{"id":3695,"npaid":"NPA003695","original_name":"Thelephantin O","mol_formula":"C33H24O8","mol_weight":"548.5470","exact_mass":"548.1471","inchikey":"GFBVHSKVZMZGND-UHFFFAOYSA-N","smiles":"C1=CC=C(C=C1)CC(=O)OC2=C(C(=C(C(=C2C3=CC=C(C=C3)O)O)O)C4=CC=C(C=C4)O)OC(=O)C5=CC=CC=C5","cluster_id":24,"node_id":23,"has_exclusions":false,"synonyms":[],"inchi":"InChI=1S/C33H24O8/c34-24-15-11-21(12-16-24)27-29(37)30(38)28(22-13-17-25(35)18-14-22)32(41-33(39)23-9-5-2-6-10-23)31(27)40-26(36)19-20-7-3-1-4-8-20/h1-18,34-35,37-38H,19H2","m_plus_h":"549.1544","m_plus_na":"571.1363","origin_reference":{"doi":"10.1021/jf200461j","pmid":21630659,"authors":"Norikura, Toshio; Fujiwara, Kenshu; Narita, Takanobu; Yamaguchi, Shinya; Morinaga, Yae; Iwai, Kunihisa; Matsue, Hajime","title":"Anticancer activities of thelephantin O and vialinin A isolated from Thelephora aurantiotincta","journal":"Journal of Agricultural and Food Chemistry","year":2011,"volume":"59","issue":"13","pages":"6974-6979"},"origin_organism":{"id":440,"type":"Fungus","genus":"Thelephora","species":"aurantiotincta","taxon":{"id":1611,"name":"Thelephora","rank":"genus","taxon_db":"mycobank","external_id":"18640","ncbi_id":56489,"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":1603,"name":"Thelephorales","rank":"order","taxon_db":"mycobank","external_id":"90575","ncbi_id":56487},{"id":1609,"name":"Thelephoraceae","rank":"family","taxon_db":"mycobank","external_id":"81463","ncbi_id":56488}]}},"syntheses":["10.1021/jo300565s"],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.1021/jf200461j","structure_smiles":"C1=CC=C(C=C1)CC(=O)OC2=C(C(=C(C(=C2C3=CC=C(C=C3)O)O)O)C4=CC=C(C=C4)O)OC(=O)C5=CC=CC=C5","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"npmrd","external_db_code":"NP0010080"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0001645","name":"Depsides and depsidones","chemont_id":"CHEMONTID:0001645","description":"Polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone)."},"smiles":"OC1=CC=C(C=C1)C1=C(O)C(O)=C(C2=CC=C(O)C=C2)C(OC(=O)C2=CC=CC=C2)=C1OC(=O)CC1=CC=CC=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=GFBVHSKVZMZGND-UHFFFAOYSA-N","subclass":null,"ancestors":["1-hydroxy-2-unsubstituted benzenoids","Benzene and substituted derivatives","Benzenediols","Benzenoids","Benzoic acid esters","Benzoic acids and derivatives","Benzoyl derivatives","Biphenyls and derivatives","Carbonyl compounds","Carboxylic acid derivatives","Carboxylic acid esters","Carboxylic acids and derivatives","Catechols","Chemical entities","Depsides and depsidones","Dicarboxylic acids and derivatives","Hydrocarbon derivatives","Monocarboxylic acids and derivatives","Organic acids and derivatives","Organic compounds","Organic oxides","Organic oxygen compounds","Organooxygen compounds","P-terphenyls","Phenol esters","Phenols","Phenoxy compounds","Phenylpropanoids and polyketides","Terphenyls"],"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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