| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Antifungal activity of a series of 1,2-benzisothiazol-3(2H)-one derivatives
|
Dou, Dengfeng
|
|
2011
|
19 |
19 |
p. 5782-5787
6 p.
|
article
|
| 2 |
A ribonucleopeptide module for effective conversion of an RNA aptamer to a fluorescent sensor
|
Liew, Fong Fong
|
|
2011
|
19 |
19 |
p. 5771-5775
5 p.
|
article
|
| 3 |
1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents
|
Novikov, Mikhail S.
|
|
2011
|
19 |
19 |
p. 5794-5802
9 p.
|
article
|
| 4 |
CNS and antimalarial activity of synthetic meridianin and psammopemmin analogs
|
Lebar, Matthew D.
|
|
2011
|
19 |
19 |
p. 5756-5762
7 p.
|
article
|
| 5 |
Deep understanding of structure–solubility relationship for a diverse set of organic compounds using matched molecular pairs
|
Zhang, Liying
|
|
2011
|
19 |
19 |
p. 5763-5770
8 p.
|
article
|
| 6 |
Design and synthesis of inhibitors of noroviruses by scaffold hopping
|
Dou, Dengfeng
|
|
2011
|
19 |
19 |
p. 5749-5755
7 p.
|
article
|
| 7 |
Editorial board
|
|
|
2011
|
19 |
19 |
p. IFC-
1 p.
|
article
|
| 8 |
Evaluation of PI polyamide conjugates with eight-base pair recognition and improvement of the aqueous solubility by PEGylation
|
Takagaki, Toshiki
|
|
2011
|
19 |
19 |
p. 5896-5902
7 p.
|
article
|
| 9 |
Exploiting differences in caspase-2 and -3 S2 subsites for selectivity: Structure-based design, solid-phase synthesis and in vitro activity of novel substrate-based caspase-2 inhibitors
|
Maillard, Michel C.
|
|
2011
|
19 |
19 |
p. 5833-5851
19 p.
|
article
|
| 10 |
Graphical contents list
|
|
|
2011
|
19 |
19 |
p. 5743-5748
6 p.
|
article
|
| 11 |
Identification of novel small molecule inhibitors of 4-diphosphocytidyl-2-C-methyl-d-erythritol (CDP-ME) kinase of Gram-negative bacteria
|
Tang, M.
|
|
2011
|
19 |
19 |
p. 5886-5895
10 p.
|
article
|
| 12 |
Inhibitory effect of novel 5-O-acyl juglones on mammalian DNA polymerase activity, cancer cell growth and inflammatory response
|
Maruo, Sayako
|
|
2011
|
19 |
19 |
p. 5803-5812
10 p.
|
article
|
| 13 |
Modeling the molecular basis for α4β1 integrin antagonism
|
Hutt, Oliver E.
|
|
2011
|
19 |
19 |
p. 5903-5911
9 p.
|
article
|
| 14 |
Natural daucane sesquiterpenes with antiproliferative and proapoptotic activity against human tumor cells
|
Dall’Acqua, Stefano
|
|
2011
|
19 |
19 |
p. 5876-5885
10 p.
|
article
|
| 15 |
New aporphinoid 5-HT2A and α1A antagonists via structural manipulations of nantenine
|
Chaudhary, Sandeep
|
|
2011
|
19 |
19 |
p. 5861-5868
8 p.
|
article
|
| 16 |
Novel thiophenyl C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents
|
Lee, Suk Ho
|
|
2011
|
19 |
19 |
p. 5813-5832
20 p.
|
article
|
| 17 |
Potential AMPK activators of cucurbitane triterpenoids from Siraitia grosvenorii Swingle
|
Chen, Xu-bing
|
|
2011
|
19 |
19 |
p. 5776-5781
6 p.
|
article
|
| 18 |
Probing DNA interstrand cross-link formation by an oxidized abasic site using nonnative nucleotides
|
Sczepanski, Jonathan T.
|
|
2011
|
19 |
19 |
p. 5788-5793
6 p.
|
article
|
| 19 |
Searching for new NO-donor aspirin-like molecules: Furoxanylacyl derivatives of salicylic acid and related furazans
|
Lazzarato, Loretta
|
|
2011
|
19 |
19 |
p. 5852-5860
9 p.
|
article
|
| 20 |
Synthesis, binding and cellular uptake properties of oligodeoxynucleotides containing cationic bicyclo-thymidine residues
|
Lietard, Jory
|
|
2011
|
19 |
19 |
p. 5869-5875
7 p.
|
article
|
| 21 |
Synthesis of new six- and seven-membered 1-N-iminosugars as promising glycosidase inhibitors
|
Jabgunde, Amit M.
|
|
2011
|
19 |
19 |
p. 5912-5915
4 p.
|
article
|
Journal description