Compound ID | 1150

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Bluensomycin

Synonym(s): U-12898  |  glebomycin

Class: Aminoglycoside

Spectrum of activity: Gram-negative
Details of activity: Activity similar to other aminoglycosides
Description: Mason D. J et al. "U-12898, A new antibiotic" Program and Abstracts of the interscience science Conference on Antimicrobial Agents and Chemotherapy. 1962.
Institute where first reported: The UpJohn Company
Year first mentioned: 1962
Highest development stage: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 585.56
Iso. SMILES: C[C@H]1[C@@]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H]([C@H]2O)O)OC(=O)N)O)N=C(N)N)O[C@H]3[C@H]([C@@H]([C@H]([C@@H](O3)CO)O)O)NC)(CO)O
InChI Key: RQLDKUSQKQMFCN-AEXVNIBOSA-N
Can. SMILES: C[C@H]1[C@](CO)([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H]([C@H]2O)O)OC(=O)N)O)N=C(N)N)O[C@H]3[C@H]([C@@H]([C@H]([C@H](CO)O3)O)O)NC)O
InChI: InChI=1S/C21H39N5O14/c1-5-21(35,4-28)16(40-17-8(25-2)10(30)9(29)6(3-27)37-17)18(36-5)38-14-7(26-19(22)23)11(31)15(39-20(24)34)13(33)12(14)32/h5-18,25,27-33,35H,3-4H2,1-2H3,(H2,24,34)(H4,22,23,26)/t5-,6-,7-,8-,9-,10-,11-,12+,13+,14+,15+,16-,17-,18-,21+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/20055290
Guide to Pharmacology: bluensomycin
Citation: https://academic.oup.com/femsle/article/219/2/285/571226

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