메뉴 건너뛰기




Volumn 65, Issue 1, 2011, Pages 180-185

Four new glucosides from the aerial parts of Mediasia macrophylla

Author keywords

Glucosides; Mediasia macrophylla; Umbelliferae; Uzbekistan

Indexed keywords

1 (4 HYDROXYPHENYL)ETHANE 1',2' DIOL 2' O BETA GLUCOPYRANOSIDE; 1 O ANGELOYL BETA GLUCOPYRANOSE; 2 METHOXY 3 HYDROXY 5 PROPENYLPHENOL 1 O BETA GLUCOPYRANOSIDE; 3 (4' METHOXYPHENYL)PROPANOL 1 O BETA GLUCOPYRANOSIDE; GLUCOSIDE; UNCLASSIFIED DRUG;

EID: 78651391675     PISSN: 13403443     EISSN: 18610293     Source Type: Journal    
DOI: 10.1007/s11418-010-0444-3     Document Type: Article
Times cited : (9)

References (45)
  • 4
    • 0034097385 scopus 로고    scopus 로고
    • Sesquiterpene phenylpropanoid and sesquiterpene chromone derivatives from Ferula pallida
    • DOI 10.1021/np9904298
    • BN Su Y Takaishi G Honda M Itoh Y Takeda OK Kodzhimatov O Ashurmetov 2000 Sesquiterpene phenylpropanoid and sesquiterpene chromone derivatives from Ferula pallida J Nat Prod 63 520 522 1:CAS:528:DC%2BD3cXhs1WrsL4%3D 10785430 10.1021/np9904298 (Pubitemid 30257167)
    • (2000) Journal of Natural Products , vol.63 , Issue.4 , pp. 520-522
    • Su, B.-N.1    Takaishi, Y.2    Honda, G.3    Itoh, M.4    Takeda, Y.5    Kodzhimatov, O.K.6    Ashurmetov, O.7
  • 7
    • 0037085614 scopus 로고    scopus 로고
    • Coumarins and γ-pyrone derivatives from Prangos pabularia: Antibacterial activity and inhibition of cytokine release
    • DOI 10.1016/S0031-9422(02)00023-7, PII S0031942202000237
    • Y Tada Y Shikishima Y Takaishi H Shibata T Higuti G Honda M Ito Y Takeda OK Kodzhimatov O Ashurmetov Y Ohmoto 2002 Coumarins and γ-pyrone derivatives from Prangos pabularia: antibacterial activity and inhibition of cytokine release Phytochemistry 59 649 654 1:CAS:528:DC%2BD38XhsFaguro%3D 11867097 10.1016/S0031-9422(02)00023-7 (Pubitemid 34229379)
    • (2002) Phytochemistry , vol.59 , Issue.6 , pp. 649-654
    • Tada, Y.1    Shikishima, Y.2    Takaishi, Y.3    Shibata, H.4    Higuti, T.5    Honda, G.6    Ito, M.7    Takeda, Y.8    Kodzhimatov, O.K.9    Ashurmetov, O.10    Ohmoto, Y.11
  • 8
    • 0035900473 scopus 로고    scopus 로고
    • Sesquiterpenoids from the fruits of Ferula kuhistanica and antibacterial activity of the constituents of F. kuhistanica
    • DOI 10.1016/S0031-9422(01)00307-7, PII S0031942201003077
    • K Tamemoto Y Takaishi B Chen K Kawazoe H Shibata T Higuti G Honda M Ito Y Takeda OK Kodzhimatov O Ashurmetov 2001 Sesquiterpenoids from the fruits of Ferula kuhistanica and antibacterial activity of the constituents of F. kuhistanica Phytochemistry 58 763 767 1:CAS:528:DC%2BD3MXnslWns70%3D 11672742 10.1016/S0031-9422(01)00307-7 (Pubitemid 33055390)
    • (2001) Phytochemistry , vol.58 , Issue.5 , pp. 763-767
    • Tamemoto, K.1    Takaishi, Y.2    Chen, B.3    Kawazoe, K.4    Shibata, H.5    Higuti, T.6    Honda, G.7    Ito, M.8    Takeda, Y.9    Kodzhimatov, O.K.10    Ashurmetov, O.11
  • 10
    • 0034620736 scopus 로고    scopus 로고
