Reaction Details | |||
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Report a problem with these data | |||
Cell Reactant: | JNK2/JNK3 | ||
Syringe Reactant: | BDBM26057 | ||
Meas. Tech.: | Isothermal Titration Calorimetry | ||
Entry Date: | 12/18/08 | ||
Δ G ° : | n/a | ||
pH: | 7.4±n/a | ||
Log10Kb: | 5.09± 4.76 | ||
Temperature: | 298.15±n/a (K) | ||
ΔH° : | n/a | ||
ΔHobs: | n/a | ||
Ionic Strength: | n/a | ||
no | |||
Protons Released: | n/a | ||
ΔCp : | n/a | ||
Stoich. Param.: | n/a | ||
ΔS° : | n/a | ||
Comments: | n/a | ||
Citation | Stebbins, JL; De, SK; Machleidt, T; Becattini, B; Vazquez, J; Kuntzen, C; Chen, LH; Cellitti, JF; Riel-Mehan, M; Emdadi, A; Solinas, G; Karin, M; Pellecchia, M Identification of a new JNK inhibitor targeting the JNK-JIP interaction site. Proc Natl Acad Sci U S A105:16809-13 (2008) [PubMed] Article | ||
More Info.: | Get all data from this article , ITC RUN data , Solution Info , Data Fit Method , Instrument Info | ||
JNK2/JNK3 | |||
Source: | n/a | ||
Purity: | n/a | ||
Prep. Method: | n/a | ||
Name: | Mitogen-activated protein kinase 9 | ||
Synonyms: | JNK-55 | JNK2 | JNK2/JNK3 | MAPK9 | MK09_HUMAN | Mitogen-Activated Protein Kinase 9 (JNK2) | Mitogen-activated protein kinase 8/9 | PRKM9 | SAPK1A | Stress-activated protein kinase JNK2 | c-Jun N-terminal kinase 2 | c-Jun N-terminal kinase 2 (JNK2) | ||
Type: | Enzyme | ||
Mol. Mass.: | 48131.49 | ||
Organism: | Homo sapiens (Human) | ||
Description: | JNK-2 was purchased from Upstate Cell Signaling Solutions (formerly Upstate Biotechnology). | ||
Residue: | 424 | ||
Sequence: |
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BDBM26057 | |||
Source: | n/a | ||
Purity: | n/a | ||
Prep. Method: | n/a | ||
Name | BDBM26057 | ||
Synonyms: | 4-(2,3-dihydro-1,4-benzodioxin-6-yl)-5-[(5-nitro-1,3-thiazol-2-yl)sulfanyl]-4H-1,2,4-triazol-3-ol | BI-78D3 | ||
Type | Small organic molecule | ||
Emp. Form. | C13H9N5O5S2 | ||
Mol. Mass. | 379.371 | ||
SMILES | [O-][N+](=O)c1cnc(Sc2n[nH]c(=O)n2-c2ccc3OCCOc3c2)s1 | ||
Structure |
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