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Protocol 01

SirtCore™ 01

Energy & Cellular Defense

Precision NAD+ and cellular energy support. Clinically dosed for European biology.

Batch #MN-2026-0412: Verified Pure
€49one-time
or€41.65/monthSAVE 15%

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SirtCore™ 01 - NAD+ Precursor & Cellular Defense Protocol
EU COMPLIANTGMP CERTIFIED
The Formula

Four Precision-Dosed Compounds

Every ingredient at clinical dosage. No proprietary blends. No fillers. Full transparency.

500mg98% PURE

Trans-Resveratrol

Sirtuin Activator

Direct SIRT1 activation, enhancing NAD+ utilization efficiency

300mg99% PURE

Nicotinamide Riboside (NR)

NAD+ Precursor — EU Authorized Novel Food

Enters cells via NRK1/NRK2 kinase — directly synthesising NMN then NAD+, bypassing the rate-limiting NAMPT step that limits plain Nicotinamide. Superior cellular bioavailability.

Commission Implementing Regulation (EU) 2020/16

"Authorized Novel Food at 300 mg/day for adults"

10mg

Zinc Bisglycinate

Enzymatic Cofactor

Essential cofactor for 300+ enzymes including DNA repair

EFSA Journal 2009;7(9):1229

"Contributes to the protection of cells from oxidative stress"

300mg

Quercetin

CD38 Inhibitor

Inhibits CD38 enzyme that degrades NAD+, extending NAD+ half-life

Mechanism of Action

The NAD+ Salvage Pathway

How SirtCore™ 01 optimizes your cellular energy metabolism through precision targeting

1

NAD+ Precursor Delivery

Nicotinamide Riboside (NR) enters cells via the NRK1/NRK2 kinase pathway — converting directly to NMN and then NAD+, bypassing the rate-limiting NAMPT step that constrains plain Nicotinamide.

NR → NMN → NAD+EU 2020/16
2

Sirtuin Activation

Trans-Resveratrol directly activates SIRT1 genes — the master regulators of cellular longevity and mitochondrial biogenesis.

SIRT1 → Mitochondrial Function ↑
3

NAD+ Protection

Quercetin inhibits CD38, the enzyme responsible for 95% of NAD+ degradation. This extends NAD+ half-life significantly.

CD38 ↓ → NAD+ Half-life ↑
4

Enzymatic Support

Zinc Bisglycinate serves as an essential cofactor for 300+ enzymes, including those in DNA repair and Sirtuin function.

Oxidative Stress Protection

The Result: Optimized NAD+ levels, enhanced mitochondrial function, and activated cellular defense mechanisms.

Comparison

Precision vs. Kitchen Sink

See how targeted formulation compares to broad-spectrum approaches

FeatureSirtCore™ 01AG1Seed DS-01Generic Multi
Ingredient Count4 (Precision)75+2420-30
Precision Dosing
EFSA CompliantFullPartialYesVaries
Direct NAD+ SupportYes — NR 300mg (EU 2020/16)IndirectNoMinimal
Sirtuin Activation
CD38 Inhibition
Formula TransparencyFull DisclosureProprietary BlendsFull DisclosureVaries
Price€49€99€60€10-25
Regulatory Transparency

NMN vs NR — The EU Compliance Distinction

We publish the regulatory basis for every ingredient. Here is why SirtCore™ 01 uses NR, not NMN.

NMN — Not EU Authorized

Nicotinamide Mononucleotide (NMN) is classified as a Novel Food under Regulation (EU) 2015/2283. It has not received an authorization decision from the European Commission and cannot legally be sold as a food supplement in the EU.

Regulation (EU) 2015/2283 — Novel Food, no authorization issued

NR — EU Authorized · 300 mg/day

Nicotinamide Riboside (NR) was granted Novel Food authorization by the European Commission under Commission Implementing Regulation (EU) 2020/16 for use in food supplements at up to 300 mg per day for the general adult population. SirtCore™ 01 delivers the full authorized dose.

Commission Implementing Regulation (EU) 2020/16 — 10 January 2020

Why NR Is Biochemically Superior to Plain Nicotinamide (B3)

Nicotinamide (B3) — Limited Pathway

Relies on NAMPT — a rate-limiting enzyme that becomes a bottleneck under supplemental doses. High-dose Nicotinamide can also inhibit Sirtuins through feedback mechanisms.

Nicotinamide Riboside (NR) — Direct Route ✓

Enters cells via NRK1/NRK2 kinase — a direct, high-capacity route to NMN and then NAD+. No NAMPT bottleneck. Does not inhibit Sirtuins at supplemental doses.

References: Commission Implementing Regulation (EU) 2020/16 · Regulation (EU) 2015/2283 · Bogan & Brenner 2008 (NRK pathway) · Canto et al. 2012 (NR bioavailability) · EFSA Journal 2009;7(9):1229

GMP Certified

Germany

Third-Party Tested

Independent Verification

Made in Germany

GMP Certified Facility

EFSA Compliant

Full Documentation

Protocol Timeline

What to Expect

Supplements support your biology — they do not override it. Realistic timelines build sustainable results.

W1–2

Weeks 1–2

Baseline Period

Your body establishes baseline levels of the active compounds. No specific outcome is expected at this stage — consistent dosing is building the foundation.

Take at the same time each day to support consistent bioavailability.

W3–8

Weeks 3–8

Active Phase

With consistent use alongside a healthy diet and exercise, customers often report noticing changes. Biomarker shifts are possible during this window. Individual results vary.

Results depend on diet, sleep, exercise, and individual genetics.

W8+

Weeks 8+

Sustained Protocol

Sustained, consistent use allows the full protocol to function as intended. Most customers who see the clearest benefits use for a minimum of 90 days.

This is precision nutrition — not a pharmaceutical. Protocol duration matters.

Individual results vary based on diet, exercise, lifestyle, sleep quality, and individual genetics. This is not a pharmaceutical — it is precision nutrition. Results are not guaranteed.

Common Questions

Product FAQ

Does this work?

The ingredients are selected based on clinical evidence and EFSA-approved health claims. Supplements support healthy biological function — they do not replace diet, exercise, and sleep. Use consistently alongside a healthy lifestyle for the best outcomes.

How long until I notice results?

Timeline varies by individual. With consistent use, many customers report noticing changes within 4–8 weeks. A full 90-day protocol is recommended for sustained benefit. Individual results depend on diet, exercise, genetics, and consistency.

Is it approved by EFSA?

EFSA regulates health claims, not ingredients. All ingredients in this formula are authorised for use in EU food supplements. Every health claim we make is approved under EU Regulation 432/2012 or EFSA Regulation 1924/2006. EFSA Journal references are listed on each product page and verifiable at efsa.europa.eu.

Is it better than [competitor product]?

We don't make comparative claims — EU Regulation 1924/2006 prohibits them without rigorous substantiation. What we do: clinical doses of EFSA-approved ingredients, full ingredient transparency, and proactive compliance monitoring. You can verify every claim we make.

Full Regulatory FAQ →•What We Don't Claim →•Formulation Philosophy →
Begin Your Protocol

Precision Longevity Starts Here

Four compounds. Clinical dosages. Full EU compliance. Precision-targeted formulation for cellular energy support.

Add to Cart — €49View All Protocols

Food Supplement. This product is not intended to diagnose, treat, cure, or prevent any disease. Manufactured in Germany in accordance with EFSA standards. Do not exceed recommended daily intake. Keep out of reach of children. Store in a cool, dry place. Consult your healthcare provider before use if you are pregnant, nursing, taking medication, or have a medical condition.