Drug Information
Drug General Information | Top | |||
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Drug ID |
D02OGA
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Drug Name |
Thiadiazolidindione derivative 2
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Synonyms |
PMID27828716-Compound-5
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Drug Type |
Small molecular drug
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Structure |
Download2D MOL |
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Formula |
C14H16N2O3S
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Canonical SMILES |
C1CC(OC1)CN2C(=O)N(SC2=O)CC3=CC=CC=C3
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InChI |
1S/C14H16N2O3S/c17-13-15(10-12-7-4-8-19-12)14(18)20-16(13)9-11-5-2-1-3-6-11/h1-3,5-6,12H,4,7-10H2
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InChIKey |
AGFKNYDGTJNEDN-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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