2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-(TYROSYLAMINO)-ACETIC-ACID-N-BUTYL-AMIDE
Compound with spectra: 1 NMR
![2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-(TYROSYLAMINO)-ACETIC-ACID-N-BUTYL-AMIDE](/api/compound/7NlR4pU1JNm.png?ph=true&h=300&w=458 "2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-(TYROSYLAMINO)-ACETIC-ACID-N-BUTYL-AMIDE")
| SpectraBase Compound ID | 7NlR4pU1JNm |
|---|---|
| InChI | InChI=1S/C21H32N4O8/c1-2-3-8-23-19(30)14(15-16(27)21(31)10-33-20(17(21)28)25(15)32)24-18(29)13(22)9-11-4-6-12(26)7-5-11/h4-7,13-17,20,26-28,31-32H,2-3,8-10,22H2,1H3,(H,23,30)(H,24,29)/t13-,14?,15+,16-,17+,20-,21+/m0/s1 |
| InChIKey | YLZAEDYSARUBHX-KJLBAAIISA-N |
| Mol Weight | 468.5 g/mol |
| Molecular Formula | C21H32N4O8 |
| Exact Mass | 468.222014 g/mol |
| Enantiomer InChIKey | YLZAEDYSARUBHX-VHQRXVIVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
2-(2,4,5,8-TETRAHYDROXY-7-OXA-2-AZABICYCLO-[3.2.1]-OCT-3-YL)-2-[(N-ACETYL)-TYROSYLAMINO]-ACETIC-ACID
(5E,5BE)-METHYL-BICYCLOMYCIN-5A-PROPENOATE
(5E,5BE)-ALLYL-BICYCLOMYCIN-5A-PROPENOATE
5A-(PYRIDIN-2-YL-SULFANYL)-DIHYDROBICYCLOMYCIN;MAJOR-DIASTEREOMER
5A-(NAPHTH-2-YL-METHYLSULFANYL)-DIHYDROBICYCLOMYCIN;MAJOR-DIASTEREOMER
Ferupennin C
3,7-Dimethoxycalophyfuran
14,15,16,17-tetrahydro-7-methylthio-cis-erythrinan-8-one
Benzo[g]chrysene-1,3,4-triol, 2-bromo-1,2,3,4-tetrahydro-, 3,4-diacetate, (1.alpha.,2.beta.,3.beta.,4.alpha.)-(.+-.)-
2-(benzylthio)-3-cyclopentyl-3H-spiro[benzo[h]quinazoline-5,1'-cyclopentan]-4(6H)-one
| 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 |