• KSBB Journal
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• v.8 no.2
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• pp.110-114
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• 1993

Vinblastine, an anticancer agent was produced by chemical coupling of two different monomeric indole alkaloids, vinblastine and catharanthine in the presence of ferric ion. Vindoline was efficiently extracted from the leaves of vinca (Cafharanthus roseus) by using supercritical carbon dioxide, whereas catharanthine was chemically extracted from the in vitro cultured hairy roots. The extracted crude monomeric precursors were purified by a two-step preparative TLC. The coupling reaction was carried out in the 0.1M glycine buffer(pH 2.0, 5ml) containing 40mM FeC13 with purified vindoline(0.3mg) and catharanthine(0.3mg) at 4$^{\circ}C$. The production yields (weight %) of vinblastine and 3', 4'-anhy-drovinblastine in the products were 23.2 and 26.0, respectively. The produced vinblastine was confirmed by FAB-MS.

• The Korean Journal of Food & Health Convergence
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• v.4 no.2
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• pp.17-23
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• 2018

Carica papaya is an important medicinal plant used in the management of different disease conditions. Phytochemical screening was carried out using different chemical test, Percentage yield and total phenolic content was evaluated using Folin Ciocalteu method in different solvent system; methanol, ethanol, ethyl acetate, n-butanol and n-hexane respectively. The phytochemical screening of the studies showed the presence of flavonoids, saponins, tannins, terpenoids, glycosides, steroids, carbonhydrate, anthraquinone and alkaloids. The percentage yield of crude extract and total polyphenol content was high in methanol, ethanol and ethyl acetate when compared with n-butanol and n-hexane. The studies show that Carica papaya leave extracts is a potent source of secondary metabolites. The use of the plant in the management of diseases is justified.

• Journal of Microbiology and Biotechnology
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• v.3 no.4
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• pp.238-243
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• 1993

In the suspension cultures of Eschscholtzia californica, phytohormone effects showed that alkaloid production was increased by IAA treatment without kinetin in both volumetric and specific way. Kinetin, however, suppressed alkaloid accumulation. Addition of ethephon inhibited cell growth. However, it enhanced the alkaloid production significantly in both volumetric and specific way. IAA promoted alkaloid production during elicitation. The highest alkaloid accumulation was observed at 5 $\mu$ M of IAA. Ethephon also enhanced alkaloid production during elicitation. The highest alkaloid formation was observed at 460 mg/l of ethephon with elicitation. Elicitation with ethephon, however, altered cell growth and the pattern of benzophenanthridine alkaloids production.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1996.11a
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• pp.165-169
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• 1996

The cytochrome P450 (P450) proteins have been studied extensively because of their prominent roles as catalysts in the oxidations of drugs, carcinogens, steroids, alkaloids, vitamins, and other important chemicals (Guengerich, 1991). In the past decade the study of these enzymes has been advanced by the cloning of cDNAs and expression of the proteins in several heterologous vector systems. One approach that has been employed in this and other laboratories is expression in bacteria. To date at least 31 different mammalian P450s have been expressed in Escherichia coli-band systems (Guengerich et al., 1996). In most of these cases the N-terminus has been altered to facilitate better expression (Barnes et al., 1991).

• Natural Product Sciences
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• v.5 no.3
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• pp.142-147
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• 1999

Tiliacora racemosa Colebr. belonging to the family Menispermaceae is the biggest store-house of diphenyl bisbenzylisoquinoline (DBBI) alkaloids. Exhaustive chemical processing of the root of T. racemosa by the application of modern separation techniques yielded a DBBI alkaloid which was identified as tiliacorine using sophisticated spectroscopic methods (UV, IR, $1^H-NMR$, Mass). Tiliacorine potentiated the sleeping time induced by standard hypnotics viz. chlorpromazine (CPZ), pentobarbitone (PB) and diazepam (DZ) in a dose dependent manner. Tiliacorine potentiated the analgesic action of standard analgesic agents viz., morphine and meperidine. It was also found to possess anti convulsive activity in the strychnine induced convulsion model.

• Korean Journal of Pharmacognosy
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• v.7 no.3
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• pp.211-214
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• 1976

Basic substances were obtained from five Korean Aconitum, A. koreanum, A. chiisanense, A. ciliae, A. pseudoproliferum and unknown Aconitum species and compared TLC patterns of the substances. Soluble substances in ammonia alkali showed 8 spots on TLC, while insoluble substances in ammonia alkali 7 spots. These patterns are all similar in all species used in the investigation.

• Natural Product Sciences
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• v.9 no.3
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• pp.143-153
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• 2003

Though a great deal of secondary metabolites and their bioactivities were discovered from the plants of the genus Hovenia, the structure-activity relationship was not well defined. To facilitate further pharmacological research and development in this area, we have summarized the progress of phytochemical and pharmacological research on the plants of the genus Hovenia.

• Korean Journal of Pharmacognosy
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• v.2 no.2
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• pp.83-86
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• 1971

The effects of temperature on Vitali test for tropane alkaloids were investigated. At low temperatures, after nitration occurred at para-position, the electron force of the nitro group caused hydrolysis of ester and oxidation, p-nitrobenzoic acid being produced. At $140^{\circ}C(high{\;}temperature)$, pyrolytic deesterification first took place and then nitration followed, yielding 2,4-dinitrobenzoic and 3,5-dinitrobenzoic acids.

• Korean Journal of Pharmacognosy
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• v.29 no.2
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• pp.104-109
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• 1998

Four alkaloids were isolated from the n-BuOH extract of the bulbus of Fritillaria walujewii (Liliaceae). On the basis of spectroscopic evidences, the structures of these compounds were established as Alkaloid fr-5(11-deoxo-6-oxo-5${\alpha}$,6-dihydrojervine), delavinone, delavine and petilidine.

• Korean Journal of Pharmacognosy
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• v.1 no.2
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• pp.11-17
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• 1970

The identification methods for tropane alkaloids so far known were limited on tropic acid esters such as atropine and was unable to detect mandelic acid esters such as homatropine. The present method employing thin-layer chromatography was able to detect violet coloration developed with any of them by Vitali-reaction. It was established that this violet coloration is due to the mesomerization of carb-anion in the alkaline solution.