Hubungan Kuantitaf Struktur Aktivitas Dan Penambatan Molekul Senyawa Analog O-Metil Kuersetin Sebagai Inhibitor Epidermal Growth Factor Receptor-Tyrosine Kinase (EGFR-TK)

Aulia, Syafana Zahra and Lohita Sari, Bina and Agus Setiani, Lusi (2023) Hubungan Kuantitaf Struktur Aktivitas Dan Penambatan Molekul Senyawa Analog O-Metil Kuersetin Sebagai Inhibitor Epidermal Growth Factor Receptor-Tyrosine Kinase (EGFR-TK). Skripsi thesis, Universitas Pakuan.

[img] Text
SKRIPSI_Shafana Zahra Aulia_066118270.pdf

Download (4MB)

Abstract

Quantitative Structure-Activity Relationship and Molecular Docking of O�methyl Quercetin Analogues Compounds as EGFR-TK Inhibitor Bina Lohita Sari*, Lusi Agus Setiani, and Shafana Zahra Aulia Department of Pharmacy, Faculty of Mathematics and Natural Sciences, Universitas Pakuan, Bogor, West Java, Indonesia. Abstract: Epidermal Growth Factor Receptor-Tyrosine Kinase (EGFR-TK) is a growth factor regulating cell proliferation. Cancer arises from the uncontrolled proliferation of cells. Lung cancer stands as one example among the diverse array of cancer types. O-methyl quercetin analogs can be potential drug candidate for treating lung cancer. The activity of new compounds can be predicted using a Quantitative Structure-Activity Relationship (QSAR) model. The structures were optimized using the parameterized method 3 (PM3) and analyzed through multiple linear regression (MLR). Structures of new compounds were modified with O-alkylamino and then docked to the EGFR-TK receptor using molecular docking. The best QSAR model is expressed as LogIC50 = 23.059 + (7.397 × log P) + (0.273 × dipole moment) – (0.005 × heat of formation) – (0.733 × ELUMO) – (0.501 × EHOMO) with statistical parameters: R = 0.966; R2 = 0.933; Fcount/Ftable = 3.830; and Q2 = 0.752. The molecular docking results, in the form of grid scores for the new compounds (QC6_7 and QC6_8), were superior to quercetin base don the validated QSAR model, specifically -77.699 kcal/mol and -79.458 kcal/mol, respectively. Both compounds interact with a key residue of the EGFR-TK receptor, Met769, suggesting their potential as drugs for lung cancer. A R T I C L E H I S T O R Y Received: Revised: Accepted: DOI: Keywords: QSAR, Quercetin Analogs, Molecular Docking, EGFR-TK, Lung Cancer

Item Type: Thesis (Skripsi)
Subjects: Fakultas Ilmu Pengetahuan Alam dan Matematika > Farmasi
Divisions: Fakultas Matematika dan Ilmu Pengetahuan Alam > Farmasi
Depositing User: PERPUSTAKAAN FAKULTAS MATEMATIKA DAN ILMU PENGETAHUAN ALAM UNPAK
Date Deposited: 03 Jul 2024 06:20
Last Modified: 03 Jul 2024 06:20
URI: http://eprints.unpak.ac.id/id/eprint/7880

Actions (login required)

View Item View Item