• Archives of Pharmacal Research
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• 제28권2호
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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.

• 천문학회보
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• 제38권1호
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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.

• 천문학회보
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• 제37권1호
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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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• 제19권6호
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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.

• 대한화학회지
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• 제17권4호
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• pp.269-274
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• 1973

${\alpha}$-Cyano-${\beta}$-Piperonylacrylic Acid의 가분해 속도상수를 자외선분광기를 사용하여 구하였으며 아울러 넓은 pH범위에 잘 맞는 반응속도식도 얻었다. 이 식에 의하면 넓은 pH범위에 잘 맞는 반응속도식도 얻었다. 이 식에 의하면 넓은 pH범위, 특히 종전에 잘 규명된 바 없는 산성용매 속에서의 반응 및 hydroxide ion의 촉매역활 등도 정략적으로 잘 설명할 수 있음을 알았다. 즉 pH4.0이하에서의 가수분해반응은 ${\alpha}$-Cyano-${\beta}$-Piperonylacrylic Acid에 물분자가 첨가되므로써 시작되며 pH $5.0{\sim}7.5$ 에서는 ${\alpha}$-Cyano-${\beta}$-Piperonylacrylic Acid와 ${\alpha}$-Cyano-${\beta}$${\alpha}$-Cyano-${\beta}$-piperonylacrylate anion에 물분자만이 첨가되며 pH 12.0 이상에서는 hydroxide ion만이 ${\alpha}$-Cyano-${\beta}$-piperonylacrylate anion에 첨가됨을 알았다.

• 한국식품영양학회지
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• 제14권3호
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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

• 호남수학학술지
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• 제32권3호
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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.

• 한국미생물·생명공학회지
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• 제30권4호
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• pp.332-338
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• 2002

토양으로부터 세포외로 $\alpha$-galactosidase를 분비 생산하는 방선균 YB-4가 분리되었으며, 분리균의 배양ㆍ형태ㆍ생리적 특성을 조사한 결과 Streptomyces 속 균주로 확인되었다. 분리균의 배양상등액으로부터 부분정제된 $\alpha$-galactosidase를 조효소액으로 사용하였을 때 para-nitrophenyl-$\alpha$-D-galacto-pyranoside는 pH 6.0과 6$0^{\circ}C$의 반응조건에서 가장 잘 분해되었으며, 조효소액을 pH 4.0에서 pH 10.0범위에서 1시간 이상 방치한 후에도 약 90% 이상의 $\alpha$-galactosidase 활성을 유지하였다. 또한 분리균이 생산하는 $\alpha$-galactosidase는 melibiose, raffinose와 stachyose와 같은 저당류를 가수분해 할 수 있으며 분해산물로 galactose를 방출하는 것으로 보아 $\alpha$-1,6 결합을 분해한 것으로 확인되었다.

• 한국미생물·생명공학회지
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• 제20권6호
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• pp.647-654
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• 1992

장내 세균의 생리적 연구를 목적으로 한국인의 장내 상재균을 분리하여 효소 pattern을 관찰하였다. 분리된 Bifidobacterium sp. Int-57은 다른 장내 균종에 비하여 $\alpha$-glucosidase, $\beta$-glucosidase, $\alpha$-galactosidase, $\beta$-galactosidase, $\beta$-xylosidase, $\alpha$-arabinofuranosidase역가가 높았다. Bifidobacterium sp. Int-57의 각 효소 생산에 미치는 탄소원의 영향을 조사하였다. $\alpha$-glucosidase는 maltose, $\beta$-glucosidase는 cellobiose, $\alpha$-galactosidase는 raffinose, 는 lactose, $\beta$-xylosidase와 $\alpha$-arabinofuranosidase는 xyloserk 각각 최적의 탄소원이었다. 또한 각 효소들의 최적 조건과 pH 안정성을 조사 하였다. $\alpha$-glucosidase는 pH 6.0 $40^{\circ}C$에서 $\beta$-glucosidasessm pH 7.0 50에서, $\beta$-galactosidase는 pH 7.0 50에서, $\beta$-xylosidase는 pH 6.0 $40^{\circ}C$에서, $\alpha$-arabinofurnaosidase는 pH 5.0 $50^{\circ}C$에서 각각 최적이었다. $\alpha$-glucosidase는 pH 4.0~9.0 $\beta$-glucosidase는 pH 4.0~7.0 $\beta$-galactosidase는 pH 4.0~9.0, $\beta$-xylosidase는 pH 4.0~6.0, $\alpha$-arabinofuranosidase는 pH 7.0~9.0에서 각각 안정하였다.

• 대한수학회논문집
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• 제15권1호
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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/$\alpha$.