52448-17-6 | (S)-2-Amino-3-(6-bromo-1h-indol-3-yl)propanoic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$53.00	$38.00
250mg	95%	in stock	$82.00	$58.00
1g	95%	in stock	$283.00	$198.00
5g	95%	in stock	$977.00	$684.00

Description

• Catalog Number: AG21418
• Chemical Name: (S)-2-Amino-3-(6-bromo-1h-indol-3-yl)propanoic acid
• CAS Number: 52448-17-6
• Molecular Formula: C11H11BrN2O2
• Molecular Weight: 283.1212
• MDL Number: MFCD17214433
• SMILES: OC(=O)[C@H](Cc1c[nH]c2c1ccc(c2)Br)N

Computed Properties

• Complexity: 275
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3
• XLogP3: -0.2

Literature

• Correlation between posttranslational modification and intrinsic disorder in protein.

  Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 20120101

• Characterization of the Conus bullatus genome and its venom-duct transcriptome.

  BMC genomics 20110101

• Bioactive dehydrotyrosyl and dehydrodopyl compounds of marine origin.

  Marine drugs 20100101

• Site-specific incorporation of tryptophan analogues into recombinant proteins in bacterial cells.

  Journal of the American Chemical Society 20070829

• Novel gamma-carboxyglutamic acid-containing peptides from the venom of Conus textile.

  The FEBS journal 20060601

• Screening for post-translational modifications in conotoxins using liquid chromatography/mass spectrometry: an important component of conotoxin discovery.

  Toxicon : official journal of the International Society on Toxinology 20060501

• A novel conotoxin from Conus delessertii with posttranslationally modified lysine residues.

  Biochemistry 20050823

• Total chemical synthesis and NMR characterization of the glycopeptide tx5a, a heavily post-translationally modified conotoxin, reveals that the glycan structure is alpha-D-Gal-(1-->3)-alpha-D-GalNAc.

  European journal of biochemistry 20041201

• Multiple 6-bromotryptophan residues in a sleep-inducing peptide.

  Biochemistry 20040928

• Cathelicidin family of antimicrobial peptides: proteolytic processing and protease resistance.

  Bioorganic chemistry 20031201

• Natural Peptide antibiotics from tunicates: structures, functions and potential uses.

  Integrative and comparative biology 20030401