lavendamycin has been researched along with streptonigrin in 16 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (18.75) | 18.7374 |
1990's | 2 (12.50) | 18.2507 |
2000's | 8 (50.00) | 29.6817 |
2010's | 3 (18.75) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hibino, S; Ichikawa, M; Motoshima, A; Okazaki, M; Sato, K; Ueki, H | 1 |
Boger, DL; Drake, SD; Kitos, PA; Mitscher, LA; Thompson, SC; Yasuda, M | 1 |
Balitz, DM; Bradner, WT; Bush, JA; Doyle, TW; Nettleton, DE; O'Herron, FA | 1 |
Abe, N; Enoki, N; Munekata, M; Nakakita, Y; Nakamura, T; Takeo, S; Uchida, H | 1 |
Abe, N; Enoki, N; Munekata, M; Nakakita, Y; Nakamura, T; Uchida, H | 1 |
Abraham, RT; Behforouz, M; Cai, W; Fang, Y; Linardic, CM; Richardson, DA | 1 |
DeShong, P; McElroy, WT | 1 |
Behforouz, M; Behforouz, NC; Briere, D; Cai, W; Jung, JY; Katen, KS; Lucas, JS; Stocksdale, MG; Wang, A | 1 |
Behforouz, M; Cai, W; Chenault, DV; Erasga, NO; Knuckles, KA; Ragains, JR; Seradj, H | 1 |
Beall, HD; Behforouz, M; Cai, W; Ebrahimian, GR; Gerdes, JM; Hassani, M; Holley, DC; Lineswala, JP; Maharjan, BR; Marvin, CC; Mohammadi, F; Seradj, H; Stocksdale, MG | 1 |
Ahmadian, M; Al-Anzi, CH; Baty, DE; Behforouz, M; Behforouz, NC; Cai, W; Etling, MR; Gu, Z; Merriman, RL; Mohammadi, F; Stocksdale, MG; Swiftney, TM; Tanzer, LR | 1 |
Beall, HD; Behforouz, M; Cai, W; Gerdes, JM; Hassani, M; Holley, DC; Holloway, WG; Koelsch, KH; Lineswala, JP; Olang, F; Rose, AS | 1 |
England, DB; Padwa, A | 1 |
De Kimpe, N; Padwa, A; Verniest, G; Wang, X | 1 |
Beall, HD; Behforouz, M; Cai, W; Charkhzarrin, S; Eads, TJ; Hassani, M; Hermann, NG; Karki, R; Koelsch, KH; Lineswala, JP; Lucas, JS; Mirzaei, H; Olang, F; Rose, AS; Sedighi, M; Seradj, H; Walter, ED; York, JS | 1 |
Cong, FS; Lin, S; Xia, X; Xia, XX; Zhong, JJ | 1 |
16 other study(ies) available for lavendamycin and streptonigrin
Article | Year |
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In vitro oxidation of the 8-hydroxyquinoline moiety with metabolic activation system to a mutagenic quinoloquinone compound of lavendamycin analogs.
Topics: Animals; Biotransformation; Hydroxyquinolines; Male; Mice; Mutagens; Oxidation-Reduction; Oxyquinoline; Streptonigrin | 1986 |
Streptonigrin and lavendamycin partial structures. Probes for the minimum, potent pharmacophore of streptonigrin, lavendamycin, and synthetic quinoline-5,8-diones.
Topics: Animals; Antibiotics, Antineoplastic; Chemical Phenomena; Chemistry, Physical; Leukemia L1210; Melanoma; Mice; Microbial Sensitivity Tests; Quinolines; Streptonigrin; Structure-Activity Relationship | 1987 |
Isolation of lavendamycin, a new antibiotic from Streptomyces lavendulae.
Topics: Animals; Anti-Bacterial Agents; Antibiotics, Antineoplastic; Bacteria; Cells, Cultured; Chromatography, High Pressure Liquid; Chromatography, Thin Layer; Leukemia P388; Mice; Streptomyces; Streptonigrin | 1982 |
Novel cytocidal compounds, oxopropalines from Streptomyces sp. G324 producing lavendamycin. I. Taxonomy of the producing organism, fermentation, isolation and biological activities.
Topics: Animals; Antibiotics, Antineoplastic; Carbolines; Chromatography, High Pressure Liquid; Fermentation; Humans; Mice; Streptomyces; Streptonigrin; Tumor Cells, Cultured | 1993 |
Novel cytocidal compounds, oxopropalines from Streptomyces sp. G324 producing lavendamycin. II. Physico-chemical properties and structure elucidations.
