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. Author manuscript; available in PMC: 2020 Jul 28.
Published in final edited form as: Neurochem Res. 2009 Nov 24;35(6):888–893. doi: 10.1007/s11064-009-0098-2

Fig. 2.

Fig. 2

The compounds under studies: a Sequences of the α4 peptide and of its structural analog K156; b The oligonucleotide is designed to adopt a hairpin structure with a three thymine (T) loop (the central thymine bears the fluorophore (fluorescein) and a 17-base pair stem). The latter reproduces the end of the U5ĽTR of HIV-1 DNA but plays the role of both virus DNA and cell DNA in in vitro experiments; c The IN inhibitor TB11 includes the critical DKA group and also an aryl ring with an azide substitutent important for biological activity [3, 19]