• 제목/요약/키워드: Quantitative NMR Analysis

검색결과 98건 처리시간 0.023초

크라이신 7-O-크로토네이트의 물성 및 육모효과 (Properties and Hair-growth Effect of Chrysin 7-O-crotonate)

  • 신준수;김연희;정재훈;김양배;김박광
    • 약학회지
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    • 제43권3호
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    • pp.316-319
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    • 1999
  • Chrysin 7-Ο-crotonate was synthesized by condensing crotonic acid with chrysin in organic solvent, tetrahydrofuran (THF) using dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP). Its structure was indentified by NMR, MS, UV, IR etc. We also investigated the physico-chemical properties and set up the quantitative anytical method of this compound. The correlation coefficient of calibration curve measured at the isobestic point (340 nm) on this compound was approximately 0.9994 by absorption spetrophtometry. Detection limit was 1.6ng at S/N=3 by using a RP column by HPLC. The hair growth effect fo chrysin 7-Ο-crotonate on the hair of black mouse (C57BL/6), was carried out using paste method. When its ethanol solution was administered to this black mouse by route of skin, this compound promoted the growth of hair.

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Investigation of Germicide and Growth Enhancer Effects on Bean Sprout using NMR-based Metabolomics

  • Yoon, Dahye;Ma, Seohee;Choi, Hyeonsoo;Noh, Hyeonkyung;Ok, Youngjun;Kim, Suhkmann
    • 한국자기공명학회논문지
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    • 제20권4호
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    • pp.121-128
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    • 2016
  • Bean sprouts are often cultivated in the circumstances prevailing in the improper using of germicide and growth enhancer. The influence of ingestion those bean sprouts are unknown. The components of the bean sprouts are needed to evaluate for food safety. The extracts of the control, 0.5 g/L germicide, 1 g/L germicide, 12.5 mL/L growth enhancer and 25 mL/L growth enhancer were used to compare the components in the experiment. Nuclear Magnetic Resonance spectroscopy (NMR) was used to analyze the extracts. Statistical analysis of metabolomics showed significant changes between the control and head and the stem of the bean sprouts. Significant changes in metabolites were identified with the bean sprouts cultivated with germicide and growth enhancer by applying qualitative and quantitative analysis. Similar changes in the area of the bean sprouts were observed after treated to germicide and growth enhancer. Although treating germicide and growth enhancer showed no particular harmful metabolites changes to human, it made significant changes in the morphological and the metabolites of the bean sprouts. These changes indicate that the germicide and growth enhancer has substantially potential to influence the growth of the bean sprouts.

감귤류와 한국산 청피에 함유된 Methoxylated Flavonoids의 분석과 정량적 분포 (Quantitative Distribution and Analysis of Methoxylated Flavonoids in Citruses and Korean Chung-pi)

  • 백순옥;복진영;천현자;정승일;한완수;김일광
    • 분석과학
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    • 제14권4호
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    • pp.331-339
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    • 2001
  • 감귤류와 한국산 청피에 함유된 methoxylated flavonoids (sinenstin, nobiletin, tangeretin)를 HPLC, mass 그리고 NMR로 분리하고 분석하였다. Methoxylated flavonoids는 Chung-pi(I)과 Chung-pi(II)에 가장 풍부하게 함유되었다. 한국산 밀감에서 얻어진 Chung-pi(I), (II)의 methoxylated flavonoids 함유량은 밀감성숙도에 따라 증가하였으며, 10월 중순이후에는 서서히 감소하였다.

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참깨 종실의 항산화 성분 정량분석 연구 (Quantitative Analysis of Antioxidants in Sesame Seed)

  • 류수노;이정일;강삼식;최원열
    • 한국작물학회지
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    • 제37권4호
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    • pp.377-382
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    • 1992
  • 본 연구는 고항산화 양질 육종의 체계확립을 위해서 참깨에 있는 특수성분인 sesamin, sesamolin의 표준물질을 동정하고 그 분석기술을 개발하였는바 그 결과는 다음과 같다. 1. 한국산 참깨로부터 sesamin, sesamolin 성분을 분리하여 화학적 구조를 분광학적 방법(UV, $^1$H와 $^{13}$C-NMR, MS)으로 확인하여 sesamin, sesamolin의 표준물질을 동정하였다. 2. 참깨 lignan성분의 추출 및 분리에는 Unsaponifiable fration 보다 MeOH 냉온처리가 더 효과적이었다. 3. 검량선의 회귀직선의 방정식은 sesamin에서 y=53924.43+1277.93x(r=0.9993)이었고 sesamolin의 경우는 y=11034.95+1188.38x(r=0.9994)로 추정되었다. 4. 한국산 참깨의 lignan 성분함량은 단백깨의 경우 sesamin 0.42% sesamolin 0.3%로 나타났다.

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Phosgen-free Synthesis of Oligoureas Having Amino End-groups: Their Application to the Synthesis of Poly(urea-imide)

  • Chang, Ji-Young;Kim, Beom-Jin
    • Fibers and Polymers
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    • 제3권2호
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    • pp.55-59
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    • 2002
  • The thermal reaction of acetoacetanilide in the presence of aniline or phenol yielded carbanilide in quantitative yields. This reaction was applied to the synthesis of polyurea. Bisacetoacetamides were prepared from diamines and diketene in DMF. They were thermally polymerized in the presence of phenol or a diamine (6FDA) to yield polyureas of low molecular weights. The polymers were soluble in DMSO and NMP. $^1{H-NMR}$ analysis showed that they had amino group terminated structures. Poly(urea-imide) was synthesized by the reaction of an oligourea diamine with pyromellitic dianhydride in NMP. The concentration of terminal amino groups was determined by an acid-base titration. The thermal property of poly(urea-imide) was evaluated by thermogravimetric analysis (TGA). Initial decompisition took place at 332-$350^{\circ}C$.

