Works matching IS 17470277 AND DT 2020 AND VI 96 AND IP 6
Results: 15
Pyrrolidin‐2‐one linked benzofused heterocycles as novel small molecule monoacylglycerol lipase inhibitors and antinociceptive agents.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1418, doi. 10.1111/cbdd.13751
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A hybrid ensemble‐based technique for predicting drug–target interactions.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1447, doi. 10.1111/cbdd.13753
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- Article
Novel β‐carboline‐based indole‐4,7‐quinone derivatives as NAD(P)H: Quinone‐oxidoreductase‐1 inhibitor with potent antitumor activities by inducing reactive oxygen species, apoptosis, and DNA damage.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1433, doi. 10.1111/cbdd.13752
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- Article
Radioiodinated estradiol dimer for estrogen receptor targeted breast cancer imaging.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1332, doi. 10.1111/cbdd.13754
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- Article
A QSAR modeling approach for predicting myeloid antimicrobial peptides with high sequence similarity.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1408, doi. 10.1111/cbdd.13749
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- Article
Synthesis and evaluation of C3 substituted chalcone‐based derivatives of 7‐azaindole as protein kinase inhibitors.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1395, doi. 10.1111/cbdd.13748
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- Article
6‐Nitro‐1‐benzylquinolones exhibiting specific antitubercular activity.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1387, doi. 10.1111/cbdd.13747
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Synthesis of celastrol derivatives as potential non‐nucleoside hepatitis B virus inhibitors.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1380, doi. 10.1111/cbdd.13746
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- Article
N<sub>4</sub>‐benzyl‐N<sub>2</sub>‐phenylquinazoline‐2,4‐diamine compound presents antibacterial and antibiofilm effect against Staphylococcus aureus and Staphylococcus epidermidis.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1372, doi. 10.1111/cbdd.13745
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Design, synthesis, and biological evaluation of novel imidazo[1,2‐a]pyridinecarboxamides as potent anti‐tuberculosis agents.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1362, doi. 10.1111/cbdd.13739
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- Article
Amalgamating Isatin/Indole/Nitroimidazole with 7‐chloroquinolines via azide‐alkyne cycloaddition: Synthesis, anti‐plasmodial, and cytotoxic evaluation.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1355, doi. 10.1111/cbdd.13738
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- Article
Multimeric TAT peptides are effective in vitro inhibitors of Staphylococcus saprophyticus.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1348, doi. 10.1111/cbdd.13706
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- Article
A molecular dynamics approach on the Y393C variant of protein disulfide isomerase A1.
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- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1341, doi. 10.1111/cbdd.13700
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- Article
Issue Information.
- Published in:
- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1329, doi. 10.1111/cbdd.13563
- Publication type:
- Article
Cover Image.
- Published in:
- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. i, doi. 10.1111/cbdd.13562
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- Article