PD 158780

≥97%

Reagent Code: #99149
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CAS Number 171179-06-9

science Other reagents with same CAS 171179-06-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.19 g/mol
Formula C₁₄H₁₂BrN₅
badge Registry Numbers
MDL Number MFCD00942160
thermostat Physical Properties
Melting Point 174-178°C
Boiling Point 499.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.611±0.06 g/cm3 (20 ºC 760 Torr)
Storage -20°C

description Product Description

PD 158780 is primarily used in research settings as a selective inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase. It is employed to study the role of EGFR signaling in various cellular processes, including cell proliferation, differentiation, and survival. Researchers utilize it to investigate the mechanisms of cancer development and progression, as EGFR is often overactive in many types of tumors. Additionally, PD 158780 is used to explore potential therapeutic strategies targeting EGFR in cancer treatment. Its ability to inhibit EGFR activity makes it a valuable tool in preclinical studies aimed at understanding and developing targeted therapies for EGFR-driven cancers.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Very pale yellow to yellow crystal/powder
Purity 96.5-100
Melting Point 174.0-178.0
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿11,880.00

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PD 158780
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PD 158780 is primarily used in research settings as a selective inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase. It is employed to study the role of EGFR signaling in various cellular processes, including cell proliferation, differentiation, and survival. Researchers utilize it to investigate the mechanisms of cancer development and progression, as EGFR is often overactive in many types of tumors. Additionally, PD 158780 is used to explore potential therapeutic strategies targeting EGFR in cancer treatment. Its ability to inhibit EGFR activity makes it a valuable tool in preclinical studies aimed at understanding and developing targeted therapies for EGFR-driven cancers.
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