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Volumn 76, Issue 5, 2010, Pages 454-457

Chemical constituents from the rhizome of acorus calamus L.

Author keywords

Acorus calamus L.; Araceae; Chemical structure; NMR; Sesquiterpenes

Indexed keywords

1ALPHA,5BETA GUAIANE 10ALPHA O ETHYL 4BETA,6BETA DIOL; 1BETA,7ALPHA CADINANE 4ALPHA,6ALPHA,10ALPHA TRIOL; 6BETA,7BETA CADINANE 1ALPHA,4ALPHA,10ALPHA TRIOL; ACORUS CALAMUS EXTRACT; SESQUITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77950246579     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0029-1186217     Document Type: Article
Times cited : (22)

References (36)
  • 2
    • 0034982333 scopus 로고    scopus 로고
    • Study of antidiarrhoeal activity of four medicinal plants in castor-oil induced diarrhoea
    • Shoba F G., Thomas M. Study of antidiarrhoeal activity of four medicinal plants in castor-oil induced diarrhoea. J Ethnopharmacol 2001 76 73-76
    • (2001) J Ethnopharmacol , vol.76 , pp. 73-76
    • Shoba, F.G.1    Thomas, M.2
  • 3
    • 0031688072 scopus 로고    scopus 로고
    • Sedative and hypothermic effects induced by -asarone, a main component of Acorus calamus
    • Zanoli P, Avallone R, Baraldi M. Sedative and hypothermic effects induced by -asarone, a main component of Acorus calamus. Phytother Res 1998 12 S114-S116
    • (1998) Phytother Res , vol.12
    • Zanoli, P.1    Avallone, R.2    Baraldi, M.3
  • 4
    • 34250361782 scopus 로고    scopus 로고
    • A fraction of Acorus calamus L. extract devoid of -asarone enhances adipocyte differentiation in 3T3-L1 cells
    • Wu H S., Li Y Y., Weng L J., Zhou C X., He Q J., Lou Y J. A Fraction of Acorus calamus L. extract devoid of -asarone enhances adipocyte differentiation in 3T3-L1 cells. Phytother Res 2007 21 562-564
    • (2007) Phytother Res , vol.21 , pp. 562-564
    • Wu, H.S.1    Li, Y.Y.2    Weng, L.J.3    Zhou, C.X.4    He, Q.J.5    Lou, Y.J.6
  • 5
    • 0030484331 scopus 로고    scopus 로고
    • Sesquiterpenoids from Acorus calamus as germination inhibitors
    • Nawamaki K, Kuroyanagi M. Sesquiterpenoids from Acorus calamus as germination inhibitors. Phytochemistry 1996 43 1175-1182
    • (1996) Phytochemistry , vol.43 , pp. 1175-1182
    • Nawamaki, K.1    Kuroyanagi, M.2
  • 6
    • 0015839471 scopus 로고
    • Isolation and structure of acoragermacrone
    • Iguchi M, Niwa M, Nishiyama A. Isolation and structure of acoragermacrone. Tetrahedron Lett 1973 29 2759-2762
    • (1973) Tetrahedron Lett , vol.29 , pp. 2759-2762
    • Iguchi, M.1    Niwa, M.2    Nishiyama, A.3
  • 7
    • 0001278485 scopus 로고
    • Constituents of Acorus calamus Linn
    • Patra A, Mitra A K. Constituents of Acorus calamus Linn. Indian J Chem 1979 17B 412-414
    • (1979) Indian J Chem , vol.17 , pp. 412-414
    • Patra, A.1    Mitra, A.K.2
  • 8
    • 0542380508 scopus 로고    scopus 로고
    • Triterpenoid saponins from Acorus calamus
    • Rai R, Siddiqui I R., Singh J. Triterpenoid saponins from Acorus calamus. Indian J Chem 1998 37B 473-476
    • (1998) Indian J Chem , vol.37 , pp. 473-476
    • Rai, R.1    Siddiqui, I.R.2    Singh, J.3
  • 9
    • 0002919612 scopus 로고
    • Chemical composition of essential oil from Mongolian Acorus calamus L. rhizomes
    • Todorova M N., Ognyanov I V., Shatar S. Chemical composition of essential oil from Mongolian Acorus calamus L. rhizomes. J Essent Oil Res 1995 7 191-193
    • (1995) J Essent Oil Res , vol.7 , pp. 191-193
    • Todorova, M.N.1    Ognyanov, I.V.2    Shatar, S.3
  • 10
    • 33847309172 scopus 로고    scopus 로고
    • Acorafuran, a new sesquiterpenoid from Acorus calamus essential oil
    • Tkachev A V., Gur'ev A M., Yusubov M S. Acorafuran, a new sesquiterpenoid from Acorus calamus essential oil. Chem Nat Compd 2006 42 696-698
