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Volumn 29, Issue 1, 2014, Pages 100-108

Design, synthesis, antimicrobial activity and anti-HIV activity evaluation of novel hybrid quinazoline-triazine derivatives

Author keywords

Anti HIV; Antimicrobial; Diaryl triazine (DATA); Dibromo quinazoline; Piperazine

Indexed keywords

ANTHRANILIC ACID; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; ANTIVIRUS AGENT; CHLORINE DERIVATIVE; CYANURIC CHLORIDE; ETHYLENEDIAMINE; QUINAZOLINE; QUINAZOLINE TRIAZINE DERIVATIVE; TRIAZINE; UNCLASSIFIED DRUG;

EID: 84887495816     PISSN: 14756366     EISSN: 14756374     Source Type: Journal    
DOI: 10.3109/14756366.2012.755622     Document Type: Article
Times cited : (63)

References (51)
  • 1
    • 82255174824 scopus 로고    scopus 로고
    • Available from [last accessed 30 Oct
    • UNAIDS 2011 World AIDS Day report. Available from: Http:// www.unaids.org. [last accessed 30 Oct 2012
    • (2012) UNAIDS 2011 World AIDS Day Report
  • 2
    • 12144278681 scopus 로고    scopus 로고
    • HIV-reverse transcriptase inhibition: Inclusion of ligand-induced fit by cross-docking studies
    • Ragno R, Frasca S, Manetti F, et al. HIV-reverse transcriptase inhibition: Inclusion of ligand-induced fit by cross-docking studies. J Med Chem 2004;48:200-12
    • (2004) J Med Chem , vol.48 , pp. 200-212
    • Ragno, R.1    Frasca, S.2    Manetti, F.3
  • 3
    • 0032568207 scopus 로고    scopus 로고
    • Progress and problems in the fight against AIDS
    • Hirschel B, Francioli P. Progress and problems in the fight against AIDS. N Engl J Med 1998;338:906-8
    • (1998) N Engl J Med , vol.338 , pp. 906-908
    • Hirschel, B.1    Francioli, P.2
  • 4
    • 0035160478 scopus 로고    scopus 로고
    • New developments in anti-HIV chemotherapy
    • De Clercq E. New developments in anti-HIV chemotherapy. Curr Med Chem 2001;8:1543-72
    • (2001) Curr Med Chem , vol.8 , pp. 1543-1572
    • De Clercq, E.1
  • 5
    • 2342620790 scopus 로고    scopus 로고
    • Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-Type and drug-resistant HIV-1 variants
    • Das K, Clark AD, Lewi PJ, et al. Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-Type and drug-resistant HIV-1 variants. J Med Chem 2004;47:2550-60
    • (2004) J Med Chem , vol.47 , pp. 2550-2560
    • Das, K.1    Clark, A.D.2    Lewi, P.J.3
  • 6
    • 76749095030 scopus 로고    scopus 로고
    • Next-generation antimalarial drugs: Hybrid molecules as a new strategy in drug design
    • Muregi FW, Ishih A. Next-generation antimalarial drugs: Hybrid molecules as a new strategy in drug design. Drug Develop Res 2010;71:20-32
    • (2010) Drug Develop Res , vol.71 , pp. 20-32
    • Muregi, F.W.1    Ishih, A.2
  • 7
    • 38949106942 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel 1 3,5-Triazine derivatives as antimicrobial agents
    • Zhou C, Min J, Liu Z, et al. Synthesis and biological evaluation of novel 1,3,5-Triazine derivatives as antimicrobial agents. Bioorg Med Chem Lett 2008;18:1308-11
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 1308-1311
    • Zhou, C.1    Min, J.2    Liu, Z.3
  • 8
    • 33750498033 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of various substituted s-Triazines
    • Srinivas K, Srinivas U, Bhanuprakash K, et al. Synthesis and antibacterial activity of various substituted s-Triazines. Eur J Med Chem 2006;41:1240-6
