{"title":"The national formulary. 11th ed. Prepared by the Committee on National Formulary under the supervision of the Council, by authority of the American Pharmaceutical Association. Published by the American Pharmaceutical Association, 1960. Distributed by J. B. Lippincott Co., East Washington Square, Philadelphia 5, Pa. xxxii + 531 pp. 15 × 23 cm. Price U. S. and Foreign, $9","authors":"","doi":"10.1002/jps.3030491221","DOIUrl":"10.1002/jps.3030491221","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 788"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491221","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134879813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A method is given for partially purifying the phenolic components of Cannabis sativa resin and for separating these components by means of paper chromatography. The application of this method for the preparation of pure cannabinol and tetrahydrocannabinol is described.
{"title":"Chromatographic separation of the phenolic compounds of Cannabis sativa","authors":"Robert S. de Ropp","doi":"10.1002/jps.3030491205","DOIUrl":"10.1002/jps.3030491205","url":null,"abstract":"<div><p>A method is given for partially purifying the phenolic components of <em>Cannabis sativa</em> resin and for separating these components by means of paper chromatography. The application of this method for the preparation of pure cannabinol and tetrahydrocannabinol is described.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 756-758"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491205","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23316531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chemicals, drugs and health. By John H. Foulger. Charles C Thomas, 301–327 East Lawrence Ave., Springfield, Ill., 1960. viii + 102 pp. 13.5 × 21.5 cm","authors":"","doi":"10.1002/jps.3030491215","DOIUrl":"10.1002/jps.3030491215","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 787"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491215","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134818229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The absorption spectra of 38 cardiac glycosides, aglycones, and aglycone derivatives, have been determined in sulfuric acid. The use of these spectra may assist in differentiating between members of the A, B, and C series of digitalis glycosides and aglycones.
{"title":"Absorption spectra of cardiac glycosides and aglycones in sulfuric acid","authors":"B.T. Brown, S.E. Wright","doi":"10.1002/jps.3030491209","DOIUrl":"10.1002/jps.3030491209","url":null,"abstract":"<div><p>The absorption spectra of 38 cardiac glycosides, aglycones, and aglycone derivatives, have been determined in sulfuric acid. The use of these spectra may assist in differentiating between members of the A, B, and C series of digitalis glycosides and aglycones.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 777-779"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491209","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77189539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"General cytology. 3rd ed. By E. D. P. DeRobertis, W. W. Nowinski, and Francisco A. Saez. W. B. Saunders Co., West Washington Square, Philadelphia 5, Pa., 1960. xvi + 555 pp. 15.5 × 23.5 cm. price $10","authors":"","doi":"10.1002/jps.3030491217","DOIUrl":"10.1002/jps.3030491217","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Page 787"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491217","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134818226","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In vitro antibacterial activity of nine essential oils and one fixed oil obtained from Indian medicinal plants was determined using a filter paper disk method. The oils were tested against various Gram-positive and Gram-negative organisms. All the oils tested were found to be effective against one or more test organisms.
{"title":"In vitro antibacterial activity of oils from Indian medicinal plants I","authors":"C.L. Chopra, M.C. Bhatia, I.C. Chopra","doi":"10.1002/jps.3030491210","DOIUrl":"10.1002/jps.3030491210","url":null,"abstract":"<div><p><em>In vitro</em> antibacterial activity of nine essential oils and one fixed oil obtained from Indian medicinal plants was determined using a filter paper disk method. The oils were tested against various Gram-positive and Gram-negative organisms. All the oils tested were found to be effective against one or more test organisms.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 12","pages":"Pages 780-781"},"PeriodicalIF":0.0,"publicationDate":"1960-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491210","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23968226","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A crystalline mixture of saponins was isolated from strawberry clover (Trifolium fragiferum). Upon hydrolysis with dilute acid this product yielded the soyasapogenols B and C, a very small quantity of unidentified sapogenin, and several sugars.
{"title":"Note on Saponins and Their Sapogenins from Strawberry Clover*","authors":"E.D. Walter","doi":"10.1002/jps.3030491114","DOIUrl":"10.1002/jps.3030491114","url":null,"abstract":"<div><p>A crystalline mixture of saponins was isolated from strawberry clover (<em>Trifolium fragiferum</em>). Upon hydrolysis with dilute acid this product yielded the soyasapogenols B and C, a very small quantity of unidentified sapogenin, and several sugars.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 11","pages":"Pages 735-736"},"PeriodicalIF":0.0,"publicationDate":"1960-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491114","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84787303","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Clinical chemistry. Principles and procedures. 2nd ed. By Joseph S. Annino. Medical Book Department, Little, Brown & Co., 34 Beacon St., Boston 6, Mass., 1960. xviii + 348 pp. 15.5 × 23.5 cm. Price $8","authors":"","doi":"10.1002/jps.3030491136","DOIUrl":"10.1002/jps.3030491136","url":null,"abstract":"","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 11","pages":"Page 740"},"PeriodicalIF":0.0,"publicationDate":"1960-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491136","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134801208","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
General methods for the preparation of 1-alkyl-2,5-piperazinediones were found in the cyclization of N-alkylglycylglycines and the alkylation of the sodium salt of 1-acetyl-2,5-piperazinedione. 1-Methyl-2,5-piperazinedione showed significant antispasmodic activity.
{"title":"Preparation of 1-Alkyl-2,5-piperazinediones*","authors":"William O. Foye, Douglas H. Kay","doi":"10.1002/jps.3030491106","DOIUrl":"https://doi.org/10.1002/jps.3030491106","url":null,"abstract":"<div><p>General methods for the preparation of 1-alkyl-2,5-piperazinediones were found in the cyclization of N-alkylglycylglycines and the alkylation of the sodium salt of 1-acetyl-2,5-piperazinedione. 1-Methyl-2,5-piperazinedione showed significant antispasmodic activity.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 11","pages":"Pages 705-708"},"PeriodicalIF":0.0,"publicationDate":"1960-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491106","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90029410","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Growth and morphology were compared on plants furnished six levels of nitrate and three of ammonia in water culture. The production of dry weight with ammonia was significantly greater than with nitrate. Ratios of shoot/root and leaf/stem indicated that use of the nitrogen was very different at low vs. high levels, particularly with ammonia nitrogen.
{"title":"Growth and Differentiation of Atropa belladonna L. as Affected by Different Sources of Nitrogen*","authors":"L.J. Schermeister , F.A. Crane, R.F. Voigt","doi":"10.1002/jps.3030491104","DOIUrl":"https://doi.org/10.1002/jps.3030491104","url":null,"abstract":"<div><p>Growth and morphology were compared on plants furnished six levels of nitrate and three of ammonia in water culture. The production of dry weight with ammonia was significantly greater than with nitrate. Ratios of shoot/root and leaf/stem indicated that use of the nitrogen was very different at low vs. high levels, particularly with ammonia nitrogen.</p></div>","PeriodicalId":100839,"journal":{"name":"Journal of the American Pharmaceutical Association (Scientific ed.)","volume":"49 11","pages":"Pages 694-697"},"PeriodicalIF":0.0,"publicationDate":"1960-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jps.3030491104","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91727644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}