Loading…
Penems and Related Substances
The discovery of the penicillins, as exemplified by penicillin G (1) - one of the earliest known members of the class - and of the cephalosporins, of which the first to be isolated was cephalosporin C (2), laid the basis for one of the most spectacular chapters in the history of medicine.
Saved in:
| Published in: | Philosophical transactions of the Royal Society of London. Series B, Biological sciences Biological sciences, 1980-05, Vol.289 (1036), p.239-250 |
|---|---|
| Main Author: | |
| Format: | Article |
| Language: | English |
| Subjects: | |
| Citations: | Items that cite this one |
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| cited_by | cdi_FETCH-LOGICAL-c463t-24d15a23fa8dd8889e01c70566a848d53d73006c4ed986a89cd064fd26fe51853 |
|---|---|
| cites | |
| container_end_page | 250 |
| container_issue | 1036 |
| container_start_page | 239 |
| container_title | Philosophical transactions of the Royal Society of London. Series B, Biological sciences |
| container_volume | 289 |
| creator | Woodward, R. B. |
| description | The discovery of the penicillins, as exemplified by penicillin G (1) - one of the earliest known members of the class - and of the cephalosporins, of which the first to be isolated was cephalosporin C (2), laid the basis for one of the most spectacular chapters in the history of medicine. |
| doi_str_mv | 10.1098/rstb.1980.0042 |
| format | article |
| fullrecord | <record><control><sourceid>jstor_royal</sourceid><recordid>TN_cdi_royalsociety_journals_10_1098_rstb_1980_0042</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>2395381</jstor_id><sourcerecordid>2395381</sourcerecordid><originalsourceid>FETCH-LOGICAL-c463t-24d15a23fa8dd8889e01c70566a848d53d73006c4ed986a89cd064fd26fe51853</originalsourceid><addsrcrecordid>eNp9kEtLAzEUhYMotT62rix05W7qzXNullp8gaC0dR3SSQamtDM1mRHqr3fGloKIrsLN_c453EPIBYURBY3XIdbzEdUIIwDBDkifgRQJMIRD0gdASIRi7JicxLgAkFoz7JGearWcQZ8MXn3pV3FoSzec-KWtvRtOm3msbZn5eEaOcruM_nz3npK3-7vZ-DF5fnl4Gt88J5lQvE6YcFRaxnOLziGi9kCzFKRSFgU6yV3KAVQmvNPY_unMgRK5Yyr3kqLkp-Rq67sO1XvjY21WRcz8cmlLXzXRpFLQlGtowdEWzEIVY_C5WYdiZcPGUDBdH6brw3R9mK6PVjDYOTfzlXd7fFdAu-fbfag27YVVVvh6YxZVE8p2_Ns1_qeaTGe3VCv9wVAXFLgygJxCypAq81msv-06wLSAKWJsvPnGfsb8Tr3cpi5iXYX9KYxryZHyLzbEmM8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75417390</pqid></control><display><type>article</type><title>Penems and Related Substances</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Royal Society Publishing Jisc Collections Royal Society Journals Read & Publish Transitional Agreement 2025 (reading list)</source><creator>Woodward, R. B.</creator><creatorcontrib>Woodward, R. B.</creatorcontrib><description>The discovery of the penicillins, as exemplified by penicillin G (1) - one of the earliest known members of the class - and of the cephalosporins, of which the first to be isolated was cephalosporin C (2), laid the basis for one of the most spectacular chapters in the history of medicine.</description><identifier>ISSN: 0080-4622</identifier><identifier>ISSN: 0962-8436</identifier><identifier>EISSN: 2054-0280</identifier><identifier>DOI: 10.1098/rstb.1980.0042</identifier><identifier>PMID: 6109320</identifier><language>eng</language><publisher>London: The Royal Society</publisher><subject>Anti-Bacterial Agents - history ; Anti-Bacterial Agents - pharmacology ; Antibacterials ; Antibiotics ; Bacteria - drug effects ; Carbapenems ; Cephalosporins ; Cephalosporins - chemical synthesis ; Chemistry ; Crystal structure ; Enantiomers ; Esters ; History of medicine ; History, 20th Century ; Molecular Conformation ; Penicillin ; Penicillins - history ; Reactivity ; Staphylococcus aureus ; Stereoisomerism</subject><ispartof>Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 1980-05, Vol.289 (1036), p.239-250</ispartof><rights>Copyright 1980 The Royal Society</rights><rights>Scanned images copyright © 2017, Royal Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-24d15a23fa8dd8889e01c70566a848d53d73006c4ed986a89cd064fd26fe51853</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2395381$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2395381$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6109320$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woodward, R. B.</creatorcontrib><title>Penems and Related Substances</title><title>Philosophical transactions of the Royal Society of London. Series B, Biological sciences</title><addtitle>Phil. Trans. R. Soc. Lond. B</addtitle><addtitle>Philos Trans R Soc Lond B Biol Sci</addtitle><description>The discovery of the penicillins, as exemplified by penicillin G (1) - one of the earliest known members of the class - and of the cephalosporins, of which the first to be isolated was cephalosporin C (2), laid the basis for one of the most spectacular chapters in the history of medicine.