    • (2006) Eur J Med Chem , vol.41 , pp. 1240-1246
    • Srinivas, K.1    Srinivas, U.2    Bhanuprakash, K.3
  • 9
    • 84870510914 scopus 로고    scopus 로고
    • Synthesis and evaluation of novel 4-substituted styryl quinazolines as potential antimicrobial agents
    • Modh RP, Patel AC, Mahajan DH, et al. Synthesis and evaluation of novel 4-substituted styryl quinazolines as potential antimicrobial agents. Arch Pharm 2012;345:964-72
    • (2012) Arch Pharm , vol.345 , pp. 964-972
    • Modh, R.P.1    Patel, A.C.2    Mahajan, D.H.3
  • 10
    • 77953228682 scopus 로고    scopus 로고
    • Design, synthesis and antimicrobial evaluation of s-Triazinyl urea and thiourea derivatives
    • Kaswala PB, Chikhalia KH, Shah NK, et al. Design, synthesis and antimicrobial evaluation of s-Triazinyl urea and thiourea derivatives. Arkivoc 2009;11:326-35
    • (2009) Arkivoc , vol.11 , pp. 326-335
    • Kaswala, P.B.1    Chikhalia, K.H.2    Shah, N.K.3
  • 11
    • 84864854235 scopus 로고    scopus 로고
    • Syn thesis, antimicrobial and antimycobacterial evaluation of star shaped hydrazones derived from 1,3,5-Triazine
    • Machakanur SS, Patil BR, Pathan AH, et al. Synthesis, antimicrobial and antimycobacterial evaluation of star shaped hydrazones derived from 1,3,5-Triazine. Der Pharma Chemica 2012;4:600-7
    • (2012) Der Pharma Chemica , vol.4 , pp. 600-607
    • MacHakanur, S.S.1    Patil, B.R.2    Pathan, A.H.3
  • 12
    • 4444288821 scopus 로고    scopus 로고
    • In vitro cytotoxic activities of 2-Alkyl-4,6-diheteroalkyl-1, 3,5-Triazines: New molecules in anticancer research
    • Menicagli R, Samaritani S, Signore G, et al. In vitro cytotoxic activities of 2-Alkyl-4,6-diheteroalkyl-1,3,5-Triazines: New molecules in anticancer research. J Med Chem 2004;47:4649-52
    • (2004) J Med Chem , vol.47 , pp. 4649-4652
    • Menicagli, R.1    Samaritani, S.2    Signore, G.3
  • 13
    • 19944401083 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors: Novel sulfonamides incorporating 1, 3,5-Triazine moieties as inhibitors of the cytosolic and tumour-Associated carbonic anhydrase isozymes I, II and IX
    • Garaj V, Puccetti L, Fasolis G, et al. Carbonic anhydrase inhibitors: Novel sulfonamides incorporating 1,3,5-Triazine moieties as inhibitors of the cytosolic and tumour-Associated carbonic anhydrase isozymes I, II and IX. Bioorg Med Chem Lett 2005;15:3102-8
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 3102-3108
    • Garaj, V.1    Puccetti, L.2    Fasolis, G.3
  • 14
    • 48149090074 scopus 로고    scopus 로고
    • A combinatorial approach to 2, 4,6-Trisubstituted triazines with potent antimalarial activity: Combining conventional synthesis and microwave-Assistance
    • Melato S, Prosperi D, Coghi P, et al. A combinatorial approach to 2,4,6-Trisubstituted triazines with potent antimalarial activity: Combining conventional synthesis and microwave-Assistance. ChemMedChem 2008;3:873-6
    • (2008) ChemMedChem , vol.3 , pp. 873-876
    • Melato, S.1    Prosperi, D.2    Coghi, P.3
  • 15
    • 44349131462 scopus 로고    scopus 로고
    • Non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 11: Structural modulations of diaryltriazines with potent anti-HIV activity
