In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
July 18th, 2008 | 25 | Yes |
Popular Name: 4-Amino-5-chloro-6-ethoxy-N-(4-(methylsulfonyl)benzyl)picolinamide 4-Amino-5-chloro-6-ethoxy-N-(4-(…
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CAS Number: N/A
Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | 1.43 | 0.45 | -15.1 | 3 | 7 | 0 | 111 | 383.857 | 6 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
KPCD2-1-E | Serine/threonine-protein Kinase D2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 5200 | 0.30 | Binding ≤ 10μM |
MK01-1-E | Mitogen-activated Protein Kinase 1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 3400 | 0.31 | Binding ≤ 10μM |
MK08-1-E | Mitogen-activated Protein Kinase 8 (cluster #1 Of 5), Eukaryotic | Eukaryotes | 4 | 0.47 | Binding ≤ 10μM |
MK09-1-E | C-Jun N-terminal Kinase 2 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 74 | 0.40 | Binding ≤ 10μM |
MK10-1-E | C-Jun N-terminal Kinase 3 (cluster #1 Of 2), Eukaryotic | Eukaryotes | 120 | 0.39 | Binding ≤ 10μM |
MK08-1-E | C-Jun N-terminal Kinase 1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 480 | 0.35 | Functional ≤ 10μM |
MK09-1-E | C-Jun N-terminal Kinase 2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 480 | 0.35 | Functional ≤ 10μM |
MK10-1-E | C-Jun N-terminal Kinase 3 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 480 | 0.35 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MK08_HUMAN | P45983 | C-Jun N-terminal Kinase 1, Human | 24 | 0.43 | Binding ≤ 1μM |
MK09_HUMAN | P45984 | C-Jun N-terminal Kinase 2, Human | 74 | 0.40 | Binding ≤ 1μM |
MK10_HUMAN | P53779 | C-Jun N-terminal Kinase 3, Human | 120 | 0.39 | Binding ≤ 1μM |
MK08_HUMAN | P45983 | C-Jun N-terminal Kinase 1, Human | 24 | 0.43 | Binding ≤ 10μM |
MK09_HUMAN | P45984 | C-Jun N-terminal Kinase 2, Human | 74 | 0.40 | Binding ≤ 10μM |
MK10_HUMAN | P53779 | C-Jun N-terminal Kinase 3, Human | 120 | 0.39 | Binding ≤ 10μM |
MK01_HUMAN | P28482 | MAP Kinase ERK2, Human | 3400 | 0.31 | Binding ≤ 10μM |
KPCD2_HUMAN | Q9BZL6 | Serine/threonine-protein Kinase D2, Human | 5200 | 0.30 | Binding ≤ 10μM |
MK08_HUMAN | P45983 | C-Jun N-terminal Kinase 1, Human | 480 | 0.35 | Functional ≤ 10μM |
MK09_HUMAN | P45984 | C-Jun N-terminal Kinase 2, Human | 480 | 0.35 | Functional ≤ 10μM |
MK10_HUMAN | P53779 | C-Jun N-terminal Kinase 3, Human | 480 | 0.35 | Functional ≤ 10μM |
Description | Species |
---|---|
Activation of BIM and translocation to mitochondria | |
Activation of BMF and translocation to mitochondria | |
Activation of the AP-1 family of transcription factors | |
Advanced glycosylation endproduct receptor signaling | |
CREB phosphorylation through the activation of Ras | |
DSCAM interactions | |
ERK/MAPK targets | |
ERK2 activation | |
ERKs are inactivated | |
FCERI mediated MAPK activation | |
Gastrin-CREB signalling pathway via PKC and MAPK | |
Golgi Cisternae Pericentriolar Stack Reorganization | |
Growth hormone receptor signaling | |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human | |
NCAM signaling for neurite out-growth | |
Negative regulation of FGFR signaling | |
NRAGE signals death through JNK | |
NRIF signals cell death from the nucleus | |
Oncogene Induced Senescence | |
Oxidative Stress Induced Senescence | |
phospho-PLA2 pathway | |
Recycling pathway of L1 | |
Regulation of actin dynamics for phagocytic cup formation | |
Regulation of HSF1-mediated heat shock response | |
RSK activation | |
Senescence-Associated Secretory Phenotype (SASP) | |
Signal attenuation | |
Signal transduction by L1 | |
Signaling by FGFR | |
Thrombin signalling through proteinase activated receptors (PARs) |
No pre-computed analogs available. Try a structural similarity search.