    • (2006) Chem Nat Compd , vol.42 , pp. 696-698
    • Tkachev, A.V.1    Gur'Ev, A.M.2    Yusubov, M.S.3
  • 12
    • 0029062177 scopus 로고
    • 7-epi-Eudesmanes from Teucrium polium
    • Kamel A. 7-epi-Eudesmanes from Teucrium polium. J Nat Prod 1995 58 428-431
    • (1995) J Nat Prod , vol.58 , pp. 428-431
    • Kamel, A.1
  • 13
    • 0019198377 scopus 로고
    • Fungal metabolites. VIII: Structures of new sesquiterpenes from Lactarius scrobiculatus
    • Battaglia R, Bernardi M D., Fronza G, Mellerio G, Vidari G, Finsi P V. Fungal metabolites. VIII: Structures of new sesquiterpenes from Lactarius scrobiculatus. J Nat Prod 1980 43 319-328
    • (1980) J Nat Prod , vol.43 , pp. 319-328
    • Battaglia, R.1    Bernardi, M.D.2    Fronza, G.3    Mellerio, G.4    Vidari, G.5    Finsi, P.V.6
  • 15
    • 0343005270 scopus 로고
    • Sesquiterpenoid constituents of Meriandra benghalensis (Labiatae). X-ray structure analysis
    • Perales A, Martinez-Ripoll M, Fayos J, Savona G, Bruno M, Rodriguez B. Sesquiterpenoid constituents of Meriandra benghalensis (Labiatae). X-ray structure analysis. J Org Chem 1983 48 5318-5321
    • (1983) J Org Chem , vol.48 , pp. 5318-5321
    • Perales, A.1    Martinez-Ripoll, M.2    Fayos, J.3    Savona, G.4    Bruno, M.5    Rodriguez, B.6
  • 16
    • 0000512516 scopus 로고
    • 13C spectroscopy.
    • 13C spectroscopy. Phytochemistry 1982 21 937-938
    • (1982) Phytochemistry , vol.21 , pp. 937-938
    • Evans, F.E.1
  • 19
    • 0030797452 scopus 로고    scopus 로고
    • 7-Epi-eudesmanes, eudesmanoic acids, eudesmanolides and other sesquiterpenes from Pluchea dioscoridis
    • Mahmoud A A. 7-Epi-eudesmanes, eudesmanoic acids, eudesmanolides and other sesquiterpenes from Pluchea dioscoridis. Phytochemistry 1997 45 1633-1638
    • (1997) Phytochemistry , vol.45 , pp. 1633-1638
    • Mahmoud, A.A.1
  • 20
    • 84943913040 scopus 로고
    • Two new saturated sesquiterpene diolscadinan-3,9-diol and cadinan-3,9-diol from Taiwania cryptomerioides Hayata
    • Kuo Y H., Cheng Y S., Kao S T., Lin Y T. Two new saturated sesquiterpene diolscadinan-3,9-diol and cadinan-3,9-diol from Taiwania cryptomerioides Hayata. J Chin Chem Soc 1973 20 83-86
    • (1973) J Chin Chem Soc , vol.20 , pp. 83-86
    • Kuo, Y.H.1    Cheng, Y.S.2    Kao, S.T.3    Lin, Y.T.4
  • 22
    • 0027408104 scopus 로고
    • Marine sterols, side-chain-oxygenated sterols, possibly of abiotic origin, from the new caledonian sponge Stelodoryx chlorophylla
    • Riccardis F, Minale L, Iorizzi M, Debitus C, Lvi C. Marine sterols, side-chain-oxygenated sterols, possibly of abiotic origin, from the new caledonian sponge Stelodoryx chlorophylla. J Nat Prod 1993 56 282-287
    • (1993) J Nat Prod , vol.56 , pp. 282-287
    • Riccardis, F.1    Minale, L.2    Iorizzi, M.3    Debitus, C.4    Lvi, C.5
  • 23
    • 0008639536 scopus 로고
    • A steroid from Pistia stratiotes
    • Monaco P, Previtera L. A steroid from Pistia stratiotes. Phytochemistry 1991 30 2420-2422
    • (1991) Phytochemistry , vol.30 , pp. 2420-2422
    • Monaco, P.1    Previtera, L.2
  • 24
    • 0030020310 scopus 로고    scopus 로고
    • A sterol glycoside from leaves of Clerodendron colebrookianum
    • Goswami P, Kotoky J, Chen Z N., Lu Y. A sterol glycoside from leaves of Clerodendron colebrookianum. Phytochemistry 1996 41 279-281
    • (1996) Phytochemistry , vol.41 , pp. 279-281
    • Goswami, P.1    Kotoky, J.2    Chen, Z.N.3    Lu, Y.4
  • 25
    • 0001068365 scopus 로고
    • A sterol glycoside from marine green alga Codium iyengarii
    • Ahmad V U., Aliya R, Perveen S, Shameel M. A sterol glycoside from marine green alga Codium iyengarii. Phytochemistry 1992 31 1429-1431
    • (1992) Phytochemistry , vol.31 , pp. 1429-1431
