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Volumn 14, Issue 10, 2009, Pages 4246-4265

Investigating biological activity spectrum for novel styrylquinazoline analogues

Author keywords

In vitro antifungal activity; In vitro antimycobacterial activity; Lipophilicity; PET inhibition; Spinach chloroplasts; Structure activity relationships; Styrylquinazolinone and styrylquinazoline derivatives

Indexed keywords

2 STYRYLQUINAZOLIN 4(3H) ONE; 2-STYRYLQUINAZOLIN-4(3H)-ONE; 4 CHLORO 2 STYRYLQUINAZOLINE; 4-CHLORO-2-STYRYLQUINAZOLINE; QUINAZOLINE DERIVATIVE; STYRENE DERIVATIVE; STYRYLQUINAZOLINE; TUBERCULOSTATIC AGENT;

EID: 70350511014     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules14104246     Document Type: Article
Times cited : (60)

References (70)
  • 1
    • 70350449804 scopus 로고    scopus 로고
    • 3rd, ed.; Deutscher Apotheker Verlag: Stuttgart, Germany
    • Roth, H.J.; Fenner, H. Arzneistoffe, 3rd, ed.; Deutscher Apotheker Verlag: Stuttgart, Germany, 2000; pp. 51-114.
    • (2000) Arzneistoffe , pp. 51-114
    • Roth, H.J.1    Fenner, H.2
  • 2
    • 3242746917 scopus 로고    scopus 로고
    • Advances in the discovery of novel antibacterial agents during the year 2002
    • Harris, C.R.; Thorarensen, A. Advances in the discovery of novel antibacterial agents during the year 2002. Curr. Med. Chem. 2004, 11, 2213-2243.
    • (2004) Curr. Med. Chem. , vol.11 , pp. 2213-2243
    • Harris, C.R.1    Thorarensen, A.2
  • 4
    • 2142662107 scopus 로고    scopus 로고
    • Ring-substituted quinolines as potential anti-tuberculosis agents
    • DOI 10.1016/j.bmc.2004.03.045, PII S0968089604002470
    • Vangapandu, S.; Jain, M.; Jain, R.; Kaur, S.; Singh, P.P. Ring-substituted quinolines as potential anti-tuberculosis agents. Bioorg. Med. Chem. 2004, 12, 2501-2508. (Pubitemid 38542774)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.10 , pp. 2501-2508
    • Vangapandu, S.1    Jain, M.2    Jain, R.3    Kaur, S.4    Singh, P.P.5
  • 5
    • 44449127718 scopus 로고    scopus 로고
    • Anti-mycobacterial activity of quinolones. Triazoloquinolones a new class of potent anti-mycobacterial agents
    • Carta, A.; Piras, S.; Palomba, M.; Jabes, D.; Molicotti, P.; Zanetti, S. Anti-mycobacterial activity of quinolones. Triazoloquinolones a new class of potent anti-mycobacterial agents. Anti-Infective Agents Med. Chem. 2008, 7, 134-147.
    • (2008) Anti-infective Agents Med. Chem. , vol.7 , pp. 134-147
    • Carta, A.1    Piras, S.2    Palomba, M.3    Jabes, D.4    Molicotti, P.5    Zanetti, S.6
  • 6
    • 0141884959 scopus 로고    scopus 로고
    • The quinolone family: From antibacterial to anticancer agents
    • Sissi, C.; Palumbo, M. The quinolone family: From antibacterial to anticancer agents. Curr. Med. Chem. Anti-Canc. Agents 2003, 3, 439-450.
