BVD 10

Highly selective NPY Y1 receptor antagonist.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: R0910

CAS No:262418-00-8

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
C58H92N16O13
M.W/Mr.
1221.46
Sequence
INPIYRLRY(Modifications: Tyr-9 = Tyr-OMe)
Labeling Target
NPY Y1 receptor
Appearance
White lyophilised solid
Purity
>98%
Activity
Antagonist

BVD 10 is a synthetic peptide compound recognized for its distinctive sequence and functional properties within the realm of peptide-based research. As a member of the peptide class, it is composed of a specific arrangement of amino acids designed to mimic or modulate biological interactions in vitro. The compound's structure allows it to participate in a variety of biochemical assays, making it a valuable asset for researchers investigating peptide signaling, protein-protein interactions, or the development of peptide-based analytical tools. Its chemical stability and defined sequence facilitate precise experimental design, supporting advancements in molecular biology, biochemistry, and related disciplines.

Peptide-protein interaction studies: BVD 10 is frequently employed in investigations focused on elucidating the molecular mechanisms underlying peptide-protein interactions. By serving as a model ligand or probe, it enables researchers to map binding sites, characterize affinity parameters, and dissect the specificity of protein recognition events. Such studies are fundamental for understanding cellular signaling pathways, regulatory networks, and the molecular basis of disease-related processes, providing a foundation for the identification of novel modulatory strategies.

Receptor binding assays: The compound's well-defined sequence makes it a suitable candidate for in vitro receptor binding experiments. Utilizing BVD 10 in these assays allows for the quantitative assessment of ligand-receptor interactions, including the determination of binding kinetics, receptor specificity, and competitive inhibition profiles. Insights gained from these experiments are instrumental in the early stages of drug discovery and in the development of novel diagnostic reagents targeting peptide-responsive receptors.

Peptide synthesis validation: Researchers often use BVD 10 as a reference standard or positive control in synthetic peptide production workflows. Its established sequence and predictable physicochemical properties make it ideal for benchmarking synthesis protocols, optimizing purification strategies, and validating analytical methods such as mass spectrometry or high-performance liquid chromatography. This application is particularly valuable for laboratories striving to ensure the reliability and reproducibility of custom peptide synthesis.

Structural and conformational analysis: The compound is utilized in studies aimed at elucidating peptide secondary structure and conformational dynamics. Techniques such as circular dichroism spectroscopy, nuclear magnetic resonance, or X-ray crystallography benefit from the use of well-characterized peptides like BVD 10, as they enable the systematic investigation of sequence-structure relationships. These analyses contribute to a deeper understanding of peptide folding, stability, and interaction potential, informing the rational design of bioactive peptides.

Functional screening and assay development: BVD 10 plays a role in the development and optimization of functional assays for peptide activity screening. Its defined biological properties make it a useful tool for calibrating assay sensitivity, establishing dynamic ranges, and validating assay reproducibility. This function is essential for laboratories engaged in high-throughput screening, peptide library evaluation, or the assessment of novel peptide analogues, supporting robust and reliable experimental outcomes across a range of research applications.

Long-term Storage Conditions
Soluble in DMSO
Solubility
-20 °C
InChI
InChI=1S/C58H92N16O13/c1-8-32(5)46(60)53(83)71-42(30-45(59)77)55(85)74-26-12-15-44(74)52(82)73-47(33(6)9-2)54(84)70-41(28-34-16-20-36(75)21-17-34)51(81)68-38(13-10-24-65-57(61)62)48(78)69-40(27-31(3)4)50(80)67-39(14-11-25-66-58(63)64)49(79)72-43(56(86)87-7)29-35-18-22-37(76)23-19-35/h16-23,31-33,38-44,46-47,75-76H,8-15,24-30,60H2,1-7H3,(H2,59,77)(H,67,80)(H,68,81)(H,69,78)(H,70,84)(H,71,83)(H,72,79)(H,73,82)(H4,61,62,65)(H4,63,64,66)/t32-,33-,38-,39-,40-,41-,42-,43-,44-,46-,47-/m0/s1
InChI Key
JLQHEFJKMUJISI-QUCBMPEKSA-N
Isomeric SMILES
CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC3=CC=C(C=C3)O)C(=O)OC)N
BoilingPoint
N/A
Melting Point
N/A

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