-
1
-
-
12344269806
-
Synthesis of mono- and bisglucuronylated carboranes
-
DOI 10.1016/j.tetasy.2004.11.059, PII S0957416604009073
-
S. Ronchi D. Prosperi C. Thimon C. Morin L. Panza 2005 Tetrahedron: Asymmetry 16 39 10.1016/j.tetasy.2004.11.059 1:CAS:528:DC%2BD2MXnsVKisA%3D%3D (Pubitemid 40127073)
-
(2005)
Tetrahedron Asymmetry
, vol.16
, Issue.1
, pp. 39-44
-
-
Ronchi, S.1
Prosperi, D.2
Thimon, C.3
Morin, C.4
Panza, L.5
-
2
-
-
0000323139
-
-
(a) A. H. Soloway, W. Tyarks, B. A. Barnam, F.-G. Rong, R. F. Barh, I. M. Codogni, J. G. Wilson, Chem. Rev., 1998, 98, 1515
-
(1998)
Chem. Rev.
, vol.98
, pp. 1515
-
-
Soloway, A.H.1
Tyarks, W.2
Barnam, B.A.3
Rong, F.-G.4
Barh, R.F.5
Codogni, I.M.6
Wilson, J.G.7
-
3
-
-
33645820229
-
-
V. I. Bregadze, I. B. Sivaev, S. A. Glazun, Anti-Cancer Agents Med. Chem., 2006, 6, 75.
-
(2006)
Anti-Cancer Agents Med. Chem.
, vol.6
, pp. 75
-
-
Bregadze, V.I.1
Sivaev, I.B.2
Glazun, S.A.3
-
5
-
-
0030872450
-
-
R. S. Bresalier, P.-S. Yan, J. C. Byrd, R. Lotan, A. Raz, Cancer, 1997, 80, 776.
-
(1997)
Cancer
, vol.80
, pp. 776
-
-
Bresalier, R.S.1
Yan, P.-S.2
Byrd, J.C.3
Lotan, R.4
Raz, A.5
-
6
-
-
21244466796
-
Galectins as markers of aggressiveness of mouse mammary carcinoma: Towards a lectin target therapy of human breast cancer
-
DOI 10.1007/s10549-005-0289-8
-
E. V. Moiseeva E. M. Rapoport N. V. Bovin A. I. Miroshnikov A. V. Chaadaeva M.S. Krasilschikova V. K. Bojenko C. Bijleveld J. E. van Dijk W. van der Otter 2005 Breast Cancer Res. Treat. 91 227 10.1007/s10549-005-0289-8 1:CAS:528:DC%2BD2MXltFGqsLg%3D (Pubitemid 40896569)
-
(2005)
Breast Cancer Research and Treatment
, vol.91
, Issue.3
, pp. 227-241
-
-
Moiseeva, E.V.1
Rapoport, E.M.2
Bovin, N.V.3
Miroshnikov, A.I.4
Chaadaeva, A.V.5
Krasilshschikova, M.S.6
Bojenko, V.K.7
Bijleveld, C.8
Van Dijk, J.E.9
Den Otter, W.10
-
9
-
-
33745824193
-
Conjugates of polyhedral boron compounds with carbohydrates. 4. Hydrolytic stability of carborane-lactose conjugates depends on the structure of a spacer between the carborane cage and sugar moiety
-
DOI 10.1002/aoc.1082
-
A. V. Orlova L. O. Kononov B. G. Kimel I. B. Sivaev V. I. Bregadze 2006 Appl. Organomet. Chem. 20 416 10.1002/aoc.1082 1:CAS:528:DC%2BD28XnsFKqtrg%3D (Pubitemid 44031433)
-
(2006)
Applied Organometallic Chemistry
, vol.20
, Issue.6
, pp. 416-420
-
-
Orlova, A.V.1
Kononov, L.O.2
Kimel, B.G.3
Sivaev, B.I.4
Bregadze, V.I.5
-
10
-
-
62249094345
-
-
L. M. Likhosherstov, O. S. Novikova, L. O. Kononov, A. V. Orlova, I. B. Sivaev, V. I. Bregadze, Izv. Akad. Nauk, Ser. Khim., 2007, 2033
-
(2007)
Izv. Akad. Nauk, Ser. Khim.
, pp. 2033
-
-
Likhosherstov, L.M.1
Novikova, O.S.2
Kononov, L.O.3
Orlova, A.V.4
Sivaev, I.B.5
Bregadze, V.I.6
-
12
-
-
20244362890
-
Synthesis and self-assembly of globotriose derivatives: A model system for studies of carbohydrate-protein interactions
-
DOI 10.1021/la015643m
-
S. Svedhem I. Ohberg S. Borrelli R. Valiokas M. Andersson S. Oscarson S. C. T. Svensson B. Liedberg P. Konrandsson 2002 Langmuir 18 2848 10.1021/la015643m 1:CAS:528:DC%2BD38Xhs1Citrs%3D (Pubitemid 35390161)
-
(2002)
Langmuir
, vol.18
, Issue.7
, pp. 2848-2858
-
-
Svedhem, S.1
Ohberg, L.2
Borrelli, S.3
Valiokas, R.4
Andersson, M.5
Oscarson, S.6
Svensson, S.C.T.7
Liedberg, B.8
Konradsson, P.9
-
14
-
-
73149119682
-
-
L. M. Likhosherstov, O. S. Novikova, G. V. Mokrov, Izv. Akad. Nauk, Ser. Khim., 2008, 647
-
(2008)
Izv. Akad. Nauk, Ser. Khim.
, pp. 647
-
-
Likhosherstov, L.M.1
Novikova, O.S.2
Mokrov, G.V.3
-
16
-
-
77950284702
-
-
L. M. Likhosherstov, O. S. Novikova, G. V. Mokrov, Izv. Akad. Nauk, Ser. Khim., 2008, 2368
-
(2008)
Izv. Akad. Nauk, Ser. Khim.
, pp. 2368
-
-
Likhosherstov, L.M.1
Novikova, O.S.2
Mokrov, G.V.3
-
18
-
-
0030687892
-
Glycosylated peptoids as prototypical HIV-1 protease inhibitors
-
DOI 10.1016/S0040-4039(97)10028-4, PII S0040403997100284
-
U. K. Saha R. Roy 1997 Tetrahedron Lett. 38 7697 10.1016/S0040-4039(97) 10028-4 1:CAS:528:DyaK2sXnt1Wrsbg%3D (and references therein) (Pubitemid 27463501)
-
(1997)
Tetrahedron Letters
, vol.38
, Issue.44
, pp. 7697-7700
-
-
Saha, U.K.1
Roy, R.2
|