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)
|
3.43 |
14.23 |
-51.13 |
1 |
6 |
1 |
53 |
413.549 |
6 |
↓
|
Clustered Target Annotations
Code |
Organism Class |
Affinity (nM) |
LE (kcal/mol/atom) |
Type |
MLTK-1-E |
Mixed Lineage Kinase 7 (cluster #1 Of 1), Eukaryotic |
Eukaryotes |
4880 |
0.24 |
Binding ≤ 10μM
|
TGFR1-1-E |
TGF-beta Receptor Type I (cluster #1 Of 1), Eukaryotic |
Eukaryotes |
246 |
0.30 |
Binding ≤ 10μM
|
TGFR1-1-E |
TGF-beta Receptor Type I (cluster #1 Of 1), Eukaryotic |
Eukaryotes |
854 |
0.27 |
Functional ≤ 10μM
|
TGFR2-1-E |
TGF-beta Receptor Type II (cluster #1 Of 1), Eukaryotic |
Eukaryotes |
854 |
0.27 |
Functional ≤ 10μM
|
Reactome Annotations from Targets (via Uniprot)
Description |
Species |
Downregulation of TGF-beta receptor signaling |
|
SMAD2/3 MH2 Domain Mutants in Cancer |
|
SMAD2/3 Phosphorylation Motif Mutants in Cancer |
|
TGF-beta receptor signaling activates SMADs |
|
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
|
TGFBR1 KD Mutants in Cancer |
|
TGFBR1 LBD Mutants in Cancer |
|
TGFBR2 Kinase Domain Mutants in Cancer |
|
TGFBR2 MSI Frameshift Mutants in Cancer |
|
No pre-computed analogs available. Try a structural similarity search.