메뉴 건너뛰기




Volumn 31, Issue 6, 2016, Pages 1132-1138

Synthesis and anticancer and lipophilic properties of 10-dialkylaminobutynyl derivatives of 1,8- and 2,7-diazaphenothiazines

Author keywords

Antiproliferative activity; BACL 2 BAX ratio; dialkylaminoalkynyl substituents; dipyridothiazines; phenothiazines

Indexed keywords

1,8 DIAZAPHENOTHIAZINE DERIVATIVE; 10 (4 MORPHOLIN 4 YL BUT 2 YNYL) 1,8 DIAZAPHENOTHIAZINE; 10 (4 MORPHOLIN 4 YL BUT 2 YNYL) 2,7 DIAZAPHENOTHIAZINE; 10 (4 PIPERIDIN 1 YL BUT 2 YNYL) 1,8 DIAZAPHENOTHIAZINE; 10 (4 PIPERIDIN 1 YL BUT 2 YNYL) 2,7 DIAZAPHENOTHIAZINE; 10 (4 PYRROLIDIN 1 YL BUT 2 YNYL) 1,8 DIAZAPHENOTHIAZINE; 10 (4 PYRROLIDIN 1 YL BUT 2 YNYL) 2,7 DIAZAPHENOTHIAZINE; 10 DIALKYLAMINOBUTYNYL DERIVATIVE; 10 PROPARGYL 1,8 DIAZAPHENOTHIAZINE DERIVATIVE; 10 PROPARGYL 2,7 DIAZAPHENOTHIAZINE DERIVATIVE; 10 [4 (4 METHYLPIPERAZIN 1 YL)BUT 2 YNYL] 1,8 DIAZAPHENOTHIAZINE; 10 [4 (4 METHYLPIPERAZIN 1 YL)BUT 2 YNYL] 2,7 DIAZAPHENOTHIAZINE; 10 [4 (4 PHENYLPIPERAZIN 1 YL)BUT 2 YNYL] 1,8 DIAZAPHENOTHIAZINE; 10 [4 (4 PHENYLPIPERAZIN 1 YL)BUT 2 YNYL] 2,7 DIAZAPHENOTHIAZINE; 10 [4 (N ETHYL N METHYL)AMINO BUT 2 YNYL] 1,8 DIAZAPHENOTHIAZINE; 10 [4 (N ETHYL N METHYL)AMINO BUT 2 YNYL] 2,7 DIAZAPHENOTHIAZINE; 10 [4 (N,N DIETHYL)AMINO BUT 2 YNYL] 1,8 DIAZAPHENOTHIAZINE; 10 [4 (N,N DIETHYL)AMINO BUT 2 YNYL] 2,7 DIAZAPHENOTHIAZINE; 2,7 DIAZAPHENOTHIAZINE DERIVATIVE; ACETYLENE; AMINE; ANTINEOPLASTIC AGENT; CISPLATIN; CYCLIN DEPENDENT KINASE INHIBITOR 1A; FUNCTIONAL GROUP; PHENOTHIAZINE DERIVATIVE; PROTEIN BAX; PROTEIN BCL 2; PROTEIN P53; PROTHIPENDYL; UNCLASSIFIED DRUG; PHENOTHIAZINE;

EID: 84989316822     PISSN: 14756366     EISSN: 14756374     Source Type: Journal    
DOI: 10.3109/14756366.2015.1101092     Document Type: Article
Times cited : (24)

References (57)
  • 2
    • 33646155333 scopus 로고    scopus 로고
    • Retrosynthetic approach to the synthesis of phenothiazines
    • New York: Elsevier
    • I.A.Silberg, G.Cormos, D.C.Oniciu Retrosynthetic approach to the synthesis of phenothiazines. In:Katritzky AR, ed. Advances in heterocyclic chemistry. New York:Elsevier; 2006:205
    • (2006) Advances in heterocyclic chemistry , pp. 205
    • Silberg, I.A.1    Cormos, G.2    Oniciu, D.C.3
  • 3
    • 66349113472 scopus 로고    scopus 로고
    • Synthesis and properties of diaza-, triaza- and tetraazaphenothiazines
    • K.Pluta, B.Morak-Młodawska, M.Jeleń Synthesis and properties of diaza-, triaza- and tetraazaphenothiazines. J Heterocycl Chem 2009;46:355–91
    • (2009) J Heterocycl Chem , vol.46 , pp. 355-391
    • Pluta, K.1    Morak-Młodawska, B.2    Jeleń, M.3
  • 4
    • 79958257266 scopus 로고    scopus 로고
    • Recent progress in biological activities of synthesized phenothiazines
    • K.Pluta, B.Morak-Młodawska, M.Jeleń Recent progress in biological activities of synthesized phenothiazines. Eur J Med Chem 2011;46:3179–89
    • (2011) Eur J Med Chem , vol.46 , pp. 3179-3189
    • Pluta, K.1    Morak-Młodawska, B.2    Jeleń, M.3
  • 5
    • 0034329373 scopus 로고    scopus 로고
    • Antitumor potential and possible targets of phenothiazine-related compounds
    • N.Motohashi, M.Kawase, S.Saito, H.Sakagami Antitumor potential and possible targets of phenothiazine-related compounds. Curr Drug Targets 2000;1:237–45
    • (2000) Curr Drug Targets , vol.1 , pp. 237-245
