• Archives of Pharmacal Research
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• v.28 no.2
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• pp.172-176
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• 2005

Phytochemical investigation of the whole plant of Amberboa ramosa led to the isolation of six sesquiterpene lactones which could be identified as $8{\alpha}$-hydroxy-$11{\beta}$-methyl-$1{\alpha}H,\;5{\alpha}H,\;6{\beta}H,\;7{\alpha}H,\;11{\alpha}H-guai-10(14)$, 4(15)-dien-6, 12-olide(2), $3{\beta},\;8{\alpha}-dihydroxy-11{\alpha}-methyl-1{\alpha}H,\;5{\alpha}H,\;6{\beta}H,\;7{\alpha}H,\;11{\beta}H-guai-10(14)$, 4(15)-dien-6, 12-olide (2), $3{\beta},\;4{\alpha},\;8{\alpha}-trihydroxy-4{\beta}(hydroxymethyl)-1{\alpha}H,\;5{\alpha}H,\;6{\beta}H,\;7{\alpha}H-guai-10(14)$, 11(13)-dien-6, 12-olide (3), $3{\beta},\;4{\alpha},\;8{\alpha}-trihydroxy-4{\beta}-(chloromethyl)-1{\alpha}H,\;5{\alpha}H,\;6{\beta}H,\;7{\alpha}H-guai-10(14)$, 11(13)-dien-6, 12-olide(4), $3{\beta},\;4{\alpha},\;dihydroxy-4{\beta}-(hydroxymethyl)-1{\alpha}H,\;5{\alpha}H,\;6{\beta}H,\;7{\alpha}H-guai-10(14)$, 11(13)-dien-6, 12-olide(5), $3{\beta},\;4{\alpha}-dihydroxy-4{\beta}-(chloromethyl)-8{\alpha}-(4-hydroxymethacrylate)-1{\alpha}H,\;5{\alpha}H,\;6{\beta}H,\;7{\alpha}H-guai-10(14)$, 11(13)-dien-6, 12-olide (6) by spectroscopic methods. All of them showed inhibitory potential against butyrylcholinesterase.

• The Bulletin of The Korean Astronomical Society
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• v.38 no.1
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• pp.48.1-48.1
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• 2013

It is known that the diffuse $H{\alpha}$ emission outside of bright H II regions not only are very extended, but also can occur in distinct patches or filaments far from H II regions, and the line ratios of [S II] ${\lambda}6716/H{\alpha}$ and [N II] ${\lambda}6583/H{\alpha}$ observed far from bright H II regions are generally higher than those in the H II regions. These observations have been regarded as evidence against the dust-scattering origin of the diffuse $H{\alpha}$ emission (including other optical lines), and the effect of dust scattering has been neglected in studies on the diffuse $H{\alpha}$ emission. However, as opposed to the previous contention, the expected dust-scattered $H{\alpha}$ halos surrounding H II regions are, in fact, in good agreement with the observed $H{\alpha}$ morphology. We find that the observed line ratios of [S II]/$H{\alpha}$, [N II]/$H{\alpha}$, and He I ${\lambda}5876/H{\alpha}$ in the diffuse ISM accord well with the dust-scattered halos around H II regions, which are photoionized by late O- and/or early B-type stars. We also demonstrate that the $H{\alpha}$ absorption feature in the underlying continuum from the dust-scattered starlight ("diffuse galactic light") and unresolved stars is able to substantially increase the [S II]/$H{\alpha}$ and [N II]/$H{\alpha}$ line ratios in the diffuse ISM.

• The Bulletin of The Korean Astronomical Society
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• v.37 no.1
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• pp.74.1-74.1
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• 2012

It is known that the diffuse H${\alpha}$ halos around bright H II regions are more extended than the dust-scattered halos around point sources and the line ratios [S II] ${\lambda}$6716/H${\alpha}$ and [N II] ${\lambda}$6583/H${\alpha}$ observed outside of bright H II regions are generally higher than those in H II regions. These observational facts have been regarded as evidence against the dust-scattering origin of the diffuse H${\alpha}$ emission and the effect of dust-scattering has been neglected in studying the diffuse H${\alpha}$ emission. In this paper, we find, however, that dust-scattered halos of H II regions should be more extended than those of point sources and is in good agreement with the observed H${\alpha}$ profiles around H II regions. We also found that the observed line ratios [S II]/H${\alpha}$, [N II]/H${\alpha}$, and He I ${\lambda}$5876/H${\alpha}$ in the diffuse regions can be well reproduced with the dust-scattered halos around H II regions which are photoionized by late O- and/or early B-type stars in the interstellar medium with the abundances close to those of the warm neutral medium. Therefore, we conclude that the diffuse H${\alpha}$ emission may originate mostly from the dust-scattering.

