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Volumn 34, Issue 13, 2004, Pages 2451-2461

Regiospecific synthesis of 5-halo-substituted thiophene pyridyl thiourea compounds as non-nucleoside inhibitors of HIV-1 reverse transcriptase

Author keywords

HIV 1; Non nucleoside inhibitors; Reverse transcriptase; Thiourea compounds

Indexed keywords

CARBONYL DERIVATIVE; HALOGEN; IMIDAZOLE DERIVATIVE; N,N DIMETHYLFORMAMIDE; PHENETHYLAMINE DERIVATIVE; PYRIDINE DERIVATIVE; RNA DIRECTED DNA POLYMERASE; RNA DIRECTED DNA POLYMERASE INHIBITOR; THIOPHENE DERIVATIVE; THIOUREA DERIVATIVE;

EID: 3543147840     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120039499     Document Type: Article
Times cited : (11)

References (10)
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    • Uckun, F.M.; Pendergrass, S.; Maher, D.; Zhu, D.; Tuel-Ahlgren, L.; Mao, C.; Venkatachalam, T.K. N′-[2-(2-Thiophene)ethyl]-N′-[2-(5- bromopyridyl)] thiourea as a potent inhibitor of NNI-resistant and multi-drug-reistant human immunodeficiency virus-1. Bioorg. Med. Chem. Lett. 1999, 9, 3411.
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    • Uckun, F.M.1    Pendergrass, S.2    Maher, D.3    Zhu, D.4    Tuel-Ahlgren, L.5    Mao, C.6    Venkatachalam, T.K.7
  • 2
    • 3543128363 scopus 로고    scopus 로고
    • U.S. Patent No. 6,124,324, issued to Uckun et al., 2000
    • U.S. Patent No. 6,124,324, issued to Uckun et al., 2000.
  • 3
    • 84955838834 scopus 로고
    • Halo-substituted or 2,5-disubstituted thiophene compounds
    • Kooyman, E.C. Halo-substituted or 2,5-disubstituted thiophene compounds. Pure Appl. Chem. 1963, 7, 193.
    • (1963) Pure Appl. Chem. , vol.7 , pp. 193
    • Kooyman, E.C.1
  • 5
    • 77957042702 scopus 로고
    • Electrophilic substitution on five membered aromatic heterocycles
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    • (1971) Adv. Heterocyclic Chem. , vol.13 , pp. 235
    • Marino, G.1
  • 8
    • 0031788490 scopus 로고    scopus 로고
    • Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reserve transcriptase
    • Vig, R.; Mao, C.; Venkatachalam, T.K.; Tuel-Ahlgren, L.; Sudbeck, E.A.; Uckun, F.M. Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reserve transcriptase. Bioorg. Med. Chem. 1998, 6, 1789.
    • (1998) Bioorg. Med. Chem. , vol.6 , pp. 1789
    • Vig, R.1    Mao, C.2    Venkatachalam, T.K.3    Tuel-Ahlgren, L.4    Sudbeck, E.A.5    Uckun, F.M.6
  • 9
    • 0033532653 scopus 로고    scopus 로고
    • Rational design of N-[2-(2′,5-dimethoxyphenylethyl)]-N′-[2- (5-bromopyridyl)]-thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus
    • Mao, C.; Sudbeck, E.A.; Venkatachalam, T.K.; Uckun, F.M. Rational design of N-[2-(2′,5-dimethoxyphenylethyl)]-N′-[2-(5-bromopyridyl)]- thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus. Bioorg. Med. Chem. Lett. 1999, 9, 1593.
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , pp. 1593
    • Mao, C.1    Sudbeck, E.A.2    Venkatachalam, T.K.3    Uckun, F.M.4
  • 10
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    • Structure-based design of non-nucleoside reverse transcriptase inhibitors of drug-resistant human immunodeficiency virus
    • Mao, C.; Sudbeck, E.A.; Venkatachalam, T.K.; Uckun, F.M. Structure-based design of non-nucleoside reverse transcriptase inhibitors of drug-resistant human immunodeficiency virus. Antivir. Chem. Chemther. 1999, 10, 233.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.