Topics: Antibiotics, Antineoplastic; Carbolines; Magnetic Resonance Spectroscopy; Mass Spectrometry; Spectrophotometry; Streptomyces; Streptonigrin | 1993 |
Characterization of the cytotoxic activities of novel analogues of the antitumor agent, lavendamycin.
Topics: Antineoplastic Agents; Apoptosis; Cell Cycle; Cell Line, Tumor; Flow Cytometry; G2 Phase; Humans; Immunoblotting; Mitosis; Models, Chemical; Phosphorylation; Proto-Oncogene Proteins p21(ras); Streptonigrin; Time Factors; Tumor Suppressor Protein p53 | 2003 |
Siloxane-based cross-coupling of bromopyridine derivatives: studies for the synthesis of streptonigrin and lavendamycin.
Topics: Antibiotics, Antineoplastic; Molecular Structure; Pyridines; Siloxanes; Streptonigrin | 2003 |
Novel lavendamycin analogues as potent HIV-reverse transcriptase inhibitors: synthesis and evaluation of anti-reverse transcriptase activity of amide and ester analogues of lavendamycin.
Topics: Amides; Animals; Cells, Cultured; Dideoxynucleotides; Drug Synergism; Esters; HIV Reverse Transcriptase; Humans; Mice; Reverse Transcriptase Inhibitors; Streptonigrin; Structure-Activity Relationship; Thymine Nucleotides; Zidovudine | 2003 |
Total synthesis of novel 6-substituted lavendamycin antitumor agents.
Topics: Antibiotics, Antineoplastic; Catalysis; Indicators and Reagents; Molecular Structure; Streptomyces; Streptonigrin; Structure-Activity Relationship | 2004 |
Novel lavendamycin analogues as antitumor agents: synthesis, in vitro cytotoxicity, structure-metabolism, and computational molecular modeling studies with NAD(P)H:quinone oxidoreductase 1.
Topics: Antineoplastic Agents; Binding Sites; Cell Line, Tumor; Drug Screening Assays, Antitumor; Electrochemistry; Humans; Hydrogen Bonding; Models, Molecular; NAD(P)H Dehydrogenase (Quinone); Oxidation-Reduction; Streptonigrin; Structure-Activity Relationship | 2005 |
Synthesis and evaluation of antitumor activity of novel N-acyllavendamycin analogues and quinoline-5,8-diones.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Female; Mice; Mice, Inbred C57BL; Mice, Nude; Molecular Structure; Neoplasms; Quinolines; Rats; Stereoisomerism; Streptonigrin; Structure-Activity Relationship; Xenograft Model Antitumor Assays | 2007 |
Lavendamycin antitumor agents: structure-based design, synthesis, and NAD(P)H:quinone oxidoreductase 1 (NQO1) model validation with molecular docking and biological studies.
Topics: Antineoplastic Agents; Binding Sites; Cell Line, Tumor; Cytochromes c; Drug Screening Assays, Antitumor; Humans; Models, Molecular; NAD(P)H Dehydrogenase (Quinone); Protein Binding; Streptonigrin; Structure-Activity Relationship | 2008 |
Gold-catalyzed cycloisomerization of N-Propargylindole-2-carboxamides: application toward the synthesis of lavendamycin analogues.
Topics: Alkynes; Carbolines; Catalysis; Cyclization; Gold Compounds; Indoles; Molecular Structure; Organometallic Compounds; Palladium; Stereoisomerism; Streptonigrin | 2008 |
Heteroaryl cross-coupling as an entry toward the synthesis of lavendamycin analogues: a model study.
Topics: Antibiotics, Antineoplastic; Catalysis; Cross-Linking Reagents; Indoles; Magnetic Resonance Spectroscopy; Molecular Structure; Palladium; Quinolines; Stereoisomerism; Streptonigrin | 2010 |
Synthesis, metabolism and in vitro cytotoxicity studies on novel lavendamycin antitumor agents.
Topics: Antineoplastic Agents; Cell Line, Tumor; Humans; NAD(P)H Dehydrogenase (Quinone); Recombinant Proteins; Streptonigrin; Structure-Activity Relationship | 2010 |
Significance of agitation-induced shear stress on mycelium morphology and lavendamycin production by engineered Streptomyces flocculus.
Topics: Antibiotics, Antineoplastic; Mechanical Phenomena; Oxygen; Streptomyces; Streptonigrin; Stress, Mechanical | 2014 |