| Drug General Information |
| Drug ID |
D09OLH
|
| Former ID |
DNC006596
|
| Drug Name |
(1H-indol-2-yl)(5-methoxy-1H-indol-2-yl)methanone
|
| Drug Type |
Small molecular drug
|
| Indication |
Discovery agent
|
Investigative |
[1]
|
|---|
| Structure |
|
Download
2D MOL
3D MOL
|
| Formula |
C18H14N2O2
|
| Canonical SMILES |
COC1=CC2=C(C=C1)NC(=C2)C(=O)C3=CC4=CC=CC=C4N3
|
| InChI |
1S/C18H14N2O2/c1-22-13-6-7-15-12(8-13)10-17(20-15)18(21)16-9-11-4-2-3-5-14(11)19-16/h2-10,19-20H,1H3
|
| InChIKey |
QTIQVLAVCXXZPS-UHFFFAOYSA-N
|
| PubChem Compound ID |
|
| Target and Pathway |
| Target(s) |
FL cytokine receptor |
Target Info |
Inhibitor |
[1]
|
|---|
| Beta platelet-derived growth factor receptor |
Target Info |
Inhibitor |
[1]
|
| Alpha platelet-derived growth factor receptor |
Target Info |
Inhibitor |
[1]
|
|
KEGG Pathway
|
Cytokine-cytokine receptor interaction
|
|
Hematopoietic cell lineage
|
|
Pathways in cancer
|
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Transcriptional misregulation in cancer
|
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Acute myeloid leukemia
|
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Central carbon metabolism in cancerhsa04010:MAPK signaling pathway
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Ras signaling pathway
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Rap1 signaling pathway
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Calcium signaling pathway
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PI3K-Akt signaling pathway
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Focal adhesion
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Gap junction
|
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Regulation of actin cytoskeleton
|
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HTLV-I infection
|
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MicroRNAs in cancer
|
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Glioma
|
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Prostate cancer
|
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Melanoma
|
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Central carbon metabolism in cancer
|
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Choline metabolism in cancerhsa04010:MAPK signaling pathway
|
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Endocytosis
|
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Choline metabolism in cancer
|
|
NetPath Pathway
|
TGF_beta_Receptor Signaling Pathway
|
|
PANTHER Pathway
|
Angiogenesis
|
|
PDGF signaling pathwayP00005:Angiogenesis
|
|
PDGF signaling pathway
|
|
Pathway Interaction Database
|
Signaling events mediated by PTP1B
|
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Beta3 integrin cell surface interactions
|
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S1P3 pathway
|
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Nectin adhesion pathway
|
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Signaling events mediated by TCPTP
|
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SHP2 signaling
|
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S1P1 pathway
|
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Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling
|
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PDGFR-beta signaling pathway
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Validated targets of C-MYC transcriptional repression
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PDGF receptor signaling networkatf2_pathway:ATF-2 transcription factor network
|
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PDGFR-alpha signaling pathway
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PDGF receptor signaling network
|
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Reactome
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PIP3 activates AKT signaling
|
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Constitutive Signaling by Aberrant PI3K in Cancer
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RAF/MAP kinase cascadeR-HSA-1257604:PIP3 activates AKT signaling
|
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RAF/MAP kinase cascade
|
|
WikiPathways
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Regulation of Actin Cytoskeleton
|
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MAPK Signaling Pathway
|
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Osteoblast Signaling
|
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Focal Adhesion
|
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PIP3 activates AKT signaling
|
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PDGF Pathway
|
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Signaling Pathways in Glioblastoma
|
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Signaling by PDGFWP51:Regulation of Actin Cytoskeleton
|
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Hair Follicle Development: Organogenesis (Part 2 of 3)
|
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Cardiac Progenitor Differentiation
|
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Integrated Pancreatic Cancer Pathway
|
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Allograft Rejection
|
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Signaling by PDGF
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|
Angiogenesis
|
| References |
| REF 1 | J Med Chem. 2006 Jun 1;49(11):3101-15.Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase. |
|---|