    • Ahmad, V.U.1    Aliya, R.2    Perveen, S.3    Shameel, M.4
  • 26
    • 77950215147 scopus 로고    scopus 로고
    • Lignans in flower buds of Magnolia biondii
    • Guo Q, Fang H, Su W. Lignans in flower buds of Magnolia biondii. Chin Tradit Herb Drugs 2004 35 849-851
    • (2004) Chin Tradit Herb Drugs , vol.35 , pp. 849-851
    • Guo, Q.1    Fang, H.2    Su, W.3
  • 27
    • 0001517750 scopus 로고
    • Lignan and terpene glycosides from Epimedium sagittatum
    • Matsushita H, Miyase T, Ueno A. Lignan and terpene glycosides from Epimedium sagittatum. Phytochemistry 1991 30 2025-2027
    • (1991) Phytochemistry , vol.30 , pp. 2025-2027
    • Matsushita, H.1    Miyase, T.2    Ueno, A.3
  • 29
    • 0036103605 scopus 로고    scopus 로고
    • A mild and convenient procedure for the conversion of toxic -asarone into rare phenylpropanoids: 2,4,5-trimethoxycinnamaldehyde and -asarone
    • Sinha A K., Acharya R, Joshi B P. A mild and convenient procedure for the conversion of toxic -asarone into rare phenylpropanoids: 2,4,5- trimethoxycinnamaldehyde and -asarone. J Nat Prod 2002 65 764-765
    • (2002) J Nat Prod , vol.65 , pp. 764-765
    • Sinha, A.K.1    Acharya, R.2    Joshi, B.P.3
  • 30
    • 0019853769 scopus 로고
    • Constituents of Acorus calamus: Structure of acoramone. carbon-13 NMR spectra of cis- and trans -asarone
    • Patra A, Mitra A K. Constituents of Acorus calamus: structure of acoramone. carbon-13 NMR spectra of cis- and trans -asarone. J Nat Prod 1981 44 668-669
    • (1981) J Nat Prod , vol.44 , pp. 668-669
    • Patra, A.1    Mitra, A.K.2
  • 31
    • 0032481005 scopus 로고    scopus 로고
    • Total synthesis of maesanin and analogues
    • Poigny S, Guyot M, Samadi M. Total synthesis of maesanin and analogues. Tetrahedron 1998 54 14791-14802
    • (1998) Tetrahedron , vol.54 , pp. 14791-14802
    • Poigny, S.1    Guyot, M.2    Samadi, M.3
  • 32
    • 68049103819 scopus 로고    scopus 로고
    • Studies on chemical constituents of Acorus tatarinowii decoction
    • Yang X Y., Chen F K., Wu L J. Studies on chemical constituents of Acorus tatarinowii decoction. Chin Tradit Herb Drugs 1998 29 730-731
    • (1998) Chin Tradit Herb Drugs , vol.29 , pp. 730-731
    • Yang, X.Y.1    Chen, F.K.2    Wu, L.J.3
  • 33
    • 0036179960 scopus 로고    scopus 로고
    • Lignanamides and nonalkaloidal components of Hyoscyamus niger seeds
    • Ma C Y., Liu W K., Che C T. Lignanamides and nonalkaloidal components of Hyoscyamus niger seeds. J Nat Prod 2002 65 206-209
    • (2002) J Nat Prod , vol.65 , pp. 206-209
    • Ma, C.Y.1    Liu, W.K.2    Che, C.T.3
  • 34
    • 38349030194 scopus 로고    scopus 로고
    • Studies on the chemical constituent of Tripterygium wilfordill Hook. F
    • Chen Y, Yang G Z., Li Y C. Studies on the chemical constituent of Tripterygium wilfordill Hook. F. Nat Prod Res Dev 2005 17 301-302
    • (2005) Nat Prod Res Dev , vol.17 , pp. 301-302
    • Chen, Y.1    Yang, G.Z.2    Li, Y.C.3
  • 35
    • 33846294795 scopus 로고    scopus 로고
    • Studies on chemical constituents in root tuber of Cynanchum auriculatum
    • Zhang J F., Li Y B., Qian S H., Li C L., Jiang J Q. Studies on chemical constituents in root tuber of Cynanchum auriculatum. China J Chin Mater Med 2006 31 814-816
    • (2006) China J Chin Mater Med , vol.31 , pp. 814-816
    • Zhang, J.F.1    Li, Y.B.2    Qian, S.H.3    Li, C.L.4    Jiang, J.Q.5
  • 36
    • 4644295242 scopus 로고    scopus 로고
    • Studies on chemical constituents of Siegesbeckia pubescens
    • Fu H Z., Yang X W., Cai S Q. Studies on chemical constituents of Siegesbeckia pubescens. Chin Tradit Herb Drugs 1997 28 259-262
    • (1997) Chin Tradit Herb Drugs , vol.28 , pp. 259-262
    • Fu, H.Z.1    Yang, X.W.2    Cai, S.Q.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.