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Compounds

COMPOUND NPA027388

STRUCTURE
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PROPERTIES
NPAID NPA027388
CLUSTER ID 8263
NODE ID 4987
NAME 6-O-triacetyl(A,B,C)-α-cyclodextrin
FORMULA C42H66O33
MOLECULAR WEIGHT (Da) 1098.9570
ACCURATE MASS (Da) 1098.3486
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Anabaena
ORIGIN SPECIES sp. XSPORK2A
InChIKey WHFOCKDBMPPPNF-YFUQKLGGSA-N
InChI InChI=1S/C42H66O33/c1-10(46)61-7-16-34-23(53)29(59)41(68-16)75-36-18(9-63-12(3)48)69-42(30(60)24(36)54)74-35-17(8-62-11(2)47)67-40(28(58)22(35)52)72-33-15(6-45)65-38(26(56)20(33)50)70-31-13(4-43)64-37(25(55)19(31)49)71-32-14(5-44)66-39(73-34)27(57)21(32)51/h13-45,49-60H,4-9H2,1-3H3/t13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37?,38?,39?,40?,41?,42?/m1/s1
SMILES CC(=O)OC[C@H]1OC2O[C@@H]3[C@@H](COC(C)=O)OC(O[C@@H]4[C@@H](COC(C)=O)OC(O[C@@H]5[C@@H](CO)OC(O[C@@H]6[C@@H](CO)OC(O[C@@H]7[C@@H](CO)OC(O[C@H]1[C@H](O)[C@H]2O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O
ORIGINAL ISOLATION REFERENCE
CITATION Shishido TK; Jokela J; Kolehmainen CT; Fewer DP; Wahlsten M; Wang H; Rouhiainen L; Rizzi E; De Bellis G; Permi P; Sivonen K Antifungal activity improved by coproduction of cyclodextrins and anabaenolysins in Cyanobacteria. Proceedings of the National Academy of Sciences of the United States of America 2015 112 (44) 13669-13674.
DOI 10.1073/pnas.1510432112 PMID 26474830
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Cyanobacteria LPSN 1117
Class Cyanophyceae LPSN -
Order Nostocales LPSN 1161
Family Aphanizomenonaceae LPSN 1892259
Genus Anabaena LPSN 1163
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