떡윤노리나무로부터 분리된 Lyoniside의 함량분석과 항염증 효과 (Quantitative Analysis and Anti-inflammatory of Lyoniside from the Pourthiaea villosa var. brunnea)

  • 우경완;성태경;이혜미;장지훈;이기호;조현우;조정희;안병관
    • 생약학회지
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    • 제47권1호
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    • pp.12-17
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    • 2016
  • In this study, the purification of the MeOH extract from the stems and leaves of Pourthiaea villosa var. brunnea using column chromatography furnished a main compound, lyoniside. The structure was elucidated on the basis of $^1H$ and $^{13}C$ NMR spectroscopic data. Quantitative analysis of lyoniside was conducted by HPLC method and the highest content of lyoniside was found in 50% MeOH reflux extraction. To investigate the anti-inflammatory effect of the lyoniside, we measured nitric oxide and pro-inflammatory cytokines such as TNF-${\alpha}$, IL-$1{\beta}$, IL-6 levels in lipopolysaccharide-induced murine macrophage cell line RAW 264.7. As a results, lyoniside decreased the level of nitric oxide and IL-6 in concentration dose dependent manner in RAW 264.7 cells.

고비로부터 Cinnamtannin B-1의 분리 및 함량 분석 (Isolation and Quantitative Analysis of Cinnamtannin B-1 from Osmunda japonica Thunb)

  • 김민석;우경완;이기호;이현주;이선유;강병만;전병훈;조정희;조현우
    • 생약학회지
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    • 제47권3호
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    • pp.232-236
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    • 2016
  • In traditional Korean medicine, Osmunda japonica Thunb has been used as hemostasis and antipyretic treatment. The main compound "cinnamtannin B-1" was obtained by column chromatographic separation, and its structure was determined by spectroscopic methods, including $^1H$, $^{13}C$ NMR, and IT-TOF-ESI MS. Ash, moisture and extract content and acidinsoluble ash were monitored as identification test to establish the analytical methods. The optimum reflux extraction condition was 100% methanol extracted 30 min for 2 times. A quantitative analysis using HPLC method exhibited that the main compound at 24.7 min and its content was 0.96% in methanol extraction.

아가리쿠스 버섯에서 생리활성물질의 추출 및 정제 (Extraction and Purification of Bioactive Materials from Agaricus blazei Fruiting Bodies)

  • 최정우;류동열;김영기;홍억기;권명상;한진수
    • KSBB Journal
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    • 제15권3호
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    • pp.293-298
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    • 2000
  • ${\beta}$-Glucan a kind of polysaccharide which is particularly abundant in Agaricus blazei is known as the bioactive materials especially anticancer agents. The process development of the isolation and the purification process of water soluble ${\beta}$-glucans from A. blazei was achieved. and the process operation variables were optimized. Crude polysaccharides (CR.PS) were obtained from A. blazei by hot water extraction filtration solvent precipitation dialysis and freeze drying. Neutral and acidic fraction of polysaccharides were separated from crude polysaccharides by ion chromatography and then high molecular weight and low molecular weight fraction were separated from neutral fraction by gel chromatography. Quantitative and qualitative analysis of each compounds were performed with FT-IR NMR spectroscopy. Based on these analysis the optimal conditions of temperatures operating time organic solvent volume for precipitation and dialysis time were determined.

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Identification of Triterpenoids and Flavonoids from the Seeds of Tartary Buckwheat

  • Lee, Jeong Min;Lee, Ki Ho;Yoon, Young-Ho;Cho, Eun Ju;Lee, Sanghyun
    • Natural Product Sciences
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    • 제19권2호
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    • pp.137-144
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    • 2013
  • Phytochemical constituents were isolated from the seeds of tartary buckwheat (Fagopyrum tataricum) by open column chromatography. Their structures were elucidated as ${\beta}$-sitosterol (1), ${\beta}$-sitosterol-3-O-glucoside (2), oleanolic acid (3), kaempferol (4), quercetin (5), kaempferol-3-O-rutinoside (6), and quercetin-3-O-rutinoside (7) on the basis of spectroscopic analysis including $^1H$-, $^{13}C$-NMR, and MS. To our knowledge, oleanolic acid (3) has been isolated for the first time from the seeds of Fagopyrum species. The total contents of compounds 4 - 7 were 0.500 mg/g in Daesan maemil, 0.312 mg/g in Yangjul maemil, and 2.185 mg/g in tartary buckwheat.

Isolation and Quantitative Analysis of Chemical Constituents in Codonopsis lanceolata

  • Ju, Yeongdon;Jeon, Jeong Wook;Hyun, Kyung-Yae
    • 대한의생명과학회지
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    • 제27권3호
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    • pp.154-160
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    • 2021
  • Codonopsis lanceolata has numerous chemical constituents that includes polyphenols, saponins, tannins, triterpene, alkaloids, and steroids. The extract of C. lanceolata was partitioned with Haxane, CH2Cl2, EtOAc, n-BuOH and MeOH. The determination of structure for lancemaside G, lancemaside B, lancemaside A were based on physicochemical and HPLC chromatogram data, including NMR and HR-MS. In addition, tangshenoside I and lobetyolin were identified in the material separation process for the extract of C. lanceolata, and content analysis was performed using HPLC. The compounds were confirmed as lancemaside G, lancemaside B, lancemaside A, tangshenoside I, and lobetyolin.