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Catalogue / Neuroactive

Semax 5mg research peptide vial
Semax
5mg

Neuroactive

Semax 5mg

Neuropeptide studied for cognition and neuroprotection.

£24.95

Purity

99.2%

Batch

SE-2405-E

Format

Lyophilised powder

Assay

HPLC / MS

Lyophilised, 2–8°C. Reconstituted: 2–8°C, use within 28 days.

Research use only — not for human or veterinary consumption

What is Semax?

Semax is a synthetic heptapeptide derived from an ACTH(4-10) fragment with the Pro-Gly-Pro tail added for stability. It is a standard nootropic research compound.

How it works

It is studied for elevation of BDNF and NGF expression in hippocampal tissue and for modulation of monoamine turnover, without the corticotropic activity of the parent ACTH sequence.

How to handle and reconstitute

  1. Allow the sealed 10mg vial to reach room temperature before opening the carton to prevent condensation on the lyophilised cake.
  2. Reconstitute by running bacteriostatic water slowly down the inner wall of the vial — never inject the stream directly into the powder.
  3. Swirl gently until fully dissolved. Do not shake: agitation shears peptide bonds and can lower assayed purity.
  4. Label the vial with the reconstitution date and store at 2–8°C, protected from light. Use within 28 days.

Research applications

  • BDNF and NGF expression assays
  • Cognition and memory models
  • Neuroprotection and ischaemia research

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Background

Research context, documentation and handling

Wider context for this research area, plus the documentation, dispatch and intended-use terms that apply to every vial we ship.

Neuroactive peptide research

Neuroactive peptides are studied for their effect on neurotrophic factor expression, synaptic structure and neurotransmitter tone. The most-referenced readouts are BDNF and NGF expression in hippocampal tissue, dendritic spine density in cultured neurons, and behavioural profiles in established anxiety and memory models.

A recurring theme in this category is stability engineering. Many of these compounds are fragments of larger endogenous molecules, modified to survive peptidase activity long enough to reach their target — a Pro-Gly-Pro tail, cyclisation, or backbone substitution. Comparing a modified analogue against its parent sequence is a standard way to separate the contribution of exposure time from the contribution of intrinsic activity.

Blood–brain barrier penetration is the other central variable. A compound with excellent receptor affinity and no route into the central nervous system produces nothing in an in-vivo model while performing well in culture, so the two settings often disagree for entirely mechanical reasons.

Practical notes for this category

Neuroactive peptides are typically supplied at small masses, so reconstitution volume selection determines whether your working dilution is pipettable. Prepare an intermediate dilution rather than attempting to measure sub-microlitre volumes from a concentrated stock.

Several sequences in this group are sensitive to oxidation at methionine residues; minimise headspace exposure and do not leave reconstituted stocks at room temperature between draws.

Documentation supplied with every vial

Each vial ships with its batch code printed on the label and a matching certificate of analysis published in the certificate library. The certificate records the assay date, the purity figure returned by high-performance liquid chromatography, and the identity confirmation from mass spectrometry. Quote the batch code in any enquiry and we can retrieve the underlying chromatogram rather than the summary record.

For reproducibility, record the compound, vial size, lot number and certified purity alongside your method. If a later batch behaves differently in the same assay, that record is what makes the comparison possible rather than a matter of recollection.

Dispatch and intended use

Orders confirmed before 3pm on a working day leave the London facility the same day on a free tracked next-day service within the UK; international orders ship within forty-eight hours on a tracked courier. Lyophilised material is stable at ambient temperature for far longer than any tracked service takes, so no cold chain is required in transit — refrigeration matters on arrival and after reconstitution.

This compound is supplied strictly for in-vitro laboratory research by qualified personnel. It is not a medicine, holds no marketing authorisation, and is not intended for human or veterinary consumption. No dosing, administration or clinical guidance is provided.