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CS-W001157 4
Total: USD 88.00

MC-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH

  • CAS No. 1599440-25-1

  • Cat. No. CS-0145893
  • Purity≥98%
  • MDL No.None

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

MC-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH|CS-0145893

Structure of 1599440-25-1

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General Information

  • CAS No. 1599440-25-1
  • Cat. No. CS-0145893
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₈H₃₆N₆O₁₀
  • Molecular Weight 616.62
  • Synonym(s) (S)-10-Benzyl-23-(2,5-Dioxo-2,5-Dihydro-1H-Pyrrol-1-Yl)-6,9,12,15,18-Pentaoxo-3-Oxa-5,8,11,14,17-Pentaazatricosan-1-Oic Acid
  • SMILES OC(COCNC(CNC([C@@H](NC(CNC(CNC(CCCCCN1C(C=CC1=O)=O)=O)=O)=O)CC2=CC=CC=C2)=O)=O)=O

Description

MC-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH features a hydrophilic polyethylene glycol linker flanked by a tetrapeptide sequence, enabling efficient conjugation in bioactive molecule synthesis. This design supports stable, water-soluble derivatization under physiological conditions, ideal for peptide-based probe development and targeted delivery systems.

Application

MC-Gly-Gly-Phe-Gly-NH-CH₂-O-CH₂COOH serves as a stable, bifunctional peptide scaffold enabling site-specific conjugation in bioconjugation workflows. The N-terminal amine and C-terminal carboxylic acid facilitate efficient coupling reactions, while the glycosylated linker enhances solubility and metabolic stability. This sequence supports modular synthesis of peptide-drug conjugates and protein labeling reagents with predictable reactivity and ease of purification.

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
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501

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Computational Chemistry Data

  • TPSA   229.41
  • LogP   -2.2772
  • H_Acceptors   9
  • H_Donors   6
  • Rotatable_Bonds   20

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