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Lexicon

Andarine (S4)

One of the oldest SARMs, well described preclinically, known for a characteristic dose-dependent vision effect.

1 min read 7 sources

White tablet bottle with a black TPD label for Andarine (S4) on a white podium with a glowing rim, next to a long blue 3D molecule model in a bright lab
Preclinical · not approved

Summary

At a glance

Sources checked on 26 Oct 2026

Prostate weight (rats)
16 %

compared with intact animals, castrated rats on the lower study dose3

Muscle back to normal level
8 weeks

soleus and levator ani muscle of castrated rats as in intact animals3

Bone study (rats)
120 days

bone density maintained and less body fat after removal of the ovaries1

Oral absorption (rats)
100 %

complete at the lower doses, less at higher ones4

Human trials in the registry
0 trials

no trial with andarine on ClinicalTrials.gov, as of 26 Oct 20266

  • Andarine (S-4) is a non-steroidal selective androgen receptor modulator (SARM) from the aryl-propionamide family.72
  • In castrated rats andarine brought muscle mass and strength back to the level of intact animals over eight weeks. On the lower study dose the prostate and seminal vesicles stayed at 16 and 17 percent.3
  • After removal of the ovaries andarine maintained bone density in rats over 120 days, made the bones stronger and lowered body fat.1
  • The pituitary hormones LH and FSH fell in a dose-dependent way. This shows that andarine brakes the body's own hormone axis.3
  • ClinicalTrials.gov lists no human trial of andarine (as of October 2026). Everything here is preclinical research, not a recommendation.6
Profile

Updated May 2026

How long does it stay in the body?

Share left after one dose, calculated with a half-life of ~4 hours

Half-life ~4 hours
After 8 hours: 25 %
Hour 4 · 50 %Hour 8 · 25 %Hour 12 · 12.5 %Hour 20 · 3.1 %

Simplified model without an absorption phase, half-life from the TPD lexicon.

Class
SARM

aryl-propionamide

Use
Oral

often split

Half-life
short

approx. 4 hours

WADA
Banned

category S1.2

Sizes
10 to 25 mg

2 sizes in the shop

Contents 14 sections
  1. At a glance
  2. What is Andarine?
  3. How it works
  4. How to take it
  5. Dosing
  6. What the research shows
  7. Research status
  8. Side effects
  9. Practice
  10. Storage
  11. Related compounds
  12. FAQ
  13. Glossary
  14. Sources

What is Andarine?

Andarine, also S4 or S-4, is one of the older SARMs from the aryl-propionamide family. It was one of the first to be clinically evaluated. Clinical development was later not pursued.

Andarine is known mainly for a characteristic vision effect: a yellow tint to vision and worse night vision, occurring dose-dependently. This is not a myth but is reported consistently.

Comparison

SARMs compared

Five SARMs from the TPD lexicon, as described there. Tap a card to open its entry.

Simplified: all act on the androgen receptor and aim to address muscle and bone more than the prostate. There is no head-to-head comparison in humans. 32

How it works

Andarine binds the androgen receptor and activates it with tissue preference in muscle and bone. In animal models it was associated with maintaining bone density and reducing body fat.

The vision effect likely relates to how Andarine binds certain structures in the eye. It is reversible after stopping but bothersome during use.

Where it acts

Where andarine acted in experiments

Tap a point or a card. Colour = androgen receptor, grey = observed. All from rat studies.

  1. Skeletal muscle

    Muscle mass and strength back to intact levels (castrated rats)3

    AR
  2. Bone

    Bone density maintained, bones stronger (rats after ovary removal)1

    AR
  3. Fat tissue

    Less body fat (rats after ovary removal)1

    Observed in trials
  4. Pituitary

    LH and FSH fell in a dose-dependent way (castrated rats)3

    AR
  5. Prostate and seminal vesicles

    Only 16 and 17 percent of the weight of intact animals (lower study dose)3

    AR

Known targets7

Compound PubChem CID 9824562: one described target, Agonist in muscle, bone and pituitary, weak in the prostate.

Androgen receptor
Gene
AR
UniProt
P10275
ChEMBL
CHEMBL1871
Action
Agonist in muscle, bone and pituitary, weak in the prostate
Blue 3D molecules between a glass trabecular bone structure on the left and light blue muscle fibres on the right, golden droplets on the fibres
Action on bone and muscle, fat breakdown. Symbolic image.

How to take it

Oral, often split because of the short half-life.

  • Half-life only around 4 hours, so often morning and evening.
  • With some water, with or without food.
  • Cycles are usually kept short.
White tablet bottle with a black TPD label for Andarine (S4) next to a glass of water and a few small white tablets on a bright table
Tablet taken by mouth, according to the entry often split into two doses. Symbolic image.

Dosing

Dosing

Dosing, titration and syringe

Loading the dosing information …

  • Getting started and stepping up, drawn as a staircase
  • Units on the U-100 syringe for every step
  • How long one vial lasts

What the research shows

A preclinical study (Kearbey, 2007) showed in ovariectomized rats that S-4 maintained bone density and bone strength while reducing body fat. That is a solid animal result.

Solid modern human data on muscle building in healthy people are scarce, clinical development was discontinued. The Solomon review (2019) places Andarine in the SARM context.

Study results

What the trials measured

Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.