    • Motohashi, N.1    Kawase, M.2    Saito, S.3    Sakagami, H.4
  • 7
    • 77955552597 scopus 로고    scopus 로고
    • Bioactive phenothiazines and benzo[a]phenothiazines: spectroscopic studies and biological and biomedical properties and applications
    • J.J.Aaron, M.D.Gaye Seye, S.Trajkovska, N.Motohashi Bioactive phenothiazines and benzo[a]phenothiazines:spectroscopic studies and biological and biomedical properties and applications. Top Heterocycl Chem 2009;16:153–231
    • (2009) Top Heterocycl Chem , vol.16 , pp. 153-231
    • Aaron, J.J.1    Gaye Seye, M.D.2    Trajkovska, S.3    Motohashi, N.4
  • 8
    • 79953210160 scopus 로고    scopus 로고
    • Antibacterial activity of artificial phenothiazines and isoflavones from plants
    • A.Dasgupta, S.G.Dastridara, Y.Shirataki, N.Motohashi Antibacterial activity of artificial phenothiazines and isoflavones from plants. Top Heterocycl Chem 2008;15:67–132
    • (2008) Top Heterocycl Chem , vol.15 , pp. 67-132
    • Dasgupta, A.1    Dastridara, S.G.2    Shirataki, Y.3    Motohashi, N.4
  • 9
    • 57949111337 scopus 로고    scopus 로고
    • 10H-Phenothiazines: a new class of enzyme inhibitors for inflammatory diseases
    • Y.S.Sadandam, M.M.Shetty, A.Bhaskar Rao 10H-Phenothiazines:a new class of enzyme inhibitors for inflammatory diseases. Eur J Med Chem 2009;44:197–202
    • (2009) Eur J Med Chem , vol.44 , pp. 197-202
    • Sadandam, Y.S.1    Shetty, M.M.2    Bhaskar Rao, A.3
  • 10
    • 0035172946 scopus 로고    scopus 로고
    • Phenothiazines: potential management of Creutzfeldt-Jacob disease and its variants
    • L.Amaral, J.E.Kristiansen Phenothiazines:potential management of Creutzfeldt-Jacob disease and its variants. Int J Antimicrob Agents 2001;18:411–17
    • (2001) Int J Antimicrob Agents , vol.18 , pp. 411-417
    • Amaral, L.1    Kristiansen, J.E.2
  • 11
    • 21344462866 scopus 로고    scopus 로고
    • The in vitro activity of phenothiazines against Mycobacterium avium: potential of thioridazine for therapy of the co-infected AIDS patient
    • M.Viveiros, M.Martins, I.Couto,. The in vitro activity of phenothiazines against Mycobacterium avium:potential of thioridazine for therapy of the co-infected AIDS patient. In Vivo 2005;19:733–6
    • (2005) In Vivo , vol.19 , pp. 733-736
    • Viveiros, M.1    Martins, M.2    Couto, I.3
  • 12
    • 79955575049 scopus 로고    scopus 로고
    • Acylamino-phenothiazines: neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer’s disease
    • G.C.González-Muñoz, M.P.Arce, B.López,. Acylamino-phenothiazines:neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer’s disease. Eur J Med Chem 2011;46:2224–35
    • (2011) Eur J Med Chem , vol.46 , pp. 2224-2235
    • González-Muñoz, G.C.1    Arce, M.P.2    López, B.3
  • 13
    • 77957752527 scopus 로고    scopus 로고
    • Multiple non-psychiatric effects of phenothiazines: a review
    • G.Sudeshna, K.Parimal Multiple non-psychiatric effects of phenothiazines:a review. Eur J Pharmacol 2010;648:6–14
    • (2010) Eur J Pharmacol , vol.648 , pp. 6-14
    • Sudeshna, G.1    Parimal, K.2
  • 14
    • 84862187466 scopus 로고    scopus 로고
    • Chemical structure of phenothiazines and their biological activity
    • A.Jaszczyszy, K.Gąsiorowski, P.Świątek,. Chemical structure of phenothiazines and their biological activity. Pharmacol Rep 2012;64:16–23
