{"id":12386,"npaid":"NPA012386","original_name":"Matlystatin A","mol_formula":"C22H40N4O5","mol_weight":"440.5850","exact_mass":"440.2999","inchikey":"IWWYEUSBHSDVOX-CLWJZODNSA-N","smiles":"CCCCC[C@H](CC(=O)NO)C(=O)N1[C@@H](CCCN1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)CC","cluster_id":2909,"node_id":2234,"has_exclusions":false,"synonyms":[],"inchi":"InChI=1S/C22H40N4O5/c1-5-8-9-11-16(14-19(28)25-31)22(30)26-17(12-10-13-23-26)21(29)24-20(15(4)6-2)18(27)7-3/h15-17,20,23,31H,5-14H2,1-4H3,(H,24,29)(H,25,28)/t15-,16+,17-,20-/m0/s1","m_plus_h":"441.3072","m_plus_na":"463.2891","origin_reference":{"doi":"10.7164/antibiotics.47.1473","pmid":7844042,"authors":"Haruyama; Ohkuma; Nagaki; Ogita; Tamaki; Kinoshita","title":"Matlystatins, new inhibitors of type IV collagenases from Actinomadura atramentaria. III. Structure elucidation of matlystatins A to F","journal":"Journal of Antibiotics","year":1994,"volume":"47","issue":"12","pages":"1473-1480"},"origin_organism":{"id":4463,"type":"Bacterium","genus":"Actinomadura","species":"atramentaria","taxon":{"id":217,"name":"Actinomadura","rank":"genus","taxon_db":"lpsn","external_id":"517407","ncbi_id":1988,"ancestors":[{"id":1,"name":"Bacteria","rank":"domain","taxon_db":"lpsn","external_id":"0","ncbi_id":2},{"id":203,"name":"Actinobacteria","rank":"phylum","taxon_db":"lpsn","external_id":"0","ncbi_id":201174},{"id":204,"name":"Actinobacteria","rank":"class","taxon_db":"lpsn","external_id":"0","ncbi_id":null},{"id":205,"name":"Streptosporangiales","rank":"order","taxon_db":"lpsn","external_id":"0","ncbi_id":85012},{"id":215,"name":"Thermomonosporaceae","rank":"family","taxon_db":"lpsn","external_id":"0","ncbi_id":2012}]}},"syntheses":[],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.7164/antibiotics.47.1473","structure_smiles":"CCCCC[C@H](CC(=O)NO)C(=O)N1[C@@H](CCCN1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)CC","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"mibig","external_db_code":"BGC0001443"},{"external_db_name":"npmrd","external_db_code":"NP0022530"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000265","name":"Carboxylic acids and derivatives","chemont_id":"CHEMONTID:0000265","description":"Compounds containing a carboxylic acid group with the formula -C(=O)OH or a derivative thereof."},"smiles":"CCCCC[C@H](CC(=O)NO)C(=O)N1NCCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)CC","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=IWWYEUSBHSDVOX-CLWJZODNSA-N","subclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000013","name":"Amino acids, peptides, and analogues","chemont_id":"CHEMONTID:0000013","description":"Organic compounds containing an amino acid or a peptide backbone, or derivatives thereof."},"ancestors":["Alpha amino acids and derivatives","Amino acids and derivatives","Amino acids, peptides, and analogues","Azacyclic compounds","Carbonyl compounds","Carboxylic acid amides","Carboxylic acid derivatives","Carboxylic acid hydrazides","Carboxylic acids and derivatives","Chemical entities","Diazinanes","Hydrocarbon derivatives","Hydroxamic acids","Ketones","Organic acids and derivatives","Organic compounds","Organic nitrogen compounds","Organic oxides","Organic oxygen compounds","Organoheterocyclic compounds","Organonitrogen compounds","Organooxygen compounds","Organopnictogen compounds","Primary carboxylic acid amides","Secondary carboxylic acid amides"],"superclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000264","name":"Organic acids and derivatives","chemont_id":"CHEMONTID:0000264","description":"Compounds an organic acid or a derivative thereof."},"description":"This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. 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