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ARAPLYSILLIN_N(9)-SULFAMATE
SpectraBase Compound ID IY7fTUeS57a
InChI InChI=1S/C21H23Br4N3O8S.Na/c1-34-18-14(24)9-21(19(29)16(18)25)10-15(28-36-21)20(30)26-4-2-6-35-17-12(22)7-11(8-13(17)23)3-5-27-37(31,32)33;/h7-9,19,27,29H,2-6,10H2,1H3,(H,26,30)(H,31,32,33);/q;+1/p-1/t19-,21+;/m0./s1
InChIKey SWDXEYXTKXVRKS-LZAGWAHOSA-M
Mol Weight 819.09 g/mol
Molecular Formula C21H22Br4N3NaO8S
Exact Mass 814.775882 g/mol
Parent InChIKey VCMZCGIYWCZUJH-PZJWPPBQSA-M
Enantiomer InChIKey SWDXEYXTKXVRKS-DGXMUYMBSA-M
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD:CDCl3=1:19
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • ARAPLYSILLIN-N(9)-SULFAMATE
  • ARAPSYLLIN-I_N-(20)-SULFAMATE
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
FTICR-MS and LC-UV/MS-SPE-NMR Applications for the Rapid Dereplication of a Crude Extract from the Sponge Ianthella flabelliformis Journal of Natural Products 2009
Highly Polar Spiroisoxazolines from the Sponge Aplysina fulva Journal of Natural Products 2007

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