    • (2012) Pharmacol Rep , vol.64 , pp. 16-23
    • Jaszczyszy, A.1    Gąsiorowski, K.2    Świątek, P.3
  • 15
    • 84897441779 scopus 로고    scopus 로고
    • Harnessing the lysosome-dependent antitumor activity of phenothiazines in human small cell lung cancer
    • Z.Zong, K.Zielinska-Chomej, T.Juntti,. Harnessing the lysosome-dependent antitumor activity of phenothiazines in human small cell lung cancer. Cell Death Dis 2014;5:e1111
    • (2014) Cell Death Dis , vol.5 , pp. 1111
    • Zong, Z.1    Zielinska-Chomej, K.2    Juntti, T.3
  • 16
    • 84869222731 scopus 로고    scopus 로고
    • Anticancer (hexacarbonyldocobalt)propargyl aryl ethers: synthesis, antiproliferative activity, apoptosis induction, and effct on cellular oxidative stress
    • S.D.Schimler, D.J.Hall, S.L.Debbert Anticancer (hexacarbonyldocobalt)propargyl aryl ethers:synthesis, antiproliferative activity, apoptosis induction, and effct on cellular oxidative stress. J Inorg Biochem 2013;119:28–37
    • (2013) J Inorg Biochem , vol.119 , pp. 28-37
    • Schimler, S.D.1    Hall, D.J.2    Debbert, S.L.3
  • 17
    • 79960764010 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activity of some new 2,6-substituted purines
    • N.G.Kode, S.Phadtare Synthesis and cytotoxic activity of some new 2,6-substituted purines. Molecules 2011;16:5840–60
    • (2011) Molecules , vol.16 , pp. 5840-5860
    • Kode, N.G.1    Phadtare, S.2
  • 18
    • 84876764238 scopus 로고    scopus 로고
    • Synthesis, structure and cytotoxic activity of new acetylenic derivatives of betulin
    • S.Boryczka, E.Bębenek, J.Wietrzyk,. Synthesis, structure and cytotoxic activity of new acetylenic derivatives of betulin. Molecules 2013;18:4526–43
    • (2013) Molecules , vol.18 , pp. 4526-4543
    • Boryczka, S.1    Bębenek, E.2    Wietrzyk, J.3
  • 19
    • 84894139178 scopus 로고    scopus 로고
    • 2[N-Alkyl(R-phenyl)-aminomethyl]-3-phenyl-7-trifluoromethylquinoxalines as anticancer agents inhibitors of folateenzymes
    • S.Piras, A.Carta, I.Briguglio,. 2[N-Alkyl(R-phenyl)-aminomethyl]-3-phenyl-7-trifluoromethylquinoxalines as anticancer agents inhibitors of folateenzymes. Eur J Med Chem 2014;75:169–83
    • (2014) Eur J Med Chem , vol.75 , pp. 169-183
    • Piras, S.1    Carta, A.2    Briguglio, I.3
  • 20
    • 84895835370 scopus 로고    scopus 로고
    • A convergent synthesis of alkyneeazide cycloaddition derivatives of 4-a,b-2-propyne podophyllotoxin depicting potent cytotoxic activity
    • M.K.Zilla, D.Nayak, R.A.Vishwakarma,. A convergent synthesis of alkyneeazide cycloaddition derivatives of 4-a,b-2-propyne podophyllotoxin depicting potent cytotoxic activity. Eur J Med Chem 2014;77:47–55
    • (2014) Eur J Med Chem , vol.77 , pp. 47-55
    • Zilla, M.K.1    Nayak, D.2    Vishwakarma, R.A.3
  • 22
    • 79955473280 scopus 로고    scopus 로고
    • Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero)arylethynyl thiophene derivatives
    • R.Romagnoli, P.G.Baraldi, O.Cruz-Lopez,. Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero)arylethynyl thiophene derivatives. Bioorg Med Chem Lett 2011;21:2746–51
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 2746-2751
    • Romagnoli, R.1    Baraldi, P.G.2    Cruz-Lopez, O.3
  • 23
