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Calculated reference model · not an experimental or batch-certified structure. Backbone view: 17 of 34 atoms.

Model data & sources
  • Free tetrapeptide Arg-D-Val-Ser-Gln. Only valine is D. Free termini match catalog formula C19H36N8O7. Acetylated and amidated literature variants are different molecules and are not drawn.
  • Heavy atoms only; hydrogens are omitted from the reference display.
  • Source-defined atom stereochemistry is checked against the calculated coordinates; no energy-minimum or observed-fold claim is made.
  • Reference molecular species only; batch counterions, excipients and material composition are not certified.
Sequence
Arg-D-Val-Ser-Gln
Formula
C19H36N8O7
Method
RDKit ETKDGv3 / MMFF94s calculated reference conformer
Made
2026-01-20
Reports
2 on file
Everything shipping from this page today came off this batch. The code is printed on your label, and one certificate covers the whole batch.

N163-166 mod6

Peptides

Published formats

  • Standard Reference Vial

Supplementary product details from the published catalog, checked 2026-10-07. These reference details do not establish current availability.

Pricing

Pricing and order placement are reserved for reviewed research accounts. Log in or submit an account application to view current product pricing.

Technical Specifications

Batch COA Database ↗
CAS Registry NumberRefer to batch COA
Molecular FormulaC₁₉H₃₆N₈O₇
Molecular Weight488.5
IUPAC DesignationVDAC1-derived tetrapeptide with a D-valine
Physical FormLyophilized powder
Storage RequirementsRefer to product documentation
Capsule Concentration250mcg

Identity fields from the published product record, checked 2026-10-07. Reference information is not a batch identity certificate.

Research Overview

N163-166 mod6 (VDAC1-Derived Peptide) Research Standard

N163-166 mod6 is a specialized, synthetic VDAC1-derived tetrapeptide designed to modulate mitochondrial cholesterol transport. By targeting the interaction between the voltage-dependent anion channel 1 (VDAC1) and the steroidogenic transduceosome complex, this peptide serves as a research tool for studying the rate-limiting step of steroidogenesis. Specifically, N163-166 mod6 is utilized to investigate the selective enhancement of testosterone biosynthesis through increased mitochondrial cholesterol availability, while maintaining neutral activity regarding corticosterone production, offering a precise model for researching androgen-specific signaling.

Additional Properties

Property Specification
Origin VDAC1 (Voltage-Dependent Anion Channel 1)
Sequence Modification Arg-D-Val-Ser-Gln (R-D-V-S-Q)
Physical Appearance Lyophilized powder

Mechanism of Action (Pharmacological Context)

N163-166 mod6 functions by modulating the mitochondrial transduceosome, a multiprotein complex responsible for the translocation of cholesterol into the mitochondria—the rate-limiting step in steroidogenesis.

  • Cholesterol Transport: The peptide acts by interacting with VDAC1, which functions as a gatekeeper in the outer mitochondrial membrane. By disrupting inhibitory interactions (such as the 14-3-3epsilon binding to VDAC1), the peptide facilitates the recruitment of the Steroidogenic Acute Regulatory protein (StAR) and cholesterol import.

  • Testosterone Specificity: Research indicates that this mechanism specifically promotes androgen biosynthesis within Leydig cells. Notably, data suggests this enhancement occurs without stimulating a corresponding increase in corticosterone production, differentiating it from generalized steroidogenic stimulants.

  • D-Valine Modification: The inclusion of D-Valine in this specific "mod6" variant serves to increase proteolytic stability in in vitro and in vivo research models, preventing rapid degradation and allowing for more controlled kinetic analysis.

Research Applications

N163-166 mod6 is a pivotal tool for exploring mitochondrial dynamics and androgenic signaling.

Primary fields of in vitro and in vivo laboratory investigation include:

  • Steroidogenic Pathway Mapping: Studying the protein-protein interactions (PPIs) between VDAC1, TSPO, and StAR.

  • Mitochondrial Cholesterol Flux: Measuring the rate of cholesterol entry into the mitochondrial matrix under stimulated and basal conditions.

  • Androgen-Specific Signaling: Investigating why this peptide scaffold specifically upregulates testosterone biosynthesis while remaining selective relative to other steroid pathways (e.g., corticosterone).

  • Proteolytic Stability Research: Utilizing the D-Valine-modified tetrapeptide to benchmark how stereochemical variations improve the half-life of short-chain bioactive peptides.

Storage & Handling Guidelines

Store at controlled room temperature. Keep tightly closed.

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

References

  • Martinez-Arguelles DJ, et al. (2023) Oral administration of VDAC1-derived small molecule peptides increases circulating testosterone levels in male rats. Frontiers in Endocrinology. 13:1003017. doi:10.3389/fendo.2022.1003017.

  • Aghazadeh Y, et al. (2014) Peptide Targeting of Mitochondria Elicits Testosterone Formation. Molecular Therapy. 22(8):1511-1520.

Related Research Compounds

Research Use Disclaimer

Research Use Only Disclaimer: This product is labeled and sold "For Research Use Only — NOT FOR HUMAN CONSUMPTION." It is not a drug, dietary supplement, food, cosmetic, or medical device, and it is not approved by the FDA or any other regulator for human or veterinary use. It is supplied to approved account holders as a research chemical for laboratory use and must be handled in accordance with applicable law.

Certificates of Analysis

Currently shipping from batch KC-N63-01.

Kimera Chems

Compounds That Survive Scrutiny

Research use only. Not for human or veterinary use.