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N-[(5-S,10-R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENE-3-CARBONYL]-4-AMINOBUTANOIC_ACID

Compound with spectra: 3 NMR

N-[(5-S,10-R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENE-3-CARBONYL]-4-AMINOBUTANOIC_ACID
SpectraBase Compound ID F84y3gpMIv9
InChI InChI=1S/C14H16Br2N2O6/c1-23-11-7(15)5-14(12(21)10(11)16)6-8(18-24-14)13(22)17-4-2-3-9(19)20/h5,12,21H,2-4,6H2,1H3,(H,17,22)(H,19,20)/t12-,14+/m0/s1
InChIKey QIRBPXLEOLCMDX-GXTWGEPZSA-N
Mol Weight 468.1 g/mol
Molecular Formula C14H16Br2N2O6
Exact Mass 465.937512 g/mol
Enantiomer InChIKey QIRBPXLEOLCMDX-OCCSQVGLSA-N

View Spectrum of N-[(5-S,10-R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENE-3-CARBONYL]-4-AMINOBUTANOIC_ACID

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.

View Spectrum of N-[(5-S,10-R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENE-3-CARBONYL]-4-AMINOBUTANOIC_ACID

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD:CDCl3=2:1

View Spectrum of N-[(5-S,10-R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENE-3-CARBONYL]-4-AMINOBUTANOIC_ACID

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • N-[(5S,10R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENE-3-CARBOXY]-4-AMINOBUTANOIC-ACID
AEROTHIONINE
AEROTHIONIN
SUBEREAMOLLINE_B
SUBEREAMOLLINE_A
APLYSINAMETABOLITE;METHYL-4-[(5S,10R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENECARBOXAMIDO]-2-OXO-BUTYLCARBAMATE
QRCHFTPWKYEDNH-CJNGLKHVSA-N
METHYL-4-[(5S,10R)-7,9-DIBROMO-10-HYDROXY-8-METHOXY-1-OXA-2-AZASPIRO-[4.5]-DECA-2,6,8-TRIENECARBOXAMIDO]-3-OXO-BUTYLCARBAMATE
CAISSARINE-A
DIHYDROXY-AEROTHIONIN
11-DIHYDRO-AEROTHIONIN
Title Journal or Book Year
Brominated Compounds from Marine Sponges of the Genus Aplysina and a Compilation of Their 13C NMR Spectral Data Marine Drugs 2011
Highly Polar Spiroisoxazolines from the Sponge Aplysina fulva Journal of Natural Products 2007
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