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Home Product Protected Amino Acids, Resins & Reagents Pseudoproline Dipeptides Fmoc-Ala-Thr(psiMe,Mepro)-OH

DESCRIPTION

Fmoc-Ala-Thr(psiMe,Mepro)-OH is an Fmoc-protected Ala-Thr pseudoproline building block for solid-phase peptide synthesis (SPPS). The Thr residue is incorporated in a reversible 2,2-dimethyloxazolidine pseudoproline form that temporarily changes local backbone hydrogen-bonding and conformation during chain elongation.

The preformed Ala-Thr unit introduces the sequence motif in one coupling operation. Under standard TFA-mediated final cleavage and deprotection, the acid-labile pseudoproline ring is opened and the native Thr residue is regenerated.

Product Information

Product NameFmoc-Ala-Thr(psiMe,Mepro)-OH
Catalog No.AS4258
CAS No.252554-79-3
Molecular FormulaC25H28N2O6
Molecular Weight452.50 g/mol
Building Block TypeFmoc-protected Ala-Thr pseudoproline dipeptide
Sequence MotifAla-Thr
Primary UseFmoc-SPPS of difficult or aggregation-prone Ala-Thr-containing sequences

Why Use a Preformed Pseudoproline Dipeptide

The Ala-Thr amide bond is already present before the reagent is coupled to the growing peptide. This matters because formation of the pseudoproline oxazolidine makes the downstream Thr nitrogen sterically constrained. Supplying the unit as a protected dipeptide avoids relying on direct acylation at that hindered nitrogen and installs two residues in a single step. This should be considered alongside solid-phase peptide synthesis guide when diagnosing sequence-dependent assembly problems.

Sequence-Specific Use in Difficult SPPS

For a target containing a native Ala-Thr segment, this building block places the temporary backbone-disrupting element exactly at the Thr site. It is most relevant when synthesis around that region shows poor coupling, difficult Fmoc removal, deletion products, or other signs that chain association is limiting reagent access.

Coupling and Final Cleavage

The C-terminal carboxyl group remains available for incorporation through standard Fmoc-SPPS coupling chemistry. During final acid treatment, the pseudoproline ring is removed and the intended Ala-Thr sequence is recovered. Coupling reagent choice and cleavage cocktail should still be selected for the complete sequence rather than for this building block alone.

When to Choose This Building Block

We consider Ala-Thr pseudoproline substitution most useful when there is a sequence-specific reason to alter the physical behavior of the resin-bound chain. A routine Ala-Thr sequence that couples cleanly with conventional amino acids does not automatically require a pseudoproline strategy. Related motifs can be compared in the protected pseudoproline building blocks.

Experimental Planning

When a difficult sequence contains several possible Ser/Thr pseudoproline insertion sites, placement should be assessed together with chain length, hydrophobicity, resin loading, neighboring residues, and the stage at which coupling or deprotection performance begins to decline. The presence of an Ala-Thr motif alone does not establish that this building block is required.

For projects where building-block selection needs to be evaluated with the full target sequence, our modified peptide synthesis can support integrated planning, synthesis, purification, and QC requirements.

Product Documents

MSDS - Fmoc-Ala-Thr(psiMe,Mepro)-OH (AS4258)

The Safety Data Sheet provides product identification, hazard information, handling and storage guidance, exposure controls, transport information, and regulatory information for laboratory use.

Certificates of Analysis (COAs) are batch-specific. Please contact us to request the COA for your product, and we will provide it by email.

Frequently Asked Questions

What does psi(Me,Me)pro indicate?

It denotes a dimethyl-substituted pseudoproline formed from the downstream Thr residue. The five-membered oxazolidine temporarily changes backbone behavior during synthesis.

Why is the Ala-Thr unit supplied as a preformed building block?

The amide bond immediately before the pseudoproline nitrogen is already formed, avoiding direct acylation of a sterically hindered oxazolidine nitrogen and allowing the motif to be introduced in one coupling operation.

Does the pseudoproline remain in the final peptide?

No. Standard TFA-mediated final cleavage opens the pseudoproline ring and restores the downstream Thr residue.

Should this be used for every Ala-Thr sequence?

No. Pseudoproline use is most justified when the sequence shows aggregation, poor chain accessibility, or another reproducible assembly problem. Straightforward sequences may not require it.

Research Use Only.

Fmoc-Ala-Thr(psiMe,Mepro)-OH

Catalog No: AS4258
Cas No: 252554-79-3

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