KR19990051318A - Novel densifloric acid and preparation method thereof and composition having cell adhesion inhibitory activity including the same - Google Patents
Novel densifloric acid and preparation method thereof and composition having cell adhesion inhibitory activity including the same Download PDFInfo
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Abstract
본 발명은 솔잎으로부터 분리 정제된 세포접착 저해활성을 나타내는 세가지 신규의 화합물, 이의 제조방법 및 이를 포함하는 세포접착저해용 조성물에 관한 것으로, 본 발명에 따라 솔잎으로부터 분리 정제된 덴시플로릭산 Ⅰ, 덴시플로릭산 Ⅱ 및 덴시프로릭산 Ⅲ는 세포접착저해 작용이 우수하므로 암전이의 예방 및 치료제로서 이용될 수 있다.The present invention relates to three novel compounds exhibiting purified cell adhesion inhibitory activity isolated from pine needles, a method for preparing the same, and a composition for inhibiting cell adhesion, including the same. Floric acid II and denciprolic acid III can be used as a prophylactic and therapeutic agent for cancer metastasis because of its excellent cell adhesion inhibitory action.
Description
본 발명은 솔잎으로부터 분리한 강력한 세포 접착저해활성을 나타내며 신규의 구조를 가지는 디테르페노드화합물인 덴시플로릭산(densifloric acid)에 관한 것이다.The present invention relates to a densifloric acid, which is a diterpenoid compound exhibiting strong cell adhesion inhibitory activity isolated from pine needles and having a novel structure.
세포접착현상은 세포정보전달, 암, 면역, 신경, 발생, 세포증식, 세포분화, 세포인식 등의 여러 가지 생명현상에 관여하고 있고 염증, 암전이등과 같은 질병과 관련이 있는 것으로 밝혀져 있다. 암환자의 주된 사망요인은 초기종양에 의한 것이 아니라 암세포의 다른 조직으로의 전이에 의한 것이다. 따라서 암세포의 전이 기작에 관한 많은 연구가 진행되어 접착, 침윤, 혈관형성등의 삼단계설이 확립되어 있으며 이중 어느 하나를 차단하는 것에 의하여 암세포의 전이를 억제하는 것이 가능하다. 암세포의 모세혈관 벽의 세포외기질과의 접착은 세포외기질 구성성분인 파이브로넥틴, 라미닌, 바이트로넥틴등에 존재하는 접착에 관여하는 펩타이드와 암세포의 표면에서 발현되는 인테그린과 같은 접착분자의 상호작용에 의해 이루어지며 이러한 기능을 조절제어하여 암전이를 억제하려는 시도가 성공적으로 이루어 졌다. 즉 세포외 매트릭스인 파이브로넥틴, 라미닌, 콜라겐등에서 유래한 펩타이드는 세포독성을 나타내지 않으면서 암세포의 세포외매트릭스상의 이동이나 접착을 저해하여 암전이억제효과를 나타내는 것으로 밝혀졌다(Humpheries등 1986, Science, 233, 467 ; Iwamoto등, 1987, Science, 138, 1132). 그러나 이와같은 물질들은 혈관내에서 단백질분해효소의 작용에 의하여 분해되는 결점이 있어 새로운 구조의 화합물의 개발이 요구되어 왔다.Cell adhesion is involved in various life phenomena such as cell information transmission, cancer, immunity, nerves, development, cell proliferation, cell differentiation, cell recognition, and has been found to be related to diseases such as inflammation and cancer metastasis. The main cause of death in cancer patients is not due to early tumors, but to metastasis of cancer cells to other tissues. Therefore, many studies on the metastasis mechanism of cancer cells have been progressed, and three-stage theories such as adhesion, invasion, and angiogenesis have been established. The adhesion of cancer cells to the extracellular matrix of the capillary wall is the interaction of peptides involved in adhesion in the extracellular matrix components, such as fibronectin, laminin, and bytetronectin, and adhesion molecules such as integrins expressed on the surface of cancer cells. Attempts have been made to suppress cancer metastasis by regulating these functions. In other words, peptides derived from the extracellular matrix, fibronectin, laminin, collagen, and the like, have been shown to exhibit cancer metastasis inhibitory effects by inhibiting migration or adhesion of extracellular matrix of cancer cells without showing cytotoxicity (Humpheries et al. 1986, Science). , 233, 467; Iwamoto et al., 1987, Science, 138, 1132). However, these materials have the disadvantage of being degraded by the action of proteolytic enzymes in the blood vessels has been required to develop a compound of a new structure.
따라서, 본 발명자들은 세포의 접착을 억제하는 활성이 솔잎의 메타놀추출물에 존재하는 것을 발견하고 이들 활성성분을 추적한 결과, 하기 구조를 가지는 세가지 신규 화합물인 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ을 분리하여 본 발명을 완성하였다.Therefore, the present inventors found that the activity of inhibiting cell adhesion is present in the methanol extract of pine needles, and following these active ingredients, three novel compounds having the following structure, dendritic acid I, II and III, were isolated The present invention has been completed.
