Date published: 2026-5-12

1-800-457-3801

SCBT Portrait Logo
Seach Input

Boc-Nle-OH (CAS 6404-28-0)

0.0(0)
Write a reviewAsk a question

Application:
Boc-Nle-OH is a boc protected amino acid derivative
CAS Number:
6404-28-0
Purity:
99%
Molecular Weight:
231.29
Molecular Formula:
C11H21NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Boc-Nle-OH is an amino acid derivative with wide-ranging applications in scientific research. Its versatility makes it valuable in studying various biochemical and physiological effects. Moreover, Boc-Nle-OH is an essential component in the synthesis of diverse compounds. Notably, researchers employ it to modify the structure and activity of peptides and proteins.


Boc-Nle-OH (CAS 6404-28-0) References

  1. Chemoenzymatic synthesis of neoglycopeptides using endo beta-N-acetylglucosaminidase from Mucor hiemalis.  |  Haneda, K., et al. 2003. Methods Enzymol. 362: 74-85. PMID: 12968358
  2. Synthesis and biological activity of CCK heptapeptide analogues. Effects of conformational constraints and standard modifications on receptor subtype selectivity, functional activity in vitro, and appetite suppression in vivo.  |  Holladay, MW., et al. 1992. J Med Chem. 35: 2919-28. PMID: 1501220
  3. Synthesis and evaluation of TAC-based inhibitors of papain as mimics of cystatin B.  |  van Zoelen, DJ., et al. 2007. Chembiochem. 8: 1950-6. PMID: 17886319
  4. Synthesis and binding affinities of cyclic and related linear analogues of CCK8 selective for central receptors.  |  Charpentier, B., et al. 1989. J Med Chem. 32: 1184-90. PMID: 2724293
  5. Application of a Sulfoxonium Ylide Electrophile to Generate Cathepsin X-Selective Activity-Based Probes.  |  Mountford, SJ., et al. 2020. ACS Chem Biol. 15: 718-727. PMID: 32022538
  6. Imidazopyridine-fused [1,3]diazepinones: modulations of positions 2 to 4 and their impacts on the anti-melanoma activity.  |  Baccon-Sollier, PL., et al. 2020. J Enzyme Inhib Med Chem. 35: 935-949. PMID: 32249633
  7. Pentagastrin analogs containing alpha-aminooxy acids, I. Synthesis of analogs substituted at the N-terminus.  |  Kisfaludy, L., et al. 1978. Hoppe Seylers Z Physiol Chem. 359: 887-95. PMID: 711151
  8. Design and synthesis of thrombin substrates with modified kinetic parameters.  |  Rijkers, DT., et al. 1995. Thromb Res. 79: 491-9. PMID: 7502275
  9. Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid.  |  Amblard, M., et al. 1993. J Med Chem. 36: 3021-8. PMID: 7692048
  10. Pegylated peptides. II. Solid-phase synthesis of amino-, carboxy- and side-chain pegylated peptides.  |  Lu, YA. and Felix, AM. 1994. Int J Pept Protein Res. 43: 127-38. PMID: 8200730
  11. Synthesis of lipidic amino acid and dipeptide inhibitors of human platelet phospholipase A2.  |  Kokotos, G., et al. 1996. Int J Pept Protein Res. 48: 160-6. PMID: 8872534
  12. Synthesis and biological evaluation of potent, selective, hexapeptide CCK-A agonist anorectic agents.  |  Pierson, ME., et al. 1997. J Med Chem. 40: 4302-7. PMID: 9435899
  13. Synthesis and conformational studies of proline-containing tripeptides  |  AM Tamburro, V Guantieri, A Scatturin - International Journal of Biological …, 1984 - Elsevier. October 1984,. International Journal of Biological Macromolecules. Volume 6, Issue 5,: Pages 241-248.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Boc-Nle-OH, 1 g

sc-239400
1 g
$80.00