| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acyl selenoureido benzensulfonamides show potent inhibitory activity against carbonic anhydrases from the pathogenic bacterium Vibrio cholerae
|
Angeli, Andrea
|
|
2017
|
75 |
C |
p. 170-172
|
artikel
|
| 2 |
Application of the Morita-Baylis-Hillman reaction in the synthesis of 3-[(N-cycloalkylbenzamido)methyl]-2-quinolones as potential HIV-1 integrase inhibitors
|
Sekgota, Khethobole C.
|
|
2017
|
75 |
C |
p. 310-316
|
artikel
|
| 3 |
Chemical synthesis and in silico molecular modeling of novel pyrrolyl benzohydrazide derivatives: Their biological evaluation against enoyl ACP reductase (InhA) and Mycobacterium tuberculosis
|
Joshi, Shrinivas D.
|
|
2017
|
75 |
C |
p. 181-200
|
artikel
|
| 4 |
Coumarinyl pyranopyrimidines as new neuropeptide S receptor antagonists; design, synthesis, homology and molecular docking
|
Batran, Rasha Z.
|
|
2017
|
75 |
C |
p. 274-290
|
artikel
|
| 5 |
Cytotoxic dihydrobenzofuran neolignans from Mappianthus iodoies
|
Jiang, Zhi-Hua
|
|
2017
|
75 |
C |
p. 260-264
|
artikel
|
| 6 |
Design, synthesis and biological evaluation of 1,3-dihydroxyxanthone derivatives: Effective agents against acetylcholinesterase
|
Menéndez, Cintia A.
|
|
2017
|
75 |
C |
p. 201-209
|
artikel
|
| 7 |
Design, synthesis, and evaluation of novel ursolic acid derivatives as HIF-1α inhibitors with anticancer potential
|
Chi, Ke-Qiang
|
|
2017
|
75 |
C |
p. 157-169
|
artikel
|
| 8 |
3,4-Dimethoxybenzohydrazide derivatives as antiulcer: Molecular modeling and density functional studies
|
Taha, Muhammad
|
|
2017
|
75 |
C |
p. 235-241
|
artikel
|
| 9 |
Discovery of triazole-based uracil derivatives bearing amide moieties as novel dipeptidyl peptidase-IV inhibitors
|
Deng, Xiaoyan
|
|
2017
|
75 |
C |
p. 357-367
|
artikel
|
| 10 |
Editorial Board
|
|
|
2017
|
75 |
C |
p. i
|
artikel
|
| 11 |
Enzymatic synthesis of 1,3-dihydroxyphenylacetoyl-sn-glycerol: Optimization by response surface methodology and evaluation of its antioxidant and antibacterial activities
|
Kharrat, Nadia
|
|
2017
|
75 |
C |
p. 347-356
|
artikel
|
| 12 |
Exploration of thioxothiazolidinone–sulfonate conjugates as a new class of aldehyde/aldose reductase inhibitors: A synthetic and computational investigation
|
Andleeb, Hina
|
|
2017
|
75 |
C |
p. 1-15
|
artikel
|
| 13 |
Hit discovery of 4-amino-N-(4-(3-(trifluoromethyl)phenoxy)pyrimidin-5-yl)benzamide: A novel EGFR inhibitor from a designed small library
|
Elkamhawy, Ahmed
|
|
2017
|
75 |
C |
p. 393-405
|
artikel
|
| 14 |
Identification of new potent inhibitor of aldose reductase from Ocimum basilicum
|
Bhatti, Huma Aslam
|
|
2017
|
75 |
C |
p. 62-70
|
artikel
|
| 15 |
Inactivation of bovine plasma amine oxidase by 1,1,1–trihalo–3–aminopropanes
|
Kim, Jisook
|
|
2017
|
75 |
C |
p. 265-273
|
artikel
|
| 16 |
Issue TOC
|
|
|
2017
|
75 |
C |
p. ii-xi
|
artikel
|
| 17 |
Is the Sudlow site I of human serum albumin more generous to adopt prospective anti-cancer bioorganic compound than that of bovine: A combined spectroscopic and docking simulation approach
|
Joshi, Ritika
|
|
2017
|
75 |
C |
p. 332-346
|
artikel
|
| 18 |
Liquid phase combinatorial synthesis of 1,2,5-trisubstituted benzimidazole derivatives as human DHODH inhibitors
|
Sitwala, Nikum D.
