W0 2011/000721 A1 I||||||||||||||||||||||||||||||||||||||||||||||||||||||||| - Questel

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12. A compound according to claim 10 or 1 1 of formula wherein aj is 32 and J i s a t h i r d g e n e ratio n 2 , 2 '- bis(methoxyol)propanoic acid (bis-MPA) based dendrimer. 13. Compounds of formula [X-Y] Z -Z (I) according to claims 1 to 6 , as a medicament for the treatment and/or prevention of HIV, Ebola, Dengue, Hepatitis C, SARS or tuberculosis infections. 14. Compounds of formula [X-Y] aw -W (Ia) according to claim 7 as a medicament for the treatment and/or prevention of HIV, Ebola, Dengue, Hepatitis C, SARS or tuberculosis infections. 15. Compounds of formula [X-Y] aj -J (Ib) according to claims 10 to 12 as a medicament for the treatment and/or prevention of HIV, Ebola, Dengue, Hepatitis C, SARS or tuberculosis infections.
16. Compound of formula or of formula wherein R 1 is methoxy or is -NHR 3 , wherein R 3 is an A group selected in the group comprising cyclopropan, cyclohexil, phenyl, benzyl or benzyl meta or para substituted with methoxy (-OCH 3 ), nitro (-NO 2 ), carboxy (- COOH), methylester (-COOCH 3 ), hydroxymethyl (-CH 2 OH), methyle (-CH 3 ), methoxy (-OCH 3 ), amino (-NH 2 ), isopropyl (-CH(CH 3 ) 2 ) or R 3 is 1,3, thiazole
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(12) INTERNATIONAL APPLICATION PUBL
Page 3 and 4:
mannose disaccharide (Manα1-2Man),
Page 5 and 6:
It is a forth object of the inventi
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M' is a saccharidic or pseudo-sacch
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wherein Q and n are above disclosed
Page 12 and 13:
wherein R is as above disclosed,
Page 14 and 15: may be made of gold, silver, Fe 2 O
Page 16 and 17: Within the compound of formula (I)
Page 18 and 19: wherein R and R 2 are as above repo
Page 20 and 21: through the Y linker and n is 1 to
Page 22 and 23: and (12a) 12b. As per a third aspec
Page 24 and 25: H wherein Q is selected from — N
Page 26 and 27: According to a second object of the
Page 28 and 29: wherein aj is 32 and J is a third g
Page 30 and 31: eactions requiring anhydrous condit
Page 32 and 33: To a solution of the silylmannopyra
Page 34 and 35: 3H, CH 3 CO), 1.99 (s, 3H, CH 3 CO)
Page 36 and 37: To a solution of the compound 9 (12
Page 38 and 39: (C2 D ), 70.36 (C6 M ), 70.01 (C6 M
Page 40 and 41: EXAMPLE 2 Synthesis of compound 12a
Page 42 and 43: 13 C-NMR (100 MHz, D2 O) δ (ppm):
Page 44 and 45: (the R5 tropic laboratory-adapted s
Page 46 and 47: derived from 1 (see above); G3Man32
Page 48 and 49: CLAIMS: 1 A compound of general for
Page 50: OCH 3 ), hydroxymethyl (-CH 2 OH),
Page 53 and 54: alkyl chain, C1-C8 linear or branch
Page 55 and 56: 7 . A compound having the general f
Page 57 and 58: H wherein Q is selected from — N
Page 59: or methyl substituted 1,3-thiazole;
Page 62 and 63: wherein R 2 may be hydroxyl (-0H),
Page 66: or methyl substituted 1,3-thiazole;
Page 82 and 83: INTERNATIONAL SEARCH REPORT C(Conti
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W0 2011/000721 A1 I||||||||||||||||||||||||||||||||||||||||||||||||||||||||| - Questel

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