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Compounds

COMPOUND NPA002355

STRUCTURE
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PROPERTIES
NPAID NPA002355
CLUSTER ID 920
NODE ID 141
NAME A-1437-B
FORMULA C59H93N13O20
MOLECULAR WEIGHT (Da) 1304.4640
ACCURATE MASS (Da) 1303.6660
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Actinoplanes
ORIGIN SPECIES friuliensis
InChIKey BYWOWQCRVFUOLF-FYWRMAATSA-N
InChI InChI=1S/C59H93N13O20/c1-30(2)19-14-12-10-8-9-11-13-15-22-40(73)64-37(27-45(80)81)52(84)70-49-34(7)63-53(85)39-21-18-24-72(39)57(89)46(31(3)4)68-56(88)48(33(6)60)67-42(75)29-62-50(82)35(25-43(76)77)65-41(74)28-61-51(83)36(26-44(78)79)66-55(87)47(32(5)59(91)92)69-54(86)38-20-16-17-23-71(38)58(49)90/h13,15,30-39,46-49H,8-12,14,16-29,60H2,1-7H3,(H,61,83)(H,62,82)(H,63,85)(H,64,73)(H,65,74)(H,66,87)(H,67,75)(H,68,88)(H,69,86)(H,70,84)(H,76,77)(H,78,79)(H,80,81)(H,91,92)/b15-13+
SMILES CC1C(C(=O)N2CCCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)C)C(C)N)CC(=O)O)CC(=O)O)C(C)C(=O)O)NC(=O)C(CC(=O)O)NC(=O)C/C=C/CCCCCCCC(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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