Averlane Labs
TBL150(rad150) 100x10mg

TBL150(rad150) 100x10mg

€77.50
approx $84.50

Certificate of Analysis available on request for the current lot.

These are research-grade materials for laboratory use only. Not for human or veterinary use, consumption, or clinical application.

Complete the setup

Reconstitution and bench supplies researchers pair with TBL150(rad150) 100x10mg

NOT FOR HUMAN CONSUMPTION

TLB-150 (RAD-150 benzoate) is an investigational, non-steroidal selective androgen receptor modulator (SARM). It is widely described as the benzoate ester analogue of RAD-140 (testolone), engineered to maintain AR selectivity while potentially extending exposure versus the parent scaffold. In vitro vendor data list potent AR modulation in the sub-micromolar range; no approved medical indication or registrational trials exist. 


Additional Benefits of TLB-150 Now Under Investigation

Benefit Key take-aways
1 Duration/steadiness vs RAD-140 The benzoate ester is promoted to prolong active lifespan and smooth concentration–time curves compared with RAD-140; this remains unverified in humans. Sports Technology Labs
2 Muscle anabolism (class effect) As an AR agonist, TLB-150 is positioned to increase fat-free mass and strength similarly to first-gen SARMs, direct human efficacy data for TLB-150 are absent.
3 Bone support (class effect) SARMs up-regulate osteoblast pathways and improve BMD in animals; TLB-150 is presumed comparable pending direct studies.
4 Oral convenience Once-daily oral SARM paradigms favor adherence vs injectables; specific TLB-150 PK in humans is unknown.
5 Potentially lower androgenic “baggage” Like other non-steroidal SARMs, design intent is muscle/bone selectivity with less prostate/skin stimulation than testosterone, needs confirmation.
6 Research-use positioning Commercial listings emphasize research-use only and lack of regulatory approval. medchemexpress.com
7 SARM-class synergy with resistance training Expect additivity with structured training/protein adequacy (extrapolated from SARM literature).
8 Dosing flexibility If ester prolongation holds, lower/fewer doses could yield similar exposure (hypothesis). Sports Technology Labs
9 Doping relevance As a SARM, TLB-150 would be prohibited at all times under WADA S1 (Anabolic Agents). U.S. Anti-Doping Agency (USADA)wada-ama.org

2. Molecular Mechanism of Action

2.1 Receptor Pharmacodynamics

TLB-150 binds the androgen receptor (AR), promoting nuclear translocation and ARE-driven transcription. In muscle, AR activation up-regulates mTOR/S6K and suppresses atrogenes (MAFbx/MuRF1); in bone, AR signaling supports osteoblastogenesis and trabecular integrity (inferred from SARM class biology).

2.2 Down-stream Biology

Pathway Functional outcome Context
AR → mTOR/S6K/4E-BP1 ↑ Protein synthesis, myofiber hypertrophy Skeletal muscle
AR ↔ Wnt/β-catenin/Osterix ↑ Osteoblast activity, ↑ BMD Bone
↓ FoxO/ubiquitin ligases ↓ Proteolysis (anti-catabolic) Catabolic stress
HPG-axis feedback ↓ LH/FSH/testosterone (suppression) Pituitary–gonadal

3. Pharmacokinetics

  • Route: Oral (research use).

  • Design rationale: Benzoate esterification of RAD-140 intended to enhance stability and effective half-life; quantitative human PK is undetermined. Sports Technology Labs

  • Metabolism/clearance: Expected ester hydrolysis → RAD-140-like core + oxidative/conjugative metabolism; formal human data unavailable.

  • Detection: As a SARM, long-term metabolites may extend detection windows in doping control (extrapolated from class).


4. Pre-clinical and Translational Evidence

4.1 Identity & in-vitro profiling

Commercial technical sheets list AR modulation with sub-µM potency and CAS 1208070-53-4; peer-reviewed in-vivoefficacy for TLB-150 specifically is limited/publicly sparse. medchemexpress.com

4.2 Extrapolation from RAD-140/SARM literature

Anabolic FFM gains, strength improvements, and bone protection are well described for earlier SARMs in animals and small human studies; whether TLB-150 surpasses RAD-140 clinically is unknown.

Evidence quality note: TLB-150 data are largely vendor-level and pre-clinical; there are no authoritative human RCTs or approvals.


5. Emerging Clinical Interests

Field Rationale Current status
Sarcopenia/rehab Oral anabolic with putative longer exposure Concept/extrapolation
Osteopenia Bone-anabolic SARM class biology Pre-clinical rationale
Male contraception research Strong HPG suppression is a SARM class effect, unproven for TLB-150 Hypothesis only
Athletics (illicit use) Oral potency + duration = high misuse potential WADA-prohibited U.S. Anti-Doping Agency (USADA)

6. Safety and Tolerability

  • Known/expected class effects:
    HPG-axis suppression (↓ LH/FSH/testosterone), HDL-C reduction (± ↑ LDL/TG), possible ALT/AST elevations, acne/oily skin, mood/insomnia, mild ↑ hematocrit.

  • Unknowns for TLB-150: Human PK, dose–response, long-term hepatic/CV outcomes, neuropsychiatricsignals.

  • Quality risks: Grey-market products show adulteration/mislabeling; use outside trials is unsafe.

  • Drug interactions: Potential hepatic enzyme interactions (class consideration).

  • Pregnancy: Contraindicated (androgenic mechanism).

Comparative safety matrix

Concern TLB-150 (RAD-150) RAD-140 (testolone) Enobosarm (MK-2866)
Oral potency Presumed high (unverified) High (preclinical + forensic) Moderate–high (human Phase 2)
Duration Designed longer (ester) Shorter vs ester ~24 h
Human data None/very limited Limited (non-pivotal) Phase 2 datasets
HDL impact Expected
HPG suppression Likely strong Strong Moderate

7. Regulatory Landscape


8. Future Directions

  • Authentic PK/PD: First-in-human GMP studies to define half-life, exposure, metabolite ID, and dose–response.

  • Head-to-head vs RAD-140: Demonstrate superiority (duration/efficacy/safety), not just parity.

  • Long-term safety: Lipids/CV, hepatic, endocrine recovery; standardized monitoring.

  • Doping science: Metabolite mapping and detection windows.

  • Medicinal chemistry: Optimize lipid neutrality and reduced HPG suppression without losing anabolism.


Selected References

  • MedChemExpress technical page: “TLB-150 Benzoate (RAD-150), AR modulator; CAS 1208070-53-4; research-use only.” medchemexpress.com

  • Vendor/scientific summaries describing RAD-150 as the benzoate ester of RAD-140 with prolonged activity claims. Sports Technology LabsLawless Labs USA

  • USADA: “All SARMs are prohibited at all times (S1 ‘Other Anabolic Agents’).” U.S. Anti-Doping Agency (USADA)

  • WADA Prohibited List (2025), International Standard.

 

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