H. Kendrick

发表

Activity of bisphosphonates against Trypanosoma brucei rhodesiense.

E. Oldfield, S. Croft, Jared C. Lewis, 2002, Journal of medicinal chemistry.

Bisphosphonates inhibit the growth of Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: a potential route to chemotherapy.

E. Oldfield, V. Yardley, S. Croft, 2001, Journal of medicinal chemistry.

Synthesis and antileishmanial activity of novel buparvaquone oxime derivatives.

S. Croft, T. Nevalainen, T. Järvinen, 2004, Bioorganic & medicinal chemistry.

Squalamine analogues as potential anti-trypanosomal and anti-leishmanial compounds.

I. Gilbert, V. Yardley, S. Croft, 2000, Bioorganic & medicinal chemistry letters.

Synthesis, stability, and antimalarial activity of new hydrolytically stable and water-soluble (+)-deoxoartelinic acid.

S. Croft, B. Robinson, M. Jung, 2002, Journal of medicinal chemistry.

Metalloantimalarials: synthesis, X-ray crystal structure of potent antimalarial copper (II) complex of arylazo-4-hydroxy-1,2-naphthoquinone.

S. Croft, V. McKee, S. Padhye, 2006, Bioorganic & medicinal chemistry letters.

Design, synthesis, and biological evaluation of a series of simple and novel potential antimalarial compounds.

V. Yardley, S. Croft, H. Ren, 2001, Bioorganic & medicinal chemistry letters.

Effects of bisphosphonates on the growth of Entamoeba histolytica and Plasmodium species in vitro and in vivo.

E. Oldfield, S. Croft, R. G. Kemp, 2004, Journal of medicinal chemistry.

In vitro antiprotozoal activity of extract and compounds from the stem bark of Combretum molle

V. Yardley, S. Croft, K. Asres, 2001, Phytotherapy research : PTR.

Squalamine Analogues as Potential Anti‐Trypanosomal and Anti‐Leishmanial Compounds.

I. Gilbert, V. Yardley, S. Croft, 2000 .

Synthesis and evaluation of cryptolepine analogues for their potential as new antimalarial agents.

S. Croft, J. Brown, P. Pollet, 2001, Journal of medicinal chemistry.

Antiplasmodial activities of some Ghanaian plants traditionally used for fever/malaria treatment and of some alkaloids isolated from Pleiocarpa mutica; in vivo antimalarial activity of pleiocarpine.

C. Wright, H. Kendrick, J. Addae-Kyereme, 2001, Journal of ethnopharmacology.

Synthesis of some cryptolepine analogues, assessment of their antimalarial and cytotoxic activities, and consideration of their antimalarial mode of action.

S. Croft, S. Parapini, D. Taramelli, 2005, Journal of medicinal chemistry.

Antiprotozoal and cytotoxicity evaluation of sulfonamide and urea analogues of quinacrine.

A. Fairlamb, V. Yardley, S. Croft, 2001, Bioorganic & medicinal chemistry letters.

Design, synthesis, and biological evaluation of a series of simple and novel potential antimalarial compounds.

V. Yardley, S. Croft, H. Ren, 2001, Bioorganic & medicinal chemistry letters.

QSAR study on the contribution of log P and E(s) to the in vitro antiprotozoal activity of glutathione derivatives.

V. Yardley, S. Croft, S. Daunes, 2001, Journal of medicinal chemistry.

Transition metal complexes of buparvaquone as potent new antimalarial agents. 1. Synthesis, X-ray crystal-structures, electrochemistry and antimalarial activity against Plasmodium falciparum.

S. Croft, A. Powell, S. Padhye, 2003, Journal of inorganic biochemistry.

Synthesis and characterization of copper(II) complexes of pyridine-2-carboxamidrazones as potent antimalarial agents

S. Croft, A. Powell, S. Padhye, 2003 .

Isolation and in vitro antiplasmodial activities of alkaloids from Teclea trichocarpa: in vivo antimalarial activity and X-ray crystal structure of normelicopicine.

S. Croft, I. Scowen, W. Abraham, 2002, Journal of natural products.

Peptidomimetic inhibitors of protein farnesyltransferase show potent antimalarial activity.

S. Croft, M. Gelb, S. Sebti, 2001, Bioorganic & medicinal chemistry letters.

Drug sensitivity of Leishmania species: some unresolved problems.

V. Yardley, S. Croft, H. Kendrick, 2002, Transactions of the Royal Society of Tropical Medicine and Hygiene.

Identification and Activity of a Series of Azole-based Compounds with Lactate Dehydrogenase-directed Anti-malarial Activity*

Araceli, V. J. Winter, S. Croft, 2004, Journal of Biological Chemistry.

Plasmodium falciparum: stage specific effects of a selective inhibitor of lactate dehydrogenase.

S. Croft, J. Lavandera, David Barros, 2005, Experimental parasitology.

In vitro and in vivo antimalarial activity of peptidomimetic protein farnesyltransferase inhibitors with improved membrane permeability.

D. Chakrabarti, S. Croft, M. Gelb, 2004, Bioorganic & medicinal chemistry.

Metallocene-based antimalarials: an exploration into the influence of the ferrocenyl moiety on in vitro antimalarial activity in chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum.

S. Croft, K. Chibale, J. R. Moss, 2007, Bioorganic & medicinal chemistry.

Synthesis and in vitro anti-protozoal activity of a series of benzotropolone derivatives incorporating endocyclic hydrazines.

V. Yardley, S. Croft, H. Ren, 2003, European journal of medicinal chemistry.

Use of an additional hydrophobic binding site, the Z site, in the rational drug design of a new class of stronger trypanothione reductase inhibitor, quaternary alkylammonium phenothiazines

D. Marks, V. Yardley, S. Croft, 2000 .

Use of an additional hydrophobic binding site, the Z site, in the rational drug design of a new class of stronger trypanothione reductase inhibitor, quaternary alkylammonium phenothiazines.

D. Marks, V. Yardley, S. Croft, 2000, Journal of medicinal chemistry.