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The squalestatins: synthesis and biological activity of some C3-modified analogues; replacement of a carboxylic acid or methyl ester with an isoelectronic heterocyclic functionality. [electronic resource] by
- Bamford, M J
- Chan, C
- Craven, A P
- Dymock, B W
- Green, D
- Henson, R A
- Kirk, B E
- Lester, M G
- Procopiou, P A
- Snowden, M A
Producer: 19951004
In:
Journal of medicinal chemistry vol. 38
Availability: No items available.
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The squalestatins: novel inhibitors of squalene synthase. Enzyme inhibitory activities and in vivo evaluation of C1-modified analogues. [electronic resource] by
- Procopiou, P A
- Bailey, E J
- Bamford, M J
- Craven, A P
- Dymock, B W
- Houston, J G
- Hutson, J L
- Kirk, B E
- McCarthy, A D
- Sareen, M
Producer: 19941103
In:
Journal of medicinal chemistry vol. 37
Availability: No items available.
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5.
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A fluorescence polarization assay for inhibitors of Hsp90. [electronic resource] by
- Howes, R
- Barril, X
- Dymock, B W
- Grant, K
- Northfield, C J
- Robertson, A G S
- Surgenor, A
- Wayne, J
- Wright, L
- James, K
- Matthews, T
- Cheung, K-M
- McDonald, E
- Workman, P
- Drysdale, M J
Producer: 20060518
In:
Analytical biochemistry vol. 350
Availability: No items available.
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6.
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The squalestatins: decarboxy and 4-deoxy analogues as potent squalene synthase inhibitors. [electronic resource] by
- Chan, C
- Andreotti, D
- Cox, B
- Dymock, B W
- Hutson, J L
- Keeling, S E
- McCarthy, A D
- Procopiou, P A
- Ross, B C
- Sareen, M
- Scicinski, J J
- Sharratt, P J
- Snowden, M A
- Watson, N S
Producer: 19960301
In:
Journal of medicinal chemistry vol. 39
Availability: No items available.
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TG02, a novel oral multi-kinase inhibitor of CDKs, JAK2 and FLT3 with potent anti-leukemic properties. [electronic resource] by
- Goh, K C
- Novotny-Diermayr, V
- Hart, S
- Ong, L C
- Loh, Y K
- Cheong, A
- Tan, Y C
- Hu, C
- Jayaraman, R
- William, A D
- Sun, E T
- Dymock, B W
- Ong, K H
- Ethirajulu, K
- Burrows, F
- Wood, J M
Producer: 20120330
In:
Leukemia vol. 26
Availability: No items available.
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8.
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SB1518, a novel macrocyclic pyrimidine-based JAK2 inhibitor for the treatment of myeloid and lymphoid malignancies. [electronic resource] by
- Hart, S
- Goh, K C
- Novotny-Diermayr, V
- Hu, C Y
- Hentze, H
- Tan, Y C
- Madan, B
- Amalini, C
- Loh, Y K
- Ong, L C
- William, A D
- Lee, A
- Poulsen, A
- Jayaraman, R
- Ong, K H
- Ethirajulu, K
- Dymock, B W
- Wood, J W
Producer: 20111222
In:
Leukemia vol. 25
Availability: No items available.
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