Matches in SemOpenAlex for { <https://semopenalex.org/work/W4288035423> ?p ?o ?g. }
- W4288035423 endingPage "17" @default.
- W4288035423 startingPage "1" @default.
- W4288035423 abstract "Serotonin (5-HT) antagonists and reuptake inhibitors (SARIs) are atypical antidepressants for managing major depressive disorder. They are oftentimes applied as adjuvants for ameliorating aftereffects of SSRI antidepressants including insomnia and sexual dysfunction. The few available candidates of this class including lorpiprazole and trazodone also display some daunting side effects, making a continuous search for improved alternatives essential. Natural β-carboline alkaloids (NβCs) are interestingly renowned with broad pharmacological spectrum against several neuropsychiatric disorders including depression. However, their potentials as SARIs remain underexplored. In this study, 982 NβCs retrieved from the Ambinter-Greenpharma (Amb) database were virtually screened for potent SARI alternatives using computational and biocheminformatics approaches: homology modelling of 5-HT1A receptor, Glide HTVS, SP and XP molecular docking, molecular dynamics (MD) simulation, ADMET and mutagenicity predictions. The homology receptor was validated as a good representative of human 5HT1A receptor using the RCSB structure validation and quality protocols. From the virtual screening against the 5-HT1A receptor, Amb ligands, Amb18709727 and Amb37857532 showed higher binding affinities by XP scores of −8.725 and −7.976 kcal/mol, and MMGBSA of −87.972 and −107.585 kcal/mol respectively compared to lorpiprazole, a reference SARI with XP score and MMGBSA of −6.512 and −62.788 kcal/mol respectively. They maintained ideal contacts with pharmacologically essential amino acid residues implicated in SARI mechanisms and expressed higher stability and compactness than lorpiprazole throughout the trajectories of 100 ns MD simulation. They also displayed interesting ADME, druggability, low toxicity and mutagenicity profiles, ideal for CNS drug prospects, thus, recommended as putative SARI candidates for further study." @default.
- W4288035423 created "2022-07-27" @default.
- W4288035423 creator A5029535736 @default.
- W4288035423 creator A5040275034 @default.
- W4288035423 creator A5059076850 @default.
- W4288035423 creator A5064634732 @default.
- W4288035423 creator A5083110337 @default.
- W4288035423 date "2022-07-26" @default.
- W4288035423 modified "2023-09-24" @default.
- W4288035423 title "Structural modelling and <i>in silico</i> pharmacology of β-carboline alkaloids as potent 5-HT1A receptor antagonists and reuptake inhibitors" @default.
- W4288035423 cites W1574692482 @default.
- W4288035423 cites W1967119647 @default.
- W4288035423 cites W1971513938 @default.
- W4288035423 cites W1981737096 @default.
- W4288035423 cites W1992192767 @default.
- W4288035423 cites W2009423060 @default.
- W4288035423 cites W2017196167 @default.
- W4288035423 cites W2031168104 @default.
- W4288035423 cites W2051381895 @default.
- W4288035423 cites W2071486470 @default.
- W4288035423 cites W2075659901 @default.
- W4288035423 cites W2079953901 @default.
- W4288035423 cites W2088933990 @default.
- W4288035423 cites W2095719702 @default.
- W4288035423 cites W2102993309 @default.
- W4288035423 cites W2113623846 @default.
- W4288035423 cites W2122144012 @default.
- W4288035423 cites W2132534801 @default.
- W4288035423 cites W2148494031 @default.
- W4288035423 cites W2222589778 @default.
- W4288035423 cites W2379628571 @default.
- W4288035423 cites W2426561352 @default.
- W4288035423 cites W2516880361 @default.
- W4288035423 cites W2571978672 @default.
- W4288035423 cites W2593436234 @default.
- W4288035423 cites W2612308018 @default.
- W4288035423 cites W2695471189 @default.
- W4288035423 cites W2731817207 @default.
- W4288035423 cites W2735127571 @default.
- W4288035423 cites W2765322245 @default.
- W4288035423 cites W2773115966 @default.
- W4288035423 cites W2800892557 @default.
- W4288035423 cites W2803029512 @default.
- W4288035423 cites W2803589537 @default.
- W4288035423 cites W2804822363 @default.
- W4288035423 cites W2808053923 @default.
- W4288035423 cites W2884406458 @default.
- W4288035423 cites W2886532357 @default.
- W4288035423 cites W2908029837 @default.
- W4288035423 cites W2936757670 @default.
- W4288035423 cites W2944504593 @default.
- W4288035423 cites W2949864276 @default.
- W4288035423 cites W2971267227 @default.
- W4288035423 cites W2983552824 @default.
- W4288035423 cites W2984278087 @default.
- W4288035423 cites W3013619085 @default.
- W4288035423 cites W3015943244 @default.
- W4288035423 cites W3037526368 @default.
- W4288035423 cites W3092920235 @default.
- W4288035423 cites W3115564139 @default.
- W4288035423 cites W3123276428 @default.
- W4288035423 cites W3137816310 @default.
- W4288035423 cites W3156497785 @default.
- W4288035423 cites W3156706849 @default.
- W4288035423 cites W3197730160 @default.
- W4288035423 cites W3203812274 @default.
- W4288035423 cites W3211795435 @default.
- W4288035423 cites W4206424542 @default.
- W4288035423 cites W4230478154 @default.
- W4288035423 cites W4281482112 @default.
- W4288035423 doi "https://doi.org/10.1080/07391102.2022.2104376" @default.
- W4288035423 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35881145" @default.
- W4288035423 hasPublicationYear "2022" @default.
- W4288035423 type Work @default.
- W4288035423 citedByCount "5" @default.
- W4288035423 countsByYear W42880354232022 @default.
- W4288035423 countsByYear W42880354232023 @default.
- W4288035423 crossrefType "journal-article" @default.
- W4288035423 hasAuthorship W4288035423A5029535736 @default.
- W4288035423 hasAuthorship W4288035423A5040275034 @default.
- W4288035423 hasAuthorship W4288035423A5059076850 @default.
- W4288035423 hasAuthorship W4288035423A5064634732 @default.
- W4288035423 hasAuthorship W4288035423A5083110337 @default.
- W4288035423 hasConcept C104317684 @default.
- W4288035423 hasConcept C10679952 @default.
- W4288035423 hasConcept C159110408 @default.
- W4288035423 hasConcept C169627665 @default.
- W4288035423 hasConcept C181199279 @default.
- W4288035423 hasConcept C185592680 @default.
- W4288035423 hasConcept C2775905019 @default.
- W4288035423 hasConcept C2780035454 @default.
- W4288035423 hasConcept C2780152424 @default.
- W4288035423 hasConcept C41685203 @default.
- W4288035423 hasConcept C55493867 @default.
- W4288035423 hasConcept C69366308 @default.
- W4288035423 hasConcept C71240020 @default.
- W4288035423 hasConcept C71924100 @default.
- W4288035423 hasConcept C98274493 @default.