{"id":4336,"npaid":"NPA004336","original_name":"Ganodermaside A","mol_formula":"C28H40O2","mol_weight":"408.6260","exact_mass":"408.3028","inchikey":"MMVSNLKSAHIETF-ZZAHPFGNSA-N","smiles":"C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1C[C@@H](C2=C3C=CC4=CC(=O)CC[C@@]4(C3CC[C@]12C)C)O","cluster_id":2164,"node_id":163,"has_exclusions":false,"synonyms":[],"inchi":"InChI=1S/C28H40O2/c1-17(2)18(3)7-8-19(4)24-16-25(30)26-22-10-9-20-15-21(29)11-13-27(20,5)23(22)12-14-28(24,26)6/h7-10,15,17-19,23-25,30H,11-14,16H2,1-6H3/b8-7+/t18-,19+,23?,24+,25-,27-,28+/m0/s1","m_plus_h":"409.3101","m_plus_na":"431.2920","origin_reference":{"doi":"10.1016/j.bmc.2009.12.070","pmid":20093034,"authors":"Weng, Yufang; Xiang, Lan; Matsuura, Akira; Zhang, Yang; Huang, Qianming; Qi, Jianhua","title":"Ganodermasides A and B, two novel anti-aging ergosterols from spores of a medicinal mushroom Ganoderma lucidum on yeast via UTH1 gene","journal":"Bioorganic and Medicinal Chemistry","year":2010,"volume":"18","issue":"3","pages":"999"},"origin_organism":{"id":159,"type":"Fungus","genus":"Ganoderma","species":"lucidum","taxon":{"id":1515,"name":"Ganoderma","rank":"genus","taxon_db":"mycobank","external_id":"17639","ncbi_id":5314,"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":1511,"name":"Polyporales","rank":"order","taxon_db":"mycobank","external_id":"90565","ncbi_id":5303},{"id":1512,"name":"Ganodermataceae","rank":"family","taxon_db":"mycobank","external_id":"80782","ncbi_id":null}]}},"syntheses":[],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.1016/j.bmc.2009.12.070","structure_smiles":"C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1C[C@@H](C2=C3C=CC4=CC(=O)CC[C@@]4(C3CC[C@]12C)C)O","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"npmrd","external_db_code":"NP0008977"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000258","name":"Steroids and steroid derivatives","chemont_id":"CHEMONTID:0000258","description":"Compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. 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