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Gly-Gly-Gly-Gly-OH

  CAS No.: 637-84-3   Cat No.: BADC-01587   Purity: ≥ 99% (TLC) 4.5  

Gly-Gly-Gly-Gly-OH is a very versatile peptide mimetic compound. This cleavable linker stands out through its careful design in complex drug delivery systems, promising profound implications in the fight against a variety of diseases including cancer, neurodegenerative diseases, and cardiovascular diseases.

Gly-Gly-Gly-Gly-OH

Structure of 637-84-3

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ADC Linker
Molecular Formula
C8H14N4O5
Molecular Weight
246.22
Shipping
Store at 2-8 °C

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
Tetraglycine; Triglycyl-glycine; Glycyl-glycyl-glycyl-glycine
IUPAC Name
2-[[2-[[2-[(2-aminoacetyl)amino]acetyl]amino]acetyl]amino]acetic acid
Canonical SMILES
C(C(=O)NCC(=O)NCC(=O)NCC(=O)O)N
InChI
InChI=1S/C8H14N4O5/c9-1-5(13)10-2-6(14)11-3-7(15)12-4-8(16)17/h1-4,9H2,(H,10,13)(H,11,14)(H,12,15)(H,16,17)
InChIKey
QMOQBVOBWVNSNO-UHFFFAOYSA-N
Density
1.3853 g/cm3(rough estimate)
Melting Point
300 °C
Appearance
White powder
Storage
Store at 2-8 °C
Boiling Point
389.22°C (rough estimate)

Gly-Gly-Gly-Gly-OH is a tetrapeptide composed of four glycine units and serves as an important building block in peptide synthesis and molecular design. Its small size and simple structure make it a versatile compound in drug development, particularly in the creation of peptide-based therapeutics. This tetrapeptide can be used to explore structure-activity relationships and optimize the stability and bioavailability of larger peptides. Additionally, Gly-Gly-Gly-Gly-OH is often employed as a spacer or linker in drug conjugates, where it can help in improving the pharmacokinetic properties of the conjugated drugs, ensuring that the therapeutic agents are delivered efficiently to target tissues.

Another key application of Gly-Gly-Gly-Gly-OH lies in the field of peptide-drug conjugates (PDCs). As a simple, non-toxic sequence, it is used to connect active pharmaceutical compounds to target-specific peptides or antibodies. This allows for the selective delivery of drugs to particular tissues, enhancing the therapeutic effect while minimizing systemic side effects. The tetrapeptide's ability to link payloads with high stability yet cleave in response to specific biological conditions, such as enzyme activity, makes it an ideal candidate for the controlled release of cytotoxic agents or other therapeutic molecules within targeted cells. This approach is particularly valuable in cancer therapy, where precise drug delivery is essential.

Additionally, Gly-Gly-Gly-Gly-OH plays a role in research related to protein folding and molecular recognition. Its repetitive glycine structure is useful for studying the behavior of peptides in different environments and their interactions with other molecules. By varying the number of glycine residues or incorporating different amino acids, researchers can investigate how peptide sequences affect protein conformation and binding affinity. This has applications in drug design, biomaterials, and the development of biosensors, where precise molecular interactions are crucial for performance. In this regard, Gly-Gly-Gly-Gly-OH serves as a foundational tool in advancing both basic and applied biochemistry.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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