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Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues

Hogberg, M (author)
Sahlberg, C (author)
Engelhardt, P (author)
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Noreen, R (author)
Kangasmetsa, J (author)
Johansson, NG (author)
Oberg, B (author)
Vrang, L (author)
Zhang, H (author)
Sahlberg, BL (author)
Unge, T (author)
Uppsala universitet,Strukturell molekylärbiologi
Lovgren, S (author)
Fridborg, K (author)
Backbro, K (author)
Uppsala universitet,Strukturell molekylärbiologi
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 (creator_code:org_t)
1999
1999
English.
In: JOURNAL OF MEDICINAL CHEMISTRY. - 0022-2623. ; 42:20, s. 4150-4160
  • Journal article (other academic/artistic)
Abstract Subject headings
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  • The further development-of allosteric HIV-1 RT inhibitors in the urea analogue series of PETT (phenylethylthiazolylthiourea) derivatives is described here. The series includes derivatives with an ethyl linker (1-5) and racemic (6-16) and enantiomeric (17-

Keyword

IMMUNODEFICIENCY-VIRUS TYPE-1; NONNUCLEOSIDE INHIBITORS; WILD-TYPE; POTENT; DERIVATIVES; REPLICATION; COMBINATION; NEVIRAPINE; DRUG; ZIDOVUDINE

Publication and Content Type

vet (subject category)
art (subject category)

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