• Natural Product Sciences
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• 제13권4호
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• pp.317-321
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• 2007

Phytochemical investigation of the aerial parts of Lotus ornithopodioloides L. resulted in the isolation of six known compounds. The structures were determined utilizing physical, chemical, spectral methods as well as direct comparison with reference materials whenever possible. The compounds were identified as: ${\beta}$-sitosterol; the two triterpenes oleanolic and betulinic acids; the two cyanogenic glycosides lotaustralin and linamarin in addition to the flavonol diglycoside kaempferitin.

• Archives of Pharmacal Research
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• 제24권6호
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• pp.524-526
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• 2001

Four prostate-type triterpenes were isolated from a methanol extract of Alismatis Rhizoma by bioassay-guided isolation using in vitro cytotoxic assay. The compounds were identified as alisol B 23-acetate (1), alisol C 23-acetate (2), alisol B (3), alisol A 24-acetate (4) by spectroscopic methods. Amongst the compounds, alisol B (3) showed significant cytotoxicity against SK-OV3, B16-F10, and HT1080 cancer cell lines with $ED_50$ values of 7.5, 7.5, $4.9\mu\textrm{g}/ml$, respectively.

• 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.371.1-371.1
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• 2002

Triterpenoids. Ursolic acid (1). 23-hydroxyursolic acid (2). and tormentic acid (3) were obtained by the hydrolysis of BuOH fraction of Cussonia bancoensis extract and further chromatographic isolation to test antinociceptive and anti-inflammatory effect of C. bancoensis (Aratiaceae). Compound 1 and 2 exhibited anti-nociceptive effects, which were determined by acetic acid-induced writhing test and hot plate test. However. the effect of tormentic acid was not significant (omitted)

• 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.375.1-375.1
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• 2002

As part of a research program on the bioactive terpene constituents of Korean compositae plants. we have investigated Cacalia koraiensis (compositae). collected from Gangwon Province on August 2001. On reviewing the literatures of this species. triterpenes and pyrrolizidine alkaloids were isolated and some pharmacological activities were investigated. This species have been used for tinea and spasmolysis However. chemical constituents of this plant have not been reported. (omitted)

• Natural Product Sciences
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• 제27권2호
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• pp.134-139
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• 2021

A new cipadesin limonoid, i.e. 3-epi-cipadonoid C (1), and a new tirucallane triterpene, i.e. hispidol B 3-palmitate (3), have been isolated from the seeds and fruit peels extract of Sandoricum koetjape, respectively. Along with these compounds the known limonoid, cipaferen G (2), and two pentacyclic triterpenes, bryonolic (4) and bryononic (5) acids, were also isolated. The strucrures of the new compounds were elucidated by the analysis of NMR and mass spectral data. Compounds 1 - 5 were evaluated as the inhibitor of receptor tyrosine kinases (EGFR, Epidermal Growth Factor Receptor; HER2, HER4, Human Epidermal growth factor Receptor 2, -4; IGFR, Insulin-like Growth Factor Receptor; InsR, Insulin Receptor; KDR, Kinase insert Domain Receptor; PDGFRα, and PDGFRβ, Platelet-Derived Growth Factor Receptor-α and -β). The results showed only 1 and 3 that have weak activity against InsR.

• 한국자원식물학회지
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• 제30권2호
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• pp.240-264
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• 2017

한국산 초롱꽃과 식물의 전통지식을 확인하고, 이들의 화학성분, 약리효과에 관한 자료와의 비교 분석을 통해 종합적인 고찰을 수행하였다. 그 결과, 민속식물은 총 18분류군으로 식용, 약용, 관상용 등으로 이용되고 있으며, 이 중 약용으로는 도라지, 잔대, 더덕 등 총 12분류군이 확인되었다. 약용 전통지식은 감기, 천식, 산후조리 등 49개의 질병 및 질환을 치료하기 위해 이용된 것으로 조사되었다. 지금까지 한국산 초롱꽃과 잔대속, 더덕속, 도라지속, 초롱꽃속, 영아자속에서 총 211개의 화학성분이 선행 연구자들에 의해 밝혀졌으며, 이들은 triterpenes 109종류, sterols 8종류, polyacetylens 4종류, alkaloids 21종류, flavonoids 14종류, phenolic acids 14종류, phenolic glycosides 11종류, phenylpropanoids 8종류, 그 밖의 성분으로 organic acid 계열 등 22종류이다. 약리효과로는 면역활성, 항염증, 항천식 및 점액분비촉진, 항알레르기, 항산화, 에스트로겐 활성, 항당뇨, 간 보호, 신경 보호, 항종양, 항진통, 순환계, 항비만 등에 효과가 있는 것으로 조사되었다. 조사된 전통지식과 화학성분, 약리효과에 대한 자료를 종합해 본 결과, 한국산 초롱꽃과 식물을 호흡기 계통, 임신 출산 산후조리, 생식 배설 계통, 순환 계통, 근골격계 계통 등의 질병 및 질환에 사용된 전통지식은 해당 식물체 조추출물 및 화학성분을 이용한 약리 실험을 통해 그 효과가 입증되었다고 판단된다.