    • (2003) Curr. Med. Chem. Anti-canc. Agents , vol.3 , pp. 439-450
    • Sissi, C.1    Palumbo, M.2
  • 9
    • 3042538232 scopus 로고    scopus 로고
    • Synthesis of (2E)-2-methyl-3-(4-{[4-(quinolin-2-yl-methoxy)phenyl] sulfany}pheny)prop- 2-enoic acid (VUFB 20609) and 2-methyl-3-(4-{[4-(quinolin-2- yl-methoxy) phenyl]sulfany}phenyl)propanoic acid (VUFB 20584) as potential antileukotrienic agents
    • DOI 10.1211/0022357023484
    • Jampilek, J.; Dolezal, M.; Kunes, J.; Vichova, P.; Jun, D.; Raich, I.; ÓConnor, R.; Clynes, M. Synthesis of (2E)-2-methyl-3-(4-{[4-(quinolin-2- ylmethoxy)phenyl]sulfanyl}phenyl)prop-2-enoic acid (VUFB 20609) and 2-methyl-3-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl) propionic acid (VUFB 20584) as potential antileukotrienic agents. J. Pharm. Pharmacol. 2004, 56, 783-794. (Pubitemid 38807302)
    • (2004) Journal of Pharmacy and Pharmacology , vol.56 , Issue.6 , pp. 783-794
    • Jampilek, J.1    Dolezal, M.2    Kunes, J.3    Vichova, P.4    Jun, D.5    Hanika, J.6    O'Connor, R.7    Clynes, M.8
  • 10
    • 4444251668 scopus 로고    scopus 로고
    • Preparation of 2-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl) propionic acid (VUFB 20615) and 2-methyl-2-(4-{[4-(quinolin-2-ylmethoxy)phenyl] sulfanyl}phenyl)propionic acid (VUFB 20623) as potential antileukotrienic agents
    • Jampilek, J.; Dolezal, M.; Kunes, J.; Vichova, P.; Jun, D.; Raich, I.; ÓConnor, R.; Clynes, M. Preparation of 2-(4-{[4-(quinolin-2-ylmethoxy) phenyl]sulfanyl}phenyl)propionic acid (VUFB 20615) and 2-methyl-2-(4-{[4- (quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)propionic acid (VUFB 20623) as potential antileukotrienic agents. Curr. Org. Chem. 2004, 8, 1235-1243.
    • (2004) Curr. Org. Chem. , vol.8 , pp. 1235-1243
    • Jampilek, J.1    Dolezal, M.2    Kunes, J.3    Vichova, P.4    Jun, D.5    Raich, I.6    ÓConnor, R.7    Clynes, M.8
  • 11
    • 33645467520 scopus 로고    scopus 로고
    • 5-Lipoxygenase, leukotrienes biosynthesis and potential antileukotrienic agents
    • Jampilek, J.; Dolezal, M.; Opletalova, V.; Hartl. J. 5-Lipoxygenase, leukotrienes biosynthesis and potential antileukotrienic agents. Curr. Med. Chem. 2006, 13, 117-129.
    • (2006) Curr. Med. Chem. , vol.13 , pp. 117-129
    • Jampilek, J.1    Dolezal, M.2    Opletalova, V.3    Hartl, J.4
  • 16
    • 33645857870 scopus 로고    scopus 로고
    • Quinaldine derivatives: Preparation and biological activity
    • Jampilek, J.; Dolezal, M.; Kunes, J.; Buchta, V.; Kralova, K. Quinaldine derivatives: Preparation and biological activity. Med. Chem. 2005, 1, 591-599.
    • (2005) Med. Chem. , vol.1 , pp. 591-599
    • Jampilek, J.1    Dolezal, M.2    Kunes, J.3    Buchta, V.4    Kralova, K.5
  • 19
    • 42149168708 scopus 로고    scopus 로고
    • Investigating biological activity spectrum for novel quinoline analogues 2: Hydroxyquinolinecarboxamides with photosynthesis inhibiting activity
    • Musiol, R.; Tabak, D.; Niedbala, H.; Podeszwa, B.; Jampilek, J.; Kralova, K.; Dohnal, J.; Finster, J.; Mencel, A.; Polanski, J. Investigating biological activity spectrum for novel quinoline analogues 2: Hydroxyquinolinecarboxamides with photosynthesis inhibiting activity. Bioorg. Med. Chem. 2008, 16, 4490-4499.
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 4490-4499
    • Musiol, R.1    Tabak, D.2    Niedbala, H.3    Podeszwa, B.4    Jampilek, J.5    Kralova, K.6    Dohnal, J.7    Finster, J.8    Mencel, A.9    Polanski, J.10
  • 23
    • 0017603121 scopus 로고
    • Relationship between inhibitor binding by chloroplasts and inhibition of photosynthetic electron transport
    • Tischer, W.; Strotmann, H. Relationship between inhibitor binding by chloroplasts and inhibition of photosynthetic electron transport. Biochim. Biophys. Acta 1977, 460, 113-125.
    • (1977) Biochim. Biophys. Acta , vol.460 , pp. 113-125
    • Tischer, W.1    Strotmann, H.2
  • 24
    • 0002813617 scopus 로고
    • Structure activity correlations of recent herbicides in photosynthetic reactions
    • Greissbuehler H. Ed.; Pergamon Press: Oxford, UK
    • Trebst, A.; Draber, W. Structure activity correlations of recent herbicides in photosynthetic reactions. In Advances in Pesticide Science; Greissbuehler H. Ed.; Pergamon Press: Oxford, UK, 1979; pp. 223-234.
