Liu H, Chen H, Huang S, Li Z, Wang C, Zhang H
Mar Drugs. 2025; 23(1).
PMID: 39852527
PMC: 11766693.
DOI: 10.3390/md23010025.
Nuutila A, Xiao X, van der Heul H, van Wezel G, Dinis P, Elsayed S
ACS Chem Biol. 2024; 19(5):1131-1141.
PMID: 38668630
PMC: 11106748.
DOI: 10.1021/acschembio.4c00082.
Ma G, Xin L, Liao Y, Chong Z, Candra H, Pang L
Appl Environ Microbiol. 2022; 88(23):e0120822.
PMID: 36350133
PMC: 9746310.
DOI: 10.1128/aem.01208-22.
Wilkinson D, Cioncoloni G, Symes M, Bucher G
RSC Adv. 2022; 10(62):38004-38012.
PMID: 35515143
PMC: 9057194.
DOI: 10.1039/d0ra06519f.
Zhang J, Sun Y, Wang Y, Chen X, Xue L, Zhang J
Microb Cell Fact. 2021; 20(1):192.
PMID: 34600534
PMC: 8487521.
DOI: 10.1186/s12934-021-01681-5.
Himalaquinones A-G, Angucyclinone-Derived Metabolites Produced by the Himalayan Isolate sp. PU-MM59.
Zhang Y, Cheema M, Ponomareva L, Ye Q, Liu T, Sajid I
J Nat Prod. 2021; 84(7):1930-1940.
PMID: 34170698
PMC: 8565601.
DOI: 10.1021/acs.jnatprod.1c00192.
Bio-Guided Isolation of Antimalarial Metabolites from the Coculture of Two Red Sea Sponge-Derived and spp.
Alhadrami H, Thissera B, Hassan M, Behery F, Ngwa C, Hassan H
Mar Drugs. 2021; 19(2).
PMID: 33673168
PMC: 7918646.
DOI: 10.3390/md19020109.
Cryptic Sulfur Incorporation in Thioangucycline Biosynthesis.
Cao M, Zheng C, Yang D, Kalkreuter E, Adhikari A, Liu Y
Angew Chem Int Ed Engl. 2021; 60(13):7140-7147.
PMID: 33465268
PMC: 7969429.
DOI: 10.1002/anie.202015570.
spp. From Ethiopia Producing Antimicrobial Compounds: Characterization via Bioassays, Genome Analyses, and Mass Spectrometry.
Kibret M, Guerrero-Garzon J, Urban E, Zehl M, Wronski V, Ruckert C
Front Microbiol. 2018; 9:1270.
PMID: 29946312
PMC: 6007079.
DOI: 10.3389/fmicb.2018.01270.
Streptomyces globosus DK15 and Streptomyces ederensis ST13 as new producers of factumycin and tetrangomycin antibiotics.
Charousova I, Medo J, Hleba L, Javorekova S
Braz J Microbiol. 2018; 49(4):816-822.
PMID: 29705162
PMC: 6175699.
DOI: 10.1016/j.bjm.2017.12.007.
Monacyclinones, New Angucyclinone Metabolites Isolated from Streptomyces sp. M7_15 Associated with the Puerto Rican Sponge Scopalina ruetzleri.
Vicente J, Stewart A, Wagoner R, Elliott E, Bourdelais A, Wright J
Mar Drugs. 2015; 13(8):4682-700.
PMID: 26230704
PMC: 4556999.
DOI: 10.3390/md13084682.
Cytotoxic and antibacterial angucycline- and prodigiosin-analogues from the deep-sea derived Streptomyces sp. SCSIO 11594.
Song Y, Liu G, Li J, Huang H, Zhang X, Zhang H
Mar Drugs. 2015; 13(3):1304-16.
PMID: 25786061
PMC: 4377985.
DOI: 10.3390/md13031304.
Identification of Streptomyces sp. nov. WH26 producing cytotoxic compounds isolated from marine solar saltern in China.
Liu H, Xiao L, Wei J, Schmitz J, Liu M, Wang C
World J Microbiol Biotechnol. 2013; 29(7):1271-8.
PMID: 23420111
DOI: 10.1007/s11274-013-1290-8.
Angucyclines: Biosynthesis, mode-of-action, new natural products, and synthesis.
Kharel M, Pahari P, Shepherd M, Tibrewal N, Nybo S, Shaaban K
Nat Prod Rep. 2011; 29(2):264-325.
PMID: 22186970
PMC: 11412254.
DOI: 10.1039/c1np00068c.
Aminopyrimidoisoquinolinequinone (APIQ) redox cycling is potentiated by ascorbate and induces oxidative stress leading to necrotic-like cancer cell death.
Vasquez D, Verrax J, Valderrama J, Buc Calderon P
Invest New Drugs. 2011; 30(3):1003-11.
PMID: 21465233
DOI: 10.1007/s10637-011-9661-1.
Screening natural products for inhibitors of quinone reductase-2 using ultrafiltration LC-MS.
Choi Y, Jermihov K, Nam S, Sturdy M, Maloney K, Qiu X
Anal Chem. 2011; 83(3):1048-52.
PMID: 21192729
PMC: 3034444.
DOI: 10.1021/ac1028424.
Landomycins P-W, cytotoxic angucyclines from Streptomyces cyanogenus S-136.
Shaaban K, Srinivasan S, Kumar R, Damodaran C, Rohr J
J Nat Prod. 2010; 74(1):2-11.
PMID: 21188999
PMC: 3070852.
DOI: 10.1021/np100469y.
11-Deoxylandomycinone and landomycins X-Z, new cytotoxic angucyclin(on)es from a Streptomyces cyanogenus K62 mutant strain.
Shaaban K, Stamatkin C, Damodaran C, Rohr J
J Antibiot (Tokyo). 2010; 64(1):141-50.
PMID: 20978514
PMC: 3030652.
DOI: 10.1038/ja.2010.121.
Moromycins A and B, isolation and structure elucidation of C-glycosylangucycline-type antibiotics from Streptomyces sp. KY002.
Abdelfattah M, Kharel M, Hitron J, Baig I, Rohr J
J Nat Prod. 2008; 71(9):1569-73.
PMID: 18666798
PMC: 2562265.
DOI: 10.1021/np800281f.
Identification of the function of gene lndM2 encoding a bifunctional oxygenase-reductase involved in the biosynthesis of the antitumor antibiotic landomycin E by Streptomyces globisporus 1912 supports the originally assigned structure for....
Zhu L, Ostash B, Rix U, Nur-E-Alam M, Mayers A, Luzhetskyy A
J Org Chem. 2005; 70(2):631-8.
PMID: 15651811
PMC: 2884283.
DOI: 10.1021/jo0483623.