In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
August 19th, 2004 | 23 | Yes |
Popular Name: 3-(4-methoxyphenyl)-2-(6-methyl-2-pyridyl)-5,6-dihydro-4H-pyrrolo[2,1-e]pyrazole 3-(4-methoxyphenyl)-2-(6-methyl-…
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) | 3.30 | 0.72 | -12.25 | 0 | 4 | 0 | 39 | 305.381 | 3 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MK14-1-E | MAP Kinase P38 Alpha (cluster #1 Of 3), Eukaryotic | Eukaryotes | 4600 | 0.32 | Binding ≤ 10μM |
THB-1-E | Thyroid Hormone Receptor Beta-1 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 121 | 0.42 | Binding ≤ 10μM |
Z80951-1-O | NIH3T3 (Fibroblasts) (cluster #1 Of 4), Other | Other | 397 | 0.39 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
THB_HUMAN | P10828 | Thyroid Hormone Receptor Beta-1, Human | 121 | 0.42 | Binding ≤ 1μM |
MK14_HUMAN | Q16539 | MAP Kinase P38 Alpha, Human | 4600 | 0.32 | Binding ≤ 10μM |
THB_HUMAN | P10828 | Thyroid Hormone Receptor Beta-1, Human | 121 | 0.42 | Binding ≤ 10μM |
Z80951 | Z80951 | NIH3T3 (Fibroblasts) | 397 | 0.39 | 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 | |
KSRP destabilizes mRNA | |
NOD1/2 Signaling Pathway | |
Nuclear Receptor transcription pathway | |
Oxidative Stress Induced Senescence | |
p38MAPK events | |
Platelet sensitization by LDL | |
VEGFA-VEGFR2 Pathway |