Benzylpenicillin (English Wikipedia)

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

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8nih.gov

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acs.org

"Benzylpenicillin". Molecule of the Week. American Chemical Society. Retrieved 9 November 2022.
Barros J (4 January 2016). "Use Extraction to Improve Penicillin G Recovery". Discover Chemistry. American Chemical Society. Archived from the original on 6 May 2019. Retrieved 6 May 2019.

diaion.com

"Separation and Purification of Pharmaceuticals and Antibiotics" (PDF). Mitsubishi Chemical Corporation. pp. 312–324.

doi.org

Dexter DD, van der Veen JM (1978). "Conformations of penicillin G: crystal structure of procaine penicillin G monohydrate and a refinement of the structure of potassium penicillin G". Journal of the Chemical Society, Perkin Transactions 1. 3 (3): 185–190. doi:10.1039/p19780000185. PMID 565366.
Fossieck Jr B, Parker RH (October 1974). "Neurotoxicity during intravenous infusion of penicillin. A review". Journal of Clinical Pharmacology. 14 (10): 504–12. doi:10.1002/j.1552-4604.1974.tb01364.x. PMID 4610013. S2CID 40884225.
Liu Q, Li Y, Li W, Liang X, Zhang C, Liu H (February 2016). "Efficient Recovery of Penicillin G by a Hydrophobic Ionic Liquid". ACS Sustainable Chemistry & Engineering. 4 (2): 609–615. doi:10.1021/acssuschemeng.5b00975.
Saino Y, Kobayashi F, Inoue M, Mitsuhashi S (October 1982). "Purification and properties of inducible penicillin beta-lactamase isolated from Pseudomonas maltophilia". Antimicrobial Agents and Chemotherapy. 22 (4): 564–570. doi:10.1128/AAC.22.4.564. PMC 183794. PMID 6983856.
Robinson FA (July 1947). "Chemistry of penicillin". The Analyst. 72 (856): 274–276. Bibcode:1947Ana....72..274R. doi:10.1039/an9477200274. PMID 20259048.

drugs.com

"Penicillin G Injection - FDA prescribing information, side effects and uses". www.drugs.com. Archived from the original on 20 December 2016. Retrieved 10 December 2016.

handle.net

hdl.handle.net

Stuart MC, Kouimtzi M, Hill SR, eds. (2009). WHO Model Formulary 2008. World Health Organization. pp. 98, 105. hdl:10665/44053. ISBN 9789241547659.
World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.

harvard.edu

ui.adsabs.harvard.edu

Robinson FA (July 1947). "Chemistry of penicillin". The Analyst. 72 (856): 274–276. Bibcode:1947Ana....72..274R. doi:10.1039/an9477200274. PMID 20259048.

nih.gov

pubmed.ncbi.nlm.nih.gov

Dexter DD, van der Veen JM (1978). "Conformations of penicillin G: crystal structure of procaine penicillin G monohydrate and a refinement of the structure of potassium penicillin G". Journal of the Chemical Society, Perkin Transactions 1. 3 (3): 185–190. doi:10.1039/p19780000185. PMID 565366.
Yip DW, Gerriets V (2023). "Penicillin". StatPearls. StatPearls Publishing. PMID 32119447. Retrieved 7 December 2023.
Fossieck Jr B, Parker RH (October 1974). "Neurotoxicity during intravenous infusion of penicillin. A review". Journal of Clinical Pharmacology. 14 (10): 504–12. doi:10.1002/j.1552-4604.1974.tb01364.x. PMID 4610013. S2CID 40884225.
Saino Y, Kobayashi F, Inoue M, Mitsuhashi S (October 1982). "Purification and properties of inducible penicillin beta-lactamase isolated from Pseudomonas maltophilia". Antimicrobial Agents and Chemotherapy. 22 (4): 564–570. doi:10.1128/AAC.22.4.564. PMC 183794. PMID 6983856.
Robinson FA (July 1947). "Chemistry of penicillin". The Analyst. 72 (856): 274–276. Bibcode:1947Ana....72..274R. doi:10.1039/an9477200274. PMID 20259048.

ncbi.nlm.nih.gov

Yip DW, Gerriets V (2023). "Penicillin". StatPearls. StatPearls Publishing. PMID 32119447. Retrieved 7 December 2023.
Saino Y, Kobayashi F, Inoue M, Mitsuhashi S (October 1982). "Purification and properties of inducible penicillin beta-lactamase isolated from Pseudomonas maltophilia". Antimicrobial Agents and Chemotherapy. 22 (4): 564–570. doi:10.1128/AAC.22.4.564. PMC 183794. PMID 6983856.

pubchem.ncbi.nlm.nih.gov

"Penicillin G". PubChem. National Center for Biotechnology Information, National Library of Medicine. Retrieved 26 December 2020.

sciencedirect.com

Flaherty DK (2012). "Immunogenicity and Antigenicity". Immunology for Pharmacy. Mosby. ISBN 978-0-323-06947-2. Natural penicillin (PenG), penicillinase-resistant penicillin (methicillin), extended-spectrum penicillin (amoxicillin), and broad-spectrum penicillin (carbenicillin) all have the same core β-lactam ring, which is essential for antimicrobial activity.

semanticscholar.org

api.semanticscholar.org

Fossieck Jr B, Parker RH (October 1974). "Neurotoxicity during intravenous infusion of penicillin. A review". Journal of Clinical Pharmacology. 14 (10): 504–12. doi:10.1002/j.1552-4604.1974.tb01364.x. PMID 4610013. S2CID 40884225.

seqirus.com

labeling.seqirus.com

"Australian Product Information – BENPEN" (PDF). Seqirus Pty Ltd.

toku-e.com

"Penicillin G" (PDF). Toku-E. 10 October 2010. Archived from the original (PDF) on 3 March 2016. Retrieved 11 June 2012.

web.archive.org

"Penicillin G Injection - FDA prescribing information, side effects and uses". www.drugs.com. Archived from the original on 20 December 2016. Retrieved 10 December 2016.
"Penicillin G" (PDF). Toku-E. 10 October 2010. Archived from the original (PDF) on 3 March 2016. Retrieved 11 June 2012.
Barros J (4 January 2016). "Use Extraction to Improve Penicillin G Recovery". Discover Chemistry. American Chemical Society. Archived from the original on 6 May 2019. Retrieved 6 May 2019.