</description><subject>Anti-Bacterial Agents - history</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterials</subject><subject>Antibiotics</subject><subject>Bacteria - drug effects</subject><subject>Carbapenems</subject><subject>Cephalosporins</subject><subject>Cephalosporins - chemical synthesis</subject><subject>Chemistry</subject><subject>Crystal structure</subject><subject>Enantiomers</subject><subject>Esters</subject><subject>History of medicine</subject><subject>History, 20th Century</subject><subject>Molecular Conformation</subject><subject>Penicillin</subject><subject>Penicillins - history</subject><subject>Reactivity</subject><subject>Staphylococcus aureus</subject><subject>Stereoisomerism</subject><issn>0080-4622</issn><issn>0962-8436</issn><issn>2054-0280</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLAzEUhYMotT62rix05W7qzXNullp8gaC0dR3SSQamtDM1mRHqr3fGloKIrsLN_c453EPIBYURBY3XIdbzEdUIIwDBDkifgRQJMIRD0gdASIRi7JicxLgAkFoz7JGearWcQZ8MXn3pV3FoSzec-KWtvRtOm3msbZn5eEaOcruM_nz3npK3-7vZ-DF5fnl4Gt88J5lQvE6YcFRaxnOLziGi9kCzFKRSFgU6yV3KAVQmvNPY_unMgRK5Yyr3kqLkp-Rq67sO1XvjY21WRcz8cmlLXzXRpFLQlGtowdEWzEIVY_C5WYdiZcPGUDBdH6brw3R9mK6PVjDYOTfzlXd7fFdAu-fbfag27YVVVvh6YxZVE8p2_Ns1_qeaTGe3VCv9wVAXFLgygJxCypAq81msv-06wLSAKWJsvPnGfsb8Tr3cpi5iXYX9KYxryZHyLzbEmM8</recordid><startdate>19800516</startdate><enddate>19800516</enddate><creator>Woodward, R. B.</creator><general>The Royal Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19800516</creationdate><title>Penems and Related Substances</title><author>Woodward, R. B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-24d15a23fa8dd8889e01c70566a848d53d73006c4ed986a89cd064fd26fe51853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Anti-Bacterial Agents - history</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibacterials</topic><topic>Antibiotics</topic><topic>Bacteria - drug effects</topic><topic>Carbapenems</topic><topic>Cephalosporins</topic><topic>Cephalosporins - chemical synthesis</topic><topic>Chemistry</topic><topic>Crystal structure</topic><topic>Enantiomers</topic><topic>Esters</topic><topic>History of medicine</topic><topic>History, 20th Century</topic><topic>Molecular Conformation</topic><topic>Penicillin</topic><topic>Penicillins - history</topic><topic>Reactivity</topic><topic>Staphylococcus aureus</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woodward, R. B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Philosophical transactions of the Royal Society of London. Series B, Biological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woodward, R. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Penems and Related Substances</atitle><jtitle>Philosophical transactions of the Royal Society of London. Series B, Biological sciences</jtitle><stitle>Phil. Trans. R. Soc. Lond. B</stitle><addtitle>Philos Trans R Soc Lond B Biol Sci</addtitle><date>1980-05-16</date><risdate>1980</risdate><volume>289</volume><issue>1036</issue><spage>239</spage><epage>250</epage><pages>239-250</pages><issn>0080-4622</issn><issn>0962-8436</issn><eissn>2054-0280</eissn><abstract>The discovery of the penicillins, as exemplified by penicillin G (1) - one of the earliest known members of the class - and of the cephalosporins, of which the first to be isolated was cephalosporin C (2), laid the basis for one of the most spectacular chapters in the history of medicine.</abstract><cop>London</cop><pub>The Royal Society</pub><pmid>6109320</pmid><doi>10.1098/rstb.1980.0042</doi><tpages>12</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0080-4622 |
| ispartof | Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 1980-05, Vol.289 (1036), p.239-250 |
| issn | 0080-4622 0962-8436 2054-0280 |
| language | eng |
| recordid | cdi_royalsociety_journals_10_1098_rstb_1980_0042 |
| source | JSTOR Archival Journals and Primary Sources Collection; Royal Society Publishing Jisc Collections Royal Society Journals Read & Publish Transitional Agreement 2025 (reading list) |
| subjects | Anti-Bacterial Agents - history Anti-Bacterial Agents - pharmacology Antibacterials Antibiotics Bacteria - drug effects Carbapenems Cephalosporins Cephalosporins - chemical synthesis Chemistry Crystal structure Enantiomers Esters History of medicine History, 20th Century Molecular Conformation Penicillin Penicillins - history Reactivity Staphylococcus aureus Stereoisomerism |
| title | Penems and Related Substances |
| url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T22%3A23%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_royal&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Penems%20and%20Related%20Substances&rft.jtitle=Philosophical%20transactions%20of%20the%20Royal%20Society%20of%20London.%20Series%20B,%20Biological%20sciences&rft.au=Woodward,%20R.%20B.&rft.date=1980-05-16&rft.volume=289&rft.issue=1036&rft.spage=239&rft.epage=250&rft.pages=239-250&rft.issn=0080-4622&rft.eissn=2054-0280&rft_id=info:doi/10.1098/rstb.1980.0042&rft_dat=%3Cjstor_royal%3E2395381%3C/jstor_royal%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c463t-24d15a23fa8dd8889e01c70566a848d53d73006c4ed986a89cd064fd26fe51853%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=75417390&rft_id=info:pmid/6109320&rft_jstor_id=2395381&rfr_iscdi=true |