Cyclosporin D, 95%, from Micromonospora

95%

Reagent Code: #162770
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CAS Number 63775-96-2

science Other reagents with same CAS 63775-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1216.64 g/mol
Formula C₆₃H₁₁₃N₁₁O₁₂
badge Registry Numbers
MDL Number MFCD11111526
thermostat Physical Properties
Melting Point 148-151 °C (lit.)
inventory_2 Storage & Handling
Storage −20°C

description Product Description

Used in immunosuppressive research to study T-cell activation and immune response modulation. Employed in pharmaceutical development for organ transplant models due to its ability to inhibit calcineurin, a key enzyme in immune signaling. Also utilized in cancer research for its potential to reverse multidrug resistance in tumor cells by inhibiting P-glycoprotein efflux pumps. Commonly applied in in vitro studies requiring selective immunosuppression or investigation of cellular transport mechanisms.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿19,220.00

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Cyclosporin D, 95%, from Micromonospora
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Used in immunosuppressive research to study T-cell activation and immune response modulation. Employed in pharmaceutical development for organ transplant models due to its ability to inhibit calcineurin, a key enzyme in immune signaling. Also utilized in cancer research for its potential to reverse multidrug resistance in tumor cells by inhibiting P-glycoprotein efflux pumps. Commonly applied in in vitro studies requiring selective immunosuppression or investigation of cellular transport mechanisms.

Used in immunosuppressive research to study T-cell activation and immune response modulation. Employed in pharmaceutical development for organ transplant models due to its ability to inhibit calcineurin, a key enzyme in immune signaling. Also utilized in cancer research for its potential to reverse multidrug resistance in tumor cells by inhibiting P-glycoprotein efflux pumps. Commonly applied in in vitro studies requiring selective immunosuppression or investigation of cellular transport mechanisms.

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