Alloc-Val-Ala-PAB-OH

≥97%(LC&N)

Reagent Code: #137288
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CAS Number 1343407-91-9

science Other reagents with same CAS 1343407-91-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 377.44 g/mol
Formula C₁₉H₂₇N₃O₅
thermostat Physical Properties
Melting Point 227 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents to cancer cells. The Alloc group acts as a protecting group that can be selectively removed under mild conditions, allowing precise control during synthesis. The PAB (para-aminobenzyloxycarbonyl) spacer enables efficient release of the drug payload inside the cell through enzymatic cleavage, enhancing therapeutic efficacy while minimizing off-target effects. Commonly employed in the development of novel anticancer agents where controlled drug activation is critical.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,850.00

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Alloc-Val-Ala-PAB-OH
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Used as a linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents to cancer cells. The Alloc group acts as a protecting group that can be selectively removed under mild conditions, allowing precise control during synthesis. The PAB (para-aminobenzyloxycarbonyl) spacer enables efficient release of the drug payload inside the cell through enzymatic cleavage, enhancing therapeutic efficacy while minimizing off-target effects. Commonly employed in the development of novel an

Used as a linker in antibody-drug conjugates (ADCs), enabling targeted delivery of cytotoxic agents to cancer cells. The Alloc group acts as a protecting group that can be selectively removed under mild conditions, allowing precise control during synthesis. The PAB (para-aminobenzyloxycarbonyl) spacer enables efficient release of the drug payload inside the cell through enzymatic cleavage, enhancing therapeutic efficacy while minimizing off-target effects. Commonly employed in the development of novel anticancer agents where controlled drug activation is critical.

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