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ONTOLOGY REPORT - ANNOTATIONS


Term:spiramycin II
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Accession:CHEBI:31168 term browser browse the term
Definition:A macrolide antibiotic produced by various Streptomyces species.
Synonyms:exact_synonym: (4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-{[(2S,3R,4R,5S,6R)-5-{[(2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy}-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-10-{[(2R,5S,6S)-5-(dimethylamino)-6-methyloxan-2-yl]oxy}-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-4-yl acetate
 related_synonym: Acetylspiramycin;   Acetylspiramycinum;   Formula=C45H76N2O15;   Foromacidin B;   Foromacidine B;   InChI=1S/C45H76N2O15/c1-25-22-31(20-21-48)41(62-44-39(51)38(47(10)11)40(28(4)58-44)61-37-24-45(7,53)43(52)29(5)57-37)42(54-12)34(59-30(6)49)23-35(50)55-26(2)16-14-13-15-17-33(25)60-36-19-18-32(46(8)9)27(3)56-36/h13-15,17,21,25-29,31-34,36-44,51-53H,16,18-20,22-24H2,1-12H3/b14-13+,17-15+/t25-,26-,27-,28-,29+,31+,32+,33+,34-,36+,37+,38-,39-,40-,41+,42+,43+,44+,45-/m1/s1;   InChIKey=ZPCCSZFPOXBNDL-RSMXASMKSA-N;   SMILES=CO[C@H]1[C@@H](CC(=O)O[C@H](C)C\\C=C\\C=C\\[C@H](O[C@H]2CC[C@@H]([C@H](C)O2)N(C)C)[C@H](C)C[C@H](CC=O)[C@@H]1O[C@@H]1O[C@H](C)[C@@H](O[C@H]2C[C@@](C)(O)[C@@H](O)[C@H](C)O2)[C@@H]([C@H]1O)N(C)C)OC(C)=O;   Spiramycin 2;   Spiramycin B
 xref: CAS:24916-51-6 "ChemIDplus";   CAS:24916-51-6 "KEGG COMPOUND";   KEGG:C12891;   KEGG:D02420;   LIPID_MAPS_instance:LMPK05000002 "LIPID MAPS";   PMID:15127585 "Europe PMC";   PMID:16496680 "Europe PMC";   PMID:20843520 "Europe PMC";   PMID:2232146 "Europe PMC";   PMID:23866271 "Europe PMC";   PMID:24790408 "Europe PMC";   PMID:25081985 "Europe PMC";   PMID:25164320 "Europe PMC";   PMID:3793330 "Europe PMC";   PMID:4077347 "Europe PMC";   PMID:6655800 "Europe PMC";   PMID:7154255 "Europe PMC";   PMID:7321185 "Europe PMC";   PMID:7321187 "Europe PMC";   Patent:WO2011147316;   Reaxys:25081792 "Reaxys"


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          spiramycin II 0
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    subatomic particle 0
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              atomic nucleus 0
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                    p-block element atom 0
                      carbon group element atom 0
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                          organic molecular entity 0
                            organic group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      carboxylic acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            formyl group 0
                                              aldehyde 0
                                                spiramycin II 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.