InChI=1S/C31H51NO9/c1-9-25-20(5)29-31(6,41-29)12-10-23(34)17(2)14-21(11-13-33)28(19(4)24(35)16-26(36)39-25)40-30-27(37)22(32(7)8)15-18(3)38-30/h10,12-13,17-22,24-25,27-30,35,37H,9,11,14-16H2,1-8H3/b12-10+/t17-,18-,19+,20-,21+,22+,24-,25-,27-,28-,29+,30+,31+/m1/s1 |
IUPCWCLVECYZRV-JZMZINANSA-N |
CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@@H](CC=O)C[C@@H](C)C(=O)\C=C\[C@]2(C)O[C@H]2[C@@H]1C |
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Micromonospora rosaria
(NCBI:txid47874)
|
See:
DOI
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bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via macrolide antibiotic )
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View more via ChEBI Ontology
(1S,2R,3R,7R,8S,9S,10R,12R,14E,16S)-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-10-(2-oxoethyl)-4,17-dioxabicyclo[14.1.0]heptadec-14-en-9-yl 3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranoside
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rosaramicin
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ChemIDplus
|
rosaramicina
|
ChemIDplus
|
rosaramicine
|
ChemIDplus
|
rosaramicinum
|
ChemIDplus
|
4'-Deoxycirramycin A1
|
ChemIDplus
|
Antibiotic 67-694
|
ChemIDplus
|
Antibiotic M 4365A2
|
ChemIDplus
|
Juvenimicin A3
|
ChemIDplus
|
M 4365A2
|
ChemIDplus
|
M-4365A2
|
ChemIDplus
|
NSC 175150
|
ChemIDplus
|
Rosamicin
|
ChemIDplus
|
Sch 14947
|
ChemIDplus
|
35834-26-5
|
CAS Registry Number
|
SUBMITTER
|
35834-26-5
|
CAS Registry Number
|
ChemIDplus
|
4731365
|
Reaxys Registry Number
|
Reaxys
|
2088343
|
PubMed citation
|
Europe PMC
|
3890223
|
PubMed citation
|
Europe PMC
|
3988965
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PubMed citation
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Europe PMC
|
43705
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PubMed citation
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Europe PMC
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6141912
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PubMed citation
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Europe PMC
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6517543
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PubMed citation
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Europe PMC
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6625312
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PubMed citation
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Europe PMC
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6648747
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PubMed citation
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Europe PMC
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6786880
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PubMed citation
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Europe PMC
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7039760
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PubMed citation
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Europe PMC
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7221804
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PubMed citation
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Europe PMC
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7235684
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PubMed citation
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Europe PMC
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7444711
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PubMed citation
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Europe PMC
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7447432
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PubMed citation
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Europe PMC
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903212
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PubMed citation
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Europe PMC
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