Barka EA, Vatsa P, Sanchez L, Gaveau-Vaillant N, Jacquard C, Meier-Kolthoff JP, et al. Taxonomy, physiology, and natural products of actinobacteria. Microbiol Mol Biol Rev. 2015;80:1–43.
Google ScholarÂ
Tiwari K, Gupta RK. Rare actinomycetes: a potential storehouse for novel antibiotics. Crit Rev Biotechnol. 2012;32:108–32.
Google ScholarÂ
Saito S, Atsumi K, Zhou T, Fukaya K, Urabe D, Oku N, et al. A cyclopeptide and three oligomycin-class polyketides produced by an underexplored actinomycete of the genus Pseudosporangium. Beilstein J Org Chem. 2020;6:1100–10.
Google ScholarÂ
Lu S, Zhou T, Fukaya K, Harunari E, Oku N, Urabe D, et al. Krasilnikolides A and B and detalosylkrasilnikolide A, cytotoxic 20-membered macrolides from the genus Krasilnikovia: assignment of anomeric configuration by J-based configuration analysis. J Nat Prod. 2022;85:2796–803.
Google ScholarÂ
Liu C, Zhang Z, Fukaya K, Urabe D, Harunari E, Oku N, et al. Catellatolactams A–C, plant growth-promoting ansamacrolactam from a rare actinomycete of the genus Catellatospora. J Nat Prod. 2022;85:1993–9.
Google ScholarÂ
Liu C, Zhang Z, Fukaya K, Oku N, Harunari E, Urabe D, et al. Isolation and structure determination of allopteridic acids A–C and allokutzmicin from an unexplored actinomycete of the genus Allokutzneria. J Antibiot. 2023;76:305–15.
Google ScholarÂ
Kudo T, Itoh T, Miyadoh S, Shomura T, Seino A. Herbidospora gen. nov., new genus of the family Streptosporangiaceae Goodfellow et al. 1990. Int J Syst Bacteriol. 1993;43:319–28.
Google ScholarÂ
Kudo T. Establisment of the genus Herbidospora and some new taxa of actinomycetes. Actinomycetol. 1995;9:66–74.
Google ScholarÂ
Tseng M, Yang SF, Yuan GF. Herbidospora yilanensis sp. nov. and Herbidospora daliensis sp. nov., from sediment. Int J Syst Evol Microbiol. 2010;60:1168–72.
Google ScholarÂ
Boondaeng A, Suriyachadkun C, Ishida Y, Tamura T, Tokuyama S, Kitpreechavanich V. Herbidospora sakaeratensis sp. nov., isolated from soil, and reclassification of Streptosporangium claviforme as a later synonym of Herbidospora cretacea. Int J Syst Evol Microbiol. 2011;61:777–80.
Google ScholarÂ
Ara I, Tsetseg B, Daram D, Suto M, Ando K. Herbidospora mongoliensis sp. nov., isolated from soil, and reclassification of Herbidospora osyris and Streptosporangium claviforme as synonyms of Herbidospora cretacea. Int J Syst Evol Microbiol. 2012;62:2322–9.
Google ScholarÂ
Niemhom N, Thawai C. Herbidospora soli sp. nov., isolated from soil. Int J Syst Evol Microbiol. 2018;68:294–8.
Google ScholarÂ
Han L, Yu M, Zhao J, Jiang H, Guo X, Shen G, et al. Herbidospora galbida sp. nov., a novel actinobacterium isolated from soil. Int J Syst Evol Microbiol. 2020;70:1364–71.
Google ScholarÂ
Yu M, Zhou R, Li J, Han L, Wang H, Zhang S, et al. Herbidospora solisilvae sp. nov., a novel cellulose-degrading actinobacterium isolated from forest soil. Int J Syst Evol Microbiol. 2021;114:581–90.
Google ScholarÂ
Cheng MJ, Wu MD, Chen JJ, Su YS, Kuo YH. Secondary metabolites with antimycobacterial activities from one actinobacteria: Herbidospora yilanensis. Molecules. 2021;26:6236.
Google ScholarÂ
Chen JJ, Lee TH, Cheng MJ. Secondary metabolites with anti-inflammatory activities from an actinobacteria Herbidospora daliensis. Molecules. 2022;27:1887.
Google ScholarÂ
Biological Resource Center, NITE (NBRC). https://www.nite.go.jp/nbrc/ (accessed Sep. 25, 2020).
Tanemura K, Suzuki T, Horaguchi T, Sudo M. Synthesis and properties of furo[4,3,2-de][1]benzopyran. J Heterocycl Chem. 1991;28:305-9.
