Zobrazeno 1 - 10
of 10
pro vyhledávání: '"H. Yasmin Godage"'
Autor:
Marco Falasca, Paolo Innocenti, Barry V.L. Potter, Stefano Iacobelli, Massimo Broggini, Cosmo Rossi, H. Yasmin Godage, Adolfo Saiardi, Andrew M. Riley, Manuela Iezzi, Albana Cumashi, Enza Piccolo, Tania Maffucci
Supplementary Fig. S1 from Inhibition of the Phosphatidylinositol 3-Kinase/Akt Pathway by Inositol Pentakisphosphate Results in Antiangiogenic and Antitumor Effects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a8fbfbfba95d5728cd8bcb9b0c4de93
https://doi.org/10.1158/0008-5472.22363659.v1
https://doi.org/10.1158/0008-5472.22363659.v1
Autor:
Marco Falasca, Paolo Innocenti, Barry V.L. Potter, Stefano Iacobelli, Massimo Broggini, Cosmo Rossi, H. Yasmin Godage, Adolfo Saiardi, Andrew M. Riley, Manuela Iezzi, Albana Cumashi, Enza Piccolo, Tania Maffucci
Supplementary Fig. S3 from Inhibition of the Phosphatidylinositol 3-Kinase/Akt Pathway by Inositol Pentakisphosphate Results in Antiangiogenic and Antitumor Effects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c1e9cedf937182c937b078b0d7495e
https://doi.org/10.1158/0008-5472.22363653
https://doi.org/10.1158/0008-5472.22363653
Autor:
Marco Falasca, Paolo Innocenti, Barry V.L. Potter, Stefano Iacobelli, Massimo Broggini, Cosmo Rossi, H. Yasmin Godage, Adolfo Saiardi, Andrew M. Riley, Manuela Iezzi, Albana Cumashi, Enza Piccolo, Tania Maffucci
Supplementary Fig. S2 from Inhibition of the Phosphatidylinositol 3-Kinase/Akt Pathway by Inositol Pentakisphosphate Results in Antiangiogenic and Antitumor Effects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba2e015294d08cc86f77ad5a6c10c24c
https://doi.org/10.1158/0008-5472.22363656.v1
https://doi.org/10.1158/0008-5472.22363656.v1
Publikováno v:
Tetrahedron: Asymmetry. 17:171-174
Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate via the formation of diastereoisomeric bis[(1S)-(−)-camphanate] esters provides a convenient and fast route to precursors for biologically important inositol phosphates and lipids, and to
Publikováno v:
Org. Biomol. Chem.. 1:3772-3786
A variety of beta- or alpha-C-glycosides may be readily accessed in an entirely stereoselective fashion from esters derived from the reaction of carboxylic acids and 3-hydroxy glycals, by way of a tandem reaction sequence of Tebbe methylenation and C
Autor:
H. Yasmin Godage, Antony J. Fairbanks
Publikováno v:
Tetrahedron Letters. 41:7589-7593
A variety of β- C -glycosides may be readily accessed in a stereoselective fashion from 3-OH glycal esters, via the use of Tebbe methylenation and subsequent thermal Claisen rearrangement. The use of carbohydrate ester substrates allows the formatio
Autor:
Andrew M. Riley, Alexander W. Cheesman, Barry V. L. Potter, H. Yasmin Godage, Benjamin L. Turner
Publikováno v:
Environmental Science & Technology
The inositol phosphates are an abundant but poorly understood group of organic phosphorus compounds found widely in the environment. Four stereoisomers of inositol hexakisphosphate (IP(6)) occur, although for three of these (scyllo, neo, and D-chiro)
Autor:
Albana Cumashi, Manuela Iezzi, Paolo Innocenti, Enza Piccolo, Adolfo Saiardi, Massimo Broggini, Barry V. L. Potter, Andrew M. Riley, Stefano Iacobelli, Marco Falasca, Cosmo Rossi, Tania Maffucci, H. Yasmin Godage
Publikováno v:
Cancer research. 65(18)
The purpose of this study was to investigate the antiangiogenic and in vivo properties of the recently identified phosphatidylinositol 3-kinase (PI3K)/Akt inhibitor Inositol(1,3,4,5,6) pentakisphosphate [Ins(1,3,4,5,6)P5]. Because activation of the P
Autor:
Antony J. Fairbanks, H. Yasmin Godage
Publikováno v:
ChemInform. 34
A variety of α-C-glycosides may be accessed in an entirely stereoselective fashion from 3-OH glycal esters, by way of the tandem reaction sequence of Tebbe methylenation and Claisen rearrangement. In contrast with previous studies in the correspondi
Autor:
H. Yasmin Godage, Antony J. Fairbanks
Publikováno v:
ChemInform. 31
A variety of β- C -glycosides may be readily accessed in a stereoselective fashion from 3-OH glycal esters, via the use of Tebbe methylenation and subsequent thermal Claisen rearrangement. The use of carbohydrate ester substrates allows the formatio