2020
DOI: 10.1080/07391102.2020.1775701
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Inhibition of fibrillation of human γ d -crystallin by a flavonoid morin

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Cited by 4 publications
(3 citation statements)
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“…Several studies by others have reported the existence of small molecules that bind to γ-crystallins, including lanosterol ( 59 ), cochineal carmine ( 60 ), ortho-Vanilin ( 61 ), quercetin ( 62 ), hesperetin ( 63 ), and sodium citrate ( 64 ). Moreover, small molecules with either demonstrated potential anticataract properties involving antiaggregation activity against crystallins include rosemarinic acid ( 65 ), morin ( 66 , 67 ), 25-hydrocholesterol ( 68 ), epigallocatechin gallate ( 69 ), and myoinositol ( 70 ). Among these compounds, those that were included in the screen included epigallocatechin gallate, which improved aggregation, whereas morin, lanosterol, hesperetin, and carmine had no impact.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies by others have reported the existence of small molecules that bind to γ-crystallins, including lanosterol ( 59 ), cochineal carmine ( 60 ), ortho-Vanilin ( 61 ), quercetin ( 62 ), hesperetin ( 63 ), and sodium citrate ( 64 ). Moreover, small molecules with either demonstrated potential anticataract properties involving antiaggregation activity against crystallins include rosemarinic acid ( 65 ), morin ( 66 , 67 ), 25-hydrocholesterol ( 68 ), epigallocatechin gallate ( 69 ), and myoinositol ( 70 ). Among these compounds, those that were included in the screen included epigallocatechin gallate, which improved aggregation, whereas morin, lanosterol, hesperetin, and carmine had no impact.…”
Section: Discussionmentioning
confidence: 99%
“…18,19 Several groups previously reported that various small molecules can prevent γD-crystallin aggregation in vitro. 20,21 However, only a few have shown potential to be tried in clinical trials. In therapeutic treatment, polyphenols, which are secondary metabolites obtained from plants, have gained tremendous attention owing to their unique mode of action.…”
Section: ■ Introductionmentioning
confidence: 99%
“…The best possible option could be to have a drug molecule preventing or delaying the aggregation of the protein. It is a well-known fact that small molecules/peptides can effectively delay and/or inhibit amyloid aggregation in other amyloid diseases. , Several groups previously reported that various small molecules can prevent γD-crystallin aggregation in vitro. , However, only a few have shown potential to be tried in clinical trials. In therapeutic treatment, polyphenols, which are secondary metabolites obtained from plants, have gained tremendous attention owing to their unique mode of action .…”
Section: Introductionmentioning
confidence: 99%