    • Coumarins and bicoumarin from Ferula sumbul: Anti-HIV activity and inhibition of cytokine release
    • DOI 10.1016/S0031-9422(99)00554-3, PII S0031942299005543
    • P Zhou Y Takaishi H Duan B Chen G Honda M Itoh Y Takeda OK Kodzhimatov KH Lee 2000 Coumarins and bicoumarin from Ferula sumbul: anti-HIV activity and inhibition of cytokine release Phytochemistry 53 689 697 1:CAS:528: DC%2BD3cXitVeiurg%3D 10746882 10.1016/S0031-9422(99)00554-3 (Pubitemid 30148788)
    • (2000) Phytochemistry , vol.53 , Issue.6 , pp. 689-697
    • Zhou, P.1    Takaishi, Y.2    Duan, H.3    Chen, B.4    Honda, G.5    Itoh, M.6    Takeda, Y.7    Kodzhimatov, O.K.8    Lee, K.-H.9
  • 11
    • 0035818769 scopus 로고    scopus 로고
    • A bis-sesquiterpene and sesquiterpenolides from Inula macrophylla
    • DOI 10.1016/S0031-9422(01)00334-X, PII S003194220100334X
    • B Fu BN Su Y Takaishi G Honda M Ito Y Takeda OK Kodzhimatov O Ashurmetov 2001 A bis-sesquiterpene and sesquiterpenolides from Inula macrophylla Phytochemistry 58 1121 1128 1:CAS:528:DC%2BD3MXos1Wrt74%3D 11730877 10.1016/S0031-9422(01)00334-X (Pubitemid 33130975)
    • (2001) Phytochemistry , vol.58 , Issue.7 , pp. 1121-1128
    • Fu, B.1    Su, B.-N.2    Takaishi, Y.3    Honda, G.4    Ito, M.5    Takeda, Y.6    Kodzhimatov, O.K.7    Ashurmetov, O.8
  • 12
    • 0034716538 scopus 로고    scopus 로고
    • Macrophyllidimers A and B, two novel sesquiterpene dimers from the bark of Inula macrophylla
    • DOI 10.1016/S0040-4039(99)02321-7, PII S0040403999023217
    • BN Su Y Takaishi M Tori S Takaoka G Honda M Itoh Y Takeda OK Kodzhimatov O Ashurmetov 2000 Macrophyllidimers A and B, two novel sesquiterpene dimers from the bark of Inula macrophylla Tetrahedron Lett 41 1475 1479 1:CAS:528:DC%2BD3cXhslSms7s%3D 10.1016/S0040-4039(99)02321-7 (Pubitemid 30126540)
    • (2000) Tetrahedron Letters , vol.41 , Issue.9 , pp. 1475-1479
    • Su, B.-N.1    Takaishi, Y.2    Tori, M.3    Takaoka, S.4    Honda, G.5    Itoh, M.6    Takeda, Y.7    Kodzhimatov, O.K.8    Ashurmetov, O.9
  • 13
    • 0034707972 scopus 로고    scopus 로고
    • Macrophyllols A and B, two unusual novel sesquiterpene and monoterpene dimers from the bark of Inula macrophylla
    • 1:CAS:528:DC%2BD3cXms1WksQ%3D%3D 10814359 10.1021/ol990401n
    • BN Su Y Takaishi M Tori S Takaoka G Honda M Itoh Y Takeda OK Kodzhimatov O Ashurmetov 2000 Macrophyllols A and B, two unusual novel sesquiterpene and monoterpene dimers from the bark of Inula macrophylla Org Lett 2 493 496 1:CAS:528:DC%2BD3cXms1WksQ%3D%3D 10814359 10.1021/ol990401n
    • (2000) Org Lett , vol.2 , pp. 493-496
    • Su, B.N.1    Takaishi, Y.2    Tori, M.3    Takaoka, S.4    Honda, G.5    Itoh, M.6    Takeda, Y.7    Kodzhimatov, O.K.8    Ashurmetov, O.9
  • 19
    • 43049161277 scopus 로고    scopus 로고
    • Monoterpene glycosides from Paeonia hybrida
    • 1:CAS:528:DC%2BD1cXlslOrs70%3D 18400238 10.1016/j.phytochem.2008.02.016
    • M Okasaka Y Kashiwada OK Kodzhimatov O Ashurmetov Y Takaishi 2008 Monoterpene glycosides from Paeonia hybrida Phytochemistry 69 1767 1772 1:CAS:528:DC%2BD1cXlslOrs70%3D 18400238 10.1016/j.phytochem.2008.02.016