    • 62849118422 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activity of 7-alkynyl camptothecin derivatives
    • F.Xiao, Y.Xue, Y.Luo,. Synthesis and cytotoxic activity of 7-alkynyl camptothecin derivatives. Chinese Chem Lett 2009;20:566–8
    • (2009) Chinese Chem Lett , vol.20 , pp. 566-568
    • Xiao, F.1    Xue, Y.2    Luo, Y.3
  • 24
    • 67650178255 scopus 로고    scopus 로고
    • Efficient synthesis of the first betulonic acid-acetylene hybrids and their hepatoprotective and anti-inflammatory activity
    • S.F.Vasilevsky, A.I.Govdi, E.E.Shults,. Efficient synthesis of the first betulonic acid-acetylene hybrids and their hepatoprotective and anti-inflammatory activity. Bioorg Med Chem 2009;17:5164–9
    • (2009) Bioorg Med Chem , vol.17 , pp. 5164-5169
    • Vasilevsky, S.F.1    Govdi, A.I.2    Shults, E.E.3
  • 25
    • 84871431464 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of 4,5-diaryl-2-[4-(tamino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-ones
    • E.N.Al-Kaissi, N.F.Al-Ghrary, N.K.Al-Kaisi,. Synthesis and antimicrobial evaluation of 4,5-diaryl-2-[4-(tamino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-ones. Bioorg Med Chem Lett 2012;21:3390–5
    • (2012) Bioorg Med Chem Lett , vol.21 , pp. 3390-3395
    • Al-Kaissi, E.N.1    Al-Ghrary, N.F.2    Al-Kaisi, N.K.3
  • 26
    • 84864623309 scopus 로고    scopus 로고
    • Synthesis and antibacterial evaluation of a new series of N-alkyl-2-alkynyl/(E)-alkenyl-4-(1H)-quinolones
    • A.Wube, J.D.Guzman, A.Hüfner,. Synthesis and antibacterial evaluation of a new series of N-alkyl-2-alkynyl/(E)-alkenyl-4-(1H)-quinolones. Molecules 2012;17:8217–40
    • (2012) Molecules , vol.17 , pp. 8217-8240
    • Wube, A.1    Guzman, J.D.2    Hüfner, A.3
  • 27
    • 34250790689 scopus 로고    scopus 로고
    • Synthesis and anti-HIV-1 activity of new MKC-442 analogues with an alkynyl-substituted 6-benzyl group
    • Y.L.Aly, E.B.Pedersen, P.La Colla, R.Lodda Synthesis and anti-HIV-1 activity of new MKC-442 analogues with an alkynyl-substituted 6-benzyl group. Arch Pharm 2007;340:225–35
    • (2007) Arch Pharm , vol.340 , pp. 225-235
    • Aly, Y.L.1    Pedersen, E.B.2    La Colla, P.3    Lodda, R.4
  • 28
    • 34250888819 scopus 로고    scopus 로고
    • 5Alkynyl analogs of arabinouridine and 2‘-deoxyuridine: cytostatic activity against herpes simplex virus and varicella-zoster thymidine kinase gene-transfected cells
    • W.A.Cristofoli, L.I.Wiebe, E.De Clercq,. 5Alkynyl analogs of arabinouridine and 2‘-deoxyuridine:cytostatic activity against herpes simplex virus and varicella-zoster thymidine kinase gene-transfected cells. J Med Chem 2007;50:2851–7
    • (2007) J Med Chem , vol.50 , pp. 2851-2857
    • Cristofoli, W.A.1    Wiebe, L.I.2    De Clercq, E.3
  • 29
    • 0036189146 scopus 로고    scopus 로고
    • Antioxidant activity of synthetic cytokinin analogues: 6-alkynyl- and 6-alkenylpurines as novel 15-lipoxygenase inhibitors
    • A.Bräthe, G.Andresen, L.L.Gundersen,. Antioxidant activity of synthetic cytokinin analogues:6-alkynyl- and 6-alkenylpurines as novel 15-lipoxygenase inhibitors. Bioorg Med Chem 2002;10:1581–6
    • (2002) Bioorg Med Chem , vol.10 , pp. 1581-1586
    • Bräthe, A.1    Andresen, G.2    Gundersen, L.L.3
  • 30
    • 44849117020 scopus 로고    scopus 로고
