Physical Representations
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)
|
3.66 |
8.19 |
-10.64 |
2 |
6 |
0 |
76 |
358.398 |
6 |
↓
|
Clustered Target Annotations
Code |
Organism Class |
Affinity (nM) |
LE (kcal/mol/atom) |
Type |
AKT3-2-E |
Serine/threonine-protein Kinase AKT3 (cluster #2 Of 2), Eukaryotic |
Eukaryotes |
7400 |
0.29 |
Binding ≤ 10μM
|
ChEMBL Target Annotations
Uniprot |
Swissprot |
Affinity (nM) |
LE (kcal/mol/atom) |
Type |
AKT3_HUMAN |
Q9Y243
|
Serine/threonine-protein Kinase AKT3, Human |
7400 |
0.29 |
Binding ≤ 10μM
|
Reactome Annotations from Targets (via Uniprot)
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 |
|
CD28 dependent PI3K/Akt signaling |
|
Constitutive PI3K/AKT Signaling in Cancer |
|
CTLA4 inhibitory signaling |
|
Downregulation of ERBB2:ERBB3 signaling |
|
G beta:gamma signalling through PI3Kgamma |
|
GPVI-mediated activation cascade |
|
Negative regulation of the PI3K/AKT network |
|
PIP3 activates AKT signaling |
|
VEGFR2 mediated vascular permeability |
|
No pre-computed analogs available. Try a structural similarity search.