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PubPharm (269)
261
Novel inhibitors of bacterial protein synthesis : structure-activity relationships for 1,8-naphthyridine derivatives incorporating position 3 and 4 variants
enthalten in:
Bioorganic & medicinal chemistry letters
| 2004
von
Clark, R.
|
Wang, S.
|
Ma, Z.
| +18
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262
Structure-activity relationships of novel potent MurF inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2004
von
Gu, Y.
|
Florjancic, A.
|
Clark, R.
| +10
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263
Structure-activity relationships of novel potent MurF inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2004
von
Gu, Y.
|
Florjancic, A.
|
Clark, R.
| +6
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264
Identification of a monoacid-based, cell permeable, selective inhibitor of protein tyrosine phosphatase 1B
enthalten in:
Bioorganic & medicinal chemistry letters
| 2003
von
Xin, Z.
|
Liu, G.
|
Abad-Zapatero, C.
| +11
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265
Cloning and expression of human canstatin and its purification and bioactivity
enthalten in:
Wei sheng wu xue bao = Acta microbiologica Sinica
| 2003
von
He, G.
|
Luo, J.
|
Zhang, T.
| +2
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266
Discovery and SAR of novel, potent and selective protein tyrosine phosphatase 1B inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2003
von
Pei, Z.
|
Li, X.
|
Liu, G.
| +7
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267
Discovery and SAR of novel, potent and selective protein tyrosine phosphatase 1B inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2003
von
Pei, Z.
|
Li, X.
|
Liu, G.
| +6
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268
Identification of a monoacid-Based, cell permeable, selective inhibitor of protein tyrosine phosphatase 1B
enthalten in:
Bioorganic & medicinal chemistry letters
| 2003
von
Xin, Z.
|
Liu, G.
|
Abad-Zapatero, C.
| +6
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269
PROTEIN CHEMISTRY AND STRUCTURE - CCR5 HIV-1 coreceptor activity. Role of cooperativity between residues in N-terminal extracellular and intracellular domains
enthalten in:
The journal of biological chemistry
| 1999
von
Wang, Z.
|
Lee, B.
|
Murray, J.
| +5
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