Ecdysterone vs RAD-140
Moderate Research vs Emerging
avoid Mechanism-based · 53% Both Ecdysterone and RAD-140 carry hepatotoxic risk. Combining hepatotoxic compounds significantly increases liver damage potential. If unavoidable, include liver support (TUDCA/NAC) and monitor ALT/AST frequently.
Molecular Data
Ecdysterone RAD-140
Weight 480.64 Da 393.83 Da
Half-life ~4-9 hours ~60 hours
Type Ecdysteroid (C27H44O7) Nonsteroidal selective androgen receptor modulator (C20H16ClN5O2)
Key Benefits
Ecdysterone
01 Activation of muscle protein synthesis through ERbeta/PI3K/Akt/mTOR signaling without androgen receptor binding
02 Statistically significant increases in lean muscle mass demonstrated in a controlled human trial in trained subjects
03 No hormonal suppression -- does not affect testosterone, LH, or FSH levels, eliminating the need for post-cycle therapy
04 No androgenic side effects (no hair loss, acne, prostate issues, or virilization in women)
05 No hepatotoxicity, unlike oral anabolic steroids that undergo 17-alpha alkylation
06 Naturally occurring in common foods (spinach, quinoa), with a long history of safe dietary exposure
07 Compatible with other performance compounds due to its non-hormonal mechanism
08 Available as a dietary supplement without prescription in most jurisdictions
RAD-140
01 Potent anabolic activity in muscle tissue with high oral bioavailability
02 Tissue-selective action sparing the prostate and other androgen-sensitive organs
03 No aromatization to estrogen (no estrogen-related side effects such as water retention or gynecomastia)
04 No conversion to DHT (reduced risk of hair loss and prostate stimulation compared to testosterone)
05 Long half-life (~60 hours) permitting convenient once-daily oral dosing
06 Neuroprotective properties observed in preclinical models
07 Increased lean body mass and reduced fat mass in preclinical studies
Dosing Protocols
Ecdysterone
500-1000 mg/day (oral) or 50-100 mg/day (injectable) / 1-2x daily
Enhanced Anabolic Effect / Higher Bioavailability 50-100 mg/day Once daily
RAD-140
10-20 mg/day / Once daily (oral)
Side Effects
Ecdysterone
Mild gastrointestinal discomfort (nausea, bloating, or stomach upset) with oral doses, particularly at higher dosages taken without food
Injection site pain, redness, or mild swelling with injectable administration
RAD-140
Testosterone suppression (dose-dependent, occurs in virtually all users by week 4-6)
Liver enzyme elevation (ALT, AST increases reported in clinical and anecdotal data)
Hair shedding (temporary, typically resolves after discontinuation)
Headaches (most common in the first 1-2 weeks, often transient)
Nausea (mild, usually with initial doses or on an empty stomach)
Lipid disruption (HDL suppression, LDL elevation)
Mild insomnia or sleep disturbance
Reduced libido and mood changes related to testosterone suppression
Contraindications
Known allergy to ecdysteroids or spinach-derived compounds
Pregnancy and breastfeeding (insufficient safety data)
Individuals with estrogen-sensitive conditions should consult a physician, though ERbeta activation is generally considered protective rather than proliferative
Pre-existing liver disease or elevated liver enzymes at baseline
Hormone-sensitive cancers (prostate cancer, certain breast cancers not being treated under clinical supervision)
Pregnancy or potential pregnancy (teratogenic risk from androgen receptor agonism)
Breastfeeding
Age under 25 (incomplete endocrine system maturation and higher risk of HPG axis disruption)
Concurrent use of hepatotoxic medications without medical supervision
Known cardiovascular disease (insufficient safety data for this population)
Research Evidence
Ecdysterone RAD-140
Status Moderate Research Emerging
References 5 studies 5 studies
Latest 2020 July 2020
FDA Approved No No
This comparison is for educational and research purposes only. Consult a healthcare professional before use.