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)
|
7.25 |
13.85 |
-39.59 |
2 |
4 |
1 |
43 |
458.553 |
7 |
↓
|
ChEMBL Target Annotations
Uniprot |
Swissprot |
Affinity (nM) |
LE (kcal/mol/atom) |
Type |
ESR1_RAT |
P06211
|
Estrogen Receptor Alpha, Rat |
0.25 |
0.40 |
Binding ≤ 1μM
|
ESR1_HUMAN |
P03372
|
Estrogen Receptor Alpha, Human |
0.24 |
0.40 |
Binding ≤ 1μM
|
ESR2_HUMAN |
Q92731
|
Estrogen Receptor Beta, Human |
0.28 |
0.39 |
Binding ≤ 1μM
|
ESR2_RAT |
Q62986
|
Estrogen Receptor Beta, Rat |
0.3 |
0.39 |
Binding ≤ 1μM
|
ESR1_RAT |
P06211
|
Estrogen Receptor Alpha, Rat |
0.25 |
0.40 |
Binding ≤ 10μM
|
ESR1_HUMAN |
P03372
|
Estrogen Receptor Alpha, Human |
0.24 |
0.40 |
Binding ≤ 10μM
|
ESR2_HUMAN |
Q92731
|
Estrogen Receptor Beta, Human |
0.28 |
0.39 |
Binding ≤ 10μM
|
ESR2_RAT |
Q62986
|
Estrogen Receptor Beta, Rat |
0.3 |
0.39 |
Binding ≤ 10μM
|
ESR1_HUMAN |
P03372
|
Estrogen Receptor Alpha, Human |
0.34 |
0.39 |
Functional ≤ 10μM
|
ESR2_HUMAN |
Q92731
|
Estrogen Receptor Beta, Human |
0.34 |
0.39 |
Functional ≤ 10μM
|
Z81068 |
Z81068
|
Ishikawa (Uterine Carcinoma Cells) |
3.2 |
0.35 |
Functional ≤ 10μM
|
Z80224 |
Z80224
|
MCF7 (Breast Carcinoma Cells) |
0.34 |
0.39 |
Functional ≤ 10μM
|
Reactome Annotations from Targets (via Uniprot)
Description |
Species |
Nuclear Receptor transcription pathway |
|
Nuclear signaling by ERBB4 |
|
No pre-computed analogs available. Try a structural similarity search.