In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
February 18th, 2006 | 25 | Yes |
Popular Name: 2-benzooxazol-2-ylsulfanyl-N-(4-tetrazol-1-ylphenyl)-acetamide 2-benzooxazol-2-ylsulfanyl-N-(4-…
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) | 1.91 | -0.76 | -18.02 | 1 | 8 | 0 | 98 | 352.379 | 5 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MK01-1-E | Mitogen-activated Protein Kinase 1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 5000 | 0.30 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MK01_HUMAN | P28482 | MAP Kinase ERK2, Human | 5000 | 0.30 | Binding ≤ 10μM |
Description | Species |
---|---|
Activation of the AP-1 family of transcription factors | |
Advanced glycosylation endproduct receptor signaling | |
CREB phosphorylation through the activation of Ras | |
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 | |
NCAM signaling for neurite out-growth | |
Negative regulation of FGFR signaling | |
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.