Singh J, Zeller W, Zhou N, Hategan G, Mishra RK, Polozov A, et al. Structure−activity relationship studies leading to the identification of (2E)-3-[l-[(2,4-dichlorophenyl)methyl]-5-fluoro-3-methyl-lH-indol-7-yl]-N-[(4,5-dichloro-2-thienyl)sulfonyl]-2-propenamide (DG-041), a potent and selective prostanoid EP3 receptor antagonist, as a novel antiplatelet agent that does not prolong bleeding. J Med Chem. 2010:53;18–36.
Katritzky, AR, Denisko, OV Heterocyclic compound. Encyclopedia Britannica, 1 December 2023. https://www.britannica.com/science/heterocyclic-compound (accessed January 19, 2024).
Dangles O, Fenger JA. The chemical reactivity of anthocyanins and its consequences in food science and nutrition. Molecules. 2018;23:1970.
Google ScholarÂ
Mattioli R, Francioso A, Mosca L, Silva P. Anthocyanins: a comprehensive review of their chemical properties and health effects on cardiovascular and neurodegenerative diseases. Molecules. 2020;25:3809.
Google ScholarÂ
Matsunaga H, Kamisuki S, Kaneko M, Yamaguchi Y, Takeuchi T, Watashi K, et al. Isolation and structure of vanitaracin A, a novel anti-hepatitis B virus compound from Talaromyces sp. Bioorg Med Chem Lett. 2015;25:4325–8.
Google ScholarÂ
Ma J, Cao B, Chen X, Xu M, Bi X, Guan P, et al. Violacin A, a new chromanone produced by Streptomyces violaceoruber and its anti-inflammatory activity. Bioorg Med Chem Lett. 2018;28:947–51.
Google ScholarÂ
Jiang L, Pu H, Xiang J, Su M, Yan X, Yang D, et al. Huanglongmycin A–C, cytotoxic polyketides biosynthesized by a putative type II polyketide synthase from Streptomyces sp. CB09001. Front Chem. 2018;6:254.
Google ScholarÂ
Zhang H, Xiao X, Conte MM, Khalila Z, Capon RJ, Spiralisones A–D acylphloroglucinol hemiketals from an Australian marine brown alga, Zonaria spiralis. Org Biomol Chem 2012;10:9671–6.
Google ScholarÂ
Suthiwong J, Sribuhom T, Wongphakham P, Senawong T, Yenjai C. Cytotoxicity of acylphloroglucinol derivatives from the fruits of Horsfieldia irya. Nat Prod Res. 2021;35:4930–8.
Google ScholarÂ
Hu M, Yang XQ, Zhou QY, Li SQ, Wang BY, Ruan BH, et al. Benzopyran derivatives from endophytic Daldinia eschscholtzii JC-15 in Dendrobium chrysotoxum and their bioactivities. Nat Prod Res. 2019;33:1431–5.
Google ScholarÂ
Ding L, Maier A, Fiebig HH, Görls H, Lin WH, Peschel G, et al. Divergolides A–D from a mangrove endophyte reveal an unparalleled plasticity in ansa-macrolide biosynthesis. Angew Chem Int Ed. 2011;50:1630–4.
Google ScholarÂ
Dreyer DL, Munderloh KP, Thiessen WE. Extractives of Dalea species (Leguminosae). Tetrahedron. 1975;31:287–93.
Google ScholarÂ
Roitman JN, Jurd L. Biomimetic synthesis of dalrubone and of a new pigment from Dalea emoryi. Phytochemistry. 1978;1978:161–3.
Google ScholarÂ
Zhang H, Li X, Ashendel CL, Chang C. Bioactive compounds from Psorothamnus junceus. J Nat Prod. 2000;63:1244–8.
Google ScholarÂ
Facundo VA, Sá AL, Silva SAF, Morais SM, Matos CRR, Braz-Filho R. Three new natural cyclopentenedione derivatives from Piper carnoconnectivum. J Braz Chem Soc. 2004;15:140–5.
Google ScholarÂ
Karim MRU, Harunari E, Oku N, Akasaka K, Igarashi Y. Bulbimidazoles A–C, antimicrobial and cytotoxic alkanoyl imidazoles from a marine gammaproteobacterium microbulbifers species. J Nat Prod. 2020;83:1295–9.
Google ScholarÂ
Sharma AR, Zhou T, Harunari E, Oku N, Trianto A, Igarashi Y. Labrenzbactin from a coral-associated bacterium Labrenzia sp. J Antibiot. 2019;72:634–9.
Google ScholarÂ