Cumulative CAMAG Bibliography Service CCBS

Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.

The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:

  • Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
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      96 091
      Phenolic compounds in the flowers of Lavatera trimestris L
      K. Glowniak*, K. Skalicka, A. Ludwiczuk, K. Jop (*Department of Pharmacognosy with Medicinal Plant Garden, Medical University, 1 Chodzki Str., 20-093 Lublin, Poland)

      (Malvaceae). J. Planar Chromatogr. 18, 264-268 (2005). TLC in horizontal chambers of phenolic acids (caffeic, p-coumaric, ferulic, protocatechuic, gentisic, chlorogenic, isovanillic, gallic, syringic, vanillic and p-hydroxybenzoic acid) from Lavatera trimestris flowers on cellulose with water - acetic acid 3:17, toluene - ethyl formate - formic acid 5:4:1, chloroforrm - acetic acid - water 4:1:1 and of flavonoids (rutoside, kaempferol 3-rhamnoglucoside, hyperoside, isoquercetin, luteolin 7-glucoside, quercitrin, isorhamnetin 3-glucoside, luteolin, apigenin, quercetin, kaempferol) on silica gel with n-propanol - ethyl acetate - water 7:2:1, ethanol - 25 % ammonia - water 20:1:4, ethyl acetate - formic acid - water 10:2:3, ethyl acetate - formic acid - glacial acetic acid - water 100:11:11:27 and 50:5:5:9. Also two-dimensional TLC of phenolic acids on cellulose (after conditioning in the chamber for 5 min with benzene - methanol - acetic acid 94:1:5) with benzene - methanol - acetic acid - acetonitrile 16:2:1:1 in the first direction and with sodium formate - formic acid - water 1:0.1:20 in the second direction. Detection under UV light at 254 and 366 nm before and after treatment with ammonia vapor. Also derivatization by spraying with a 2 % aqueous solution of iron(III) chloride, diazotized sulfanilic acid in 20 % sodium carbonate solution, and diazotized p-nitroaniline for phenolics and with a 1 % methanolic solution of natural products reagent A for flavonoids.

      Classification: 8a, 11a, 32e
      96 133
      (Study of the quality Standard for Compound Songluo granules) (Chinese)
      Q. QIN (Qin Qing)*, B. GAO (Gao Baoshuan), (*Hebei Inst. Cont. Med. App. and Drug Package Materials, Shijiazhuang, Hebei 050061, China)

      J. Chinese Trad. Patent Med. (Zhongchengyao) 27 (3), 272-275 (2005). TLC of the extracts on silica gel with 1) n-hexane - chloroform - methanol 15:8:2; 2) n-hexane - ethyl acetate 9:1; 3) chloroform - benzene - glacial acetic acid 7:2:1. Detection 1) by exposing to iodine vapours; 2) under UV 365 and 254 nm. Identification by comparison with the standard. Quantification of usnic acid by densitometry at 290 nm. Validation by investigating the linearity range (0.50 - 2.50 µg/spot, r = 0.999), precision (RSD = 2.26 %, n= 5, within plate, and 2.97 %, n = 5, plate-to-plate), and standard addition recovery (97.5 %, RSD = 2.61, n = 5).

      Classification: 32c
      97 017
      Planar chromatographic study of flavonoids and soyasaponins for validation of fingerprints of Desmodium adscendens of different origin
      J. Pothier*, J. Ragot, N. Galand (*University Francois Rabelais, Laboratory of Pharmacognosy, Faculty of Pharmacy, 31 Avenue Monge, F-37200 Tours, France)

      J. Planar Chromatogr. 19, 191-194 (2006). TLC of the flavonoid and triterpenoid soyasaponin content (rutin, vitexine, isovitexine, soyasaponin I and VI as standards) on silica gel in a twin-trough chamber with ethyl acetate - formic acid - acetic acid - water 100:11:11:26 for flavonoids. Detection with diphenylboric acid 2-aminoethylester (natural products reagent) followed by PEG reagent. For soyasaponins chloroform - methanol - water 6:4:1 was used. Detection by spraying with anisaldehyde - sulfuric acid reagent followed by heating at 115 °C.

