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Virus adsorption inhibitors
Virus co-receptor antagonists
Virus fusion inhibitors
HIV
Nucleocapsid protein
Zn-finger-targeted agents
Reverse transcriptase
inhibitors
HIV integrase inhibitors
Transcription
(transactivation) inhibitors
HIV protease inhibitors
Figure 3: Life cycle of HIV (human immunodeficiency virus) and representation of the targets for anti-HIV drugs. Adapted from ref [12b].
The CBAs can be divided in two categories: lectins that specifically recognize glycan structures, and non-peptidic
small-size agents (Fig. 4 ) that may have an efficient and often specific affinity for monosaccharide and/or
oligosaccharide structures [16]. Besides, various research groups have developed the synthesis and characterization
of synthetic CBAs.
CH 3
(A)
O
H
COOH
O HO
CH 3
O
O
H 3 C
O HO
O
CH 3
OH
O
OH
NH
O
Pradicimin A
O
HO
HO
HO
CH 3
(B)
O
H
COOH
O HO
CH 3
O
O
H 3 C
OH
O
OH
HO
O
CH 3
O
O
H HO
O
OH
OH
Figure 4: Small-size non-peptidic carbohydrate-binding antigens (CBAs). Pradimicin A ( A ) and benanomicin A ( B ) are
produced by Actinomadura hibiscus and Actinomadura spadix , respectively [16].
Benanomicin A
 
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