List of works - Ana-Isabel Hernández

5'-O-Tritylated Nucleoside Derivatives: Inhibition of Thymidine Phosphorylase and Angiogenesis

scientific article published on 04 May 2006

5‘-O-Tritylinosine and Analogues as Allosteric Inhibitors of Human Thymidine Phosphorylase

scientific article published on 01 September 2006

Acyclic nucleoside analogues as novel inhibitors of human mitochondrial thymidine kinase.

scientific article

Bromovinyl-deoxyuridine: A selective substrate for mitochondrial thymidine kinase in cell extracts

scientific article published on 01 May 2006

Chemical interrogation of FOXO3a nuclear translocation identifies potent and selective inhibitors of phosphoinositide 3-kinases

scientific article published on 18 August 2009

Exploring acyclic nucleoside analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase.

scientific article

Identification of ETP-46321, a potent and orally bioavailable PI3K α, δ inhibitor.

scientific article

Imidazo[1,2-a]pyrazines as novel PI3K inhibitors

scientific article published on 28 January 2012

Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamides

scientific article published in September 2003

Mitochondrial thymidine kinase inhibitors

scientific article

N1-Substituted Thymine Derivatives as Mitochondrial Thymidine Kinase (TK-2) Inhibitors

scientific article published on 01 December 2006

Non-nucleoside inhibitors of mitochondrial thymidine kinase (TK-2) differentially inhibit the closely related herpes simplex virus type 1 TK and Drosophila melanogaster multifunctional deoxynucleoside kinase

scientific article published in February 2003

Rapid identification of ETP-46992, orally bioavailable PI3K inhibitor, selective versus mTOR.

scientific article

Structure, physiological role, and specific inhibitors of human thymidine kinase 2 (TK2): present and future.

scientific article published on September 2008

The nucleoside derivative 5'-O-trityl-inosine (KIN59) suppresses thymidine phosphorylase-triggered angiogenesis via a noncompetitive mechanism of action

scientific article

Thymidine phosphorylase inhibitors: recent developments and potential therapeutic applications

scientific article

List of works by Ana-Isabel Hernández

5'-O-Tritylated Nucleoside Derivatives: Inhibition of Thymidine Phosphorylase and Angiogenesis

5‘-O-Tritylinosine and Analogues as Allosteric Inhibitors of Human Thymidine Phosphorylase

Acyclic nucleoside analogues as novel inhibitors of human mitochondrial thymidine kinase.

Bromovinyl-deoxyuridine: A selective substrate for mitochondrial thymidine kinase in cell extracts

Chemical interrogation of FOXO3a nuclear translocation identifies potent and selective inhibitors of phosphoinositide 3-kinases

Exploring acyclic nucleoside analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase.

Identification of ETP-46321, a potent and orally bioavailable PI3K α, δ inhibitor.

Imidazo[1,2-a]pyrazines as novel PI3K inhibitors

Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamides

Mitochondrial thymidine kinase inhibitors

N1-Substituted Thymine Derivatives as Mitochondrial Thymidine Kinase (TK-2) Inhibitors

Non-nucleoside inhibitors of mitochondrial thymidine kinase (TK-2) differentially inhibit the closely related herpes simplex virus type 1 TK and Drosophila melanogaster multifunctional deoxynucleoside kinase

Rapid identification of ETP-46992, orally bioavailable PI3K inhibitor, selective versus mTOR.

Structure, physiological role, and specific inhibitors of human thymidine kinase 2 (TK2): present and future.

The nucleoside derivative 5'-O-trityl-inosine (KIN59) suppresses thymidine phosphorylase-triggered angiogenesis via a noncompetitive mechanism of action

Thymidine phosphorylase inhibitors: recent developments and potential therapeutic applications