    • (2008) Phytochemistry , vol.69 , pp. 1767-1772
    • Okasaka, M.1    Kashiwada, Y.2    Kodzhimatov, O.K.3    Ashurmetov, O.4    Takaishi, Y.5
  • 20
    • 0036925954 scopus 로고    scopus 로고
    • Lipids from Mediasia macrophylla leaves
    • 1:CAS:528:DC%2BD38XpsFCis7Y%3D 10.1023/A:1021657520719
    • TV Chernenko AI Glushenkova AM Nigmatullaev 2002 Lipids from Mediasia macrophylla leaves Chem Nat Compd 38 307 309 1:CAS:528:DC%2BD38XpsFCis7Y%3D 10.1023/A:1021657520719
    • (2002) Chem Nat Compd , vol.38 , pp. 307-309
    • Chernenko, T.V.1    Glushenkova, A.I.2    Nigmatullaev, A.M.3
  • 21
    • 77949820632 scopus 로고    scopus 로고
    • 10-polyacetylenic glucosides from Mediasia macrophylla
    • 1:CAS:528:DC%2BC3cXjvF2ksLg%3D 20074759 10.1016/j.phytochem.2009.12.007
    • 10-polyacetylenic glucosides from Mediasia macrophylla Phytochemistry 71 688 692 1:CAS:528:DC%2BC3cXjvF2ksLg%3D 20074759 10.1016/j.phytochem.2009.12.007
    • (2010) Phytochemistry , vol.71 , pp. 688-692
    • Kurimoto, S.1    Okasaka, M.2    Kashiwada, Y.3    Kodzhimatov, O.K.4    Takaishi, Y.5
  • 22
    • 0037699915 scopus 로고    scopus 로고
    • Water-soluble constituents of coriander
    • DOI 10.1248/cpb.51.32
    • T Ishikawa K Kondo J Kitajima 2003 Water-soluble constituents of coriander Chem Pharm Bull 51 32 39 1:CAS:528:DC%2BD3sXjsFCqtbY%3D 12520125 10.1248/cpb.51.32 (Pubitemid 41702013)
    • (2003) Chemical and Pharmaceutical Bulletin , vol.51 , Issue.1 , pp. 32-39
    • Ishikawa, T.1    Kondo, K.2    Kitajima, J.3
  • 24
    • 0030062249 scopus 로고    scopus 로고
    • Monoterpene glycosides from Paeonia suffruticosa
    • DOI 10.1016/0031-9422(95)00526-9
    • HC Lin HY Ding TS Wu PL Wu 1996 Monoterpene glycosides from Paeonia suffruticosa Phytochemistry 41 237 242 1:CAS:528:DyaK28XisVaisw%3D%3D 10.1016/0031-9422(95)00526-9 (Pubitemid 3010587)
    • (1996) Phytochemistry , vol.41 , Issue.1 , pp. 237-242
    • Lin Hang-Ching1    Ding, H.-Y.2    Wu Tian-Shung3    Wu Pei-Lin4
  • 25
    • 0031772859 scopus 로고    scopus 로고
    • Water-soluble constituents of fennel. III. Fenchane-type monoterpenoid glycosides
    • T Ishikawa J Kitajima Y Tanaka 1998 Water-soluble constituents of fennel. III. Fenchane-type monoterpenoid glycosides Chem Pharm Bull 46 1599 1602 1:CAS:528:DyaK1cXntVSlt7Y%3D (Pubitemid 28531021)
    • (1998) Chemical and Pharmaceutical Bulletin , vol.46 , Issue.10 , pp. 1599-1602
    • Ishikawa, T.1    Kitajima, J.2    Tanaka, Y.3
  • 26
    • 0028011493 scopus 로고
    • Biotransformation of 1,8-cineole by cultured cells of Eucalyptus perriniana
    • DOI 10.1016/S0031-9422(00)90578-8
    • Y Orihara T Furuya 1994 Biotransformation of 1, 8-cineole by cultured cells of Eucalyptus perriniana Phytochemistry 35 641 644 1:CAS:528: DyaK2cXktlWhsr4%3D 10.1016/S0031-9422(00)90578-8 (Pubitemid 2044171)
    • (1994) Phytochemistry , vol.35 , Issue.3 , pp. 641-644
    • Orihara, Y.1    Furuya, T.2
  • 27
    • 0035851028 scopus 로고    scopus 로고
