• Research in Plant Disease
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• v.19 no.1
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• pp.45-48
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• 2013

Rusts are plant diseases caused by pathogenic fungi of the order Pucciniales. Rusts can affect a variety of plants. Development of new effective and environmentally benign agents against rusts is of great interest. In this study, we investigated the disease control efficacy of the emulsion concentrate (EC10) and wettable powder (WP20) type formulations of the extract of Magnolia officinalis (Magjia90; containing honokiol and magnolol at 90%) against rust diseases of perilla and zoysiagrass in fields. The treatment of EC10 and WP20 of Magjia90 showed control values of 47.9% to 69.6% and Magjia90-WP20 reduced more effectively the development of rust symptoms on perilla plants than Magjia90-EC10. Magjia90-WP20 also highly suppressed zoysiagrass rust with control values of 65.7% to 80.5%. On the other hand, no harmful effect of Magjia90-EC10 and Magjia90-WP20 was observed on the perilla and zoysiagrass plants tested. The results strongly indicate that the extract of M. officinalis (Magjia90) can be used as a natural fungicide for the control of rust diseases.

• Journal of Applied Biological Chemistry
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• v.58 no.3
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• pp.233-236
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• 2015

The flowers of Magnolia obovata were extracted with aqueous MeOH and fractionated into EtOAc, n-BuOH, and $H_2O$ fractination. Three alkyl glycosides were isolated from the EtOAc fraction through repeated silica gel and ODS column chromatography. The structures were identified to be 2-methylbutan-1-ol-${\beta}$-$\small{D}$-galacto-pyranoside (1), 2-methylbutan-1-ol-${\beta}$-$\small{D}$-glucopyranoside (2), and 2-methylpropan-1-ol-${\beta}$-$\small{D}$-glucopyranoside (3) on the basis of spectroscopic analyses such as fast atom bombardment mass spectrometry, infrared spectroscopy, 1D nuclear magnetic resonance (NMR) ($^1H$ and $^{13}C-NMR$), and 2D NMR (gCOSY, gHSQC, and gHMBC). These compounds were isolated for the first time from the flower of M. obovata in this study.

• Journal of Applied Biological Chemistry
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• v.58 no.4
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• pp.391-391
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• 2015

• Proceedings of the PSK Conference
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• 2002.10a
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• pp.362.4-363
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• 2002

Costunolide which is known as a chemopreventive drug is a sesquiterpene compound isolated from Magnolia Sieboldii. and has antitumor and antiinflamatory activities. it is very hard to collect enough amount of natural extracts of costunolide for the activity studies. therfore. synthesis of costunolide derivatives is honestly needed. the aim of this research is to develope new methods for costunolide synthesis and to test biological activities. (omitted)

• Proceedings of the PSK Conference
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• 2001.04a
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• pp.197.3-198
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• 2001

• Korean Journal of Pharmacognosy
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• v.7 no.1
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• pp.69-71
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• 1976

New or noteworthy medicinal plants were found in Korea, such as 1. Magnolia sieboldii K. KOCH f. dupliflora $C_{HI}$ (Magnoliaceae) 2. Peucedanum insolens $K_{ITAGAWA}$ (Umbelliferae) 3. Panax japonicus C.A. $M_{EYER}$ (Araliaceae) 4. Phytolacca americana L. (Phytolaccaceae) 5. Polygonum ellipticum $M_{IGO}$ (Polygonaceae).

• Proceedings of the Korean Society of Toxicology Conference
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• 2005.05a
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• pp.204-204
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• 2005

• Archives of Pharmacal Research
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• v.4 no.2
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• pp.123-127
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• 1981

The method extracts of Patriniae radix, Dianthii herba, Melandrii herba, Echinopii radix, Siegesbeckiae herba and Magnoliae cortex showed a significant elevation of serum transam inase activity accompanied by fatty degeneration and Kupffer accompanied by fatty degeneration and Kupffer cell activation in hepatic cells.

• Asian Journal of Turfgrass Science
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• v.12 no.2
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• pp.93-98
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• 1998

동아시아와 북미에 분포하는 조경수목을 형태적 특성 및 분자생물학적 특성에 따른 연구 결과를 토대로 분류한 결과 8종에서 밀접한 관련성을 갖고 있었다. 자주받침꽃, 능소화, 산딸나무, 보리밥나무, 가래나무, 튤립나무, 일본목련, 잣나무는 동아시아와 북미에서 각각 밀접한 유연성을 가진 종들이 있어 이들을 조경수목쌍으로 분류할 수 있었다. 그리고, 형태적 특성이 매우 흡사한 종으로는 중국단풍나무, 고로쇠, 들메나무, 야광나무, 소나무와 곰솔, 상수리나무, 갈참나무, 떡갈나무, 신갈나무, 굴참나무, 피나무, 참느릅나무 등에서 동아시아와 북미 조경수목쌍이 존재하는 것으로 판단되었다.

• Proceedings of the PSK Conference
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• 2002.10a
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• pp.363.1-363.1
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• 2002

Costunolide. a sesquiterpene lactone is isolated from Magnolia Sieboldi. It is known to possess antitumour and anti-inflammatory activities. This compound is synthesized from Ihe easily available decalin dione using the ring cleavage approach to construct the ten-membered ring system. The two keys points in this work are the chiral inductionon the allyl alcohol moiety using Sharpless epoxidation reaction and opening of the eopxide with an organocuprate reagent which leads to a $\alpha$-exomethylene lactone. (omitted)