    • (1979) Advances in Pesticide Science , pp. 223-234
    • Trebst, A.1    Draber, W.2
  • 26
    • 4243841714 scopus 로고    scopus 로고
    • Inhibition of photosynthetic electron transport in spinach chloroplasts by 3-and 4-halogeno substituted benzanilides and thiobenzanilides
    • Kralova, K.; Sersen, F.; Kubicova, L.; Waisser, K. Inhibition of photosynthetic electron transport in spinach chloroplasts by 3-and 4-halogeno substituted benzanilides and thiobenzanilides. J. Trace Microprobe Techn. 2000, 18, 251-256.
    • (2000) J. Trace Microprobe Techn. , vol.18 , pp. 251-256
    • Kralova, K.1    Sersen, F.2    Kubicova, L.3    Waisser, K.4
  • 27
    • 0036395603 scopus 로고    scopus 로고
    • Inhibitory effects of substituted benzanilides on photosynthetic electron transport in spinach chloroplasts
    • Kralova, K.; Sersen, F.; Miletin, M., Dolezal, M. Inhibitory effects of substituted benzanilides on photosynthetic electron transport in spinach chloroplasts. Chem. Pap. 2002, 56, 214-217.
    • (2002) Chem. Pap. , vol.56 , pp. 214-217
    • Kralova, K.1    Sersen, F.2    Miletin, M.3    Dolezal, M.4
  • 28
    • 3242787449 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some amides of pyrazine-2-carboxylic acids
    • Dolezal, M.; Miletin, M.; Kunes, J.; Kralova, K. Synthesis and biological evaluation of some amides of pyrazine-2-carboxylic acids. Molecules 2002, 7, 363-373.
    • (2002) Molecules , vol.7 , pp. 363-373
    • Dolezal, M.1    Miletin, M.2    Kunes, J.3    Kralova, K.4
  • 29
    • 33646406340 scopus 로고    scopus 로고
    • Substituted pyrazinecarboxamides: Synthesis and biological evaluation
    • Dolezal, M.; Palek, L.; Vinsova, J.; Buchta, V.; Jampilek, J.; Kralova, K. Substituted pyrazinecarboxamides: synthesis and biological evaluation. Molecules 2006, 11, 242-256.
    • (2006) Molecules , vol.11 , pp. 242-256
    • Dolezal, M.1    Palek, L.2    Vinsova, J.3    Buchta, V.4    Jampilek, J.5    Kralova, K.6
  • 30
    • 70350469455 scopus 로고    scopus 로고
    • 21 September
    • http://www.who.int/tb/publications/global-report/2008/summary/en/index. html/ (21 September 2009).
    • (2009)
  • 31
    • 0037841362 scopus 로고    scopus 로고
    • The global situation of MDR-TB
    • Espinal, M.A. The global situation of MDR-TB. Tuberculosis 2003, 83, 44-51.
    • (2003) Tuberculosis , vol.83 , pp. 44-51
    • Espinal, M.A.1
  • 32
    • 33745131823 scopus 로고    scopus 로고
    • Lung disease due to the more common nontuberculous mycobacteria
    • Field, S.K.; Cowie, R.L. Lung disease due to the more common nontuberculous mycobacteria. Chest 2006, 129, 1653-1672.
    • (2006) Chest , vol.129 , pp. 1653-1672
    • Field, S.K.1    Cowie, R.L.2
  • 33
    • 4844224397 scopus 로고    scopus 로고
    • Nontuberculous mycobacterial infections: A clinical review
    • Wagner, D.; Young, L.S. Nontuberculous mycobacterial infections: A clinical review. Infection 2004, 32, 257-270.
    • (2004) Infection , vol.32 , pp. 257-270
    • Wagner, D.1    Young, L.S.2
  • 35
    • 70350436833 scopus 로고    scopus 로고
    • 21 September
    • http://www.doctorfungus.org/ (21 September 2009).
    • (2009)
  • 36
    • 4444267246 scopus 로고    scopus 로고
    • Synergistic mixtures of fungitoxic monochloro- and dichloro-8-quinolinols against five fungi
    • Gershon, H; Gershon, M; Clarke, D.D. Synergistic mixtures of fungitoxic monochloro- and dichloro-8-quinolinols against five fungi. Mycopathologia 2004, 158, 131-135.