    • Glycosides and xanthine oxidase inhibitors from Conyza bonariensis
    • DOI 10.1016/S0031-9422(01)00176-5, PII S0031942201001765
    • LD Kong Z Abliz CX Zhou LJ Li CHK Cheng RX Tan 2001 Glycosides and xanthine oxidase inhibitors from Conyza bonariensis Phytochemistry 58 645 651 1:CAS:528:DC%2BD3MXntVeiu7s%3D 11576616 10.1016/S0031-9422(01)00176-5 (Pubitemid 32904889)
    • (2001) Phytochemistry , vol.58 , Issue.4 , pp. 645-651
    • Kong, L.D.1    Abliz, Z.2    Zhou, C.X.3    Li, L.J.4    Cheng, C.H.K.5    Tan, R.X.6
  • 28
    • 0031760515 scopus 로고    scopus 로고
    • Water-soluble constituents of fennel VII. Acyclic monoterpenoid glycosides
    • 1:CAS:528:DyaK1cXnsFyjsb4%3D
    • T Ishikawa Y Tanaka J Kitajima 1998 Water-soluble constituents of fennel VII. Acyclic monoterpenoid glycosides Chem Pharm Bull 46 1748 1751 1:CAS:528:DyaK1cXnsFyjsb4%3D
    • (1998) Chem Pharm Bull , vol.46 , pp. 1748-1751
    • Ishikawa, T.1    Tanaka, Y.2    Kitajima, J.3
  • 29
    • 0344515360 scopus 로고    scopus 로고
    • The synthesis of the anti-malarial natural product polysphorin and analogues using polymer-supported reagents and scavengers
    • 1:CAS:528:DC%2BD3sXoslyjsrk%3D 14664385 10.1039/b308761a
    • AL Lee SV Ley 2003 The synthesis of the anti-malarial natural product polysphorin and analogues using polymer-supported reagents and scavengers Org Biomol Chem 1 3957 3966 1:CAS:528:DC%2BD3sXoslyjsrk%3D 14664385 10.1039/b308761a
    • (2003) Org Biomol Chem , vol.1 , pp. 3957-3966
    • Lee, A.L.1    Ley, S.V.2
  • 30
    • 0742287179 scopus 로고    scopus 로고
    • Isolation of α-glusosidase inhibitors from hyssop (Hyssopus officinalis)
    • DOI 10.1016/j.phytochem.2003.10.009
    • H Matsuura H Miyazaki C Asakawa M Amano T Yoshihara J Mizutani 2004 Isolation of α-glucosidase inhibitors from hyssop (Hyssopus officinalis) Phytochemistry 65 91 97 1:CAS:528:DC%2BD3sXpvFynsL8%3D 14697274 10.1016/j.phytochem.2003.10.009 (Pubitemid 38155895)
    • (2004) Phytochemistry , vol.65 , Issue.1 , pp. 91-97
    • Matsuura, H.1    Miyazaki, H.2    Asakawa, C.3    Amano, M.4    Yoshihara, T.5    Mizutani, J.6
  • 31
    • 45549111795 scopus 로고
    • Caffeoyl conjugates from Echinacea species: Structures and biological activity
    • 10.1016/0031-9422(88)80664-2
    • A Cheninat R Zawatzky H Becker R Brouillard 1988 Caffeoyl conjugates from Echinacea species: structures and biological activity Phytochemistry 27 2787 2794 10.1016/0031-9422(88)80664-2
    • (1988) Phytochemistry , vol.27 , pp. 2787-2794
    • Cheninat, A.1    Zawatzky, R.2    Becker, H.3    Brouillard, R.4
  • 32
    • 0027947989 scopus 로고
    • Phenolic constituents of Phellodendron amurense bark
    • DOI 10.1016/S0031-9422(00)90536-3
    • Y Ida Y Satoh M Ohtsuka M Nagasao J Shoji 1994 Phenolic constituents of Phellodendron amurense bark Phytochemistry 35 209 215 1:CAS:528: DyaK2cXis1Grsr8%3D 10.1016/S0031-9422(00)90536-3 (Pubitemid 2032300)
    • (1994) Phytochemistry , vol.35 , Issue.1 , pp. 209-215
