Bemethyl Free Base

Bemethyl free base is a scientifically recognized actoprotector and metabolic enhancer, exerting ergogenic, neuroprotective, and antioxidant effects. Its applications extend to military, sports science, and neuropharmacology research, making it a promising investigational compound for optimizing physiological and cognitive performance under stressful conditions.

For a more detailed description and lab analysis, please see the sections below.

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Bemethyl Free Base, Powder

Bemethyl free base, chemically known as 2-(ethylthio)benzimidazole, is a synthetic benzimidazole derivative exhibiting actoprotective, antihypoxic, and metabolic-modulating properties. It was initially synthesized in the Soviet Union for military, cosmonaut, and sports applications, particularly for enhancing physiological endurance and cognitive resilience under extreme conditions.

Pharmacodynamics and Mechanism of Action

Bemethyl exhibits actoprotective activity, which is characterized by its ability to enhance adaptive metabolic responses under hypoxic stress conditions. The compound exerts its effects primarily through:

  1. Mitochondrial Biogenesis and Metabolic Modulation
    • Increases mitochondrial enzyme activity, enhancing oxidative phosphorylation efficiency and ATP synthesis.
    • Upregulates RNA and protein synthesis, improving cellular metabolism and repair mechanisms under physiological stress.
  2. Antioxidant and Free Radical Scavenging Activity
    • Upregulates endogenous superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT), mitigating oxidative stress-induced cellular damage.
    • Reduces lipid peroxidation and protein carbonylation, preserving membrane integrity and enzyme activity.
  3. Neuroprotective and Psychostimulant Effects
    • Enhances cholinergic neurotransmission and modulates dopaminergic pathways, contributing to cognitive enhancement and mental endurance.
    • Attenuates neuroinflammatory processes, reducing glial activation and neurodegeneration.

Pharmacokinetics and Metabolism

  • Absorption: Bemethyl demonstrates rapid gastrointestinal absorption, reaching peak plasma concentrations within 1-2 hours post-administration.
  • Distribution: The compound exhibits high lipid solubility, facilitating efficient blood-brain barrier (BBB) penetration and accumulation in neural and muscular tissues.
  • Metabolism: Primary metabolic transformation occurs via glutathione conjugation, yielding benzimidazole-acetylcysteine metabolites.
  • Excretion: Eliminated primarily via renal clearance, with metabolites detected in urine up to 48 hours post-ingestion.

Applications and Research Context

1. Military and Aerospace Medicine

  • Used by cosmonauts and military personnel to enhance physiological resilience in hypoxic and high-G force environments.
  • Supports adaptation to extreme climates, including high-altitude and deep-sea conditions.

2. Sports Science and Exercise Physiology

  • Investigated for its ergogenic potential, increasing VO₂ max and mitochondrial oxidative capacity.
  • Enhances recovery rates post-exercise by reducing lactic acid accumulation.

3. Neuropharmacology and Cognitive Enhancement

  • Studied for its potential in cognitive enhancement, particularly in neurodegenerative conditions such as Alzheimer’s and Parkinson’s disease.
  • Reduces mental fatigue and improves working memory, possibly via modulation of acetylcholine synthesis.
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Description

Bemethyl Free Base, Powder

Bemethyl free base, chemically known as 2-(ethylthio)benzimidazole, is a synthetic benzimidazole derivative exhibiting actoprotective, antihypoxic, and metabolic-modulating properties. It was initially synthesized in the Soviet Union for military, cosmonaut, and sports applications, particularly for enhancing physiological endurance and cognitive resilience under extreme conditions.

Pharmacodynamics and Mechanism of Action

Bemethyl exhibits actoprotective activity, which is characterized by its ability to enhance adaptive metabolic responses under hypoxic stress conditions. The compound exerts its effects primarily through:

  1. Mitochondrial Biogenesis and Metabolic Modulation
    • Increases mitochondrial enzyme activity, enhancing oxidative phosphorylation efficiency and ATP synthesis.
    • Upregulates RNA and protein synthesis, improving cellular metabolism and repair mechanisms under physiological stress.
  2. Antioxidant and Free Radical Scavenging Activity
    • Upregulates endogenous superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT), mitigating oxidative stress-induced cellular damage.
    • Reduces lipid peroxidation and protein carbonylation, preserving membrane integrity and enzyme activity.
  3. Neuroprotective and Psychostimulant Effects
    • Enhances cholinergic neurotransmission and modulates dopaminergic pathways, contributing to cognitive enhancement and mental endurance.
    • Attenuates neuroinflammatory processes, reducing glial activation and neurodegeneration.

Pharmacokinetics and Metabolism

  • Absorption: Bemethyl demonstrates rapid gastrointestinal absorption, reaching peak plasma concentrations within 1-2 hours post-administration.
  • Distribution: The compound exhibits high lipid solubility, facilitating efficient blood-brain barrier (BBB) penetration and accumulation in neural and muscular tissues.
  • Metabolism: Primary metabolic transformation occurs via glutathione conjugation, yielding benzimidazole-acetylcysteine metabolites.
  • Excretion: Eliminated primarily via renal clearance, with metabolites detected in urine up to 48 hours post-ingestion.

Applications and Research Context

1. Military and Aerospace Medicine

  • Used by cosmonauts and military personnel to enhance physiological resilience in hypoxic and high-G force environments.
  • Supports adaptation to extreme climates, including high-altitude and deep-sea conditions.

2. Sports Science and Exercise Physiology

  • Investigated for its ergogenic potential, increasing VO₂ max and mitochondrial oxidative capacity.
  • Enhances recovery rates post-exercise by reducing lactic acid accumulation.

3. Neuropharmacology and Cognitive Enhancement

  • Studied for its potential in cognitive enhancement, particularly in neurodegenerative conditions such as Alzheimer’s and Parkinson’s disease.
  • Reduces mental fatigue and improves working memory, possibly via modulation of acetylcholine synthesis.

Additional information

Size

10g, 20g, 50g

Lab Analysis


Product PDF Preview

COA_Bemethyl_lot-221024_2024-10-25

Chemical Informations

CAS 14610-11-8
Molar Mass 178.26 g/mol
Chemical Formula C₉H₁₀N₂S
IUPAC Name 2-Ethylsulfanyl-1H-benzimidazole
Synonyms 1H-Benzimidazole,2-(ethylthio)-(9CI)/2-mercaptoethylbenzimidazole/MFCD00223154/2-(Ethylthio)benzimidazole/2S44TEQ96E/2-(ethylsulfanyl)-1H-benzimidazole/Bemithyl/2-ethylthiobenzimidazole/Bemetil/Bemythyl/2-(Ethylsulfanyl)benzimidazole; 2-(Ethylthio)benzimidazole; /2-Mercaptoethylbenzimidazole/CDS1_000187/Maybridge1_002475
PubChem SID
Solubility

Soluble in dimethyl sulfoxide (DMSO), slightly soluble in ethanol, and insoluble in water

Organoleptic Profile Off-white powder
Physical Form Solid
Specification ≥99%

Storage Conditions

  • Temperature: Store at 2-8°C for long-term stability. Can be stored at ambient temperature (15-25°C) for short periods.
  • Light Sensitivity: Keep away from direct sunlight and UV exposure.
  • Moisture Protection: Store in an airtight container to prevent degradation.
  • Shelf Life: Stable for up to 2 years under recommended conditions.

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