    • Multidrug resistance reverting activity and antitumor profile of new phenothiazine derivatives
    • A.Bisi, M.Meli, S.Gobbi,. Multidrug resistance reverting activity and antitumor profile of new phenothiazine derivatives. Bioorg Med Chem 2008;16:6474–82
    • (2008) Bioorg Med Chem , vol.16 , pp. 6474-6482
    • Bisi, A.1    Meli, M.2    Gobbi, S.3
  • 31
    • 84872904588 scopus 로고    scopus 로고
    • Lipophilicity-methods of determination and its role in medicinal chemistry
    • E.Rutkowska, K.Pająk, K.Jóźwiak Lipophilicity-methods of determination and its role in medicinal chemistry. Acta Pol Pharm 2013;70:13–18
    • (2013) Acta Pol Pharm , vol.70 , pp. 13-18
    • Rutkowska, E.1    Pająk, K.2    Jóźwiak, K.3
  • 32
    • 84943657905 scopus 로고    scopus 로고
    • Lipophilic study of eight cephalosporins by reversed-phase thin-layer chromatographic method
    • M.Dąbrowska, Ł.Komsta, J.Krzek, K.Kokoszka Lipophilic study of eight cephalosporins by reversed-phase thin-layer chromatographic method. Biomed Chromatogr 2015. [Epub ahead of print]. DOI:10.1002/bmc.3490
    • (2015) Biomed Chromatogr
    • Dąbrowska, M.1    Komsta, Ł.2    Krzek, J.3    Kokoszka, K.4
  • 33
    • 79955599163 scopus 로고    scopus 로고
    • Lipophilicity and its relationship with passive drug permeation
    • X.Liu, B.Testa, A.Fahr Lipophilicity and its relationship with passive drug permeation. Pharm Res 2011;28:962–77
    • (2011) Pharm Res , vol.28 , pp. 962-977
    • Liu, X.1    Testa, B.2    Fahr, A.3
  • 34
    • 84866879823 scopus 로고    scopus 로고
    • The influence of lipophilicity in drug discovery and design
    • J.A.Arnot, S.L.Planey The influence of lipophilicity in drug discovery and design. Expert Opin Drug Discov 2012;7:863–75
    • (2012) Expert Opin Drug Discov , vol.7 , pp. 863-875
    • Arnot, J.A.1    Planey, S.L.2
  • 35
    • 77749315417 scopus 로고    scopus 로고
    • Lipophilicity in drug discovery
    • M.J.Waring Lipophilicity in drug discovery. Expert Opin Drug Discov 2010;5:235–48
    • (2010) Expert Opin Drug Discov , vol.5 , pp. 235-248
    • Waring, M.J.1
  • 36
    • 0023917242 scopus 로고
    • Derivatives of amsacrine: determinants required for high activity against Lewis lung carcinoma
    • B.C.Baguley, G.J.Finlay Derivatives of amsacrine:determinants required for high activity against Lewis lung carcinoma. J Natl Cancer Inst 1988;80:195–9
    • (1988) J Natl Cancer Inst , vol.80 , pp. 195-199
    • Baguley, B.C.1    Finlay, G.J.2
  • 37
    • 0026341704 scopus 로고
    • Influence of lipophilicity on cytotoxicity of anthracyclines in LoVo and LoVo/Dx human cell lines
    • I.Facchetti, M.Grandi, P.Cucchi,. Influence of lipophilicity on cytotoxicity of anthracyclines in LoVo and LoVo/Dx human cell lines. Anticancer Drug Des 1991;6:385–97
    • (1991) Anticancer Drug Des , vol.6 , pp. 385-397
    • Facchetti, I.1    Grandi, M.2    Cucchi, P.3
  • 38
    • 0026759286 scopus 로고
    • Role of lipophilicity in the in vitro antitumour activity of a series of new mitosene compounds
    • M.Maliepaard, N.J.de Mol, L.H.M.Janssen,. Role of lipophilicity in the in vitro antitumour activity of a series of new mitosene compounds. Anticancer Drug Des 1992;7:415–25
    • (1992) Anticancer Drug Des , vol.7 , pp. 415-425
    • Maliepaard, M.1    de Mol, N.J.2    Janssen, L.H.M.3
