(Q46081234)

English

Design, synthesis, and evaluation of carnosine derivatives as selective and efficient sequestering agents of cytotoxic reactive carbonyl species

scientific article published in June 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

Design, synthesis, and evaluation of carnosine derivatives as selective and efficient sequestering agents of cytotoxic reactive carbonyl species (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

0 references

1

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

4

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

object named as

Marica Orioli

2

0 references

object named as

Marina Carini

7

0 references

Giancarlo Aldini

object named as

Giancarlo Aldini

8

0 references

Alessandro Pedretti

3

object named as

Alessandro Pedretti

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

author name string

Renato Canevotti

5

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

Gianpaolo Negrisoli

6

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

publication date

1 June 2009

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

4

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

6

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

967-975

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

4-hydroxynonenal: a membrane lipid oxidation product of medicinal interest.

1 reference

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Intervention strategies to inhibit protein carbonylation by lipoxidation-derived reactive carbonyls.

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4-hydroxynonenal as a bioactive marker of pathophysiological processes

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Mechanisms for oxidative stress in diabetic cardiovascular disease

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Role of oxidative carbonylation in protein quality control and senescence

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Molecular mechanisms of the conjugated alpha,beta-unsaturated carbonyl derivatives: relevance to neurotoxicity and neurodegenerative diseases

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Lipoxidation-derived reactive carbonyl species as potential drug targets in preventing protein carbonylation and related cellular dysfunction

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Advanced lipid peroxidation end products in oxidative damage to proteins. Potential role in diseases and therapeutic prospects for the inhibitors.

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HNE Michael adducts to histidine and histidine-containing peptides as biomarkers of lipid-derived carbonyl stress in urines: LC-MS/MS profiling in Zucker obese rats.

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Homology Modeling of Human Serum Carnosinase, a Potential Medicinal Target, and MD Simulations of Its Allosteric Activation by Citrate

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Synthesis and evaluation of neuroprotective alpha,beta-unsaturated aldehyde scavenger histidyl-containing analogues of carnosine

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Ability of carnosine and other skeletal muscle components to quench unsaturated aldehydic lipid oxidation products

1 reference

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Carnosine is a quencher of 4-hydroxy-nonenal: through what mechanism of reaction?

1 reference

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Carnosine inhibits (E)-4-hydroxy-2-nonenal-induced protein cross-linking: structural characterization of carnosine-HNE adducts

1 reference

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Efficient scavenging of fatty acid oxidation products by aminoguanidine

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Molecular lipophilicity potential, a tool in 3D QSAR: method and applications.

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Transport characteristics of L-carnosine and the anticancer derivative 4-toluenesulfonylureido-carnosine in a human epithelial cell line

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Kinetics and mechanism of the reaction of aminoguanidine with the alpha-oxoaldehydes glyoxal, methylglyoxal, and 3-deoxyglucosone under physiological conditions.

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Angiotensin II receptor antagonists and angiotensin-converting enzyme inhibitors lower in vitro the formation of advanced glycation end products: biochemical mechanisms

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In vivo formation of a Schiff base of aminoguanidine with pyridoxal phosphate

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pH-metric log P. II: Refinement of partition coefficients and ionization constants of multiprotic substances

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VEGA: a versatile program to convert, handle and visualize molecular structure on Windows-based PCs.

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Scalable molecular dynamics with NAMD

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Identifiers

10.1002/CMDC.200800433

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19301317

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