Androgenic organs after eight weeks3

Organ weight in percent of intact animals (intact = 100%)

Prostate3
Intact animals (comparison) 100%
With andarine, lower study dose 16%
Seminal vesicles3
Intact animals (comparison) 100%
With andarine, lower study dose 17%

Values from the abstract. In the same experiment andarine brought the soleus and levator ani muscle to the level of intact animals. The comparison androgen DHT made the prostate and seminal vesicles grow to more than double. Rat model, not tested in humans.

Glass eye with a blue and yellow iris, surrounded by glowing yellow and white arcs of light on a light blue background
The described vision effect has not been studied. Symbolic image.

Research status

Where the research stands

Where the compound stands on the way from lab research to approval. As of 26 Oct 2026. 6

  1. Preclinical Rat studies on muscle, bone, fat and pharmacokinetics (2004 to 2007)
  2. Phase 1 no registered trial
  3. Phase 2 no registered trial
  4. Phase 3 no registered trial
  5. Approval not yet
Not approved and no registered human trial. Development was not pursued further.6

So far there is no registered trial in humans. 6

Side effects

  • Characteristic vision effect: yellow tint, worse night vision, dose-dependent and reversible after stopping.
  • Dose-dependent suppression of the testosterone axis.
  • Falling HDL values.

Practice

  1. Stay low, the vision effect scales directly with the dose.

  2. Short cycles, then a break.

  3. Banned in official competition and detectable (WADA S1.2).

Light blue skipping rope, folded white towels and a water bottle on a wooden table in a bright room

Storage

Store dry, cool and protected from light, out of reach of children. Keep the original container closed and mind the expiry date.

Three white bottles on a bright shelf next to a folded light blue towel
Store dry, cool and out of reach of children. Symbolic image.

Related

Related compounds

Same targets or a different path: all in the TPD lexicon.

FAQ

Common questions about Andarine (S4)

Short answers, each backed by the sources below.

Is andarine approved or studied in humans?

There is no approval. As of 26 October 2026 ClinicalTrials.gov lists no trial with andarine and we found no published study in humans. Development was not pursued further.62

What do the rat studies show on muscle?

Rats received andarine for eight weeks, starting twelve weeks after castration. The soleus and levator ani muscle regained the mass and strength of intact animals and lean mass came back. On the lower study dose the prostate and seminal vesicles stayed at 16 and 17 percent, while the comparison androgen DHT made them grow to more than double.3

And on bone?

In rats after removal of the ovaries, a model of fast bone loss, andarine maintained whole-body and trabecular bone density over 120 days and made the bones stronger. At the same time body fat fell. In castrated male rats bone density rose more than with DHT.13

Why is the half-life considered short?

In rats the half-life was between 2.6 and 5.3 hours depending on the dose. At low doses an oral dose reached the blood completely. Neither has been measured in humans.4

What about the vision effect?

The entry describes a dose-dependent yellow tint and poorer night vision that fades after stopping. We found no published study in PubMed that measures this. The information rests on reports from the research community.2

Does andarine brake the body's own hormone axis?

Yes, at least in rats: LH and FSH from the pituitary fell in a dose-dependent way. In humans a brake on the body's own testosterone production should be expected, but it has not been measured for andarine.3

What do analyses of purchased SARM products show?

Andarine was one of the SARMs found in an analysis of 44 products bought online. Only 52 percent of the products contained any SARM at all and in 59 percent the amount differed markedly from the label.5

Glossary

Terms explained briefly

Dotted words in the text open these explanations directly.

Androgen receptor
Binding site for testosterone and related hormones in many tissues, such as muscle, bone, prostate and brain.
Aryl-propionamide
The chemical backbone of a SARM family that ostarine also belongs to.
Bone density
Mineral content of bone, a measure of its strength.
DHT
Dihydrotestosterone, a strong androgen. In the studies it served as a comparison because it makes the prostate grow strongly.
Half-life
The time until the amount in the blood has fallen by half.
LH and FSH
Pituitary hormones that stimulate the testes to make testosterone and sperm.
Preclinical
Research before first use in humans, in cell cultures and animal models. Results cannot be transferred directly to humans.
Removal of the ovaries
Animal model of menopause: without estrogen the animals lose bone mass quickly.
SARM
Selective androgen receptor modulator. A non-steroidal compound meant to address the androgen receptor mainly in muscle and bone.
WADA
World Anti-Doping Agency. Its prohibited list includes SARMs under S1.2, other anabolic agents.

Evidence

Sources

Show all 7 sourcesHide sources 5 Studies1 Trial registry1 Database checked 26 Oct 2026

Studies

  1. Bone preserved, less body fat in rats after ovary removal

    Kearbey et al., Pharmaceutical Research, 2007

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  2. Review of SARMs: pharmacology and clinical evidence

    Solomon et al., Sexual Medicine Reviews, 2019

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  3. Muscle, bone and pituitary in castrated rats

    Gao et al., Endocrinology, 2005

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  4. Pharmacokinetics in rats: absorption, half-life, distribution

    Kearbey et al., Xenobiotica, 2004

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  5. Analysis of SARM products sold online

    Van Wagoner et al., JAMA, 2017

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed

Trial registry

  1. Search on ClinicalTrials.gov (no trial with andarine)

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 26 Oct 2026 via ClinicalTrials.gov API v2

Database

  1. Structure of andarine in PubChem

    PubChem, U.S. National Library of Medicine (CID 9824562)

    Checked 26 Oct 2026 via PubChem

In the shop

Andarine (S4) in the catalog

Sizes, prices and shipping times are on the product page.

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