In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 22nd, 2008 | 31 | No |
Popular Name: 3-[(E)-3-(1H-benzimidazol-2-yl)prop-2-enoyl]-6-chloro-4-phenyl-1H-quinolin-2-one 3-[(E)-3-(1H-benzimidazol-2-yl)p…
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) | 5.06 | 11.39 | -15.33 | 2 | 5 | 0 | 79 | 425.875 | 4 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
AKT1-2-E | RAC-alpha Serine/threonine-protein Kinase (cluster #2 Of 3), Eukaryotic | Eukaryotes | 4500 | 0.24 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
AKT1_HUMAN | P31749 | Serine/threonine-protein Kinase AKT, Human | 3900 | 0.24 | Binding ≤ 10μM |
Description | Species |
---|---|
Activation of BAD and translocation to mitochondria | |
AKT phosphorylates targets in the cytosol | |
AKT phosphorylates targets in the nucleus | |
AKT-mediated inactivation of FOXO1A | |
Butyrate Response Factor 1 (BRF1) destabilizes mRNA | |
CD28 dependent PI3K/Akt signaling | |
Constitutive PI3K/AKT Signaling in Cancer | |
CTLA4 inhibitory signaling | |
deactivation of the beta-catenin transactivating complex | |
Downregulation of ERBB2:ERBB3 signaling | |
eNOS activation | |
G beta:gamma signalling through PI3Kgamma | |
GPVI-mediated activation cascade | |
Integrin alphaIIb beta3 signaling | |
KSRP destabilizes mRNA | |
Negative regulation of the PI3K/AKT network | |
PIP3 activates AKT signaling | |
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | |
Translocation of GLUT4 to the plasma membrane | |
VEGFR2 mediated vascular permeability |
No pre-computed analogs available. Try a structural similarity search.