• Archives of Pharmacal Research
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• v.19 no.6
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• pp.507-513
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• 1996

Three sesquiterpene lactone compounds, two novel(1.betha.,3.betha.-dihydroxy-6.betha.,11.betha.,4.alpha.,5.alpha.,7.alpha.H -eudesm-12, 6-olide-1-O-.betha.-D-glucopyranoside, 1.betha.,3.betha.-dihydroxy-6.betha.,11.betha.,4.alpha.,5.alpha.,7.alpha.H-eudes m-12,6-olide-1-O-.betha.-D-glucopyranoside) and 1.betha.,3.betha.-dihydroxy-6.betha.,11.betha.,4.alpha.,5.alpha., 7.alpha.H-eudesm-12,6-olide were isolated from the aqueous fraction of MeOH extract of the roots from Taraxacum hallaisanensis (Compositae) employing Amberlite XAD-2, ODS-gel, silica gel and Sephadex LH-20 column chromatographics. Another known compound, (-)-epicatechin, was isolated from the aqueous fraction of the MeOH extract. The total MeOH extract also contained phytosterol and a mixture of .betha.-amyrin acetate, .alpha.-amyrin acetate and lupeol acetate. Structures of isolated compounds were elucidated by spectroscopic parameters of IR, Mass, /sup 13/C-NMR, /sup 1/H-NMR, /sup 1/H-/sup 1/H COSY, /sup 13/C-/sup 1/H COSY and HMBC.

• Journal of the Korean Chemical Society
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• v.17 no.4
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• pp.269-274
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• 1973

The rate constants of the hydrolysis of ${\alpha}$-Cyano-${\beta}$-piperonylacrylic acid were determined by Ultraviolet spectrophotometry at various pH and a rate equation which can be applied over wide pH range was obtained. The reaction mechanism of hydrolysis of ${\alpha}$-Cyano-${\beta}$-piperonylic acid and especially the catalytic contribution of hydroxide ion which not studied carefully before in acidic media, can be fully explained by the rate equation obtained. The rate equation reveals that; below pH 4.0, the reaction is initiated by the addition of water molecule to ${\alpha}$-Cyano-${\beta}$-piperonyl acrylic acid. At pH $5.0{\sim}7.5$, ${\alpha}$-Cyano-${\beta}$-piperonylacrylic acid compete with ${\alpha}$-Cyano-${\beta}$-piperonyl acrylate ion in adding of water. At pH 8.0, water is the only nucleophile for ${\alpha}$-Cyano-${\beta}$-piperonylacrylate ion, however, above pH 12.0, hydroxide ion is an addendum and the accepter is ${\alpha}$-Cyano-${\beta}$-piperonylacrylate ion.

• The Korean Journal of Food And Nutrition
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• v.14 no.3
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• pp.263-268
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• 2001

NaIO$_4$-산화 전분당을 Bacillus licheniformis의 $\alpha$-아밀라아제의 반응시켜서 시프염기 형성으로 당단백질로 변형시켜서 안정성을 확인하였다. 10$0^{\circ}C$에서의 열안정성은 10분 뒤에, pH 9.7에서 변형한 효소 비변형 효소의 순으로 높았다. 그러나 변형 및 안정성에 $\alpha$-cyclodextrin($\alpha$-CD)을 사용한 결과 큰 차이는 나지 않았다. pH 8.0에서 $\alpha$-CD 존재하에 변형한 효소는 pH 8~11dml 알칼리쪽에서 가장 높은 안정성을 나타냈으나, pH 5~7사이에는 다른 효소보다 낮았다. pH 9.7에서 변형하지 않은 효소는 pH 5부터 pH 13까지 서서히 증가하였고 pH 9.7에서 $\alpha$-CD존재 하의 효소는 pH 5부터 7까지 증가하다가 그 후 pH13까지 서서히 감소하였다. $\alpha$-CD존재하의 비변형 효소는 pH 7과 10에서 피크를나타낸 다음 pH12이후에는 급격히 낮아졌다. 변형한 효소는 HPLC 의 유출시간이 빨라wu서 변형하지 않은 효소보다 분자량이 큰 것으로 나타났다. 분자량 크기는 비변형 효소

