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Compounds

COMPOUND NPA033136

STRUCTURE
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PROPERTIES
NPAID NPA033136
CLUSTER ID 248
NODE ID 11
NAME Potashchelin A
FORMULA C43H72N10O23
MOLECULAR WEIGHT (Da) 1097.0960
ACCURATE MASS (Da) 1096.4772
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Halomonas
ORIGIN SPECIES sp. MG34
InChIKey WRQCDTBWGNVZFM-RZNIIMBFSA-N
InChI InChI=1S/C43H72N10O23/c1-3-4-5-6-7-8-9-11-21(59)14-27(60)50-30(32(62)42(72)73)39(69)48-23(16-54)34(64)44-15-28(61)45-24(17-55)35(65)47-26(19-57)37(67)52-31(33(63)43(74)75)40(70)51-29(20(2)58)38(68)49-25(18-56)36(66)46-22-12-10-13-53(76)41(22)71/h20-26,29-33,54-59,62-63,76H,3-19H2,1-2H3,(H,44,64)(H,45,61)(H,46,66)(H,47,65)(H,48,69)(H,49,68)(H,50,60)(H,51,70)(H,52,67)(H,72,73)(H,74,75)/t20-,21?,22+,23-,24-,25+,26+,29-,30+,31+,32+,33-/m1/s1
SMILES CCCCCCCCCC(O)CC(=O)N[C@H](C(=O)N[C@H](CO)C(=O)NCC(=O)N[C@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@@H](CO)C(=O)N[C@H]1CCCN(O)C1=O)[C@@H](C)O)[C@@H](O)C(=O)O)[C@H](O)C(=O)O
ORIGINAL ISOLATION REFERENCE
CITATION Li, Yihong; Liu, Li; Zhang, Gengxin; He, Ning; Guo, Wenqiang; Hong, Bin; Xie, Yunying Potashchelins, a Suite of Lipid Siderophores Bearing Both L-threo and L-erythro Beta-Hydroxyaspartic Acids, Acquired From the Potash-Salt-Ore-Derived Extremophile Halomonas sp. MG34 Frontiers in Chemistry 2020 8 (None) None.
DOI 10.3389/fchem.2020.00197 PMID 32266214
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Proteobacteria LPSN 1224
Class Gammaproteobacteria LPSN 1236
Order Oceanospirillales LPSN 135619
Family Halomonadaceae LPSN 28256
Genus Halomonas LPSN 2745
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