    • Xiong YZ, Chen FE, Balzarini J, et al. Non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 11: Structural modulations of diaryltriazines with potent anti-HIV activity. Eur J Med Chem 2008;43:1230-6
    • (2008) Eur J Med Chem , vol.43 , pp. 1230-1236
    • Xiong, Y.Z.1    Chen, F.E.2    Balzarini, J.3
  • 16
    • 14444286696 scopus 로고    scopus 로고
    • New azole antifungals. 3. Synthesis and antifungal activity of 3-substituted-4(3H)-quinazolinones1, 2
    • Bartroli J, Turmo E, Algueró M, et al. New azole antifungals. 3. synthesis and antifungal activity of 3-substituted-4(3H)-quinazolinones1,2. J Med Chem 1998;41:1869-82
    • (1998) J Med Chem , vol.41 , pp. 1869-1882
    • Bartroli, J.1    Turmo, E.2    Algueró, M.3
  • 17
    • 0009709634 scopus 로고    scopus 로고
    • Aminoacids in the synthesis of heterocyclic systems: The synthesis of triazinoquinazolinones, triazepinoquinazolinones and triazocinoquinazolinones of potential biological interest
    • El-Sharief A, Ammar Y, Zahran M, et al. Aminoacids in the synthesis of heterocyclic systems: The synthesis of triazinoquinazolinones, triazepinoquinazolinones and triazocinoquinazolinones of potential biological interest. Molecules 2001;6:267-78
    • (2001) Molecules , vol.6 , pp. 267-278
    • El-Sharief, A.1    Ammar, Y.2    Zahran, M.3
  • 18
    • 84861920293 scopus 로고    scopus 로고
    • Design, synthesis biological evaluation of some novel quinazolinone scaffolds
    • Modh RP, Patel AC, Chikhalia KH. Design, synthesis biological evaluation of some novel quinazolinone scaffolds. Med Chem 2012;8:182-92
    • (2012) Med Chem , vol.8 , pp. 182-192
    • Modh, R.P.1    Patel, A.C.2    Chikhalia, K.H.3
  • 19
    • 84861585894 scopus 로고    scopus 로고
    • Synthesis of 5-Arylaminosulpho-N-Acetylanthranilic acid, 6-Arylaminosulpho-2-methyl-3-Amino/3-Nchloroacetamido/ 3-N-Arylaminoacetamido-4- (3H)-quinazolones as potential anti-HIV, anticancer and antimicrobial agents
    • Purohit DM, Bhuva VR, Shah VH. Synthesis of 5-Arylaminosulpho-N- Acetylanthranilic acid, 6-Arylaminosulpho-2-methyl-3-Amino/3-Nchloroacetamido/ 3-N-Arylaminoacetamido-4-(3H)-quinazolones as potential anti-HIV, anticancer and antimicrobial agents. Chem Indian J 2003;1:233-45
    • (2003) Chem Indian J , vol.1 , pp. 233-245
    • Purohit, D.M.1    Bhuva, V.R.2    Shah, V.H.3
  • 20
    • 84861602512 scopus 로고    scopus 로고
    • Design, synthesis and antiviral activity of novel quinazolinones
    • Wang Z, Wang M, Yao X, et al. Design, synthesis and antiviral activity of novel quinazolinones. Eur J Med Chem 2012;53:275-82
    • (2012) Eur J Med Chem , vol.53 , pp. 275-282
    • Wang, Z.1    Wang, M.2    Yao, X.3
  • 21
    • 34250473557 scopus 로고
    • Synthesis and tuberculostatic activity of aminoquinazoline derivatives
    • Murav'eva KM, Arkhangel'skaya NV, Shchukina MN, et al. Synthesis and tuberculostatic activity of aminoquinazoline derivatives. Pharm Chem J 1971;5:339-41
    • (1971) Pharm Chem J , vol.5 , pp. 339-341
    • Murav'eva, K.M.1    Arkhangel'skaya, N.V.2    Shchukina, M.N.3
  • 23
    • 69949169680 scopus 로고    scopus 로고
    • A new therapeutic approach in Parkinson's disease: Some novel quinazoline derivatives as dual selective phosphodiesterase 1 inhibitors and anti-inflammatory agents
