nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A new cerebroside from the twigs of Lindera glauca (Sieb. et Zucc.) Blume
|
Yu, Jae Sik |
|
2017 |
74 |
C |
p. 122-125 4 p. |
artikel |
2 |
A new lignan and a new alkaloid, and α-glucosidase inhibitory compounds from the grains of Echinochloa utilis Ohwi & Yabuno
|
Nguyen, Thi Trang |
|
2017 |
74 |
C |
p. 221-227 7 p. |
artikel |
3 |
Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies
|
Taha, Muhammad |
|
2017 |
74 |
C |
p. 1-9 9 p. |
artikel |
4 |
Catalytic amidolysis of amino acid p-nitroanilides using transition state analogue imprinted artificial enzymes: Cooperative effect of pyridine moiety
|
Divya, Mathew |
|
2017 |
74 |
C |
p. 91-103 13 p. |
artikel |
5 |
Corrigendum to “Designing structural-motifs for the preparation of acylated proinsulin and their regiospecific conversion into insulin modified at Lys29 (K29)” [Bioorg. Chem. 73 (2017) 147–153]
|
Ahmad, Munir |
|
2017 |
74 |
C |
p. 284- 1 p. |
artikel |
6 |
Design, synthesis and α-amylase inhibitory activity of novel chromone derivatives
|
Valentina, Parthiban |
|
2017 |
74 |
C |
p. 158-165 8 p. |
artikel |
7 |
Design, synthesis and biological evaluation of some novel benzothiazole/benzoxazole and/or benzimidazole derivatives incorporating a pyrazole scaffold as antiproliferative agents
|
Abdelgawad, Mohamed A. |
|
2017 |
74 |
C |
p. 82-90 9 p. |
artikel |
8 |
Design, synthesis and evaluation of newer 5,6-dihydropyrimidine-2(1H)-thiones as GABA-AT inhibitors for anticonvulsant potential
|
Sahu, Meeta |
|
2017 |
74 |
C |
p. 166-178 13 p. |
artikel |
9 |
Design, synthesis, in vitro Evaluation and docking studies on dihydropyrimidine-based urease inhibitors
|
Iftikhar, Fatima |
|
2017 |
74 |
C |
p. 53-65 13 p. |
artikel |
10 |
Editorial Board
|
|
|
2017 |
74 |
C |
p. i- 1 p. |
artikel |
11 |
Exploration of aroyl/heteroaroyl iminothiazolines featuring 2,4,5-trichlorophenyl moiety as a new class of potent, selective, and in vitro efficacious glucosidase inhibitors
|
Kazmi, Madiha |
|
2017 |
74 |
C |
p. 134-144 11 p. |
artikel |
12 |
Is literature data useful for identifying enzyme catalysts for new substrates? A case study on reduction of 1-aryl-2-alkanoates
|
Hoff, Bård Helge |
|
2017 |
74 |
C |
p. 260-271 12 p. |
artikel |
13 |
Issue TOC
|
|
|
2017 |
74 |
C |
p. ii-ix nvt p. |
artikel |
14 |
New carbazole linked 1,2,3-triazoles as highly potent non-sugar α-glucosidase inhibitors
|
Iqbal, Shazia |
|
2017 |
74 |
C |
p. 72-81 10 p. |
artikel |
15 |
New heterocyclic compounds from Ranunculus ternatus Thunb.
|
Feng, Zi-ming |
|
2017 |
74 |
C |
p. 10-14 5 p. |
artikel |
16 |
New 1,3,4-oxadiazole/oxime hybrids: Design, synthesis, anti-inflammatory, COX inhibitory activities and ulcerogenic liability
|
Abd-Ellah, Heba S. |
|
2017 |
74 |
C |
p. 15-29 15 p. |
artikel |
17 |
Novel antioxidant bromophenols with acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase inhibitory actions
|
Öztaskın, Necla |
|
2017 |
74 |
C |
p. 104-114 11 p. |
artikel |
18 |
Novel dehydroabietylamine derivatives as potent inhibitors of acetylcholinesterase
|
Wiemann, Jana |
|
2017 |
74 |
C |
p. 145-157 13 p. |
artikel |
19 |
Pyrazole-hydrazone derivatives as anti-inflammatory agents: Design, synthesis, biological evaluation, COX-1,2/5-LOX inhibition and docking study
|
Abdelgawad, Mohamed A. |
|
2017 |
74 |
C |
p. 212-220 9 p. |
artikel |
20 |
Structure-activity relationships and molecular docking of thirteen synthesized flavonoids as horseradish peroxidase inhibitors
|
Mahfoudi, Reguia |
|
2017 |
74 |
C |
p. 201-211 11 p. |
artikel |
21 |
Structure-based design of competitive ligands to target Spon2 in gastric cancer: An integration of molecular modeling and in vitro assay
|
Xu, Zhenglei |
|
2017 |
74 |
C |
p. 115-121 7 p. |
artikel |
22 |
5-Substituted 2-benzylidene-1-tetralone analogues as A1 and/or A2A antagonists for the potential treatment of neurological conditions
|
Janse van Rensburg, H.D. |
|
2017 |
74 |
C |
p. 251-259 9 p. |
artikel |
23 |
Synthesis and anticancer activity of new thiazolo[3,2-a]pyrimidines: DNA binding and molecular modeling study
|
Hassan, Ghada S. |
|
2017 |
74 |
C |
p. 41-52 12 p. |
artikel |
24 |
Synthesis and antioxidant ability of 6,6′-diamino-6,6′-dideoxytrehalose
|
Tan, Wenqiang |
|
2017 |
74 |
C |
p. 66-71 6 p. |
artikel |
25 |
Synthesis and biological evaluation of quinazolinone-based hydrazones with potential use in Alzheimer’s disease
|
Haghighijoo, Zahra |
|
2017 |
74 |
C |
p. 126-133 8 p. |
artikel |
26 |
Synthesis and study of the α-amylase inhibitory potential of thiadiazole quinoline derivatives
|
Taha, Muhammad |
|
2017 |
74 |
C |
p. 179-186 8 p. |
artikel |
27 |
Synthesis, characterization and DNA binding studies of platinum(II) complexes with benzimidazole derivative ligands
|
Tarı, Özden |
|
2017 |
74 |
C |
p. 272-283 12 p. |
artikel |
28 |
Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes mellitus
|
Taha, Muhammad |
|
2017 |
74 |
C |
p. 30-40 11 p. |
artikel |
29 |
Synthesis, molecular docking studies of coumarinyl-pyrazolinyl substituted thiazoles as non-competitive inhibitors of mushroom tyrosinase
|
Saeed, Aamer |
|
2017 |
74 |
C |
p. 187-196 10 p. |
artikel |
30 |
Tannic acid affects the phenotype of Staphylococcus aureus resistant to tetracycline and erythromycin by inhibition of efflux pumps
|
Tintino, Saulo R. |
|
2017 |
74 |
C |
p. 197-200 4 p. |
artikel |
31 |
The synthesis of novel sulfamides derived from β-benzylphenethylamines as acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase enzymes inhibitors
|
Akıncıoğlu, Akın |
|
2017 |
74 |
C |
p. 238-250 13 p. |
artikel |
32 |
Thiazolo[4,5-d]pyridazine analogues as a new class of dihydrofolate reductase (DHFR) inhibitors: Synthesis, biological evaluation and molecular modeling study
|
Ewida, Menna A. |
|
2017 |
74 |
C |
p. 228-237 10 p. |
artikel |