In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 21st, 2008 | 37 | No |
Popular Name: methylBLAHdione methylBLAHdione
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) | 3.46 | 10.69 | -60.01 | 2 | 8 | 1 | 83 | 499.591 | 0 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
GSK3B-1-E | Glycogen Synthase Kinase-3 Beta (cluster #1 Of 7), Eukaryotic | Eukaryotes | 71 | 0.27 | Binding ≤ 10μM |
KPCA-1-E | Protein Kinase C Alpha (cluster #1 Of 6), Eukaryotic | Eukaryotes | 300 | 0.25 | Binding ≤ 10μM |
KPCB-1-E | Protein Kinase C Beta (cluster #1 Of 4), Eukaryotic | Eukaryotes | 47 | 0.28 | Binding ≤ 10μM |
KPCE-1-E | Protein Kinase C Epsilon (cluster #1 Of 5), Eukaryotic | Eukaryotes | 250 | 0.25 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
GSK3B_HUMAN | P49841 | Glycogen Synthase Kinase-3 Beta, Human | 71 | 0.27 | Binding ≤ 1μM |
KPCA_HUMAN | P17252 | Protein Kinase C Alpha, Human | 300 | 0.25 | Binding ≤ 1μM |
KPCB_HUMAN | P05771 | Protein Kinase C Beta, Human | 41 | 0.28 | Binding ≤ 1μM |
KPCE_HUMAN | Q02156 | Protein Kinase C Epsilon, Human | 250 | 0.25 | Binding ≤ 1μM |
GSK3B_HUMAN | P49841 | Glycogen Synthase Kinase-3 Beta, Human | 71 | 0.27 | Binding ≤ 10μM |
KPCA_HUMAN | P17252 | Protein Kinase C Alpha, Human | 300 | 0.25 | Binding ≤ 10μM |
KPCB_HUMAN | P05771 | Protein Kinase C Beta, Human | 41 | 0.28 | Binding ≤ 10μM |
KPCE_HUMAN | Q02156 | Protein Kinase C Epsilon, Human | 250 | 0.25 | Binding ≤ 10μM |
Description | Species |
---|---|
Acetylcholine regulates insulin secretion | |
Activation of NF-kappaB in B cells | |
AKT phosphorylates targets in the cytosol | |
APC truncation mutants have impaired AXIN binding | |
AXIN missense mutants destabilize the destruction complex | |
Beta-catenin phosphorylation cascade | |
Ca2+ pathway | |
Calmodulin induced events | |
Constitutive PI3K/AKT Signaling in Cancer | |
CRMPs in Sema3A signaling | |
DAG and IP3 signaling | |
Degradation of beta-catenin by the destruction complex | |
Depolymerisation of the Nuclear Lamina | |
disassembly of the destruction complex and recruitment of AXIN to the membrane | |
Disinhibition of SNARE formation | |
Effects of PIP2 hydrolysis | |
EGFR Transactivation by Gastrin | |
G alpha (z) signalling events | |
HuR stabilizes mRNA | |
Inactivation, recovery and regulation of the phototransduction cascade | |
misspliced GSK3beta mutants stabilize beta-catenin | |
Regulation of HSF1-mediated heat shock response | |
Regulation of KIT signaling | |
Response to elevated platelet cytosolic Ca2+ | |
Role of phospholipids in phagocytosis | |
S33 mutants of beta-catenin aren't phosphorylated | |
S37 mutants of beta-catenin aren't phosphorylated | |
S45 mutants of beta-catenin aren't phosphorylated | |
Signaling by SCF-KIT | |
Syndecan interactions | |
T41 mutants of beta-catenin aren't phosphorylated | |
Trafficking of GluR2-containing AMPA receptors | |
truncations of AMER1 destabilize the destruction complex | |
VEGFR2 mediated cell proliferation | |
WNT5A-dependent internalization of FZD4 |