N-((S)-1-(((S)-4-Hydroxy-3-oxo-1-((S)-2-oxopyrrolidin-3-yl)butan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)-4-methoxy-1H-indole-2-carboxamide

95%

Reagent Code: #219922
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CAS Number 870153-29-0

science Other reagents with same CAS 870153-29-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 944.0599999999999 g/mol
Formula C₂₄H₃₂N₄O₆
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used in pharmaceutical research as a proteolysis targeting chimera (PROTAC) linker component, enabling targeted protein degradation. Demonstrates potential in oncology for modulating disease-causing proteins by facilitating their ubiquitination and subsequent degradation via the proteasome pathway. Exhibits cell permeability and stability in biological systems, making it suitable for in vitro and in vivo studies focused on cancer therapeutics. Also employed in the development of molecular glues and bifunctional molecules designed to induce protein-protein interactions for therapeutic intervention.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿16,080.00
N-((S)-1-(((S)-4-Hydroxy-3-oxo-1-((S)-2-oxopyrrolidin-3-yl)butan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)-4-methoxy-1H-indole-2-carboxamide
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Used in pharmaceutical research as a proteolysis targeting chimera (PROTAC) linker component, enabling targeted protein degradation. Demonstrates potential in oncology for modulating disease-causing proteins by facilitating their ubiquitination and subsequent degradation via the proteasome pathway. Exhibits cell permeability and stability in biological systems, making it suitable for in vitro and in vivo studies focused on cancer therapeutics. Also employed in the development of molecular glues and bifun

Used in pharmaceutical research as a proteolysis targeting chimera (PROTAC) linker component, enabling targeted protein degradation. Demonstrates potential in oncology for modulating disease-causing proteins by facilitating their ubiquitination and subsequent degradation via the proteasome pathway. Exhibits cell permeability and stability in biological systems, making it suitable for in vitro and in vivo studies focused on cancer therapeutics. Also employed in the development of molecular glues and bifunctional molecules designed to induce protein-protein interactions for therapeutic intervention.

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