In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
March 5th, 2009 | 14 | Yes |
Popular Name: isoquinoline-5-sulfonamide isoquinoline-5-sulfonamide
Find On: PubMed — Wikipedia — Google
CAS Number: 109547-31-1
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) | 0.70 | -0.04 | -12.54 | 2 | 4 | 0 | 73 | 208.242 | 1 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
MP | 222 - 224 | Enamine Building Blocks |
MP | 222...224 | Enamine Building Blocks |
purity | 9.500000000000000e+001 | Enamine Building Blocks Enamine Building Blocks |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
AKT2-2-E | Serine/threonine-protein Kinase AKT2 (cluster #2 Of 2), Eukaryotic | Eukaryotes | 590 | 0.62 | Binding ≤ 10μM |
KAPCA-2-E | CAMP-dependent Protein Kinase Alpha-catalytic Subunit (cluster #2 Of 4), Eukaryotic | Eukaryotes | 73 | 0.71 | Binding ≤ 10μM |
KAPCB-2-E | CAMP-dependent Protein Kinase Beta-1 Catalytic Subunit (cluster #2 Of 3), Eukaryotic | Eukaryotes | 73 | 0.71 | Binding ≤ 10μM |
KAPCG-1-E | CAMP-dependent Protein Kinase, Gamma Catalytic Subunit (cluster #1 Of 2), Eukaryotic | Eukaryotes | 73 | 0.71 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
KAPCA_HUMAN | P17612 | CAMP-dependent Protein Kinase Alpha-catalytic Subunit, Human | 73 | 0.71 | Binding ≤ 1μM |
KAPCB_HUMAN | P22694 | CAMP-dependent Protein Kinase Beta-1 Catalytic Subunit, Human | 73 | 0.71 | Binding ≤ 1μM |
KAPCG_HUMAN | P22612 | CAMP-dependent Protein Kinase, Gamma Catalytic Subunit, Human | 73 | 0.71 | Binding ≤ 1μM |
AKT2_HUMAN | P31751 | Serine/threonine-protein Kinase AKT2, Human | 590 | 0.62 | Binding ≤ 1μM |
KAPCA_HUMAN | P17612 | CAMP-dependent Protein Kinase Alpha-catalytic Subunit, Human | 73 | 0.71 | Binding ≤ 10μM |
KAPCB_HUMAN | P22694 | CAMP-dependent Protein Kinase Beta-1 Catalytic Subunit, Human | 73 | 0.71 | Binding ≤ 10μM |
KAPCG_HUMAN | P22612 | CAMP-dependent Protein Kinase, Gamma Catalytic Subunit, Human | 73 | 0.71 | Binding ≤ 10μM |
AKT2_HUMAN | P31751 | Serine/threonine-protein Kinase AKT2, Human | 590 | 0.62 | Binding ≤ 10μM |
Description | Species |
---|---|
Activation of BAD and translocation to mitochondria | |
Activation of PKB | |
AKT phosphorylates targets in the cytosol | |
AKT phosphorylates targets in the nucleus | |
AKT-mediated inactivation of FOXO1A | |
CD28 dependent PI3K/Akt signaling | |
Constitutive PI3K/AKT Signaling in Cancer | |
CREB phosphorylation through the activation of Adenylate Cyclase | |
CTLA4 inhibitory signaling | |
DARPP-32 events | |
deactivation of the beta-catenin transactivating complex | |
Downregulation of ERBB2:ERBB3 signaling | |
Factors involved in megakaryocyte development and platelet production | |
G beta:gamma signalling through PI3Kgamma | |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | |
Gluconeogenesis | |
GPVI-mediated activation cascade | |
Hormone-sensitive lipase (HSL)-mediated triacylglycerol hydrolysis | |
Inhibition of TSC complex formation by PKB | |
Interleukin-3, 5 and GM-CSF signaling | |
Loss of Nlp from mitotic centrosomes | |
Loss of proteins required for interphase microtubule organization from the ce | |
Negative regulation of the PI3K/AKT network | |
PDE3B signalling | |
PIP3 activates AKT signaling | |
PKA activation | |
PKA activation in glucagon signalling | |
PKA-mediated phosphorylation of CREB | |
PKA-mediated phosphorylation of key metabolic factors | |
Rap1 signalling | |
Recruitment of mitotic centrosome proteins and complexes | |
Regulation of insulin secretion | |
Regulation of PLK1 Activity at G2/M Transition | |
Translocation of GLUT4 to the plasma membrane | |
Vasopressin regulates renal water homeostasis via Aquaporins | |
VEGFA-VEGFR2 Pathway | |
VEGFR2 mediated vascular permeability |
No pre-computed analogs available. Try a structural similarity search.