In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 21st, 2008 | 38 | Yes |
Popular Name: 1-(5-tert-butyl-2-phenyl-pyrazol-3-yl)-3-[4-(2-morpholinoethoxy)-1-naphthyl]urea 1-(5-tert-butyl-2-phenyl-pyrazol…
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) | 5.98 | 11.78 | -17.61 | 2 | 8 | 0 | 81 | 513.642 | 8 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MK14-1-E | MAP Kinase P38 Alpha (cluster #1 Of 3), Eukaryotic | Eukaryotes | 5 | 0.31 | Binding ≤ 10μM |
TNFA-1-E | TNF-alpha (cluster #1 Of 1), Eukaryotic | Eukaryotes | 9 | 0.30 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MK14_HUMAN | Q16539 | MAP Kinase P38 Alpha, Human | 0.1 | 0.37 | Binding ≤ 1μM |
MK14_MOUSE | P47811 | MAP Kinase P38 Alpha, Mouse | 0.23 | 0.36 | Binding ≤ 1μM |
TNFA_HUMAN | P01375 | TNF-alpha, Human | 9 | 0.30 | Binding ≤ 1μM |
MK14_HUMAN | Q16539 | MAP Kinase P38 Alpha, Human | 0.1 | 0.37 | Binding ≤ 10μM |
MK14_MOUSE | P47811 | MAP Kinase P38 Alpha, Mouse | 0.23 | 0.36 | Binding ≤ 10μM |
TNFA_HUMAN | P01375 | TNF-alpha, Human | 3400 | 0.20 | Binding ≤ 10μM |
Description | Species |
---|---|
activated TAK1 mediates p38 MAPK activation | |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation | |
Activation of the AP-1 family of transcription factors | |
ADP signalling through P2Y purinoceptor 1 | |
CDO in myogenesis | |
DSCAM interactions | |
ERK/MAPK targets | |
KSRP destabilizes mRNA | |
NOD1/2 Signaling Pathway | |
Oxidative Stress Induced Senescence | |
p38MAPK events | |
Platelet sensitization by LDL | |
TNF signaling | |
Transcriptional regulation of white adipocyte differentiation | |
VEGFA-VEGFR2 Pathway |