• 제목/요약/키워드: Rutaceae

검색결과 82건 처리시간 0.024초

왕초피나무의 성분연구(成分硏究) (A Study on the Chemical Components of Zanthoxylum coreanum Nakai(Rutaceae))

  • 김창민;허인옥
    • 생약학회지
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    • 제12권1호
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    • pp.5-11
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    • 1981
  • The five fractions from the barks of Zanthoxylum coreanum in Je-ju Island are examined in detail chromatographically in this paper. 37 compounds are detected in all of the fractions, and the compounds from each of fractions are found to be presumed that this plant is classified into the same group as that of the temperate Zanthoxylum taxa but is different from the tropical zanthoxylum taxa by its chemical components.

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Aromatic Acid and Flavonoids from the Leaves of Zanthoxylum piperitum

  • Hur, Jong-Moon;Park, Jong-Cheol;Hwang, Young-Hee
    • Natural Product Sciences
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    • 제7권1호
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    • pp.23-26
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    • 2001
  • Five flavonoids and one aromatic acid were isolated from the leaves of Zanthoxylum piperitum. The structures of compounds were elucidated as quercetin, afzelin, quercitrin, hyperoside, hesperidin and protocatechuic acid on the basis of spectral evidence.

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Antineopastic Natural products and the analogues IV

  • Kang, Kyu-Sang;Ryu, Sung-Ho;Ahn, Byung-Zun
    • Archives of Pharmacal Research
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    • 제8권3호
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    • pp.187-190
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    • 1985
  • A cytotoxic coumarin against L1210 cell was isolated from the unripe fruit of Poncirus trifoliata ($ED_{5}$) = 10.2 $\mu$ g/ml. Its structure was identified as aurapten, 7-geranyloxycoumarin. Hydrolysis of the substance gave umbelliferone and geraniol. Only geraniol showed the cytotoxic activity ($ED_{53}$ = 6.5 $\mu$g/ml) while umbelliferone and its methyl or allyl derivatives were not active.

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Synthetic Approaches to Benzophenanthridines

  • Gang, Seong-Gyoung;Le NguyenThanh;Cho, Won-Jea
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.355.2-355.2
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    • 2002
  • Benzo[c] phenanthridine alkaloids occurring in the Fumariaceae, Papaveraceae, and Rutaceae. posses numerous pharmacological activities, such as antitumor. antimicrobal and antifungal activities. Thus, they have attracted much interests of chemists and as the result, several total syntheses of these heterocycle structure were accomplished. Among that, procedures which involve 3-arylisoquinoline intermediates are useful methods and these synthons could be also applied to the preparation of other alkaloids. (omitted)

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Erysiphe orixae, a Powdery Mildew Occurring on Orixa japonica in Korea

  • Ji-Hyun Park;In-Young Choi;Lamiya Abasova;Hyeon-Dong Shin
    • 한국균학회지
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    • 제51권4호
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    • pp.307-311
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    • 2023
  • Powdery mildew anamorphs were collected from Orixa japonica (Rutaceae) in Korea. Based on the morphology and molecular phylogeny derived from the internal transcribed spacer regions and the large subunit gene of the rDNA, the fungus was identified as Erysiphe orixae. This powdery mildew species has been known to be endemic to Japan. This is the first report on E. orixae in Korea.

trnL-trnF 서열에 의한 한국 귤나무속과 두 근연 식물종의 계통분류학적 연구 (Phylogenic Study of Genus Citrus and Two Relative Genera in Korea by trnL-trnF Sequence)

