Date published: 2026-2-7

1-800-457-3801

SCBT Portrait Logo
Seach Input

4-Methyl-L-phenylalanine (CAS 1991-87-3)

0.0(0)
Write a reviewAsk a question

Alternate Names:
H-Phe(4-Me)-OH
CAS Number:
1991-87-3
Molecular Weight:
179.22
Molecular Formula:
C10H13NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4-Methyl-L-phenylalanine (4-MLPA) is a derivative of the essential amino acid phenylalanine, and it holds great significance in scientific research. Its versatility makes it useful in various biochemical and physiological experiments. Researchers rely on the wide-ranging applications of 4-Methyl-L-phenylalanine, and its ability to be synthesized in the lab adds to its appeal. In scientific research, 4-Methyl-L-phenylalanine finds utility as a substrate in enzyme assays and as a reagent in biochemical and physiological experiments. 4-Methyl-L-phenylalanine aids in investigating protein structure, function, and metabolic pathways. It serves as a substrate for enzymes, facilitating the study of their activities and inhibition. Additionally, 4-Methyl-L-phenylalanine can act as a probe to delve into the intricacies of protein structure and function.


4-Methyl-L-phenylalanine (CAS 1991-87-3) References

  1. Studies on crenarchaeal tyrosylation accuracy with mutational analyses of tyrosyl-tRNA synthetase and tyrosine tRNA from Aeropyrum pernix.  |  Iwaki, J., et al. 2012. J Biochem. 152: 539-48. PMID: 23024156
  2. Polymorphism and Modulation of Para-Substituted l-Phenylalanine.  |  Sögütoglu, LC., et al. 2017. Cryst Growth Des. 17: 6231-6238. PMID: 29234239
  3. Discovery of a Manduca sexta Allatotropin Antagonist from a Manduca sexta Allatotropin Receptor Homology Model.  |  Kai, ZP., et al. 2018. Molecules. 23: PMID: 29614008
  4. Initiation of Protein Synthesis with Non-Canonical Amino Acids In Vivo.  |  Tharp, JM., et al. 2020. Angew Chem Int Ed Engl. 59: 3122-3126. PMID: 31828898
  5. Molecular basis for activation and biased signaling at the thrombin-activated GPCR proteinase activated receptor-4 (PAR4).  |  Thibeault, PE., et al. 2020. J Biol Chem. 295: 2520-2540. PMID: 31892516
  6. Hijacking Translation Initiation for Synthetic Biology.  |  Tharp, JM., et al. 2020. Chembiochem. 21: 1387-1396. PMID: 32023356
  7. Highly selective synthesis of D-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory.  |  Zhang, DP., et al. 2021. Microb Cell Fact. 20: 11. PMID: 33422055
  8. A new thermostable Cu(II) coordination polymer: photocatalytic activity and application values on diabetes.  |  Jin, CL., et al. 2021. Des Monomers Polym. 24: 136-144. PMID: 34104071
  9. Mapping and Exploiting the Promiscuity of OxyB toward the Biocatalytic Production of Vancomycin Aglycone Variants.  |  Forneris, CC., et al. 2020. ACS Catal. 10: 9287-9298. PMID: 34422446
  10. Mechanism of metal-independent hydroxylation by Chromobacterium violaceum phenylalanine hydroxylase.  |  Carr, RT., et al. 1995. Biochemistry. 34: 7525-32. PMID: 7779797

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Methyl-L-phenylalanine, 250 mg

sc-267649
250 mg
$55.00