In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
September 26th, 2005 | 26 | Yes |
Popular Name: 4-[4-(4-Fluorophenyl)-2-[4-(methylthio)phenyl]-1H-imidazol-5-yl]pyridine 4-[4-(4-Fluorophenyl)-2-[4-(meth…
Find On: PubMed — Wikipedia — Google
CAS Number: 152121-44-3
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) | 4.70 | 11.23 | -8.24 | 1 | 3 | 0 | 42 | 361.445 | 4 | ↓ |
Lo Low (pH 4.5-6) | 4.70 | 11.67 | -35.88 | 2 | 3 | 1 | 43 | 362.453 | 4 | ↓ |
Lo Low (pH 4.5-6) | 4.70 | 11.66 | -35.83 | 2 | 3 | 1 | 43 | 362.453 | 4 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
GLR-2-E | Glucagon Receptor (cluster #2 Of 2), Eukaryotic | Eukaryotes | 490 | 0.34 | Binding ≤ 10μM |
LOX5-1-E | Arachidonate 5-lipoxygenase (cluster #1 Of 6), Eukaryotic | Eukaryotes | 2700 | 0.30 | Binding ≤ 10μM |
MK11-1-E | MAP Kinase P38 Beta (cluster #1 Of 1), Eukaryotic | Eukaryotes | 120 | 0.37 | Binding ≤ 10μM |
MK12-1-E | MAP Kinase P38 Gamma (cluster #1 Of 2), Eukaryotic | Eukaryotes | 120 | 0.37 | Binding ≤ 10μM |
MK13-1-E | MAP Kinase P38 Delta (cluster #1 Of 1), Eukaryotic | Eukaryotes | 120 | 0.37 | Binding ≤ 10μM |
MK14-1-E | MAP Kinase P38 Alpha (cluster #1 Of 3), Eukaryotic | Eukaryotes | 120 | 0.37 | Binding ≤ 10μM |
LOX5-1-E | Arachidonate 5-lipoxygenase (cluster #1 Of 7), Eukaryotic | Eukaryotes | 580 | 0.34 | Functional ≤ 10μM |
Z100081-1-O | PBMC (Peripheral Blood Mononuclear Cells) (cluster #1 Of 4), Other | Other | 580 | 0.34 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
GLR_HUMAN | P47871 | Glucagon Receptor, Human | 490 | 0.34 | Binding ≤ 1μM |
MK14_HUMAN | Q16539 | MAP Kinase P38 Alpha, Human | 117 | 0.37 | Binding ≤ 1μM |
MK11_HUMAN | Q15759 | MAP Kinase P38 Beta, Human | 120 | 0.37 | Binding ≤ 1μM |
MK13_HUMAN | O15264 | MAP Kinase P38 Delta, Human | 120 | 0.37 | Binding ≤ 1μM |
MK12_HUMAN | P53778 | MAP Kinase P38 Gamma, Human | 120 | 0.37 | Binding ≤ 1μM |
LOX5_RAT | P12527 | Arachidonate 5-lipoxygenase, Rat | 2700 | 0.30 | Binding ≤ 10μM |
GLR_HUMAN | P47871 | Glucagon Receptor, Human | 490 | 0.34 | Binding ≤ 10μM |
MK14_HUMAN | Q16539 | MAP Kinase P38 Alpha, Human | 117 | 0.37 | Binding ≤ 10μM |
MK11_HUMAN | Q15759 | MAP Kinase P38 Beta, Human | 120 | 0.37 | Binding ≤ 10μM |
MK13_HUMAN | O15264 | MAP Kinase P38 Delta, Human | 120 | 0.37 | Binding ≤ 10μM |
MK12_HUMAN | P53778 | MAP Kinase P38 Gamma, Human | 120 | 0.37 | Binding ≤ 10μM |
LOX5_HUMAN | P09917 | Arachidonate 5-lipoxygenase, Human | 580 | 0.34 | Functional ≤ 10μM |
Z100081 | Z100081 | PBMC (Peripheral Blood Mononuclear Cells) | 580 | 0.34 | Functional ≤ 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 | |
G alpha (q) signalling events | |
G alpha (s) signalling events | |
Glucagon signaling in metabolic regulation | |
Glucagon-type ligand receptors | |
KSRP destabilizes mRNA | |
NOD1/2 Signaling Pathway | |
Oxidative Stress Induced Senescence | |
p38MAPK events | |
Platelet sensitization by LDL | |
Synthesis of 5-eicosatetraenoic acids | |
Synthesis of Leukotrienes (LT) and Eoxins (EX) | |
Synthesis of Lipoxins (LX) | |
VEGFA-VEGFR2 Pathway |
No pre-computed analogs available. Try a structural similarity search.