{"id":423,"npaid":"NPA000423","original_name":"Myxovirescin A1","mol_formula":"C35H61NO8","mol_weight":"623.8720","exact_mass":"623.4397","inchikey":"VQWNGCSUNKJFLW-ARNOELBJSA-N","smiles":"CCC[C@H]1C(=O)NC[C@H](C[C@@H]([C@@H](CC/C(=C/C=C/C(CCCC(=O)CCCC[C@H](C[C@@H](C(=O)O1)C)C)CC)/COC)O)O)O","cluster_id":331,"node_id":300,"has_exclusions":false,"synonyms":[],"inchi":"InChI=1S/C35H61NO8/c1-6-12-33-34(41)36-23-30(38)22-32(40)31(39)20-19-28(24-43-5)16-10-14-27(7-2)15-11-18-29(37)17-9-8-13-25(3)21-26(4)35(42)44-33/h10,14,16,25-27,30-33,38-40H,6-9,11-13,15,17-24H2,1-5H3,(H,36,41)/b14-10+,28-16-/t25-,26+,27?,30+,31-,32+,33+/m1/s1","m_plus_h":"624.4470","m_plus_na":"646.4289","origin_reference":{"doi":"10.1039/c39820001340","pmid":null,"authors":"Trowitzsch, Wolfram; Wray, Victor; Gerth, Klaus; Höfle, Gerhard","title":"Structure of myxovirescin A, a new macrocylic antibiotic from gliding bacteria","journal":"Journal of the Chemical Society, Chemical Communications","year":1982,"volume":null,"issue":"23","pages":"1340-1342"},"origin_organism":{"id":372,"type":"Bacterium","genus":"Myxococcus","species":"virescens strain v48","taxon":{"id":185,"name":"Myxococcus","rank":"genus","taxon_db":"lpsn","external_id":"516145","ncbi_id":32,"ancestors":[{"id":1,"name":"Bacteria","rank":"domain","taxon_db":"lpsn","external_id":"0","ncbi_id":2},{"id":2,"name":"Proteobacteria","rank":"phylum","taxon_db":"lpsn","external_id":"0","ncbi_id":1224},{"id":168,"name":"Deltaproteobacteria","rank":"class","taxon_db":"lpsn","external_id":"0","ncbi_id":28221},{"id":169,"name":"Myxococcales","rank":"order","taxon_db":"lpsn","external_id":"0","ncbi_id":29},{"id":183,"name":"Myxococcaceae","rank":"family","taxon_db":"lpsn","external_id":"0","ncbi_id":31}]}},"syntheses":["10.1002/chem.200700926"],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.1039/c39820001340","structure_smiles":"CCC[C@H]1C(=O)NC[C@H](C[C@@H]([C@@H](CC/C(=C/C=C/C(CCCC(=O)CCCC[C@H](C[C@@H](C(=O)O1)C)C)CC)/COC)O)O)O","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"mibig","external_db_code":"BGC0001104"},{"external_db_name":"mibig","external_db_code":"BGC0001025"},{"external_db_name":"gnps","external_db_code":"CCMSLIB00000478595%Myxovirescin A%1"},{"external_db_name":"npmrd","external_db_code":"NP0178757"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0001900","name":"Macrolide lactams","chemont_id":"CHEMONTID:0001900","description":"Cyclic polyketides containing  both a cyclic amide and a cyclic ester group."},"smiles":"CCC[C@@H]1OC(=O)[C@@H](C)C[C@H](C)CCCCC(=O)CCCC(CC)\\C=C\\C=C(COC)\\CC[C@@H](O)[C@@H](O)C[C@H](O)CNC1=O","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=VQWNGCSUNKJFLW-ARNOELBJSA-N","subclass":null,"ancestors":["1,2-diols","Alcohols and polyols","Azacyclic compounds","Carbonyl compounds","Carboxylic acid amides","Carboxylic acid derivatives","Carboxylic acid esters","Carboxylic acids and derivatives","Chemical entities","Cyclic ketones","Dialkyl ethers","Ethers","Hydrocarbon derivatives","Ketones","Lactams","Lactones","Macrolactams","Macrolide lactams","Macrolides and analogues","Monocarboxylic acids and derivatives","Organic acids and derivatives","Organic compounds","Organic nitrogen compounds","Organic oxides","Organic oxygen compounds","Organoheterocyclic compounds","Organonitrogen compounds","Organooxygen compounds","Organopnictogen compounds","Oxacyclic compounds","Phenylpropanoids and polyketides","Polyols","Secondary alcohols","Secondary carboxylic acid amides"],"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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