• Journal of Life Science
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• v.3 no.1
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• pp.2-8
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• 1993

천연화합물과 합성화합물은 모두 합쳐서 식물생장조절제라 부르고 이들 화합물은 경우에 따라 식물의 기간들의 생장율을 촉진하거나 억제한다. 호르몬이란 용어는 천연적으로 발생하는 색물생장 조절제에 국한되는 것이다. 실제의 응용에 있어서 합성된 생장조절제가 사용되는 것은 이 물질이 생체내에서 안정도가 더 크기 때문이다. 따라서, 합성물질은 식물 호르몬의 구조적인 유사성으로 흉내를 내거나 내생 호르몬들의 생합성, 전류, 및 대사를 조정해서 그 수준을 조절하게 된다. 그래서, 식물생장 조절물질들의 기능과 가능력을 이해하기 위해서 분자수준에서 식물호르몬들의 작용의 양상을 고찰한다.

• The Korean Journal of Pesticide Science
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• v.5 no.3
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• pp.1-11
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• 2001

New technologies will have a large impact on the discovery of new herbicide site of action. Genomics, combinatorial chemistry, and bioinformatics help take advantage of serendipity through tile sequencing of huge numbers of genes or the synthesis of large numbers of chemical compounds. There are approximately $10^{30}\;to\;10^{50}$ possible molecules in molecular space of which only a fraction have been synthesized. Combining this potential with having access to 50,000 plant genes in the future elevates tile probability of discovering flew herbicidal site of actions. If 0.1, 1.0 or 10% of total genes in a typical plant are valid for herbicide target, a plant with 50,000 genes would provide about 50, 500, and 5,000 targets, respectively. However, only 11 herbicide targets have been identified and commercialized. The successful design of novel herbicides depends on careful consideration of a number of factors including target enzyme selections and validations, inhibitor designs, and the metabolic fates. Biochemical information can be used to identify enzymes which produce lethal phenotypes. The identification of a lethal target site is an important step to this approach. An examination of the characteristics of known targets provides of crucial insight as to the definition of a lethal target. Recently, antisense RNA suppression of an enzyme translation has been used to determine the genes required for toxicity and offers a strategy for identifying lethal target sites. After the identification of a lethal target, detailed knowledge such as the enzyme kinetics and the protein structure may be used to design potent inhibitors. Various types of inhibitors may be designed for a given enzyme. Strategies for the selection of new enzyme targets giving the desired physiological response upon partial inhibition include identification of chemical leads, lethal mutants and the use of antisense technology. Enzyme inhibitors having agrochemical utility can be categorized into six major groups: ground-state analogues, group specific reagents, affinity labels, suicide substrates, reaction intermediate analogues, and extraneous site inhibitors. In this review, examples of each category, and their advantages and disadvantages, will be discussed. The target identification and construction of a potent inhibitor, in itself, may not lead to develop an effective herbicide. The desired in vivo activity, uptake and translocation, and metabolism of the inhibitor should be studied in detail to assess the full potential of the target. Strategies for delivery of the compound to the target enzyme and avoidance of premature detoxification may include a proherbicidal approach, especially when inhibitors are highly charged or when selective detoxification or activation can be exploited. Utilization of differences in detoxification or activation between weeds and crops may lead to enhance selectivity. Without a full appreciation of each of these facets of herbicide design, the chances for success with the target or enzyme-driven approach are reduced.

• Proceedings of the Korean Society of Applied Pharmacology
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• 1992.05a
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• pp.52-52
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• 1992

cisplatin 자체는 용혈작용이 고농도에서 얼었는데 반하여 호중구 자극상등액에서는 저농도에서 높은 용혈작용을 나타내 신장독성이 호중구 활성화에 기인할 것이라는 가능성을 시사하였다. In vitro에서 대부분의 활성산소 제거제는 세포독성 억제효과가 있었으며 in vivo 투여시에도 합성 항산화제인 BHA 등은 혈청 BUN, creatinine치의 현저한 감소를 나타내 좋은 신장독성억제 효과를 보여주었다.

• Korean Journal of Ichthyology
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• v.12 no.3
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• pp.173-179
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• 2000

Effects of Estradiol-$17\beta(E_2)$ and 2, 4-dichlorophenoxy acetic acid (2, 4-D) on vitellogenin(VTG) production were investigated in primary hepatocyte culture of olive flounder, Paralichthys olivaceus. Highest survival rate of hepatocyte were observed at $27^{\circ}C$, which markedly declined equal to 50% of those of $15^{\circ}C$. Vitellogenin production peaked at the concentration of $10^{-6}M\;E_2$. No effect was observed on VTG production at various concentrations of 2, 4-D. However, a low concentration of 2, 4-D (ie, $10^{-8}M$) only appeared increased VTG production. $E_2$ or $10^{-8}M$ 2, 4-D-primed VTG production was markedly inhibited by the addition of $10^{-6}M$ tamoxifen to the culture medium(P<0.01). Inhibition was not affected by combinational treatment with $10^{-6}M$ $E_2$ and $10^{-6}M$ 2, 4-D. These results from the current investigation suggest that 2, 4-D mimics $E_2$, but the mechanism of reaction in inducing the $E_2$ receptor are different in VTG production in oliver flounder hepatocytes.

