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2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-[(N-ACETYL)-TYROSYLAMINO]-ACETIC-ACID

Compound with spectra: 1 NMR

2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-[(N-ACETYL)-TYROSYLAMINO]-ACETIC-ACID
SpectraBase Compound ID G2TS7rc3L4f
InChI InChI=1S/C19H25N3O10/c1-8(23)20-11(6-9-2-4-10(24)5-3-9)16(27)21-12(18(28)29)13-14(25)19(30)7-32-17(15(19)26)22(13)31/h2-5,11-15,17,24-26,30-31H,6-7H2,1H3,(H,20,23)(H,21,27)(H,28,29)/t11-,12?,13+,14-,15+,17-,19+/m0/s1
InChIKey RMPBTJXFBUPSJJ-WLLUZDSCSA-N
Mol Weight 455.42 g/mol
Molecular Formula C19H25N3O10
Exact Mass 455.153994 g/mol
Enantiomer InChIKey RMPBTJXFBUPSJJ-QKEOVDBISA-N

View Spectrum of 2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-[(N-ACETYL)-TYROSYLAMINO]-ACETIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
SB-219383;SIGNALSET-#1;N-(L-TYROSYL)-2-AMINO-[1(S*),3(S*),5(R*),8(R*)-2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL]-ACETIC-ACID
2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-(TYROSYLAMINO)-ACETIC-ACID-N-BUTYL-AMIDE
Methyl (1S*,3R*,3aS*,6aR*)-3-benzoyl-1,5-dimethyl-4,6-dioxooctahydropyrrolo[3,4-c]pyrrole-1-carboxylate
9-(4-chlorophenyl)-6,6-dimethyl-8-oxo-5,6,7,8,8a,9-hexahydropyrazolo[5,1-b]quinazoline-3-carbonitrile
PLAGIOCHILINE-R
Spiro[5H-cyclopropa[3,4]cyclohepta[1,2-c]pyran-5,2'-oxirane]-1,8-dimethanol, 4-(acetyloxy)-4,4a,6,7,7a,8,8a,8b-octahydro-8-methyl-, diacetate, [4R-(4.alpha.,4a.alpha.,5.beta.,7a.beta.,8.alpha.,8a.beta.,8b.alpha.)]-
3'-(4-Chlorobenzyl)-2',3'-dihydro-4'-phenyl-2'-thioxo-spiro[indole-3,6'-[1,3]thiazin]-2(1H)-one
Neothiobinupharidine, 6-hydroxy-, (6.alpha.)-
JATAMANVALTRATE-L
1-OHBG-5'-SMP;1-(ORTHO-HYDROXYBENZYL)-GUANOSINE-5'-S-METHYL-PHOSHOROTHIOLATE
Title Journal or Book Year
Synthesis and Activity of Analogues of SB-219383. Novel Potent Inhibitors of Bacterial Tyrosyl tRNA Synthetase. The Journal of Antibiotics 2000
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