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CS-W001157 4
Total: USD 88.00

Boc-Val-Ala-PAB-PNP

  • CAS No. 1884578-00-0

  • Cat. No. CS-0119068
  • Purity≥98%
  • MDL No.MFCD28557281

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

Boc-Val-Ala-PAB-PNP|CS-0119068

Structure of 1884578-00-0

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General Information

  • CAS No. 1884578-00-0
  • Cat. No. CS-0119068
  • Purity ≥98%
  • MDL No. MFCD28557281
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₇H₃₄N₄O₉
  • Molecular Weight 558.58
  • Synonym(s) None
  • SMILES CC([C@H](NC(OC(C)(C)C)=O)C(N[C@H](C(NC1=CC=C(C=C1)COC(OC2=CC=C(C=C2)[N+]([O-])=O)=O)=O)C)=O)C

Description

Boc-Val-Ala-PAB-PNP serves as a key intermediate in peptide synthesis, featuring a protected N-terminal valine and an activated C-terminal PAB-PNP moiety. This combination enables efficient coupling reactions under standard conditions, with the PNP group facilitating rapid deprotection and purification. The Boc protection ensures stability during manipulation, while the Ala residue provides optimal spacing for conjugation. Ideal for solid-phase and solution-phase workflows, this reagent streamlines access to complex peptide architectures.

Application

Boc-Val-Ala-PAB-PNP serves as a versatile building block for the synthesis of peptide-based conjugates and prodrugs. The Boc group provides reliable N-terminal protection, while the Val-Ala dipeptide sequence enables enzymatic cleavage in biological systems. The PAB-PNP moiety offers a robust linker for site-specific attachment to antibodies or solid supports, facilitating efficient conjugation via nucleophilic displacement. This compound exhibits excellent bench stability, compatibility with standard peptide coupling protocols, and ease of purification, making it ideal for modular assembly of targeted therapeutics.

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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

  • TPSA   175.2
  • LogP   4.3029
  • H_Acceptors   9
  • H_Donors   3
  • Rotatable_Bonds   10

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