본 발명의 목적은 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ을 단독 또는 이들 화합물을 포함하는 솔잎 및 솔잎분획의 약학 및 식품학적으로 허용 가능한 담체 및 용액를 포함하는 조성물을 제공하는데 있다.SUMMARY OF THE INVENTION An object of the present invention is to provide a composition comprising pharmaceutic and pharmaceutically acceptable carriers and solutions of pine needles and pine needle fractions comprising densifloric acid I, II and III alone or including these compounds.
상기 발명의 목적을 달성하기 위하여 소나무(Pinus densiflora Siebold et Zuccarini)를 선택하였다. 소나무는 적송, 흑송이라 불리우며 상록교목으로 높이 30m, 지름 1.5m 안팎이며 가지가 퍼지고 윗부분의 수피가 적갈색 또는 흑갈색이며 동아는 적갈색이고 침엽은 2개씩 달리며 비틀리고 길이 6-12cm, 너비 0.5mm를 나타내는 식물로 그 잎에는 혈관 강화 물질을 함유하고 있다.Pine tree (Pinus densiflora Siebold et Zuccarini) was selected to achieve the object of the present invention. The pine is called red pine and black pine. It is an evergreen arbor, 30m high and 1.5m in diameter, with branches spreading. The bark of the upper part is reddish brown or blackish brown. Donga is reddish brown, and two conifers are twisted, 6-12cm long, and 0.5mm wide. It is a plant whose leaves contain vascular enhancing substances.
또, 솔잎으로부터 세포접착저해활성을 갖는 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ을 용매추출공정이나 실리카, 흡착수지, 역상실리카 등에 의해 정제한다.Also, dendritic acids I, II and III having cell adhesion inhibitory activity from pine needles are purified by a solvent extraction step, silica, adsorptive resin, reversed phase silica or the like.
또, 본 발명의 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ을 약제학적으로 혹은 식품제조에서 허용 가능한 담체와 부형제를 이용하고 공지의 방법으로 제제화하여 단위용량 형태 또는 다용량 용기에 내입 시킨다. 제제형태는 오일 또는 수성매질 중의 용액, 현탁액 또는 유화액형태이거나, 엑기스제, 분말제,과립제, 정제, 캅셀제 어떤 형태로든 관계없다. 또, 공지의 분산제, 현탁제 또는 안정화제를 함유 시킬 수 있다.In addition, the dendrifloric acids I, II and III of the present invention are formulated by known methods using carriers and excipients that are acceptable in pharmaceutical or food production and are incorporated into unit dosage forms or multi-dose containers. The formulation may be in the form of solutions, suspensions or emulsions in oils or aqueous media, or in any form of extracts, powders, granules, tablets, capsules. Moreover, a well-known dispersing agent, suspension agent, or stabilizer can be contained.
본 발명의 덴시플로릭산Ⅰ, Ⅱ 및 Ⅲ을 솔잎으로부터 분리 또는 조성물을 제조하는 공정 및 접착저해 생물활성등 본 발명의 구체적인 구성과 작용을 실시예를 들어 설명한다. 다만, 본 발명은 이들 실시예에만 제한되지 아니한다.The specific structure and action of the present invention, such as the process of separating the densifloric acid I, II and III of the present invention from pine needles or preparing a composition and bioadhesive inhibitory activity, will be described with examples. However, the present invention is not limited only to these examples.
도 1은 중수소클로로포름(CDCl3)용액에서 덴시프로릭산(Ⅰ)의 프로톤 핵자기 공명 스펙트럼을 나타낸 것이다.1 shows proton nuclear magnetic resonance spectra of dendritic acid (I) in deuterium chloroform (CDCl 3 ) solution.
도 2는 중수소메타놀(CD3OD)용액에서 덴시프로릭산(Ⅱ)의 프로톤 핵자기 공명 스펙트럼을 나타낸 것이다.Figure 2 shows the proton nuclear magnetic resonance spectra of dendritic acid (II) in deuterium methanol (CD 3 OD) solution.
도 3은 중수소메타놀(CD3OD)용액에서 덴시프로릭산(Ⅲ)의 프로톤 핵자기 공명 스펙트럼을 나타낸 것이다.Figure 3 shows the proton nuclear magnetic resonance spectra of dendritic acid (III) in deuterium methanol (CD 3 OD) solution.
도 4는 중수소클로로포름(CDCl3)용액에서 덴시프로릭산(Ⅰ)의 탄소 핵자기 공명 스펙트럼을 나타낸 것이다.Figure 4 shows the carbon nuclear magnetic resonance spectra of dendritic acid (I) in deuterium chloroform (CDCl 3 ) solution.