      Classification: 8a, 14
      97 067
      Gastroprotective mechanisms of indole alkaloids from Himatanthus lancifolius
      C.H. Baggio, G. de Martini Otofuji, W. M. de Souza, C. A. de Moraes Santos, L. M. B. Torres, L. Rieck, M. .de Andrade Marques, Sonia MESIA-VELA* (*Department of Pharmacology, Biological Science Sector, Universidade Federal of Paraná, UFPR, Centro Politecnico, Caixa Postal 19031, Jardim das Americas, CEP 81531-990, Curitiba-PR, Brazil; sm2418@columbia.edu)

      Planta Med. 71, 733-738 (2005). Preparative TLC of (+)-ulein on silica gel with n-hexane - dichloromethane - methanol - diethylamine 25:20:4:1 and n-hexane - ethyl acetate - methanol - diethylamine 25:20:4:1. Detection under UV light at 254 nm.

      Classification: 32e
      97 092
      Antitubercular constituents of Valeriana laxifloria
      J.-Q. GU (Jian-Qiao Gu), Y. WANG (Yuehong Wang), S. G. FRANZBLAU, G. Montenegro, D. Yang (Danzhou Yang), Barbara N. TIMMERMANN* (*Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, P. O. Box 210207, 1703 E. Mabel Street, Tucson, AZ 85721-0207, USA; btimmer@pharmacy.arizona.edu)

      Planta Med. 70, 509-514 (2004). Analytical and preparative TLC of a new iridolactone (4R,5R,7S,8S,9S)-7-hydroxy-8-hxdroxymethyl-4-methyl perhydrocyclopenta[c]pyran-1-one) on silica gel and RP18 with acetonitrile - water 1:1. Detection by dipping in phosphomolybdic acid or vanillin - sulfuric acid reagent followed by heating at 110 °C for 5 min.

      Classification: 32e
      97 120
      Five new oleanolic acid glycosides from Achyranthes bidentata with inhibitory activity on osteoclast formation
      J.-X. LI* (Jian-Xin Li), T. HAREYAMA, Y. TEZUKA, Y. ZHANG (Yuan Zhang), T. Miyahara, S, Kadota (*Key Lab of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China; lijxnju@nju.edu.cn)

      Planta Med. 71, 673-679 (2005). Analytical and preparative TLC of 18-(beta-D-glucopyranosyloxy)-28-oxoolean-12-en-3beta-yl 3-O-(beta-D-glucopyranosyl)-beta-D-glucopyranosiduronic acid methyl ester, achyranthoside C dimethyl ester, achyranthoside C butyl dimethyl ester, achyranthoside E dimethyl ester, achyranthoside E butyl methyl ester (and 10 known compounds) on silica gel and RP18 with chloroform - methanol - water 8:5:2 or methanol - water 1:1, respectively. Detection under UV light at 254 nm or by spraying with cerium sulfate - 10 % sulfuric acid 1:99.

      Classification: 32e
      97 151
      Cytotoxicities of xanthones and cinnanate esters from Hypericum hookerianum
      R. Wilairat, J. Manosroi, A. Manosroi, A. Kijjoa, M. S. J. Nascimento, M. Pinto, A. M. S. Silva, G. Eaton, W. Herz* (*Department of Chemistry and Biochemistry, Florida State University, Tallahassee FL 32306-4390, USA; jdulin@chem.fsu.edu)

      Planta Med. 71, 680-682 (2005). Analytical and preparative TLC of 5-hydroxy-2-methoxyxanthone, 2-hydroxy-3-methoxyxanthone, trans-kielcarin, 4-hydroxy-3-methoxyphenyl ferulate, and 3beta-O-caffeoylbetulinic acid on silica gel with chloroform - petroleum ether - formic acid 950:50:1, chloroform - acetone - formic acid 950:50:1, 900:100:1, and 850:150:1. Detection under UV light at 254 nm.

      Classification: 32e
      98 067
      Quantification of eugenol, luteolin, ursolic acid, and oleanolic acid in black (Krishna Tulasi) and green (Sri Tulasi) varieties of Ocimum sanctum Linn
      S. ANANDJIWALA, J. KALOLA, M. RAJANI* (*B. V. Patel Pharmaceutical Education and Research Development Centre, Pharmacognosy and Phytochemistry Department, Thaltej, Ahmedabad-380 054, Gujarat, India; rajanivenkat@hotmail.com)

      using high-performance thin-layer chromatography. J. AOAC Int. 89, 1467-1474 (2006). HPTLC of eugenol, luteolin, ursolic acid, and oleanolic acid on silica gel in a twin trough chamber with toluene - ethyl acetate - formic acid 35:15:1 at 25 °C and 40 % relative humidity. Quantitation in absorbance mode at 280 nm for eugenol, at 350 nm for luteolin, and at 530 nm for ursolic acid and oleanolic acid after derivatization with anisaldehyde-sulfuric acid reagent and heating at 105°C. The methods were validated for precision, repeatability, and accuracy.

      Classification: 32e
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