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Compounds

COMPOUND NPA001341

STRUCTURE
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PROPERTIES
NPAID NPA001341
CLUSTER ID 887
NODE ID 768
NAME Cervimycin D
FORMULA C60H79NO25
MOLECULAR WEIGHT (Da) 1214.2740
ACCURATE MASS (Da) 1213.4941
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES tendae
InChIKey YQSUNUWAYVGFKR-DIMVSIEISA-N
InChI InChI=1S/C60H79NO25/c1-24(58(70)71)59(72)84-40-13-18-45(77-30(40)7)82-37-11-16-43(75-27(37)4)81-36-10-17-44(76-26(36)3)83-38-12-19-46(78-28(38)5)85-54-33-22-31-21-32-49(35(63)23-41(73-8)51(32)64)52(65)48(31)55(67)60(33,56(68)50(53(54)66)57(61)69)86-47-20-14-39(29(6)79-47)80-42-15-9-34(62)25(2)74-42/h21,23-30,33-34,36-40,42-47,54,62,65,68H,9-20,22H2,1-8H3,(H2,61,69)(H,70,71)/t24?,25-,26+,27+,28-,29-,30+,33-,34+,36+,37+,38+,39+,40+,42+,43+,44+,45+,46+,47+,54-,60-/m1/s1
SMILES C[C@@H]1[C@H](CC[C@@H](O1)O[C@H]2CC[C@@H](O[C@@H]2C)O[C@]34[C@H](CC5=C(C3=O)C(=C6C(=C5)C(=O)C(=CC6=O)OC)O)[C@H](C(=O)C(=C4O)C(=O)N)O[C@H]7CC[C@@H]([C@H](O7)C)O[C@H]8CC[C@@H]([C@@H](O8)C)O[C@H]9CC[C@@H]([C@@H](O9)C)O[C@H]1CC[C@@H]([C@@H](O1)C)OC(=O)C(C)C(=O)O)O
ORIGINAL ISOLATION REFERENCE
CITATION Herold, Kerstin; Gollmick, Friedrich A; Groth, Ingrid; Roth, Martin; Menzel, Klaus-Dieter; Möllmann, Ute; Gräfe, Udo; Hertweck, Christian Cervimycin A-D: a polyketide glycoside complex from a cave bacterium can defeat vancomycin resistance Chemistry - A European Journal 2005 11 (19) 5523-5530.
DOI 10.1002/chem.200500320 PMID 15940739
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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