    • Laddha SS, Bhatnagar SP. A new therapeutic approach in Parkinson's disease: Some novel quinazoline derivatives as dual selective phosphodiesterase 1 inhibitors and anti-inflammatory agents. Bioorg Med Chem 2009;17:6796-802
    • (2009) Bioorg Med Chem , vol.17 , pp. 6796-6802
    • Laddha, S.S.1    Bhatnagar, S.P.2
  • 24
    • 70349194362 scopus 로고
    • Part I.I. Synthesis of novel-2-styryl-3-benzylidenimino-4(3H)-quinazolone derivatives of expected anticonvulsant activity
    • Aziza MA, Ibrahim MK, El-Helpy AG. Part II. Synthesis of novel-2-styryl-3-benzylidenimino-4(3H)-quinazolone derivatives of expected anticonvulsant activity. Al-Azhar J Pharm Sci 1994; 14:193-201
    • (1994) Al-Azhar J Pharm Sci , vol.14 , pp. 193-201
    • Aziza, M.A.1    Ibrahim, M.K.2    El-Helpy, A.G.3
  • 25
    • 50949089653 scopus 로고    scopus 로고
    • CNS depressant and anticonvulsant activities of some novel 3-[5-substituted 1, 3,4-Thiadiazole-2-yl]-2-styryl quinazoline-4(3H)-ones
    • Jatav V, Mishra P, Kashaw S, Stables JP. CNS depressant and anticonvulsant activities of some novel 3-[5-substituted 1,3,4-Thiadiazole-2-yl] -2-styryl quinazoline-4(3H)-ones. Eur J Med Chem 2008;43:1945-54
    • (2008) Eur J Med Chem , vol.43 , pp. 1945-1954
    • Jatav, V.1    Mishra, P.2    Kashaw, S.3    Stables, J.P.4
  • 26
    • 0029881470 scopus 로고    scopus 로고
    • Synthesis and hypolipidemic activities of novel 2-[4- [(diethoxyphosphoryl)methyl]phenyl]quinazolines and 4(3H)-quinazolinones
    • Kurogi Y, Inoue Y, Tsutsumi K, et al. Synthesis and hypolipidemic activities of novel 2-[4-[(diethoxyphosphoryl)methyl]phenyl]quinazolines and 4(3H)-quinazolinones. J Med Chem 1996;39:1433-7
    • (1996) J Med Chem , vol.39 , pp. 1433-1437
    • Kurogi, Y.1    Inoue, Y.2    Tsutsumi, K.3
  • 27
    • 0028811501 scopus 로고
    • Studies on antiulcer agents. IV: Antiulcer effects of 2-benzylthio-5, 6, 7, 8-Tetrahydro-4 (3H)-quinazolinones and related compounds
    • Terashima K, Shimamura H, Kawase A, et al. Studies on antiulcer agents. IV: Antiulcer effects of 2-benzylthio-5, 6, 7, 8-Tetrahydro-4 (3H)-quinazolinones and related compounds. Chem Pharm Bull 1995;43:2021-3
    • (1995) Chem Pharm Bull , vol.43 , pp. 2021-2023
    • Terashima, K.1    Shimamura, H.2    Kawase, A.3
  • 28
    • 33750949952 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted- 3Hquinazolin-4-one as analgesic, anti-inflammatory agents
    • Alagarsamy V, Raja Solomon V, Dhanabal K. Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3Hquinazolin-4-one as analgesic, anti-inflammatory agents. Bioorg Med Chem 2007;15:235-41
    • (2007) Bioorg Med Chem , vol.15 , pp. 235-241
    • Alagarsamy, V.1    Raja Solomon, V.2    Dhanabal, K.3
  • 29
    • 0031468483 scopus 로고    scopus 로고
    • Syntheses of Novel 3-Amino-2(1H)-Thioxo-4(3H)-quinazolinones and evaluation of their immunotropic activity. Part III
    • Nawrocka W, Zimecki M. Syntheses of Novel 3-Amino-2(1H)-Thioxo-4(3H)- quinazolinones and evaluation of their immunotropic activity. Part III. Arch Pharm 1997;330:399-405
    • (1997) Arch Pharm , vol.330 , pp. 399-405
    • Nawrocka, W.1    Zimecki, M.2
  • 30
    • 77949488931 scopus 로고    scopus 로고
    • Novel quinoline and naphthalene derivatives as potent antimycobacterial agents