    • Ida, Y.1    Satoh, Y.2    Ohtsuka, M.3    Nagasao, M.4    Shoji, J.5
  • 34
    • 45549112609 scopus 로고
    • Flavonoid and other constituents of Bauhinia manca
    • 1:CAS:528:DyaL1cXlt1Grsbs%3D 10.1016/0031-9422(88)80455-2
    • H Achenbach M Stoecker MA Constenla 1988 Flavonoid and other constituents of Bauhinia manca Phytochemistry 27 1835 1841 1:CAS:528:DyaL1cXlt1Grsbs%3D 10.1016/0031-9422(88)80455-2
    • (1988) Phytochemistry , vol.27 , pp. 1835-1841
    • Achenbach, H.1    Stoecker, M.2    Constenla, M.A.3
  • 35
    • 0000350129 scopus 로고
    • Aromatic glycosides from Berchemia racemosa
    • 1:CAS:528:DyaL1cXnt1Sqtg%3D%3D 10.1016/S0031-9422(00)83595-5
    • S Inoshiri M Sasaki H Kohda H Otsuka K Yamasaki 1987 Aromatic glycosides from Berchemia racemosa Phytochemistry 26 2811 2814 1:CAS:528: DyaL1cXnt1Sqtg%3D%3D 10.1016/S0031-9422(00)83595-5
    • (1987) Phytochemistry , vol.26 , pp. 2811-2814
    • Inoshiri, S.1    Sasaki, M.2    Kohda, H.3    Otsuka, H.4    Yamasaki, K.5
  • 36
    • 33749512193 scopus 로고    scopus 로고
    • Comparative phytochemical characterization of three Rhodiola species
    • DOI 10.1016/j.phytochem.2006.07.026, PII S0031942206004316
    • GG Yousef MH Grace DM Cheng IV Belolipov I Raskin MA Lila 2006 Comparative phytochemical characterization of three Rhodiola species Phytochemistry 67 2380 2391 1:CAS:528:DC%2BD28XhtVyktrbI 16956631 10.1016/j.phytochem.2006.07.026 (Pubitemid 44527929)
    • (2006) Phytochemistry , vol.67 , Issue.21 , pp. 2380-2391
    • Yousef, G.G.1    Grace, M.H.2    Cheng, D.M.3    Belolipov, I.V.4    Raskin, I.5    Lila, M.A.6
  • 37
    • 0000998721 scopus 로고
    • Aryl β-d-glucosides from Carica papaya fruit
    • 1:CAS:528:DyaL1cXlt1Grsb8%3D 10.1016/0031-9422(88)80450-3
    • W Schwab P Schreier 1988 Aryl β-d-glucosides from Carica papaya fruit Phytochemistry 27 1813 1816 1:CAS:528:DyaL1cXlt1Grsb8%3D 10.1016/0031-9422(88)80450-3
    • (1988) Phytochemistry , vol.27 , pp. 1813-1816
    • Schwab, W.1    Schreier, P.2
  • 38
    • 0001537550 scopus 로고
    • Ionone and lignan glycosides from Epimedium diphyllum
    • 1:CAS:528:DyaK3cXhslGmurg%3D 10.1016/0031-9422(89)80369-3
    • T Miyase A Ueno N Takizawa H Kobayashi H Oguchi 1989 Ionone and lignan glycosides from Epimedium diphyllum Phytochemistry 28 3483 3485 1:CAS:528:DyaK3cXhslGmurg%3D 10.1016/0031-9422(89)80369-3
    • (1989) Phytochemistry , vol.28 , pp. 3483-3485
    • Miyase, T.1    Ueno, A.2    Takizawa, N.3    Kobayashi, H.4    Oguchi, H.5
  • 39
    • 0036773833 scopus 로고    scopus 로고
    • Water-soluble constituents of caraway: Aromatic compound, aromatic compound glucoside and glucides
    • DOI 10.1016/S0031-9422(02)00288-1, PII S0031942202002881
    • T Matsumura T Ishikawa J Kitajima 2002 Water-soluble constituents of caraway: aromatic compound, aromatic compound glucoside and glucosides Phytochemistry 61 455 459 1:CAS:528:DC%2BD38XnsF2ltbc%3D 12377243 10.1016/S0031-9422(02)00288-1 (Pubitemid 35230807)
    • (2002) Phytochemistry , vol.61 , Issue.4 , pp. 455-459
