117467-73-9

Basic information

• Product Name: CBZ-D-4-FLUOROPHENYLALANINE
• Synonyms: N-Benzyloxycarbonyl-3-(4-fluorophenyl)-D-alanine;(R)-2-(((Benzyloxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid;4-Fluoro-N-[(phenylmethoxy)carbonyl]-D-phenylalanine;(R)-Z-2-amino-3-(4-fluorophenyl)propionic acid;Z-4-fluoro-D-phenylalanine≥ 99% (HPLC);Z-π-fluoro-D-Phe-OH
• CAS NO: 117467-73-9
• Molecular Formula: C₁₇H₁₆FNO₄
• Molecular Weight: 317.31
• Mol File: 117467-73-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: CBZ-D-4-FLUOROPHENYLALANINE(CAS DataBase Reference)
• NIST Chemistry Reference: CBZ-D-4-FLUOROPHENYLALANINE(117467-73-9)
• EPA Substance Registry System: CBZ-D-4-FLUOROPHENYLALANINE(117467-73-9)

Safety Data

• Hazardous Substances Data: 117467-73-9(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 127862-81-1 Z-DL-Phe(4F)-OCH₂CF₃ 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 51-65-0 4-Fluorophenylalanine 
• 141971-11-1 Z-DL-Phe(4F)OMe 
• 18125-46-7 (R)-4-fluorophenylalanine 
• 501-53-1 benzyl chloroformate 
• 394210-36-7 4-(4-fluoro-benzyl)-2,5-dioxo-oxazolidine-3-carboxylic acid benzyl ester 
• 64-17-5 ethanol 
• 404-32-0 DL-Z-4-F-Phe-OH 

Downstream Products

• 152929-92-5 [(R)-2-(4-Fluoro-phenyl)-1-formyl-ethyl]-carbamic acid benzyl ester 
• 152929-91-4 [(R)-2-(4-Fluoro-phenyl)-1-(methoxy-methyl-carbamoyl)-ethyl]-carbamic acid benzyl ester 
• 152929-93-6 (2R,3S,4S,5R)-2.5-bis(N-Cbz-amino)-3,4-dihydroxy-1,6-di(4-fluorophenyl)hexane 
• 1053528-20-3 (4R,5S,6S,7R)-1,3-Bis-cyclopropylmethyl-4,7-bis-(4-fluoro-benzyl)-5,6-bis-(2-trimethylsilanyl-ethoxymethoxy)-[1,3]diazepan-2-one 
• 1054644-41-5 (4R,5S,6S,7R)-4,7-Bis-(4-fluoro-benzyl)-1,3-bis-(4-hydroxymethyl-benzyl)-5,6-bis-(2-trimethylsilanyl-ethoxymethoxy)-[1,3]diazepan-2-one 

Relevant articles and documents

Synthesis, in vitro biological activity, hydrolytic stability and docking of new analogs of BIM-23052 containing halogenated amino acids

One of the potent somatostatin analogs, BIM-23052 (DC-23-99) d-Phe-Phe-Phe-d-Trp-Lys-Thr-Phe-Thr-NH2, has established in vitro growth hormone inhibitory activity in nM concentrations. It is also characterized by high affinity to some somatostatin receptors which are largely distributed in the cell membranes of many tumor cells. Herein, we report the synthesis of a series of analogs of BIM-23052 containing halogenated Phe residues using standard solid-phase peptide method Fmoc/OtBu-strategy. The cytotoxic effects of the compounds were tested in vitro against two human tumor cell lines—breast cancer cell line and hepatocellular cancer cell line, as well as on human non-tumorigenic epithelial cell line. Analogs containing fluoro-phenylalanines are cytotoxic in μM range, as the analog containing Phe (2-F) showed better selectivity against human hepatocellular cancer cell line. The presented study also reveals that accumulation of halogenated Phe residues does not increase the cytotoxicity according to tested cell lines. The calculated selective index reveals different mechanisms of antitumor activity of the parent compound BIM-23052 and target halogenated analogs for examined breast tumor cell lines. All peptides tested have high antitumor activity against the HepG2 cell line (IC50 ≈ 100?μM and SI > 5) compared to breast cells. This is probably due to the high permeability of the cell membrane and the higher metabolic activity of hepatocytes. In silico docking studies confirmed that all obtained analogs bind well with the somatostatin receptors with preference to ssrt3 and ssrt5. All target compounds showed high hydrolytic stability at acid and neutral pH, which mimic physiological condition in stomach and human plasma.

Asymmetric synthesis of α-amino acids via cinchona alkaloid-catalyzed kinetic resolution of urethane-protected α-amino acid N-carboxyanhydrides

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PAPAIN-ASSISTED RESOLUTION OF NATURAL AND XENOBIOTIC α-AMINO ACIDS

A new and convenient method for the preparation of pure enantiomers of α-amino acids is described.Industrial papain, catalyzes the synthesis of L-Z-amino acid ethyl esters in ethanolic medium, with good yields.These esters are obtained from DL-Z-amino acids with 100percent optical purity.Unreactive D-Z-amino acids are readily isolated from reaction medium.Physical constants of natural and xenobiotic L-Z-amino acid esters and D-Z-amino acids are described.