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Gross H; Goeger D; Musafija-Girt M; McPhail K; Leal RM; Mooberry SL; Gerwick WH","title":"Isolation of swinholide A and related glycosylated derivatives from two field collections of marine cyanobacteria.","journal":"Organic Letters","year":2005,"volume":"7","issue":"7","pages":"1375-1378"},"origin_organism":{"id":1515,"type":"Bacterium","genus":"Symploca","species":"sp.","taxon":{"id":488,"name":"Symploca","rank":"genus","taxon_db":"lpsn","external_id":"0","ncbi_id":105591,"ancestors":[{"id":1,"name":"Bacteria","rank":"domain","taxon_db":"lpsn","external_id":"0","ncbi_id":2},{"id":417,"name":"Cyanobacteria","rank":"phylum","taxon_db":"lpsn","external_id":"0","ncbi_id":1117},{"id":418,"name":"Cyanophyceae","rank":"class","taxon_db":"lpsn","external_id":"0","ncbi_id":null},{"id":473,"name":"Oscillatoriales","rank":"order","taxon_db":"lpsn","external_id":"0","ncbi_id":1150},{"id":486,"name":"Microcoleaceae","rank":"family","taxon_db":"lpsn","external_id":"0","ncbi_id":1892252}]}},"syntheses":[],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.1021/ol050188x","structure_smiles":"CO[C@@H]1C[C@H](C)O[C@@H](CC[C@H](C)[C@H](O)[C@H](C)C2OC(=O)/C=C/C(C)=C/C[C@@H](O)C[C@H]3C=CC[C@H](C[C@@H](OC)[C@H](C)[C@H](O)C[C@H](O)[C@@H](C)C([C@@H](C)[C@@H](O)[C@@H](C)CC[C@H]4C[C@H](OC)C[C@H](C)O4)OC(=O)/C=C/C(C)=C/C[C@@H](O)C[C@H]4C=CC[C@H](C[C@@H](OC)[C@H](C)[C@H](O)C[C@H](O)[C@H]2C)O4)O3)C1","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"mibig","external_db_code":"BGC0001795"},{"external_db_name":"gnps","external_db_code":"CCMSLIB00005436034%Swinholide A%3"},{"external_db_name":"gnps","external_db_code":"CCMSLIB00005463853%Swinholide A%3"},{"external_db_name":"gnps","external_db_code":"CCMSLIB00005463854%Swinholide A%3"},{"external_db_name":"gnps","external_db_code":"CCMSLIB00005467778%Swinholide F putative%3"},{"external_db_name":"npmrd","external_db_code":"NP0005797"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000147","name":"Macrolides and analogues","chemont_id":"CHEMONTID:0000147","description":"Organic compounds containing a lactone ring of at least twelve members."},"smiles":"CO[C@@H]1C[C@H](C)O[C@@H](CC[C@H](C)[C@H](O)[C@H](C)C2OC(=O)\\C=C\\C(\\C)=C\\C[C@@H](O)C[C@@H]3O[C@H](CC=C3)C[C@@H](OC)[C@H](C)[C@H](O)C[C@H](O)[C@@H](C)C(OC(=O)\\C=C\\C(\\C)=C\\C[C@@H](O)C[C@@H]3O[C@H](CC=C3)C[C@@H](OC)[C@H](C)[C@H](O)C[C@H](O)[C@H]2C)[C@@H](C)[C@@H](O)[C@@H](C)CC[C@H]2C[C@@H](C[C@H](C)O2)OC)C1","kingdom":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000000","name":"Organic compounds","chemont_id":"CHEMONTID:0000000","description":"Compounds that contain at least one carbon atom, excluding isocyanide/cyanide and their non-hydrocarbyl derivatives, thiophosgene, carbon diselenide, carbon monosulfide, carbon disulfide, carbon subsulfide, carbon monoxide, carbon dioxide, Carbon suboxide, and dicarbon monoxide."},"inchikey":"InChIKey=RJVBVECTCMRNFG-YGHILOOQSA-N","subclass":null,"ancestors":["Alcohols and polyols","Alpha,beta-unsaturated carboxylic esters","Carbonyl compounds","Carboxylic acid derivatives","Carboxylic acid esters","Carboxylic acids and derivatives","Chemical entities","Dialkyl ethers","Dicarboxylic acids and derivatives","Enoate esters","Ethers","Hydrocarbon derivatives","Lactones","Macrolides and analogues","Organic acids and derivatives","Organic compounds","Organic oxides","Organic oxygen compounds","Organoheterocyclic compounds","Organooxygen compounds","Oxacyclic compounds","Oxanes","Phenylpropanoids and polyketides","Polyols","Pyrans","Secondary alcohols"],"superclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000261","name":"Phenylpropanoids and polyketides","chemont_id":"CHEMONTID:0000261","description":"Organic compounds that are synthesized either from the amino acid phenylalanine (phenylpropanoids) or the decarboxylative condensation of malonyl-CoA (polyketides). 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