1268837-82-6

Basic information

• Product Name: C₆₃H₁₁₈O₅
• Synonyms: C₆₃H₁₁₈O₅
• CAS NO: 1268837-82-6
• Molecular Weight: 955.627
• Mol File: 1268837-82-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₆₃H₁₁₈O₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₃H₁₁₈O₅(1268837-82-6)
• EPA Substance Registry System: C₆₃H₁₁₈O₅(1268837-82-6)

Safety Data

• Hazardous Substances Data: 1268837-82-6(Hazardous Substances Data)

Upstream product

• 831-61-8 Ethyl gallate 
• 112-89-0 1-Bromooctadecane 
• 149-91-7 3,4,5-trihydroxybenzoic acid 

Downstream Products

• 1268837-86-0 C₆₇H₁₁₇NO₇ 
• 1268837-88-2 C₆₇H₁₁₉NO₅ 
• 126229-90-1 3,4,5-tris(n-octadecan-1-yloxy)benzoic acid 
• 188685-36-1 3,4,5-tris(n-octadecan-1-yloxy)benzoyl chloride 
• 1221072-22-5 5-(azidomethyl)-1,2,3-tris(octadecyloxy)benzene 
• 256927-09-0 5-(chloromethyl)-1,2,3-tris(octadecyloxy)benzene 
• 955095-33-7 5-(bromomethyl)-1,2,3-tris(octadecyloxy)benzene 
• 233281-31-7 (3,4,5-trioctadecyloxyphenyl)methan-1-ol 

Relevant articles and documents

Rational Design of Supramolecular Dynamic Protein Assemblies by Using a Micelle-Assisted Activity-Based Protein-Labeling Technology

The self-assembly of proteins into higher-order superstructures is ubiquitous in biological systems. Genetic methods comprising both computational and rational design strategies are emerging as powerful methods for the design of synthetic protein complexes with high accuracy and fidelity. Although useful, most of the reported protein complexes lack a dynamic behavior, which may limit their potential applications. On the contrary, protein engineering by using chemical strategies offers excellent possibilities for the design of protein complexes with stimuli-responsive functions and adaptive behavior. However, designs based on chemical strategies are not accurate and therefore, yield polydisperse samples that are difficult to characterize. Here, we describe simple design principles for the construction of protein complexes through a supramolecular chemical strategy. A micelle-assisted activity-based protein-labeling technology has been developed to synthesize libraries of facially amphiphilic synthetic proteins, which self-assemble to form protein complexes through hydrophobic interaction. The proposed methodology is amenable for the synthesis of protein complex libraries with molecular weights and dimensions comparable to naturally occurring protein cages. The designed protein complexes display a rich structural diversity, oligomeric states, sizes, and surface charges that can be engineered through the macromolecular design. The broad utility of this method is demonstrated by the design of most sophisticated stimuli-responsive systems that can be programmed to assemble/disassemble in a reversible/irreversible fashion by using the pH or light as trigger.

HYDROPHOBIN MIMICS: PROCESS FOR PREPARATION THEREOF

The present invention discloses hydrophobin mimics of formula (I) comprising a protein head group, hydrophilic linker and hydrophobic tail and to a process for synthesis of library of hydrophobin mimics thereof. The hydrophobin mimics of the present invention self-assemble to form protein nanoparticles/nanocontainer either alone or in a specified chemical environment. The hydrophobin mimics (I) of the present invention find application in area of bio-nanotechnology.