메뉴 건너뛰기




Volumn 70, Issue 6, 2004, Pages 509-514

Antitubercular constituents of Valeriana laxiflora

Author keywords

Antimycobacterial activity; Cytotoxicity; Iridolactone; Lignan; Triterpene; Valeriana laxiflora; Valerianaceae

Indexed keywords

1 HYDROXY 2,6 BISEPIPINORESINOL; 1 HYDROXYPINORESINOL; 23 HYDROXYURSOLIC ACID; 5,7,3' TRIHYDROXY 4' METHOXYFLAVONE; 7 HYDROXY 8 HYDROXYMETHYL 4 METHYLPERHYDROCYCLOPENTAPYRAN 1 ONE; BETULIC ACID; BETULIN; ESTER; FERULIC ACID; FLAVONE DERIVATIVE; HEXANE; LACTONE DERIVATIVE; LIGNAN DERIVATIVE; OLEANOLIC ACID; PINORESINOL; PLANT EXTRACT; PYRAN DERIVATIVE; SANTIN; TRICIN; UNCLASSIFIED DRUG; URSOLIC ACID; VALERIAN; VALERIANA LAXIFLORA EXTRACT;

EID: 3042748326     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-827149     Document Type: Article
Times cited : (99)

References (22)
  • 3
    • 0030903133 scopus 로고    scopus 로고
    • Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium
    • Collins L, Franzblau SG. Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium. Antimicrob Agents Chemother 1997; 41: 1004-9
    • (1997) Antimicrob Agents Chemother , vol.41 , pp. 1004-1009
    • Collins, L.1    Franzblau, S.G.2
  • 4
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • Ohtani I, Kusumi T, Kashman Y, Kakisawa H. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J Am Chem Soc 1991; 113: 4092-6
    • (1991) J Am Chem Soc , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 5
    • 0036741302 scopus 로고    scopus 로고
    • New chemical constituents of Euphorbia quinquecostata and absolute configuration assignment by a convenient Mosher ester procedure carried out in NMR tubes
    • Su BN, Park EJ, Mbwambo ZH, Santarsiero BD, Mesecar AD, Fong HHS et al. New chemical constituents of Euphorbia quinquecostata and absolute configuration assignment by a convenient Mosher ester procedure carried out in NMR tubes. J Nat Prod 2002; 65: 1278-82
    • (2002) J Nat Prod , vol.65 , pp. 1278-1282
    • Su, B.N.1    Park, E.J.2    Mbwambo, Z.H.3    Santarsiero, B.D.4    Mesecar, A.D.5    Fong, H.H.S.6
  • 9
    • 85008119850 scopus 로고
    • Carbon-13 nuclear magnetic resonance spectral study. Effect of O-methylation of ortho-substituted phenols on the aryl carbon shielding and its application to interpretation of the spectra of some flavonoids
    • Fujita M, Nagai M, Inoue T. Carbon-13 nuclear magnetic resonance spectral study. Effect of O-methylation of ortho-substituted phenols on the aryl carbon shielding and its application to interpretation of the spectra of some flavonoids. Chem Pharm Bull 1982; 30: 1151-6
    • (1982) Chem Pharm Bull , vol.30 , pp. 1151-1156
    • Fujita, M.1    Nagai, M.2    Inoue, T.3
  • 10
    • 0024118754 scopus 로고
    • Phytochemical studies of seeds of medicinal plants. I. Two sulfated triterpenoid glycosides, sulfapatrinosides I and II, from seeds of Patrinia scabiosaefolia Fischer
    • Inada A, Yamada M, Murata H, Kobayashi M, Toya H, Kato Y et al. Phytochemical studies of seeds of medicinal plants. I. Two sulfated triterpenoid glycosides, sulfapatrinosides I and II, from seeds of Patrinia scabiosaefolia Fischer. Chem Pharm Bull 1988; 36: 4269-74
    • (1988) Chem Pharm Bull , vol.36 , pp. 4269-4274
    • Inada, A.1    Yamada, M.2    Murata, H.3    Kobayashi, M.4    Toya, H.5    Kato, Y.6
  • 12
    • 0017233727 scopus 로고
    • Polyphenolic acids of Lithospermum ruderale. II. Carbon-13 nuclear magnetic resonance of lithospermic and rosmarinic acids
    • Kelley CJ, Harruff RC, Carmack M. Polyphenolic acids of Lithospermum ruderale. II. Carbon-13 nuclear magnetic resonance of lithospermic and rosmarinic acids. J Org Chem 1976; 41: 449-55
    • (1976) J Org Chem , vol.41 , pp. 449-455
    • Kelley, C.J.1    Harruff, R.C.2    Carmack, M.3
  • 14
    • 33845279415 scopus 로고
    • Oleanderol, a new pentacyclic triterpene from the leaves of Nerium oleander
    • Siddiqui S, Hafeez F, Begum S, Siddiqui BS. Oleanderol, a new pentacyclic triterpene from the leaves of Nerium oleander. J Nat Prod 1988; 51: 229-33
    • (1988) J Nat Prod , vol.51 , pp. 229-233
    • Siddiqui, S.1    Hafeez, F.2    Begum, S.3    Siddiqui, B.S.4
  • 15
    • 0017380369 scopus 로고
    • Synthesis of polyhydroxyflavonol methyl ethers with potential cyclotoxic activity. I. Synthesis of quercetagetin and gossypetin dimethyl ethers for the structure determination of new flavonols from Parthenium, Chrysosplenium, Larrea, and Spinacia species
    • Wagner H, Maurer I, Farkas L, Strelisky J. Synthesis of polyhydroxyflavonol methyl ethers with potential cyclotoxic activity. I. Synthesis of quercetagetin and gossypetin dimethyl ethers for the structure determination of new flavonols from Parthenium, Chrysosplenium, Larrea, and Spinacia species. Tetrahedron 1977; 33: 1405-9
    • (1977) Tetrahedron , vol.33 , pp. 1405-1409
    • Wagner, H.1    Maurer, I.2    Farkas, L.3    Strelisky, J.4
  • 18
    • 0001128893 scopus 로고
    • Absolute structure of gibboside, an iridoid glucoside from Patrinia gibbosa
    • Uesato S, Shan X, Inouye H, Shingu T, Inoue M, Doi M. Absolute structure of gibboside, an iridoid glucoside from Patrinia gibbosa. Phytochemistry 1987; 26: 561-4
    • (1987) Phytochemistry , vol.26 , pp. 561-564
    • Uesato, S.1    Shan, X.2    Inouye, H.3    Shingu, T.4    Inoue, M.5    Doi, M.6
  • 21
    • 0013915502 scopus 로고
    • Studies on constituents of medicinal plants. VIII. The stereochemistry of paulownin and isopaulownin
    • Takahashi K, Nakagawa T. Studies on constituents of medicinal plants. VIII. The stereochemistry of paulownin and isopaulownin. Chem Pharm Bull 1966; 14: 641-7
    • (1966) Chem Pharm Bull , vol.14 , pp. 641-647
    • Takahashi, K.1    Nakagawa, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.