In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
March 2nd, 2009 | 23 | No |
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) | 3.36 | 5.09 | -6.07 | 2 | 2 | 0 | 40 | 320.448 | 1 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
ANDR-2-E | Androgen Receptor (cluster #2 Of 4), Eukaryotic | Eukaryotes | 11 | 0.48 | Binding ≤ 10μM |
ESR1-2-E | Estrogen Receptor Alpha (cluster #2 Of 5), Eukaryotic | Eukaryotes | 4280 | 0.33 | Binding ≤ 10μM |
ESR2-2-E | Estrogen Receptor Beta (cluster #2 Of 4), Eukaryotic | Eukaryotes | 25 | 0.46 | Binding ≤ 10μM |
ESR1-2-E | Estrogen Receptor Alpha (cluster #2 Of 3), Eukaryotic | Eukaryotes | 622 | 0.38 | Functional ≤ 10μM |
ESR2-1-E | Estrogen Receptor Beta (cluster #1 Of 2), Eukaryotic | Eukaryotes | 4 | 0.51 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
ANDR_HUMAN | P10275 | Androgen Receptor, Human | 11 | 0.48 | Binding ≤ 1μM |
ESR2_HUMAN | Q92731 | Estrogen Receptor Beta, Human | 25 | 0.46 | Binding ≤ 1μM |
ANDR_HUMAN | P10275 | Androgen Receptor, Human | 11 | 0.48 | Binding ≤ 10μM |
ESR1_HUMAN | P03372 | Estrogen Receptor Alpha, Human | 4280 | 0.33 | Binding ≤ 10μM |
ESR2_HUMAN | Q92731 | Estrogen Receptor Beta, Human | 25 | 0.46 | Binding ≤ 10μM |
ESR1_HUMAN | P03372 | Estrogen Receptor Alpha, Human | 622 | 0.38 | Functional ≤ 10μM |
ESR2_HUMAN | Q92731 | Estrogen Receptor Beta, Human | 3.8 | 0.51 | Functional ≤ 10μM |
Description | Species |
---|---|
Nuclear Receptor transcription pathway | |
Nuclear signaling by ERBB4 |