  • 허만규;윤혜정;최주수
    • 생명과학회지
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    • 제21권10호
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    • pp.1452-1459
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    • 2011
  • 귤나무속은 운향과(Rutaceae)에 속한다. 동남아시아, 미얀마, 중국 운남에서 기원된 것으로 알려져 있다. 이 속의 분류관계는 복잡한데 클론번식과 야생식물과 교잡이 빈번하다. 식물에서 속간 속내 계통관계 추론을 위해 널리 이용되고 있는 엽록체 trnL-trnF 부위가 있다. 이 귤나무속과 두 근연한 탱자나무속과 금감속에 속하는 7종간 계통 관계를 평가하였다. 많은 삽입이 발견되었고 속내 종간 변이는 결실/삽입에 의한 것으로 밝혀졌다. 이 속의 레몬과 당귤나무은 네 계통도(MP, ML, ME, and NJ)에서 모두 같은 분지군을 형성하여 가장 근연관계에 있었고 광귤나무(향귤나무)과 자매군을 형성하였다. 유자나무는 이들과 많은 서열 차이를 나타내었다. 외부 분지군은 낮은 지지도를 나타내었다.

국내 나비온실의 식물 식재현황 분석과 적용방안 연구 (The Analysis of the Butterfly Greenhouse Plant for the Butterfly Gardening)

  • 손진관;강동현;이시영;윤성욱;김남춘;김창현;공민재
    • 한국환경복원기술학회지
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    • 제20권1호
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    • pp.35-53
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    • 2017
  • This study analyzed the relationship between butterflies and plants. We examined 8 butterfly greenhouse. Butterflies are 5 families, 22 species found in 8 locations. Papilio xuthus, Pieris rapae, Papilio bianor etc. was expected to be introduced in the garden. Plants were identified in the 8 greenhouse with a total 249 taxa to 82 families 186 gunus 224 species 23 variety 2 forma. The main planting species were Compositae, Liliaceae, Rosaceae, Umbelliferae, Crassulaceae, Rutaceae and Etc. A main life forms are Hemicryptophytes. The naturalized plants have been identified 7 families 11 species. And planting in the garden, we propose appropriate management. Host plant is confirmed Rutaceae, Umbelliferae Leguminosae, Cruciferae, Ulmaceae, Aristolochiaceae Etc.. Main nectar plant is Compositae, Liliaceae, Rosaceae, Crassulaceae, Labiatae. Nectar plant is proposed to be planted in consideration of the flowering period. Zanthoxylum piperitum, Zanthoxylum schinifolium, Phellodendron amurense, Poncirus trifoliata, Citrus junos, Ruta graveolens proposed design reflects the woody. Spiraea(Rosaceae) and Rhododendron(Ericaceae) proposed by Nectar plants of woody. We hope to be utilized in the planning and construction of a butterfly garden.

Effect of Citrus aurantium var amara on weight change in mice

  • Sarker, Satyajit Dey;Habibi, Bohlol;Sharifi, Tohid;Asnaashari, Solmaz;Nahar, Lutfun;Delazar, AndAbbas
    • Advances in Traditional Medicine
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    • 제8권3호
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    • pp.222-227
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    • 2008
  • Citrus aurantium var. amara L., commonly known as 'bitter orange' or 'sour orange', of the family Rutaceae, has traditionally been used in the treatment of various ailments, and it possesses different types of pharmacological properties. As a part of our on-going studies on the plantsfrom the Iranian flora, the extract of C. aurantium var. amara has been studied for its weight lossproperties using the mice model. While the Sep-Pak fraction, 20% methanol (MeOH) in water, of the hydro-methanolic extract of the peels of C. aurantium var. amara fruits, when injectedintraperitoneal (i.p.) at a dose of 10 mg/kg, significantly decreased the level of weight gain of the mice in comparison with control the group (P < 0.01), the Sep-Pak fraction 80% MeOH in water decreased the initial weight of mice by 0.44% in six weeks. The administration of the total extract(10 and 20 mg/kg, i.p.), and the Sep-Pak fractions, 40% and 60% MeOH in water (10 mg/kg, i.p.)did not show any significant change of weight of the test mice. Of the two active fractions, the80% MeOH in water fraction did not show any noticeable adverse effects on mice, and was therefore analysed by reversed-phase preparative high performance liquid chromatography resulting in the isolation and identification of four major components, two coumarins, meranzin hydrate (1) and bergamottin (2), and two flavonoids, xanthomicrol 5,4'-di-methyl ether (tangeritin, 3) and hymenoxin 5,7-di-methyl ether (nobiletin, 4).