    • (2004) Mycopathologia , vol.158 , pp. 131-135
    • Gershon H1    Gershon M2    Clarke, D.D.3
  • 37
    • 1342279423 scopus 로고    scopus 로고
    • Antileishmanial activity of a new 8-hydroxyquinoline derivative designed 7-[5'-(3'-phenylisoxazolino)methyl]-8-hydroxyquinoline: Preliminary study
    • Dardari, Z.; Lemrani, M.; Bahloul, A.; Sebban, A.; Hassar, M.; Kitane, S.; Berrada, M.; Boudouma, M. Antileishmanial activity of a new 8-hydroxyquinoline derivative designed 7-[5'-(32 -phenylisoxazolino)methyl]-8- hydroxyquinoline: preliminary study. Farmaco 2004, 59, 195-199.
    • (2004) Farmaco , vol.59 , pp. 195-199
    • Dardari, Z.1    Lemrani, M.2    Bahloul, A.3    Sebban, A.4    Hassar, M.5    Kitane, S.6    Berrada, M.7    Boudouma, M.8
  • 38
    • 33748673779 scopus 로고    scopus 로고
    • An efficient microwave-assisted synthesis of structurally diverse styrylquinolines
    • Musiol, R.; Podeszwa, B.; Finster, J.; Niedbala, H.; Polanski; J. An efficient microwave-assisted synthesis of structurally diverse styrylquinolines. Monatsh. Chem. 2006, 137, 1211-1217.
    • (2006) Monatsh. Chem. , vol.137 , pp. 1211-1217
    • Musiol, R.1    Podeszwa, B.2    Finster, J.3    Niedbala, H.4    Polanski, J.5
  • 42
    • 0035468033 scopus 로고    scopus 로고
    • Physicochemical profiling (permeability, solubility, charge state)
    • Avdeef, A. Physicochemical profiling (permeability, solubility, charge state). Curr. Topics Med. Chem. 2001, 1, 277-351.
    • (2001) Curr. Topics Med. Chem. , vol.1 , pp. 277-351
    • Avdeef, A.1
  • 43
    • 84946900757 scopus 로고    scopus 로고
    • Lipophilicity in drug action and toxicology
    • 1st ed.; Pliska, V., Testa, B., van der Waterbeemd, H. Eds.; Wiley-VCH: Weinheim, DE
    • Pliska, V. Lipophilicity in drug action and toxicology. In Methods and Principles in Medicinal Chemistry, 1st ed.; Pliska, V., Testa, B., van der Waterbeemd, H. Eds.; Wiley-VCH: Weinheim, DE, 1996; Vol. 4, pp. 1-6.
    • (1996) Methods and Principles in Medicinal Chemistry , vol.4 , pp. 1-6
    • Pliska, V.1
  • 44
    • 2342635206 scopus 로고    scopus 로고
    • Application of high-performance liquid chromatography based measurements of lipophilicity to model biological distribution
    • Valko, K. Application of high-performance liquid chromatography based measurements of lipophilicity to model biological distribution. J. Chromatogr. A 2004, 1037, 299-310.
    • (2004) J. Chromatogr. A , vol.1037 , pp. 299-310
    • Valko, K.1
  • 46
    • 0031838093 scopus 로고    scopus 로고
    • Role of stationary phase and eluent composition on the determination of log P values of N-hydroxyethylamide of aryloxyalkylen and pyridine carboxylic acids by reversed-phase high-performance liquid chromatography
    • Cimpan, G.; Irimie, F.; Gocan, S.; Claessens, H.A. Role of stationary phase and eluent composition on the determination of log P values of N-hydroxyethylamide of aryloxyalkylen and pyridine carboxylic acids by reversed-phase high-performance liquid chromatography. J. Chromatogr. B 1998, 714, 247-261.
    • (1998) J. Chromatogr. B , vol.714 , pp. 247-261
    • Cimpan, G.1    Irimie, F.2    Gocan, S.3    Claessens, H.A.4
  • 47
    • 85051689627 scopus 로고    scopus 로고
    • Lipophilicity measurements by liquid chromatography
    • Gocan, S.; Cimpan, G.; Comer, J. Lipophilicity measurements by liquid chromatography. Adv. Chromatogr. 2006, 44, 79-176.
    • (2006) Adv. Chromatogr. , vol.44 , pp. 79-176
    • Gocan, S.1    Cimpan, G.2    Comer, J.3
  • 48
    • 13244282955 scopus 로고    scopus 로고
    • Lipophilicity - Beyond octanol/water: A short comparison of modern technologies
    • Hartmann, T.; Schmitt, J. Lipophilicity - beyond octanol/water: A short comparison of modern technologies. Drug Discov. Today Technol. 2004, 1, 431-439.
