Pass and Swiss ADME collaborated in silico docking approach to the synthesis of certain pyrazoline spacer compounds for dihydrofolate reductase inhibition and antimalarial activity
New series of pyrazoline spacer compounds were prepared by the reaction between benzimidazole chalcones and (2-methyl-5-nitro-imidazole-1-yl)-acetic acid hydrazide by the sensible use of Michael addition. The building blocks used for the synthesis of pyrazoline derivatives were opted by using virtua...
Enregistré dans:
| Auteurs principaux: | , , , , |
|---|---|
| Format: | Livre |
| Publié: |
Bangladesh Pharmacological Society,
2018-01-01T00:00:00Z.
|
| Sujets: | |
| Accès en ligne: | Connect to this object online. |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
MARC
| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | doaj_cc3c23b675f54d2ba60cd0daa96f09bf | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Krishnakumar Lohidakshan |e author |
| 700 | 1 | 0 | |a Manju Rajan |e author |
| 700 | 1 | 0 | |a Andhale Ganesh |e author |
| 700 | 1 | 0 | |a Mathew Paul |e author |
| 700 | 1 | 0 | |a Jithu Jerin |e author |
| 245 | 0 | 0 | |a Pass and Swiss ADME collaborated in silico docking approach to the synthesis of certain pyrazoline spacer compounds for dihydrofolate reductase inhibition and antimalarial activity |
| 260 | |b Bangladesh Pharmacological Society, |c 2018-01-01T00:00:00Z. | ||
| 500 | |a 10.3329/bjp.v13i1.33625 | ||
| 500 | |a 1991-0088 | ||
| 520 | |a New series of pyrazoline spacer compounds were prepared by the reaction between benzimidazole chalcones and (2-methyl-5-nitro-imidazole-1-yl)-acetic acid hydrazide by the sensible use of Michael addition. The building blocks used for the synthesis of pyrazoline derivatives were opted by using virtual screening by molinspiration search engine. The hypothetically resulted pyrazoline spacer compounds from this list are checked for their reliability on other in silico drug designing online web services like PASS online bioactivity, Swiss ADME predictor. The docking study on final four pyrazoline compounds was carried out using Accelrys Discovery Studio 3.5. These synthesized compounds were, later, characterized with the help of UV, IR, mass and 1H NMR techniques. These compounds were further screened for their in vitro antimalarial effect. The PASS, Swiss ADME assisted docking approach and the use of combo heterocyclic ring with pyrazoline scaffold were found to be beneficial to derive and synthesize effective antimalarial agents in the present study. Video Clip of Methodology: 6 min 20 sec: Full Screen Alternate | ||
| 546 | |a EN | ||
| 690 | |a Antimalarial | ||
| 690 | |a Dihydrofolate reductase | ||
| 690 | |a Molecular docking | ||
| 690 | |a Pass and Swiss ADME | ||
| 690 | |a Pyrazoline | ||
| 690 | |a Therapeutics. Pharmacology | ||
| 690 | |a RM1-950 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Bangladesh Journal of Pharmacology, Vol 13, Iss 1 (2018) | |
| 787 | 0 | |n https://www.banglajol.info/index.php/BJP/article/view/33625 | |
| 787 | 0 | |n https://doaj.org/toc/1991-0088 | |
| 856 | 4 | 1 | |u https://doaj.org/article/cc3c23b675f54d2ba60cd0daa96f09bf |z Connect to this object online. |