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Available Variants1 g
CHA.38188-1g
Price
€66.64
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.38188-1g | €66.64 |
≥98% (TLC), suitable for ligand binding assays
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C23H28N2O5 |
|---|---|
| CAS Number | 4313-73-9 |
| Molecular Weight | 412.48 |
| UNSPSC Code | 12352209 |
| PubChem Substance ID | 24892360 |
| NACRES | NA.26 |
| MDL number | MFCD00038301 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
Z-Phe-Leu, also known by its CAS number 4313-73-9, is a synthetic dipeptide composed of phenylalanine and leucine. This compound is a protease inhibitor, specifically designed to inhibit the activity of certain enzymes involved in protein degradation. Z-Phe-Leu has been utilized in various biochemical and pharmacological studies to investigate its potential therapeutic applications, including the treatment of conditions characterized by excessive proteolytic activity. The compounds mechanism of action involves binding to the active site of target enzymes, thereby blocking their ability to cleave protein substrates. As a result, Z-Phe-Leu has been explored as a potential tool for understanding the role of proteases in various diseases and for developing novel therapeutic strategies to modulate their activity. Its inhibitory properties make it a valuable reagent in biomedical research and drug discovery efforts.
