(R)-Lipoamido-peg8-acid

95%

Reagent Code: #105985
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CAS Number 1334172-70-1

science Other reagents with same CAS 1334172-70-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 629.82 g/mol
Formula C₂₇H₅₁NO₁₁S₂
badge Registry Numbers
MDL Number MFCD21363243
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in bioconjugation and drug delivery systems, this compound serves as a linker to attach therapeutic agents to targeting molecules or nanoparticles. Its PEG (polyethylene glycol) chain enhances solubility and stability, while the lipoamide group facilitates binding to biomolecules. It is particularly valuable in developing targeted cancer therapies, where it helps deliver drugs specifically to tumor cells, minimizing off-target effects. Additionally, it is employed in research for modifying proteins or peptides to improve their pharmacokinetic properties.

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inventory 1g
10-20 days ฿16,002.00

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(R)-Lipoamido-peg8-acid
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Used in bioconjugation and drug delivery systems, this compound serves as a linker to attach therapeutic agents to targeting molecules or nanoparticles. Its PEG (polyethylene glycol) chain enhances solubility and stability, while the lipoamide group facilitates binding to biomolecules. It is particularly valuable in developing targeted cancer therapies, where it helps deliver drugs specifically to tumor cells, minimizing off-target effects. Additionally, it is employed in research for modifying proteins

Used in bioconjugation and drug delivery systems, this compound serves as a linker to attach therapeutic agents to targeting molecules or nanoparticles. Its PEG (polyethylene glycol) chain enhances solubility and stability, while the lipoamide group facilitates binding to biomolecules. It is particularly valuable in developing targeted cancer therapies, where it helps deliver drugs specifically to tumor cells, minimizing off-target effects. Additionally, it is employed in research for modifying proteins or peptides to improve their pharmacokinetic properties.

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