Additional file 1 of Evaluation of the anticarcinogenic potential of the endophyte, Streptomyces sp. LRE541 isolated from Lilium davidii var. unicolor (Hoog) Cotton

Additional file 1: Table S1. Antimicrobial activities of the actinomycete-like isolates from the root tissues of Lilium davidii var. unicolor (Hoog) Cotton. Table S2. Chemical constituents of antitumor-(1–39), antioxidant-(40–49), and antimicrobial-(50–65) compounds identified in the LRE541 extract by the UHPLC-MS/MS analysis. Figure S1. Total iron chromatography of the LRE541 extract by the UHPLC-MS/MS analysis. Figure S2. Chemical structures of the antitumor (1–39)-, antioxidant (40–49)-, and antimicrobial (50–65)-compounds from the LRE541 extract. Figure S3. 13C NMR spectrum of epsilon-pyrromycinone in CDCl3 (100 MHz). Figure S4. 1H NMR spectrum of Epsilon-pyrromycinone in CDCl3 (400 MHz). Figure S5. 13C NMR spectrum of 4-deoxy-ε-pyrromycinone in CDCl3 (100 MHz). Figure S6. 1H NMR spectrum of 4-deoxy-ε-pyrromycinone in CDCl3 (400 MHz). Figure S7. HMBC spectrum of 4-deoxy-ε-pyrromycinone in CDCl3. Figure S8. HSQC spectrum of 4-deoxy-ε-pyrromycinone in CDCl3. Figure S9. 13C NMR spectrum of Neoechinulin A in CDCl3 (100 MHz). Figure S10. 1H NMR spectrum of Neoechinulin A in CDCl3 (400 MHz).