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Compounds

COMPOUND NPA020436

STRUCTURE
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PROPERTIES
NPAID NPA020436
CLUSTER ID 920
NODE ID 141
NAME Friulimicin A
FORMULA C58H92N14O19
MOLECULAR WEIGHT (Da) 1289.4530
ACCURATE MASS (Da) 1288.6663
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Actinoplanes
ORIGIN SPECIES friuliensis HAG 010964
InChIKey SLJYYRCUSIXQEQ-AJAGNRCHSA-N
InChI InChI=1S/C58H92N14O19/c1-29(2)18-13-11-9-8-10-12-14-21-40(74)64-34(24-39(60)73)51(83)70-48-33(7)63-52(84)38-20-17-23-72(38)56(88)45(30(3)4)68-55(87)47(32(6)59)67-42(76)28-62-49(81)35(25-43(77)78)65-41(75)27-61-50(82)36(26-44(79)80)66-54(86)46(31(5)58(90)91)69-53(85)37-19-15-16-22-71(37)57(48)89/h12,14,29-38,45-48H,8-11,13,15-28,59H2,1-7H3,(H2,60,73)(H,61,82)(H,62,81)(H,63,84)(H,64,74)(H,65,75)(H,66,86)(H,67,76)(H,68,87)(H,69,85)(H,70,83)(H,77,78)(H,79,80)(H,90,91)/b14-12-/t31-,32+,33+,34-,35-,36-,37+,38-,45+,46-,47+,48-/m0/s1
SMILES C[C@@H]1[C@@H](C(=O)N2CCCC[C@@H]2C(=O)N[C@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)NCC(=O)N[C@@H](C(=O)N[C@@H](C(=O)N3CCC[C@H]3C(=O)N1)C(C)C)[C@@H](C)N)CC(=O)O)CC(=O)O)[C@H](C)C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)C/C=C\CCCCCCC(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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