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Compounds

COMPOUND NPA018838

STRUCTURE
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PROPERTIES
NPAID NPA018838
CLUSTER ID 4829
NODE ID 3489
NAME BE-54238B
FORMULA C22H21NO6
MOLECULAR WEIGHT (Da) 395.4110
ACCURATE MASS (Da) 395.1369
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES sp. A54238
InChIKey GROPDRMIDADBEP-UHFFFAOYSA-N
InChI InChI=1S/C22H21NO6/c1-8(24)11-4-5-12-10-3-6-13(25)18-17(10)20(23(11)12)19-16(21(18)27)9(2)28-14-7-15(26)29-22(14)19/h3,6,8-9,11,14,22,24,27H,4-5,7H2,1-2H3
SMILES CC1C2=C(C3=C4C(=C5CCC(N5C4=C2C6C(O1)CC(=O)O6)C(C)O)C=CC3=O)O
ORIGINAL ISOLATION REFERENCE
CITATION TSUKAMOTO, MASAO; NAKAJIMA, SHIGERU; MUROOKA, KUMIKO; HIRAYAMA, MIOKO; HIRANO, KAORI; YOSHIDA, SHIGEMI; KOJIRI, KATSUHISA; SUDA, HIROYUKI New Cytotoxic Agents, BE-54238A and B, Produced by a Streptomycete Journal of Antibiotics 2000 53 (1) 26-32.
DOI 10.7164/antibiotics.53.26 PMID 10724004
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Streptomycetales LPSN 85011
Family Streptomycetaceae LPSN 2062
Genus Streptomyces LPSN 1883
SYNTHESES
CITATION 1 Tatsuta K; Hirabayashi T; Kojima M; Suzuki Y; Ogura T The first total synthesis of a pyranonaphthoquinone antitumor, BE-54238B. Journal of Antibiotics 2004 57 (4) 291-7. DOI: 10.7164/antibiotics.57.291 PMID: 15217195
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