In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 23rd, 2008 | 27 | Yes |
Popular Name: 3-[4-(4-aminothieno[5,4-d]pyrimidin-5-yl)phenyl]-1-(m-tolyl)urea 3-[4-(4-aminothieno[5,4-d]pyrimi…
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) | 4.26 | 8.45 | -13.29 | 4 | 6 | 0 | 93 | 375.457 | 3 | ↓ |
Lo Low (pH 4.5-6) | 4.26 | 8.74 | -33.8 | 5 | 6 | 1 | 94 | 376.465 | 3 | ↓ |
Lo Low (pH 4.5-6) | 4.26 | 5.29 | -30.5 | 5 | 6 | 1 | 94 | 376.465 | 3 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CSF1R-1-E | Macrophage Colony-stimulating Factor 1 Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 3 | 0.44 | Binding ≤ 10μM |
FGFR1-1-E | Fibroblast Growth Factor Receptor 1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 4200 | 0.28 | Binding ≤ 10μM |
FGFR2-1-E | Fibroblast Growth Factor Receptor 2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 4200 | 0.28 | Binding ≤ 10μM |
FGFR3-1-E | Fibroblast Growth Factor Receptor 3 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 4200 | 0.28 | Binding ≤ 10μM |
FGFR4-1-E | Fibroblast Growth Factor Receptor 4 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 4200 | 0.28 | Binding ≤ 10μM |
FLT3-1-E | Tyrosine-protein Kinase Receptor FLT3 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 2 | 0.45 | Binding ≤ 10μM |
KIT-1-E | Stem Cell Growth Factor Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 6 | 0.43 | Binding ≤ 10μM |
TIE2-1-E | Tyrosine-protein Kinase TIE-2 (cluster #1 Of 2), Eukaryotic | Eukaryotes | 730 | 0.32 | Binding ≤ 10μM |
VGFR1-1-E | Vascular Endothelial Growth Factor Receptor 1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 2 | 0.45 | Binding ≤ 10μM |
VGFR2-1-E | Vascular Endothelial Growth Factor Receptor 2 (cluster #1 Of 2), Eukaryotic | Eukaryotes | 3 | 0.44 | Binding ≤ 10μM |
VGFR3-1-E | Vascular Endothelial Growth Factor Receptor 3 (cluster #1 Of 2), Eukaryotic | Eukaryotes | 13 | 0.41 | Binding ≤ 10μM |
PGFRA-1-E | Platelet-derived Growth Factor Receptor Alpha (cluster #1 Of 1), Eukaryotic | Eukaryotes | 48 | 0.38 | Functional ≤ 10μM |
PGFRB-1-E | Platelet-derived Growth Factor Receptor Beta (cluster #1 Of 1), Eukaryotic | Eukaryotes | 48 | 0.38 | Functional ≤ 10μM |
VGFR2-1-E | Vascular Endothelial Growth Factor Receptor 2 (cluster #1 Of 2), Eukaryotic | Eukaryotes | 1 | 0.47 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CSF1R_HUMAN | P07333 | Macrophage Colony Stimulating Factor Receptor, Human | 3 | 0.44 | Binding ≤ 1μM |
KIT_HUMAN | P10721 | Stem Cell Growth Factor Receptor, Human | 6 | 0.43 | Binding ≤ 1μM |
FLT3_HUMAN | P36888 | Tyrosine-protein Kinase Receptor FLT3, Human | 2 | 0.45 | Binding ≤ 1μM |
TIE2_HUMAN | Q02763 | Tyrosine-protein Kinase TIE-2, Human | 720 | 0.32 | Binding ≤ 1μM |
VGFR1_HUMAN | P17948 | Vascular Endothelial Growth Factor Receptor 1, Human | 2 | 0.45 | Binding ≤ 1μM |
VGFR2_HUMAN | P35968 | Vascular Endothelial Growth Factor Receptor 2, Human | 3 | 0.44 | Binding ≤ 1μM |
VGFR3_HUMAN | P35916 | Vascular Endothelial Growth Factor Receptor 3, Human | 13 | 0.41 | Binding ≤ 1μM |
FGFR1_HUMAN | P11362 | Fibroblast Growth Factor Receptor 1, Human | 4200 | 0.28 | Binding ≤ 10μM |
FGFR2_HUMAN | P21802 | Fibroblast Growth Factor Receptor 2, Human | 4200 | 0.28 | Binding ≤ 10μM |
FGFR3_HUMAN | P22607 | Fibroblast Growth Factor Receptor 3, Human | 4200 | 0.28 | Binding ≤ 10μM |
FGFR4_HUMAN | P22455 | Fibroblast Growth Factor Receptor 4, Human | 4200 | 0.28 | Binding ≤ 10μM |
CSF1R_HUMAN | P07333 | Macrophage Colony Stimulating Factor Receptor, Human | 3 | 0.44 | Binding ≤ 10μM |
KIT_HUMAN | P10721 | Stem Cell Growth Factor Receptor, Human | 6 | 0.43 | Binding ≤ 10μM |
FLT3_HUMAN | P36888 | Tyrosine-protein Kinase Receptor FLT3, Human | 2 | 0.45 | Binding ≤ 10μM |
TIE2_HUMAN | Q02763 | Tyrosine-protein Kinase TIE-2, Human | 720 | 0.32 | Binding ≤ 10μM |
VGFR1_HUMAN | P17948 | Vascular Endothelial Growth Factor Receptor 1, Human | 2 | 0.45 | Binding ≤ 10μM |
VGFR2_HUMAN | P35968 | Vascular Endothelial Growth Factor Receptor 2, Human | 3 | 0.44 | Binding ≤ 10μM |
VGFR3_HUMAN | P35916 | Vascular Endothelial Growth Factor Receptor 3, Human | 13 | 0.41 | Binding ≤ 10μM |
PGFRA_HUMAN | P16234 | Platelet-derived Growth Factor Receptor Alpha, Human | 48 | 0.38 | Functional ≤ 10μM |
PGFRB_HUMAN | P09619 | Platelet-derived Growth Factor Receptor Beta, Human | 48 | 0.38 | Functional ≤ 10μM |
VGFR2_HUMAN | P35968 | Vascular Endothelial Growth Factor Receptor 2, Human | 1 | 0.47 | Functional ≤ 10μM |
Description | Species |
---|---|
Activated point mutants of FGFR2 | |
betaKlotho-mediated ligand binding | |
Constitutive PI3K/AKT Signaling in Cancer | |
Downstream signal transduction | |
EPHA-mediated growth cone collapse | |
FGFR4 ligand binding and activation | |
FRS2-mediated cascade | |
Integrin cell surface interactions | |
Negative regulation of FGFR signaling | |
Neurophilin interactions with VEGF and VEGFR | |
Phospholipase C-mediated cascade | |
PI-3K cascade | |
PI3K Cascade | |
PIP3 activates AKT signaling | |
Regulation of KIT signaling | |
SHC-mediated cascade | |
Signaling by activated point mutants of FGFR1 | |
Signaling by activated point mutants of FGFR3 | |
Signaling by FGFR mutants | |
Signaling by FGFR2 amplification mutants | |
Signaling by FGFR3 mutants | |
Signaling by FGFR4 mutants | |
Signaling by PDGF | |
Signaling by SCF-KIT | |
t(4;14) translocations of FGFR3 | |
Tie2 Signaling | |
VEGF binds to VEGFR leading to receptor dimerization | |
VEGFA-VEGFR2 Pathway | |
VEGFR2 mediated cell proliferation |
No pre-computed analogs available. Try a structural similarity search.