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Compounds

COMPOUND NPA020437

STRUCTURE
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PROPERTIES
NPAID NPA020437
CLUSTER ID 920
NODE ID 141
NAME Friulimicin D
FORMULA C60H96N14O19
MOLECULAR WEIGHT (Da) 1317.5070
ACCURATE MASS (Da) 1316.6976
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Actinoplanes
ORIGIN SPECIES friuliensis HAG 010964
InChIKey YCENLAAIZVXNOG-JCDMCXPCSA-N
InChI InChI=1S/C60H96N14O19/c1-8-32(4)20-15-13-11-9-10-12-14-16-23-42(76)66-36(26-41(62)75)53(85)72-50-35(7)65-54(86)40-22-19-25-74(40)58(90)47(31(2)3)70-57(89)49(34(6)61)69-44(78)30-64-51(83)37(27-45(79)80)67-43(77)29-63-52(84)38(28-46(81)82)68-56(88)48(33(5)60(92)93)71-55(87)39-21-17-18-24-73(39)59(50)91/h14,16,31-40,47-50H,8-13,15,17-30,61H2,1-7H3,(H2,62,75)(H,63,84)(H,64,83)(H,65,86)(H,66,76)(H,67,77)(H,68,88)(H,69,78)(H,70,89)(H,71,87)(H,72,85)(H,79,80)(H,81,82)(H,92,93)/b16-14-/t32?,33-,34+,35+,36-,37-,38-,39+,40-,47+,48-,49+,50-/m0/s1
SMILES CCC(C)CCCCCCC/C=C\CC(=O)N[C@@H](CC(=O)N)C(=O)N[C@H]1[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H]3CCCCN3C1=O)[C@H](C)C(=O)O)CC(=O)O)CC(=O)O)[C@@H](C)N)C(C)C)C
ORIGINAL ISOLATION REFERENCE
CITATION VÉRTESY, LÁSZLÓ; EHLERS, EBERHARD; KOGLER, HERBERT; KURZ, MICHAEL; MEIWES, JOHANNES; SEIBERT, GERHARD; VOGEL, MARTIN; HAMMANN, PETER Friulimicins. Novel Lipopeptide Antibiotics with Peptidoglycan Synthesis Inhibiting Activity from Actinoplanes friuliensis sp. nov. II. Isolation and Structural Characterization Journal of Antibiotics 2000 53 (8) 816-827.
DOI 10.7164/antibiotics.53.816 PMID 11079804
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Micromonosporales LPSN 85008
Family Micromonosporaceae LPSN 28056
Genus Actinoplanes LPSN 1865
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