    • Upadhayaya RS, Vandavasi JK, Kardile RA, et al. Novel quinoline and naphthalene derivatives as potent antimycobacterial agents. Eur J Med Chem 2010;45:1854-67
    • (2010) Eur J Med Chem , vol.45 , pp. 1854-1867
    • Upadhayaya, R.S.1    Vandavasi, J.K.2    Kardile, R.A.3
  • 31
    • 79959608402 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of some novel 5-Alkyl-6-substituted uracils and related derivatives
    • Al-Turkistani AA, Al-Deeb OA, El-Brollosy NR,El-Emam AA. Synthesis and antimicrobial activity of some novel 5-Alkyl-6-substituted uracils and related derivatives. Molecules 2011;16:4764-74
    • (2011) Molecules , vol.16 , pp. 4764-4774
    • Al-Turkistani, A.A.1    Al-Deeb, O.A.2    El-Brollosy, N.R.3    El-Emam, A.A.4
  • 32
    • 48549105219 scopus 로고    scopus 로고
    • Synthesis and antimicrobial studies of novel 1-benzhydryl-piperazine sulfonamide and carboxamide derivatives
    • Ananda Kumar C, Vinaya K, Narendra Sharath Chandra J, et al. Synthesis and antimicrobial studies of novel 1-benzhydryl-piperazine sulfonamide and carboxamide derivatives. J Enzyme Inhib Med Chem 2008;23:462-9
    • (2008) J Enzyme Inhib Med Chem , vol.23 , pp. 462-469
    • Ananda Kumar, C.1    Vinaya, K.2    Narendra Sharath Chandra, J.3
  • 33
    • 1842787547 scopus 로고    scopus 로고
    • Optically active antifungal azoles: Synthesis and antifungal activity of (2R,3S-2-( 2,4-difluorophenyl)-3-(5-{2-[4-Aryl-piperazin-1-yl]-ethyl}-Tetrazol- 2-yl/1-yl)-1-[ 1,2,4]-Triazol-1-yl-butan-2-ol
    • Upadhayaya RS, Sinha N, Jain S, et al. Optically active antifungal azoles: Synthesis and antifungal activity of (2R,3S)-2-(2,4-difluorophenyl)-3- (5-{2-[4-Aryl-piperazin-1-yl]-ethyl}-Tetrazol-2-yl/1-yl)-1-[1,2,4] -Triazol-1-yl-butan-2-ol. Bioorg Med Chem 2004;12:2225-38
    • (2004) Bioorg Med Chem , vol.12 , pp. 2225-2238
    • Upadhayaya, R.S.1    Sinha, N.2    Jain, S.3
  • 34
    • 78650512116 scopus 로고    scopus 로고
    • Novel isatinyl thiosemicarbazones derivatives as potential molecule to combat HIV-TB co-infection
    • Banerjee D, Yogeeswari P, Bhat P, et al. Novel isatinyl thiosemicarbazones derivatives as potential molecule to combat HIV-TB co-infection. Eur J Med Chem 2011;46:106-21
    • (2011) Eur J Med Chem , vol.46 , pp. 106-121
    • Banerjee, D.1    Yogeeswari, P.2    Bhat, P.3
  • 35
    • 79951545568 scopus 로고    scopus 로고
    • Synthesis and in vitro antibacterial activity of N-Alkyl and N-Aryl piperazine derivatives
    • Singh KK, Joshi SC, Mathela CS. Synthesis and in vitro antibacterial activity of N-Alkyl and N-Aryl piperazine derivatives. Indian J Chem B 2011;50:196
    • (2011) Indian J Chem B , vol.50 , pp. 196
    • Singh, K.K.1    Joshi, S.C.2    Mathela, C.S.3
  • 36
    • 0037534121 scopus 로고    scopus 로고
    • Structural features of piperazinyl-linked ciprofloxacin dimers required for activity against drug-resistant strains of Staphylococcus aureus
    • Kerns RJ, Rybak MJ, Kaatz GW, et al. Structural features of piperazinyl-linked ciprofloxacin dimers required for activity against drug-resistant strains of Staphylococcus aureus. Bioorg Med Chem Lett 2003;13:2109-12
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 2109-2112
    • Kerns, R.J.1    Rybak, M.J.2    Kaatz, G.W.3
  • 37
    • 84862529315 scopus 로고    scopus 로고
    • Antimicrobial, anti-TB, anticancer and anti-HIV evaluation of new s-Triazine-based heterocycles