  • 39
    • 70349897753 scopus 로고    scopus 로고
    • The immunosuppressive activities of newly synthesized azaphenothiazines in human and mouse models
    • M.Zimecki, J.Artym, M.Kocięba,. The immunosuppressive activities of newly synthesized azaphenothiazines in human and mouse models. Cell Mol Biol Lett 2009;14:622–35
    • (2009) Cell Mol Biol Lett , vol.14 , pp. 622-635
    • Zimecki, M.1    Artym, J.2    Kocięba, M.3
  • 40
    • 77953303960 scopus 로고    scopus 로고
    • Anticancer activity of newly synthesized azaphenothiazines from NCI's anticancer screening bank
    • K.Pluta, M.Jeleń, B.Morak-Młodawska,. Anticancer activity of newly synthesized azaphenothiazines from NCI's anticancer screening bank. Pharmacol Rep 2010;62:319–32
    • (2010) Pharmacol Rep , vol.62 , pp. 319-332
    • Pluta, K.1    Jeleń, M.2    Morak-Młodawska, B.3
  • 42
    • 84939898373 scopus 로고    scopus 로고
    • Synthesis and selected immunological properties of 10-substituted 1,8-diazaphenothiazines
    • B.Morak-Młodawska, K.Pluta, M.Zimecki,. Synthesis and selected immunological properties of 10-substituted 1,8-diazaphenothiazines. Med Chem Res 2015;24:1408–18
    • (2015) Med Chem Res , vol.24 , pp. 1408-1418
    • Morak-Młodawska, B.1    Pluta, K.2    Zimecki, M.3
  • 43
    • 67649867158 scopus 로고    scopus 로고
    • Acyl and sulfonyl derivatives of 10-aminoalkyl-2,7-diazaphenothiazines
    • B.Morak-Młodawska, K.Pluta Acyl and sulfonyl derivatives of 10-aminoalkyl-2,7-diazaphenothiazines. Heterocycles 2009;78:1289–98
    • (2009) Heterocycles , vol.78 , pp. 1289-1298
    • Morak-Młodawska, B.1    Pluta, K.2
  • 45
    • 0032197149 scopus 로고    scopus 로고
    • Multivariate analysis of experimental and computational descriptors of molecular lipophilicity
    • R.Mannhold, G.Cruciani, K.Dross, R.Rekker Multivariate analysis of experimental and computational descriptors of molecular lipophilicity. J Comput Aided Mol Des 1998;12:573–81
    • (1998) J Comput Aided Mol Des , vol.12 , pp. 573-581
    • Mannhold, R.1    Cruciani, G.2    Dross, K.3    Rekker, R.4
  • 46
    • 0024656378 scopus 로고
    • A new method for the estimation of partition coefficient
    • N.Bodor, Z.Gabanyi, C.K.Wong A new method for the estimation of partition coefficient. J Am Chem Soc 1989;111:3783–6
    • (1989) J Am Chem Soc , vol.111 , pp. 3783-3786
    • Bodor, N.1    Gabanyi, Z.2    Wong, C.K.3
  • 48
    • 0035853811 scopus 로고    scopus 로고
    • Bax is present as a high molecular weight oligomer/complex in the mitochondrial membrane of apoptotic cells
    • B.Antonsson, S.Montessuit, B.Sanchez, J.C.Martinou Bax is present as a high molecular weight oligomer/complex in the mitochondrial membrane of apoptotic cells. J Biol Chem 2001;276:11615–23
    • (2001) J Biol Chem , vol.276 , pp. 11615-11623
    • Antonsson, B.1    Montessuit, S.2    Sanchez, B.3    Martinou, J.C.4
  • 49
    • 0037427412 scopus 로고    scopus 로고
    • Mechanisms of cytochrome c release by proapoptotic BCL-2 family members
    • L.Scorrano, S.J.Korsmeyer Mechanisms of cytochrome c release by proapoptotic BCL-2 family members. Biochem Biophys Res Commun 2003;304:437–44
    • (2003) Biochem Biophys Res Commun , vol.304 , pp. 437-444
    • Scorrano, L.1    Korsmeyer, S.J.2
  • 51
    • 43749086054 scopus 로고    scopus 로고
