16691-00-2

Basic information

• Product Name: CYCLO(-GLU-GLU)
• Synonyms: CYCLO(-GLU-GLU);CYCLO(L-GLU-L-GLU);Pidotimod Impurity 9
• CAS NO: 16691-00-2
• Molecular Formula: C10H14N2O6
• Molecular Weight: 258.23
• Mol File: 16691-00-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 151 °C
• Boiling Point: 766.0±45.0 °C(Predicted)
• Appearance: /
• Density: 1.366±0.06 g/cm3(Predicted)
• Storage Temp.: -15°C
• PKA: 4.17±0.10(Predicted)
• CAS DataBase Reference: CYCLO(-GLU-GLU)(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLO(-GLU-GLU)(16691-00-2)
• EPA Substance Registry System: CYCLO(-GLU-GLU)(16691-00-2)

Safety Data

• Hazardous Substances Data: 16691-00-2(Hazardous Substances Data)

Usage

General Description

CYCLO(-GLU-GLU) is a cyclic dipeptide made up of two glutamic acid (GLU) molecules joined together through a peptide bond. Glutamic acid is an amino acid that is a building block of proteins and is also involved in various biological functions in the body. CYCLO(-GLU-GLU) is a small, stable molecule with a cyclic structure, which may make it advantageous for use in various applications, such as drug development or as a research tool in biochemistry. Its unique structure and properties may also make it a valuable molecule for studying the behavior and interactions of cyclic peptides in biological systems. Overall, CYCLO(-GLU-GLU) is a promising compound with potential applications in the pharmaceutical and research fields.

Upstream product

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Relevant articles and documents

Rapidly Recoverable Thixotropic Hydrogels from the Racemate of Chiral OFm Monosubstituted Cyclo(Glu-Glu) Derivatives

Both chiral OFm monosubstituted cyclo(l-Glu-l-Glu) and cyclo(d-Glu-d-Glu) display a robust gelation ability in a variety of organic solvents and water. In contrast to an individual enantiomer, their racemate can form rapidly recoverable thixotropic hydrogels with a remarkably shorter thixotropic recovery time. This unexpected thixotropic behavior is induced by the random arrangement of d- and l-enantiomers in the cell units, leading to the formation of pseudoracemate , noncrystalline self-assemblies in the resulting 3D fibrous network.

Bio-based epoxy resin precursor containing cyclic amide structure, and preparation method and application thereof

The invention discloses a bio-based epoxy resin precursor containing a cyclic amide structure, and also discloses a preparation method and application of the bio-based epoxy resin precursor containingthe cyclic amide structure. The preparation method comp

Macromolecular self-assembly of diketopiperazine tetrapeptides

Basic solutions of tetrapeptides derived from L-aspartic acid diketopiperazines are shown to form microcapsules when acidified to pH 2.4. An initial structure-activity study clearly demonstrates that a very delicate balance exists between the tetrapeptide