Welcome to LookChem.com Sign In|Join Free
  • or
"Z-Phe-gGly-D-COCH(CH3)C6H5" is a complex organic compound, which can be broken down into its constituent parts for better understanding. "Z" refers to the benzyloxycarbonyl group, a protecting group used in peptide synthesis to prevent unwanted side reactions. "Phe" stands for phenylalanine, an amino acid that is one of the 20 standard amino acids common in proteins. "gGly" represents glycine, another amino acid, with "g" indicating that it is in the gamma position, which is not common in standard peptide sequences and may suggest a cyclic or unusual peptide structure. "D" signifies that the following amino acid is in its D-configuration, which is the non-natural, or mirror-image, form of the standard L-amino acids found in proteins. "COCH(CH3)C6H5" describes a substituted benzyl group, where a methyl group (CH3) is attached to the benzyl ring, which can act as a protecting group or a handle for further chemical modifications. Z-Phe-gGly-D-COCH(CH3)C6H5 is likely used in advanced peptide chemistry, possibly for the synthesis of pharmaceuticals or for research into protein structure and function.

95617-49-5

Post Buying Request

95617-49-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

95617-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95617-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,1 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95617-49:
(7*9)+(6*5)+(5*6)+(4*1)+(3*7)+(2*4)+(1*9)=165
165 % 10 = 5
So 95617-49-5 is a valid CAS Registry Number.

95617-49-5Relevant academic research and scientific papers

Synthesis and Pharmacological Activity of Partially Modified Retro-Inverso Dermorphin Tetrapeptides

Salvadori, Severo,Marastoni, Mauro,Balboni, Gianfranco,Sarto, Gian Pietro,Tomatis, Roberto

, p. 769 - 774 (2007/10/02)

We studied the effect of partial retro-inverso modification of selected peptide bonds of N-terminal tetrapeptide analogues of dermorphin (H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2).Among the 14 compounds synthesized and tested for opioid activity, some tetrapeptides have the C-terminus carrying different amide moieties; retromodifications concern the Phe-Gly bond (Ia-f) and/or the C-terminal carboxamide function (IIIa-d, IIa-d).All pseudotetrapeptide derivatives showed opioid activity in vitro and in vivo.The most potent compounds (II) have a biological potency comparable with that of the original tetrapeptides in the guinea pig ileum preparation and in the mouse tail-flick test after intracerebral or subcutaneous administration.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 95617-49-5