메뉴 건너뛰기




Volumn 26, Issue 5, 2011, Pages 668-680

Synthesis, QSAR and anti-HIV activity of new 5-benzylthio-1,3,4-oxadiazoles derived from α-amino acids

Author keywords

amino acids; 3,4 oxadiazoles; 5 benzylthio 1; Anti HIV activity; QSAR

Indexed keywords

5 BENZYLTHIO 1,3,4 OXADIAZOLE; ALANINE; ALPHA AMINO ACID; ANTIVIRUS AGENT; HYDRAZIDE; METHIONINE; OXADIAZOLE DERIVATIVE; PHENYLALANINE; UNCLASSIFIED DRUG;

EID: 80052830960     PISSN: 14756366     EISSN: 14756374     Source Type: Journal    
DOI: 10.3109/14756366.2010.546792     Document Type: Article
Times cited : (14)

References (26)
  • 1
    • 0031858933 scopus 로고    scopus 로고
    • Instability of the NS5A ISDR of hepatitis C virus during natural course: Take-over of wild type by mutant type or vice-versa driven by immune pressure
    • PII S138663469800014X
    • Hijikata M, Ohta Y, Baba K. Iwata K, Matsumoto M, Mishiro S, Kanai K. Instability of the NS5A ISDR of hepatitis C virus during natural course: take-over of wild type by mutant type or vice-versa driven by immune pressure. Hepatology Res 1998;11:19-25. (Pubitemid 28234440)
    • (1998) Hepatology Research , vol.11 , Issue.1 , pp. 19-25
    • Hijikata, M.1    Ohta, Y.2    Baba, K.3    Iwata, K.4    Matsumoto, M.5    Mishiro, S.6    Kanai, K.7
  • 2
    • 0034877411 scopus 로고    scopus 로고
    • Novel cell culture systems for the hepatitis C virus
    • DOI 10.1016/S0166-3542(01)00164-4, PII S0166354201001644
    • Bartenschlager R, Lohmann V. Novel cell culture systems for the hepatitis C virus. Antiviral Res 2001;52:1-17. (Pubitemid 32800687)
    • (2001) Antiviral Research , vol.52 , Issue.1 , pp. 1-17
    • Bartenschlager, R.1    Lohmann, V.2
  • 4
    • 34047171977 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and anti-HIV activity of some novel benzenesulfonamides bearing 2,5-disubstituted-1-3,4-oxadiazole moiety
    • Iqbal R, Zareef M, Ahmed S, Zaidi JH, Arfan M, Shafque M, Al-Masoudi NA. Synthesis, antimicrobial and anti-HIV activity of some novel benzenesulfonamides bearing 2,5-disubstituted-1,3,4-oxadiazole moiety. J Chin Chem Soc 2006;53:689-696.
    • (2006) J Chin Chem Soc , vol.53 , pp. 689-696
    • Iqbal, R.1    Zareef, M.2    Ahmed, S.3    Zaidi, J.H.4    Arfan, M.5    Shafque, M.6    Al-Masoudi, N.A.7
  • 5
    • 4444361143 scopus 로고    scopus 로고
    • Synthesis, antimicrobial, and anti-HIV-1 activity of certain 5-(1-adamantyl)-2-substituted thio-1,3,4-oxadiazoles and 5-(1-adamantyl)-3- substituted aminomethyl-1,3,4-oxadiazoline-2-thiones
    • DOI 10.1016/j.bmc.2004.07.033, PII S0968089604005395
    • El-Emam AA, Al-Deeb OA, Al-Omar M, Lehmann J. Synthesis, antimicrobial, and anti-HIV-1 activity of certain 5-(1-adamantyl)-2-substituted thio-1,3,4-oxadiazoles and 5-(1-adamantyl)-3-substituted aminomethyl-1,3,4- oxadiazoline-2-thiones. Bioorg Med Chem 2004;12:5107-5113. (Pubitemid 39206283)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.19 , pp. 5107-5113
    • El-Emam, A.A.1    Al-Deeb, O.A.2    Al-Omar, M.3    Lehmann, J.4
  • 7
    • 69449101785 scopus 로고    scopus 로고
    • STARTMRK investigators Safety and efcacy of raltegravir-based versus efavirenz-based combination therapy in treatment-naive patients with HIV-1 infection: A multicentre, double-blind randomised controlled trial
    • Lennox JL, DeJesus E, Lazzarin A, Pollard RB, Madruga JV, Berger DS et al.; STARTMRK investigators. Safety and efcacy of raltegravir-based versus efavirenz-based combination therapy in treatment-naive patients with HIV-1 infection: a multicentre, double-blind randomised controlled trial. Lancet 2009;374:796-806.
    • (2009) Lancet , vol.374 , pp. 796-806
    • Lennox, J.L.1    Dejesus, E.2    Lazzarin, A.3    Pollard, R.B.4    Madruga, J.V.5    Berger, D.S.6
  • 8
    • 33847612920 scopus 로고    scopus 로고
    • Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: Convergence of structure-based drug design and X-ray crystallographic study
    • DOI 10.1016/j.bmcl.2007.01.024, PII S0960894X07000728
    • Yan S, Appleby T, Larson G, Wu JZ, Hamatake RK, Hong Z et al. Tiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: convergence of structure-based drug design and X-ray crystallographic study. Bioorg Med Chem Lett 2007;17:1991-1995. (Pubitemid 46367660)
    • (2007) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.7 , pp. 1991-1995
    • Yan, S.1    Appleby, T.2    Larson, G.3    Wu, J.Z.4    Hamatake, R.K.5    Hong, Z.6    Yao, N.7
  • 10
    • 33845462055 scopus 로고    scopus 로고
    • Anti-influenza virus activities of 4-[(1,2-dihydro-2-oxo-3H-indol-3- ylidene)amino]-N-(4,6-dimethyl-2-pyrimidin-2-yl)benzenesulphonamide and its derivatives
    • Selvam P, Murugesh N, Chandramohan M, Sidwell RW, Wandersee MK, Smee D F. Anti-infuenza virus activities of 4-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene) amino]-N-(4,6-dimethyl-2-pyrimidin-2-yl)benzenesulphonamide and its derivatives. Antiviral Chem Chemother 2006;17:269-274. (Pubitemid 44901471)
    • (2006) Antiviral Chemistry and Chemotherapy , vol.17 , Issue.5 , pp. 269-274
    • Selvam, P.1    Murugesh, N.2    Chandramohan, M.3    Sidwell, R.W.4    Wandersee, M.K.5    Smee, D.F.6
  • 12
    • 23844469822 scopus 로고    scopus 로고
    • Cyclotriazadisulfonamides: Promising new CD4-targeted anti-HIV drugs
    • DOI 10.1093/jac/dki208
    • Vermeire K, Schols D. Cyclotriazadisulfonamides: promising new CD4-targeted anti-HIV drugs. J Antimicrob Chemother 2005;56:270-272. (Pubitemid 41158511)
    • (2005) Journal of Antimicrobial Chemotherapy , vol.56 , Issue.2 , pp. 270-272
    • Vermeire, K.1    Schols, D.2
  • 13
    • 44649091552 scopus 로고    scopus 로고
    • In vitro antitumor and antiviral activities of new benzothiazole and 1,3,4-oxadiazole-2-thione derivatives
    • DOI 10.2478/v10007-008-0007-2, PII X517Q7H577174482
    • Akhtar T, Hameed S, Al-Masoudi NA, Loddo R, La Colla P. In vitro antitumor and antiviral activities of new benzothiazole and 1,3,4-oxadiazole-2- thione. Acta Pharm 2008;58:135-149. (Pubitemid 351777172)
    • (2008) Acta Pharmaceutica , vol.58 , Issue.2 , pp. 135-149
    • Akhtar, T.1    Hameed, S.2    Al-Masoudi, N.A.3    Loddo, R.4    Colla, P.L.5
  • 14
    • 34248162841 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of new chiral 1,2,4-triazoles and 1,3,4-thiadiazoles
    • DOI 10.1002/hc.20282
    • Akhtar T, Hameed S, Al-Masoudi NA, Khan KM. Synthesis, and anti-HIV activity of new chiral 1,2,4-triazoles and 1,3,4-thiadiazoles. Heteroatom Chem 2007;18:316-322. (Pubitemid 46716670)
    • (2007) Heteroatom Chemistry , vol.18 , Issue.3 , pp. 316-322
    • Akhtar, T.1    Hameed, S.2    Al-Masoudi, N.A.3    Khan, K.M.4
  • 15
    • 77949871457 scopus 로고    scopus 로고
    • New 2-(4-aryl)-5-(2-adamantylthiazol-4-yl)-1,3,4-oxadiazoles as potential antiproliferative and antiviral agents
    • Zahid M, Yasin KA, Akhtar T, Rama NH, Hameed S, Al-Masoudi NA., Loddo R, La Colla P. New 2-(4-aryl)-5-(2-adamantylthiazol-4-yl)-1,3,4-oxadiazoles as potential antiproliferative and antiviral agents, ARKIVOC 2009;xi: 85-93.
    • (2009) ARKIVOC , vol.11 , pp. 85-93
    • Zahid, M.1    Yasin, K.A.2    Akhtar, T.3    Rama, N.H.4    Hameed, S.5    Al-Masoudi, N.A.6    Loddo, R.7    La Colla, P.8
  • 16
    • 67649846462 scopus 로고    scopus 로고
    • Synthesisurease inhibition and antimicrobial activities of some chiral 5-aryl-4-(1-phenylpropyl)-2H-1,2,4-triazole-3-(4H)-thione
    • Serwar M, Akhtar T, Hameed S, Khan KM. Synthesis, urease inhibition and antimicrobial activities of some chiral 5-aryl-4-(1-phenylpropyl)-2H-1,2,4- triazole-3-(4H)-thione. ARKIVOC 2009;vii:210-221.
    • (2009) ARKIVOC , vol.7 , pp. 210-221