    • (2004) Drug Discov. Today Technol. , vol.1 , pp. 431-439
    • Hartmann, T.1    Schmitt, J.2
  • 49
    • 0037278031 scopus 로고    scopus 로고
    • Chromatographic retention parameters in medicinal chemistry and molecular pharmacology
    • Nasal, A.; Siluk, D.; Kaliszan, R. Chromatographic retention parameters in medicinal chemistry and molecular pharmacology. Curr. Med. Chem. 2003, 10, 381-426.
    • (2003) Curr. Med. Chem. , vol.10 , pp. 381-426
    • Nasal, A.1    Siluk, D.2    Kaliszan, R.3
  • 50
    • 0032406026 scopus 로고    scopus 로고
    • Determination of the lipophilicity of aroma compounds by RP-HPLC
    • Piraprez, G.; Herent, M.F.; Collin, S. Determination of the lipophilicity of aroma compounds by RP-HPLC. Flavour Fragr. J. 1998, 13, 400-408.
    • (1998) Flavour Fragr. J. , vol.13 , pp. 400-408
    • Piraprez, G.1    Herent, M.F.2    Collin, S.3
  • 51
    • 0030668789 scopus 로고    scopus 로고
    • Hydrophobicity parameters determined by reversedphase liquid chromatography. XII. Comparison of capacity factors and octane/methanol-water partition coefficients for monosubstituted pyrazines, and effect of octanol added to both partitioning systems
    • Yamagami, C.; Iwasaki, K.; Ishikawa, A. Hydrophobicity parameters determined by reversedphase liquid chromatography. XII. Comparison of capacity factors and octane/methanol-water partition coefficients for monosubstituted pyrazines, and effect of octanol added to both partitioning systems. Chem. Pharm. Bull. 1997, 45, 1653-1658.
    • (1997) Chem. Pharm. Bull. , vol.45 , pp. 1653-1658
    • Yamagami, C.1    Iwasaki, K.2    Ishikawa, A.3
  • 52
    • 0032732592 scopus 로고    scopus 로고
    • Measurement and prediction of hydrophobicity parameters for highly lipophilic compounds: Application of the HPLC column-switching technique to measurement of log P of diarylpyrazines
    • Yamagami, C.; Araki, K.; Ohnishi, K.; Hanasato, K.; Inaba, H.; Aono, M.; Ohta, A. Measurement and prediction of hydrophobicity parameters for highly lipophilic compounds: Application of the HPLC column-switching technique to measurement of log P of diarylpyrazines. J. Pharm. Sci. 1999, 88, 1299-1304.
    • (1999) J. Pharm. Sci. , vol.88 , pp. 1299-1304
    • Yamagami, C.1    Araki, K.2    Ohnishi, K.3    Hanasato, K.4    Inaba, H.5    Aono, M.6    Ohta, A.7
  • 56
    • 0142248977 scopus 로고    scopus 로고
    • Substituted 5-aroylpyrazine-2-carboxylic acid derivatives: Synthesis and biological activity
    • Dolezal, M.; Jampilek, J.; Osicka, Z.; Kunes, J.; Buchta, V.; Vichova, P. Substituted 5-aroylpyrazine-2-carboxylic acid derivatives: Synthesis and biological activity. Farmaco 2003, 58, 1105-1111.
    • (2003) Farmaco , vol.58 , pp. 1105-1111
    • Dolezal, M.1    Jampilek, J.2    Osicka, Z.3    Kunes, J.4    Buchta, V.5    Vichova, P.6
  • 58
    • 70350469454 scopus 로고    scopus 로고
    • Synthesis and hydrophobic properties of substituted 2-aryl- 5,7-di-tert-butylbenzoxazoles
    • November 1-30, [CD-ROM ed.]; Seijas, J.A., Tato, M.P.V., Eds.; MDPI: Basel, Switzerland, 2006; a003
    • Jampilek, J.; Vinsova, J.; Dohnal, J. Synthesis and hydrophobic properties of substituted 2-aryl- 5,7-di-tert-butylbenzoxazoles. In Proceedings of the 10th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-10), November 1-30, 2006 [CD-ROM ed.]; Seijas, J.A., Tato, M.P.V., Eds.; MDPI: Basel, Switzerland, 2006; a003.