• Natural Product Sciences
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• 제21권3호
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• pp.150-154
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• 2015

Phytochemical investigation of Kandelia candel resulted in the isolation of six triterpenes (1 - 5) and two glyceryl glycosides (6 and 7) and their structures were determined by comparing the spectroscopic data with those of reported values. In present study, we described the inhibitory effects of fractions and isolated compounds from K. candel on pro-inflammatory cytokines (IL-12 p40, IL-6, and TNF-α) production in lipopolysaccharide (LPS) stimulated bone marrow-derived dendritic cells (BMDCs). Results indicated that compounds 3, 6, and 7 showed potent inhibition on IL-6 production (IC₅₀ values at less than 0.5 μM, respectively). Meanwhile, compounds 6 and 7 exhibited strong inhibitory effects on the production of TNF-α (IC₅₀ values of 1.7 ± 0.1 and 5.5 ± 0.2 μM). Compounds 1 and 3 were also showed the inhibitory effects on IL-12 p40 production (IC₅₀ values of 8.9 ± 0.4 and 3.3 ± 0.1 μM, respectively).

• 한국작물학회지
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• 제67권4호
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• pp.335-341
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• 2022

기장에 있는 트리테르페노이드류인 밀리아신 성분은 각질 세포의 증식을 촉진하는 등의 특성을 가지고 있어 탈모에 효과가 있다고 알려져 있다. 이 연구에서는 기장의 기름을 추출하여 검화 반응을 거쳐 불검화물의 추출 방법을 이용하여 GC/MS로 분석하였다. 기장 기름 성분을 GC/MS의 정성분석을 통해 확인하였으며, 기장 5품종과 비교를 위한 조 2품종의 밀리아신 함량을 분석하였다. 1. 기장에서는 β-amyrine, lupeol 등의 pentacyclic triterpene 류의 성분들이 검출되었다. 2. 밀리아신 함량은 기장의 한라찰에서 370.38±0.04 ㎍/100 mg oil으로 가장 높은 함량을 나타내었다. 3. 특히 조의 품종인 삼다찰과 삼다메에서는 밀리아신 함량이 검출되지 않았다.

• Journal of Ginseng Research
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• 제37권1호
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• pp.74-79
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• 2013

In continuation of our research to find biological components from Panax stipuleanatus, four oleanane-type triterpenes (12 to 15) were isolated successively. Fifteen oleanane-type saponins (1 to 15) were evaluated for nuclear factor (NF)-${\kappa}B$ activity using a luciferase reporter gene assay in HepG2 cells. Compounds 6 to 11 inhibited NF-${\kappa}B$, with $IC_{50}$ values between 3.1 to 18.9 ${\mu}M$. The effects on inducible nitric oxide synthase and cyclooxygenase-2 by compounds 8, 10, and 11 were also examined using reverse transcription-polymerase chain reaction. Three compounds (8, 10, and 11) inhibited NF-${\kappa}B$ activity by reducing the concentration of inflammatory factors in HepG2 cells.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2012년도 정기총회 및 춘계학술발표회
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• pp.20-20
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• 2012

Isoprenoids represent the most diverse group of metabolites, which are functionally and structurally identified in plant organism to date. Ginsenosides, glycosylated triterpenes, are considered to be the major pharmaceutically active ingredient of ginseng. Its backbones, categorized as protopanaxadiol (PPD), protopanaxatriol (PPT), and oleanane saponin, are synthesized via the isoprenoid pathway by cyclization of 2,3-oxidosqualene mediated with dammarenediol synthase or beta-amyrin synthase. The rate-limiting 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR), which is the first committed step enzyme catalyzes the cytoplasmic mevalonate (MVA) pathway for isoprenoid biosynthesis. DXP reductoisomerese (DXR), yields 2-C-methyl-D-erythritol 4-phosphate (MEP), is partly involved in isoprenoid biosynthesis via plastid. Squalene synthase and squalene epoxidase are involved right before the cyclization step. The triterpene backbone then undergoes various modifications, such as oxidation, substitution, and glycosylation. Here we will discuss general biosynthesis pathway for the production of ginsenoside and its modification based on their subcellular biological functions.