Drug Information
Drug General Information | Top | |||
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Drug ID |
D03ETN
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Drug Name |
PMID27828716-Compound-18
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Drug Type |
Small molecular drug
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Structure |
Download2D MOL |
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Formula |
C16H16ClN5
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Canonical SMILES |
CC1=CC(=NN1)NC2=NC(=NC(=C2C)C)C3=CC=CC=C3Cl
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InChI |
1S/C16H16ClN5/c1-9-8-14(22-21-9)19-15-10(2)11(3)18-16(20-15)12-6-4-5-7-13(12)17/h4-8H,1-3H3,(H2,18,19,20,21,22)
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InChIKey |
ONBXAMQNBSFIQS-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Glycogen synthase kinase-3 alpha (GSK-3A) | Target Info | Inhibitor | [1] |
Target's Patent Info | Glycogen synthase kinase-3 alpha (GSK-3A) | Target's Patent Info | [1] | |
NetPath Pathway | TGF_beta_Receptor Signaling Pathway | |||
Panther Pathway | Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | |||
Insulin/IGF pathway-protein kinase B signaling cascade | ||||
PDGF signaling pathway | ||||
Ras Pathway | ||||
Pathway Interaction Database | Degradation of beta catenin | |||
Canonical Wnt signaling pathway | ||||
FOXM1 transcription factor network | ||||
Class I PI3K signaling events mediated by Akt | ||||
Reactome | AKT phosphorylates targets in the cytosol | |||
XBP1(S) activates chaperone genes | ||||
Constitutive Signaling by AKT1 E17K in Cancer |
References | Top | |||
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REF 1 | Glycogen synthase kinase 3 (GSK-3) inhibitors: a patent update (2014-2015).Expert Opin Ther Pat. 2017 Jun;27(6):657-666. |
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