    • RPTLC determination of log P of structurally diverse neutral compounds
    • G.Völgyi, K.Deák, J.Válmos,. RPTLC determination of log P of structurally diverse neutral compounds. J Planar Chromatogr 2008;21:143–9
    • (2008) J Planar Chromatogr , vol.21 , pp. 143-149
    • Völgyi, G.1    Deák, K.2    Válmos, J.3
  • 52
    • 80054926399 scopus 로고    scopus 로고
    • Evaluation of the lipophilicity and prediction of biological activity of some N-cyclohexyl-N-substituted-2-phenylacetamide derivatives using RP-TLC
    • D.Vaštag, N.Perišić-Janjić, J.Tomić, S.Petrović Evaluation of the lipophilicity and prediction of biological activity of some N-cyclohexyl-N-substituted-2-phenylacetamide derivatives using RP-TLC. J Planar Chromatog 2011;24:435–40
    • (2011) J Planar Chromatog , vol.24 , pp. 435-440
    • Vaštag, D.1    Perišić-Janjić, N.2    Tomić, J.3    Petrović, S.4
  • 53
    • 84861128866 scopus 로고    scopus 로고
    • Comprehensive evaluation of lipophilicity of biogenic amines and related compounds using different chemically bonded phases and various descriptors
    • D.Casoni, C.Sârbu Comprehensive evaluation of lipophilicity of biogenic amines and related compounds using different chemically bonded phases and various descriptors. J Sep Sci 2012;35:915–21
    • (2012) J Sep Sci , vol.35 , pp. 915-921
    • Casoni, D.1    Sârbu, C.2
  • 54
    • 84861521197 scopus 로고    scopus 로고
    • Evaluation of the lipophilicity of selected uridine derivatives by use of RP-TLC, shake flask, and computational methods
    • J.Paszkowska, B.Kania, I.Wandzik Evaluation of the lipophilicity of selected uridine derivatives by use of RP-TLC, shake flask, and computational methods. J Liq Chromatogr Rel Technol 2012;35:1202–12
    • (2012) J Liq Chromatogr Rel Technol , vol.35 , pp. 1202-1212
    • Paszkowska, J.1    Kania, B.2    Wandzik, I.3
  • 55
    • 0029845112 scopus 로고    scopus 로고
    • Calculation procedures for molecular lipophilicity: a comparative study
    • R.Mannhold, K.Dross Calculation procedures for molecular lipophilicity:a comparative study. Quant Struct-Act Relat 1996;15:403–9
    • (1996) Quant Struct-Act Relat , vol.15 , pp. 403-409
    • Mannhold, R.1    Dross, K.2
  • 56
    • 0032903082 scopus 로고    scopus 로고
    • Ionisation constants and distribution coefficients of phenothiazines and calcium channel antagonists determined by a pH-metric method and correlation with calculated partition coefficients
    • U.Franke, A.Munk, M.Wiese Ionisation constants and distribution coefficients of phenothiazines and calcium channel antagonists determined by a pH-metric method and correlation with calculated partition coefficients. J Pharm Sci 1999;88:89–95
    • (1999) J Pharm Sci , vol.88 , pp. 89-95
    • Franke, U.1    Munk, A.2    Wiese, M.3
  • 57
    • 84941626703 scopus 로고    scopus 로고
    • Estimation of the lipophilicity of new anticancer and immunosuppressive 1,8-diazaphenothiazine derivatives
    • B.Morak-Młodawska, K.Pluta, M.Jeleń Estimation of the lipophilicity of new anticancer and immunosuppressive 1,8-diazaphenothiazine derivatives. J Chromatogr Sci 2015;53:462–6
    • (2015) J Chromatogr Sci , vol.53 , pp. 462-466
    • Morak-Młodawska, B.1    Pluta, K.2    Jeleń, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.