Romidepsin

98%

Reagent Code: #54001
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CAS Number 128517-07-7

science Other reagents with same CAS 128517-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 540.70 g/mol
Formula C₂₄H₃₆N₄O₆S₂
badge Registry Numbers
MDL Number MFCD18433404
thermostat Physical Properties
Melting Point 219-224°C
inventory_2 Storage & Handling
Density 1.174g/cm3
Storage -20°C

description Product Description

Romidepsin is primarily used in the treatment of cutaneous T-cell lymphoma (CTCL) and peripheral T-cell lymphoma (PTCL), particularly in patients who have not responded to other therapies. It works by inhibiting histone deacetylase, which helps to regulate gene expression and can lead to the death of cancer cells. This makes it a valuable option for those with relapsed or refractory forms of these cancers. Additionally, its ability to induce cell cycle arrest and apoptosis in malignant cells has sparked interest in exploring its potential for treating other types of cancers and diseases involving abnormal cell growth. Research is ongoing to evaluate its efficacy in combination with other therapies and in broader oncological applications.

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Test Parameter Specification
Appearance White Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿22,990.00
inventory 1mg
10-20 days ฿6,570.00

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Romidepsin
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Romidepsin is primarily used in the treatment of cutaneous T-cell lymphoma (CTCL) and peripheral T-cell lymphoma (PTCL), particularly in patients who have not responded to other therapies. It works by inhibiting histone deacetylase, which helps to regulate gene expression and can lead to the death of cancer cells. This makes it a valuable option for those with relapsed or refractory forms of these cancers. Additionally, its ability to induce cell cycle arrest and apoptosis in malignant cells has sparked

Romidepsin is primarily used in the treatment of cutaneous T-cell lymphoma (CTCL) and peripheral T-cell lymphoma (PTCL), particularly in patients who have not responded to other therapies. It works by inhibiting histone deacetylase, which helps to regulate gene expression and can lead to the death of cancer cells. This makes it a valuable option for those with relapsed or refractory forms of these cancers. Additionally, its ability to induce cell cycle arrest and apoptosis in malignant cells has sparked interest in exploring its potential for treating other types of cancers and diseases involving abnormal cell growth. Research is ongoing to evaluate its efficacy in combination with other therapies and in broader oncological applications.

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