    • (2006) Proceedings of the 10th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-10)
    • Jampilek, J.1    Vinsova, J.2    Dohnal, J.3
  • 60
    • 0016592909 scopus 로고
    • Physicochemical-activity relations in practice. 1. Rational and self-consistent data bank
    • Norrington, F.E.; Hyde, R.M.; Williams, S.G.; Wotton, R. Physicochemical-activity relations in practice. 1. Rational and self-consistent data bank. J. Med. Chem. 1975, 18, 604-607.
    • (1975) J. Med. Chem. , vol.18 , pp. 604-607
    • Norrington, F.E.1    Hyde, R.M.2    Williams, S.G.3    Wotton, R.4
  • 61
    • 20844460406 scopus 로고    scopus 로고
    • Estimation of Hammett sigma constants of substituted benzenes through accurate density-functional calculation of core-electron binding energy shifts
    • Takahata, Y.; Chong, D.P. Estimation of Hammett sigma constants of substituted benzenes through accurate density-functional calculation of core-electron binding energy shifts. Int. J. Quantum Chem. 2005, 103, 509-515.
    • (2005) Int. J. Quantum Chem. , vol.103 , pp. 509-515
    • Takahata, Y.1    Chong, D.P.2
  • 62
    • 0000567650 scopus 로고
    • Phosphoramides. XII. Phosphorus pentaoxide - Amine hydrochloride as reagents in the synthesis of 4-(3H)-quinazolinones and 4-quinazolinamines
    • Nielsen, K.E.; Pedersen, E.B. Phosphoramides. XII. Phosphorus pentaoxide - amine hydrochloride as reagents in the synthesis of 4-(3H)-quinazolinones and 4-quinazolinamines. Acta Chem. Scand. Ser. B 1980, 34, 637-642.
    • (1980) Acta Chem. Scand. Ser. B , vol.34 , pp. 637-642
    • Nielsen, K.E.1    Pedersen, E.B.2
  • 64
    • 0142010661 scopus 로고    scopus 로고
    • Search for substances with antioxidant and antiamnestic activities among 2-substituted 4-(3H)-quinazolones
    • Kovalenko, S.; Belenichev, I.; Nikitin, V.; Karpenko, A. Search for substances with antioxidant and antiamnestic activities among 2-substituted 4-(3H)-quinazolones. Acta Pol. Pharm. Drug Design 2003, 60, 275-279.
    • (2003) Acta Pol. Pharm. Drug Design , vol.60 , pp. 275-279
    • Kovalenko, S.1    Belenichev, I.2    Nikitin, V.3    Karpenko, A.4
  • 65
    • 0018028466 scopus 로고
    • Synthesis of some 2-styrylquinazoline derivatives structurally related to certain chemotherapeutic agents
    • Botros, S.; Shaban, M. Synthesis of some 2-styrylquinazoline derivatives structurally related to certain chemotherapeutic agents. Pharmazie 1978, 33, 646-647.
    • (1978) Pharmazie , vol.33 , pp. 646-647
    • Botros, S.1    Shaban, M.2
  • 66
    • 77958522863 scopus 로고    scopus 로고
    • Approaches to measuring plant photosynthesis activity
    • 2nd Ed.; Pessarakli, M., Eds.; Taylor & Francis Group: Boca Raton, London-New York-Singapore
    • Masarovicova, E.; Kralova, K. Approaches to measuring plant photosynthesis activity. In Handbook of Photosynthesis, 2nd Ed.; Pessarakli, M., Eds.; Taylor & Francis Group: Boca Raton, London-New York-Singapore, 2005; pp. 617-656.
    • (2005) Handbook of Photosynthesis , pp. 617-656
    • Masarovicova, E.1    Kralova, K.2
  • 67
    • 0000873980 scopus 로고
    • Photosynthesis inhibition produced by 2-alkylthio-6-Rbenzothiazoles
    • Kralova, K.; Sersen, F.; Sidoova, E. Photosynthesis inhibition produced by 2-alkylthio-6-Rbenzothiazoles. Chem. Pap. 1992, 46, 348-350.
    • (1992) Chem. Pap. , vol.46 , pp. 348-350
    • Kralova, K.1    Sersen, F.2    Sidoova, E.3
  • 70
    • 0003443223 scopus 로고    scopus 로고
    • National Committee for Clinical Laboratory standards. Approved Standard, NCCLS document M27-A; NCCLS: Villanova, PA, USA
    • National Committee for Clinical Laboratory standards. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeast. Approved Standard, NCCLS document M27-A; NCCLS: Villanova, PA, USA, 1997.
    • (1997) Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeast


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