• Honam Mathematical Journal
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• v.32 no.3
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• pp.413-439
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• 2010

W. A. Dudek, M. Shabir and M. Irfan Ali discussed the properties of (${\alpha},{\beta}$)-fuzzy ideals of hemirings in [9]. In this paper, we discuss the generalization of their results on (${\alpha},{\beta}$)-fuzzy ideals of hemirings. As a generalization of the notions of $({\alpha},\;\in{\vee}q)$-fuzzy left (right) ideals, $({\alpha},\;\in{\vee}q)$-fuzzy h-ideals and $({\alpha},\;\in{\vee}q)$-fuzzy k-ideals, the concepts of $({\alpha},\;\in{\vee}q_m)$-fuzzy left (right) ideals, $({\alpha},\;\in{\vee}q_m)$-fuzzy h-ideals and $({\alpha},\;\in{\vee}q_m)$-fuzzy k-ideals are defined, and their characterizations are considered. Using a left (right) ideal (resp. h-ideal, k-ideal), we construct an $({\alpha},\;\in{\vee}q_m)$-fuzzy left (right) ideal (resp. $({\alpha},\;\in{\vee}q_m)$-fuzzy h-ideal, $({\alpha},\;\in{\vee}q_m)$-fuzzy k-ideal). The implication-based fuzzy h-ideals (k-ideals) of a hemiring are considered.

• Microbiology and Biotechnology Letters
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• v.30 no.4
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• pp.332-338
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• 2002

A strain YB-4 producing the extracellular $\alpha$-galactosidase was isolated from soil, and has been identified as Streptomyces sp. on the basis of its cultural, morphological and physiological properties. The partially purified $\alpha$-galactosidase was most active on paranitrophenyl-$\alpha$-D-galactopyranoside at pH 6.0 and 6$0^{\circ}C$. The enzyme retained 90% of its maximum activity between pH 4.0 and pH 10.0 after pre-incubation for 1 h. The enzyme was able to hydrolyze oligomeric substrates such as melibiose, raffinose and stachyose to liberate galactose residue, indicating that the $\alpha$-galactosidase of Steptomyces sp. YB-4 hydrolyzed $\alpha$-1,6 linkage.

• Microbiology and Biotechnology Letters
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• v.20 no.6
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• pp.647-654
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• 1992

In order to study the physiological properties of the intestinal bacteria, we isolated the intestinal bacteria of Koreans and tested the enzymatic patterns. Isolated Bifidobacterium sp. Int-57 had the higher activity of $\alpha$-glucosidase, $\beta$-glucosidase, $\alpha$-galactosidase, $\beta$-galactosidase. $\beta$-xylosidase and $\alpha$-arabinofuranosidase than other intestinal microorganisms. The effect of the carbon sources on the production of each enzymes of Bijidobacterium sp. Int-57 was investigated. The most suitable carbon source for the production of $\beta$-glucosidase was maltose, for a-glucosidase cellobiose, for $\alpha$-galactosidase raffinose, for $\beta$-galactosidase lactose, and for $\beta$-xylosidase and $\alpha$-arabinofuranosidase xylose, respectively. In addition, we investigated the optimal conditions and pH stability of each crude enzymes. The optimal condition of a-glucosidase was pH 6.0 and $40^{\circ}C$. that of Jj-glucosidase pH 7.0 and 50oe, that of $\beta$-galactosidase pH 7.0 and $50^{\circ}C$, that of $\beta$-xylosidase pH 6.0 and $40^{\circ}C$ , and that of $\alpha$-arabinofuranosidase pH 5.0 and $50^{\circ}C$. respectively. a-Glucosidase was stable at pH 4.0-9.0. Jj-glucosidase at pH 4.0-7.0. $\beta$-galactosidase at pH 4.0-9.0, $\beta$-xylosidase at pH 4.0-6.0, and /3-arabinofuranosidase at pH 7.0-9.0, respectively.

• Communications of the Korean Mathematical Society
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• v.15 no.1
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• pp.123-131
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• 2000

Let {X(t) : t $\geq$B 0} be a Symmetric $\alpha$ Stable and H-Self-similar process with stationary increments. We examine a.s. Holder unboundedness of S$\alpha$S H-sssi Chentsov processes and H-sssi Chentsov fields for order ${\gamma}$>H. Finally, we prove a.s. Holder continuity of S$\alpha$S H-sssi processes with ergodic seating transformations for the case of H>1/$\alpha$.