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GGN (Melatonin)

CAS
73-31-4
Molecular wt
232.28 g/mol
Compound class
Indoleamine (N-acetyl-5-methoxytryptamine)

GGN (Melatonin)

Amount Per ML

GABA 100mg

L-Histidine 100mg

Theanine 50mg

Taurine 100mg

Melatonin 200mcg

20ml vial

Solution In Deionized Water And 1% Benzyl Alcohol

Store at controlled room temperature

GGN (Melatonin) is sold for laboratory research use only. Terms of sale apply. Not for human consumption, nor medical, veterinary, or household uses. Please familiarize yourself with our Terms and Conditions prior to ordering.

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HPLC and mass spectrometry

Description

GGN: Synergistic Neuro-Modulatory Matrix (Optimized Research Reference)

GGN is a standardized, multi-component solution specifically engineered for investigating complex neurochemical crosstalk. By integrating melatonin within a precise matrix of inhibitory neurotransmitters and neuromodulatory amino acids (GABA, L-Theanine, Taurine, and L-Histidine), GGN provides a controlled biochemical environment for researchers to establish non-linear, synergistic interaction profiles that isolated single-ligand assays cannot replicate.

This formulation is optimized for Concentration-Response (C-R) studies, serving as a stable baseline for establishing EC₅₀ shifts when comparing melatonin’s activity in isolation versus its performance within an integrated amino acid matrix.

Analytical Formulation Matrix

Each milliliter of the solution is prepared in a deionized water base with 1% benzyl alcohol, calibrated to the following concentrations:

Component Function within Matrix Concentration (per mL)
Melatonin Circadian Signaling / MT1/MT2 Ligand 200 mcg
GABA Primary Inhibitory Neurotransmitter 100 mg
L-Histidine Histamine Precursor / Neuro-modulator 100 mg
Taurine Osmotic Regulator / Neuromodulator 100 mg
L-Theanine Alpha-wave / Neurotransmitter Balancer 50 mg

Experimental Utility: EC₅₀ Shift Modeling

GGN is primarily intended for use in comparative pharmacological assays designed to isolate the potential potentiation of melatonin by its accompanying matrix.

  • Potentiation Mapping: Enables researchers to conduct parallel concentration-response curves to quantify potential left-ward shifts in the EC₅₀ of melatonin when sequestered within the GGN matrix, providing a clear numerical value for synergistic efficacy.

  • Signaling Cross-talk: Facilitates the study of how GABAergic inhibitory tone and taurine-mediated osmotic regulation concurrently influence the downstream sensitivity of the circadian pathway.

  • Matrix Baseline Control: Provides a standardized reference for establishing a “matrix effect” baseline, allowing for the subtraction of individual amino acid noise to isolate specific melatonin-matrix interactions.

Storage & Handling Guidelines

Store at controlled room temperature.

Storage guidance is a house recommendation. Analytical documentation is per-lot release testing.

Related Research Compounds

Analytical Documentation

Purity, identity, and composition vary by manufacturing lot. Kimera Chems does not publish a single fixed purity figure for this item; refer to the batch-specific Certificate of Analysis (COA) issued for the lot received, which reflects third-party analytical testing for that lot. Contact us if a COA for your lot is required.

Research Use Only Disclaimer: This product is developed, compounded, and distributed strictly as a Research Use Only (RUO) laboratory reagent intended exclusively for non-clinical analytical and scientific investigation. It is not an FDA-approved drug formulation, therapeutic medication, dietary supplement, or food additive, and is strictly prohibited for human or veterinary consumption. Kimera Chems supplies these calibrated solutions solely to accredited institutional laboratories and qualified scientific investigators.

Compound Class Indoleamine (N-acetyl-5-methoxytryptamine)
CAS Number 73-31-4
Other Names Melatonin, Melatonine, N-Acetyl-5-methoxytryptamine, Circadin, 5-Methoxy-N-acetyltryptamine, Melatol
IUPAC Name N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide
Molecular Formula C13H16N2O2
Molecular Weight 232.28 g/mol