PROFILPELAJAR.COM

Spenolimycin
Names
	IUPAC name (1R,3S,5R,8S,10R,11S,12S,13R,14S)-7-methoxy-5-methyl-11,13-bis(methylamino)-2,4,9-trioxatricyclo[8.4.0.03,8]tetradec-6-ene-8,12,14-triol
Identifiers
CAS Number	95041-97-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:81421;
ChemSpider	111484;
KEGG	C17970;
PubChem CID	125257;
CompTox Dashboard (EPA)	DTXSID60241735 ;
	InChI InChI=1S/C15H26N2O7/c1-6-5-7(21-4)15(20)14(22-6)23-13-11(19)8(16-2)10(18)9(17-3)12(13)24-15/h5-6,8-14,16-20H,1-4H3/t6-,8-,9+,10+,11+,12-,13-,14+,15+/m1/s1 Key: JXUOVTMVWNHOAJ-XLBYJKOOSA-N;
	SMILES C[C@@H]1C=C([C@]2([C@@H](O1)O[C@@H]3[C@H]([C@@H]([C@@H]([C@@H]([C@H]3O2)NC)O)NC)O)O)OC;
Properties
Chemical formula	C15H26N2O7
Molar mass	346.380 g·mol−1
Solubility in water	Soluble
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Spenolimycin is a spectinomycin-type antibiotic which has been isolated from the bacterium Streptomyces gilvospiralissp.^[2]^[3]^[1] Spenolimycin has the molecular formula C₁₅H₂₆N₂O₇.^[1]^[3]^[4]

References

^ ^a ^b ^c "Spenolimycin". Pubchem.ncbi.NLM.nih.gov.
^ Collins, Peter M. (29 November 2005). Dictionary of Carbohydrates. CRC Press. p. 63. ISBN 978-1-000-61156-4.
^ ^a ^b Fernandes, Prabhavathi B.; Vojtko, Charlene M.; Bower, Robert R.; Weisz, Jonina (1984). "Spenolimycin, a new spectinomycin-type antibiotic. III. Biological properties". The Journal of Antibiotics. 37 (12): 1525–1527. doi:10.7164/antibiotics.37.1525. PMID 6241193.
^ Arya, Dev P. (17 September 2007). Aminoglycoside Antibiotics: From Chemical Biology to Drug Discovery. John Wiley & Sons. p. 33. ISBN 978-0-470-14966-9.