Dipeptide Diaminobutyroyl Benzylamide Diacetate

CosmeticCosmetic nicotinic antagonist mimeticExperimental

Also known as: Waglerin-1 mimetic, Tripeptide-3

Dipeptide Diaminobutyroyl Benzylamide Diacetate (also called Waglerin-1 mimetic or Tripeptide-3) is a cosmetic nicotinic antagonist mimetic. This dipeptide is a synthetic mimetic of waglerin-1, a component of temple viper venom that antagonises the muscle-type nicotinic acetylcholine receptor. In vitro it shows reversible antagonist-like activity at the postsynaptic receptor of the neuromuscular junction, reducing the depolarisation that initiates muscle contraction.

Calculate Dose

For research use only.

Key Facts

CAS
823202-99-9
Molecular Weight (MW)
—
Half-life
Topical; systemic PK not established
FDA status
Not Approved
Administration Route
Topical
Frequency
—
Last updated
Sep 26, 2026
Reviewed
Aug 30, 2026
Targets
Muscle nAChR (model systems)

Vendor price snapshot

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Vendors listing this peptide
1
Listed offers
1
Price per mg
$1.05/mg

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Research summary

Waglerin-1–inspired tripeptide used in cosmetics to reduce expression-line appearance. Topical cosmetic active, not an FDA drug.

Peptide Library's Dipeptide Diaminobutyroyl Benzylamide Diacetate profile summarises 4 cited studies listed in the Science section, the compound's regulatory status, and research-protocol parameters reported for it. It is a research reference, not medical advice.

Protocol

Dosage Range
Per cosmetic formulation
Frequency
—
Cycle
—
Administration Route
Topical
Reconstitution Guide
—

Not yet checked against primary sources

These figures are compiled from earlier reference material. They have not been verified against FDA labelling, registered trials or published literature, no citation is attached to them, and none of them is a recommended dose. Dipeptide Diaminobutyroyl Benzylamide Diacetate is queued for dosage evidence review.

Compare reported doses across the whole library

Sequence & molecular data

Sequence and molecular data for Dipeptide Diaminobutyroyl Benzylamide Diacetate
Molecular formulaC23H37N5O7 (salt forms vary)
Molecular weight—
CAS number823202-99-9
Half-lifeTopical; systemic PK not established
AppearanceClear solution or powder (cosmetic grade)
FormulationTopical Cream
PubChem CID71465152
FDA UNII38H206R00R

Identifiers link to the public PubChem, FDA Substance Registration (UNII), ChEMBL and DrugBank records for the same entity.

Science

Mechanism of Action

This dipeptide is a synthetic mimetic of waglerin-1, a component of temple viper venom that antagonises the muscle-type nicotinic acetylcholine receptor. In vitro it shows reversible antagonist-like activity at the postsynaptic receptor of the neuromuscular junction, reducing the depolarisation that initiates muscle contraction. Applied topically the intent is to reduce the microcontractions of facial expression muscles that produce dynamic lines, giving a mechanism conceptually parallel to botulinum toxin but acting on the receptor rather than on vesicle fusion, and far weaker. Whether a topically applied dipeptide reaches the neuromuscular junction in meaningful concentration is the central unresolved question; evidence is largely supplier-derived.

Origin

Synthetic tripeptide analog of temple-viper waglerin-1.

Targets

Muscle nAChR (model systems)

Regulatory & research status

Dipeptide Diaminobutyroyl Benzylamide Diacetate is not an FDA-approved product. It is sold for laboratory research and has no approved medical use.

Regulatory and research status for Dipeptide Diaminobutyroyl Benzylamide Diacetate
FDA statusNot Approved
AvailabilityOTC / Supplement
WADA (sport)Permitted
Library classificationResearch-Only

Benefits

Topical expression-line cosmetics

Dipeptide Diaminobutyroyl Benzylamide Diacetate side effects

Side Effects

  • Irritation
  • Redness

Storage & stability

Lyophilized (freeze-dried) peptide powder is far more stable than the reconstituted solution. Keep sealed vials cold, dry and away from light; long-term storage is typically frozen, with short-term refrigeration for vials in use.

Once reconstituted in bacteriostatic water, keep the solution refrigerated, avoid repeated freeze–thaw cycles and agitation, and label the vial with the reconstitution date and concentration. Discard any solution that turns cloudy or shows particulates.

Degradation rates differ by sequence: peptides containing methionine, cysteine, asparagine or glutamine are more prone to oxidation and deamidation, so shelf life after reconstitution is compound-specific rather than universal.

Cosmetic peptides in this library are formulated into topical products; follow the product label rather than the reconstitution guidance above.

Read the full guide: how to store peptides before and after reconstitution →

Source: Manning MC, Chou DK, Murphy BM, Payne RW, Katayama DS. Stability of protein pharmaceuticals: an update. Pharm Res. 2010;27(4):544–575. (PMID 20143256). General guidance for research handling; not product-specific instructions.

Dipeptide Diaminobutyroyl Benzylamide Diacetate: frequently asked questions

What is Dipeptide Diaminobutyroyl Benzylamide Diacetate?

Waglerin-1–inspired tripeptide used in cosmetics to reduce expression-line appearance. Topical cosmetic active, not an FDA drug.

How does Dipeptide Diaminobutyroyl Benzylamide Diacetate work?

This dipeptide is a synthetic mimetic of waglerin-1, a component of temple viper venom that antagonises the muscle-type nicotinic acetylcholine receptor. In vitro it shows reversible antagonist-like activity at the postsynaptic receptor of the neuromuscular junction, reducing the depolarisation that initiates muscle contraction.

Is Dipeptide Diaminobutyroyl Benzylamide Diacetate FDA approved?

No. Dipeptide Diaminobutyroyl Benzylamide Diacetate is not approved by the FDA for any indication and is categorised as otc / supplement. It has not been reviewed for safety or efficacy as a medicine, and published research should be read as investigation rather than established use.

What is the half-life of Dipeptide Diaminobutyroyl Benzylamide Diacetate?

Reported half-life for Dipeptide Diaminobutyroyl Benzylamide Diacetate is Topical; systemic PK not established. Half-life describes how long the compound persists in circulation, not how long any effect lasts, and published figures vary with route of administration, formulation and the population studied.

Is Dipeptide Diaminobutyroyl Benzylamide Diacetate banned in sport?

Dipeptide Diaminobutyroyl Benzylamide Diacetate is recorded here as permitted in sport. Anti-doping status is revised annually, so athletes subject to testing should confirm against the current WADA Prohibited List before use.

What peptides are similar to Dipeptide Diaminobutyroyl Benzylamide Diacetate?

Compounds most often compared with Dipeptide Diaminobutyroyl Benzylamide Diacetate include Acetyl Hexapeptide-8, Acetyl Octapeptide-3, Acetyl Tetrapeptide-3 and AHK-Cu. They are grouped by shared mechanism or research area rather than by equivalence, and their regulatory status and evidence base differ.

References

Related research, comparisons & guides

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Compiled by Peptide Library Editorial · Reviewed Aug 30, 2026 · Updated Sep 26, 2026 · Version 3

This Dipeptide Diaminobutyroyl Benzylamide Diacetate profile is compiled from published literature (4 cited studies linked above), public regulatory records and chemical registries. It describes what research reports; it is not medical advice, and nothing here is a dosing recommendation for humans. Peptide Library does not sell peptides. Editorial policy · How profiles are compiled · Report an error

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