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DC Field | Value | Language |
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dc.contributor.author | Wangchuk P. | |
dc.contributor.author | Keller P.A. | |
dc.contributor.author | Pyne S.G. | |
dc.contributor.author | Sastraruji T. | |
dc.contributor.author | Taweechotipatr M. | |
dc.contributor.author | Rattanajak R. | |
dc.contributor.author | Tonsomboon A. | |
dc.contributor.author | Kamchonwongpaisan S. | |
dc.date.accessioned | 2021-04-05T03:34:19Z | - |
dc.date.available | 2021-04-05T03:34:19Z | - |
dc.date.issued | 2012 | |
dc.identifier.issn | 1934578X | |
dc.identifier.other | 2-s2.0-84861505544 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14347 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84861505544&doi=10.1177%2f1934578x1200700507&partnerID=40&md5=32ca02c41f971064f9320f03e533e056 | |
dc.description.abstract | The chemical constituents and biological activities of Corydalis crispa (Fumariaceae) were investigated for the first time. The phytochemical study resulted in the isolation of nine known isoquinoline alkaloids: protopine (1), 13-oxoprotopine (2), 13-oxocryptopine (3), stylopine (4), coreximine (5), rheagenine (6), ochrobirine (7), sibiricine (8) and bicuculline (9), with complete NMR data for 2 and 3 provided here for the first time. Crude extracts exhibited significant anti-inflammatory (p<0.01) activity against TNF-α production in LPS activated THP-1 cells. The acetylcholinesterase inhibitory activity of compounds 2, 4 and 7 and the antiplasmodial activity of compound 5 against P. falciparum strains TM4/8.2 and K1CB1 (multidrug resistant strain) are reported here for the first time. Stylopine (4) did not show antimalarial activity against the K1CB1 strain in contrast to a previous report. This study generated a scientific basis for the use of this plant in Bhutanese traditional medicine, either individually or in combination with other medicinal ingredients to treat a broad range of disorders. This study also identified compound 5 as potential new antimalarial lead compound. | |
dc.subject | 13 oxocryptopine | |
dc.subject | 13 oxoprotopine | |
dc.subject | amoxicillin | |
dc.subject | amphotericin B | |
dc.subject | antibiotic agent | |
dc.subject | antiflagellate agent | |
dc.subject | antifungal agent | |
dc.subject | antiinflammatory agent | |
dc.subject | antimalarial agent | |
dc.subject | antitrypanosomal agent | |
dc.subject | bicuculline | |
dc.subject | chloroquine | |
dc.subject | coreximine | |
dc.subject | Corydalis crispa extract | |
dc.subject | cycloguanil | |
dc.subject | dexamethasone | |
dc.subject | galantamine | |
dc.subject | ochrobirine | |
dc.subject | pb 113 | |
dc.subject | plant extract | |
dc.subject | plant medicinal product | |
dc.subject | protopine | |
dc.subject | pyrimethamine | |
dc.subject | rheagenine | |
dc.subject | sibiricine | |
dc.subject | stylopine | |
dc.subject | unclassified drug | |
dc.subject | vancomycin | |
dc.subject | antibacterial activity | |
dc.subject | antifungal activity | |
dc.subject | antiinflammatory activity | |
dc.subject | antiprotozoal activity | |
dc.subject | article | |
dc.subject | Bhutan | |
dc.subject | biological activity | |
dc.subject | controlled study | |
dc.subject | Corydalis crispa | |
dc.subject | cytokine production | |
dc.subject | drug isolation | |
dc.subject | drug mechanism | |
dc.subject | drug screening | |
dc.subject | drug structure | |
dc.subject | enzyme inhibition | |
dc.subject | nonhuman | |
dc.subject | nuclear magnetic resonance | |
dc.subject | Papaveraceae | |
dc.subject | phytochemistry | |
dc.subject | Plasmodium falciparum | |
dc.subject | Corydalis | |
dc.subject | Fumariaceae | |
dc.subject | Plasmodium falciparum | |
dc.title | Phytochemical and biological activity studies of the Bhutanese medicinal plant corydalis crispa | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Natural Product Communications. Vol 7, No.5 (2012), p.575-580 | |
dc.identifier.doi | 10.1177/1934578x1200700507 | |
Appears in Collections: | Scopus 1983-2021 |
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