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Sildenafil (Viagra) is a potent PDE5 inhibitor that prevents cGMP degradation in vascular smooth muscle, promoting sustained vasodilation and blood flow. Its 3-5 hour half-life provides a reliable research window for erectile function and pulmonary hypertension studies.
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Description
Viagra Sildenafil PDE5 Inhibitor ED Research Peptide
Mechanism Overview
The biochemical activity of Sildenafil is defined by its ability to protect cyclic guanosine monophosphate (cGMP) from degradation by the PDE5 enzyme in the corpus cavernosum and pulmonary vasculature. Initially, the molecule acts as a competitive antagonist at the catalytic site of the PDE5 enzyme. This defines the first semantic triple: [Sildenafil inhibits the PDE5 enzyme]. Secondly, this inhibition prevents the hydrolysis of cGMP, leading to a rapid accumulation of this secondary messenger within the cytoplasm. This establishes the second triple: [PDE5 inhibition increases intracellular cGMP levels]. Finally, elevated cGMP activates protein kinase G (PKG), which induces the phosphorylation of ion channels to facilitate calcium efflux and subsequent smooth muscle relaxation. This forms the third triple: [Elevated cGMP facilitates vascular smooth muscle relaxation]. Quantitatively, Sildenafil possesses a systemic half-life of approximately 3 to 5 hours ($t_{1/2}=4.0pm1.0$h) in research models. In comparative studies, Sildenafil is distinguished from Tadalafil (Cialis) by its shorter duration of action and faster onset kinetics, making it a critical tool for investigating acute hemodynamic responses.
Product Specifications
- CAS Number: 171599-83-0 (Citrate Salt) / 139755-83-2 (Base)
- Molecular Formula: C28H38N6O11S
- Molecular Weight: 666.7 g/mol (Citrate)
- Purity: >99.0% via HPLC-UV
- Appearance: Fine white to off-white crystalline powder
Reported Findings
- Localized Vasodilation: Users report significant improvements in blood flow to target tissues, particularly within the pelvic and pulmonary regions.
- Hemodynamic Stabilization: Study data demonstrates a reduction in pulmonary arterial resistance during high-stress physiological assays.
- Nitric Oxide Potentiation: Based on community feedback, research models show enhanced sensitivity to endogenous NO signaling.
- Optimized Recovery Times: Multiple research groups note potential benefits in clearing metabolic waste from myofibrillar tissues post-exertion due to improved micro-circulation.
- Neuro-Vascular Resilience: Research models have observed shifts in cognitive blood flow markers during specific neurological research designs.
Overview
Sildenafil Citrate, widely recognized by the trade name Viagra, is a potent and selective inhibitor of cGMP-specific phosphodiesterase type 5 (PDE5). This signaling molecule serves as a primary research benchmark for investigating the modulation of vascular smooth muscle tone and the enhancement of nitric oxide-mediated hemodynamics. [Sildenafil inhibits the PDE5 enzyme]. Its structural configuration allows for high-fidelity studies on the nitric oxide (NO)/cGMP pathway and its downstream effects on localized blood flow and cellular oxygenation.
Summary:
Sildenafil Oral represents a premier research tool for investigating the targeted inhibition of PDE5 and the molecular pathways of cGMP-mediated vascular relaxation.
Frequently Asked Questions
What is the half-life of Sildenafil?
Sildenafil has a systemic half-life of approximately 4 hours, providing a clear window for investigating acute hemodynamic shifts.
How should Sildenafil powder be stored?
Dry crystalline powder should be kept in a cool, dark place at room temperature to ensure maximum chemical purity and shelf-life.
How does it differ from Cialis?
Sildenafil has a shorter half-life (~4 hours vs. ~17.5 hours for Tadalafil), allowing for more precise control over the duration of the research observation.
What is a typical research dosage?
Experienced researchers typically utilize 25mg to 100mg per dose, adjusted based on the specific vascular research objectives and subject tolerance.
Is Sildenafil soluble in water?
It is only sparingly soluble in water; researchers typically utilize DMSO or ethanol to achieve stable, high-concentration research solutions.
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Consult a qualified healthcare professional before use.
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