|
|
2017
|
75 |
C |
p. 118-126
|
artikel
|
| 19 |
Molecular docking and QSAR analyses of aromatic heterocycle thiosemicarbazone analogues for finding novel tyrosinase inhibitors
|
Dong, Huanhuan
|
|
2017
|
75 |
C |
p. 106-117
|
artikel
|
| 20 |
New indole-based chalconoids as tubulin-targeting antiproliferative agents
|
Mirzaei, Hassan
|
|
2017
|
75 |
C |
p. 86-98
|
artikel
|
| 21 |
New iridoid glycosides from the fruits of Forsythia suspensa and their hepatoprotective activities
|
Shao, Si-Yuan
|
|
2017
|
75 |
C |
p. 303-309
|
artikel
|
| 22 |
Nitric oxide inhibitory daphnane diterpenoids as potential anti-neuroinflammatory agents for AD from the twigs of Trigonostemon thyrsoideus
|
Liu, Feng
|
|
2017
|
75 |
C |
p. 149-156
|
artikel
|
| 23 |
Novel diphenylthiazole derivatives with multi-target mechanism: Synthesis, docking study, anticancer and anti-inflammatory activities
|
Abdelazeem, Ahmed H.
|
|
2017
|
75 |
C |
p. 127-138
|
artikel
|
| 24 |
Novel quinoline-3-carboxamides (Part 2): Design, optimization and synthesis of quinoline based scaffold as EGFR inhibitors with potent anticancer activity
|
Aly, Rasha M.
|
|
2017
|
75 |
C |
p. 368-392
|
artikel
|
| 25 |
Novel quinoline incorporating 1,2,4-triazole/oxime hybrids: Synthesis, molecular docking, anti-inflammatory, COX inhibition, ulceroginicity and histopathological investigations
|
Mohassab, Aliaa M.
|
|
2017
|
75 |
C |
p. 242-259
|
artikel
|
| 26 |
N-Sulfamoylphenyl- and N-sulfamoylphenyl-N-thiazolyl-β-alanines and their derivatives as inhibitors of human carbonic anhydrases
|
Vaškevičienė, Irena
|
|
2017
|
75 |
C |
p. 16-29
|
artikel
|
| 27 |
Phytochemicals with NO inhibitory effects and interactions with iNOS protein from Trigonostemon howii
|
Ma, Jun
|
|
2017
|
75 |
C |
p. 71-77
|
artikel
|
| 28 |
Polycyclic phloroglucinols as PTP1B inhibitors from Hypericum longistylum: Structures, PTP1B inhibitory activities, and interactions with PTP1B
|
Cao, Xiangrong
|
|
2017
|
75 |
C |
p. 139-148
|
artikel
|
| 29 |
Reactivity improvement of cellulolytic enzyme lignin via mild hydrothermal modification
|
Ma, Zhuoming
|
|
2017
|
75 |
C |
p. 173-180
|
artikel
|
| 30 |
SAR studies of some acetophenone phenylhydrazone based pyrazole derivatives as anticathepsin agents
|
Raghav, Neera
|
|
2017
|
75 |
C |
p. 38-49
|
artikel
|
| 31 |
Sulfonyl hydrazones derived from 3-formylchromone as non-selective inhibitors of MAO-A and MAO-B: Synthesis, molecular modelling and in-silico ADME evaluation
|
Abid, Syed Mobasher Ali
|
|
2017
|
75 |
C |
p. 291-302
|
artikel
|
| 32 |
Syntheses of 4,6-dihydroxypyrimidine diones, their urease inhibition, in vitro, in silico, and kinetic studies
|
Muhammad, Munira Taj
|
|
2017
|
75 |
C |
p. 317-331
|
artikel
|
| 33 |
Synthesis and bioelectrochemical behavior of aromatic amines
|
Shabbir, Muhammad
|
|
2017
|
75 |
C |
p. 224-234
|
artikel
|
| 34 |
Synthesis and cholinesterase inhibitory activity study of new piperidone grafted spiropyrrolidines
|
Basiri, Alireza
|
|
2017
|
75 |
C |
p. 210-216
|
artikel
|
| 35 |
Synthesis and in vitro study of benzofuran hydrazone derivatives as novel alpha-amylase inhibitor
|
Taha, Muhammad
|
|
2017
|
75 |
C |
p. 78-85
|
artikel
|
| 36 |
Synthesis of thiobarbituric acid derivatives: In vitro α-glucosidase inhibition and molecular docking studies
|
Barakat, Assem
|
|
2017
|
75 |
C |
p. 99-105
|
artikel
|
| 37 |
Synthetic and medicinal perspective of thiazolidinones: A review
|
Kaur Manjal, Sundeep
|
|
2017
|
75 |
C |
p. 406-423
|
artikel
|
| 38 |
The anthraquinone emodin inhibits the non-exported FIKK kinase from Plasmodium falciparum
|
Lin, Benjamin C.
|
|
2017
|
75 |
C |
p. 217-223
|
artikel
|
| 39 |
The inhibitory activity of HL-7 and HL-10 peptide from scorpion venom (Hemiscorpius lepturus) on angiotensin converting enzyme: Kinetic and docking study
|
Setayesh-Mehr, Zahra
|
|
2017
|
75 |
C |
p. 30-37
|
artikel
|
| 40 |
Traditional Chinese medicinal herbs as potential AChE inhibitors for anti-Alzheimer’s disease: A review
|
Jiang, Yingying
|
|
2017
|
75 |
C |
p. 50-61
|
artikel
|
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