Design, Synthesis and Docking Studies of New 4-hydroxyquinoline-3-carbohydrazide Derivatives as Anti-HIV-1 Agents
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Design, Synthesis and Docking Studies of New 4-hydroxyquinoline-3-carbohydrazide Derivatives as Anti-HIV-1 Agents ; volume:63 ; number:04 ; year:2013 ; pages:192-197
Drug research ; 63, Heft 04 (2013), 192-197
- Contributor
-
Hajimahdi, Z.
Zabihollahi, R.
Aghasadeghi, M. R.
Zarghi, A.
- DOI
-
10.1055/s-0033-1334964
- URN
-
urn:nbn:de:101:1-2018121215322895818403
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hajimahdi, Z.
- Zabihollahi, R.
- Aghasadeghi, M. R.
- Zarghi, A.
Other Objects (12)
Model-based anti-HIV therapy
Dual anti-HIV mechanism of clofarabine
Universal access to anti-HIV therapy
Docking studies of flavonoid derivatives as potent HIV-1 integrase inhibitors
Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents
Anti-HIV nucleosides : past, present and future
The role of the glycosyl moiety of myricetin derivatives in anti-HIV-1 activity in vitro
6-Bromo quinazoline derivatives as cytotoxic agents: design, synthesis, molecular docking and MD simulation
Anti-HIV and immune modulating activities of IND02
SHIVs, monkeys, and anti-HIV-1 neutralizing antibodies
Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents
Design, efficient synthesis and molecular docking of some novel thiazolyl-pyrazole derivatives as anticancer agents
Model-based anti-HIV therapy
Dual anti-HIV mechanism of clofarabine
Universal access to anti-HIV therapy
Docking studies of flavonoid derivatives as potent HIV-1 integrase inhibitors
Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents
Anti-HIV nucleosides : past, present and future
The role of the glycosyl moiety of myricetin derivatives in anti-HIV-1 activity in vitro
6-Bromo quinazoline derivatives as cytotoxic agents: design, synthesis, molecular docking and MD simulation
Anti-HIV and immune modulating activities of IND02
SHIVs, monkeys, and anti-HIV-1 neutralizing antibodies
Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents
Design, efficient synthesis and molecular docking of some novel thiazolyl-pyrazole derivatives as anticancer agents
Model-based anti-HIV therapy
Dual anti-HIV mechanism of clofarabine
Universal access to anti-HIV therapy
Docking studies of flavonoid derivatives as potent HIV-1 integrase inhibitors
Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents
Anti-HIV nucleosides : past, present and future
The role of the glycosyl moiety of myricetin derivatives in anti-HIV-1 activity in vitro
6-Bromo quinazoline derivatives as cytotoxic agents: design, synthesis, molecular docking and MD simulation
Anti-HIV and immune modulating activities of IND02
SHIVs, monkeys, and anti-HIV-1 neutralizing antibodies
Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents