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Compounds

COMPOUND NPA020317

STRUCTURE
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EXTERNAL LINKS
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PROPERTIES
NPAID NPA020317
CLUSTER ID 2059
NODE ID 1648
NAME CDA3a
FORMULA C66H76N14O26
MOLECULAR WEIGHT (Da) 1481.4060
ACCURATE MASS (Da) 1480.5055
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES coelicolor A3(2)
InChIKey SLGCKWXDQZMUCF-SSNLTMHJSA-N
InChI InChI=1S/C66H76N14O26/c1-3-8-44-54(106-44)65(103)77-43(27-81)61(99)79-50-28(2)105-66(104)42(20-31-25-69-36-12-7-5-10-34(31)36)76-57(95)37(17-18-46(84)85)71-64(102)52(53(92)55(67)93)78-45(83)26-70-56(94)39(21-47(86)87)75-63(101)51(29-13-15-32(82)16-14-29)80-60(98)41(23-49(90)91)73-59(97)40(22-48(88)89)72-58(96)38(74-62(50)100)19-30-24-68-35-11-6-4-9-33(30)35/h4-7,9-16,20,24-25,28,37-41,43-44,50-54,68-69,81-82,92H,3,8,17-19,21-23,26-27H2,1-2H3,(H2,67,93)(H,70,94)(H,71,102)(H,72,96)(H,73,97)(H,74,100)(H,75,101)(H,76,95)(H,77,103)(H,78,83)(H,79,99)(H,80,98)(H,84,85)(H,86,87)(H,88,89)(H,90,91)/b42-20-/t28-,37+,38-,39+,40+,41+,43+,44?,50+,51-,52-,53+,54?/m1/s1
SMILES CCCC1C(O1)C(=O)N[C@@H](CO)C(=O)N[C@H]2[C@H](OC(=O)/C(=C/C3=CNC4=CC=CC=C43)/NC(=O)[C@@H](NC(=O)[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](NC2=O)CC5=CNC6=CC=CC=C65)CC(=O)O)CC(=O)O)C7=CC=C(C=C7)O)CC(=O)O)[C@@H](C(=O)N)O)CCC(=O)O)C
ORIGINAL ISOLATION REFERENCE
CITATION Hojati Z, Milne C, Harvey B, Gordon L, Borg M, Flett F, Wilkinson B, Sidebottom PJ, Rudd BA, Hayes MA, Smith CP, Micklefield J Structure, Biosynthetic Origin, and Engineered Biosynthesis of Calcium-Dependent Antibiotics from Streptomyces coelicolor Chemistry & Biology 2002 9 (11) 1175-1187.
DOI 10.1016/S1074-5521(02)00252-1 PMID 12445768
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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