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Kalkitoxin (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kalkitoxin" in English language version.

refsWebsite
Global rank English rank
14nih.gov
4th place
4th place
12doi.org
2nd place
2nd place
1researchgate.net
120th place
125th place
1chemspider.com
8,573rd place
low place

chemspider.com

doi.org

  • Berman; et al. (1999). "Antillatoxin and kalkitoxin, ichthyotoxins from the tropical cyanobacterium Lyngbya majuscula, induce distinct temporal patterns of NMDA receptor-mediated neurotoxicity". Toxicon. 37 (11): 1645–8. doi:10.1016/s0041-0101(99)00108-7. PMID 10482399.
  • Morgan; et al. (2015). "Kalkitoxin inhibits angiogenesis, disrupts cellular hypoxic signaling and blocks mitochondrial electron transport in tumor cells". Marine Drugs. 13 (3): 1552–1568. doi:10.3390/md13031552. PMC 4377999. PMID 25803180.
  • Nogle and Gerwick (2003). "Diverse Secondary Metabolites from a Puerto Rican Collection of Lyngbya Majuscula". Journal of Natural Products. 66 (2): 217–20. doi:10.1021/np020332c. PMID 12608852.
  • Wu; et al. (2000). "Structure, Synthesis, and Biological Properties of Kalkitoxin, a Novel Neurotoxin from the Marine Cyanobacterium Lyngbya majuscule". Journal of the American Chemical Society. 122 (48): 12041–12042. doi:10.1021/ja005526y.
  • Umezawa; et al. (2011). "Synthesis and Biological Activity of Kalkitoxin and its Analogues". Journal of Organic Chemistry. 77 (1): 357–70. doi:10.1021/jo201951s. PMID 22111947.
  • Hawkins, Clifford J.; Lavin, Martin F.; MarshallKaren A., Karen A.; Van den Brenk, Anna L.; Watters, Diane J. (1990-06-01). "Structure-activity relationships of the lissoclinamides: cytotoxic cyclic peptides from the ascidian Lissoclinum patella". Journal of Medicinal Chemistry. 33 (6): 1634–1638. doi:10.1021/jm00168a016. PMID 2342056.
  • White, James D.; Xu, Qing; Lee, Chang-Sun; Valeriote, Frederick A (2004). "Total synthesis and biological evaluation of (+)-kalkitoxin, a cytotoxic metabolite of the cyanobacterium Lyngbya majuscula". Organic & Biomolecular Chemistry. 2 (14): 2092–2102. doi:10.1039/B404205K. PMID 15254638.
  • White, James D; Lee, Chang-Sun; Xu, Qing (2003). "Total synthesis of (+)-kalkitoxin". Chemical Communications (16): 2012–2013. doi:10.1039/B306124H. PMID 12934887.
  • Burns; et al. (2014). "High Precision Assembly Line Synthesis for Molecules with Tailored Shapes". Nature. 513 (7517): 183–188. doi:10.1038/nature13711. PMC 4167605. PMID 25209797.
  • Balieu; et al. (2015). "Toward Ideality: The Synthesis of (+)-Kalkitoxin and (+)-Hydroxyphthioceranic Acid by Assembly-Line Synthesis". Journal of the American Chemical Society. 137 (13): 4398–4403. doi:10.1021/ja512875g. PMID 25625684.
  • LePage; et al. (2005). "The neurotoxic lipopeptide kalkitoxin interacts with voltage-sensitive sodium channels in cerebellar granule neurons". Toxicology Letters. 158 (2): 133–9. doi:10.1016/j.toxlet.2005.03.007. PMID 16039402.
  • de Bono; et al. (2003). "The future of cytotoxic therapy: selective cytotoxicity based on biology is the key". Breast Cancer Research. 5 (3): 154–9. doi:10.1186/bcr597. PMC 165009. PMID 12793897.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Berman; et al. (1999). "Antillatoxin and kalkitoxin, ichthyotoxins from the tropical cyanobacterium Lyngbya majuscula, induce distinct temporal patterns of NMDA receptor-mediated neurotoxicity". Toxicon. 37 (11): 1645–8. doi:10.1016/s0041-0101(99)00108-7. PMID 10482399.
  • Morgan; et al. (2015). "Kalkitoxin inhibits angiogenesis, disrupts cellular hypoxic signaling and blocks mitochondrial electron transport in tumor cells". Marine Drugs. 13 (3): 1552–1568. doi:10.3390/md13031552. PMC 4377999. PMID 25803180.
  • Nogle and Gerwick (2003). "Diverse Secondary Metabolites from a Puerto Rican Collection of Lyngbya Majuscula". Journal of Natural Products. 66 (2): 217–20. doi:10.1021/np020332c. PMID 12608852.
  • Umezawa; et al. (2011). "Synthesis and Biological Activity of Kalkitoxin and its Analogues". Journal of Organic Chemistry. 77 (1): 357–70. doi:10.1021/jo201951s. PMID 22111947.
  • Hawkins, Clifford J.; Lavin, Martin F.; MarshallKaren A., Karen A.; Van den Brenk, Anna L.; Watters, Diane J. (1990-06-01). "Structure-activity relationships of the lissoclinamides: cytotoxic cyclic peptides from the ascidian Lissoclinum patella". Journal of Medicinal Chemistry. 33 (6): 1634–1638. doi:10.1021/jm00168a016. PMID 2342056.
  • White, James D.; Xu, Qing; Lee, Chang-Sun; Valeriote, Frederick A (2004). "Total synthesis and biological evaluation of (+)-kalkitoxin, a cytotoxic metabolite of the cyanobacterium Lyngbya majuscula". Organic & Biomolecular Chemistry. 2 (14): 2092–2102. doi:10.1039/B404205K. PMID 15254638.
  • White, James D; Lee, Chang-Sun; Xu, Qing (2003). "Total synthesis of (+)-kalkitoxin". Chemical Communications (16): 2012–2013. doi:10.1039/B306124H. PMID 12934887.
  • Burns; et al. (2014). "High Precision Assembly Line Synthesis for Molecules with Tailored Shapes". Nature. 513 (7517): 183–188. doi:10.1038/nature13711. PMC 4167605. PMID 25209797.
  • Balieu; et al. (2015). "Toward Ideality: The Synthesis of (+)-Kalkitoxin and (+)-Hydroxyphthioceranic Acid by Assembly-Line Synthesis". Journal of the American Chemical Society. 137 (13): 4398–4403. doi:10.1021/ja512875g. PMID 25625684.
  • LePage; et al. (2005). "The neurotoxic lipopeptide kalkitoxin interacts with voltage-sensitive sodium channels in cerebellar granule neurons". Toxicology Letters. 158 (2): 133–9. doi:10.1016/j.toxlet.2005.03.007. PMID 16039402.
  • de Bono; et al. (2003). "The future of cytotoxic therapy: selective cytotoxicity based on biology is the key". Breast Cancer Research. 5 (3): 154–9. doi:10.1186/bcr597. PMC 165009. PMID 12793897.

ncbi.nlm.nih.gov

researchgate.net