Bluensomycin

Synonym(s): U-12898

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 developmental phase:	Preclinical
Development status:	Inactive

Chemical structure(s):
Canonical 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
Isomeric 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:	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
InChI Key:	RQLDKUSQKQMFCN-AEXVNIBOSA-N
Structure link:	https://pubchem.ncbi.nlm.nih.gov/compound/20055290

External links:
Guide to Pharmacology:	bluensomycin
Citation:	https://academic.oup.com/femsle/article/219/2/285/571226