In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 21st, 2011 | 32 | No |
Popular Name: (3Z)-5-fluoro-3-[[3-methyl-4-(2-morpholinoethoxy)azulen-1-yl]methylene]indolin-2-one (3Z)-5-fluoro-3-[[3-methyl-4-(2-…
None
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) | 3.72 | 9.26 | -18.53 | 1 | 5 | 0 | 55 | 432.495 | 5 | ↓ |
Mid Mid (pH 6-8) | 3.72 | 11.61 | -53.64 | 2 | 5 | 1 | 56 | 433.503 | 5 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
FLT3-1-E | Tyrosine-protein Kinase Receptor FLT3 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 19 | 0.34 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
FLT3_HUMAN | P36888 | Tyrosine-protein Kinase Receptor FLT3, Human | 19 | 0.34 | Binding ≤ 1μM |
FLT3_HUMAN | P36888 | Tyrosine-protein Kinase Receptor FLT3, Human | 19 | 0.34 | Binding ≤ 10μM |
No pre-computed analogs available. Try a structural similarity search.