ChemInform Abstract: THE SYNTHESIS AND ANTI‐INFLAMMATORY ACTIVITY OF SUBSTITUTED 2‐(4‐HYDROXYPHENYL)‐1,3‐INDANDIONES

Goot, H. Van Der; Eriks, J. Ch.; Schaar, P. J. Van Rhijn‐Van Der; Zuiderveld, Obbe P.; Nauta, W. Th.

doi:10.1002/chin.197911218

Cited by 2 publications

(3 citation statements)

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“…t-Bu 2c 3-Tert-butyl-4-hydroxy-5-methylbenzaldehyde (2c): [4] white solid, 0.80 g (83% yield), m.p. 146-148 o C (lit [4] m.p.…”

Section: Cho Ohmentioning

confidence: 99%

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Environmentally Friendly and Highly Efficient Co(OAc)₂-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Jiang

Zhang

et al. 2014

Synthetic Communications

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“…t-Bu 2c 3-Tert-butyl-4-hydroxy-5-methylbenzaldehyde (2c): [4] white solid, 0.80 g (83% yield), m.p. 146-148 o C (lit [4] m.p.…”

Section: Cho Ohmentioning

confidence: 99%

“…t-Bu 2c 3-Tert-butyl-4-hydroxy-5-methylbenzaldehyde (2c): [4] white solid, 0.80 g (83% yield), m.p. 146-148 o C (lit [4] m.p. 152-153 °C); 1 H NMR (400 MHz, CDCl 3,5-Dimethoxy-4-hydroxybenzaldehyde (2d): [1] yellow solid, 0.83 g (91%), m.p.…”

Section: Cho Ohmentioning

confidence: 99%

Environmentally Friendly and Highly Efficient Co(OAc)₂-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Jiang

Zhang

et al. 2014

Synthetic Communications

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“…2‐Substituted‐1,3‐indandiones are biologically active compounds which are used in the medicine and biology (4). Studies on their biological activity indicate the presence of anticoagulant (5), anti‐inflammatory (6), antibacterial (7), protein binding (4), antineoplastic (8,9) and neuroprotective action (10). 2‐Carbamido‐1,3‐indanedione (CAID), also known as 1,3‐dioxo‐2‐indane‐carboxamide, belongs to the group of 2‐substituted indan‐1,3‐dione.…”

Section: Introductionmentioning

confidence: 99%

Binding Expedient of 2‐carbamido‐1,3‐indandione to Nucleic Acids: Potential Fluorescent Probe

Stoyanova

Маркова

Angelov

et al. 2021

Photochem & Photobiology

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Fluorescent and computational methods were used to elucidate the binding expedient of 2‐carbamido‐1,3‐indandione (CAID) tautomers to nucleotides. The dependence of the fluorescence emission of CAID loaded nucleic acids sequences to compound concentration, temperature and time variation was investigated. It was found that the subject compound binds to nucleic acids but does not intercalate. According to our quantum‐chemical calculations on the conjugation between CAID and nucleotides, the binding in the formed complexes may be through hydrogen bonds. Two possible types of complexes were considered—CAID to the phosphate group and CAID to the nucleobase. To estimate the binding affinity, the interaction energies of the formed complexes were calculated. Tautomer 2‐carboamide‐1‐hydroxy‐3‐oxo‐indane is preferred in the formation of complexes, and the phosphate group complexes were more stable. Generally, the guanosine and deoxyguanosine monophosphate complexes were the most preferred regardless of the complex type. Because of the lack of cytotoxic effect on untransformed cell lines of mouse embryo fibroblasts Balb/c 3T3 according to our previous report (Markova et al, (2017) Bulg Chem Commun, 49D, 221–226) and the affinity to nucleic acids, we can suggest that the subject compound could be suitable to be used as a novel type of fluorescent biomarker.

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ChemInform Abstract: THE SYNTHESIS AND ANTI‐INFLAMMATORY ACTIVITY OF SUBSTITUTED 2‐(4‐HYDROXYPHENYL)‐1,3‐INDANDIONES

Abstract: Olefinierung der Hydroxybenzaldehyde (II) mit dem Wittig‐ Reagenz (I) ergibt die Hydroxybenzyliden‐phthalide (III), die beim Erhitzen mit.

Cited by 2 publications

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Environmentally Friendly and Highly Efficient Co(OAc)₂-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Environmentally Friendly and Highly Efficient Co(OAc)₂-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Binding Expedient of 2‐carbamido‐1,3‐indandione to Nucleic Acids: Potential Fluorescent Probe

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ChemInform Abstract: THE SYNTHESIS AND ANTI‐INFLAMMATORY ACTIVITY OF SUBSTITUTED 2‐(4‐HYDROXYPHENYL)‐1,3‐INDANDIONES

Abstract: Olefinierung der Hydroxybenzaldehyde (II) mit dem Wittig‐ Reagenz (I) ergibt die Hydroxybenzyliden‐phthalide (III), die beim Erhitzen mit.

Cited by 2 publications

References 0 publications

Environmentally Friendly and Highly Efficient Co(OAc)2-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Environmentally Friendly and Highly Efficient Co(OAc)2-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Binding Expedient of 2‐carbamido‐1,3‐indandione to Nucleic Acids: Potential Fluorescent Probe

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Environmentally Friendly and Highly Efficient Co(OAc)₂-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes

Environmentally Friendly and Highly Efficient Co(OAc)₂-Catalyzed Aerobic Oxidation to Access 2,6-Di-Electron-Donating Group Substituted 4-Hydroxybenzaldehydes