    • Matsumura, T.1    Ishikawa, T.2    Kitajima, J.3
  • 40
    • 51849146531 scopus 로고    scopus 로고
    • Characterization of polyketide metabolites from foliar endophytes of Picea glauca
    • 1:CAS:528:DC%2BD1cXos1ahsrg%3D 18636777 10.1021/np800192f
    • MW Sumarah E Puniani BA Blackwell JD Miller 2008 Characterization of polyketide metabolites from foliar endophytes of Picea glauca J Nat Prod 71 1393 1398 1:CAS:528:DC%2BD1cXos1ahsrg%3D 18636777 10.1021/np800192f
    • (2008) J Nat Prod , vol.71 , pp. 1393-1398
    • Sumarah, M.W.1    Puniani, E.2    Blackwell, B.A.3    Miller, J.D.4
  • 41
    • 85007810327 scopus 로고
    • Determination of constituents in fruit juice by near infrared spectroscopy Part I. Determination of sugar and acid contents in fruit juice of satsuma mandarin by near infrared spectroscopy
    • Fujiwara T, Honjo T (1995) Determination of constituents in fruit juice by near infrared spectroscopy Part I. Determination of sugar and acid contents in fruit juice of satsuma mandarin by near infrared spectroscopy. Nippon Shokuhin Kagaku Kogaku Kaishi 42:109-117
    • (1995) Nippon Shokuhin Kagaku Kogaku Kaishi , vol.42 , pp. 109-117
    • Fujiwara, T.1    Honjo, T.2
  • 42
    • 49349138226 scopus 로고
    • Carbon-13 NMR studies of flavonoids-III: Naturally occurring flavonoid glycosides and their acylated derivatives
    • 1:CAS:528:DyaE1MXht1Wqt74%3D 10.1016/0040-4020(78)88336-7
    • KR Markham B Ternai R Stanley H Geiger TJ Mabry 1978 Carbon-13 NMR studies of flavonoids-III: naturally occurring flavonoid glycosides and their acylated derivatives Tetrahedron 34 1389 1397 1:CAS:528:DyaE1MXht1Wqt74%3D 10.1016/0040-4020(78)88336-7
    • (1978) Tetrahedron , vol.34 , pp. 1389-1397
    • Markham, K.R.1    Ternai, B.2    Stanley, R.3    Geiger, H.4    Mabry, T.J.5
  • 43
    • 0021978927 scopus 로고
    • Coumarin and secoiridoid glucosides from bark of Olea africana and Olea capensis
    • 1:CAS:528:DyaL2MXht1yrtLc%3D
    • H Tsukamoto S Hisada S Nishibe 1985 Coumarin and secoiridoid glucosides from bark of Olea africana and Olea capensis Chem Pharm Bull 33 396 399 1:CAS:528:DyaL2MXht1yrtLc%3D
    • (1985) Chem Pharm Bull , vol.33 , pp. 396-399
    • Tsukamoto, H.1    Hisada, S.2    Nishibe, S.3
  • 44
    • 0001504711 scopus 로고
    • 9α-Hydroxypinoresinol, 9α-hydroxymedioresinol and related lignans from Allamanda neriifolia
    • F Abe T Yamauchi 1988 9α-Hydroxypinoresinol, 9α- hydroxymedioresinol and related lignans from Allamanda neriifolia Phytochemistry 27 75 77
    • (1988) Phytochemistry , vol.27 , pp. 75-77
    • Abe, F.1    Yamauchi, T.2
  • 45
    • 0001003716 scopus 로고
    • Characterization of lariciresinol glucosides from Osmanthus asiaticus
    • 10.3987/COM-92-6187
    • M Sugiyama M Kikuchi 1993 Characterization of lariciresinol glucosides from Osmanthus asiaticus Heterocycles 36 117 121 10.3987/COM-92-6187
    • (1993) Heterocycles , vol.36 , pp. 117-121
    • Sugiyama, M.1    Kikuchi, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.