Β-ラクタム (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Β-ラクタム" in Japanese language version.

refsWebsite

Global rank Japanese rank

9doi.org

2^nd place

6^th place

3nih.gov

4^th place

24^th place

1nature.com

234^th place

363^rd place

1asahi.com

141^st place

9^th place

1ukim.edu.mk

low place

asahi.com (Global: 141^st place; Japanese: 9^th place)

“中国依存の抗生物質、目指せ国産化　かぎは熟練の「職人技」”. 朝日新聞DIGITAL (2024年6月7日). 2024年9月29日閲覧。

doi.org (Global: 2^nd place; Japanese: 6^th place)

Brandt, C. (2017). “In silico serine β-lactamases analysis reveals a huge potential resistome in environmental and pathogenic species”. SciRep 7 (43232). doi:10.1038/srep43232.
Ehmann, David E. (2012). “Avibactam is a covalent, reversible, non-β-lactam β-lactamase inhibitor”. PNAS 109 (29): 11663–11668. doi:10.1073/pnas.1205073109.
Tidwell, Thomas T. (2008). “Hugo (Ugo) Schiff, Schiff Bases, and a Century of β-Lactam Synthesis”. Angewandte Chemie International Edition 47 (6): 1016–20. doi:10.1002/anie.200702965. PMID 18022986.
Hermann Staudinger (1907). “Zur Kenntniss der Ketene. Diphenylketen”. Justus Liebigs Ann. Chem. 356 (1-2): 51–123. doi:10.1002/jlac.19073560106.
Woodward, R.B. (1980). “Penems and related substances”. Phil Trans Royal Soc Chem B 289 (1036): 239–50. doi:10.1098/rstb.1980.0042. PMID 6109320.
Nangia, A. (1996). “Correlation of biological activity in β-lactam antibiotics with Woodward and Cohen structural parameters: A Cambridge database study”. J Chem Soc, Perkin Trans 2 (5): 943–53. doi:10.1039/p29960000943.
Mowery, Brendan P., et al. (2009). “Structure− activity relationships among random nylon-3 copolymers that mimic antibacterial host-defense peptides”. Journal of the American Chemical Society 131 (28): 9735-9745. doi:10.1021/ja901613g.
O'Boyle, Niamh (December 2010). “Synthesis and Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents”. Journal of Medicinal Chemistry 53 (24): 8569–8584. doi:10.1021/jm101115u. PMID 21080725.
O'Boyle, Niamh (2011). “Synthesis, evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones”. Bioorganic and Medicinal Chemistry 19 (7): 2306–2625. doi:10.1016/j.bmc.2011.02.022.

nature.com (Global: 234^th place; Japanese: 363^rd place)

Brandt, C. (2017). “In silico serine β-lactamases analysis reveals a huge potential resistome in environmental and pathogenic species”. SciRep 7 (43232). doi:10.1038/srep43232.

nih.gov (Global: 4^th place; Japanese: 24^th place)

pubmed.ncbi.nlm.nih.gov

Tidwell, Thomas T. (2008). “Hugo (Ugo) Schiff, Schiff Bases, and a Century of β-Lactam Synthesis”. Angewandte Chemie International Edition 47 (6): 1016–20. doi:10.1002/anie.200702965. PMID 18022986.
Woodward, R.B. (1980). “Penems and related substances”. Phil Trans Royal Soc Chem B 289 (1036): 239–50. doi:10.1098/rstb.1980.0042. PMID 6109320.
O'Boyle, Niamh (December 2010). “Synthesis and Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents”. Journal of Medicinal Chemistry 53 (24): 8569–8584. doi:10.1021/jm101115u. PMID 21080725.

ukim.edu.mk (Global: low place; Japanese: low place)

pmf.ukim.edu.mk

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Β-ラクタム (Japanese Wikipedia)

asahi.com (Global: 141st place; Japanese: 9th place)

doi.org (Global: 2nd place; Japanese: 6th place)

nature.com (Global: 234th place; Japanese: 363rd place)

nih.gov (Global: 4th place; Japanese: 24th place)