Betiatide

Betiatide is a short regulatory peptide containing charged and hydrophobic residues that create a balanced conformational profile. The sequence supports exploration of reversible structural transitions, hydrogen bonding, and intermolecular interactions. Researchers use it in mapping ligand-recognition motifs and dynamic folding landscapes. Its compact design aids detailed structural analysis.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Betiatide(CAS 103725-47-9)

CAT No: R2273

CAS No:103725-47-9

Synonyms/Alias:Betiatide;103725-47-9;UNII-9NV2SR34P8;MP-600;S-benzoyl-MAG3;9NV2SR34P8;S-Benzoylmercaptoacetyltriglycine;DTXSID3048788;MP 600;DTXCID3028714;Betiatide (USAN);Glycine, N-(N-(N-((benzoylthio)acetyl)glycyl)glycyl);Glycine, N-(N-(N-((benzoylthio)acetyl)glycyl)glycyl)-;NCGC00182993-01;BETIATIDE [USAN];Thiobenzoic acid, S-ester with N-(N-(N-(mercaptoacetyl)glycyl)glycyl)glycine;N-(N-(N-(Mercaptoacetyl)glycyl)glycyl)glycine benzoate (ester);1,4,7,10-tetraoxo-1-phenyl-2-thia-5,8,11-triazatridecan-13-oic acid;betiatidum;Betiatida;Betiatide [USAN:INN:BAN];N-[N-[N-(Mercaptoacetyl)glycyl]glycyl]glycine benzoate (ester);2-[[2-[[2-[(2-benzoylsulfanylacetyl)amino]acetyl]amino]acetyl]amino]acetic acid;benzoylmercaptoacetylglycylglycylglycine;BETIATIDE [INN];BETIATIDE [WHO-DD];Technescan Tc 99m Mertiatide;SCHEMBL1055212;CHEMBL3183117;CHEBI:136015;VDPYMEBVIDZKMD-UHFFFAOYSA-N;Tox21_113265;HY-P10369;MFCD00868930;AKOS016340732;DB14082;SS-4620;CAS-103725-47-9;CS-1051684;N-[(benzoylthio)-acetyl]glycylglycyl-glycine;NS00070179;D03105;EN300-18567860;Q27272797;Kit for the Preparation of Technetium Tc99m Mertiatide;2-(2-{2-[2-(benzoylsulfanyl)acetamido]acetamido}acetamido)acetic acid;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C15H17N3O6S
M.W/Mr.
367.4
Sequence
One Letter Code:GGG

Betiatide is a synthetic peptide compound recognized for its unique sequence and bioactive properties, making it a valuable tool in biochemical and molecular research. As a member of the peptide family, it is characterized by its defined amino acid arrangement, which enables specific interactions with biological targets. Researchers are increasingly interested in its functional roles and mechanisms, particularly in the context of cellular signaling and protein-protein interactions. Its stability and synthetic accessibility further enhance its utility across a range of experimental protocols, positioning it as a versatile resource for peptide-focused investigations.

Peptide signaling studies: Betiatide is frequently employed in studies aimed at elucidating the mechanisms of peptide-mediated signaling pathways. Due to its defined structure, it serves as a model substrate or ligand for probing interactions with receptors or enzymes involved in cellular communication. By incorporating it into in vitro assays, researchers can dissect the specificity and affinity of peptide-receptor binding, contributing to a deeper understanding of signal transduction processes and the modulation of downstream biological responses.

Structure-activity relationship (SAR) analysis: The compound is often utilized in SAR studies to investigate how modifications to peptide sequences influence biological activity. By systematically altering residues within Betiatide or comparing its activity to related analogs, scientists can map critical determinants of function. This approach is instrumental in identifying key motifs responsible for binding, activation, or inhibition of target proteins, thereby guiding the rational design of novel peptides with enhanced or tailored properties.

Protease substrate profiling: Owing to its peptide backbone, Betiatide is a suitable substrate for evaluating the activity and specificity of proteolytic enzymes. Researchers incorporate it into enzymatic assays to monitor cleavage patterns, assess protease kinetics, and distinguish between different classes of proteolytic activity. Such studies are essential for characterizing enzyme-substrate interactions, validating protease inhibitors, and advancing knowledge of protein turnover and regulation in biological systems.

Peptide synthesis optimization: The compound is also valued as a reference or test peptide in the development and optimization of solid-phase peptide synthesis protocols. Its sequence complexity and physicochemical properties provide a practical benchmark for assessing coupling efficiency, resin compatibility, and purification strategies. By monitoring yield and purity outcomes with Betiatide, peptide chemists can refine synthetic workflows, troubleshoot challenges, and establish robust methodologies for producing more complex or sensitive sequences.

Analytical method development: Analytical laboratories leverage Betiatide as a standard or calibration peptide in the validation of chromatographic and mass spectrometric techniques. Its well-characterized nature makes it ideal for testing system performance, optimizing separation conditions, and verifying detection sensitivity. Use of such reference peptides ensures reproducibility and accuracy in peptide quantification, identification, and quality control applications, supporting the reliability of analytical data in both research and industrial settings.

InChI
InChI=1S/C15H17N3O6S/c19-11(16-6-12(20)18-8-14(22)23)7-17-13(21)9-25-15(24)10-4-2-1-3-5-10/h1-5H,6-9H2,(H,16,19)(H,17,21)(H,18,20)(H,22,23)
InChI Key
VDPYMEBVIDZKMD-UHFFFAOYSA-N

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