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Volumn 5, Issue 2, 2010, Pages 211-217

Anti-tuberculosis compounds from Mallotus philippinensis

Author keywords

Chromenes; Mallotophilippen; Mallotus philippinensis; Mycobacterium tuberculosis; Phloroglucinols; Rottlerin

Indexed keywords

8 CINNAMOYL 2,2 DIMETHYL 7 HYDROXY 5 METHOXYCHROMENE; 8 CINNAMOYL 5,7 DIHYDROXY 2,2 DIMETHYL 6 GERANYLCHROMENE; 8 CINNAMOYL 5,7 DIHYDROXY 2,2,6 TRIMETHYLCHROMENE; ISOALLOROTTLERIN; ROTTLERIN; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

EID: 77951922188     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1000500208     Document Type: Article
Times cited : (19)

References (41)
  • 2
    • 65249188733 scopus 로고    scopus 로고
    • Mycobacterial subversion of chemotherapeutic reagents and host defense tactics: Challenges in tuberculosis drug development
    • Nguyen L, Pieters J. (2009) Mycobacterial subversion of chemotherapeutic reagents and host defense tactics: challenges in tuberculosis drug development. Annual Review of Pharmacology and Toxicology, 49, 427-453.
    • (2009) Annual Review of Pharmacology and Toxicology , vol.49 , pp. 427-453
    • Nguyen, L.1    Pieters, J.2
  • 5
    • 77954109848 scopus 로고    scopus 로고
    • Anti-tuberculosis compounds from two Bolivian medicinal plants, Senecio mathewsii and Usnea florida
    • Hong Q, Minter DE, Franzblau SG, Reinecke MG. (2008) Anti-tuberculosis compounds from two Bolivian medicinal plants, Senecio mathewsii and Usnea florida. Natural Product Communications, 3, 1377-1384.
    • (2008) Natural Product Communications , vol.3 , pp. 1377-1384
    • Hong, Q.1    Minter, D.E.2    Franzblau, S.G.3    Reinecke, M.G.4
  • 8
    • 42549122922 scopus 로고    scopus 로고
    • Potential anti-tumor-promoting activity of 3.alpha.-hydroxy-D:A- friedooleanan-2-one from the stem bark of Mallotus philippensis
    • Tanaka R, Nakata T, Yamaguchi C, Wada S-i, Yamada T, Tokuda H. (2008) Potential anti-tumor-promoting activity of 3.alpha.-hydroxy-D:A-friedooleanan-2- one from the stem bark of Mallotus philippensis. Planta Medica, 74, 413-416.
    • (2008) Planta Medica , vol.74 , pp. 413-416
    • Tanaka, R.1    Nakata, T.2    Yamaguchi, C.3    Wada, S.-I.4    Yamada, T.5    Tokuda, H.6
  • 9
    • 1442315196 scopus 로고    scopus 로고
    • Anti-allergic agents from natural sources (4): Anti-allergic activity of new phloroglucinol derivatives from Mallotus philippensis (Euphorbiaceae)
    • Daikonya A, Katsuki S, Wu J-B, Kitanaka S. (2002) Anti-allergic agents from natural sources (4): Anti-allergic activity of new phloroglucinol derivatives from Mallotus philippensis (Euphorbiaceae). Chemical & Pharmaceutical Bulletin, 50, 1566-1569.
    • (2002) Chemical & Pharmaceutical Bulletin , vol.50 , pp. 1566-1569
    • Daikonya, A.1    Katsuki, S.2    Wu, J.-B.3    Kitanaka, S.4
  • 10
    • 20344402268 scopus 로고    scopus 로고
    • Antiallergic agents from natural sources 9. Inhibition of nitric oxide production by novel chalcone derivatives from Mallotus philippinensis (Euphorbiaceae)
    • Daikonya A, Katsuki S, Kitanaka S. (2004) Antiallergic agents from natural sources 9. Inhibition of nitric oxide production by novel chalcone derivatives from Mallotus philippinensis (Euphorbiaceae). Chemical & Pharmaceutical Bulletin, 52, 1326-1329.
