Abstract
Hypercholesterolemia has posed a serious threat of heart diseases and stroke worldwide. Xanthine oxidase (XO), the rate-limiting enzyme in uric acid biosynthesis, is regarded as the root of reactive oxygen species (ROS) that generates atherosclerosis and cholesterol crystals. β-Hydroxy β-methylglutaryl-coenzyme A reductase (HMGR) is a rate-limiting enzyme in cholesterol biosynthesis. Although some commercially available enzyme inhibiting drugs have effectively reduced the cholesterol level, most of them have failed to meet the requirements of being apt drug candidates. Here, we have carried out an in-silico analysis of secondary metabolites that have already shown good inhibitory activity against XO and HMGR. Out of 118 secondary metabolites reviewed, sixteen molecules inhibiting XO and HMGR were taken based on IC50 values reported in vitro assays. Further, receptor-based virtual screening was carried out against secondary metabolites using GOLD Protein-Ligand Docking Software, combined with subsequent post-docking, to study the binding affinities of ligands to the enzymes. In-Silico ADMET analysis was carried out to study their pharmacokinetic properties, followed by toxicity prediction through ProTox-II. The molecular docking of amentoflavone (1) (GOLD score 70.54), and ganomycin I (9) (GOLD score 59.61) evinced that the drug has effectively bind at the competitive site of XO and HMGR, respectively. Besides, 6-paradol (3) and selgin (4) could be potential drug candidates to inhibit XO. Likewise, n-octadecanyl-O-α-D-glucopyranosyl(6’→1”)-O-α-D-glucopyranoside (10) could be potential drug candidates to maintain serum cholesterol. In-silico ADMET analysis showed that the sixteen metabolites were optimal within the categorical range in comparison to commercially available XO and HMGR inhibitors, respectively. Toxicity analysis through Protox-II revealed that 6-gingerol (2), ganoleucoin K (11), and ganoleucoin Z (12) are toxic for human use. This computational analysis supports earlier experimental evidence towards the inhibition of XO and HMGR by natural products. Further study is necessary to explore the clinical efficacy of these secondary molecules, which might be alternatives for the treatment of hypercholesterolemia.
Competing Interest Statement
The authors have declared no competing interest.
List of abbreviations
- ACAT-2
- Acyl-CoA cholesterol acyltransferase 2
- AI
- Artificial intelligence
- ANGPTL3
- Angiopoietin-like protein 3
- ATP
- Adenosine triphosphate
- BBB
- Blood-brain barrier
- CVDs
- Cardiovascular diseases
- CYP
- Cytochrome P450
- DGAT-2
- Diglyceride acyltransferase 2
- ER
- Endoplasmic reticulum
- GOLD
- Genetic optimization for ligand docking
- HDL
- High-density lipoproteins
- HMG-CoA
- β-Hydroxy β-methylglutaryl-coenzyme A
- HMGR
- HMG-CoA reductase
- IHD
- Ischemic heart disease
- kDa
- Kilodalton
- LDL
- Low-density lipoprotein
- MACE
- Major adverse cardiovascular events
- MOE
- Molecular Operating Environment
- NOS
- Nitric oxide synthase
- PCSK9
- Proprotein convertase subtilisin kexin type 9
- ROS
- Reactive oxygen species
- SREBPs
- Sterol regulatory element-binding proteins
- TC
- Total cholesterol
- TG
- Triglyceride
- TPSA
- Total polar surface area
- VLDL
- Very low-density lipoprotein
- WHO
- World Health Organization
- XO
- Xanthine oxidase