"Succinimides" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A subclass of IMIDES with the general structure of pyrrolidinedione. They are prepared by the distillation of ammonium succinate. They are sweet-tasting compounds that are used as chemical intermediates and plant growth stimulants.
Descriptor ID |
D013388
|
MeSH Number(s) |
D02.478.770 D03.383.773.812.852
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Succinimides".
Below are MeSH descriptors whose meaning is more specific than "Succinimides".
This graph shows the total number of publications written about "Succinimides" by people in this website by year, and whether "Succinimides" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
1999 | 0 | 1 | 1 |
2002 | 1 | 0 | 1 |
2003 | 0 | 1 | 1 |
2009 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Succinimides" by people in Profiles.
-
M?ndez J, Morales Cruz M, Delgado Y, Figueroa CM, Orellano EA, Morales M, Monteagudo A, Griebenow K. Delivery of chemically glycosylated cytochrome c immobilized in mesoporous silica nanoparticles induces apoptosis in HeLa cancer cells. Mol Pharm. 2014 Jan 06; 11(1):102-11.
-
Carson MJ, Wilson EH. Visualizing chemokine-dependent T cell activation and migration in response to central nervous system infection. Methods Mol Biol. 2013; 1013:171-83.
-
Phillips JA, Morgan EL, Dong Y, Cole GT, McMahan C, Hung CY, Sanderson SD. Single-step conjugation of bioactive peptides to proteins via a self-contained succinimidyl bis-arylhydrazone. Bioconjug Chem. 2009 Oct 21; 20(10):1950-7.
-
Xie H, Tkachenko AG, Glomm WR, Ryan JA, Brennaman MK, Papanikolas JM, Franzen S, Feldheim DL. Critical flocculation concentrations, binding isotherms, and ligand exchange properties of peptide-modified gold nanoparticles studied by UV-visible, fluorescence, and time-correlated single photon counting spectroscopies. Anal Chem. 2003 Nov 01; 75(21):5797-805.
-
Chockalingam PS, Gadgil H, Jarrett HW. DNA-support coupling for transcription factor purification. Comparison of aldehyde, cyanogen bromide and N-hydroxysuccinimide chemistries. J Chromatogr A. 2002 Jan 04; 942(1-2):167-75.
-
Chen X, Eswaran D, Smith MA, Perry G, Anderson VE. Universal isolation of cross-linked peptides: application to neurofibrillary tangles. Bioconjug Chem. 1999 Jan-Feb; 10(1):112-8.
-
Faust FM, Slisz M, Jarrett HW. Calmodulin is labeled at lysine 148 by a chemically reactive phenothiazine. J Biol Chem. 1987 Feb 15; 262(5):1938-41.
-
Jarrett HW. Response of three enzymes to oleic acid, trypsin, and calmodulin chemically modified with a reactive phenothiazine. J Biol Chem. 1986 Apr 15; 261(11):4967-72.
-
Ward WS, Schmidt WN, Schmidt CA, Hnilica LS. Cross-linking of Novikoff ascites hepatoma cytokeratin filaments. Biochemistry. 1985 Jul 30; 24(16):4429-34.
-
Jarrett HW. The synthesis and reaction of a specific affinity label for the hydrophobic drug-binding domains of calmodulin. J Biol Chem. 1984 Aug 25; 259(16):10136-44.