Name: SLU-PP-332 - 250mcg (60 capsules) (preorder)
Brand: Peptide Revolution
SKU: NH136
Price: 89.99 EUR
Availability: BackOrder
Rating: 5 (1 reviews)

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Product Description

Research Compound

SLU-PP-332 250 mcg Capsules

Research-grade capsule formulation supplied in a secure resealable container. SLU-PP-332 is an investigational REV-ERBα agonist studied in controlled laboratory settings for its relationship to circadian rhythm signaling, inflammatory regulation, metabolic balance, lipid handling, and neuroinflammation-associated pathways.

Research Use Only

This product is intended strictly for laboratory and scientific investigation. Not for human consumption, therapeutic use, or veterinary application.

Specifications

Form

Capsules

Content

250 mcg SLU-PP-332 per capsule

Quantity

60 capsules

Packaging

Resealable container

Storage

Store in a dry, dark place at room temperature

Molecular Formula

C₂₂H₂₃N₃O₂S

Molecular Weight

393.51 g·mol⁻¹

Other Names

SLUPP-332, REV-ERB agonist

Research Overview

SLU-PP-332 is studied as a selective REV-ERBα research compound with strong interest in circadian regulation, inflammatory control, and metabolic signaling. In experimental settings, it is investigated for its relationship to clock-gene expression, lipid metabolism, glucose handling, neuroinflammation, and broader energy-homeostasis pathways. No therapeutic or clinical claims are made or implied.

Primary Research Areas

Circadian Rhythm Modulation

Experimental investigation of REV-ERB-linked clock-gene signaling, biological rhythm regulation, and sleep-cycle-associated laboratory pathways.

Inflammation & Cytokine Signaling

Preclinical research focused on inflammatory mediators, cytokine expression, neuroinflammation, and immune-associated signaling balance.

Metabolic Balance & Glucose Regulation

Laboratory studies involving insulin sensitivity, glucose tolerance, energy expenditure, and broader metabolic homeostasis pathways.

Lipid & Neurodegeneration Research

Research involving lipid-profile modulation, fat-mass-related models, neuroprotective signaling, and neurodegeneration-associated experimental pathways.