    • Serwar, M.1    Akhtar, T.2    Hameed, S.3    Khan, K.M.4
  • 17
    • 57349145856 scopus 로고    scopus 로고
    • Synthesesurease inhibition, and antimicrobial studies of some chiral 3-substituted-4-amino-5-thioxo-1H,4H-1, 2,4-triazoles
    • Akhtar T, Hameed S, Khan KM, Choudhary MI. Syntheses, urease inhibition, and antimicrobial studies of some chiral 3-substituted-4-amino-5-thioxo-1H,4H-1, 2,4-triazoles. Med Chem 2008;4:539-543.
    • (2008) Med Chem , vol.4 , pp. 539-543
    • Akhtar, T.1    Hameed, S.2    Khan, K.M.3    Choudhary, M.I.4
  • 18
    • 84988129057 scopus 로고
    • Optimization of parameters for semi-empirical methods
    • Stewart JJP. Optimization of parameters for semi-empirical methods. I Method J Comput Chem 1989;10:209-220.
    • (1989) I Method J Comput Chem , vol.10 , pp. 209-220
    • Stewart, J.J.P.1
  • 19
    • 37549039510 scopus 로고    scopus 로고
    • Short history of SHELX
    • Sheldrick GMA. Short history of SHELX. Acta Cryst 2008;A64:112-122.
    • (2008) Acta Cryst , vol.A64 , pp. 112-122
    • Sheldrick, G.M.A.1
  • 21
    • 19944369750 scopus 로고    scopus 로고
    • Design and Synthesis of New 2-substituted-5-(2-benzylthiophenyl)-1,3,4- oxadiazoles As Benzodiazepine Receptor Agonists
    • Zarghi A, Faizi M, Shafaghi B, Ahadian A, Khojastehpoor HR, Zanganeh V et al. Design and synthesis of new 2-substituted-5-(2-benzylthiophenyl)-1,3,4- oxadiazoles as benzodiazepine receptor agonists. Bioorg Med Chem Lett 2005;15:3126-3129.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 3126-3129
    • Zarghi, A.1    Faizi, M.2    Shafaghi, B.3    Ahadian, A.4    Khojastehpoor, H.R.5    Zanganeh, V.6
  • 22
    • 18244410412 scopus 로고    scopus 로고
    • 5-Furan-2yl[1,3,4]oxadiazole-2-thiol, 5-furan-2yl-4h [1,2,4] triazole-3-thiol and their thiol-thione tautomerism
    • Koparir M, Cetin A, Cansiz A. 5-Furan-2-yl[1,3,4]oxadiazole-2-thiol, 5-furan-2yl-4H [1,2,4] triazole-3-thiol and their thiol-thione tautomerism. Molecules 2005;10:475-480. (Pubitemid 40632788)
    • (2005) Molecules , vol.10 , Issue.2 , pp. 475-480
    • Koparir, M.1    Cetin, A.2    Cansiz, A.3
  • 23
    • 0025740266 scopus 로고
    • Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. Tricyclic pyridobenzo-and dipyridodiazepinones
    • Hargrave KD, Proudfoot JR, Grozinger KG, Cullen E, Kapadia SR, Patel UR et al. Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. Tricyclic pyridobenzo-and dipyridodiazepinones. J Med Chem 1991;34:2231-2241.
    • (1991) J Med Chem , vol.34 , pp. 2231-2241
    • Hargrave, K.D.1    Proudfoot, J.R.2    Grozinger, K.G.3    Cullen, E.4    Kapadia, S.R.5    Patel, U.R.6
  • 24
    • 0001707601 scopus 로고
    • 3'-Azido-3'-deoxythymidine (BW A509U): An antiviral agent that inhibits the infectivity and cytopathic effect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro
    • DOI 10.1073/pnas.82.20.7096
    • Mitsuya H, Weinhold KJ, Furman PA, St Clair MH, Lehrman SN, Gallo RC et al. 3′-Azido-3′-deoxythymidine (BW A509U): an antiviral agent that inhibits the infectivity and cytopathic efect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro. Proc Natl Acad Sci USA 1985;82:7096-7100. (Pubitemid 16209699)
    • (1985) Proceedings of the National Academy of Sciences of the United States of America , vol.82 , Issue.20 , pp. 7096-7100
    • Mitsuya, H.1    Weinhold, K.J.2    Furman, P.A.3
  • 26
    • 39149103710 scopus 로고    scopus 로고
    • 2D-QSAR studies on phenoxybenzoic acid derivatives: A novel class of 5α-reductase inhibitors
    • Rui OM, Qian L. I. 2D-QSAR studies on phenoxybenzoic acid derivatives: A novel class of 5α-reductase inhibitors. Chinese J Struct Chem 2008; 27: 105-111.
    • (2008) Chinese J Struct Chem , vol.27 , pp. 105-111
    • Rui, O.M.1    Qian, L.I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.