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Chemical structure of Cyclo(-His-Phe)

GA21334

Cyclo(-His-Phe)

Also known as 3-benzyl-6-(1H-imidazol-5-ylmethyl)piperazine-2,5-dione

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

ChemicalCAS56586-95-9MW284.32FormulaC15H16N4O2
CAS number
56586-95-9
Molecular weight
284.32
Formula
C15H16N4O2
Solubility
Soluble in DMSO
InChIKey
HLXXMJDWTBXTOR-UHFFFAOYSA-N
Catalogue number
GA21334
Brand
GLPBIO
Computed properties PubChem CID 3611370 · XLogP 0.8 · TPSA 86.9 Ų · H-bond donors 3
XLogP
0.8
TPSA
86.9 Ų
H-bond donors
3
H-bond acceptors
3
Rotatable bonds
4
Heavy atoms
21

SMILES C1=CC=C(C=C1)CC2C(=O)NC(C(=O)N2)CC3=CN=CN3

Computed descriptors from PubChem (CID 3611370), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

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