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CS-W001157 4
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Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH

  • CAS No. 1599440-20-6

  • Cat. No. CS-0168722
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH|CS-0168722

Structure of 1599440-20-6

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General Information

  • CAS No. 1599440-20-6
  • Cat. No. CS-0168722
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, stored under nitrogen, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₈H₂₅N₅O₇
  • Molecular Weight 423.42
  • Synonym(s) None
  • SMILES OC(COCNC(CNC([C@@H](NC(CNC(CN)=O)=O)CC1=CC=CC=C1)=O)=O)=O

Description

This tetrapeptide derivative features a C-terminal ester-linked carboxylic acid, combining peptide backbone stability with enhanced solubility. The Gly-Gly-Phe-Gly sequence provides a rigid, hydrophobic core, while the N-terminal amidation and O-alkylated side chain enable controlled reactivity in bioconjugation workflows.

Application

Gly-Gly-Phe-Gly-NH-CH₂-O-CH₂COOH serves as a stable, readily accessible peptide-based building block for the synthesis of bioactive oligopeptide scaffolds. Its N-terminal hydroxymethyl carbamate functionality enables selective derivatization and conjugation in solid-phase and solution-phase peptide coupling protocols. The sequence exhibits good bench stability and facilitates orthogonal functional group manipulation, supporting efficient access to cyclic analogs and peptidomimetic architectures in medicinal chemistry campaigns.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   188.95
  • LogP   -2.9201
  • H_Acceptors   7
  • H_Donors   6
  • Rotatable_Bonds   13

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