    • Patel RV, Kumari P, Rajani DP, et al. Antimicrobial, anti-TB, anticancer and anti-HIV evaluation of new s-Triazine-based heterocycles. Future Med Chem 2012;4:1053-65
    • (2012) Future Med Chem , vol.4 , pp. 1053-1065
    • Patel, R.V.1    Kumari, P.2    Rajani, D.P.3
  • 38
    • 33748259410 scopus 로고    scopus 로고
    • Synthesis and studies of novel homoveratryl based thiohydantoins as antibacterial as well as anti-HIV agents
    • Patel RB, Desai KR, Chikhalia KH. Synthesis and studies of novel homoveratryl based thiohydantoins as antibacterial as well as anti-HIV agents. Indian J Chem B 2006;45B:1716
    • (2006) Indian J Chem B , vol.45 B , pp. 1716
    • Patel, R.B.1    Desai, K.R.2    Chikhalia, K.H.3
  • 39
    • 34247511550 scopus 로고    scopus 로고
    • Synthesis of novel PETT analogues: 3, 4-dimethoxy phenyl ethyl 1, 3, 5-Triazinyl thiourea derivatives and their antibacterial and anti-HIV studies
    • Patel RB, Chikhalia KH, Pannecouque C, Clercq E. Synthesis of novel PETT analogues: 3, 4-dimethoxy phenyl ethyl 1, 3, 5-Triazinyl thiourea derivatives and their antibacterial and anti-HIV studies. J Braz Chem Soc 2007;18:312-21
    • (2007) J Braz Chem Soc , vol.18 , pp. 312-321
    • Patel, R.B.1    Chikhalia, K.H.2    Pannecouque, C.3    Clercq, E.4
  • 40
    • 33750321456 scopus 로고    scopus 로고
    • Synthesis of heterocyclic and nonheterocyclic entities as antibacterial and anti-HIV agents
    • Patel RB, Chikhalia KH. Synthesis of heterocyclic and nonheterocyclic entities as antibacterial and anti-HIV agents. Indian J Chem B 2006;45B:1871
    • (2006) Indian J Chem B , vol.45 B , pp. 1871
    • Patel, R.B.1    Chikhalia, K.H.2
  • 41
    • 66349109052 scopus 로고    scopus 로고
    • Synthesis and studies of new 2-(coumarin-4-yloxy)-4, 6-(substituted)-s- Triazine derivatives as potential anti-HIV agents
    • Mahajan DH, Pannecouque C, De Clercq E, Chikhalia KH. Synthesis and studies of new 2-(coumarin-4-yloxy)-4, 6-(substituted)-s-Triazine derivatives as potential anti-HIV agents. Arch Pharm 2009;342:281-90
    • (2009) Arch Pharm , vol.342 , pp. 281-290
    • Mahajan, D.H.1    Pannecouque, C.2    De Clercq, E.3    Chikhalia, K.H.4
  • 42
    • 84855303822 scopus 로고    scopus 로고
    • Synthesis of a novel class of some 1, 3, 5-Triazine derivatives and their anti-HIV activity
    • Desai SD, Desai KR, Chikhalia KH, et al. Synthesis of a novel class of some 1, 3, 5-Triazine derivatives and their anti-HIV activity. Int J Drug Des Dis 2011;2:361-8
    • (2011) Int J Drug des Dis , vol.2 , pp. 361-368
    • Desai, S.D.1    Desai, K.R.2    Chikhalia, K.H.3
  • 43
    • 84861575661 scopus 로고    scopus 로고
    • Design syn thesis, anti-HIV evaluation and molecular modeling of piperidine-linked amino-Triazine derivatives as potent non-nucleoside reverse transcriptase inhibitors
    • Chen X, Zhan P, Liu X, et al. Design, synthesis, anti-HIV evaluation and molecular modeling of piperidine-linked amino-Triazine derivatives as potent non-nucleoside reverse transcriptase inhibitors. Bioorg Med Chem 2012;20:3856-64
    • (2012) Bioorg Med Chem , vol.20 , pp. 3856-3864
    • Chen, X.1    Zhan, P.2    Liu, X.3
  • 44
    • 0037006623 scopus 로고    scopus 로고
    • Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-Transcriptase inhibitor abacavir
