33599-61-0 Usage
Uses
Used in Pharmaceutical Research:
6-BROMO-DL-TRYPTOPHAN is used as a research tool for studying protein structure and enzyme kinetics, aiding in the understanding of fundamental biological processes and the development of new therapeutic strategies.
Used in Neurological Disorder Treatment:
6-BROMO-DL-TRYPTOPHAN is used as a potential therapeutic agent for neurological disorders, leveraging its biochemical properties to address specific conditions affecting the nervous system.
Used in Oncology:
6-BROMO-DL-TRYPTOPHAN is used as an investigational compound in cancer treatment, with studies exploring its effects on tumor growth and its potential synergistic benefits when combined with conventional chemotherapy.
Used in Inflammatory Condition Management:
6-BROMO-DL-TRYPTOPHAN is used in the research and potential treatment of inflammatory conditions, examining its impact on inflammatory pathways and immune responses.
Used in Synthesis of Novel Pharmaceuticals:
6-BROMO-DL-TRYPTOPHAN is used as a key component in the synthesis of new pharmaceuticals, contributing to the discovery of innovative drugs with unique mechanisms of action.
Used in Fluorescent Probe Development:
6-BROMO-DL-TRYPTOPHAN is used as a fluorescent probe in various biological assays, providing a means to track and visualize specific molecular interactions and cellular processes.
Used in Synthesis of Biologically Active Compounds:
6-BROMO-DL-TRYPTOPHAN is used as a precursor in the synthesis of other biologically active compounds, expanding its utility in the creation of new therapeutic agents and diagnostic tools.
Check Digit Verification of cas no
The CAS Registry Mumber 33599-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,9 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33599-61:
(7*3)+(6*3)+(5*5)+(4*9)+(3*9)+(2*6)+(1*1)=140
140 % 10 = 0
So 33599-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrN2O2/c12-7-1-2-8-6(3-9(13)11(15)16)5-14-10(8)4-7/h1-2,4-5,9,14H,3,13H2,(H,15,16)/t9-/m0/s1
33599-61-0Relevant academic research and scientific papers
Total synthesis of (-)-aspergilazine A
Boyd, Emily M.,Sperry, Jonathan
supporting information, p. 5056 - 5059 (2015/02/19)
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.
TOTAL SYNTHESIS OF TETRAACETYL CLIONAMIDE
Schmidt, Ulrich,Lieberknecht, Albrecht,Griesser, Helmut,Boekens, Hilmar
, p. 4911 - 4914 (2007/10/02)
Tetraacetyl clionamide, a 6-bromotryptophan derivative from the sponge Cliona celata was synthesized from gallic acid.
