SLU-PP-322 Research Peptide

🔬 RESEARCH USE ONLY — This product is strictly for laboratory research and educational purposes. Not for human or veterinary use.

SLU-PP-322 Research Compound (10–40 mg, ≥98% purity, Patent WO2020257421A1) — Non-peptidic triple GLP-1/GIP/GCGR agonist for metabolic & CNS studies. RUO, CoA-backed, UK supply.

Recommended products for reconstitution will be automatically added to the cart → Adjust quantities before checkout.

SLU-PP-322 Research Peptide

SLU-PP-322 is a synthetic, non-peptidic small-molecule triple agonist targeting the glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon (GCGR) receptors, engineered to investigate integrated metabolic signalling, energy expenditure, and biased receptor activation. It has emerged as a high-priority compound in preclinical obesity and type 2 diabetes research due to its oral bioavailability, central permeability, and differentiated pharmacokinetic profile vs. peptide triple agonists (e.g., retatrutide). This SLU-PP-322 research compound is supplied as a lyophilised solid to ensure stability, purity, and reproducibility in laboratory and investigative settings.

Supplied in lyophilised (freeze-dried) form to preserve stability.


What is the SLU-PP-322 Research Compound?

SLU-PP-322 (C₂₈H₃₅F₃N₄O₅S, MW: 610.66 g/mol) is a low-molecular-weight compound (structure per WO2020257421A1, Example 12) with balanced in vitro potency at human GLP-1R (EC₅₀ = 3.1 nM), GIPR (EC₅₀ = 4.8 nM), and GCGR (EC₅₀ = 2.9 nM) [WO2020257421A1, World Intellectual Property Organization, 2020; DOI: 10.1111/eci.13892 (TOS 2023 abstract)]. Unlike peptide incretin mimetics, SLU-PP-322 demonstrates oral activity, brain penetration, and reduced nausea liability in rodent models. Supplied exclusively for in vitro, ex vivo, and preclinical researchnot for human or veterinary use.

🔬 Note: SLU-PP-322 is an investigational research compound with no INN, no MHRA/FDA/EMA approval, and no public clinical data. This material is for mechanistic pharmacology research only.


Scientific Identifiers

Field
Value
Product Name
SLU-PP-322 Research Compound
Catalogue Numbers
NV-SLU322-5
CAS Number
Provisional internal code only (INN pending; patent WO2020257421A1)
Molecular Formula
C₂₈H₃₅F₃N₄O₅S
Molecular Weight
610.66 g/mol (monoisotopic)
Chemical Structure
N-(4-((2S)-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyrrolidin-1-yl)butyl)-1H-indole-2-carboxamide (per WO2020257421A1, Example 12)
Form
Lyophilised Solid (white to off-white powder)
Purity
≥98% (HPLC-UV, gradient elution)
Storage
Store at −20°C, protected from light and moisture
Unit Sizes
5 mg

 


Usage and Reconstitution

The SLU-PP-322 research compound is supplied freeze-dried for stability. For experimental protocols, reconstitute using:
DMSO (anhydrous, ≥99.9%) — stock solution (e.g., 10 mM)
Dilute in assay buffer (e.g., HBSS + 0.1% BSA) for working solutions

⚠️ Critical Handling Notes:
– Dissolve in DMSO first (gentle vortexing OK), then dilute ≥100-fold into aqueous buffer.
Avoid water-only reconstitution — poor solubility (<5 µg/mL in H₂O).
– Filter through 0.22 µm PVDF for cell-based assays.

Post-Reconstitution Storage:
– DMSO stock: −80°C, desiccated, ≤6 months (≤3 freeze–thaw cycles)
– Aqueous working solutions: 2–8°C, ≤24 hours

🛒 Recommended: [Add Anhydrous DMSO – 5 mL, LC-MS Grade] → Auto-added to cart.


SLU-PP-322 Research Compound: Key Investigational Pathways

SLU-PP-322 is actively studied for its triple-incretin, small-molecule pharmacology. Key research applications include:

  • Triple Receptor Bias & Signalling
    Investigated in:
    → HEK293 cells expressing hGLP-1R/hGIPR/hGCGR for cAMP, β-arrestin, and ERK bias profiling
    → BRET/FRET for receptor heteromerisation (e.g., GLP-1R:GCGR)
    → Brain-penetrance studies (LC-MS/MS in rodent CSF)
  • Metabolic & Weight-Loss Mechanisms
    Explored via:
    → DIO murine models (body weight, food intake, RER, energy expenditure via CLAMS)
    → Hepatic glucose output (HGO) assays in perfused liver
    → Brown adipose tissue (BAT) thermogenesis (UCP1, mitochondrial respiration)
  • CNS-Mediated Effects
    Studied in:
    → Hypothalamic slice electrophysiology (POMC/NPY neuron firing)
    → Conditioned taste aversion (CTA) vs. retatrutide (nausea liability comparison)
    → Microdialysis for monoamine flux (dopamine, serotonin in NAc)
  • Oral Bioavailability & PK/PD Modelling
    Evaluated in:
    → Oral vs. IP dosing (plasma/brain AUC, t₁/₂)
    → Caco-2 permeability and metabolic stability (microsomes)
    → Target engagement biomarkers (plasma GLP-1, glucagon, FGF21)

⚠️ All accessories (syringes, filters, vials) are for laboratory use only — not medical devices.


Why Order SLU-PP-322 from NovaVitality?

  • 🔬 Patent-aligned validation: Every lot includes CoA with HPLC, LC-MS (610.7 ±1.0 Da), and triple-receptor cAMP bioassay
  • 🇬🇧  UK-based & compliant: MHRA-aligned documentation, GMP-adjacent handling, discreet tracked dispatch
  • 📚 Research-first ethos: No clinical claims — full support for mechanistic pharmacology
  • 🛡️ RUO integrity: Meets MHRA GMP Guide, FDA 21 CFR 1271, ICH M7 (genotoxic impurities screened)
  • 💬 Expert support: Get help with solubility in CNS media, bias factor calculation, or DIO model dosing

Legal and Safety Information

NovaVitality supplies SLU-PP-322 strictly for laboratory research, assay development, and educational purposes (RUO).

❌ This product is not approved by the MHRA, FDA, EMA, or any regulatory authority for:
→ Human use
→ Veterinary use
→ Diagnostic, therapeutic, or supplement use

⚠️ Critical Responsibilities for Researchers:
– Use only under approved institutional biosafety protocols
– Comply with local ethics oversight (e.g., AWERB for in vivo work)
– Maintain full chain-of-custody documentation
– Do not compound, dispense, or administer to living subjects

🔒 NovaVitality disclaims all liability for unauthorised or off-label use. By purchasing, you affirm compliance with all applicable laws and institutional policies.


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Weight 5 g
Dimensions 1.55 × 3.85 cm
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