• Title/Summary/Keyword: Carpesium

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Thymol Derivatives form Carpesium divaricatum

  • Zee, Ok-Pyo;Kim, Dae-Keun;Lee, Kang-Ro
    • Archives of Pharmacal Research
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    • v.21 no.5
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    • pp.618-620
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    • 1998
  • Four thymol derivatives, 2,5-dimethoxythymol (1), 2-methoxythymol isobutyrate (2), 10-isobutyloxy-8,9-epoxythymolisobutyrate (3) and 10-(2-methylbutyloxy)-8,9-eposythymolisobutyrate (4) were isolated from the aerial parts of Carpesium divaricatum. the structures were elucidated by high field 1D and 2D NMR techniques.

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Phytochemical Constituents of Carpesium macrocephalum $F_R$. et $S_{AV}$.

  • Kim, Mi-Ran;Lee, Seung-Kyu;Kim, Chang-Soo;Kim, Kyung-Soon;Moon , Dong-Cheul
    • Archives of Pharmacal Research
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    • v.27 no.10
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    • pp.1029-1033
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    • 2004
  • From the methanol extract of the whole plants of Carpesium macrocephalum $F_R$. et $S_{AV}$., five sesquiterpene lactones (1: carabron, 2: tomentosin, 3: ivalin, 4: 4H-tomentosin, 5: carabrol) and three terpenoids (6: loliolide, 7: vomifoliol, 8: citrusin C) were isolated. The structures and stereochemistry of compounds 1-8 were established on the basis of chemical analysis as well as 1D- and 2D-NMR spectroscopy. Among them, compounds 2, 4, and 6-8 were isolated for the first time from Carpesium species.

A Phylogenetic Study of Korean Carpesium L. Based on nrDNA ITS Sequences (ITS 염기서열에 의한 한국산 담배풀속(Carpesium L.)의 계통분류학적 연구)

  • Yoo, Kwang-Pil;Park, Seon-Joo
    • Korean Journal of Plant Resources
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    • v.25 no.1
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    • pp.96-104
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    • 2012
  • Phylogenetic analyses were conducted to evaluate relationships of 7 taxa of Korean Carpesium including three outgroup (Inula britannica L., Inula germanica L., Rhanteriopsis lannginosa (DC.) Rauschert) by using ITS (internal transcribed spacer) sequences of nuclear ribosomal DNA. Phylogenetic studies used maximum parsimony, neighbor-joining and maximum likelihood methods analysis. The length of the ITS sequences was 731 bp, and the lengths of the ITS1, ITS2 and 5.8S regions were 284~297 bp, 264~266 bp and 164 bp, respectively. The total number of variable sites was 111 for the entire sequences, and a parsimony informative sites of 64 are valid. Base change appeared variously in ITS1 rather than in ITS2. As the result, Korean Carpesium were formed monophyletic group and C. abrotanoides situated as the most basal clade. The results show that C. macrocephalum is closely related with C. triste. C. rosulatum has the closest relationship with C. glossophyllum. C. cernuum is close to C. divaricatum. These results suggest that the ITS data used in this study could be useful for the phylogenetic analysis of Korean Carpesium.

A New Cytotoxic Acyclic Diterpene from Carpesium divaricatum

  • Zee, Ok-Pyo;Kim, Dae-Keun;Choi, Sang-Un;Lee, Chong-Ock;Lee, Kang-Ro
    • Archives of Pharmacal Research
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    • v.22 no.2
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    • pp.225-227
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    • 1999
  • A new acylcic deterpene (1) and a known acyclic diterpene 12(S)-hydroxygeranyleraniol (2) were isolated form the aerial parts of Carpesium divaricatum. The structure of 1 was determined to be (2E, 10E)-1, 12-dihydroxy-18-acetoxy-3,7,15-trimethylhexadeca-2,10,14-triene (1) on the basis of spectroscopic studies. Compounds 1 and 2 exhibited cytotoxicity against cultured human tumor cell lines, A549, SK-OV-3, SK-MEL-2, XF498, and $HCT_{15}$, with $ED_{50}$ values ranging from 4.3-10.2 ${\mu}g/ml$ and 4.1-8.3 ${\mu}g/ml$, respectively.

