Fmoc-D-Aph(Cbm)-OH
  • Fmoc-D-Aph(Cbm)-OH
  • Fmoc-D-Aph(Cbm)-OH

Fmoc-D-Aph(Cbm)-OH | CAS 324017-22-3

  • cas:324017-22-3
  • Molecular Formula:C25H23N3O5
  • Purity:99%
  • Molecular Weight:445.46722
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This product is for research and development use only.

Product Details;

CasNo: 324017-22-3

Molecular Formula: C25H23N3O5

4-[(AMinocarbonyl)aMino]-N-[(9H-fluoren-9-ylMethoxy)carbonyl]-D-phenylalanine Chemical Properties

Melting point 

163℃ (decomposition)

Boiling point 

699.1±55.0 °C(Predicted)

density 

1.376±0.06 g/cm3(Predicted)

storage temp. 

2-8°C

solubility 

DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)

pka

3.82±0.10(Predicted)

form 

Solid

color 

White to Off-White

Stability:

Hygroscopic

InChIKey

HFPDOFBZCSQAEJ-JOCHJYFZSA-N

SMILES

C(O)(=O)[C@@H](CC1=CC=C(NC(N)=O)C=C1)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O

4-[(AMinocarbonyl)aMino]-N-[(9H-fluoren-9-ylMethoxy)carbonyl]-D-phenylalanine Usage And Synthesis

Uses

Fmoc-D-4-Aph(cBm)-OH is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize biologically active peptide mimetics, such as Ac-D2Nal-D4Cpa-D3Pal-Ser-4Aph/4Amf(P)-D4Aph/D4Amf(Q)-Leu-ILys-Pro-DAla-NH2 with gonadotropin-releasing hormone (GnRH) antagonist activity[1].

References

[1] Guangcheng Jiang, et al. "GnRH antagonists: a new generation of long acting analogues incorporating p-ureido-phenylalanines at positions 5 and 6." Journal of medicinal chemistry 44.3 (2001): 453-467. DOI:10.1021/jm0003900

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