 
| In ZINC since | Heavy atoms | Benign functionality | 
|---|---|---|
| August 19th, 2011 | 17 | Yes | 
None
| 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) | 2.30 | 5.2 | -11.72 | 1 | 5 | 0 | 59 | 227.271 | 3 | ↓ | 
| Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type | 
|---|---|---|---|---|---|
| GSK3B-1-E | Glycogen Synthase Kinase-3 Beta (cluster #1 Of 7), Eukaryotic | Eukaryotes | 2026 | 0.47 | Binding ≤ 10μM | 
| JAK2-1-E | Tyrosine-protein Kinase JAK2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 756 | 0.50 | Binding ≤ 10μM | 
| PIM1-1-E | Serine/threonine-protein Kinase PIM1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 8359 | 0.42 | Binding ≤ 10μM | 
| ROCK2-2-E | Rho-associated Protein Kinase 2 (cluster #2 Of 2), Eukaryotic | Eukaryotes | 108 | 0.57 | Binding ≤ 10μM | 
| Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type | 
|---|---|---|---|---|---|
| ROCK2_HUMAN | O75116 | Rho-associated Protein Kinase 2, Human | 108 | 0.57 | Binding ≤ 1μM | 
| JAK2_HUMAN | O60674 | Tyrosine-protein Kinase JAK2, Human | 756 | 0.50 | Binding ≤ 1μM | 
| GSK3B_HUMAN | P49841 | Glycogen Synthase Kinase-3 Beta, Human | 2026 | 0.47 | Binding ≤ 10μM | 
| ROCK2_HUMAN | O75116 | Rho-associated Protein Kinase 2, Human | 108 | 0.57 | Binding ≤ 10μM | 
| PIM1_HUMAN | P11309 | Serine/threonine-protein Kinase PIM1, Human | 8359 | 0.42 | Binding ≤ 10μM | 
| JAK2_HUMAN | O60674 | Tyrosine-protein Kinase JAK2, Human | 756 | 0.50 | Binding ≤ 10μM | 
| Description | Species | 
|---|---|
| AKT phosphorylates targets in the cytosol | |
| APC truncation mutants have impaired AXIN binding | |
| AXIN missense mutants destabilize the destruction complex | |
| Beta-catenin phosphorylation cascade | |
| Constitutive PI3K/AKT Signaling in Cancer | |
| CRMPs in Sema3A signaling | |
| Degradation of beta-catenin by the destruction complex | |
| disassembly of the destruction complex and recruitment of AXIN to the membrane | |
| EPHA-mediated growth cone collapse | |
| EPHB-mediated forward signaling | |
| Factors involved in megakaryocyte development and platelet production | |
| G alpha (12/13) signalling events | |
| Growth hormone receptor signaling | |
| Interferon gamma signaling | |
| Interleukin receptor SHC signaling | |
| Interleukin-3, 5 and GM-CSF signaling | |
| Interleukin-6 signaling | |
| misspliced GSK3beta mutants stabilize beta-catenin | |
| Prolactin receptor signaling | |
| Regulation of HSF1-mediated heat shock response | |
| Regulation of IFNG signaling | |
| RMTs methylate histone arginines | |
| S33 mutants of beta-catenin aren't phosphorylated | |
| S37 mutants of beta-catenin aren't phosphorylated | |
| S45 mutants of beta-catenin aren't phosphorylated | |
| Sema4D induced cell migration and growth-cone collapse | |
| Signaling by Leptin | |
| Signaling by SCF-KIT | |
| T41 mutants of beta-catenin aren't phosphorylated | |
| truncations of AMER1 destabilize the destruction complex | |
| VEGFA-VEGFR2 Pathway | 
No pre-computed analogs available. Try a structural similarity search.