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Compounds

COMPOUND NPA033054

STRUCTURE
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PROJECT MOLECULE TO GLOBAL VIEW See Global
EXTERNAL LINKS
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PROPERTIES
NPAID NPA033054
CLUSTER ID 9531
NODE ID 6381
NAME Corbomycin
FORMULA C79H66N10O22
MOLECULAR WEIGHT (Da) 1507.4450
ACCURATE MASS (Da) 1506.4353
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES sp. WAC01529
InChIKey YPKFJNUZFFXJND-OUBAQASASA-N
InChI InChI=1S/C79H66N10O22/c1-33(90)81-64(36-5-9-43(91)10-6-36)76(105)86-66-40-21-46(94)29-49(22-40)111-61-26-38(8-15-59(61)97)65-77(106)87-67-41-23-51(37-7-13-50-42(32-80-54(50)24-37)25-57(73(102)85-65)84-74(66)103)70(99)62(27-41)110-48-11-2-34(3-12-48)17-55-72(101)89-69(78(107)88-68(79(108)109)39-19-44(92)28-45(93)20-39)53-30-47(95)31-60(98)63(53)52-16-35(4-14-58(52)96)18-56(71(100)82-55)83-75(67)104/h2-16,19-24,26-32,55-57,64-69,80,91-99H,17-18,25H2,1H3,(H,81,90)(H,82,100)(H,83,104)(H,84,103)(H,85,102)(H,86,105)(H,87,106)(H,88,107)(H,89,101)(H,108,109)/t55-,56+,57+,64-,65+,66-,67+,68-,69-/m0/s1
SMILES CC(=O)N[C@H](C(=O)N[C@@H]1C(=O)N[C@@H]2CC3=CNC4=C3C=CC(=C4)C3=CC4=CC(=C3O)OC3=CC=C(C=C3)C[C@@H]3NC(=O)[C@@H](CC5=CC=C(O)C(=C5)C5=C(C=C(O)C=C5O)[C@@H](C(=O)N[C@H](C(=O)O)C5=CC(O)=CC(O)=C5)NC3=O)NC(=O)[C@@H]4NC(=O)[C@H](NC2=O)C2=CC(=C(O)C=C2)OC2=CC1=CC(O)=C2)C1=CC=C(O)C=C1
ORIGINAL ISOLATION REFERENCE
CITATION Culp, Elizabeth J; Waglechner, Nicholas; Wang, Wenliang; Fiebig-Comyn, Aline A; Hsu, Yen-Pang; Koteva, Kalinka; Sychantha, David; Coombes, Brian K; Van Nieuwenhze, Michael S; Brun, Yves V; Wright, Gerard D Evolution-guided discovery of antibiotics that inhibit peptidoglycan remodelling. Nature 2020 578 (7796) 582-587.
DOI 10.1038/s41586-020-1990-9 PMID 32051588
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Streptomycetales LPSN 85011
Family Streptomycetaceae LPSN 2062
Genus Streptomyces LPSN 1883
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