1104606-57-6 Usage
Uses
Used in Medicinal Chemistry:
Boc-6-bromo-DL-tryptophan is used as a building block for the synthesis of peptides and proteins, allowing researchers to create novel compounds with potential therapeutic applications. Its unique structure, featuring the bromine substitution and the Boc protecting group, enables the development of modified peptides and proteins with enhanced or altered biological activities.
Used in Drug Development:
In the pharmaceutical industry, Boc-6-bromo-DL-tryptophan is utilized as a key component in the design and synthesis of new drugs. Its incorporation into peptide sequences can lead to the discovery of innovative therapeutic agents with improved efficacy, selectivity, and pharmacokinetic properties.
Used in Research and Development:
Boc-6-bromo-DL-tryptophan serves as an important tool for researchers who are interested in studying the structure and function of peptides and proteins. By incorporating Boc-6-bromo-DL-tryptophan into peptide sequences, scientists can gain insights into the relationship between peptide structure and biological activity, which can inform the design of new drugs and therapeutic agents.
Overall, Boc-6-bromo-DL-tryptophan is a versatile and valuable compound in the fields of medicinal chemistry, drug development, and research, offering numerous applications for the creation and study of novel peptides and proteins with potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 1104606-57-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,6,0 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1104606-57:
(9*1)+(8*1)+(7*0)+(6*4)+(5*6)+(4*0)+(3*6)+(2*5)+(1*7)=106
106 % 10 = 6
So 1104606-57-6 is a valid CAS Registry Number.
1104606-57-6Relevant academic research and scientific papers
Boyd, Emily M.,Sperry, Jonathan
, p. 5056 - 5059 (2014)
The total synthesis of (-)-aspergilazine A, an alkaloid possessing a rare N1′ to C6 bisindole bond, is described. A palladium-catalyzed N-arylation was used to selectively install the N1′-C6 bond in the presence of three other possible arylation sites. The ligand XPhos displayed a unique capability to efficiently carry out the N-arylation while simultaneously suppressing epimerization of the sensitive C9 stereocenters. This total synthesis has confirmed that aspergilazine A is a dimer of brevianamide F.
Shaker, Kamel H.,G?hl, Matthias,Müller, Tobias,Seifert, Karlheinz
, p. 1746 - 1755 (2015)
The two new indole alkaloids 2-amino-1,5-dihydro-5-(1H-indol-3-ylmethyl)-4H-imidazol-4-one (1), 2-amino-5-[(6-bromo-1H-indol-3-yl)methyl]-3,5-dihydro-3-methyl-4H-imidazol-4-one (2), and auramine (3) have been isolated from the sea anemone Heteractis auror