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Comparison of Biological Activities on Extracts and Fractions in Compositae Plants (국화류 추출물 및 분획물의 생리활성 비교연구)

  • Kang, Jeong-Ran;Yu, Eun-Mi;Han, Kap-Hoon
    • Journal of Convergence for Information Technology
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    • v.9 no.9
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    • pp.245-251
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    • 2019
  • This study was conducted to investigate the anti-oxidative, anti-oxidative and tyrosinase inhibitory effects of MeOH 80% extract and hexane, chloroform, ethyl acetate, butanol and aqueous fraction on three kinds of compositae plants in Korea. In the antimicrobial effect, the extract and chloroform fraction of Eclipta prostrata and hexane fraction of Carpesium abrotanoides L. and chloroform fraction of Siegesbeckia glabrescens exhibited significant inhibition. The antioxidant activity of ethyl acetate and butanol fractions was more than 90% in all three plants. In case of tyrosinase activity, showed a potent inhibition ethlyacetate fraction of Siegesbeckia glabrescens and Carpesium abrotanoides L, which were higher than control group. In MeOH 80% extracts, there was not found to have antimicrobial, anti-oxidant and tyrosinase inhibitory activity, however there was ethylacetate fraction of Siegesbeckia glabrescens to show effectss commonly in the three assay system.

Flora of Gwanmae Island (관매도의 식물상)

  • Sun, Eun-Mi;Son, Hyun-Deok;Park, Han-Su;Im, Hyoung-Tak
    • Korean Journal of Plant Resources
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    • v.35 no.1
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    • pp.109-133
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    • 2022
  • We investigated the flora of Gwanmae island and discussed important vascular plants found on the island. We made plant list using voucher specimens collected from Gwanmae island from 2016 to 2021 and deposited in CNU. There are 500 taxa in Gwanmae island, comprising 103 families, 307 genera, 461 species, 4 subspecies, 32 varieties and 3 forms. Eight endemic plants of Korea were found including Saussurea polylepis Nakai. There are 15 red list plants designated by Ministry of Environment including Cleisostoma scolopendrifolium (Makino) Garay and Woodwardia japonica (L. f.) Sm. There are total 126 taxa of floristic regional indicator plants including 4 taxa of level V such as Juniperus procumbens (Siebold ex Endl.) Miq., 4 taxa of level IV such as Wisteria japonica Siebold & Zucc., 45 taxa of level III such as Rubus trifidus Thunb., 16 taxa of level II such as Glehnia littoralis F. Schmidt and 56 taxa of level I such as Carpesium glossophyllum Maxim. There are 32 invasive plants including Cerastium glomeratum Thuill.

Synthesis and in vitro Cytotoxicity Monoterpenoid as New Antitumor Agents (Monoterpenoid계의 새로운 항암제 합성 및 In vitro 세포독성 평가)

  • 이민정;김대근;백형근;이강노;정규혁
    • Biomolecules & Therapeutics
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    • v.9 no.3
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    • pp.143-155
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    • 2001
  • Many attention has been focused on developing new chemotherapeutic agents for a treatment of cancer from natural products. From Carpesium divaricatum S. et Z. (Compositae), various monoterpenoid compounds were isolated and exhibited mild antitumor activity against human tumor cell lines. These facts prompted us to explore the structure-activity relationship of these compounds. The synthesis of monoterpenoid compound was accomplished by Fries rearrangement, Grignard reaction, elimination, allylic oxidation, esterification and epoxidation as key steps. The results of in vitro cytotoxicity (A549, SK-OV-3, SK-MEL-2, XF498, HCT15) of the synthesised compounds are as follows: First of all, epoxide moiety is prerequisite for cytotoxic activity in diester compound. Any kind of compounds with olefin or diol moiety instead of epoxide ring exhibited poor or mild cytotoxic activity respectively. Of o-acetoxy and isobutoxy epoxy esters, p-sub-stituted phenylacetate compounds exhibited high cytotoxic activities against SK-MEL-2 and HCT15.

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