scholarly journals Bone Sialoprotein Binding to Matrix Metalloproteinase-2 Alters Enzyme Inhibition Kinetics†

Biochemistry ◽  
2008 ◽  
Vol 47 (22) ◽  
pp. 5986-5995 ◽  
Author(s):  
Alka Jain ◽  
Larry W. Fisher ◽  
Neal S. Fedarko
Keyword(s):  
Matrix Metalloproteinase ◽  
Enzyme Inhibition ◽  
Bone Sialoprotein ◽  
Matrix Metalloproteinase 2 ◽  
Inhibition Kinetics ◽  
Enzyme Inhibition Kinetics

Longan seed polyphenols inhibit α-amylase activity and reduce postprandial glycemic response in mice

2021 ◽  
Author(s):  
Ting He ◽  
lei zhao ◽  
Yan Chen ◽  
Xin Zhang ◽  
Zhuoyan Hu ◽  
...  
Keyword(s):  
Enzyme Inhibition ◽  
Amylase Activity ◽  
Glycemic Response ◽  
Inhibition Assay ◽  
Inhibition Kinetics ◽  
Enzyme Inhibition Kinetics ◽  
Longan Seed ◽  
Kinetics Of

The effects of longan seed polyphenols (LSPs) on postprandial glycemic response in mice were investigated, enzyme inhibition kinetics of LSPs against α-amylase were studied using an inhibition assay in vitro,...

scholarly journals Increased Matrix Metalloproteinase-2 and Bone Sialoprotein Response to Human Coronal Caries

2011 ◽  
Vol 45 (5) ◽  
pp. 453-459 ◽  
Author(s):  
L.W. Boushell ◽  
H. Nagaoka ◽  
H. Nagaoka ◽  
M. Yamauchi
Keyword(s):  
Matrix Metalloproteinase ◽  
Bone Sialoprotein ◽  
Matrix Metalloproteinase 2

scholarly journals Selective Interactions of O-Methylated Flavonoid Natural Products with Human Monoamine Oxidase-A and -B

Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5358
Author(s):  
Narayan D. Chaurasiya ◽  
Jacob Midiwo ◽  
Pankaj Pandey ◽  
Regina N. Bwire ◽  
Robert J. Doerksen ◽  
...  
Keyword(s):  
Natural Products ◽  
Enzyme Inhibition ◽  
Selective Inhibition ◽  
Monoamine Oxidase A ◽  
Inhibition Kinetics ◽  
Free Energies ◽  
Mao B ◽  
Mao A ◽  
Enzyme Inhibition Kinetics ◽  
Binding Free Energies

A set of structurally related O-methylated flavonoid natural products isolated from Senecio roseiflorus (1), Polygonum senegalense (2 and 3), Bhaphia macrocalyx (4), Gardenia ternifolia (5), and Psiadia punctulata (6) plant species were characterized for their interaction with human monoamine oxidases (MAO-A and -B) in vitro. Compounds 1, 2, and 5 showed selective inhibition of MAO-A, while 4 and 6 showed selective inhibition of MAO-B. Compound 3 showed ~2-fold selectivity towards inhibition of MAO-A. Binding of compounds 1–3 and 5 with MAO-A, and compounds 3 and 6 with MAO-B was reversible and not time-independent. The analysis of enzyme-inhibition kinetics suggested a reversible-competitive mechanism for inhibition of MAO-A by 1 and 3, while a partially-reversible mixed-type inhibition by 5. Similarly, enzyme inhibition-kinetics analysis with compounds 3, 4, and 6, suggested a competitive reversible inhibition of MAO-B. The molecular docking study suggested that 1 selectively interacts with the active-site of human MAO-A near N5 of FAD. The calculated binding free energies of the O-methylated flavonoids (1 and 4–6) and chalcones (2 and 3) to MAO-A matched closely with the trend in the experimental IC50′s. Analysis of the binding free-energies suggested better interaction of 4 and 6 with MAO-B than with MAO-A. The natural O-methylated flavonoid (1) with highly potent inhibition (IC50 33 nM; Ki 37.9 nM) and >292 fold selectivity against human MAO-A (vs. MAO-B) provides a new drug lead for the treatment of neurological disorders.

Understanding the bioaccessibility, α-amylase and α-glucosidase enzyme inhibition kinetics of Allmania nodiflora (L.) R.Br. ex Wight polyphenols during in vitro simulated digestion

2022 ◽  
Vol 372 ◽  
pp. 131294
Author(s):  
Gayathri Jagadeesan ◽  
Kasipandi Muniyandi ◽  
Ashwini Lydia Manoharan ◽  
Gayathri Nataraj ◽  
Parimelazhagan Thangaraj
Keyword(s):  
Enzyme Inhibition ◽  
Inhibition Kinetics ◽  
Simulated Digestion ◽  
Enzyme Inhibition Kinetics ◽  
Kinetics Of

Evaluation of enzyme inhibition kinetics in drug–drug interactions

2014 ◽  
Vol 222 ◽  
pp. 133-134 ◽  
Author(s):  
Ang Chen ◽  
Xuan Qin ◽  
Yu Tang ◽  
Mingyao Liu ◽  
Xin Wang
Keyword(s):  
Drug Interactions ◽  
Enzyme Inhibition ◽  
Inhibition Kinetics ◽  
Enzyme Inhibition Kinetics

A study of ad-proline peptidomimetic inhibitor of melanoma and endothelial cell invasion through activity towards MMP-2 and MMP-9

MedChemComm ◽  
2015 ◽  
Vol 6 (2) ◽  
pp. 277-282 ◽  
Author(s):  
Francesca Bianchini ◽  
Chiara Calugi ◽  
Jessica Ruzzolini ◽  
Gloria Menchi ◽  
Lido Calorini ◽  
...  
Keyword(s):  
Endothelial Cell ◽  
Enzyme Inhibition ◽  
Cell Invasion ◽  
Network Formation ◽  
Capillary Network ◽  
Inhibition Kinetics ◽  
Enzyme Inhibition Kinetics

Ad-proline peptidomimetic targeting MMP-2 and MMP-9 was identified from a pool of compounds following enzyme inhibition kinetics and Matrigel sponge assays, showing the capacity of blocking capillary network formationin vivo.

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