| Bioactivity | Cyclo(L-Phe-L-Pro), isolated from Pseudomonas fluorescens and Pseudomonas alcaligenes cell-free culture supernatants is an antifungal cyclic dipeptide[1]. Cyclo(L-Phe-L-Pro) inhibits IFN-β production by interfering with retinoic-acid-inducible gene-I (RIG-I) activation[2]. Cyclo(L-Phe-L-Pro) exhibits free-radical scavenging activity with the IC50 of 24 µM in the DPPH assay[3]. | ||||||
| Name | Cyclo(L-Phe-L-Pro) | ||||||
| CAS | 3705-26-8 | ||||||
| Shortening | Cyclo(FP) | ||||||
| Formula | C14H16N2O2 | ||||||
| Molar Mass | 244.29 | ||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||
| Storage | Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
Cyclo(L-Phe-L-Pro)
CAS: 3705-26-8 F: C14H16N2O2 W: 244.29
Cyclo(L-Phe-L-Pro), isolated from Pseudomonas fluorescens and Pseudomonas alcaligenes cell-free culture supernatants is
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