    • (2004) Chemical & Pharmaceutical Bulletin , vol.52 , pp. 1326-1329
    • Daikonya, A.1    Katsuki, S.2    Kitanaka, S.3
  • 13
    • 39649091205 scopus 로고    scopus 로고
    • Rottlerin inhibits chlamydial intracellular growth and blocks chlamydial acquisition of sphingolipids from host cells
    • Shivshankar P, Lei L, Wang J, Zhong G. (2008) Rottlerin inhibits chlamydial intracellular growth and blocks chlamydial acquisition of sphingolipids from host cells. Applied and Environmental Microbiology, 74, 1243-1249.
    • (2008) Applied and Environmental Microbiology , vol.74 , pp. 1243-1249
    • Shivshankar, P.1    Lei, L.2    Wang, J.3    Zhong, G.4
  • 14
    • 65249165416 scopus 로고    scopus 로고
    • Potent bactericidal constituents from Mallotus philippinensis against clarithromycin and metronidazole resistant strains of Japanese and Pakistani Helicobacter pylori
    • Zaidi SFH, Yoshida I, Butt F, Yusuf MA, Usmanghani K, Kadowaki M, Sugiyama T. (2009) Potent bactericidal constituents from Mallotus philippinensis against clarithromycin and metronidazole resistant strains of Japanese and Pakistani Helicobacter pylori. Biological & Pharmaceutical Bulletin, 32, 631-636.
    • (2009) Biological & Pharmaceutical Bulletin , vol.32 , pp. 631-636
    • Zaidi, S.F.H.1    Yoshida, I.2    Butt, F.3    Yusuf, M.A.4    Usmanghani, K.5    Kadowaki, M.6    Sugiyama, T.7
  • 15
    • 0025084496 scopus 로고
    • Detection of antituberculous activity in plant extracts
    • Grange JM, Davey RW. (1990) Detection of Anti-tuberculosis Activity in Plant Extracts. Journal of Applied Bacteriology, 68, 587-591. (Pubitemid 20331909)
    • (1990) Journal of Applied Bacteriology , vol.68 , Issue.6 , pp. 587-591
    • Grange, J.M.1    Davey, R.W.2
  • 19
    • 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 LA, Franzblau SG. (1997) Microplate Alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium. Antimicrobial Agents and Chemotherapy, 41, 1004-1009.
    • (1997) Antimicrobial Agents and Chemotherapy , vol.41 , pp. 1004-1009
    • Collins, L.A.1    Franzblau, S.G.2
  • 20
    • 77954137709 scopus 로고
    • The chemical shifts of chelated hydroxyl protons in unsymmetrically substituted acylphloroglucinols
    • Cann MR, Shannon PVR. (1982) The chemical shifts of chelated hydroxyl protons in unsymmetrically substituted acylphloroglucinols. Chemistry & Industry (London, United Kingdom), 779-780.
    • (1982) Chemistry & Industry (London, United Kingdom) , pp. 779-780
    • Cann, M.R.1    Shannon, P.V.R.2
  • 23
    • 44949246436 scopus 로고    scopus 로고
    • Concise Total Synthesis of Biologically Interesting Mallotophilippens C and E
    • Lee YR, Li X, Kim JH. (2008) Concise Total Synthesis of Biologically Interesting Mallotophilippens C and E. Journal of Organic Chemistry, 73, 4313-4316.
    • (2008) Journal of Organic Chemistry , vol.73 , pp. 4313-4316
    • Lee, Y.R.1    Li, X.2    Kim, J.H.3
  • 24
    • 84986840493 scopus 로고
    • Carbon-13 substituent effects in monosubstituted benzenes
    • Ewing DF. (1979) Carbon-13 substituent effects in monosubstituted benzenes. Organic Magnetic Resonance, 12, 499-524.
    • (1979) Organic Magnetic Resonance , vol.12 , pp. 499-524
    • Ewing, D.F.1
  • 25
    • 0004780214 scopus 로고
    • Naturally occurring dimethylchromenes. I. Chromenes of Medicosma cunninghamii
