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INTERNATIONAL SEARCH REPORT C(Continuation). DOCUMENTS CONSIDERED TO BE RELEVANT International application No PCT/EP2010/058662 Category * Citation ol document, with indication, where appropriate, of the relevant passages Relevant to claim No. MARI ET AL: "Synthesis and conformational 1-20 analysis of an alpha-d-mannopyranosyl-(l >2 )-al pha-d-mannopyranosyl - (l->6 )-al pha-dmannopyranose mimic" CARBOHYDRATE RESEARCH, ELSEVIER SCIENTIFIC PUBLISHING COMPANY. AMSTERDAM, NL, vol. 342, no. 12-13, 16 July 2007 (2007-07-16), pages 1859-1868, XP022155737 ISSN: 0008-6215 cited in the application the whole document J . ROJO, R . DELGADO: "Dendrimers and 1-20 Dendritic Polymers as Anti-infective Agents: New Antimicrobial Strategies for Therapeutic Drugs" ANTI-INFECTIVE AGENTS IN MEDICINAL CHEMISTRY, vol. 6 , 2007, pages 151-174, XP002554588 the whole document J . ROJO, R . DELGADO: "Glycodendritic 1-20 structures: promising new antiviral drugs" JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, vol. 54, 2004, pages 579-581, XP002554589 the whole document WO 2007/033329 A (UNIV MARYLAND BIOTECH 1-20 INST [US]; WANG LAI-XI [US]; WANG JINGSONG [US];) 22 March 2007 (2007-03-22) page 4 - page 5 ; figure 2 Form PCT/ISA/210 (continuation of second sheet) (April 2005)
INTERNATIONAL SEARCH REPORT Information on patent family members International application No PCT/EP2010/058662 Patent document Publication Patent family Publication cited in search report date member(s) date WO 2007033329 22-03-2007 CA 2663633 A l 22-03-2007 EP 1937308 A l 02-07-2008 US 2009117154 A l 07-05-2009 Form PCT/ISA/210 (patent family annex) (April 2005)
Page 1 and 2:
(12) INTERNATIONAL APPLICATION PUBL
Page 3 and 4:
mannose disaccharide (Manα1-2Man),
Page 5 and 6:
It is a forth object of the inventi
Page 7 and 8:
M' is a saccharidic or pseudo-sacch
Page 9 and 10:
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 64 and 65: 12. A compound according to claim 1
Page 66: or methyl substituted 1,3-thiazole;
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W0 2011/000721 A1 I||||||||||||||||||||||||||||||||||||||||||||||||||||||||| - Questel

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