Vesilute
Also known as: Peptídeo da bexiga, Peptídeo urinário
Molecular Identifiers
Molecular Formula
C9H14N2O7
CAS Number
3918-84-1
PubChem CID
99716UNII
38Y324JU2X
Molecular Weight
262.22 Da
Overview
Urinary tract bioregulatory dipeptide developed by the Khavinson group. Acts on the bladder epithelium, regulating gene expression and supporting bladder function. Marketed in Russian pharmacies as an oral capsule formulation for urological support in short cycles.
Vesilute is presented as a short urinary tract bioregulator acting on the bladder epithelium, with proposed normalization of gene expression in vesical tissue. The clinical effect described in the Russian literature is support for urinary function, particularly in lower urinary tract aging and mild functional complaints.
Outside Russia, Vesilute has no regulatory approval or recognized clinical indication. The product is marketed in Russian pharmacies as oral capsules (RLS registry), typically in short cycles of 20–30 days, repeated every 4–6 months. In other markets it is dispensed by compounding pharmacies as off-label use. The evidence base is predominantly Russian, with few independent human clinical trials.
Within the Khavinson family, Vesilute sits on the urogenital axis alongside Prostamax (prostate) and Testagen (testicular): each is proposed as a tissue-specific bioregulator of the urogenital apparatus, distinguished more by proposed target tissue than by overall mechanism. All of this comparative literature is largely Russian and preclinical.
ED Glu-Asp Half-life
~2-4 hours
Administration Route
Subcutaneous or intramuscular
Category
Specialized Research
Mechanism of Action
- Regulation of gene expression in the bladder epithelium
- Support for detrusor and trigone function
- Modulation of urothelium cell renewal
- Bioregulatory effect on the lower urinary tract
- Protection of the bladder epithelium against age-related changes
Dosage Protocol
Data compiled from the literature. This does not constitute medical advice.
| Parameter | Value |
|---|---|
| Dose | 1-2 capsules orally (0.2 g per capsule, containing AKS-M peptide complex) |
| Frequency | 1-2 times daily, with meals |
| Timing | With meals |
| Duration | 20-30 days per cycle, repeat the course every 4-6 months |
Reported Side Effects
Adverse effects described in the literature. Severity and frequency vary between individuals.
- Injection site pain
- Local redness (rare)
Product Properties
| Purity | >95% |
| Appearance | White lyophilized powder |
| Solubility | Soluble in water and bacteriostatic water |
| Source | Solid-phase peptide synthesis (SPPS) |
| Storage | Lyophilized: -20°C for up to 2 years, 2-8°C for up to 6 months. Reconstituted: 2-8°C for up to 4 weeks. Protect from light and moisture. Avoid repeated freeze-thaw cycles. |
Presentations & Preparation
Vials of Vesilute found in the research market:
Reconstitution
- Diluent: Bacteriostatic water
- Volume: 2 ml per vial
- Inject the diluent slowly against the vial wall
- Gently swirl until fully dissolved
- Never shake
Storage
- Lyophilized: Refrigerated 2-8°C
- Reconstituted: Refrigerated 2-8°C (up to 30 days)
- Protect from direct light
- Do not freeze after reconstitution
Scientific Studies
Published studies on Vesilute.
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50-150 mcg per administration (IV or subcutaneous) · 1-3 times daily per protocol
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Bronchogen
1-2 capsules orally (0.2 g per capsule, containing AKS-B peptide complex) · 1-2 times daily, with meals
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