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CYCLO-(L-PRO-L-TYR)-(MACULOSIN-1)

Compound with spectra: 2 NMR

CYCLO-(L-PRO-L-TYR)-(MACULOSIN-1)
SpectraBase Compound ID HZ0vgPThSKv
InChI InChI=1S/C14H16N2O3/c17-10-5-3-9(4-6-10)8-11-14(19)16-7-1-2-12(16)13(18)15-11/h3-6,11-12,17H,1-2,7-8H2,(H,15,18)/t11-,12-/m0/s1
InChIKey LSGOTAXPWMCUCK-RYUDHWBXSA-N
Mol Weight 260.29 g/mol
Molecular Formula C14H16N2O3
Exact Mass 260.116092 g/mol
Enantiomer InChIKey LSGOTAXPWMCUCK-VXGBXAGGSA-N

View Spectrum of CYCLO-(L-PRO-L-TYR)-(MACULOSIN-1)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N

View Spectrum of CYCLO-(L-PRO-L-TYR)-(MACULOSIN-1)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • ML1532-II;CYCLO-(L-TYR-L-PRO)
CYCLO-(L-PROLINYL-L-TYROSINE)
CYClO-(L-PRO-L-TYR)
Cyclo-L-prolyl-L-phenylalanine
CYCLO-(R-PROLINE-R-PHENYLALANINE)
3-BENZYLHEXAHYDROPYRROLO-(1,2-A)-PYRAZINE-1,4-DIONE
CYClO-(D-PROLYL-D-PHENYLALANYL)
Cyclo[-L-Pro-L-Glu(Bzl)-]
METHYL-N-ACETYL-D-PHENYLALANYL-L-TRANS-PROLINE
CYCLO-(S-PROLINE-S-ISOLEUCINE)
CYCLO-(L-ILE-D-PRO)
Title Journal or Book Year
Lahorenoic Acids A–C, ortho-Dialkyl-Substituted Aromatic Acids from the Biocontrol Strain Pseudomonas aurantiaca PB-St2 Journal of Natural Products 2013
The selective inhibitors against SV40-transformed cells. selective inhibition of SV40-transformed cell growth by diketopiperazines. Agricultural and Biological Chemistry 1981

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