도 5는 중수소메타놀(CD3OD)용액에서 덴시프로릭산(Ⅱ)의 탄소 핵자기 공명 스펙트럼을 나타낸 것이다.Figure 5 shows the carbon nuclear magnetic resonance spectra of dendritic acid (II) in deuterium methanol (CD 3 OD) solution.
도 6은 중수소메타놀(CD3OD)용액에서 덴시프로릭산(Ⅲ)의 탄소 핵자기 공명 스펙트럼을 나타낸 것이다.Figure 6 shows the carbon nuclear magnetic resonance spectra of dendritic acid (III) in deuterium methanol (CD 3 OD) solution.
실시예 1: 솔잎으로부터 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ의 분리 및 정제Example 1 Separation and Purification of Dencifloric Acids I, II, and III from Pine Needles
소나무로부터 채취한 신선한 솔잎을 0.5- 1센티미터로 절단한 후 알코올용액에 침지하여 얻은 추출액을 감압건조하여 동량의 물과 에틸아세테이트를 첨가하여 잘 교반한후 방치한후 형성된 에틸아세테이트층을 농축하고 50% 아세토니이트릴에 녹여 50% 아세토나이트릴로 충진된 역상의 카이셀겔(kieselgel)인 유로프렙(europrep) 60-60 C18 칼럼에 흡착시켜 50%아세토나이트릴, 80%아세토나이트릴, 100%아세토나이트릴을 이용하여 순차적으로 탈착시킨후 그 활성을 측정하여 활성을 갖는 분획을 YMC-ODS-A의 HPLC칼럼에 75%아세토나이트릴로 용출하여 활성있는 분획으로 다섯 피이크를 얻었다. 이중에서 가장 먼저 나온 피이크를 덴시플로릭산 Ⅲ, 두 번째 피이크를 덴시플로릭산 Ⅱ, 네 번째 피이크를 덴시프로릭산 Ⅰ이라 명명하였다. 세 번째 피이크와 다섯 번째 피이크는 각각 기존물질인 데하이드로아베이틱산(dehydroabeitic acid)와 산다라코피마린산(Sandaracopimaric acid)으로 밝혀졌다. 상기 세가지 물질은 하기 실시예2의 화학물질의 구조해석을 통하여 신규의 물질임을 확인할 수 있었다.The fresh pine needles collected from pines are cut to 0.5-1 cm, and the extract obtained by dipping in alcohol solution is dried under reduced pressure, and the same amount of water and ethyl acetate are added. After stirring well, the resulting ethyl acetate layer is concentrated. 50% acetonitrile, 80% acetonitrile, 100% acetonitrile by adsorption on europrep 60-60 C18 column, reverse phase kieselgel filled with 50% acetonitrile, dissolved in% acetonitrile Desorption was carried out sequentially using a reel, and the activity was measured. The active fraction was eluted with 75% acetonitrile in an HPLC column of YMC-ODS-A to obtain five peaks as an active fraction. The first peak was named dencifloric acid III, the second peak was dencifloric acid II, and the fourth peak was denciproric acid I. The third and fifth peaks were identified as dehydroabeitic acid and Sandaracopimaric acid, respectively. The three materials were confirmed to be novel through the structural analysis of the chemicals of Example 2 below.
실시예 2: 덴시플로릭산Ⅰ, Ⅱ 및 Ⅲ의 구조해석Example 2 Structural Analysis of Dencifloric Acid I, II, and III
신규 화합물 덴시플로릭산Ⅰ, Ⅱ 및 Ⅲ은 흰색분말로 메탄올, 에틸아세테이트, 클로르포름에 잘 녹았으나 물에는 녹지 않았다. 질량분석결과, 분자량은 각각 302, 318, 318로 나타났고 구조식은 프로톤갯수, 카본갯수 등을 바탕으로 하여 각각C20H30O2, C20H30O3, C20H30O3으로 나타났다. 메탄올에서 자외선 최대 흡수파장은 각각 231과 208, 216, 213이었다. 탄소와 양성자핵자기공명 스펙트럼 분석결과는 하기 표1에 나타내었고 기타, 양성자-양성자 코지(1H-1H COSY), HMBC, DEPT, 양성자-탄소 코지(1H-13C COSY), ROESY 등의 기기분석기술에 의하여 상기의 덴시플로릭산의 구조를 결정하였다.The new compounds dencifloric acid I, II and III are white powders, soluble in methanol, ethyl acetate, and chloroform, but not in water. As a result of mass spectrometry, the molecular weights were 302, 318 and 318, respectively, and the structural formulas were C 20 H 30 O 2 , C 20 H 30 O 3 and C 20 H 30 O 3 based on the number of protons and carbons, respectively. . The maximum UV absorption wavelengths in methanol were 231, 208, 216 and 213, respectively. Carbon and proton nuclear magnetic resonance spectral analysis results were shown in Table 1, other proton-proton koji (1 H- 1 H COSY), HMBC, DEPT, proton-carbon koji (1 H- 13 C COSY), ROESY , etc. The structure of the densifloric acid was determined by the instrumental analysis technique.
