{"id":2548,"npaid":"NPA002548","original_name":"Schizostatin","mol_formula":"C20H30O2","mol_weight":"302.4580","exact_mass":"302.2246","inchikey":"HZGINAUBYAMOBF-AVNCOZOESA-N","smiles":"CC(=CCC/C(=C/CC/C(=C/CC/C(=C\\C=O)/C=O)/C)/C)C","cluster_id":1507,"node_id":1239,"has_exclusions":false,"synonyms":[],"inchi":"InChI=1S/C20H30O2/c1-17(2)8-5-9-18(3)10-6-11-19(4)12-7-13-20(16-22)14-15-21/h8,10,12,14-16H,5-7,9,11,13H2,1-4H3/b18-10+,19-12+,20-14+","m_plus_h":"303.2319","m_plus_na":"325.2138","origin_reference":{"doi":"10.7164/antibiotics.49.624","pmid":8784420,"authors":"KOGEN, HIROSHI; TAGO, KEIKO; KANEKO, SATORU; HAMANO, KIYOSHI; ONODERA, KAORI; HARUYAMA, HIDEYUKI; MINAGAWA, KATSUHIRO; KINOSHITA, TAKESHI; ISHIKAWA, TOMIO; TANIMOTO, TATSUO; TSUJITA, YOSHIO","title":"Schizostatin, a Novel Squalene Synthase Inhibitor Produced by the Mushroom, Schizophylllum commune. II. Structure Elucidation and Total Synthesis","journal":"Journal of Antibiotics","year":1996,"volume":"49","issue":"7","pages":"624-630"},"origin_organism":{"id":1672,"type":"Fungus","genus":"Schizophyllum","species":"commune","taxon":{"id":1483,"name":"Schizophyllum","rank":"genus","taxon_db":"mycobank","external_id":"18512","ncbi_id":5333,"ancestors":[{"id":599,"name":"Eukarya","rank":"domain","taxon_db":"mycobank","external_id":"0","ncbi_id":2759},{"id":600,"name":"Fungi","rank":"kingdom","taxon_db":"mycobank","external_id":"90157","ncbi_id":4751},{"id":1365,"name":"Basidiomycota","rank":"phylum","taxon_db":"mycobank","external_id":"90050","ncbi_id":5204},{"id":1366,"name":"Agaricomycetes","rank":"class","taxon_db":"mycobank","external_id":"501297","ncbi_id":155619},{"id":1367,"name":"Agaricales","rank":"order","taxon_db":"mycobank","external_id":"90508","ncbi_id":5338},{"id":1482,"name":"Schizophyllaceae","rank":"family","taxon_db":"mycobank","external_id":"81263","ncbi_id":5332}]}},"syntheses":["10.7164/antibiotics.49.624"],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.7164/antibiotics.49.624","structure_smiles":"CC(=CCC/C(=C/CC/C(=C/CC/C(=C\\C=O)/C=O)/C)/C)C","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"npmrd","external_db_code":"NP0023220"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000259","name":"Prenol lipids","chemont_id":"CHEMONTID:0000259","description":"Lipids synthesized from the five-carbon-unit precursors isopentenyl diphosphate and dimethylallyl diphosphate."},"smiles":"CC(C)=CCC\\C(C)=C\\CC\\C(C)=C\\CC\\C(C=O)=C/C=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=HZGINAUBYAMOBF-AVNCOZOESA-N","subclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0001551","name":"Diterpenoids","chemont_id":"CHEMONTID:0001551","description":"Terpene compounds formed by four isoprene units."},"ancestors":["Acyclic diterpenoids","Aldehydes","Alpha,beta-unsaturated aldehydes","Alpha,beta-unsaturated carbonyl compounds","Carbonyl compounds","Chemical entities","Diterpenoids","Enals","Fatty Acyls","Fatty aldehydes","Hydrocarbon derivatives","Lipids and lipid-like molecules","Organic compounds","Organic oxides","Organic oxygen compounds","Organooxygen compounds","Prenol lipids"],"superclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000012","name":"Lipids and lipid-like molecules","chemont_id":"CHEMONTID:0000012","description":"Fatty acids and their derivatives, and substances related biosynthetically or functionally to these compounds."},"description":"This compound belongs to the class of organic compounds known as acyclic diterpenoids. 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