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Results:
1-13
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Results: 13
Authors:
Matthews, SE
Pouton, CW
Threadgill, MD
Citation: Se. Matthews et al., Formation of hybrid polymethylene-poly(oxyethylene) macrocycles, TETRAHEDR L, 42(7), 2001, pp. 1355-1357
Authors:
Wayman, N
McDonald, MC
Thompson, AS
Threadgill, MD
Thiemermann, C
Citation: N. Wayman et al., 5-aminoisoquinolinone, a potent inhibitor of poly (adenosine 5 '-diphosphate ribose) polymerase, reduces myocardial infarct size, EUR J PHARM, 430(1), 2001, pp. 93-100
Authors:
Garrett, SW
Davies, OR
Milroy, DA
Wood, PJ
Pouton, CW
Threadgill, MD
Citation: Sw. Garrett et al., Synthesis and characterisation of polyamine-poly(ethylene glycol) constructs for DNA binding and gene delivery, BIO MED CH, 8(7), 2000, pp. 1779-1797
Authors:
Parveen, I
Threadgill, MD
Citation: I. Parveen et Md. Threadgill, Labelled compounds of interest as antitumour agents - VII. [H-2]- and [C-14]-curcumin, J LABEL C R, 43(9), 2000, pp. 883-889
Authors:
Matthews, SE
Pouton, CW
Threadgill, MD
Citation: Se. Matthews et al., A biodegradable multiblock co-polymer derived from an alpha,omega-bis(methylamino)peptide and an alpha,omega-bis(oxiranylmethyl)poly(ethylene glycol), J CONTR REL, 67(2-3), 2000, pp. 129-139
Authors:
McDonald, MC
Mota-Filipe, H
Wright, JA
Abdelrahman, M
Threadgill, MD
Thompson, AS
Thiemermann, C
Citation: Mc. Mcdonald et al., Effects of 5-aminoisoquinolinone, a water-soluble, potent inhibitor of theactivity of poly (ADP-ribose) polymerase on the organ injury and dysfunction caused by haemorrhagic shock, BR J PHARM, 130(4), 2000, pp. 843-850
Authors:
Matthews, SE
Pouton, CW
Threadgill, MD
Citation: Se. Matthews et al., Synthesis of porphyrin alpha,omega-bis(methylamino)peptide constructs, NEW J CHEM, 23(11), 1999, pp. 1087-1096
Authors:
Ulhaq, S
Chinje, EC
Naylor, MA
Jaffar, M
Stratford, IJ
Threadgill, MD
Citation: S. Ulhaq et al., Heterocyclic analogues of L-citrulline as inhibitors of the isoforms of nitric oxide synthase (NOS) and identification of N-delta-(4,5-dihydrothiazol-2-yl)ornithine as a potent inhibitor, BIO MED CH, 7(9), 1999, pp. 1787-1796
Authors:
Shinkwin, AE
Whish, WJD
Threadgill, MD
Citation: Ae. Shinkwin et al., Synthesis of thiophenecarboxamides, thieno [3,4-c] pyridin-4(5H)-ones and thieno[3,4-d]pyrimidin-4(3H)-ones and preliminary evaluation as inhibitors of poly(ADP-ribose)polymerase (PARP), BIO MED CH, 7(2), 1999, pp. 297-308
Authors:
Parveen, I
Naughton, DP
Whish, WJD
Threadgill, MD
Citation: I. Parveen et al., 2-Nitroimidazol-5-ylmethyl as a potential bioreductively activated prodrugsystem: Reductively triggered release of the PARP inhibitor 5-bromoisoquinolinone, BIOORG MED, 9(14), 1999, pp. 2031-2036
Authors:
Singh, SP
Kumar, D
Jones, BG
Threadgill, MD
Citation: Sp. Singh et al., Formation and dehydration of a series of 5-hydroxy-5-trifluoromethyl-4,5-dihydropyrazoles, J FLUORINE, 94(2), 1999, pp. 199-203
Authors:
Ulhaq, S
Chinje, EC
Naylor, MA
Jaffar, M
Stratford, IJ
Threadgill, MD
Citation: S. Ulhaq et al., S-2-amino-5-azolylpentanoic acids related to L-ornithine as inhibitors of the isoforms of nitric oxide synthase (NOS), BIO MED CH, 6(11), 1998, pp. 2139-2149
Authors:
Mahmud, NP
Garrett, SW
Threadgill, MD
Citation: Np. Mahmud et al., The 5-nitrofuran-2-ylmethylidene group as a potential bioreductively activated prodrug system for diol-containing drugs, ANTI-CAN DR, 13(6), 1998, pp. 655-662
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