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Synthesis of unnatural amino acids and other blocks

c(His-Phe)

Name
c(His-Phe)
Molecular structural formula
Purity
95%
CAS Number
56586-95-9
Formula
C15H16N4O2
MW
284.31
Sequence
cyclo(His-Phe)(main chain cyclo)
Sequence Shortening
cyclo(HF)(main chain cyclo)
InChIKey
HLXXMJDWTBXTOR-UHFFFAOYSA-N
References
[1].An investigation into the biological activity of the selected histidine-containing diketopiperazines cyclo(His-Phe) and cyclo(His-Tyr).
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Catalyst for asymmetric cyanohydrin synthesis. The addition of hydrogen cyanide to benzaldehyde gives the highest optical yield ever obtained for the corresponding cyanohydrin. In a study of McCleland et al., Cyclo(His-Phe) showed significant anti-tumour activity, causing reduction of cell viability in cervical cancer cells. In isolated rat hearts, the diketopiperazine caused a gradual reduction of heart rate and a decrease in coronary flow rate.