실시예3: 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ의 생물활성Example 3 Bioactivity of Dencifloric Acids I, II and III
암세포접착저해활성은 라미닌으로 코팅시킨 96웰의 마이크로플래이트를 1%소혈장알부민으로 세척하고 0.1%의 소혈장알부민을 함유하는 엠이엠(MEM)배지 50마이크로리터를 첨가한후 시료와 105개의 생쥐흑색종세포 B16-F1세포현탁액을 첨가하고 5% CO2존재하에서 37oC에서 한시간 동안 반응시켜서 킴텍스 타월에 뒤집어 엎어 부착하지 않은 세포를 버리고 100마이크로리터의 따뜻한 인산완충식염수 와 0.5%소혈장알부민으로 세척하고 나서 다시 100마이크로리터의 인산완충생리식염수로 다시 세척하고 부착세포는 2.5% 글루타르알데하이드 40마이크로리터로 30분동안 고정화시키고 수도수로서 세척하고 건조시킨다. 건조된 부착세포를 20%메타놀용액에 0.4%되게 크리스탈비이올렛용액 100미이크로리터로 20분 동안 염색하고 다시 수도수로서 세척하고 건조시킨다. 건조된 세포를 30%에탄올로 만든 1mM염산용액을 첨가하여 마이크로플래이트리더(microplate reader)를 사용하여 570nm에서 흡광도를 측정하였다. 이때 세포접착저해율은 하기 식과 같이 계산하였으며, IC50값은 세포접착의 저해율이 50%에 달하는 저해제의 농도로 결정하였다.After cancer cell adhesion inhibitory activity washing the micro-plate with 96 wells were coated with laminin with 1% bovine serum albumin and added to M EM (MEM) culture medium of 50 microliters containing bovine serum albumin 0.1% of the sample with 10 5 Mouse melanoma cell B16-F1 cell suspension was added and reacted for 1 hour at 37 o C in the presence of 5% CO 2 to invert the Kimtex towel to dispose of unattached cells and 100 microliter warm phosphate buffered saline and 0.5% After washing with plasma albumin, it is washed again with 100 microliters of phosphate buffered saline, and adherent cells are fixed with 40 microliters of 2.5% glutaraldehyde for 30 minutes, washed with tap water, and dried. Dried adherent cells are stained for 20 minutes with 100 microliters of crystal violet solution in 0.4% in 20% ethanol solution, washed again with tap water and dried. The absorbed cells were measured at 570 nm using a microplate reader by adding 1 mM hydrochloric acid solution made of 30% ethanol to the dried cells. At this time, the cell adhesion inhibition rate was calculated as shown in the following formula, IC 50 value was determined by the concentration of inhibitors that the inhibition rate of cell adhesion reaches 50%.
저해율(%) = (B-A)/B X 100% Inhibition = (B-A) / B X 100
여기에서 , A는 저해물질을 넣은 시료의 흡광도이고 B는 저해물질을 넣지 않은 대조구의 흡광도를 나타낸다.Here, A is the absorbance of the sample containing the inhibitor and B is the absorbance of the control without the inhibitor.
분리된 덴시플로릭산Ⅰ, Ⅱ 및 Ⅲ의 세포접착을 50% 저해하는 농도를 측정한 결과, 각각 4.2㎍/mL, 11.7㎍/mL, 및 14.7㎍/mL인 것으로 나타났다.As a result of measuring the concentration of 50% inhibition of cell adhesion of isolated dendritic acid I, II and III, it was found to be 4.2 µg / mL, 11.7 µg / mL and 14.7 µg / mL, respectively.
이상 실시예에서 상세히설명한 바와같이, 솔잎으로부터 분리 정제된 세가지의 신규 화합물 덴시플로릭산 Ⅰ, Ⅱ 및 Ⅲ은 암세포가 세포외매트릭스의 일종인 라미닌에 결합하는 것을 저해하는 작용이 있으므로 암전이의 예방 및 치료제로 이용될 수 있는 효과가 있고 기타 세포접착에 의해 야기되는 염증반응의 치료 및 예방제로 사용될 수 있으므로 생물의약산업상 매우 유용한 발명인 것이다.As described in detail in the above examples, the three novel compounds, densifloric acid I, II and III, separated and purified from pine needles, have the effect of inhibiting the binding of cancer cells to laminin, which is a type of extracellular matrix. It is a very useful invention in the biopharmaceutical industry because it can be used as a therapeutic agent and can be used as a treatment and prevention agent for inflammatory reactions caused by other cell adhesion.
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