yasser M.			80	C	p. 461-471	artikel
69	Synthesis, characterization, monoamine oxidase inhibition, molecular docking and dynamic simulations of novel 2,1-benzothiazine-2,2-dioxide derivatives	Ahmad, Shakeel			80	C	p. 498-510	artikel
70	Synthesis, in vitro and in silico evaluation of diaryl heptanones as potential 5LOX enzyme inhibitors	Meka, Bharani			80	C	p. 408-421	artikel
71	Synthesis, in vitro urease inhibitory activity, and molecular docking studies of thiourea and urea derivatives	Bano, Bilquees			80	C	p. 129-144	artikel
72	Synthesis of Bis-indolylmethane sulfonohydrazides derivatives as potent α-Glucosidase inhibitors	Gollapalli, Mohammed			80	C	p. 112-120	artikel
73	Synthesis of C-2 and C-3 substituted quinolines and their evaluation as anti-HIV-1 agents	Shah, Purvi			80	C	p. 591-601	artikel
74	Synthesis of novel isoindoline-1,3-dione-based oximes and benzenesulfonamide hydrazones as selective inhibitors of the tumor-associated carbonic anhydrase IX	Abdel-Aziz, Alaa A.-M.			80	C	p. 706-713	artikel
75	Synthesis of spherical Fe2O3 nanoparticles from the thermal decomposition of iron (III) nano-structure complex: DFT studies and evaluation of the biological activity	Zare, Nahid			80	C	p. 334-346	artikel
76	Targeting oncogenic transcriptional corepressor Nac1 POZ domain with conformationally constrained peptides by cyclization and stapling	Wu, Tao			80	C	p. 1-10	artikel
77	Tetrahydroindolocarbazoles (THICZs) as new class of urokinase (uPA) inhibitors: Synthesis, anticancer evaluation, DNA-damage determination, and molecular modelling study	El-Sharief, Marwa A.M.Sh.			80	C	p. 545-554	artikel
78	The first activation studies of the η-carbonic anhydrase from the malaria parasite Plasmodium falciparum with amines and amino acids	Angeli, Andrea			80	C	p. 94-98	artikel
79	The zinc – but not cadmium – containing ζ-carbonic from the diatom Thalassiosira weissflogii is potently activated by amines and amino acids	Angeli, Andrea			80	C	p. 261-265	artikel

79 gevonden resultaten

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