Cellular influx, efflux, and anabolism of 3-carboranyl thymidine analogs: potential boron delivery agents for neutron capture therapy

E Sjuvarsson, VL Damaraju, D Mowles… - … of Pharmacology and …, 2013 - ASPET
3-[5-{2-(2, 3-Dihydroxyprop-1-yl)-o-carboran-1-yl} pentan-1-yl] thymidine (N5-2OH) is a first
generation 3-carboranyl thymidine analog (3CTA) that has been intensively studied as a …

Preparation and Biological Evaluation of 10B-Enriched 3-[5-{2-(2,3-Dihydroxyprop-1-yl)-o-carboran-1-yl}pentan-1-yl]thymidine (N5-2OH), a New Boron Delivery …

Y Byun, BTS Thirumamagal, W Yang… - Journal of medicinal …, 2006 - ACS Publications
3-[5-{2-(2, 3-Dihydroxyprop-1-yl)-o-carboran-1-yl} pentan-1-yl] thymidine (compound 1, N5-
2OH) belongs to a novel class of boron delivery agents for neutron capture therapy, which …

Synthesis and biological evaluation of neutral and zwitterionic 3-carboranyl thymidine analogues for boron neutron capture therapy

Y Byun, J Yan, AS Al-Madhoun… - Journal of medicinal …, 2005 - ACS Publications
Novel 3-carboranyl thymidine analogues (3CTAs) were synthesized as potential boron
delivery agents for boron neutron capture therapy (BNCT). This library includes six …

Thymidine kinase 1 as a molecular target for boron neutron capture therapy of brain tumors

RF Barth, W Yang, G Wu, M Swindall… - Proceedings of the …, 2008 - National Acad Sciences
The purpose of the present study was to evaluate the effectiveness of a 3-carboranyl
thymidine analogue (3CTA), 3-[5-{2-(2, 3-dihydroxyprop-1-yl)-o-carboran-1-yl} pentan-1-yl] …

Cellular Pharmacology of the D- and L-Enantiomers of β-5-o-Carboranyl-2′-deoxyuridine

SJ Hurwitz, L Ma, A Eleuteri, J Wright… - … Nucleotides & Nucleic …, 2000 - Taylor & Francis
The cellular pharmacology of the D-and L-enantiomers of β-5-o-carboranyl-2′-
deoxyuridine (CDU), compounds designed for boron neutron capture therapy (BNCT), were …

The synthesis and biochemical evaluation of thymidine analogues substituted with nido carborane at the N-3 position

Y Byun, J Yan, AS Al-Madhoun, J Johnsamuel… - Applied radiation and …, 2004 - Elsevier
Several thymidine analogues substituted with closo-and nido-carborane at the N-3 position
were synthesized. The nido-carboranyl thymidine analogues were designed to be effective …

Synthesis and biological evaluation of 3′-carboranyl thymidine analogues

J Yan, C Naeslund, AS Al-Madhoun, J Wang… - Bioorganic & medicinal …, 2002 - Elsevier
Boron neutron capture therapy (BNCT) is a chemoradio-therapeutic method for the treatment
of cancer. It depends on the selective targeting of tumor cells by boron-containing …

N3-substituted thymidine bioconjugates for cancer therapy and imaging

A Khalil, K Ishita, T Ali, W Tjarks - Future medicinal chemistry, 2013 - Taylor & Francis
The compound class of 3-carboranyl thymidine analogues (3CTAs) are boron delivery
agents for boron neutron capture therapy (BNCT), a binary treatment modality for cancer …

Synthesis and evaluation of thymidine kinase 1-targeting carboranyl pyrimidine nucleoside analogs for boron neutron capture therapy of cancer

HK Agarwal, A Khalil, K Ishita, W Yang… - European journal of …, 2015 - Elsevier
A library of sixteen 2nd generation amino-and amido-substituted carboranyl pyrimidine
nucleoside analogs, designed as substrates and inhibitors of thymidine kinase 1 (TK1) for …

Hydrophilically enhanced 3-carboranyl thymidine analogues (3CTAs) for boron neutron capture therapy (BNCT) of cancer

S Narayanasamy, BTS Thirumamagal… - Bioorganic & medicinal …, 2006 - Elsevier
Five novel 3-carboranyl thymidine analogues (3CTAs) were designed and synthesized for
boron neutron capture therapy (BNCT) of cancer. Phosphorylation of all five 3CTAs was …