21 results on '"Posteri, Helena"'
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2. Discovery of Stereospecific PARP-1 Inhibitor Isoindolinone NMS-P515
3. Abstract 3795: Novel and selective MELK kinase inhibitors active in breast cancer cell lines
4. Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP-1 Inhibitor for Cancer Therapy
5. Synthesis and SAR of new pyrazolo[4,3- h]quinazoline-3-carboxamide derivatives as potent and selective MPS1 kinase inhibitors
6. NMS-P937, a 4,5-dihydro-1 H-pyrazolo[4,3- h]quinazoline derivative as potent and selective Polo-like kinase 1 inhibitor
7. 4,5-Dihydro-1H-pyrazolo[4,3-h]quinazolines as potent and selective Polo-like kinase 1 (PLK1) inhibitors
8. Abstract 1775: Characterization of new highly selective and potent PARP-1 inhibitors
9. NMS-P937, a 4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline derivative as potent and selective Polo-like kinase 1 inhibitor
10. Identification of 4,5-Dihydro-1H-pyrazolo[4,3-h]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors
11. Abstract 691: In vitro and in vivo characterization of selective orally available Parp-1 inhibitors with demonstrated antitumor efficacy in BRCA negative cancer models
12. Poly(ADP-ribose) polymerase inhibition in cancer therapy: are we close to maturity?
13. Nicotinoyl Azide
14. A New Glycociamidine Ring Precursor: Syntheses of (Z)-Hymenialdisine (Ia), (Z)-2-Debromohymenialdisine (Ib), and (.+-.)-endo-2-Debromohymenialdisine (II).
15. A New Glycociamidine Ring Precursor: Syntheses of (Z)-Hymenialdisine, (Z)-2-Debromohymenialdisine, and (±)-endo-2-Debromohymenialdisine
16. Nicotinoyl Azide (NCA)‐Mediated Mitsunobu Reaction: An Expedient One‐Pot Transformation of Alcohols into Azides.
17. Synthesis, Conformational Studies and Mannosidase Stability of a Mimic of 1,2-Mannobioside
18. Nicotinoyl Azide (NCA)-Mediated Mitsunobu Reaction: An Expedient One-Pot Transformation of Alcohols into Azides
19. Mimics of Ganglioside GM1 as Cholera Toxin Ligands: Replacement of the GalNAc Residue.
20. Mimics of ganglioside GM1 as cholera toxin ligands: replacement of the GalNAc residueElectronic supplementary information (ESI) available: synthetic details, product characterisations and full NOE contact list. See http://www.rsc.org/suppdata/ob/b2/b210503a/
21. A new glycociamidine ring precursor: syntheses of (Z)-hymenialdisine, (Z)-2-debromohymenialdisine, and (+/-)-endo-2-debromohymenialdisine.
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