• Journal of Korean Society of Steel Construction
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• v.28 no.5
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• pp.365-371
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• 2016

In the case of the superstructure which is consist of two I girders and slab, the section can behave as II section, so that the neutral axis with respect to out of plane direction flexure can be regarded as major axis. Therefore in-plane flexural mode might govern the free vibration mode. Meanwhile, horizontally curved girders always experience not only bending moments but also torsional moments although the primary load is usually supposed to be gravitational load. The interaction due to bending and torsional moments make the behavior complicated and torsional mode may govern the free vibration mode. In other words, structure can have different dynamic characteristic due to its initial curvature. In this research, using 3-dimensional sell elements, free-vibration analyses are carried out due to initial curvature. The analysis models are assumed to be composite and non-composite and finally natural frequency and eigen mode are discussed.

• Food Industry
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• s.1
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• pp.82-84
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• 1971

• Journal of Life Science
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• v.21 no.11
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• pp.1631-1635
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• 2011

The capability of synthesizing polyphenol glycosides was examined using recombinant amylosucrase from the hyperthermophilic bacterium Deinococcus geothermalis. Based on the action mode of amylosucrase, sucrose and twenty-one polyphenols were used as a donor and acceptors respectively. The transglycosylation reaction by amylosucrase produced one or two major polyphenol glycosides depending on the type of polyphenols used. The synthesized polyphenol glycosides were detected by thin-layer chromatography. The structures of the newly synthesized polyphenol glycosides were predicted based on the transglycosylation mechanism of the enzyme. According to the acceptability of the polyphenols, the structural characteristics of polyphenol as an efficient acceptor were evaluated. The results indicate that amylosucrase is an efficient catalyst for the enzymatic synthesis of polyphenol glycosides, which have high potentials in food, cosmetics, and pharmaceutical industries.

• Proceedings of the Korean Information Science Society Conference
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• 2006.10b
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• pp.88-91
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• 2006

웹 브라우징은 상호작용으로 이루어진다. 계면의 구조나 상호작용은 잘 구조화 되어야 브라우징하기에 유리하고, 한편으로는 계면을 합성하기에 유리하다. 본 논문에서는 브라우징에 있어서 상호작용을 4가지 원시구조인 순차구조, 분기구조, 복귀구조, 반복구조 등으로 분류하였고, 이러한 4가지 구조를 지원하는 다양한 2차원 계면을 5가지 유형으로 분류하여 정의하였다. 순차형, 분기형, 복귀형, 반복형, 진화형이 5가지 계면 유형으로 19가지 계면구조를 정의하였다. 사용자의 인식흐름은 하나로 가정하였다.

• YAKHAK HOEJI
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• v.21 no.2
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• pp.55-61
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• 1977

호르몬과 효소와의 관계를 포함하는 사항은 다음과 같이 고려할 수 있다. 즉, 1. 효소생성에 미치는 호르몬의 작용, 2. 효소활성에 미치는 호르몬의 작용, 3. 효소활성에 관여하는 제인자(조효소, activator, inhibitor)에 대한 호르몬의 작용, 4. 효소에 의한 호르몬의 합성, 5. 효소에 의한 호르몬의 분해등이다. 최근 50년간의 이 분야의 발전상은 실로 괄목할 만하며 또 그에 관한 보문도 매거할 수 없을 정도이다. 본고에 주어진 본제에 대하여는 최근에 거론되어 있는 호르몬의 표적세포의 receptor에 대하여, 호르몬의 제2의 messenger로서의 cyclic AMP및 그의 유사체인 DBC-AMP 그리고 호르몬에 의한 효소유도에 대하여 소개하고자 한다.

• Proceedings of the Korea Institute of Fire Science and Engineering Conference
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• 2013.11a
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• pp.115-116
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• 2013

본 연구에서는 유기인 유도체 중 생리활성이 커서 독성이 있는 화합물의 구조를 분석하였다. 5-[(b-monoaza-15-crown-5)ethyloxy]-2iodosbenzoic acid의 IBA 촉매를 합성하여 그 반응성을 p-nitrophenyldiphenylphosphate (PNPDPP)와 Isopropyl methylphosphonofluoridate (Sarin GB), Pinacolyl methylphosphonofluoridate (Soman, GD)를 기질로 하여 연구하였다. PNPDPP 가수분해 반응에서는 긴 알킬작용기로 친유성을 증가시킨 촉매가 더 상전이 촉매로 작용함이 확인되었다.(t1/2 = 5 sec, pH = 8.07)