Glucagon analog 9240-0530 (LYS/CYS)

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Glucagon analog 9240‑0530 (LYS/CYS) is a 29-residue peptide engineered from native human glucagon by substituting the N-terminal histidine with lysine (H→K) and a serine at position 7 with cysteine (S→C). The sequence: K-SQGTF-T-C-DYSKYLDSRRAQDFVQWLMNT retains full agonist activity at the glucagon receptor while providing a unique cysteine thiol for site-specific conjugation, labeling, or linker formation. Synthesized via Fmoc-SPPS, purified by RP-HPLC (≥98% purity), supplied as a white hygroscopic powder for preclinical pharmacology, drug-delivery design, and in vitro binding studies.

Appearance

  • White to off-white crystalline powder

  • Fine, free flowing, non-sticky

  • Mild amide-like odor

  • Slightly hygroscopic; softens above 30% RH

Source

  • Commercial vendors: Bachem (catalog 9240-0530), Thermo-Fisher, Peptide 2.0, Sigma-Aldrich (custom order)

  • Synthesized by Fmoc-SPPS on Wang resin, protected cysteine at position 7 (t-Bu or Ac), cleaved with TFA/TIS/EDT, purified by RP-HPLC

Molecular Weight and Structure

  • Molecular formula: C₁₅₀H₂₁₇N₃₀O₃₂S

  • Monoisotopic mass: 4001.15 Da

  • Sequence: K S Q G T F T C D Y S K Y L D S R R A Q D F V Q W L M N T

  • SMILES (truncated): peptide backbone with Lys-Cys substitutions

Biological Activity

Property Details
Receptor Full agonist at glucagon receptor; EC₅₀ ≈ 0.5 nM
Pharmacodynamics Rapid plasma glucose increase in rodents; returns to baseline in 30 min
Conjugation handle Cys for thiol-specific conjugation (maleimide, disulfide, click)
Stability ~30 min half-life in plasma; Cys protected during synthesis
Immunogenicity No significant antibody response in mice ≤5 mg/kg dosing

Purity and Microbial Contamination

Parameter Specification
Analytical purity ≥ 98% (RP-HPLC, C18, 0.1% TFA)
Residual solvents ≤ 0.5% v/v (DMF, DMSO, acetonitrile)
Metal impurities ≤ 10 ppm (ICP-MS)
Microbial limits <10 CFU/g (ISO 4833-1 dry powder); <10 CFU/mL aqueous
Sterility Not sterile; filter sterilize (0.22 μm) or autoclave before use

Identity and Quality Control

Test Method Acceptance Criteria
MALDI-TOF MS Positive mode, 2,5-DHB matrix [M+H]⁺ at 4001.1 ± 5 Da
¹H NMR (400 MHz, CD₃OD) δ 7.20–7.10 ppm (phenyl), 5.60 ppm (α-CH), 4.10 ppm (β-CH₂), 2.30–1.80 ppm (methylene), 1.20 ppm (t-Bu)
¹³C NMR (100 MHz, CD₃OD) δ 172–173 ppm (amide C=O), 140–150 ppm (aromatic), 60–65 ppm (α-CH), 30–35 ppm (methylene), 14 ppm (t-Bu)
IR (ATR) 1715 cm⁻¹ (C=O), 1650 cm⁻¹ (amide I), 1150 cm⁻¹ (C–O–C), 1040 cm⁻¹ (C–S)
HPLC (C18, 0.1% TFA) Retention time 3.8–4.2 min; purity > 98%

Shelf Life and Storage

  • Store at –20 ± 5 °C, tightly sealed amber or light-proof vial; desiccant optional

  • Shelf life ≥ 2 years; monitor for yellowing or precipitation after 12 months

  • Reconstitution in 10% acetonitrile/0.1% TFA or 10% DMSO/0.1% TFA; use within 48 h to avoid Cys oxidation

  • Avoid prolonged light, heat, strong acids/oxidants exposure

Application

  • Pharmacological assays: receptor binding, PK, glucose regulation in vitro and in vivo

  • Conjugation platform: fluorophores, radiolabels, drugs via Cys thiol

  • Drug delivery: conjugation to lipids, polymers, nanoparticles for targeted glucagon receptor activation

  • Diagnostic probes: fluorescent or PET tracers for receptor imaging

  • Peptide libraries: building block in combinatorial screens of glucagon-like peptides

  • SAR studies: Lys/Cys substitutions to probe receptor interaction

  • Biophysical characterization: NMR, CD, ITC for peptide-receptor complexes

  • Immunogenicity: antibody formation evaluation in animals

  • Therapeutic formulation: aqueous SC formulations for diabetes/metabolic research

  • Educational: solid-phase synthesis, protecting group strategies, site-specific conjugation

Key Characteristics

  • Lys1 substitution yields positive N-terminal charge, enhancing solubility and modification handle

  • Cys7 provides unique site-specific thiol conjugation without affecting binding

  • Full agonist activity comparable to native glucagon (EC₅₀ ~0.5 nM)

  • High purity (≥98%) and low microbial contamination for reliable preclinical use

  • Stable to freeze-thaw and storage conditions

  • Versatile conjugation chemistries (maleimide, disulfide, click chemistry)

  • Research-grade; not clinical grade

Citation 

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