75768-66-0

Basic information

• Product Name: N-Benzyl-L-tyrosine
• Synonyms: N-Benzyl-L-tyrosine
• CAS NO: 75768-66-0
• Molecular Formula: C₁₆H₁₇NO₃
• Molecular Weight: 271.31108
• Product Categories: Amino Acids & Derivatives, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 75768-66-0.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Benzyl-L-tyrosine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyl-L-tyrosine(75768-66-0)
• EPA Substance Registry System: N-Benzyl-L-tyrosine(75768-66-0)

Safety Data

• Hazardous Substances Data: 75768-66-0(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

Protected L-Tyrosine (T899975), an amino acid, N-Benzyl-L-tyrosine is used by cells to synthesize proteins. L-Tyrosine is biologically converted from L-phenylalanine and is in turn is converted to L-DOPA and further converted into the neurotransmitters: dopamine, norepinephrine, and epinephrine.

Upstream product

• 100-39-0 benzyl bromide 
• 60-18-4 L-tyrosine 
• 138585-28-1 N-benzylTyrOtBu 
• 100-52-7 benzaldehyde 
• 16874-12-7 Tyr(tBu) 
• 100-44-7 benzyl chloride 
• 179188-06-8 N-benzyltyrosine tert-butyl ester 

Downstream Products

• 174906-30-0 methyl (S)-N-benzyl-L-tyrosinate 
• 1192754-68-9 PhCH₂-Tyr-Gly-Gly-Phe-Leu-D-Asn-Arg-Ile-Dap(Ac)-Pro-Lys-NH₂; Dap = 2,3-diaminopropionic acid 
• 1192754-64-5 PhCH2-Tyr-Gly-Gly-Phe-Leu-Arg-N(α)MeArg-D-Ala-Arg-Pro-Lys-NH2 
• 1192754-65-6 PhCH2-Tyr-Gly-Gly-Phe-Leu-Arg-N(α)MeArg-Ile-Arg-D-Pro-Lys-NH2 
• 524935-37-3 PhCH2-Tyr-Gly-Gly-Phe-Leu-Arg-N(α)MeArg-D-Ala-Arg-D-Pro-Lys-NH2 
• 1192754-67-8 PhCH₂-Tyr-Gly-Gly-Phe-Leu-D-Asp-Arg-Ile-Dap-Pro-Lys-NH₂, cylclo[D-Asp⁽⁵⁾,Dap⁽⁸⁾]; Dap = 2,3-diaminopropionic acid 
• 524935-34-0 PhCH₂-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-OH 
• 1192754-63-4 PhCH₂-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-D-Ala-Arg-Pro-Lys-NH₂ 
• 524935-36-2 PhCH₂-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-D-Pro-Lys-NH₂ 
• 1192754-66-7 PhCH₂-Tyr-Gly-Gly-Phe-Leu-Arg-Arg-D-Ala-Arg-D-Pro-Lys-NH₂ 

Relevant articles and documents

Aminoacid-derivatized Cu (II) complexes: Synthesis, DNA interactions and in vitro cytotoxicity

Two different series of copper complexes, [Cu(MFL)(FcAA)H2O] (C1-C4) and [Cu(MFL) (BzAA)H2O] (C5-C8), where FcAA = ferrocenyl amino acid mannich base conjugates and BzAA = benzaldehyde amino acid mannich base conjugates have been syn

Structure-Activity Relationships of the Peptide Kappa Opioid Receptor Antagonist Zyklophin

The dynorphin (Dyn) A analogue zyklophin ([N-benzyl-Tyr1-cyclo(d-Asp5,Dap8)]dynorphin A(1-11)NH2) is a kappa opioid receptor (KOR)-selective antagonist in vitro, is active in vivo, and antagonizes KOR in the CNS

The effects of C-terminal modifications on the opioid activity of [N-benzylTyr1]dynorphin A-(1-11) analogues

Structural modifications affecting the efficacy of analogues of the endogenous opioid peptide dynorphin (Dyn) A have focused on the N-terminal "message" sequence based on the "message-address" concept. To test the hypothesis that changes in the C-terminal