    • Mallal S, Nolan D, Witt C, et al. Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-Transcriptase inhibitor abacavir. Lancet 2002; 359:727-32
    • (2002) Lancet , vol.359 , pp. 727-732
    • Mallal, S.1    Nolan, D.2    Witt, C.3
  • 45
    • 0033836982 scopus 로고    scopus 로고
    • Characterization of novel glutathione adducts of a non-nucleoside reverse transcriptase inhibitor, (s)-6-chloro-4-(cyclopropylethynyl)-4- (trifluoromethyl)-3,4-dihydro-2(1h)-quinazolinone (dpc 961), in rats. Possible formation of an oxirene metabolic intermediate from a disubstituted alkyne
    • Mutlib A, Chen H, Shockcor J, et al. Characterization of novel glutathione adducts of a non-nucleoside reverse transcriptase inhibitor, (s)-6-chloro-4-(cyclopropylethynyl)-4-(trifluoromethyl)-3,4-dihydro-2(1h) -quinazolinone (dpc 961), in rats. possible formation of an oxirene metabolic intermediate from a disubstituted alkyne. Chem Res Toxicol 2000;13:775-84
    • (2000) Chem Res Toxicol , vol.13 , pp. 775-784
    • Mutlib, A.1    Chen, H.2    Shockcor, J.3
  • 47
    • 0023709207 scopus 로고
    • Sulfated polysaccharides are potent and selective inhibitors of various enveloped viruses, including herpes simplex virus, cytomegalovirus, vesicular stomatitis virus, human immunodeficiency virus
    • Baba M, Snoeck R, Pauwels R, De Clercq E. Sulfated polysaccharides are potent and selective inhibitors of various enveloped viruses, including herpes simplex virus, cytomegalovirus, vesicular stomatitis virus, human immunodeficiency virus. Antimicrob Agents Chemother 1988;32:1742-5
    • (1988) Antimicrob Agents Chemother , vol.32 , pp. 1742-1745
    • Baba, M.1    Snoeck, R.2    Pauwels, R.3    De Clercq, E.4
  • 48
    • 40749129190 scopus 로고    scopus 로고
    • Tetrazolium-based colorimetric assay for the detection of HIV replication inhibitors: Revisited 20 years later
    • Pannecouque C, Daelemans D, De Clercq E. Tetrazolium-based colorimetric assay for the detection of HIV replication inhibitors: Revisited 20 years later. Nat Protoc 2008;3:427-34
    • (2008) Nat Protoc , vol.3 , pp. 427-434
    • Pannecouque, C.1    Daelemans, D.2    De Clercq, E.3
  • 49
    • 0021237243 scopus 로고
    • Detection, isolation, continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS
    • Popovic M, Sarngadharan MG, Read E, Gallo RC. Detection, isolation, continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. Science 1984;224:497-500
    • (1984) Science , vol.224 , pp. 497-500
    • Popovic, M.1    Sarngadharan, M.G.2    Read, E.3    Gallo, R.C.4
  • 50
    • 0020596551 scopus 로고
    • Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS
    • Barré-Sinoussi F, Chermann JC, Rey F, et al. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science 1983; 220:868-71
    • (1983) Science , vol.220 , pp. 868-871
    • Barré-Sinoussi, F.1    Chermann, J.C.2    Rey, F.3
  • 51
    • 0020261516 scopus 로고
    • Type C virus-producing cell lines derived from adult T cell leukemia
    • Miyoshi I, Taguchi H, Kubonishi I, et al. Type C virus-producing cell lines derived from adult T cell leukemia. Gann Monogr 1982;28:219-28
    • (1982) Gann Monogr , vol.28 , pp. 219-228
    • Miyoshi, I.1    Taguchi, H.2    Kubonishi, I.3


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