    • Sutherland MD. (1949) Naturally occurring dimethylchromenes. I. Chromenes of Medicosma cunninghamii. Queensland University Papers, Chemistry, 1 (35), 1-10.
    • (1949) Queensland University Papers, Chemistry , vol.1 , Issue.35 , pp. 1-10
    • Sutherland, M.D.1
  • 26
    • 35548947031 scopus 로고    scopus 로고
    • Concise total synthesis of biologically interesting pyranochalcone natural products: Citrunobin, boesenbergin A, boesenbergin B, xanthohumol C, and glabrachromene
    • Lee YR, Xia L. (2007) Concise total synthesis of biologically interesting pyranochalcone natural products: citrunobin, boesenbergin A, boesenbergin B, xanthohumol C, and glabrachromene. Synthesis, 20, 3240-3246.
    • (2007) Synthesis , vol.20 , pp. 3240-3246
    • Lee, Y.R.1    Xia, L.2
  • 28
    • 84942706567 scopus 로고
    • Obovatin, obovatin methyl ether and obovatachalcone, new piscicidal flavonoids from Tephrosia obovata
    • Chen Y-L, Wang Y-S, Lin Y-L, Munakata K, Ohta K. (1978) Obovatin, obovatin methyl ether and obovatachalcone, new piscicidal flavonoids from Tephrosia obovata. Agricultural and Biological Chemistry, 42, 2431-2432.
    • (1978) Agricultural and Biological Chemistry , vol.42 , pp. 2431-2432
    • Chen, Y.-L.1    Wang, Y.-S.2    Lin, Y.-L.3    Munakata, K.4    Ohta, K.5
  • 30
    • 0000112588 scopus 로고
    • Mixtecacin, a prenylated flavanone, and oaxacacin, its chalcone, from the roots of Tephrosia woodii
    • Dominguez XA, Tellez O, Ramirez EG. (1983) Mixtecacin, a prenylated flavanone, and oaxacacin, its chalcone, from the roots of Tephrosia woodii. Phytochemistry, 22, 2047-2049.
    • (1983) Phytochemistry , vol.22 , pp. 2047-2049
    • Dominguez, X.A.1    Tellez, O.2    Ramirez, E.G.3
  • 33
    • 0011387929 scopus 로고
    • Pyrano flavanone from Millettia ovalifolia seeds
    • Gupta RK, Krishnamurti M. (1976) Pyrano flavanone from Millettia ovalifolia seeds. Phytochemistry, 15, 1795.
    • (1976) Phytochemistry , vol.15 , pp. 1795
    • Gupta, R.K.1    Krishnamurti, M.2
  • 34
    • 34547637845 scopus 로고    scopus 로고
    • An efficient and rapid synthetic route to biologically interesting pyranochalcone natural products
    • Lee YR, Wang X, Xia L. (2007) An efficient and rapid synthetic route to biologically interesting pyranochalcone natural products. Molecules, 12, 1420-1429.
    • (2007) Molecules , vol.12 , pp. 1420-1429
    • Lee, Y.R.1    Wang, X.2    Xia, L.3
  • 37
    • 77954138285 scopus 로고    scopus 로고
    • Personal communication, 9/15/09
    • Tanaka R (2009). Personal communication, 9/15/09.
    • (2009)
    • Tanaka, R.1
  • 39
    • 77954117307 scopus 로고
    • Synthesis of 2′,4′-dihydroxy-3′-methyl-2″, 2″-dimethylpyrano(5″,6″;5′,6′)-chalcone
    • Manchanda VP, Gupta RB, Khanna RN. (1979) Synthesis of 2′,4′-dihydroxy-3′-methyl-2″,2″- dimethylpyrano(5″,6″;5′,6′)-chalcone. Current Science, 48, 663-665.
    • (1979) Current Science , vol.48 , pp. 663-665
    • Manchanda, V.P.1    Gupta, R.B.2    Khanna, R.N.3
  • 41
    • 37049167525 scopus 로고
    • Rottlerin. VI. Spectrographic study of rottlerin and its derivatives
    • Morton RA, Sawires Z. (1940) Rottlerin. VI. Spectrographic study of rottlerin and its derivatives. Journal of the Chemical Society 1052-64.
    • (1940) Journal of the Chemical Society , pp. 1052-1064
    • Morton, R.A.1    Sawires, Z.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.