2g01: Difference between revisions
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[[Image:2g01. | {{Seed}} | ||
[[Image:2g01.png|left|200px]] | |||
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{{STRUCTURE_2g01| PDB=2g01 | SCENE= }} | {{STRUCTURE_2g01| PDB=2g01 | SCENE= }} | ||
===Pyrazoloquinolones as Novel, Selective JNK1 inhibitors=== | |||
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{{ABSTRACT_PUBMED_16527482}} | |||
==About this Structure== | ==About this Structure== | ||
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[[Category: Jnk1]] | [[Category: Jnk1]] | ||
[[Category: Protein kinase jnk1 inhibitor]] | [[Category: Protein kinase jnk1 inhibitor]] | ||
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 15:09:55 2008'' | |||
Revision as of 12:09, 28 July 2008
Pyrazoloquinolones as Novel, Selective JNK1 inhibitors
Template:ABSTRACT PUBMED 16527482
About this Structure
2G01 is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Synthesis and SAR of 1,9-dihydro-9-hydroxypyrazolo[3,4-b]quinolin-4-ones as novel, selective c-Jun N-terminal kinase inhibitors., Liu M, Xin Z, Clampit JE, Wang S, Gum RJ, Haasch DL, Trevillyan JM, Abad-Zapatero C, Fry EH, Sham HL, Liu G, Bioorg Med Chem Lett. 2006 May 15;16(10):2590-4. Epub 2006 Mar 9. PMID:16527482
Page seeded by OCA on Mon Jul 28 15:09:55 2008
